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Author: Siddharth Banka

  • ORCiD: http://orcid.org/0000-0002-8527-2210
  • Most recently observed institution: Division of Evolution and Genomic Sciences, School of Biological Sciences, University of Manchester

Rankings

  • All-time downloads: 9,045 (rank: 17,164 (tie) out of 509,520)
  • Categories:
    • genetic and genomic medicine: 710 (rank: 1,435 (tie) out of 6,821)
    • genetics: 8,335 (rank: 2,006 out of 38,578)

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Preprints

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

genetics more details view paper
  • Downloaded 7,329 times
  • Download rankings, all-time:
    • Site-wide: 959 out of 118,102
    • In genetics: 34 out of 5,131
  • Year to date:
    • Site-wide: 21,772 out of 118,102
  • Since beginning of last month:
    • Site-wide: 29,088 out of 118,102

Heterozygous variants in KMT2E cause a spectrum of neurodevelopmental disorders and epilepsy

genetics more details view paper
  • Downloaded 611 times
  • Download rankings, all-time:
    • Site-wide: 33,931 out of 118,102
    • In genetics: 1,741 out of 5,131
  • Year to date:
    • Site-wide: 68,890 out of 118,102
  • Since beginning of last month:
    • Site-wide: 85,112 out of 118,102

Non-coding variants upstream of MEF2C cause severe developmental disorder through three distinct loss-of-function mechanisms

genetic and genomic medicine more details view paper
  • Downloaded 491 times
  • Download rankings, all-time:
    • Site-wide: 44,237 out of 118,102
    • In genetic and genomic medicine: 102 out of 480
  • Year to date:
    • Site-wide: 14,260 out of 118,102
  • Since beginning of last month:
    • Site-wide: 1,381 out of 118,102

Delineation of the First Human Mendelian Disorder of the DNA Demethylation Machinery: TET3 Deficiency

genetics more details view paper
  • Downloaded 395 times
  • Download rankings, all-time:
    • Site-wide: 55,895 out of 118,102
    • In genetics: 2,755 out of 5,131
  • Year to date:
    • Site-wide: 64,472 out of 118,102
  • Since beginning of last month:
    • Site-wide: 57,528 out of 118,102

Genotype-phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders

genetic and genomic medicine more details view paper
  • Downloaded 219 times
  • Download rankings, all-time:
    • Site-wide: 87,002 out of 118,102
    • In genetic and genomic medicine: 251 out of 480
  • Year to date:
    • Site-wide: 38,190 out of 118,102
  • Since beginning of last month:
    • Site-wide: 8,117 out of 118,102

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