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Genetics

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

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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