Standout Papers

The variant call format and VCFtools 1999 2026 2008 2017 9.5k
  1. The variant call format and VCFtools (2011)
    Petr Danecek, Adam Auton et al. Bioinformatics
  2. dbSNP: the NCBI database of genetic variation (2001)
    Stephen T. Sherry Nucleic Acids Research
  3. ClinGen — The Clinical Genome Resource (2015)
    Heidi L. Rehm, Jonathan S. Berg et al. New England Journal of Medicine
  4. dbSNP—Database for Single Nucleotide Polymorphisms and Other Classes of Minor Genetic Variation (1999)
    Stephen T. Sherry, Minghong Ward et al. Genome Research

Immediate Impact

8 by Nobel laureates 42 from Science/Nature 105 standout
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Citing Papers

Probiotic neoantigen delivery vectors for precision cancer immunotherapy
2024 StandoutNature
Disease variant prediction with deep generative models of evolutionary data
2021 StandoutNature

Works of Stephen T. Sherry being referenced

ClinGen — The Clinical Genome Resource
2015 Standout
dbSNP: the NCBI database of genetic variation
2001 Standout

Author Peers

Author Last Decade Papers Cites
Stephen T. Sherry 9130 10190 526 3305 96 20.4k
Adam Auton 7677 10688 241 3624 33 18.7k
David Reich 9475 21959 516 3106 176 33.1k
Matthew G. Hanna 8259 6887 278 3361 68 19.4k
Gerton Lunter 7148 7288 104 3454 77 14.9k
Manuel A. R. Ferreira 7520 14333 817 2403 84 26.1k
Shaun Purcell 11413 21712 1163 3165 135 38.0k
Carlos D. Bustamante 8477 15319 388 5185 205 24.3k
D.B. Bender 6562 12535 672 2296 33 23.9k
Steve Rozen 16272 10151 398 8067 112 33.3k
Andrey Sivachenko 14768 10618 437 4456 48 28.0k

All Works

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2026