Author: Tarjinder Singh
- ORCiD: http://orcid.org/0000-0003-0601-6815
- Most recently observed institution: Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA
Rankings
- All-time downloads: 29,285 (rank: 4,473 )
- Categories:
- genetic and genomic medicine: 2,380 (rank: 305 (tie) )
- genetics: 25,902 (rank: 244 )
- genomics: 1,003 (rank: 20,508 (tie) )
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 9,959 times
- Download rankings, all-time:
- Site-wide: 703
- In genetics: 22
- Year to date:
- Site-wide: 3,953
- Since beginning of last month:
- Site-wide: 3,336
Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation
genetics more details view paper- Downloaded 7,391 times
- Download rankings, all-time:
- Site-wide: 1,035
- In genetics: 36
- Year to date:
- Site-wide: 12,918
- Since beginning of last month:
- Site-wide: 25,218
Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia
genetic and genomic medicine more details view paper- Downloaded 2,380 times
- Download rankings, all-time:
- Site-wide: 5,081
- In genetic and genomic medicine: 12
- Year to date:
- Site-wide: 1,093
- Since beginning of last month:
- Site-wide: 1,394
Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals
genetics more details view paper- Downloaded 1,979 times
- Download rankings, all-time:
- Site-wide: 6,629
- In genetics: 334
- Year to date:
- Site-wide: 24,004
- Since beginning of last month:
- Site-wide: 37,768
De novo Variants In Neurodevelopmental Disorders With Epilepsy
genetics more details view paper- Downloaded 1,901 times
- Download rankings, all-time:
- Site-wide: 7,054
- In genetics: 347
- Year to date:
- Site-wide: 27,351
- Since beginning of last month:
- Site-wide: 43,598
ASD and ADHD have a similar burden of rare protein-truncating variants
genetics more details view paper- Downloaded 1,685 times
- Download rankings, all-time:
- Site-wide: 8,463
- In genetics: 431
- Year to date:
- Site-wide: 18,038
- Since beginning of last month:
- Site-wide: 65,174
Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders
genomics more details view paper- Downloaded 1,003 times
- Download rankings, all-time:
- Site-wide: 18,483
- In genomics: 1,931
- Year to date:
- Site-wide: 74,501
- Since beginning of last month:
- Site-wide: 91,371
Rare schizophrenia risk variants are enriched in genes shared with neurodevelopmental disorders
genetics more details view paper- Downloaded 982 times
- Download rankings, all-time:
- Site-wide: 19,051
- In genetics: 969
- Year to date:
- Site-wide: 95,212
- Since beginning of last month:
- Site-wide: 92,715
Schizophrenia risk conferred by protein-coding de novo mutations
genetics more details view paper- Downloaded 819 times
- Download rankings, all-time:
- Site-wide: 24,720
- In genetics: 1,243
- Year to date:
- Site-wide: 67,996
- Since beginning of last month:
- Site-wide: 71,474
Contribution of Retrotransposition to Developmental Disorders
genetics more details view paper- Downloaded 776 times
- Download rankings, all-time:
- Site-wide: 26,651
- In genetics: 1,348
- Year to date:
- Site-wide: 116,879
- Since beginning of last month:
- Site-wide: 66,101
Meta-analysis of Scandinavian Schizophrenia Exomes
genetics more details view paper- Downloaded 410 times
- Download rankings, all-time:
- Site-wide: 58,383
- In genetics: 2,801
- Year to date:
- Site-wide: 82,719
- Since beginning of last month:
- Site-wide: 94,942
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