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exaly
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Wellcome Centre for Human Genetics
›
Top Articles
Wellcome Centre for Human Genetics
United Kingdom
(well.ox.ac.uk)
5.2K
(top 5%)
articles
462.9K
(top 2%)
citations
1,910
(top 3%)
★★
articles
504
(top 1%)
★★★
articles
7.5
(top 1%)
Avg IF
298
(top 1%)
H-Index
522
(top 1%)
G-Index
954
journals
Most Cited Articles of Wellcome Centre for Human Genetics in 2014
Title
Journal
Year
Citations
Defining the role of common variation in the genomic and biological architecture of adult human height
Nature Genetics
2014
1.3K
Ancient human genomes suggest three ancestral populations for present-day Europeans
Nature
2014
812
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
Nature Genetics
2014
784
Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications
Nature Genetics
2014
671
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
American Journal of Human Genetics
2014
635
Crystal structure of a human GABAA receptor
Nature
2014
512
Innate immune activity conditions the effect of regulatory variants upon monocyte gene expression
Science
2014
507
A genetic atlas of human admixture history
Science
2014
492
Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data
BMJ, The
2014
406
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
Nature
2014
401
The genetics of major depression
Neuron
2014
400
A general approach for haplotype phasing across the full spectrum of relatedness
PLoS Genetics
2014
377
Pancreatic islet enhancer clusters enriched in type 2 diabetes risk-associated variants
Nature Genetics
2014
366
Loss-of-function mutations in SLC30A8 protect against type 2 diabetes
Nature Genetics
2014
351
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments
PLoS Genetics
2014
340
Quality control and conduct of genome-wide association meta-analyses
Nature Protocols
2014
278
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
Nature Communications
2014
253
Association of vitamin D status with arterial blood pressure and hypertension risk: a mendelian randomisation study
Lancet Diabetes and Endocrinology,the
2014
250
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants
Stroke
2014
245
Distribution and medical impact of loss-of-function variants in the Finnish founder population
PLoS Genetics
2014
243
Colorectal cancer cell lines are representative models of the main molecular subtypes of primary cancer
Cancer Research
2014
240
Impact of type 2 diabetes susceptibility variants on quantitative glycemic traits reveals mechanistic heterogeneity
Diabetes
2014
235
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks
American Journal of Human Genetics
2014
233
A genome-wide association study of anorexia nervosa
Molecular Psychiatry
2014
224
Mosaic loss of chromosome Y in peripheral blood is associated with shorter survival and higher risk of cancer
Nature Genetics
2014
213
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