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Academic Journal

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Authors : Marshall, CR; Howrigan, DP; Merico, D

Subjects: Medicin och hälsovetenskap

Source: Nature genetics. 49(1):27-35

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Academic Journal

The impact of low-frequency and rare variants on lipid levels

Authors : Surakka, I; Horikoshi, M; Magi, R

Subjects: Medicin och hälsovetenskap

Source: Nature genetics. 47(6):589-597

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Academic Journal

Defining the role of common variation in the genomic and biological architecture of adult human height

Authors : Wood, AR; Esko, T; Yang, J

Subjects: Medicin och hälsovetenskap

Source: Nature genetics. 46(11):1173-1186

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Academic Journal

Genetic analyses identify widespread sex-differential participation bias

Authors : Pirastu, N; Cordioli, M; Nandakumar, P

Subjects: Medicin och hälsovetenskap

Source: Nature genetics. 53(5):663

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Academic Journal

New insights into the genetic etiology of Alzheimer’s disease and related dementias

Authors : Bellenguez C.; Küçükali F.; Jansen I.E.

Subjects: genome-wide association; necrosis-factor-alpha; risk loci

Source: Nature Genetics

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Academic Journal

Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

Authors : Huckins, LM; Dobbyn, A; Ruderfer, DM

Subjects: Medicin och hälsovetenskap

Source: Nature genetics. 51(4):659

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Academic Journal

Systematic identification of trans eQTLs as putative drivers of known disease associations.

Authors : Westra HJ; Department of Genetics, University Medical Center Groningen, University of Groningen, Hanzeplein 1, Groningen, the Netherlands.; Peters MJ

Subjects: Genetic Predisposition to Disease* ; Quantitative Trait Loci*; Diabetes Mellitus, Type 1/Diabetes Mellitus, Type 1/Diabetes Mellitus, Type 1/genetics

Source: Nature genetics [Nat Genet] 2013 Oct; Vol. 45 (10), pp. 1238-1243. Date of Electronic Publication: 2013 Sep 08.Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

SMIM1 underlies the Vel blood group and influences red blood cell traits.

Authors : Cvejic A; Department of Haematology, University of Cambridge, CB2 0PT, United Kingdom.; Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1HH, United Kingdom.

Subjects: Gene Deletion* ; Homozygote* ; Quantitative Trait Loci*

Source: Nature genetics [Nat Genet] 2013 May; Vol. 45 (5), pp. 542-545. Date of Electronic Publication: 2013 Apr 07.Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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