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