Thomas Liehr (2019)
web-presence: https://cs-tl.de/Start.html
Created by Dr. Thomas Liehr (PhD),
affiliation: Institute of Human Genetics, 07740 Jena, Germany;
e-mail: Thomas.Liehr@med.uni-jena.de or LiehrT@web.de
| at
home university |
at
courses (self organized) |
at
courses (invited) |
| invited
lectures |
online
courses/ videos |
other lectures (at congress) |
Teaching for students of medicine, dentists, master molecular medicine and others since 1998 (present offers available here).
Also involved in supervision of students before at Inst. of Human Genetics in Erlangen.
|
1995 -1996 |
Supervision of the student course at the Institute of Human Genetics in Erlangen |
|
since 1998 |
Participation
in the following courses at the
Institute of Human Genetics in Jena: |
|
2004
to 2015 |
Lecture
series genetics (with other
lecturers from human genetics and
genetics) |
|
since 2006 |
Human genetic seminar for doctors (with other lecturers from human genetics) |
|
2008
to 2018 |
Biology
for medical students (lecture) |
|
since 2009 |
Human
Genetics’ for Master Molecular Medicine
(lecture) |
|
since 2012 |
Biology for medical students (seminar) |
2007 to 2017 scientific coach as part of the OPSIS program for the support of foreign students.
Practical and/or administrative supervison of graduation works
| # | name of
student |
graduation
to |
topic |
time |
| 90 |
Nogueira Correia Maria Inês |
Master
Genetic Clinical Laboratorial
(Coimbra, Portugal)
|
Characterization of centromere
near sequences of chromosome 15 |
2023-2024 |
| 89 | Nurul Aida Binti Ariffen | Bachelor (Biology) | Characterization of centromeric
sequences in FFPE sections |
2022-2023 |
| 88 | Joana Seixas |
Master Genetic Clinical
Laboratorial (Coimbra, Portugal) |
Insights into molecular
cytogenetic routine diagnostics and
characterization of repeatedly showing up
contritutive chromsomal inversions |
2022-2023 |
| 87 | Khensuwan Sudarat | PhD (Biology at Khon Kaen University, Thailand) | Classical and molecular
cytogenetics of the subfamily Cyprininae in Thailand |
2021-2023 |
| 86 | Mohammed Abdulazeez | Bachelor (Biology) | Characterization of acrocentric
p-arms added to other chromosomes |
2021-2021 |
| 85 | Seria Tsan |
Bachelor (Medicintechniques & Biotechnology) | Cryptic rearrangements in
acrocentric chromosomes of infertile pairs |
2020-2020 |
| 84 | Viktoria Musienko |
MD | Functional relevance of
non-homologous chromosomal contacts (NHCCs) |
2019–2022 |
| 83 | Fritz Kramer |
Bachelor (Biochemistry) | Molecular cytogenetic characterization of the murine cell line TSC2_ang1 | 2018–2019 |
| 82 | Ralf Steinacker |
Dentistry | On murine tumor cell lines | 2017– |
| 81 | Sandra Schöner |
MD | Fragile sites |
2017- |
| 80 |
Emanuele G. Coci |
MD | Neuro-developmental syndrome at
the border between CANPMR syndrome and chromosome
1p32-p31 deletion syndrome |
2017–2018 |
| 79 | Lioba Hergenhahn |
MD | Cytogenetic characterization
murine tumor cell lines |
2016– |
| 78 | Hans Rhode |
MD | Cytogenetic characterization
and in silico translation of two murine intestinal
tumor cell lines |
2016–2018 |
| 77 | Eva Wahlbuhl |
MD | Characterization of karyotypes of murine tumor cell lines | 2015–2021 |
| 76 | Shaymaa S.H. Azawi |
PhD (biology) |
Murine solid tumors compared to human ones | 2015– |
| 75 | Sharon Löhmer |
Master Biology from Kassel |
Gen and genome evolution through fragile sites mediated copy number mutability - with special attention to fragile sites on chromosome 1 | 2015–2016 |
| 74 | Lisa-Marie Barf |
Bachelor (biochemistry) | Cytogenetic characterization of
two solid murine tumor cell line |
2015–2016 |
| 73 |
Romy Rietschel |
Bachelor (biochemistry) | Is there an influence of sSMCs of acrocentric chromosomes 21 and 22 on the activity of the nucleolus organizer region? | 2015–2015 |
| 72 | Katja Piaszinski |
Master Molecular Medicine | Molecular cytogenetic characterization of murine cell lines from solid hepatocarcinoma and melanoma tumors | 2014–2018 |
| 71 |
Julia Lichtenwald |
Master Molecular Lifescience | Characterization of the interphase core architecture taking into account cis and long range trans chromatin interactions using the example of autosomal dominant hypertension with brachydactyly type E | 2014–2016 |
| 70 |
Katharina Rittscher |
Master Molecular Lifescience | Characterization of MLL rearrangements in acute myeloid leukemia in cases with normal and complex karyotype | 2014–2016 |
| 69 |
Felix Eilenberger |
Master Molecular Lifescience |
Small supernumerary marker chromosomes and their influence on nucleolus-organizing regions | 2014–2015 |
| 68 |
Ayham Alhaj Darouich |
MD | Alpha fetoprotein and ultrasound in the prenatal diagnosis | 2013–2015 |
| 67 |
Franziska Mallek |
Bachelor (biology) | Interphase fluorescence in situ hybridization studies on liver tissue sections from Mus musculus. | 2013–2014 |
| 66 |
Katja Piaszinski |
Bachelor (biology) | Studies on the metaphase and interphase architecture using parental karyotyping and parental origin determination fluorescence in situ hybridization | 2013–2013 |
| 65 |
Hannes Spittel |
Bachelor (biotechnology) | Stability of marker chromosomes (sSMC) in human cell lines | 2013–2013 |
| 64 |
Eyad Alhourani |
PhD (biology) |
Cryptic chromosomal rearrangements in chronic lymphocytic leukemia | 2012-2016 |
| 63 |
Nadine Aust |
Diploma (biology) | Analysis of cryptic chromosomal
aberrations in colorectal liver metastases |
2012–2013 |
| 62 |
Gopakumar Radhakrishnan |
Bachelor (biotechnology) from Chennai, India |
Molecular characterization of sSMC | 2012–2013 |
| 61 |
Claudia Venner |
Bachelor (biotechnology) | Establishment of an immunohistochemical method to characterize functional telomeres on ring chromosomes | 2012–2013 |
| 60 |
Carolin Schindler |
Bachelor (biotechnology) | Detection of micro rearrangements as a molecular cause of autosomal dominant hypertension with brachydactyly | 2012–2012 |
| 59 |
Maria Bucksch |
Bachelor (biotechnology) | Establishment of a cytogenetic probe set for the detection of aberrant metaphases | 2012–2012 |
| 58 |
Annemarie Klein |
Bachelor (biology) | Characterization of aberrant chromosomes using high-resolution FISH techniques | 2011–2012 |
| 57 |
Sharon Löhmer |
Bachelor (biology) | Characterization of evolutionarily conserved chromosome breakpoints in Hylobates lar | 2011–2012 |
| 56 |
Anja Werther |
Bachelor (biology) | Subtelomer screening using multiplex ligation-dependent probe amplification (MLPA) in mentally retarded patients | 2011–2011 |
| 55 |
Luise Theuss |
MD | Fanconi anemia as a model
system for mapping rare fragile sites on
chromosome 1 |
2010–2017 |
| 54 |
Moneeb Abdullah Kassem Othman |
PhD (biology) |
Cryptic chromosomal rearrangements in acute leukemia | 2010–2016 |
| 53 |
Martin Voigt |
Master Molecular Medicine |
Delineation of chromosomal
breakpoints in clinical and basic reserach by
microarray based comparative genomic
hybridization. |
2010–2011 |
| 52 |
Franziska Dorka |
Diploma (biology) |
Studies on the colocalization
of the transcription partners bcr and abl in
three-dimensionally obtained interphase nuclei in
patients with chronic myeloid leukemia. |
2010–2011 |
| 51 |
Julia Gebhart |
Diploma (nutritional sciences) | Evidence of cryptic aberrations in band cytogenetically normal acute lymphoblastic leukaemias | 2010–2011 |
| 50 |
Xiaobo Fan |
PhD (biology) |
Karyotype evolution in monkeys
compared to human Note: parts of this work was awarded posterpreis auf der 20th ICACGM |
2009-2016 |
| 49 |
Ahmed B. Hamid |
PhD (biology) |
Small supernumerary marker chromosomes (sSMC) - why and where do they break, and how can one differentiate between harmful and harmless sSMC? | 2009–2015 |
| 48 |
Christine Leibiger |
Diploma (nutritional sciences) |
Characterization of murine cell
lines using high-resolution multicolor banding |
2009–2010 |
| 47 |
Joscha Schröder |
Diploma (biology) |
Molecular characterization of
breakpoints of the chromosomal bands 3p25, 9q21
and 11q23 in selected clinical cases. |
2009–2010 |
| 46 |
Susann Junker |
Diploma (biology) | Colocalization of chromosomal
translocation partners in interphase nuclei of
patients with acute myeloid leukemia |
2009–2010 |
| 45 |
Kathleen Wilhelm |
MD | Fanconi anemia as a model
system for mapping rare fragile sites |
2008–2014 |
| 44 |
Elisabeth Klein |
PhD (biology) |
Mechanisms of gene regulation in imbalances close to the centrometer | 2008–2013 |
| 43 |
Jennifer Römer |
MD |
Fine structure analysis for bcr-abl rearrangements in chronic myeloid leukemia | 2008–2012 |
| 42 |
Pornarong Siripiyasing |
PhD (biology) from Khon Kaen, Thailand |
Molecular analysis for species identification of the gebus Cymbidium (Orchidaceae) in Thailand | 2008–2012 |
| 41 |
Philipp Kempf |
MD |
Evidence of cryptic aberrations in AML with trisomy 8 | 2008–2011 |
| 40 |
Annett Johne |
MD | M-FISH studies in patients with
ataxia telangiektasia |
2008–2010 |
| 39 |
Cornelius Wölfel |
Diploma (biology) | Interphase characterization of
chromosomal breakpoints |
2008–2010 |
| 38 |
Nancy Blaurock |
Diploma (biology) | Characterization of 'fragile
sites' in Fanconi anemia |
2008–2010 |
| 37 |
Rebecca Wagner |
Diploma (biology) | Centromere-near
probe sets |
2008–2010 |
| 36 |
Jörn Erlecke |
Dentistry | Automated detection of
recipient cells after countersex Konchemark or
blood stem cell transplantation with the help of
FISH |
2008–2009 |
| 35 |
Franziska Rietz |
Diploma (biology) | Studies on histion code |
2008–2009 |
| 34 |
Daniela Reich |
Diploma (biology) | Molecular biological
characterization of small supernumerary
marker chromosomes. |
2008–2009 |
| 33 |
Amelie Lier |
Diploma (biology) | Micro-CGH on AML cases with
trisomy 8 |
2008–2009 |
| 32 |
Christiane Schoder |
MD |
Breakpoints in Fanconi anemia - are they molecularly identical to 'fragile sites'? | 2007–2009 |
| 31 |
Anne-Christin Teichmann |
Diploma (environmental
engineering) from Mitweida |
Molecular cytogenetic correlation of fragile sites and neoplasia-associated breakpoints | 2007–2009 |
| 30 |
Vivian Klaschka |
Diploma (biology) | Detection of cryptic
centromere-near rearrangements in the human genome |
2007–2009 |
| 29 |
Nadine Rüdiger |
Magister (biology) | Clinical consequences of centromere-near gene dosage gains | 2007–2008 |
| 28 |
Elisabeth Ewers |
Magister (biology) | Epigenetic variations in the centromeric region of small supernumerary marker chromosomes | 2007–2008 |
| 27 |
Maria Joana Lima Barbosa de Melo |
PhD (biology) from Coimbra, Portugal |
Cytogenetic and molecular studies on small supernumerary marker chromosomes | 2006–2011 |
| 26 |
Lisbeth Backx |
PhD (biology) from Leuven, Belgium |
Implementation of arraypainting for the identification of candidate genes for (non-)syndromic intellectual disability. | 2006–2010 |
| 25 |
Katja Behr |
MD | Characterization of leukemia-associated breakpoints and their molecular genetic location with regard to 'fragile sites' | 2006–2009 |
| 24 |
Madeleine Groß |
PhD (biology) |
Evidence of cryptic chromosomal rearrangements in acute myeloid leukemia | 2006–2008 |
| 23 |
Samarth Bhatt |
PhD (biology) |
Studies on meiotic segregation
of inversions in male carriers of an inversion Cotutuelle international de these with the University of Montpellier |
2006–2008 |
| 22 |
Vera Witthuhn |
Diploma (biochemistry) | Evidence for epigenetic change
in acute myeloid leukemia with trisomy 8 |
2006–2008 |
| 21 |
Sophie Hinreiner |
Diploma (human biology) from Marburg |
Establishment of single cell-specific evidence of epigenetic changes in the human genome | 2006–2007 |
| 20 |
Britta Franze |
Diploma (biology) | Characterization of "Common
Fragile Sites" (# 1, # 13, # 16) and comparison
with neoplasia-associated and evolutionarily
conserved breakpoints |
2006–2007 |
| 19 |
Constanze Karst |
PhD (biology) |
Identification and characterization of hitherto unknown, possibly prognostic, cryptic chromosomal aberrations in ALL using molecular cytogenetic methods. | 2005–2012 |
| 18 |
Frederike Hunstig |
MD | The location of the sex chromosomes in different tissues of humans | 2005–2010 |
| 17 |
Kristin Mrasek |
PhD (biology) |
Identification and characterization of 'fragile sites' and their relationship to tumor- and evolution-associated chromosomal breakpoints | 2004–2009 |
| 16 |
Klara Müller |
Diploma (biology) | Characterization of small
supernumerary marker chromosomes using modern
molecular and molecular-cytogenetic methods |
2004–2007 |
| 15 |
Ina Fickelscher |
Diploma (biology) | Characterization of the
breakpoints of human norm variant inversions -
inv(2)(p11.2q13) and inv(9)(p11q13) |
2004–2006 |
| 14 |
Franziska Reichelt |
Diploma (biology) | Characterization of putatively
evolutionarily relevant genome regions of the
genus Pongo and comparison of evolutionary
breakpoints with “Common Fragile Sites” |
2004–2006 |
| 13 |
Melanie Glaser |
Diploma (biology) | Cryptic chromosomal
rearrangements and imbalances in acute myeloid
leukemia |
2003–2004 |
| 12 |
Sabine Schmidt |
Diploma (biology) | Molecular characterization of
the chromosomal breakpoint regions 2p11.2 ~ 12,
2q12 ~ 13, 9p11 and 9q13 involved in the norm
variants of humans |
2003–2004 |
| 11 |
Madeleine Groß |
Diploma (biology) | Identification and
characterization of putatively evolutionarily
relevant genome areas in the genus Pan |
2003–2004 |
| 10 |
Ulf Steinhäuser |
MD | Fluorescence in situ
hybridization on three-dimensional interphase
nuclei |
2002–2007 |
| 9 |
Heike Nelle |
MD | Characterization of the
chromosomal band splitting on human chromosomes 5,
6, 18, 19, 20 and X |
2002–2005 |
| 8 |
Constanze Karst |
Diploma (biology) | Detection of cryptic
chromosomal aberrations in myeloid leukemia |
2002-2003 |
| 7 |
Anja Weise |
PhD (biology) |
Identification and
characterization of putatively evolutionarily
relevant genomic regions of the Hominidae |
2001–2004 |
| 6 |
Axel Göhlert |
MD | Multiphoton multicolor
fluorescence in situ hybridization |
2000–2002 |
| 5 |
Angela Nietzel |
MD | cenM-FISH, a newly developed method for the characterization of small supernumerary marker chromosomes | 2000–2002 |
| 4 |
Kristin Mrasek |
Diploma (biology) | Comparative molecular
cytogenetic studies of the karyotypes of Homo
sapiens, Gorilla gorilla and Hylobates lar using
"multicolor banding" (MCB) Note: this work was awarded the poster prize of the ECA conference, Paris 2001 |
2000–2001 |
| 3 |
Anja Weise |
Diploma (biology) | Molecular cytogenetic
analysis of the human chromosome 2 with special
regard to high resolution multi-color banding
(MCB) |
2000–2001 |
| 2 |
Anita Heller |
PhD (biology) |
Genetic characterization of
chromosomal breakpoints Note: this work was awarded the Herbert-Hartmann-Price for PhD-works |
1999-2004 |
| 1 |
Heike Starke |
PhD (biology) |
Centromere-near
chromosomal rearrangements in the human genome |
1999-2004 |
External referee for students and pupils working in Jena lab
| # | name of
student |
graduation
to |
topic |
time |
| 4 |
Padutsch Niklas |
BTA (staatl. berufsbildende Schulzentrum Jena-Göschwitz) |
Advantages of automatization in
a molecular cytogenetic laboratory |
2017-2018 |
| 3 |
Donat Marcus | BTA (staatl. berufsbildende Schulzentrum Jena-Göschwitz) |
Detection of X inactivation on human metaphase chromosomes (lymphocytes) using 5-ethynyl-2'-deoxyuridine (EdU) and fluorescence in situ hybridization (FISH) | 2016-2017 |
| 2 | Shchegolevska Anna ,
Heyer Christian and Bossert
Josi |
Facharbeit (Carl-Zeiss-Gymnasium Jena) |
Molecular cytogenetics and its
diagnostic applications |
2008-2009 |
| 1 | Dreer Julia |
BTA (staatl. berufsbildende Schulzentrum Jena-Göschwitz) |
Localization of specific
sequences in human chromosomes by means of
Bacterial Artificial Chromosome probes and fluorescence in situ hybridization |
2007 |
External referee for guest in Jena lab for CLG education
| # | name of
student |
graduation
to |
topic |
time |
| 1 | Sy Alodi |
Australian CLG |
training via QUT student
agreement in Diagnostic Laboratory or research
Laboratory |
2021-2022 |
| # |
date |
congress |
place |
| 32 |
04.-08.09.2022 | 6 course on Basics in human genetic
diagnostics – a course for CLGs* in education
(*Clinical Laboratory Geneticists -see here) - as co-advisor |
Figueira da Foz, Portugal |
| 31 |
05.-09.09.2022 | 5 course on Basics in human genetic
diagnostics – a course for CLGs* in education
(*Clinical Laboratory Geneticists -see here) - as co-advisor |
Figueira da Foz, Portugal (online lectures) |
| 30 |
09.-13.09.2019 | 4. course on Basics in human genetic
diagnostics – a course for CLGs* in education
(*Clinical Laboratory Geneticists -see here) - as co-advisor |
Figueira da Foz, Portugal |
| 29 |
05.07.2019 | 7. PWG (permanent working group) of
marker chromosomes |
6th European Cytogenetics Conference, Salzburg, Austria |
| 28 |
30.-07.09.2018 | 3. course on Basics in human genetic
diagnostics – a course for CLGs* in education
(*Clinical Laboratory Geneticists -see here) |
Zagreb, Croatia |
| 27 |
25.-29.09.2017 | 2. course on Basics in human genetic
diagnostics – a course for CLGs* in education
(*Clinical Laboratory Geneticists -see here) |
Athens, Greece (supervised from Jena) |
| 26 |
01.07.2017 | 6. PWG (permanent working group) of
marker chromosomes |
11th European Cytogenetics Conference, Firence, Italy |
| 25 |
09.09-10.09.2016 | Human genetic FISH course (pre- and postnatal) - an Abbott Vysis FISH training | Kollegiengasse 10, Jena, Germany |
| 24 |
20.-24.06.2016 | 1. course on Basics in human genetic
diagnostics – a course for CLGs* in education
(*Clinical Laboratory Geneticists -see here) |
Nicosia, Cyprus |
| 23 |
13.11.-14.11.2015 | 6. International course on fluorescence in situ hybridization (FISH + aCHG + microdissection) | Kollegiengasse 10, Jena, Germany |
| 22 |
04.07.2015 | 5. PWG (permanent working group) of
marker chromosomes |
10th European Cytogenetics Conference, Straßburg, France |
| 21 |
22.11.-23.11.2013 | 5. International course on fluorescence in situ hybridization (FISH + aCHG + microdissection) | Kollegiengasse 10, Jena, Germany |
| 20 |
29.06.2013 | 4. PWG (permanent working group) of
marker chromosomes |
9th European Cytogenetics Conference, Dublin, Irland |
| 19 |
19.04.-20.04.2013 | 7. Course "FISH, (a)CGH and
microdissection" |
Kollegiengasse 10, Jena, Germany |
| 18 |
11.05.-12.05.2012 | 4. International course on fluorescence in situ hybridization (FISH + aCHG + microdissection) | Kollegiengasse 10, Jena, Germany |
| 17 |
08.09.-09.09.2011 | 3. International course on fluorescence in situ hybridization (FISH + microdissection) of marker chromosomes | Kollegiengasse 10, Jena, Germany |
| 16 |
02.07.2011 |
3. PWG (permanent working group) of
marker chromosomes |
8th European Cytogenetics Conference, Porto, Portugal |
| 15 |
15.10.-16.10.2010 | 6. Course "FISH and microdissection" (report in
Arab) |
Kollegiengasse 10, Jena, Germany |
| 14 |
08.11.-09.11.2009 | 2. International course on fluorescence in situ hybridization (FISH + microdissection) of marker chromosomes | Kollegiengasse 10, Jena, Germany |
| 13 |
07.11.2009 | 1. international course on small supernumeray marker chromosomes (sSMC) (see here and here) | Kollegiengasse 10, Jena, Germany |
| 12 |
05.11.-06.11.2009 | 1. International course on fluorescence in situ hybridization (FISH + microdissection) of marker chromosomes | Kollegiengasse 10, Jena, Germany |
| 11 |
06.07.2009 |
2. PWG (permanent working group) of
marker chromosomes |
7th European Cytogenetics Conference, Stockholm, Schweden |
| 10 |
08.05.-09.05.2009 | 5. Course "FISH and microdissection" |
Kollegiengasse 10, Jena, Germany |
| 9 |
17.10-18.10.2008 | 1. Course Postnatal Clinical Genetics -
an Abbott Vysis FISH course |
Kollegiengasse 10, Jena, Germany |
| 8 |
20.06-21.06.2008 | 1. Prenatal Clinical Genetics course - an
Abbott Vysis FISH course |
Kollegiengasse 10, Jena, Germany |
| 7 |
07.07.2007 |
1. PWG (permanent working group) of
marker chromosomes |
6th European Cytogenetics Conference, Istanbul,Turkey |
| 6 |
14.06.-16.06.2007 | 4. Course "FISH and microdissection" |
Kollegiengasse 10, Jena, Germany |
| 5 |
18.03.2006 | Course in the framework of the Academy of
Human Genetics on 'Small supernumerary marker chromosomes' |
Kollegiengasse 10, Jena, Germany |
| 4 |
16.06.-18.06.2005 | 3. Course "FISH and microdissection" |
Kollegiengasse 10, Jena, Germany |
| 3 |
31.03.-02.04.2005 | 2. Course "FISH and microdissection" |
Kollegiengasse 10, Jena, Germany |
| 2 |
17.-18.04 2004 | XIV. Workshop on Fetal Cells and Fetal
DNA (200 participants from 27 states) |
Ernst-Abbe-Platz, Jena, Germany |
| 1 |
31.07.-02.08.2003 | 1. Course "FISH and microdissection" |
Kollegiengasse 10, Jena, Germany |
Advisory member of the Scientific committee
| # |
date |
congress |
place |
| 1 |
21-24.01 2024 | 48th Annual meeting of Indian society of
Human Genetics |
Ahmedabad, India |
| # |
date |
congress |
place |
| 35 |
01.12.2023 | Qualifikation zur fachgebundenen
genetischen Beratung; 72 UE Kurs gem. den
Anforderungen an die Qualifikation zur genetischen
Beratung nach § 7 Abs. 3 GenDG |
Akademie f. med. Fortbildung der
Ärztekammer Westfalen-Lippe - life online talk |
| 34 |
21.07.2023 | 21 Course Curriculum Jenense Refresher - all medical specialtis | Am Klinikum 1, Jena, Germany |
| 33 |
23.-24.03.2022 | Second 72 hour course Curriculum Jenense - all medical specialtis (4 lectures) |
Am Klinikum 1, Jena, Germany |
| 32 |
13.10.2021 | Practical part of curriculum Jenense Refresher - all medical specialtis | Am Klinikum 1, Jena, Germany |
| 31 |
29.-30.09.2021 | First 72 hour course Curriculum Jenense - all medical specialtis (4 lectures) |
Am Klinikum 1, Jena, Germany |
| 30 |
21.07.2021 | 20 Course Curriculum Jenense Refresher - all medical specialtis | Am Klinikum 1, Jena, Germany |
| 29 |
25.09.2019 | 19. Course Curriculum Jenense Refresher - all medical specialtis | Am Klinikum 1, Jena, Germany |
| 28 |
18.04.2018 | 18. Course Curriculum Jenense Refresher - all medical specialtis | Am Klinikum 1, Jena, Germany |
| 27 |
26.04.2017 | 17. Course Curriculum Jenense Refresher - all medical specialtis | Kollegiengasse 10, Jena, Germany |
| 26 |
28.05.2016 | 16. Course Curriculum Jenense Refresher - all medical specialtis | Kollegiengasse 10, Jena, Germany |
| 25 |
03.11.2015 | 15. Course Curriculum Jenense Refresher - Hematology | Kollegiengasse 10, Jena, Germany |
| 24 |
28.10.2015 | 14. Course Curriculum Jenense Refresher - all medical specialtis | Kollegiengasse 10, Jena, Germany |
| 23 |
09.09.2015 | 13. Course Curriculum Jenense Refresher - all medical specialtis | Kollegiengasse 10, Jena, Germany |
| 22 |
26.03.2015 | 12. Course Curriculum Jenense Refresher - Neurology | Kollegiengasse 10, Jena, Germany |
| 21 |
17.09.2014 | 11. Course Curriculum Jenense Refresher - all medical specialtis | Kollegiengasse 10, Jena, Germany |
| 20 |
21.-22.01.2014 | Indo German
Pre-Conference FISH Workshop and Advisor of the 39th conference of Indian Society of Human Genetics, Ahmedabad, India, 23.-25.01.2014 - Meeting with Prof. Kalam (see here) |
Ahmedabad, India |
| 19 |
18.09.2013 | 10. Course Curriculum Jenense Refresher - all medical specialtis | Kollegiengasse 10, Jena, Germany |
| 18 |
11.09.2013 | 9. Course Curriculum Jenense Refresher - all medical specialtis | Kollegiengasse 10, Jena, Germany |
| 17 |
08.05.2013 | 8. Course Curriculum Jenense Refresher - Diabetologists | Leipzig, Germany |
| 16 |
09.01.2013 | 7. Course Curriculum Jenense Refresher - all medical specialtis | Kollegiengasse 10, Jena, Germany |
| 15 |
03.11.2012 | 6. Course Curriculum Jenense Refresher - for Otolaryngologists | Mannheim, Germany |
| 14 |
12.09.2012 | 5. Course Curriculum Jenense Refresher - all medical specialtis | Kollegiengasse 10, Jena, Germany |
| 13 |
09.05.2012 | 4. Course Curriculum Jenense Refresher - all medical specialtis | Kollegiengasse 10, Jena, Germany |
| 12 |
29.02.2012 | 3. Course Curriculum Jenense Refresher - all medical specialtis | Kollegiengasse 10, Jena, Germany |
| 11 |
25.01.2012 | 2. Course Curriculum Jenense Refresher - Prenatal Risk Assessment | Kollegiengasse 10, Jena, Germany |
| 10 |
30.11.2011 | 1. Course Jenense Curriculum - Prenatal Risk Assessment | Kollegiengasse 10, Jena, Germany |
| 9 |
29.-31.10.2010 | 2 . course Advanced training in cytogenetics (including molecular and tumor cytogenetics) | Akademie Humangenetik, Hamburg, Germany |
| 8 |
04.06.2010 | Perspectives on the future of clinical genetic applications | Advisor at Abbott, Rosemont, Il, USA |
| 7 |
13.-15.06.2008 | 1 . course Advanced training in cytogenetics (including molecular and tumor cytogenetics) | Akademie Humangenetik, Kiel, Germany |
| 6 |
20.-24.02.2006 | 1. course on Genetics of the nucleus; Doctoral Programme in Experimental Biology and Biomedicine, Center for Neuroscience and Cell Biology (CNC) | Speaker and advisor at University of Coimbra, Portugal |
| 5 |
12.-15.02.2005 | 1. Course in prenatal
and postnatal clinical cytogenetics (see also here) |
Speaker at European School of Medical Genetics (EGF) in Beirut, Lebanon |
| 4 |
27.-29.09.2004 | 6. Course
in Molecular Cytogenetics der European Genetics
Foundation (see also here) |
Speaker at European School of Medical Genetics (EGF) in Bertinoro, Italy |
| 3 |
19.-22.11.2000 | 2. Course in Molecular Cytogenetics der European Genetics Foundation | Speaker at European School of Medical Genetics (EGF) in Sestri Levante, Italy |
| 2 |
14.-19.11.1999 | 1. Course in Molecular Cytogenetics der European Genetics Foundation | Speaker at European School of Medical Genetics (EGF) in Sestri Levante, Italy |
| 1 |
14.-19.09.1999 | UICC-Training Course „Novel Approaches for Cancer Therapy and Diagnostics“ | Kollegiengasse 10, Jena, Germany |
| # |
date |
topic |
place |
| 129 |
10.11.2023 | Report on activities quality control Molecular Cytogenetics in Germany | BVDH
Herbsttagung, Berlin,
Germany |
| 128 |
25.11.2022 | Report on activities quality control Molecular Cytogenetics in Germany | BVDH
Herbsttagung, Köln,
Germany - online participation |
| 127 |
10.11.2022 | Necessity and advantages of (molecular) cytogenetic analyses on stem cell cultures | 6th
Pluricore meeting 2022, Berlin, Germany |
| 126 |
23.09.2022 | Grenzen und Möglichkeiten des nonm invasive prenatal testing (NIPT) | 20.
Ostsächsisches Fortbildungsseminar
Ultraschall in Gynekologie und
Geburtshilfe, Kamenz, Germany |
| 125 |
27.05.2022 | About the need to comprehensively characterize the chromosomic nature of microdeletions and microduplicatons | XVI
Jornada Interhospitalaria de
Genética,Hospital Universitario HM
Sanchinarro, Madrid, Spain -
online |
| 124 |
02.07.2021 | When molecular cytogenetic cannot be replaced by and/or is less costly than modern genetic high throughput tests. | online
available under http://bgciconference.com/Access-Previous-Talks.html Day 1 - choosing the right test - at 6:18:00 |
| 123 122 |
02.12.2019 | Necessity to use (molecular)
cytogenetics for diagnostics in a world of
nect generation sequencing and array CGH. Tumor cytogenetic reserch in murine tumor models and human diagnostic cases. |
Hematologu Asociaciju, Symposium "Molecular diagnostic methods used in hematolgiic genetics: where does the way go? Riga, Latvija, Latvija |
| 121 |
16.-17.06.2019 | Report on activities, ErCLG | National Human Genetics Society Meeting‘ ; ‚Open CLG Meeting‘ and Boardmeetings of the ESHG ‘ , ESHG meeting Götheburg, Sweden |
| 120 |
23.04.2019 | Trends in Human Genetics | Lecture at YSU, Yerevan, Armenia |
| 119 |
22.04.2019 | Trends in Human Genetics | Slavonic university Yerevan, Armenia |
| 118 |
2.03.2019 | A Clinical Laboratory Geneticist view on German and European systems on rare disease/ cancer management. | JARC WP8 Expert meeting, Budapest, Hungary |
| 117 |
07.03.2019 | The status of the ErCLG | GfH
conference - meeting of natural
scientists; Weimar,
Germany |
| 116 115 |
23.10.2018 | Parental origin of deletions
and duplications – about the necessity to
check for cryptic inversions. News about the sSMC database. |
Medical Faculty, Children Hospital, Belgrade, Serbia |
| 114 113 |
22.10.2018 | Chromosomal imbalances versus gene
mutations. What can we learn from murine tumor models? |
Medical Faculty Belgrade, Tumorgenetics, Serbia |
| 112 |
09.05.2018 | New developments in the field of Human Genetics – how to keep diagnostic quality | Institute of Human Genetics,
Magdeburg, Germany |
| 111 |
13.04.2018 | How to study chromosomal breakpoints
in clinical routine and research (see also here) |
Lecture at YSU, Department of Genetics and Cytology,
Yerevan, Armenia (the lecture was simultaneously translated into Armenian) |
| 110 |
08.12.2017 | New developments in the field of
Human Genetics – how to keep diagnostic
quality Surrogate motherhood and genetics – who is to be considered as genetic parents. (see also here) |
Mother and Child Health Care Institute of Serbia, Belgrade, Serbia |
| 109 |
27.05.2017 | Next generation phenotyping in Emanuel and Pallister Killian syndrome using computer-aided facial dysmorphology analysis of 2D photos | Face2Gene meeting Copenhagen, SHG conference Copenhagen, Denmark |
| 108 |
27.05.2017 | Next generation phenotyping in Emanuel and Pallister Killian syndrome using computer-aided facial dysmorphology analysis of 2D photos. | Best posterpresentation on P14.003C/C; ESHG conference Copenhagen, Denmark |
| 107 |
03.05.2017 | Human genetic aspects in patients with radiation exposure. | Radiologist round table: Clinic
meets practice 'of the Thuringian Society for
Radiology and Nuclear Medicine e.V., Jena,
Germany |
| 106 |
18.11.2016 | Report on activities quality control Molecular Cytogenetics in Germany | BVDH
Herbsttagung, Köln,
Germany |
| 105 |
17.10.2016 | New Trends in Molecular Human Genetics | Lecture at YSU, Department of Molecular Genetics, Yerevan, Armenia |
| 104 |
17.10.2016 | New Trends in Molecular (Cyto) Genetics. | Lecture at YSU, Department of Genetics and Cytology,
Yerevan, Armenia (the lecture was simultaneously translated into Armenian) |
| 103 |
02.06.2016 | What does human genetics do in Jena? | Lions
Club Jena Paradies, Haus im Sack, Jena,
Germany |
| 102 |
23.05.2016 | The Clinical Laboratory Geneticist branch | EBMG general assembly., ESHG annunal meeting, Barcelona, Spain |
| 101 |
13.05.2016 | Small supernumerary marker chromosomes – a group of rare diseases | Rett Syndrome World Congress, Kasan, Russia |
| 100 |
15.04.2016 | Mosaisim in sSMC | ‘Il Mosaicismo somatico: Implicationi per la pathologia umana e metodi per l’identificazione’, Istituto Auxologica Italiano; Milano, Italy |
| 99 |
15.01.2016 | Surrogacy and genetics | Congress on family and surrogacy;
Rosensäle, Jena, Germany |
| 98 |
18.12.2015 | Small supernumerary marker chromosomes have a story to tell | University of Pavia, Department of Molecular Medicine, Pavia, Italy |
| 97 |
04.12.2015 | CNvs. Importance in cancer research | Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil. |
| 96 |
01.12.2015 | Supernumerary markers: an update. (see also here) |
„1st international meeting on oncology research“, Belem, Para, Brazil |
| 95 |
10.11.2015 | Small supernumerary marker chromosomes (sSMC); genotype-phenotype correlation complicated by a yet underestimated factor: their discontinuous structure | Symposium ‚Translational biomedicine: exploring modern techniques of interdisciplinary research in implication to applied medicine‘, St. Petersburg, Russia |
| 94 |
04.07.2015 | Quality assessment platform for Human Genetics in Germany; HGQN = Human Genetics Quality Network. | Permanent Working Group ‚Quality Issues and Training in Cytogenetics‘ on 10th European Cytogenetics Conference, Straßburg, France |
| 93 92 91 |
07.-08.06.2015 | ‚Meeting of the EBMG board Clinical
Laboratory Geneticist (CLG): Report on activities EBMG board Clinical Laboratory Geneticist (CLG): The Clinical Laboratory Geneticist branch EBMG general assembly: The Clinical Laboratory Geneticist branch. |
ESHG Conference Glasgow, UK |
| 90 |
15.05.2015 | Small supernumerary marker chromosomes (sSMC): an update | Dar Al Baraa Medical Center, Kuwait |
| 89 |
05.05.2015 | MLPA in CLL-diagnostics | ‚Tumorgesprächsrunde‘
, Kollegiengasse
10, Jena,
Germany |
| 88 |
22.04.2015 | FISH in prental diagnostics |
‚Pränatalen Gesprächsrunde‘ , Kollegiengasse
10, Jena,
Germany |
| 87 |
03.04.2015 | Principle of fluorescence in situ hybridization (FISH) technique and applications towards biodiversity (and fishery) researches | Nong Khai Campus, Khon Kaen, Thailand |
| 86 |
02.04.2015 | Benign and pathological chromosomal imbalances - microscopic and submicroscopic copy number variations (CNVs) in human genetics | Department of Biology Faculty of Science, Khon Kaen, Thailand |
| 85 |
31.03.2015 | FISH in
Human Cytogenetics or Molecular
cytogenetics – Perspectives in Biology
and Medicine |
Surin Rajabhat University, Thailand |
| 84 |
31.03.2015 | FISH in Human Cytogenetics or Molecular cytogenetics – Perspectives in Biology and Medicine | Buriram Rajabhat University, Thailand |
| 83 |
17.10.2014 | Molecular cytogenetics applied to uncover cryptic rearrangements in leukemia research - results of a 10 year German-Brazil cowork | Instituto Nacional de Câncer (INCA), Rio de Janeiro, Brazil |
| 82 |
16.10.2014 | Benign and pathological chromosomal imbalances - microscopic and submicroscopic copy number variations (CNVs) in human genetics | Anatomia Patolgica e Patologia Clinica, Universidade Estadual do Rio de Janeiro (UERJ), Brazil |
| 81 |
05.09.2014 | Benign and pathological chromosomal imbalances - microscopic and submicroscopic copy number variations (CNVs) in human genetics | 47. Annual Assembly and Conference of the Cytogenetic Section of the Czech-Slovak Biological Society (CSBS), Prague, Czech |
| 80 |
09.05.2014 | Molecular Cytogenetics in clinical
genetics and other research fields. Small supernumerary marker chromosomes – towards genotype-phenotype correlations. |
Centre de génomique humaine de la Faculté de médecine et pharmacie, Université Mohammed V Souissi Rabat, Moroc |
| 79 |
05.02.2014 | Principles of FISH and multicolor FISH (mFISH) | Rajabhat Maha Sarakham University, Thailand |
| 78 77 76 |
28.01.2014 | Are there B-chromosomes in human? The long shadow of parental genomes – organizing the next generation nuclei Principles of FISH and multicolor FISH (mFISH) |
Department of Biology Faculty of Science, Khon Kaen, Thailand |
| 75 |
13.01.2014 | Small supernumerary marker
chromosomes - towards genotype-phenotype
correlations |
Lab Synlab, Laboratory for Molecular Diagnostics, Prague, Czech |
| 74 |
11.11.2013 | Benign and
pathological chromosomal
imbalances - microscopic and
submicroscopic copy number
variations (CNVs) in human
genetics |
Institute of Health Sciences, Kocaeli University, Kocaeli, Turkey |
| 73 |
11.11.2013 | Small
supernumerary marker chromosomes -
towards genotype-phenotype correlations (see also here) |
Symposium ‚Human Genetics Meeting’, Inst. of Health Sciences, Kocaeli University, Kocaeli, Turkey |
| 72 |
26.10.2013 | Principles of FISH and multicolor
FISH (mFISH) |
Institute for Cytology, St. Petersburg (divison in Peterhof), Russia |
| 71 |
25.10.2013 | The
long shadow of parental genomes –
organizing the next generation nuclei |
Institute for Cytology, St. Petersburg, Russia |
| 70 |
23.10.2013 | The
long shadow of parental genomes –
organizing the next generation nuclei |
XII Russian Federation Congress “Modern technologies in pediatrics and pediatric surgery”, Moscow, Russia |
| 69 |
17.10.2013 | Molecular cytogenetics in nowadays biology and medicine. | Lecture at YSU, Department of Genetics and Cytology,
Yerevan, Armenia (the lecture was simultaneously translated into Armenian) |
| 68 |
02.09.2013 | The
long shadow of parental genomes –
organizing the next generation nuclei |
Institute of Mother and Child Health Care“ dr Vukan Čupić, Belgrad, Serbia |
| 67 |
07.05.2013 | The
long shadow of parental genomes –
organizing the next generation nuclei |
Institute of Human Genetics, Göttingen,
Germany |
| 66 |
20.03.2013 | Report on activities quality control Molecular Cytogenetics in Germany | BVDH
Herbsttagung, Köln,
Germany |
| 65 64 |
31.05.2012 |
Principles of FISH and multicolor FISH
(mFISH) Modern molecular cytogenetic approaches in diagnostics and research |
Department of Biology Faculty of Science, Khon Kaen, Thailand |
| 63 |
22.05.2012 | Small supernumerary marker chromosomes – an update | Institute of Hereditary Diseases, Minsk, Belarus |
| 62 |
08.05.2012 | Small supernumerary marker chromosomes – an update | Institute of Human Genetics, Hannover,
Germany |
| 61 |
24.04.2012 | Molecular cytogenetics in clinical genetics and other research fields | Universidade Federal de Sao Carlos, Fish cytogenetics, Sao Carlos, SP, Brazil |
| 60 |
20.04.2012 | Recent developments, routine and research applications in molecular tumor cytogenetics | State University, Pathology Department, Rio de Janeiro, Brazil |
| 59 |
27.01.2012 | Are there B-chromosomes in human? | Leibnitz Institute for Plant
Genetics (IPK), Gatersleben, Germany |
| 58 |
27.10.2011 | Small supernumerary marker chromosomes and uniparental disomy have a story to tell. | Instituto Fernandes Figueira – IFF/FIOCRUZ Genetics Department, Rio de Janeiro, Brazil |
| 57 |
24.10.2011 | Molecular cytogenetics (FISH) and array-techniques (chips). | Anatomia Patolgica e Patologia Clinica, Universidade Estadual do Rio de Janeiro (UERJ), Brazil |
| 56 |
18.10.2011 | Prader-Willi-Syndrom and Angelman syndrome | Military Hospital associated with "Universidad de la República(UDELAR)", Montevideo, Uruguay |
| 55 |
13.09.2011 | Small supernumerary marker chromosomes and uniparental disomy have a story to tell. | Institute of Mental Health, Belgrade, Serbia |
| 54 53 |
04.06.2011 | Two European approaches to the
recognition of natural scientists in medicine,
EurProBiol, Laboratory genetics core committee Report on activities quality control Molecular Cytogenetics in Germany |
Meeting of CLGs in human genetics,
Würzburg, Germany |
| 52 |
11.11.2010 | Molecular Cytogenetics in tumor cells (Tumorcytogenetics) | Rio de Janeiro State University, Pathology Department, Rio de Janeiro, Brazil |
| 51 |
11.11.2010 | Molecular Cytogenetics in tumor cells (Tumorcytogenetics) | Instituto Nacional de Câncer (INCA), Rio de Janeiro, Brazil |
| 50 |
10.11.2010 | Molecular cytogenetics - some interesting cases solved by multicolor FISH approaches | Instituto Fernandes Figueira – IFF/FIOCRUZ Genetics Department, Rio de Janeiro, Brazil |
| 49 |
08.09.2010 | New molecular cytogenetics possibilities in clinical genetics - Lots of FISH and not so much CHIPS (see also here) | Institute of Mental Health, Belgrade, Serbia |
| 48 |
01.10.2009 | New molecular cytogenetics
possibilities in clinical genetics - Lots of
FISH and not so much CHIPS. |
Lecture at YSU, Department of Genetics and Cytology,
Yerevan, Armenia (the lecture was simultaneously translated into Armenian) |
| 47 46 |
28.09.2009 | Small supernumerary marker
chromosomes, chromosome heteromorphisms and
infertility; The work of cytogenetic servce in the Institute of Human Genetics and Anthropology, Jena |
Seminar ‚Medical-genetic aspects of reproductive function’, Research Center of Maternal and Child Health Protection, Yerevan, Armenia |
| 45 |
19.08.2009 | New molecular cytogenetics possibilities in clinical genetics - Lots of FISH and not so much CHIPS. | Inst. de ciencias biologicas, Universidade de Pernambuco, Recife, Brazil |
| 44 |
11.08.2009 | New molecular cytogenetics possibilities in clinical genetics - Lots of FISH and not so much CHIPS. | Inst. Fernandes Figueira, FIOCRUZ, Flamengo, Rio de Janeiro, Brazil |
| 43 |
11.05.2009 | Epigenetic changes in chromosomes 8, 11 and 16 in acute myeloid leukemia (AML) | 36th meeting of the board of the
competence network "Acute and Chronic
Leukemia" in Frankfurt am Main, Germany |
| 42 |
08.01.2009 | Single cell analysis using targeted molecular cytogenetics in tumor diagnostics and research. | IZKF-Seminar
Oncology, Jena,
Germany |
| 41 |
02.10.2008 | Recent developments and applications in multicolor fluorescence in situ hybridization | Instituto Nacional de Câncer (INCA), Rio de Janeiro, Brazil |
| 40 |
23.09.2008 | Recent developments and applications in multicolor fluorescence in situ hybridization | 38th Annual Meeting of the European Environmental Mutagen Society, Cavtat, Croatia |
| 39 |
08.02.2008 | Molecular Tumorcytogenetics. | 27th Annual Convention of Indian Association for Cancer Research and International Symposium on Functional Genomics, Ahmedabad, India |
| 38 |
17.10.2007 | Small supernumerary marker chromosomes | 113th Berlin Meeting of
Cytogeneticists, Berlin, Charité, Germany |
| 37 |
10.11.2006 | Characterization of the parental origin of human chromosomes on a single cell leve | 10a Reunioia da Sociedade Portuguesa de Genetica Humana, Coimbra, Portugal; |
| 36 |
08.11.2006 | New
molecular techniques in chromosome
research |
Institute of Hereditary Diseases, Minsk, Belarus |
| 35 |
06.10.2006 | Towards a genotype-phenotype correlation of small supernumerary marker chromosomes (sSMC) | VII Croatian Pediatric Congress, Osijek, Croatia |
| 34 |
02.08.2006 | Towards a genotype-phenotype correlation of small supernumerary marker chromosomes (sSMC) | Cytogenetics
Laboratory of the 'Sullivan &
Nicholaides Pathology', Brisbane, Australia |
| 33 |
13.07.2006 | Molecular cytogenetic analysis of (marker) chromosomes in humans | Institute of Human Genetics, Philipps-Universität Marburg, Germany |
| 32 |
05.07.2006 | Towards a genotype-phenotype correlation of small supernumerary marker chromosomes (sSMC) | Cambridge Veterinary School Department of Veterinary Medicine; Cambridge, UK |
| 31 |
13.06.2006 | Characterization of human (marker) chromosomes using molecular cytogenetics | Institute of Human Genetics, Hamburg-Eppendorf, Germany |
| 30 |
28.04.2006 | Molecular Cytogenetics applied in tumor cells | 4th annual Conference of South District of Russian Federation, Russian Ministry of Health and Social Development Rostov State Medical Universty, Kislovodsk, Russia |
| 29 |
24.04.2006 | New molecular techniques in chromosome research | Research Centre for Medical Genetics, Russian Academy of Medical Sciences, Moscow, Russia |
| 28 |
24.02.2006 | When are chromosomes chromosomes? Or FISH-banding applied to resolve the nature of metaphase and interphase-chromosomes. | Faculdade de Medicina da Universidade de Coimbra, Portugal |
| 27 |
19.10.2005 | New
molecular techniques in chromosome
research (see also here) |
International Alumni Seminar „Biotechnology and Health“; Lecture at YSU, Russian Armenian (Slavonic) University, Yerevan, Armenia (the lecture was simultaneously translated into Armenian) |
| 26 |
17.10.2005 | New molecular techniques in chromosome research | Lecture at YSU, Department of Genetics and Cytology,
Yerevan, Armenia (the lecture was simultaneously translated into Armenian) |
| 25 |
14.05.2005 | Recent possibilites of prenatal molecular cytogenetic diagnostics, | Lecture at Mother and Child Clinic, Yerevan, Armenia (the lecture was simultaneously translated into Russian) |
| 24 |
12.05.2005 | Human evolution from the chromosomal point of view? The karyotypic evolution in Hominoids | Lecture at YSU, Department of Genetics and Cytology,
Yerevan, Armenia (the lecture
was simultaneously translated into Russian) |
| 23 |
08.06.2005 | Characterization of (marker) chromosomes using molecular cytogenetics | Seminar 'Scientific lectures' at the
Children's Hospital Jena, Germany |
| 22 |
09.05.2005 | Centromere specific 24-color FISH and multicolor banding in the charcaterization of mini-marker chromosomes and complex chromosomal rearrangements | ESHG-meeting, Prague, Czech |
| 21 |
02.04.2005 | Detection of cryptic chromosomal changes in acute myeloid leukemia | IZKF
weekend seminars "Clinical Experimental
Oncology" Castle Oppurg, Germany |
| 20 |
04.03.2005 | Detecting chromosomal territories and individual genes in interphase nuclei | Annual Meeting of the European Consortium ‚Molecular Imaging’, ETH-Hönngerberg, Zürich, Switzerland |
| 19 |
30.10.2004 | Multi-color FISH techniques in human cytogenetics | VBMF Colloquiums ‘Confocal and
Living Cell Microscopy’ IMB, Jena, Germany |
| 18 |
22.06.2004 | Small and minor supernumerary marker chromosomes – is this ~40 year old problem of human cytogenetics solved finally by FISH? | Institute of Human Genetics,
Göttingen, Germany |
| 17 |
04.06.2004 | Multicolor fluorescence in situ hybridization and its application in human genetics | Institute of Human Genetics, Jena,
Germany |
| 16 |
16.04.2004 | Organization of the EU-COPERNICUS coordination meeting and talks | Institute of Human Genetics, Jena,
Germany |
| 15 |
18.11.2003 | Small and smallest supernumerary marker chromosomes - an old problem of cytogenetics solved with FISH? | Institute of Human Genetics,
Erlangen, Germany |
| 14 |
15.04.2003 | Characterization of (small) human marker chromosomes by recently developed molecular cytogenetic approaches | Center for Human Genetics, U.Z. Gasthuisberg, Leuven, Belgium |
| 13 12 11 |
11.04.-12.04.2003 | Multicolor FISH and new FISH
methods Recent progress in detection of chromosomal aneuploidies in pre- and postnatal diagnosis Strategies for the characterization of small human marker chromosomes |
COPERNICUS 2 ICA2-CT-2000-1001, Grand Chalet Hotel, and Gaia Centre, Athens, Greece |
| 10 |
23.01.2003 | Characterization of marker chromosomes using new molecular cytogenetic methods | Institute of Human Genetics,
Tübingen, Germany |
| 9 |
29.11.2002 | Multicolor FISH techniques in molecular cytogenetic diagnostics and research | 1. Workshop "Microscopic
Techniques", Institute for Anatomy II, Jena, Germany |
| 8 |
20.11.2002 | FISH - from the prenatal rapid test to the interpretation of unclear findings | Center for Human Genetics, Bremen,
Germany |
| 7 |
29.10.2002 | Recent developments in molecular cytogenetics | Institute of Human Genetics,
Göttingen, Germany |
| 6 |
10.10.2002 | Characterization of (small) human marker chromosomes by recently developed molecular cytogenetic approaches | Institute of Human Genetics, Essen,
Germany |
| 5 |
26.09.2002 | New possibilities in molecular cytogenetics | 12th annual meeting of the regional
association of vdbiol Thuringia, Lecture Hall
Zoology, Jena, Germany |
| 4 |
24.01.2002 | M-FISH and MCB in a complex case - case presentation. | Women's clinic, Jena, Germany |
| 3 |
15.01.2002 | Bioethics and human genetics | Parish center, Adelsdorf, Germany |
| 2 |
13.06.2001 | Multicolor FISH methods and their application in clinical and leukemia cytogenetics | Institute of Human Genetics,
Magdeburg, Germany |
| 1 |
08.07.2000 | FISH method and areas of application | Women's clinic, Jena, Germany |
| # |
date |
topic |
place |
| 85 | 06.09.2023 | Small supernumerary marker chromosomes in infertile patients | XXXIII
Annual International conference of
the RAHR - online participation |
| 86 85 |
22.06.2023 | Noninvasive prenatal testing (NIPT)
- about challenges and ethical issues Why results of chromosomal microarray always should be checked by molecular cytogenetics (recorded talks) |
Russian cytogenomics conference 2023 |
| 84 | 03.05.2023 | Noninvasive prenatal testing (NIPT)
- challenges and ethical issues (recorded talk) |
1st International Azerbaijan Laboratory Medicine Congress & Lab Expo http://www.micebaku.com/ |
| 83 |
26.04.2023 | Grundlagen des Noninvasive prenatal testing (NIPT) - und die damit verbundenen (ethischen) Probleme | Virtual: PRAEnatal & GENial, 1 Online Symposium - Nürnberg, Germany |
| 82 | 23.03.2023 | Limits and possibilities of
noninvasive prenatal testing (NIPT) (recorded talk) |
1st Symposium of Laboratory Geneticists and Molecular Biologists in Bosnia and Herzegovina, Sarajevo - see here |
| 81 | 21.03.2023 | Noninvasive prenatal testing (NIPT)
- challenges and ethical issues (recorded talk) |
International conference: Medical genetics and genomics: multidisciplinary aspects. St. Petersburg, Russia - see here and here |
| 80 |
21.11.2022 | Limits and possibilities of non-invasive prenatal testing (NIPT) | XIII Scientific Conference «Human Genetics and Pathology», Tomsk, Russia - online participation |
| 79 | 19.11.2022 | Limits and possibilities of non-invasive prenatal testing (NIPT) | 2nd Annual MSERM Worldwide Congress: "Moroccan Society for Endometriosis and Reproductive Medicine - (MSERM)" - Hybrid 2022, Fes - Morocco - online participation |
| 78 | 12.11.2022 | Small supernumerary marker chromosomes and chromothripsis | 15th Biannual Congress of the Turkish Medical Genetics Society, Istanbul, Turkey - online participation |
| 77 | 20.04.2022 | EBMG registration system for CLGs | Virtual: meeting of DSKA (short for Danish Society for Clinical Academics) https://dska.nu/ |
| 76 | 24.03.2022 | Human Ring Chromosome Disorders: An international Collaboration Towards Better Diagnosis, Interpretations, and Clinical Management (ONLINE) : Small supernumerary marker chromosomes with ring-chromosome shape | Virtual: ACMG Annual Clinical Genetics Meeting, nashville, TN, USA |
| 75 | 24.11.2021 | Was man zu Grenzen und Möglichkeiten des Noninvasive prenatal testing (NIPT) unbedingt wissen muss | Virtual: 30. Kongress der Deutschen Gesellschaft für Perinatale Medizin |
| 74 | 03.07.2021 | An International Collaboration for Human Ring chromosomes (ICHRC) towards developing standards and guidelines for best practice in laboratory diagnosis clinical management and collaborative research | Virtual: 13th ECA conference. Talk in Permanent Working Group Quality Issues, Training and Cytogenomics |
| 73 | 02.07.2021 | When molecular cytogenetics cannot be replaced by and/or is less costly than modern genetic high throughput tests. | Virtual: Board of Genetic Counseling India – 6th Annual International Conference on ‘Genomics and Genetic Counseling: Value in Health Care’. |
| 72 | 22.11.2019 | Report on activities quality control Molecular Cytogenetics in Germany | BVDH Herbsttagung, Köln, Germany |
| 71 |
04.10.2019 | Molecular cytogenetics – indispensability of the approach highlighted by sSMC characterization. | 19. Jahrestagung der
Österreichischen Gesellschaft für
Humangenetik, Salzburg, Austria |
| 70 |
06.-09.07.2019 | European certification and continuous education of clinical laboratory geneticists working in cytogenetics. | 12th ECA meeting,
Salzburg, Austria |
| 69 |
18.-22.06.2019 | Small supernumerary marker
chromosomes (sSMC) - genotype-phenotype
correlation complicated by chromothripsis
leading to discontinuous structure. |
VII Congress of Vavilov Society of Geneticist and Breeders (VSG&B) and associate symposium. St. Petersburg, Russia |
| 68 |
27.05.2019 | About the necessities to use (molecular) cytogenetics for clinical genetic diagnostics in a world of next generation sequencing. | Congress «Genetics of 21st century», Moscow, Russia |
| 67 |
09.11.2018 | Report on activities quality control Molecular Cytogenetics in Germany | BVDH Herbsttagung, Köln, Germany |
| 66 |
20.-24.08.2018 | Parental origin of deletions and
duplications; about the necessity to check for
cryptic inversions |
International Chromosome Conference Chromosome 2018. Novosibirsk, Russia |
| 65 |
9–12.06.2018 | Molecular cytogenetics in Zoo-FISH-studies – still urgently needed. | 23rd International Colloquium on Animal Cytogenetics and Genomics (23 ICACG), St. Petersburg, Russia |
| 64 |
26.-29.01.2018 | What about benign chromosomal
imbalances in cancer genetics. |
3rd Conference on
Aneuploidy and Cancer: Clinical and
Experimental Aspects, Berkeley, USA |
| 63 |
07.11.2017 | Report on activities quality control Molecular Cytogenetics in Germany | BVDH Herbsttagung, Köln, Germany |
| 62 |
27.-30.05.2017 | Next generation phenotyping in
Emanuel and Pallister Killian syndrome using
computer-aided facial dysmorphology analysis
of 2D photos |
European Society of Human Genetics. Copenhagen, Denmark |
| 61 |
26.-29.01.2017 | What about benign chromosomal
imbalances in cancer genetics? |
rd Conference on Aneuploidy and Cancer – Clinical and Experimental Aspects. Berkeley, US |
| 60 | 18.11.2016 | Report on activities quality control Molecular Cytogenetics in Germany | BVDH Herbsttagung, Köln, Germany |
| 59 |
10.-13.07.2016 | Cytogenetically visible copy number
variations (CG-CNVs) in banding and molecular
cytogenetics of human: About heteromorphisms
and euchromatic variants |
21st International Chromosome Conference (ICC), Foz de Iguazu, Brazil |
| 58 |
16.10.2015 | Report on activities quality control Molecular Cytogenetics in Germany | BVDH Herbsttagung, Köln, Germany |
| 57 |
17.-20.09.2015 |
Small supernumerary
marker chromosomes (sSMC);
genotype-phenotype correlation complicated
by a yet underestimated factor: their
discontinuous structure (see also here) |
11. Balkan Congress of Human Genetics. Belgrade, Serbia; |
| 56 |
24-28.08.2015 | Benign and pathological
chromosomal imbalances - microscopic and
submicroscopic copy number variations (CNVs) in
human genetics |
The International Conference Chromosome 2015. Novosibirsk, Russia |
| 55 |
04.-07.07.2015 | European standards for clinical
laboratory geneticist. |
11th ECA meeting, Strassburg, France |
| 54 |
28.09.-02.10.2014 | Small supernumerary marker chromosomes – an update. | VI Meeting of Vavilov Society of Geneticists and Breeders and Associated Genetics Symposia. Belgrade (moved from Kladovo), Serbia |
| 53 52 |
23.-25.01.2013 | Uniparental disomy - clinical
consequences due to imprinting and activation
of recessive genes. Small supernumerary marker chromosomes – an update. |
International Conference on Human Genetics and 39th Annual Meeting of the Indian Society of Human Genetics, Ahmedabad, India |
| 51 | 18.10.2013 | Benign and pathological chromosomal imbalances – microscopic and submicroscopic copy number variations (CNVs) in human genetics | Symposium at YSU, Yerevan, Armenia |
| 50 | 29.06.-02.07.2013 | Small supernumerary
marker chromosomes (sSMC) – what about the
genotype-phenotype correlation? |
9th ECA meeting, Dublin, Ireland |
| 49 |
20.-22.3.2013 | The Clinical Laboratory Geneticists
Section of the European Board of Medical
Genetics (EBMG). |
GfH-meeting, Dresden, Germany |
| 48 |
26.-29.11.2012 | Small supernumerary marker
chromosomes (sSMC) – what about the
genotype-phenotype correlation? (see also here) |
2. Reuniao de Citogenetica do Brasil Central, Goiana, Brazil |
| 47 |
02.-07.09.2012 | Small supernumerary marker chromosomes | 2. International Conference Chromosome. Novosibirsk, Russia |
| 46 |
23.06.2012 | Report on activities quality control Molecular Cytogenetics in Germany | GfH meeting, Nürnberg, Germany |
| 45 |
22.04.2012 | Small supernumerary marker
chromosomes (sSMC) in genetic diagnostics |
II EPACITO - ENCONTRO PAULISTA DE CITOGENÉTICA: Centro de Convenções de Ribeirão Preto. Ribeirão Preto, Brazil. 2 |
| 44 |
25.-29.08.2011 | Do position effects
drive t(8;21) in acute myelogenous leukemia? |
22nd Wilhelm Bernhard Workshop, Riga, Latvia |
| 43 |
16.-18.09.2010 | Comparative cytogenetic technologies. | Annual Conference of the German Genetics Society (GfG), Evolution of Primates. Jena, Germany |
| 42 |
28.-29.06.2010 | Small supernumerary marker
chromosomes in humans. |
The Young Scientists School Bioinformatics and Systems Biology. Novosibirsk, Russia |
| 41 |
20.-27.06.2010 | Detailed characterization of
small supernumerary marker chromosomes reveals
breakpoint hot spots. |
7. International Conference on Bioinformatics of Genome Regulation and Structur /System Biology. Novosibirsk, Russia |
| 40 |
06.-09.06.2010 | Murine FISH-banding – mcb probe
development and application. (see also here) |
19th international colloquium on animal cytogenetics and gene mapping, Balice/Krakow, Poland |
| 39 |
20.-24.10.2009 | Low grade mosaicism in marker
chromosomes. |
59th ASHG-conference, Honolulu, USA |
| 38 |
18.-22.04.2009 | Multi-color FISH assays for characterization of marker chromosomes and epigenetic changes | Experimental Biology, New Orleans, USA |
| 37 |
01.-03.04.2009 | 3-dimensional multicolor
banding (3D-MCB) reveals the distribution of
chromosomes in human sperm |
GfH-meeting, Aachen, Germany |
| 36 |
21-25.09.2008 | Recent developments and
applications in multicolor fluorescence in situ
hybridization. |
38. Annual Meeting of the European Environmental Mutagen Society. Cavtat, Croatia |
| 35 |
07.-09.02.2008 | Molecular cytogenetics in
tumor cells - A review. |
27. Annual Convention of Indian Association for Cancer Research and International Symposium on Functional Genomics. Ahmedabad, India |
| 34 |
01.-03.03.2007 | Towards a genotype-phenotype
correlation of small supernumerary marker
chromosomes (sSMC) in human. |
12. Southafrican Society of Human Genetics (SASHG) Congress. Golden Gate, South-Africa |
| 33 |
07.-10.03.2007 | Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics. | GfH-meeting, Bonn, Germany |
| 32 |
10.-11.11.2006 | Characterization of the
parental origin of human chromosomes on a single
cell level. |
10. Reunioia da Sociedade Portuguesa de Genetica Humana. Coimbra, Portugal |
| 31 |
27-29.04.2006 | Multicolor-FISH approaches
applied in tumor cytogenetics. |
IV Annual conference of south district of Russian Federation: Current advances in human genetics: clinical aspects. Kislovodsk, Russia |
| 30 |
08.-11.03.2006 | Towards a molecular
genotype-phenotype correlation of small
supernumerary marker chromosomes (sSMC) by
applying microdissected sSMC probes on a 21.5k
BAC array-CGH. |
GfH-meeting, Heidelberg, Germany |
| 29 |
09.-12.03.2005 | Towards a first
genotype-phenotype correlation of small
supernumerary marker chromosomes (sSMC). |
GfH-meeting, Halle, Germany |
| 28 |
13.-15.09.2004 | The genetic content of mosaic
and non-mosaic small supernumerary marker
chromosomes (sSMC). |
British Human Genetics Conference, York, UK |
| 27 |
01.-04.10.2003 | Giemsa-dark bands split into
dark and light subbands as demonstrated by
multicolor banding (MCB). |
GfH-meeting, Marburg, Germany |
| 26 |
29.09.-02.10.2002 | Characterization of
human small marker-chromosomes by
centromere-specific multicolor-FISH (cenM-FISH)
and high resolution multicolor banding (MCB). |
GfH-meeting, Leipzig, Germany |
| 25 |
10.-13.08.2002 | Straight-forward
characterization of small human
marker-chromosomes by centromere-specific
multicolor-FISH (cenM-FISH), high resolution
multicolor banding (MCB) and analysis for
uniparental disomy (UPD). |
Molecular Medicine 2002, XXVIII Nordic Congress in Clinical Chemistry and XXXV Nordic Conference on Coagulation, Reykjavik, Iceland |
| 24 |
14.-17.04.2002 | Multicolor banding (MCB) - a
versatile tool for characterization of exact
chromosomal breakpoints |
HGM2002 (Human Genome Meeting). Shanghai, China |
| 23 22 |
12.-13. 05.2001 | Present state and
perspectives of centromere specific multicolor
FISH (cenM-FISH) – a new approach for the PGD
and prenatal diagnosis. Centromere specific multicolor FISH (cenM-FISH) – a new approach for the characterization of marker chromosomes. |
12. Fetal Cell Workshop. Prague, Czech Republic |
| 21 |
26.-28.04.2001 | High resolution multicolour
banding (MCB) for the entire human
karyotype. (see also here) |
2. Euroconference on Quantitative Molecular Cytogenetics. Salamanca, Spain |
| 20 |
13-15.04.2000 | A new M-FISH technique: centromere specific 24-color FISH (cenM-FISH). | 1. Euroconference on quantitative molecular cytogenetics. Bari, Italy |
| 19 |
01.-03.03.2000 | Zentromer-spezifische
24-Farben FISH: Einsatz einer neuen M-FISH
Technik in der Tumorzytogenetik. |
"13. Tumorzytogenetische Arbeitstagung". Otzenhausen, Germany |
| 18 |
27.-29.05.1999 | Einsatz der p53 FISH-Sonde
zur Prognosedifferenzierung bei Leukämien |
"12. Tumorzytogenetische Arbeitstagung". Berlin, Germany |
| 17 |
18.-22. 2009 | Multi-color FISH assays for
characterization of marker chromosomes and
epigenetic changes. |
Experimental Biology New Orleans, USA |
| 16 |
?.1999 | Do patterns of genomic
imbalances in human solid tumors reflect
environmental influences on tumor formation? |
4th World Congress on Advances in Oncology", Vouliagmeni, Athens, Greece |
| 15 |
03.-06.07.1999 | Multicolor banding (MCB) of
human chromosome 13 based on region specific YAC
clones and microdissection libraries. |
2. ECA meeting, Vienna, Austria |
| 14 |
15.-18.10.1998 | Nucleus extraction from one
paraffin-embedded section mounted on a slide for
two-color FISH. |
6. European Conference on Cytogenetics and Molecular Genetics of Solid Tumors. Saarbrücken, Germany |
| 13 |
20.-22.08.1998 | An efficient nucleus
extraction method from paraffin- and cryo-fixed
material for up to three color-FISH analysis. |
1. Nordic Meeting on Molecular Cytogenetics. Aarhus, Denmark |
| 12 11 |
?.1998 |
High resolution mulitcolor
banding (hrM-FISH) for human chromosome 13 using
YAC libraries as probes. Centromere specific 24-color-FISH - a new approach for the characterization of marker chromosomes. |
GfH-meeting, Nürnberg, Germany |
| 10 |
03.-05.07.1998 | Two-color interphase FISH for
CMT1A- and HNPP-diagnostics on archival nerve
biopsies. |
7th Annual Symposium of the European Charcot-Marie-Tooth Consortium, Antwerp, Belgium |
| 9 |
22.-24.05.1998 | HN-SCCs verschiedener
Lokalisation charakterisiert mittels CGH und
Telomerase-Assay. |
11. "Tumorzytogenetische Arbeitstagung", Jena, Germany; |
| 8 |
27.10.1997 | Mosaicism for two unrelated
CMT1A patients - two casereports suggesting
somatic reversion. |
MDA Charcot-Marie-Tooth Disease Workshop. Baltimore, USA |
| 7 |
22.-24.05.1997 | Das Periphere Myelin Protein
22kDa (PMP22) Gen liegt einer Glioblastom- und
einer Osteosarkom-Zellinien amplifiziert vor;
ein neuer Kandidat für ein Onkogen? |
10. "Tumorzytogenetische Arbeitstagung". Friedrichsdorf, Germany |
| 6 |
09.-11.05.1996 | Eine effiziente
Kern-Extraktionsmethodik aus paraffin- und
cryo-fixiertem Archivmaterial für anschliessende
Mehrfarb-FISH Analysen. (see also here) |
9. "Tumorzytogenetische Arbeitstagung". Kitzbühel, Austria |
| 5 |
14.04.1996 | Mosaicism for a CMT1A patient
detected in four different tissue-types - a
casereport suggesting somatic reversion. |
5. Annual European Charcot-Marie-Tooth-Consortium Meeting. London, UK |
| 4 |
03.-06.05.1995 | Zweifarb-FISH-Analysen an
alten zytogenetischen Präparaten solider Tumore
(Interphasezytogenetik). |
8. "Tumorzytogenetische Arbeitstagung". Bremen, Germany |
| 3 |
28.-30.04.1994 | Vergleichende
Interphasezytogenetik an klassischen
Knochenmarks - Ausstrichen und -
Suspensionspräparaten mittels FISH. |
7. "Tumorzytogenetische Arbeitstagung". Schloß Salzau/Holstein, Germany |
| 2 |
16.-18.05.1993 | Interphasenzytogenetik
mittels FISH bei menschlichen
Ovarial-Karzinomen. |
6. "Tumorzytogenetische Arbeitstagung". Kloster Banz, Germany |
| 1 |
21.-23.05.1992 | Onkogen-Amplifikation in
Ovarialkarzinomen - molekulare Identifizierung
und zytogenetische Aspekte. |
5. "Tumorzytogenetische Arbeitstagung". Vienna, Austria |
| # |
available
from |
topic |
http-address |
| 3 |
01/2022 | "Genetics of monogenic and
mitochondrial disorders and imprinting" for European Federation of Clinical Chemistry and Laboratory Medicine (EFLM) in frame of "The EFLM Syllabus Course" (https://www.eflm-elearning.eu/site/syllabus-course) |
www.eflm-elearning.eu |
| 2 |
07/2021 | When molecular cytogenetics
cannot be replaced by and/or is less costly than
modern genetic high throughput tests. Board of Gentic Counseling India, 6th annual international conference |
http://bgciconference.com/Access-Previous-Talks.html
Day 1 - choosing the right test - at 6:18:00 |
| 1 |
05/2019 | An update on small
supernumerary marker chromosomes (sSMC) - online
lecture on conference in memory of Prof. Yuri
Yurov |
https://www.youtube.com/watch?v=H2kNU8zyKbc |
