A population genetic approach to mapping neurological disorder genes using deep resequencing

PLoS Genetics

Volumn 7, Issue 2, 2011, Pages

  Myers, Rachel A ^a,b,c   Casals, Ferran ^a   Gauthier, Julie ^a,d   Hamdan, Fadi F ^a,d   Keebler, Jon ^a,b,c   Boyko, Adam R ^e   Bustamante, Carlos D ^e   Piton, Amelie M ^a,d   Spiegelman, Dan ^a,d   Henrion, Edouard ^a,d   Zilversmit, Martine ^a   Hussin, Julie ^a   Quinlan, Jacklyn ^a   Yang, Yan ^a,d   Lafrenière, Ronald G ^a,d   Griffing, Alexander R ^c   Stone, Eric A ^c   Rouleau, Guy A ^a,b,d   Awadalla, Philip ^a,b,c,d  

^a UNIVERSITÉ DE MONTRÉAL   (Canada)

^b UNIVERSITY OF MONTREAL   (Canada)

^c NORTH CAROLINA STATE UNIVERSITY   (United States)

^d UNIVERSITY OF MONTREAL   (Canada)

^e STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; AUTISM; CACNA1F GENE; COHORT ANALYSIS; CONTROLLED STUDY; DEEP RESEQUENCING; DEMOGRAPHY; FEMALE; GENE; GENE FREQUENCY; GENE MAPPING; GENE SEQUENCE; GENETIC ASSOCIATION; GRIN2B GENE; HUMAN; MAJOR CLINICAL STUDY; MALE; MAP1A GENE; MISSENSE MUTATION; NONSENSE MUTATION; POPULATION GENETICS; SCHIZOPHRENIA; SINGLE NUCLEOTIDE POLYMORPHISM; CHILD; CHROMOSOME MAP; DNA SEQUENCE; GENE LOCUS; GENETIC SELECTION; GENETICS; MUTATION;

CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; CHROMOSOME MAPPING; COHORT STUDIES; FEMALE; GENETIC LOCI; GENETICS, POPULATION; HUMANS; MALE; MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; SCHIZOPHRENIA; SELECTION, GENETIC; SEQUENCE ANALYSIS, DNA;

EID: 79952254931     PISSN: 15537390     EISSN: 15537404     Source Type: Journal    
DOI: 10.1371/journal.pgen.1001318     Document Type: Article

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