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D-Index & Metrics

Genetics

D-Index
70
Citations
57174
World Ranking
2224
National Ranking
12

Overview

Stacy Steinberg is affiliated with deCODE Genetics in Iceland, focusing on research intersecting medicine and biochemistry, genetics, and molecular biology. Their work spans multiple fields of study with a particular emphasis on genetics and psychiatry and mental health, complemented by subfields including cognitive neuroscience, endocrine and autonomic systems, and molecular biology.

The scientist has contributed extensively to topics such as migraine and headache studies, genetic associations and epidemiology, bipolar disorder and treatment, neuroscience of respiration and sleep, genetics and neurodevelopmental disorders, hemispheric asymmetry in neuroscience, and genetics and physical performance.

Recent publications by Steinberg include:

  • Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology (2021, Nature Genetics)
  • Genome-wide association study identifies 48 common genetic variants associated with handedness (2020, Nature Human Behaviour)
  • Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache (2020, International Journal of Epidemiology)
  • A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine (2020, Nature Communications)
  • Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology (2020, bioRxiv - Cold Spring Harbor Laboratory)

Steinberg frequently publishes in venues including UNC Libraries, Nature Genetics, Nature Human Behaviour, International Journal of Epidemiology, and Nature Communications.

Collaborations form an important part of Steinberg's research network. Frequent coauthors include:

  • Hreinn Stefánsson
  • Scott D. Gordon
  • Bendik S. Winsvold
  • Jouke-Jan Hottenga
  • Nicholas G. Martin

Best Publications

  • Biological insights from 108 schizophrenia-associated genetic loci

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

  • 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

  • Variant of TREM2 associated with the risk of Alzheimer's disease

    Thorlakur Jonsson;Hreinn Stefansson;Stacy Steinberg;Ingileif Jonsdottir

  • Genome-wide association study identifies five new schizophrenia loci

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

  • Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk.

    Iris E. Jansen;Jeanne E. Savage;Kyoko Watanabe;Julien Bryois

  • Rate of de novo mutations and the importance of father’s age to disease risk

    Augustine Kong;Michael L. Frigge;Gisli Masson;Soren Besenbacher;Soren Besenbacher

  • Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease.

    Paul Hollingworth;Denise Harold;Rebecca Sims;Amy Gerrish

  • A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline

    Thorlakur Jonsson;Jasvinder K. Atwal;Stacy Steinberg;Jon Snaedal

  • Large recurrent microdeletions associated with schizophrenia

    Hreinn Stefansson;Dan Rujescu;Sven Cichon;Olli P. H. Pietilainen

  • Common variants conferring risk of schizophrenia

    Hreinn Stefansson;Hreinn Stefansson;Roel A. Ophoff;Roel A. Ophoff;Roel A. Ophoff;Stacy Steinberg;Stacy Steinberg;Ole A. Andreassen

  • Genome-wide association analysis identifies 13 new risk loci for schizophrenia

    Stephan Ripke;Stephan Ripke;Colm T. O'Dushlaine;Kimberly D. Chambert;Jennifer L. Moran

  • Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

    Antonio F. Pardiñas;Peter Holmans;Andrew J. Pocklington;Valentina Escott-Price

  • Genome-wide association study identifies 30 loci associated with bipolar disorder

    Eli A. Stahl;Eli A. Stahl;Gerome Breen;Andreas J. Forstner;Andrew McQuillin

  • Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

    Pamela Sklar;Pamela Sklar;Stephan Ripke;Stephan Ripke;Laura J. Scott;Ole A. Andreassen

  • Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

    Niamh Mullins;Andreas J. Forstner;Andreas J. Forstner;Andreas J. Forstner;Kevin S. O'Connell;Kevin S. O'Connell;Brandon Coombes

  • Genetic determinants of hair, eye and skin pigmentation in Europeans.

    Patrick Sulem;Daniel F Gudbjartsson;Simon N Stacey;Agnar Helgason

  • Many sequence variants affecting diversity of adult human height

    Daniel F Gudbjartsson;G Bragi Walters;Gudmar Thorleifsson;Hreinn Stefansson

  • CNVs conferring risk of autism or schizophrenia affect cognition in controls

    Hreinn Stefansson;Andreas Meyer-Lindenberg;Stacy Steinberg;Brynja Magnusdottir

  • Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases

    Alexander Gusev;S. Hong Lee;Gosia Trynka;Hilary Finucane

  • A mega-analysis of genome-wide association studies for major depressive disorder

    S. Ripke;N. R. Wray;C. M. Lewis;S. P. Hamilton

Frequent Co-Authors

Kari Stefansson
Kari Stefansson deCODE Genetics (Iceland)
Hreinn Stefansson
Hreinn Stefansson deCODE Genetics (Iceland)
Thomas Werge
Thomas Werge University of Copenhagen
Stephan Ripke
Stephan Ripke Massachusetts General Hospital
Srdjan Djurovic
Srdjan Djurovic Oslo University Hospital
Anders D. Børglum
Anders D. Børglum Aarhus University
Ole A. Andreassen
Ole A. Andreassen Oslo University Hospital
Roel A. Ophoff
Roel A. Ophoff University of California, Los Angeles
Ole Mors
Ole Mors Aarhus University
David M. Hougaard
David M. Hougaard Statens Serum Institut

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