Suchergebnisse - "Attwood, Antony P"

PubPharm (28)

1

A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders

enthalten in: Blood | 2016

von Simeoni, I. | Stephens, J. | Hu, F. | +76

CommentIn: Blood. 2016 Jun 9;127(23 ):2781-2. - PMID 27282940

2

A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders

enthalten in: Blood | 2016

von Simeoni, I. | Stephens, J. | Hu, F. | +76

3

Genetic studies of body mass index yield new insights for obesity biology

enthalten in: Nature | 2015

von Locke, A. | Kahali, B. | Berndt, S. | +112

CommentIn: Cell Metab. 2015 Apr 7;21(4):507-8. - PMID 25863240

4

Genetic studies of body mass index yield new insights for obesity biology

enthalten in: Nature | 2015

von Locke, A. | Kahali, B. | Berndt, S. | +98

5

Quality control and conduct of genome-wide association meta-analyses

enthalten in: Nature protocols | 2014

von Winkler, T. | Day, F. | Croteau-Chonka, D. | +119

6

Meta-analysis of gene-level associations for rare variants based on single-variant statistics

enthalten in: American journal of human genetics | 2013

von Hu, Y. | Berndt, S. | Gustafsson, S. | +106

7

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

enthalten in: Nature genetics | 2013

von Berndt, S. | Gustafsson, S. | Mägi, R. | +98

8

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

enthalten in: Nature genetics | 2013

von Berndt, S. | Gustafsson, S. | Mägi, R. | +96

9

Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis : two genome-wide association studies

enthalten in: Lancet (London, England) | 2011

von Reilly, M. | Li, M. | He, J. | +131

CommentIn: Lancet. 2011 Jan 29;377(9763):356-8. - PMID 21239053

10

Rare copy number variants : a point of rarity in genetic risk for bipolar disorder and schizophrenia

enthalten in: Archives of general psychiatry | 2010

von Grozeva, D. | Kirov, G. | Ivanov, D. | +113