Marc Delepine

Genome sequencing in cytogenetics: Comparison of short‐read and linked‐read approaches for germline structural variant detection and characterization

Patrick Callier, Antonio Vitobello, Yannis Duffourd, 2020, Molecular genetics & genomic medicine.

Refscope: A reference sequence, prior-knowledge system used to assess 10X Genomic Chromium System efficiency in neutralizing repeat noise

Jean-François Deleuze, Robert Olaso, Vincent Meyer, 2018, RECOMB 2018.

Performance of thunniform propulsion : a high bio-fidelity experimental study

Marc Delepine, 2013 .

The origin of a developmentally regulated Igh replicon is located near the border of regulatory domains for Igh replication and expression

Marc Delepine, Fumihiko Matsuda, Roy Riblet, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders

Elodie Ey, Thomas Bourgeron, Roberto Toro, 2012, PLoS genetics.

Lung cancer susceptibility locus at 5p15.33

Simon Heath, Tomas Axelsson, Jolanta Lissowska, 2008, Nature Genetics.

A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25

Paolo Vineis, Wolfgang Ahrens, Antonio Agudo, 2008, Nature.

Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments

Elodie Ey, Thomas Bourgeron, Roberto Toro, 2014, PLoS genetics.

SRPX2 mutations in disorders of language cortex and cognition.

Marie-Noëlle Metz-Lutz, Edouard Hirsch, Sandrine Pereira, 2006, Human molecular genetics.

Plasma fibrinogen and fibrinogen genotypes in 4685 cases of myocardial infarction and in 6002 controls: Test of causality by "Mendelian randomisation"

Sarah Parish, John Danesh, Marc Delepine, 2000 .

Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populations

Hilkka Soininen, Sandro Sorbi, Philippe Amouyel, 2011, Neurobiology of Aging.