Suchergebnisse - "Jolley, Jennifer D"

PubPharm (31)

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

Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders

enthalten in: Genome medicine | 2015

von Westbury, S. | Turro, E. | Greene, D. | +37

4

Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders

enthalten in: Genome medicine | 2015

von Westbury, S. | Turro, E. | Greene, D. | +37

5

Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders

enthalten in: Genome medicine | 2015

von Westbury, S. | Turro, E. | Greene, D. | +38

6

Estimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip data

enthalten in: Human molecular genetics | 2014

von Chen, G. | Lee, S. | Brion, M. | +105

7

Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer

enthalten in: Nature | 2013

von Ruark, E. | Snape, K. | Humburg, P. | +161

8

Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease

enthalten in: PloS one | 2013

von Huertas-Vazquez, A. | Nelson, C. | Guo, X. | +121

9

Bayesian refinement of association signals for 14 loci in 3 common diseases

enthalten in: Nature genetics | 2012

von Wellcome Trust Case Control Consortium | Maller, J. | McVean, G. | +135

10

Seven newly identified loci for autoimmune thyroid disease

enthalten in: Human molecular genetics | 2012

von Cooper, J. | Simmonds, M. | Walker, N. | +110