Corinne Gehrig

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

Jean-Louis Blouin, Beth A. Dombroski, Swapan K. Nath et al. · Nature Genetics · 1998 · 535 citations

Psychiatry, Genetic Disorder, Genetics +5

Passive and active DNA methylation and the interplay with genetic variation in gene regulation

María Gutiérrez‐Arcelus, Tuuli Lappalainen, Stephen B. Montgomery et al. · eLife · 2013 · 474 citations · Full text

Exome sequencing identifies recurrent somatic MAP2K1 and MAP2K2 mutations in melanoma

Sergey I. Nikolaev, Donata Rimoldi, Christian Iseli et al. · Nature Genetics · 2011 · 395 citations

Tumor Biology, Map2k2 Mutations, Engineering +11

Mutations in the <i>DNAH11</i> (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia

Lucia Bartoloni, Jean‐Louis Blouin, Yanzhen Pan et al. · Proceedings of the National Academy of Sciences · 2002 · 359 citations · Full text

Genotype–phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21

Robert Lyle, Frédérique Béna, Sarantis Gagos et al. · European Journal of Human Genetics · 2008 · 325 citations · Full text

Down Syndrome, Array Cgh, Cytogenetics +6