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exaly
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Wellcome Centre for Human Genetics
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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 2018
Title
Journal
Year
Citations
The UK Biobank resource with deep phenotyping and genomic data
Nature
2018
2.1K
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
Nature Genetics
2018
1.3K
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
Nature Genetics
2018
675
Analysis of shared heritability in common disorders of the brain
Science
2018
666
Genomic atlas of the human plasma proteome
Nature
2018
529
The nature of nurture: Effects of parental genotypes
Science
2018
409
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
Nature Genetics
2018
386
Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults: Implications for Primary Prevention
Journal of the American College of Cardiology
2018
285
Multi-ethnic genome-wide association study for atrial fibrillation
Nature Genetics
2018
277
The global distribution and spread of the mobilized colistin resistance gene mcr-1
Nature Communications
2018
268
Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks
Nature Genetics
2018
246
HLA variation and disease
Nature Reviews Immunology
2018
246
Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation
Nature Genetics
2018
239
Are whole-exome and whole-genome sequencing approaches cost-effective? A systematic review of the literature
Genetics in Medicine
2018
238
Structural Remodeling of the Human Colonic Mesenchyme in Inflammatory Bowel Disease
Cell
2018
224
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
Nature Genetics
2018
221
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
Nature Genetics
2018
186
Risk for and consequences of endometriosis: A critical epidemiologic review
Best Practice and Research in Clinical Obstetrics and Gynaecology
2018
186
Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
PLoS Genetics
2018
166
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders
American Journal of Human Genetics
2018
151
53BP1 cooperation with the REV7-shieldin complex underpins DNA structure-specific NHEJ
Nature
2018
148
Long reads: their purpose and place
Human Molecular Genetics
2018
146
A community approach to mortality prediction in sepsis via gene expression analysis
Nature Communications
2018
106
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 genetics
Human Molecular Genetics
2018
98
Impact of spliceosome mutations on RNA splicing in myelodysplasia: dysregulated genes/pathways and clinical associations
Blood
2018
90
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