Author details

Full Name

Emma Gray

Affiliation

ORCID

Career Start Year

2000

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
34757812	Quality of Life in Men With Prostate Cancer Randomly Allocated to Receive Docetaxel or Abiraterone in the STAMPEDE Trial.	J Clin Oncol	2022
35796042	Cost-effectiveness of pembrolizumab plus chemotherapy as first-line treatment in PD-L1-positive metastatic triple-negative breast cancer.	Immunotherapy	2022
28578639	Abiraterone for Prostate Cancer Not Previously Treated with Hormone Therapy.	N Engl J Med	2017
27236921	Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children.	Am J Hum Genet	2016
25671699	Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes.	PLoS Genet	2015
25003214	The correlation between reading and mathematics ability at age twelve has a substantial genetic component.	Nat Commun	2014
23996224	Cognitive-behavioral therapy for bulimia nervosa and atypical bulimic nervosa: effectiveness in clinical settings.	International Journal of Eating Disorders	2014
23871474	A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation.	Biol Psychiatry	2014
23717212	Imputation-based meta-analysis of severe malaria in three African populations.	PLoS Genet	2013
23974872	Genome-wide association analysis identifies 13 new risk loci for schizophrenia.	Nat Genet	2013
23835762	Pegylated liposomal doxorubicin for relapsed epithelial ovarian cancer.		2013
23291585	Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis.	Nat Genet	2013
21989056	Long-range DNA looping and gene expression analyses identify DEXI as an autoimmune disease candidate gene.	Hum Mol Genet	2012
22306652	Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke.	Nat Genet	2012
22961001	Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.	Nat Genet	2012
21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Nature	2011
21044948	Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.	Hum Mol Genet	2011
21186350	Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes.	Nat Genet	2011
20360734	Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.	Nature	2010
20953190	A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.	Nat Genet	2010
20395598	Association of the 9p21.3 locus with risk of first-ever myocardial infarction in Pakistanis: case-control study in South Asia and updated meta-analysis of Europeans.	Arterioscler Thromb Vasc Biol	2010
19915572	Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.	Nat Genet	2009
18185940	Cortical alpha-synuclein load is associated with amyloid-beta plaque burden in a subset of Parkinson's disease patients.	Acta Neuropathol	2008
11030696	Family histories of cancer in primary care. Nurse led clinic may provide better service than computer program.		2000