Alexandre Reymond

Research interests

Publications

• A cross-disorder dosage sensitivity map of the human genome

  Cell · 2022 · 10.1016/j.cell.2022.06.036

• Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome

  Nature Communications · 2021 · https://doi.org/10.1038/s41467-021-25805-y

• Chromatin three-dimensional interactions mediate genetic effects on gene expression

  Science · 2019 · https://doi.org/10.1126/science.aat8266

• GENCODE reference annotation for the human and mouse genomes

  Nucleic Acids Research · 2018 · https://doi.org/10.1093/nar/gky955

• Population Variation and Genetic Control of Modular Chromatin Architecture in Humans

  Cell · 2015 · https://doi.org/10.1016/j.cell.2015.08.001

• Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities

  JAMA Psychiatry · 2015 · 10.1001/jamapsychiatry.2015.2123

• Comparative analysis of the transcriptome across distant species

  Nature · 2014 · 10.1038/nature13424

• Coordinated Effects of Sequence Variation on DNA Binding, Chromatin Structure, and Transcription

  Science · 2013 · 10.1126/science.1242463

• Landscape of transcription in human cells

  Nature · 2012 · https://doi.org/10.1038/nature11233

• KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant

  Nature · 2012 · 10.1038/nature11091

• A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders

  Journal of Medical Genetics · 2012 · 10.1136/jmedgenet-2012-101203

• The GENCODE pseudogene resource

  Genome biology · 2012 · 10.1186/gb-2012-13-9-r51

• GENCODE: The reference human genome annotation for The ENCODE Project

  Genome Research · 2012 · https://doi.org/10.1101/gr.135350.111

• Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

  Nature · 2011 · 10.1038/nature10406

• A High-Resolution Anatomical Atlas of the Transcriptome in the Mouse Embryo

  PLoS Biology · 2011 · https://doi.org/10.1371/journal.pbio.1000582

• A new highly penetrant form of obesity due to deletions on chromosome 16p11.2

  Nature · 2010 · 10.1038/nature08727

• Segmental copy number variation shapes tissue transcriptomes

  Nature Genetics · 2009 · 10.1038/ng.345

• The Genome Sequence of Taurine Cattle: A Window to Ruminant Biology and Evolution

  Science · 2009 · https://doi.org/10.1126/science.1169588

• Copy number variants, diseases and gene expression

  Human Molecular Genetics · 2009 · 10.1093/hmg/ddp011

• EGASP: the human ENCODE Genome Annotation Assessment Project.

  Genome biology · 2006 · 10.1186/gb-2006-7-s1-s2

• GENCODE: producing a reference annotation for ENCODE

  Genome biology · 2006 · 10.1186/gb-2006-7-s1-s4

• Conserved non-genic sequences — an unexpected feature of mammalian genomes

  Nature Reviews Genetics · 2005 · 10.1038/nrg1527

• Emergence of Young Human Genes after a Burst of Retroposition in Primates

  PLoS Biology · 2005 · 10.1371/journal.pbio.0030357

• Chromosome 21 and Down syndrome: from genomics to pathophysiology

  Nature Reviews Genetics · 2004 · 10.1038/nrg1448

• The tripartite motif family identifies cell compartments

  The EMBO Journal · 2001 · 10.1093/emboj/20.9.2140

Current projects

No projects listed.