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

TitleJournalYearCitations
Defining the role of common variation in the genomic and biological architecture of adult human heightNature Genetics20141.3K
Ancient human genomes suggest three ancestral populations for present-day EuropeansNature2014812
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibilityNature Genetics2014784
Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applicationsNature Genetics2014671
Convergence of genes and cellular pathways dysregulated in autism spectrum disordersAmerican Journal of Human Genetics2014635
Crystal structure of a human GABAA receptorNature2014512
Innate immune activity conditions the effect of regulatory variants upon monocyte gene expressionScience2014507
A genetic atlas of human admixture historyScience2014492
Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant dataBMJ, The2014406
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarcheNature2014401
The genetics of major depressionNeuron2014400
A general approach for haplotype phasing across the full spectrum of relatednessPLoS Genetics2014377
Pancreatic islet enhancer clusters enriched in type 2 diabetes risk-associated variantsNature Genetics2014366
Loss-of-function mutations in SLC30A8 protect against type 2 diabetesNature Genetics2014351
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairmentsPLoS Genetics2014340
Quality control and conduct of genome-wide association meta-analysesNature Protocols2014278
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panelNature Communications2014253
Association of vitamin D status with arterial blood pressure and hypertension risk: a mendelian randomisation studyLancet Diabetes and Endocrinology,the2014250
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variantsStroke2014245
Distribution and medical impact of loss-of-function variants in the Finnish founder populationPLoS Genetics2014243
Colorectal cancer cell lines are representative models of the main molecular subtypes of primary cancerCancer Research2014240
Impact of type 2 diabetes susceptibility variants on quantitative glycemic traits reveals mechanistic heterogeneityDiabetes2014235
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacksAmerican Journal of Human Genetics2014233
A genome-wide association study of anorexia nervosaMolecular Psychiatry2014224
Mosaic loss of chromosome Y in peripheral blood is associated with shorter survival and higher risk of cancerNature Genetics2014213