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Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 65,403 bioRxiv papers from 289,694 authors.

Author: Anubha Mahajan

Rankings

  • All-time downloads: 28,063 (rank: 692 out of 289,694)
  • Categories:
    • bioinformatics: 1,757 (rank: 4,385 (tie) out of 25,220)
    • epidemiology: 958 (rank: 1,052 out of 9,549)
    • genetics: 18,580 (rank: 344 out of 28,745)
    • genomics: 6,768 (rank: 1,762 out of 32,932)

Downloads per author, site-wide

Preprints

A reference panel of 64,976 haplotypes for genotype imputation

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Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

genomics more details view paper
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Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

genetics more details view paper
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Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

genetics more details view paper
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Genetic discovery and translational decision support from exome sequencing of 20,791 type 2 diabetes cases and 24,440 controls from five ancestries

genetics more details view paper
  • Downloaded 1,411 times
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New genetic signals for lung function highlight pathways and pleiotropy, and chronic obstructive pulmonary disease associations across multiple ancestries

genomics more details view paper
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Developing a network view of type 2 diabetes risk pathways through integration of genetic, genomic and functional data

bioinformatics more details view paper
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PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

genetics more details view paper
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    • In genetics: 475 out of 3,699
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Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

genetics more details view paper
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Influence of genetic variants on gene expression in human pancreatic islets – implications for type 2 diabetes

genomics more details view paper
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Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure

genetics more details view paper
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    • In genetics: 640 out of 3,699
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Narrow-sense heritability estimation of complex traits using identity-by-descent information.

genetics more details view paper
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    • In genetics: 655 out of 3,699
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    • Site-wide: 30,832 out of 65,403

Identification of type 2 diabetes loci in 433,540 East Asian individuals

genetics more details view paper
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Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci

genomics more details view paper
  • Downloaded 869 times
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Large-Scale Genome-Wide Meta Analysis of Polycystic Ovary Syndrome Suggests Shared Genetic Architecture for Different Diagnosis Criteria.

genetics more details view paper
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Causal relationships between obesity and the leading causes of death in women and men

epidemiology more details view paper
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Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

genomics more details view paper
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    • Site-wide: 54,831 out of 65,403

Trans-ethnic genome-wide association study provides insight into effector genes and molecular mechanisms for kidney function and highlights a causal effect on kidney-specific disease aetiologies

genetics more details view paper
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    • In genetics: 1,126 out of 3,699
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Deep learning models predict regulatory variants in pancreatic islets and refine type 2 diabetes association signals

bioinformatics more details view paper
  • Downloaded 526 times
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    • In bioinformatics: 2,840 out of 6,484
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    • Site-wide: 6,692 out of 65,403

Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

genetics more details view paper
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Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 are associated with gestational duration

genetics more details view paper
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    • In genetics: 1,695 out of 3,699
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    • Site-wide: 44,020 out of 65,403

Meta-analysis of exome array data identifies six novel genetic loci for lung function

genetics more details view paper
  • Downloaded 382 times
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    • In genetics: 1,786 out of 3,699
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Multi-ancestry GWAS of the electrocardiographic PR interval identifies 210 loci underlying cardiac conduction

genetics more details view paper
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    • In genetics: 2,191 out of 3,699
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Discovery of biomarkers for glycaemic deterioration before and after the onset of type 2 diabetes: an overview of the data from the epidemiological studies within the IMI DIRECT Consortium

epidemiology more details view paper
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Variation in the plasma membrane monoamine transporter (PMAT, encoded in SLC29A4) and organic cation transporter 1 (OCT1, encoded in SLC22A1) and gastrointestinal intolerance to metformin in type 2 diabetes: an IMI DIRECT study

genetics more details view paper
  • Downloaded 236 times
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    • In genetics: 2,546 out of 3,699
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Elevated risk of invasive group A streptococcal disease and host genetic variation in the human leukocyte antigen locus

genetics more details view paper
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    • In genetics: 2,935 out of 3,699
  • Year to date:
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    • Site-wide: 27,314 out of 65,403

Multifaceted genome-wide study identifies novel regulatory loci for body mass index in Indians

genomics more details view paper
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    • In genomics: 4,202 out of 4,463
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