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 2018

TitleJournalYearCitations
The UK Biobank resource with deep phenotyping and genomic dataNature20182.1K
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depressionNature Genetics20181.3K
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome mapsNature Genetics2018675
Analysis of shared heritability in common disorders of the brainScience2018666
Genomic atlas of the human plasma proteomeNature2018529
The nature of nurture: Effects of parental genotypesScience2018409
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traitsNature Genetics2018386
Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults: Implications for Primary PreventionJournal of the American College of Cardiology2018285
Multi-ethnic genome-wide association study for atrial fibrillationNature Genetics2018277
The global distribution and spread of the mobilized colistin resistance gene mcr-1Nature Communications2018268
Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marksNature Genetics2018246
HLA variation and diseaseNature Reviews Immunology2018246
Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variationNature Genetics2018239
Are whole-exome and whole-genome sequencing approaches cost-effective? A systematic review of the literatureGenetics in Medicine2018238
Structural Remodeling of the Human Colonic Mesenchyme in Inflammatory Bowel DiseaseCell2018224
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetesNature Genetics2018221
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesityNature Genetics2018186
Risk for and consequences of endometriosis: A critical epidemiologic reviewBest Practice and Research in Clinical Obstetrics and Gynaecology2018186
Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteriaPLoS Genetics2018166
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex DisordersAmerican Journal of Human Genetics2018151
53BP1 cooperation with the REV7-shieldin complex underpins DNA structure-specific NHEJNature2018148
Long reads: their purpose and placeHuman Molecular Genetics2018146
A community approach to mortality prediction in sepsis via gene expression analysisNature Communications2018106
Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal geneticsHuman Molecular Genetics201898
Impact of spliceosome mutations on RNA splicing in myelodysplasia: dysregulated genes/pathways and clinical associationsBlood201890