Výsledky vyhledávání - Andrew Polyak
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Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants Autor Lucilla Pizzo, Matthew Jensen, Andrew Polyak, Jill A. Rosenfeld, Katrin Männik, Arjun Krishnan, M. Elizabeth McCready, Olivier Pichon, Cédric Le Caignec, Anke Van Dijck, Kate Pope, Els Voorhoeve, Jieun Yoon, Paweł Stankiewicz, Sau Wai Cheung, Damian Pazuchanics, Emily Huber, Vijay Kumar, Rachel L. Kember, Francesca Mari, Aurora Currò, Lucia Castiglia, Ornella Galesi, Emanuela Avola, Teresa Mattina, Marco Fichera, Luana Mandarà, Marie Vincent, Mathilde Nizon, Sandra Mercier, Claire Bénéteau, Sophie Blesson, Dominique Martin–Coignard, Anne-Laure Mosca-Boidron, Jean-Hubert Caberg, Maja Bućan, Susan Zeesman, Małgorzata J.M. Nowaczyk, Mathilde Lefebvre, Laurence Faivre, Patrick Callier, Cindy Skinner, Boris Keren, Perrine Charles, Paolo Prontera, Nathalie Marle, Alessandra Renieri, Alexandre Reymond, R. Frank Kooy, Bertrand Isidor, Charles E. Schwartz, Corrado Romano, Erik A. Sistermans, David J. Amor, Joris Andrieux, Santhosh Girirajan
Vydáno 2018Artigo
Vyhledávací nástroje:
Související témata
Medicine
Psychiatry
Autism
Bioinformatics
Biology
Gene
Genetics
Clinical psychology
Comorbidity
Computational biology
Copy-number variation
Disease
Epilepsy
Exome
Exome sequencing
Gene expression
Genetic heterogeneity
Genetic syndromes
Genome
Human genetics
Intellectual disability
Internal medicine
Microarray
Mutation
Neurology
Pediatrics
Phenotype
Proband
Psychology