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

TitleJournalYearCitations
Genetic effects on gene expression across human tissuesNature20172.1K
10 Years of GWAS Discovery: Biology, Function, and TranslationAmerican Journal of Human Genetics20171.7K
Association analysis identifies 65 new breast cancer risk lociNature2017643
Scater: pre-processing, quality control, normalization and visualization of single-cell RNA-seq data in RBioinformatics2017563
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjectsNature Genetics2017530
Epigenome-wide association study of body mass index, and the adverse outcomes of adiposityNature2017511
Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel diseaseNature Genetics2017462
An Expanded Genome-Wide Association Study of Type 2 Diabetes in EuropeansDiabetes2017414
Rare and low-frequency coding variants alter human adult heightNature2017412
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samplesGenetics in Medicine2017386
Oncostatin M drives intestinal inflammation and predicts response to tumor necrosis factor-neutralizing therapy in patients with inflammatory bowel diseaseNature Medicine2017344
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular riskNature Genetics2017313
Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistanceNature Genetics2017312
Fine-mapping inflammatory bowel disease loci to single-variant resolutionNature2017311
Exome-wide association study of plasma lipids in >300,000 individualsNature Genetics2017310
Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization StudyJAMA Oncology2017236
Comprehensive comparison of Pacific Biosciences and Oxford Nanopore Technologies and their applications to transcriptome analysisF1000Research2017236
A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's diseaseNature Neuroscience2017228
PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation studyLancet Diabetes and Endocrinology,the2017225
A reference data set of 5.4 million phased human variants validated by genetic inheritance from sequencing a three-generation 17-member pedigreeGenome Research2017223
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysisPLoS Medicine2017223
Same-Day Diagnostic and Surveillance Data for Tuberculosis via Whole-Genome Sequencing of Direct Respiratory SamplesJournal of Clinical Microbiology2017221
Genetic markers associated with dihydroartemisinin-piperaquine failure in Plasmodium falciparum malaria in Cambodia: a genotype-phenotype association studyLancet Infectious Diseases, The2017212
Effects of control interventions on Clostridium difficile infection in England: an observational studyLancet Infectious Diseases, The2017202
British Society of Gastroenterology position statement on serrated polyps in the colon and rectumGut2017187