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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 67,594 bioRxiv papers from 298,144 authors.

Author: Tarjinder Singh

  • ORCiD: http://orcid.org/0000-0003-0601-6815
  • Most recently observed institution: Analytic and Translational Genetics Unit, Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA 02114, USA; 2Program in Medical and Population Genetics, Broad Institute of MIT and Harvard

Rankings

  • All-time downloads: 21,628 (rank: 1,179 out of 298,067)
  • Categories:
    • genetics: 20,716 (rank: 288 out of 29,770)
    • genomics: 912 (rank: 14,804 (tie) out of 33,991)

Downloads per author, site-wide

Preprints

Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism

genetics more details view paper
  • Downloaded 7,094 times
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    • Site-wide: 234 out of 67,591
    • In genetics: 23 out of 3,799
  • Year to date:
    • Site-wide: 99 out of 67,591
  • Since beginning of last month:
    • Site-wide: 205 out of 67,591

Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation

genetics more details view paper
  • Downloaded 6,969 times
  • Download rankings, all-time:
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    • In genetics: 25 out of 3,799
  • Year to date:
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  • Since beginning of last month:
    • Site-wide: 23,072 out of 67,591

De novo Variants In Neurodevelopmental Disorders With Epilepsy

genetics more details view paper
  • Downloaded 1,556 times
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    • In genetics: 321 out of 3,799
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  • Since beginning of last month:
    • Site-wide: 23,868 out of 67,591

Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals

genetics more details view paper
  • Downloaded 1,529 times
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    • In genetics: 333 out of 3,799
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    • Site-wide: 914 out of 67,591
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    • Site-wide: 7,129 out of 67,591

ASD and ADHD have a similar burden of rare protein-truncating variants

genetics more details view paper
  • Downloaded 1,315 times
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    • In genetics: 403 out of 3,799
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Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

genomics more details view paper
  • Downloaded 912 times
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    • In genomics: 1,382 out of 4,581
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Rare schizophrenia risk variants are enriched in genes shared with neurodevelopmental disorders

genetics more details view paper
  • Downloaded 835 times
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Contribution of Retrotransposition to Developmental Disorders

genetics more details view paper
  • Downloaded 631 times
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    • Site-wide: 31,217 out of 67,591

Schizophrenia risk conferred by protein-coding de novo mutations

genetics more details view paper
  • Downloaded 620 times
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Meta-analysis of Scandinavian Schizophrenia Exomes

genetics more details view paper
  • Downloaded 167 times
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    • In genetics: 3,132 out of 3,799
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