News & events - Topic : iGE3 Seminars

Chronological order of publication in this website

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iGE3 seminar - José Luis Gómez-Skarmeta

Gene regulation dynamics and chromatin architecture during development and evolution

José Luis Gómez-Skarmeta portrait

Prof. José Luis Gómez-Skarmeta
Centro Andaluz de Biología del Desarrollo
CSIC / Universidad Pablo de Olavide
Sevilla, Spain

Monday, April 11, 2016 – 12 h 15
Sciences III – Auditorium 1S059

Host: Denis Duboule

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iGE3 seminar - Stanislas Lyonnet

Non-coding genomic alterations in human development anomalies

Stanislas Lyonnet portrait © Inserm / Patrice Latron

Stanislas Lyonnet, Professor
Imagine Institute & University Paris Descartes
& Department of Medical Genetics
at Hôpital Necker-Enfants Malades
Paris, France

Thursday, September 24, 2015 – 14 h 15
CMU – Auditorium C150

Host: Stylianos E. Antonarakis
Information: Nema Bliggenstorfer (disabled)

Stanislas Lyonnet is Professor of Genetics at Paris Descartes University since 1995, and a clinical geneticist at Hôpital Necker-Enfants Malades. As the principal investigator of an INSERM group (Genetics and embryology of malformations), founding member of the Imagine Institute, he has conducted several studies aiming to localize and identify the genes involved in inborn errors of development. He is the author or co-author of 350 publications in peer-reviewed journals.

He is responsible for the European Master of Genetics (Paris Descartes-Paris Diderot), and served as a member of the INSERM Scientific Advisory Board. He was responsible for launching the Rare Diseases Research Program of the French National Agency for Research (ANR). He is a section editor of the European Journal of Human Genetics, and a member of the editorial board of Human Molecular Genetics.

Stanislas Lyonnet was awarded the Jean Hamburger prize in 2006, the INSERM Research Prize in 2009, and the Collery Prize (National Academy of Medicine) in 2012. He was elected President of the European Society of Human Genetics in 2013.

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iGE3 seminar - Detlef Weigel

Origin and consequences of (epi)genetic variation in Arabidopsis thaliana and relatives

Detlef Weigel portrait

Detlef Weigel, PhD
Director of the Molecular Biology Department
Max Planck Institute for Developmental Biology
Tübingen, Germany

Wednesday, February 4, 2015 – 16 h 15
Sciences II – Auditorium A100

Host: Luis Lopez-Molina

Dr Detlef Weigel is a world-renowned plant biologist and currently director of the Department of Molecular Biology at the Max Planck Institute for Developmental Biology in Tübingen.

Working with the model organism Arabidopsis thaliana, Dr Weigel has made seminal contributions to our understanding of the onset of flowering, but also flower development itself, notably with the discovery of the flower regulator LEAFY and the flower inducer FT. Furthermore, Dr Weigel demonstrated the importance of microRNAs for plant development notably by isolating the first microRNA mutant in Arabidopsis.

More recently, Dr Weigel has pioneered the use of massively parallel sequencing (Illumina) to study genetic variation in the model organism Arabidopsis thaliana and to address more general plant evolution issues. Dr Weigel's group built the first haplotype map outside mammals and generated comprehensive whole-genome databases for numerous Arabidopsis accessions (e.g. the 1001 Genomes project). This notably allowed the research community to conduct genome-wide association studies (GWAS). More recently, Dr Weigel's group has become interested in how epistatic interactions lead to plant autoimmune responses (hybrid necrosis).