Author details

Full Name

Jennifer Sambrook

Affiliation

ORCID

Career Start Year

2002

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37563721	Evaluation of interventions to prevent vasovagal reactions among whole blood donors: rationale and design of a large cluster randomised trial.	Trials	2023
37596262	A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology.	Nat Commun	2023
33341984	Comparison of four methods to measure haemoglobin concentrations in whole blood donors (COMPARE): A diagnostic accuracy study.	Transfus Med	2021
32750130	Development and validation of a universal blood donor genotyping platform: a multinational prospective study.	Blood Adv	2020
31715324	The Genetic Links to Anxiety and Depression (GLAD) Study: Online recruitment into the largest recontactable study of depression and anxiety.	Behav Res Ther	2019
29091079	NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease.	Mucosal Immunol	2018
27992413	Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease.	Nat Genet	2017
27863252	The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.	Cell	2016
26974950	Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.	Nat Neurosci	2016
27479907	Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.	Nat Genet	2016
27645285	Recruitment and representativeness of blood donors in the INTERVAL randomised trial assessing varying inter-donation intervals.	Trials	2016
25817829	Corrigendum: Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis.	Nat Commun	2015
25230735	The INTERVAL trial to determine whether intervals between blood donations can be safely and acceptably decreased to optimise blood supply: study protocol for a randomised controlled trial.	Trials	2014
24219970	Common genetic variants do not associate with CAD in familial hypercholesterolemia.	Eur J Hum Genet	2014
24588550	The impact on utilities of differences in body weight among Canadian patients with type 2 diabetes.	Current Medical Research and Opinion	2014
23563608	SMIM1 underlies the Vel blood group and influences red blood cell traits.	Nat Genet	2013
23754948	Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits.	PLoS Genet	2013
23563607	Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.	Nat Genet	2013
21989056	Long-range DNA looping and gene expression analyses identify DEXI as an autoimmune disease candidate gene.	Hum Mol Genet	2012
22972982	A GWAS sequence variant for platelet volume marks an alternative DNM3 promoter in megakaryocytes near a MEIS1 binding site.	Blood	2012
22366785	Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome.	Nat Genet	2012
23300628	Powerful identification of cis-regulatory SNPs in human primary monocytes using allele-specific gene expression.	PLoS One	2012
23222517	Seventy-five genetic loci influencing the human red blood cell.	Nature	2012
22017232	Indirect comparison of the efficacy of cetuximab and cisplatin in squamous cell carcinoma of the head and neck.	Current Medical Research and Opinion	2011
21167188	The serotonin transporter gene polymorphism and the effect of baseline on amygdala response to emotional faces.	Neuropsychologia	2011
21853107	Association between walking speed and age in healthy, free-living individuals using mobile accelerometry--a cross-sectional study.	PLoS One	2011
22200769	Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry.	Nat Genet	2011
22139419	New gene functions in megakaryopoiesis and platelet formation.	Nature	2011
22100073	Blood pressure loci identified with a gene-centric array.	Am J Hum Genet	2011
21738480	Multiple loci are associated with white blood cell phenotypes.	PLoS Genet	2011
20360734	Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.	Nature	2010
20881960	Hundreds of variants clustered in genomic loci and biological pathways affect human height.	Nature	2010
20624866	The cost-effectiveness of screening for colorectal cancer.	CMAJ	2010
19862010	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.	Nat Genet	2009
19376310	Fondaparinux versus Enoxaparin in non-ST-elevation acute coronary syndromes: short-term cost and long-term cost-effectiveness using data from the Fifth Organization to Assess Strategies in Acute Ischemic Syndromes Investigators (OASIS-5) trial.	Am Heart J	2009
19820697	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Nat Genet	2009
19915572	Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.	Nat Genet	2009
17884420	Evolutionary vignettes of natural killer cell receptors.	Curr Opin Immunol	2007
17092261	The LRC haplotype project: a resource for killer immunoglobulin-like receptor-linked association studies.	Tissue Antigens	2006
16911775	Identification of the ancestral killer immunoglobulin-like receptor gene in primates.	BMC Genomics	2006
16738944	Identification of a single killer immunoglobulin-like receptor (KIR) gene in the porcine leukocyte receptor complex on chromosome 6q.	Immunogenetics	2006
16271140	A genome-wide survey of Major Histocompatibility Complex (MHC) genes and their paralogues in zebrafish.	BMC Genomics	2005
15632087	Single haplotype analysis demonstrates rapid evolution of the killer immunoglobulin-like receptor (KIR) loci in primates.	Genome Res	2005
12909342	Characterisation of a gene cluster in Fugu rubripes containing the complement component C4 gene.	Gene	2003
12242588	Fugu orthologues of human major histocompatibility complex genes: a genome survey.	Immunogenetics	2002