ChromosOmics - About the Author

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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

Teaching Activities of Thomas Liehr


at home university
at courses (self organized)
at courses (invited)
invited lectures
online courses/ videos
other lectures (at congress)

at home university


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:
- cytogenetic internship
- clinical cytogenetics (seminar) 
-
instructions for scientific work (seminar) 
- human genetic colloquium
- molecular and clinical cytogenetics

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
93
Luis Dario Dourado Master Molecular Medicine Cytogenomic characterization of three human tumor cell lines
2024-2025
92
Piyatrakulchai Paveen PhD (Biology at  Khon Kaen University, Thailand) Classical and molecular cytogenetics in
Thai spiders
2024-2025
91
Mahmoud Mariam
Master Molecular Medicine
Characterization of centromeric sequences in FFPE sections of breast cancer 2024-2025
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 of prostate cancer
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 - not finished
81 Sandra
Schöner
MD Fragile sites
2017 - not finished
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
2016–2025
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
2 Prahlad Balakrishnan ErCLG
training
2024
1 Sy Alodi
Australian CLG
training via QUT student agreement in Diagnostic Laboratory or research Laboratory
2021-2022


at congress (self organized)
 
#
date
congress
place
32
04.-08.09.2023 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


at courses (invited)


#
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
 

invited lectures

#
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

other lectures (at congress)

#
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


online courses

#
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



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