Works matching IS 03406717 AND DT 2015 AND VI 134 AND IP 11/12

Results: 10

Heritabilities, proportions of heritabilities explained by GWAS findings, and implications of cross-phenotype effects on PR interval.

Published in:

Human Genetics, 2015, v. 134, n. 11/12, p. 1211, doi. 10.1007/s00439-015-1595-9

By:

Silva, Claudia;
Kors, Jan;
Amin, Najaf;
Dehghan, Abbas;
Witteman, Jacqueline;
Willemsen, Rob;
Oostra, Ben;
van Duijn, Cornelia;
Isaacs, Aaron

Publication type:

Article

Pervasive pleiotropy between psychiatric disorders and immune disorders revealed by integrative analysis of multiple GWAS.

Published in:

Human Genetics, 2015, v. 134, n. 11/12, p. 1195, doi. 10.1007/s00439-015-1596-8

By:

Wang, Qian;
Yang, Can;
Gelernter, Joel;
Zhao, Hongyu

Publication type:

Article

Ghazi M Rayan and Joseph Upton III: Congenital Hand Anomalies and Associated Syndromes.

Published in:

2015

By:

Newbury-Ecob, Ruth

Publication type:

Book Review

A genome-wide association study for colorectal cancer identifies a risk locus in 14q23.1.

Published in:

Human Genetics, 2015, v. 134, n. 11/12, p. 1249, doi. 10.1007/s00439-015-1598-6

By:

Lemire, Mathieu;
Qu, Conghui;
Loo, Lenora;
Zaidi, Syed;
Wang, Hansong;
Berndt, Sonja;
Bézieau, Stéphane;
Brenner, Hermann;
Campbell, Peter;
Chan, Andrew;
Chang-Claude, Jenny;
Du, Mengmeng;
Edlund, Christopher;
Gallinger, Steven;
Haile, Robert;
Harrison, Tabitha;
Hoffmeister, Michael;
Hopper, John;
Hou, Lifang;
Hsu, Li

Publication type:

Article

Scrutinizing the FTO locus: compelling evidence for a complex, long-range regulatory context.

Published in:

Human Genetics, 2015, v. 134, n. 11/12, p. 1183, doi. 10.1007/s00439-015-1599-5

By:

Rask-Andersen, Mathias;
Almén, Markus;
Schiöth, Helgi

Publication type:

Article

Computational functional genomics based analysis of pain-relevant micro-RNAs.

Published in:

Human Genetics, 2015, v. 134, n. 11/12, p. 1221, doi. 10.1007/s00439-015-1600-3

By:

Lötsch, Jörn;
Niederberger, Ellen;
Ultsch, Alfred

Publication type:

Article

A review of genome-wide association studies for multiple sclerosis: classical and hypothesis-driven approaches.

Published in:

Human Genetics, 2015, v. 134, n. 11/12, p. 1143, doi. 10.1007/s00439-015-1601-2

By:

Bashinskaya, V.;
Kulakova, O.;
Boyko, A.;
Favorov, A.;
Favorova, O.

Publication type:

Article

Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family.

Published in:

Human Genetics, 2015, v. 134, n. 11/12, p. 1239, doi. 10.1007/s00439-015-1602-1

By:

Einarsdottir, Elisabet;
Svensson, Idor;
Darki, Fahimeh;
Peyrard-Janvid, Myriam;
Lindvall, Jessica;
Ameur, Adam;
Jacobsson, Christer;
Klingberg, Torkel;
Kere, Juha;
Matsson, Hans

Publication type:

Article

Association between telomere length and chromosome 21 nondisjunction in the oocyte.

Published in:

Human Genetics, 2015, v. 134, n. 11/12, p. 1263, doi. 10.1007/s00439-015-1603-0

By:

Albizua, I.;
Rambo-Martin, B.;
Allen, E.;
He, W.;
Amin, A.;
Sherman, S.

Publication type:

Article

Copy number variants in patients with intellectual disability affect the regulation of ARX transcription factor gene.

Published in:

Human Genetics, 2015, v. 134, n. 11/12, p. 1163, doi. 10.1007/s00439-015-1594-x

By:

Ishibashi, Minaka;
Manning, Elizabeth;
Shoubridge, Cheryl;
Krecsmarik, Monika;
Hawkins, Thomas;
Giacomotto, Jean;
Zhao, Ting;
Mueller, Thomas;
Bader, Patricia;
Cheung, Sau;
Stankiewicz, Pawel;
Bain, Nicole;
Hackett, Anna;
Reddy, Chilamakuri;
Mechaly, Alejandro;
Peers, Bernard;
Wilson, Stephen;
Lenhard, Boris;
Bally-Cuif, Laure;
Gecz, Jozef

Publication type:

Article