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D-Index & Metrics

Genetics

D-Index
131
Citations
187090
World Ranking
242
National Ranking
125

Medicine

D-Index
135
Citations
190106
World Ranking
2006
National Ranking
1143

Overview

Shaun Purcell is affiliated with Harvard Medical School in the United States. Their research primarily focuses on Neuroscience, with a strong emphasis on Cognitive Neuroscience. They have also contributed to the fields of Experimental and Cognitive Psychology, Genetics, Physiology, and Molecular Biology.

The researcher's work covers a range of topics related to sleep and neurological function. Key areas include Sleep and Related Disorders, Sleep and Wakefulness Research, Obstructive Sleep Apnea Research, EEG and Brain-Computer Interfaces, Genetic Associations and Epidemiology, Genomics and Rare Diseases, and Genetics and Neurodevelopmental Disorders.

Shaun Purcell has coauthored numerous papers with several frequent collaborators. Notable coauthors include Susan Redline with 40 joint works, Nataliia Kozhemiako (26), Pamela Sklar (24), Tamar Sofer (19), and Jen Q. Pan (18).

The researcher's publications appear repeatedly in certain well-known venues. These include UNC Libraries with 28 publications, SLEEP with 27, bioRxiv (Cold Spring Harbor Laboratory) with 10, Alzheimer's & Dementia with 3, and Nature Human Behaviour with 2.

Several recent and significant papers feature Shaun Purcell's contributions. These include:

  • Macro and micro sleep architecture and cognitive performance in older adults, 2020, Nature Human Behaviour
  • Sleep Architecture, Obstructive Sleep Apnea, and Cognitive Function in Adults, 2023, JAMA Network Open
  • Analysis of protein-coding genetic variation in 60,706 humans, 2020, UNC Libraries
  • Effects of a patient-derived de novo coding alteration of CACNA1I in mice connect a schizophrenia risk gene with sleep spindle deficits, 2020, Translational Psychiatry
  • Sources of Variation in the Spectral Slope of the Sleep EEG, 2022, eNeuro

Best Publications

  • PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses

    Shaun Purcell;Shaun Purcell;Benjamin Neale;Benjamin Neale;Kathe Todd-Brown;Lori Thomas

  • Analysis of protein-coding genetic variation in 60,706 humans

    Monkol Lek;Konrad J. Karczewski;Konrad J. Karczewski;Eric V. Minikel;Eric V. Minikel;Kaitlin E. Samocha

  • Second-generation PLINK: rising to the challenge of larger and richer datasets

    Christopher C. Chang;Carson C. Chow;Laurent C.A.M. Tellier;Shashaank Vattikuti

  • Biological insights from 108 schizophrenia-associated genetic loci

    Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Aiden Corvin;James T. R. Walters

  • A haplotype map of the human genome

    John W. Belmont;Andrew Boudreau;Suzanne M. Leal;Paul Hardenbol

  • A second generation human haplotype map of over 3.1 million SNPs

    Kelly A. Frazer;Dennis G. Ballinger;David R. Cox;David A. Hinds

  • Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

    Shaun M. Purcell;Shaun M. Purcell;Naomi R. Wray;Jennifer L. Stone;Jennifer L. Stone;Peter M. Visscher

  • Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis

    Jordan W. Smoller;Kenneth Kendler;Nicholas John Craddock;Phil Hyoun Lee

  • Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

    Elizabeth K. Speliotes;Elizabeth K. Speliotes;Cristen J. Willer;Sonja I. Berndt;Keri L. Monda

  • Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence

    Giulio Genovese;Anna K. Kähler;Robert E. Handsaker;Johan Lindberg

  • Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

    Naomi R. Wray;Stephan Ripke;Stephan Ripke;Stephan Ripke;Manuel Mattheisen;MacIej Trzaskowski

  • Synaptic, transcriptional and chromatin genes disrupted in autism

    Silvia De Rubeis;Xin-Xin He;Arthur P Goldberg;Christopher S. Poultney

  • Genome-Wide Association Analysis Identifies Loci for Type 2 Diabetes and Triglyceride Levels

    Richa Saxena;Benjamin F. Voight;Valeriya Lyssenko;Noël P. Burtt

  • Genome-wide association study identifies five new schizophrenia loci

    Stephan Ripke;Alan R. Sanders;Kenneth S. Kendler;Douglas F. Levinson

  • Plasma HDL cholesterol and risk of myocardial infarction: A mendelian randomisation study

    Benjamin F. Voight;Benjamin F. Voight;Benjamin F. Voight;Gina M. Peloso;Gina M. Peloso;Marju Orho-Melander;Ruth Frikke-Schmidt

  • Genome-wide detection and characterization of positive selection in human populations

    Pardis C. Sabeti;Pardis C. Sabeti;Patrick Varilly;Patrick Varilly;Ben Fry;Jason Lohmueller

  • 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

  • Partitioning heritability by functional annotation using genome-wide association summary statistics.

    Hilary K Finucane;Hilary K Finucane;Brendan Bulik-Sullivan;Brendan Bulik-Sullivan;Alexander Gusev;Gosia Trynka

  • Hundreds of variants clustered in genomic loci and biological pathways affect human height

    Hana Lango Allen;Karol Estrada;Guillaume Lettre;Sonja I. Berndt

  • Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

    Shaun Purcell;Stacey S. Cherny;Pak Chung Sham

Frequent Co-Authors

Pamela Sklar
Pamela Sklar Icahn School of Medicine at Mount Sinai
Mark J. Daly
Mark J. Daly Massachusetts General Hospital
Benjamin M. Neale
Benjamin M. Neale Harvard University
Patrick F. Sullivan
Patrick F. Sullivan University of North Carolina at Chapel Hill
Douglas M. Ruderfer
Douglas M. Ruderfer Vanderbilt University Medical Center
Jordan W. Smoller
Jordan W. Smoller Harvard University
Steven A. McCarroll
Steven A. McCarroll Harvard University
Menachem Fromer
Menachem Fromer Broad Institute
Michael Conlon O'Donovan
Michael Conlon O'Donovan Cardiff University
Christina M. Hultman
Christina M. Hultman Karolinska Institute

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