World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
84
Citations
55383
World Ranking
1332
National Ranking
631

Shrikant Mane publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where Shrikant Mane sits on this spectrum.

45–54 publications: 6 scientists 55–64 publications: 10 scientists 65–74 publications: 35 scientists 75–84 publications: 84 scientists 85–94 publications: 102 scientists 95–104 publications: 151 scientists 105–114 publications: 175 scientists 115–124 publications: 203 scientists 125–134 publications: 217 scientists 135–144 publications: 205 scientists 145–154 publications: 193 scientists 155–164 publications: 188 scientists 165–174 publications: 170 scientists 175–184 publications: 178 scientists 185–194 publications: 164 scientists 195–204 publications: 173 scientists 205–214 publications: 159 scientists 215–224 publications: 134 scientists 225–234 publications: 143 scientists 235–244 publications: 105 scientists 245–254 publications: 114 scientists 255–264 publications: 92 scientists 265–274 publications: 88 scientists 275–284 publications: 87 scientists 285–294 publications: 80 scientists 295–304 publications: 62 scientists 305–314 publications: 75 scientists 315–324 publications: 67 scientists 325–334 publications: 60 scientists 335–344 publications: 52 scientists 345–354 publications: 40 scientists 355–364 publications: 48 scientists 365–374 publications: 47 scientists 375–384 publications: 46 scientists 385–394 publications: 31 scientists 395–404 publications: 27 scientists 405–414 publications: 40 scientists 415–424 publications: 30 scientists 425–434 publications: 43 scientists 435–444 publications: 29 scientists 445–454 publications: 14 scientists 455–464 publications: 28 scientists 465–474 publications: 21 scientists 475–484 publications: 21 scientists 485–494 publications: 22 scientists 495–504 publications: 17 scientists 505–514 publications: 12 scientists 515–524 publications: 11 scientists 525–534 publications: 8 scientists 535–544 publications: 8 scientists 545–554 publications: 14 scientists 555–564 publications: 4 scientists 565–574 publications: 11 scientists 575–584 publications: 5 scientists 585–594 publications: 11 scientists 595–604 publications: 12 scientists 605–614 publications: 7 scientists 615–624 publications: 6 scientists 625–634 publications: 10 scientists 635–644 publications: 9 scientists 645–654 publications: 10 scientists 655–664 publications: 6 scientists 665–674 publications: 6 scientists 675–684 publications: 6 scientists 685–694 publications: 4 scientists 695–702 publications: 6 scientists 703+ publications: 100 scientists
45 publications 703+

This scientist: 193 publications — 48th percentile

48% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 703 publications or more.

Shrikant Mane D-index placement in Genetics in 2026

The chart shows the D-index (discipline H-index) distribution of Genetics scientists ranked by Research.com in 2026. The highlighted bar marks where Shrikant Mane sits on this spectrum.

40–41 D-Index: 24 scientists 42–43 D-Index: 52 scientists 44–45 D-Index: 84 scientists 46–47 D-Index: 112 scientists 48–49 D-Index: 118 scientists 50–51 D-Index: 141 scientists 52–53 D-Index: 143 scientists 54–55 D-Index: 145 scientists 56–57 D-Index: 179 scientists 58–59 D-Index: 162 scientists 60–61 D-Index: 175 scientists 62–63 D-Index: 191 scientists 64–65 D-Index: 172 scientists 66–67 D-Index: 184 scientists 68–69 D-Index: 164 scientists 70–71 D-Index: 158 scientists 72–73 D-Index: 150 scientists 74–75 D-Index: 136 scientists 76–77 D-Index: 127 scientists 78–79 D-Index: 127 scientists 80–81 D-Index: 111 scientists 82–83 D-Index: 110 scientists 84–85 D-Index: 110 scientists 86–87 D-Index: 84 scientists 88–89 D-Index: 102 scientists 90–91 D-Index: 66 scientists 92–93 D-Index: 72 scientists 94–95 D-Index: 70 scientists 96–97 D-Index: 54 scientists 98–99 D-Index: 60 scientists 100–101 D-Index: 49 scientists 102–103 D-Index: 55 scientists 104–105 D-Index: 45 scientists 106–107 D-Index: 42 scientists 108–109 D-Index: 28 scientists 110–111 D-Index: 39 scientists 112–113 D-Index: 25 scientists 114–115 D-Index: 31 scientists 116–117 D-Index: 29 scientists 118–119 D-Index: 34 scientists 120–121 D-Index: 29 scientists 122–123 D-Index: 29 scientists 124–125 D-Index: 18 scientists 126–127 D-Index: 27 scientists 128–129 D-Index: 22 scientists 130–131 D-Index: 16 scientists 132–133 D-Index: 11 scientists 134–135 D-Index: 17 scientists 136–137 D-Index: 12 scientists 138–139 D-Index: 21 scientists 140–141 D-Index: 4 scientists 142–143 D-Index: 9 scientists 144–145 D-Index: 14 scientists 146–147 D-Index: 6 scientists 148–149 D-Index: 10 scientists 150–151 D-Index: 7 scientists 152–153 D-Index: 9 scientists 154–155 D-Index: 8 scientists 156–157 D-Index: 8 scientists 158–159 D-Index: 9 scientists 160+ D-Index: 96 scientists
40 D-Index 160+

This scientist: 84 D-Index — 69th percentile

69% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 160 D-Index or more.

Overview

Shrikant Mane is affiliated with Yale University in the United States. Their research spans across multiple disciplines within medicine and biochemistry, genetics, and molecular biology, reflecting a diverse and interdisciplinary scientific profile.

Their primary fields of study include:

  • Medicine
  • Biochemistry, Genetics and Molecular Biology

Within these broader areas, Shrikant Mane concentrates on several subfields, notably:

  • Molecular Biology
  • Genetics
  • Pulmonary and Respiratory Medicine
  • Infectious Diseases
  • Nephrology

The main research topics addressed by Mane include:

  • Renal and related cancers
  • Renal Diseases and Glomerulopathies
  • SARS-CoV-2 and COVID-19 Research
  • Genetic and Kidney Cyst Diseases
  • Genomics and Rare Diseases
  • Congenital heart defects research
  • COVID-19 Clinical Research Studies

Among Shrikant Mane's recent published papers are:

  • "Neuroinvasion of SARS-CoV-2 in human and mouse brain," 2020, The Journal of Experimental Medicine
  • "X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19," 2021, Science Immunology
  • "Impact of circulating SARS-CoV-2 variants on mRNA vaccine-induced immunity," 2021, Nature
  • "Neuroinvasion of SARS-CoV-2 in human and mouse brain," 2020, bioRxiv (Cold Spring Harbor Laboratory)
  • "Mutations disrupting neuritogenesis genes confer risk for cerebral palsy," 2020, Nature Genetics

Shrikant Mane frequently collaborates with several researchers, including:

  • Richard P. Lifton
  • Shirlee Shril
  • Kaya Bilgüvar
  • Friedhelm Hildebrandt
  • Christopher Castaldi

Publication venues where Mane's work appears most often include:

  • Journal of the American Society of Nephrology
  • bioRxiv (Cold Spring Harbor Laboratory)
  • Genetics in Medicine
  • The American Journal of Human Genetics
  • Proceedings of the National Academy of Sciences

Best Publications

  • Complement Factor H Polymorphism in Age-Related Macular Degeneration

    Robert J. Klein;Caroline J. Zeiss;Emily Y. Chew;Jen-yue Tsai

  • RNA-seq: An assessment of technical reproducibility and comparison with gene expression arrays

    John C. Marioni;Christopher E. Mason;Shrikant M. Mane;Matthew Stephens

  • The contribution of de novo coding mutations to autism spectrum disorder

    Ivan Iossifov;Brian J. O'Roak;Stephan J. Sanders;Stephan J. Sanders;Michael Ronemus

  • De novo mutations revealed by whole-exome sequencing are strongly associated with autism

    Stephan J. Sanders;Michael T. Murtha;Abha R. Gupta;John D. Murdoch

  • Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

    S. Hong Lee;Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Stephen V. Faraone

  • Spatio-temporal transcriptome of the human brain

    Hyo Jung Kang;Yuka Imamura Kawasawa;Feng Cheng;Ying Zhu

  • Analysis of shared heritability in common disorders of the brain

    Verneri Anttila;Verneri Anttila;Brendan Bulik-Sullivan;Brendan Bulik-Sullivan;Hilary K. Finucane;Raymond K. Walters;Raymond K. Walters

  • Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

    Murim Choi;Ute I. Scholl;Weizhen Ji;Tiewen Liu

  • Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.

    Stephan J. Sanders;Xin He;A. Jeremy Willsey;A. Gulhan Ercan-Sencicek

  • Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

    Stephan J. Sanders;A. Gulhan Ercan-Sencicek;Vanessa Hus;Rui Luo

  • Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma.

    Michael Krauthammer;Yong Lin Kong;Byung Hak Ha;Perry Evans

  • K+ Channel Mutations in Adrenal Aldosterone-Producing Adenomas and Hereditary Hypertension

    Murim Choi;Ute I. Scholl;Peng Yue;Peyman Björklund;Peyman Björklund

  • Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism

    A. Jeremy Willsey;A. Jeremy Willsey;Stephan J. Sanders;Stephan J. Sanders;Mingfeng Li;Shan Dong;Shan Dong

  • A Novel miRNA Processing Pathway Independent of Dicer Requires Argonaute2 Catalytic Activity

    Daniel Cifuentes;Huiling Xue;David W. Taylor;Heather Patnode

  • De novo mutations in histone-modifying genes in congenital heart disease

    Samir Zaidi;Murim Choi;Hiroko Wakimoto;Lijiang Ma

  • Genomic Analysis of Non-NF2 Meningiomas Reveals Mutations in TRAF7, KLF4, AKT1, and SMO

    Victoria E. Clark;E. Zeynep Erson-Omay;Akdes Serin;Jun Yin

  • De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies.

    Jason Homsy;Samir Zaidi;Yufeng Shen;James S. Ware;James S. Ware;James S. Ware

  • Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands

    Sheng Chih Jin;Jason Homsy;Samir Zaidi;Qiongshi Lu

  • Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

    Colm O'Dushlaine;Lizzy Rossin;Phil H. Lee;Laramie Duncan;Laramie Duncan

  • Complement factor H polymorphism in age-related macular degeneration

    R.J. Klein;C. Zeiss;E.Y. Chew;J.Y. Tsai

Frequent Co-Authors

Richard P. Lifton
Richard P. Lifton Rockefeller University
Kaya Bilguvar
Kaya Bilguvar Yale University
Murim Choi
Murim Choi Seoul National University
Murat Gunel
Murat Gunel Yale University
Matthew W. State
Matthew W. State University of California, San Francisco
Friedhelm Hildebrandt
Friedhelm Hildebrandt Boston Children's Hospital
Hongyu Zhao
Hongyu Zhao Yale University
Bernie Devlin
Bernie Devlin University of Pittsburgh
Daniel H. Geschwind
Daniel H. Geschwind University of California, Los Angeles
Christopher A. Walsh
Christopher A. Walsh Howard Hughes Medical Institute

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