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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 2017
Title
Journal
Year
Citations
Genetic effects on gene expression across human tissues
Nature
2017
2.1K
10 Years of GWAS Discovery: Biology, Function, and Translation
American Journal of Human Genetics
2017
1.7K
Association analysis identifies 65 new breast cancer risk loci
Nature
2017
643
Scater: pre-processing, quality control, normalization and visualization of single-cell RNA-seq data in R
Bioinformatics
2017
563
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
Nature Genetics
2017
530
Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity
Nature
2017
511
Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease
Nature Genetics
2017
462
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
Diabetes
2017
414
Rare and low-frequency coding variants alter human adult height
Nature
2017
412
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples
Genetics in Medicine
2017
386
Oncostatin M drives intestinal inflammation and predicts response to tumor necrosis factor-neutralizing therapy in patients with inflammatory bowel disease
Nature Medicine
2017
344
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
Nature Genetics
2017
313
Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance
Nature Genetics
2017
312
Fine-mapping inflammatory bowel disease loci to single-variant resolution
Nature
2017
311
Exome-wide association study of plasma lipids in >300,000 individuals
Nature Genetics
2017
310
Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study
JAMA Oncology
2017
236
Comprehensive comparison of Pacific Biosciences and Oxford Nanopore Technologies and their applications to transcriptome analysis
F1000Research
2017
236
A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease
Nature Neuroscience
2017
228
PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study
Lancet Diabetes and Endocrinology,the
2017
225
A reference data set of 5.4 million phased human variants validated by genetic inheritance from sequencing a three-generation 17-member pedigree
Genome Research
2017
223
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
PLoS Medicine
2017
223
Same-Day Diagnostic and Surveillance Data for Tuberculosis via Whole-Genome Sequencing of Direct Respiratory Samples
Journal of Clinical Microbiology
2017
221
Genetic markers associated with dihydroartemisinin-piperaquine failure in Plasmodium falciparum malaria in Cambodia: a genotype-phenotype association study
Lancet Infectious Diseases, The
2017
212
Effects of control interventions on Clostridium difficile infection in England: an observational study
Lancet Infectious Diseases, The
2017
202
British Society of Gastroenterology position statement on serrated polyps in the colon and rectum
Gut
2017
187
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