M Koochek

15q Duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array‐CGH

M Koochek, Chansonette Harvard, MJ Hildebrand et al. · Clinical Genetics · 2006 · 101 citations

Iron Deficiency in Cyanobacteria Causes Monomerization of Photosystem I Trimers and Reduces the Capacity for State Transitions and the Effective Absorption Cross Section of Photosystem I in Vivo

Alexander G. Ivanov, Marianna Król, Dmitry Sveshnikov et al. · PLANT PHYSIOLOGY · 2006 · 76 citations · Full text

Phenomic determinants of genomic variation in autism spectrum disorders

Ying Qiao, Noémie Riendeau, M Koochek et al. · Journal of Medical Genetics · 2009 · 39 citations

A variant Cri du Chat phenotype and autism spectrum disorder in a subject with<i>de novo</i>cryptic microdeletions involving 5p15.2 and 3p24.3‐25 detected using whole genomic array CGH

Chansonette Harvard, Patrick Malenfant, M Koochek et al. · Clinical Genetics · 2005 · 33 citations

Large-scale copy number variants (CNVs): Distribution in normal subjects and FISH/real-time qPCR analysis

Ying Qiao, Xudong Liu, Chansonette Harvard et al. · BMC Genomics · 2007 · 19 citations · Full text