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Giulio Genovese

Giulio Genovese

D-Index & Metrics

Genetics

D-Index
66
Citations
74822
World Ranking
2557
National Ranking
1135

Overview

Giulio Genovese is affiliated with the Broad Institute in the United States. Their research spans across the fields of Biochemistry, Genetics, and Molecular Biology, with a significant focus on Genetics and Molecular Biology. They have contributed substantially to Medicine as well.

The scientist's work covers several specific subfields, including Genetics, Molecular Biology, Cancer Research, Hematology, and Immunology. Their main research topics encompass:

  • Genetic Associations and Epidemiology
  • Genomics and Rare Diseases
  • Cancer Genomics and Diagnostics
  • Genomic variations and chromosomal abnormalities
  • Acute Myeloid Leukemia Research
  • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
  • Single-cell and spatial transcriptomics

Genovese's recent publications include:

  • "Mapping genomic loci implicates genes and synaptic biology in schizophrenia," 2022, Nature
  • "Rare coding variants in ten genes confer substantial risk for schizophrenia," 2022, Nature
  • "Monogenic and polygenic inheritance become instruments for clonal selection," 2020, Nature
  • "A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts," 2021, Biological Psychiatry
  • "Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations," 2020, Nature Neuroscience

The frequent publication venues where Genovese's work appears include:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • UNC Libraries
  • Nature
  • Biological Psychiatry
  • European Neuropsychopharmacology

Genovese collaborates regularly with several co-authors, with the most frequent including:

  • Steven A. McCarroll
  • Tim B. Bigdeli
  • Saiju Pyarajan
  • Bryan R. Gorman
  • Ayman H. Fanous

Best Publications

  • A global reference for human genetic variation.

    Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin

  • An integrated map of genetic variation from 1,092 human genomes

    Goncalo R Abecasis;Adam Auton;Lisa D Brooks

  • Biological insights from 108 schizophrenia-associated genetic loci

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

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

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

  • Schizophrenia risk from complex variation of complement component 4

    Aswin Sekar;Aswin Sekar;Allison R. Bialas;Heather de Rivera;Heather de Rivera;Avery Davis;Avery Davis

  • Association of trypanolytic ApoL1 variants with kidney disease in African Americans.

    Giulio Genovese;Giulio Genovese;David J. Friedman;Michael D. Ross;Laurence Lecordier

  • A polygenic burden of rare disruptive mutations in schizophrenia

    Shaun M Purcell;Jennifer L Moran;Menachem Fromer;Douglas Ruderfer

  • Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

    Bjarni J. Vilhjálmsson;Jian Yang;Hilary K. Finucane;Alexander Gusev

  • Chromosomal instability drives metastasis through a cytosolic DNA response.

    Samuel F. Bakhoum;Samuel F. Bakhoum;Bryan Ngo;Ashley M. Laughney;Julie Ann Cavallo;Julie Ann Cavallo

  • Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

    Christian R Marshall;Daniel P Howrigan;Daniel P Howrigan;Daniele Merico;Bhooma Thiruvahindrapuram

  • A global reference for human genetic variation

    Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin

  • Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types.

    Hilary K Finucane;Hilary K Finucane;Hilary K Finucane;Yakir A Reshef;Verneri Anttila;Verneri Anttila;Kamil Slowikowski;Kamil Slowikowski;Kamil Slowikowski

  • APOL1 Genetic Variants in Focal Segmental Glomerulosclerosis and HIV-Associated Nephropathy

    Jeffrey B. Kopp;George W. Nelson;Karmini Sampath;Randall C. Johnson;Randall C. Johnson

  • Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

    Douglas M. Ruderfer;Stephan Ripke;Stephan Ripke;Stephan Ripke;Andrew McQuillin;James Boocock

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

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

  • Human pluripotent stem cells recurrently acquire and expand dominant negative P53 mutations

    Florian T. Merkle;Sulagna Ghosh;Nolan Kamitaki;Jana Mitchell

  • Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia

    Giulio Genovese;Menachem Fromer;Eli A Stahl;Douglas M Ruderfer

  • Large multiallelic copy number variations in humans

    Robert E Handsaker;Robert E Handsaker;Vanessa Van Doren;Vanessa Van Doren;Jennifer R Berman;Giulio Genovese;Giulio Genovese

  • Deviant kinetochore microtubule dynamics underlie chromosomal instability.

    Samuel F. Bakhoum;Giulio Genovese;Duane A. Compton

  • Increased neutrophil extracellular trap formation promotes thrombosis in myeloproliferative neoplasms.

    Ofir Wolach;Ofir Wolach;Ofir Wolach;Rob S. Sellar;Rob S. Sellar;Rob S. Sellar;Kimberly Martinod;Deya Cherpokova

Frequent Co-Authors

Steven A. McCarroll
Steven A. McCarroll Harvard University
Benjamin M. Neale
Benjamin M. Neale Harvard University
Patrick F. Sullivan
Patrick F. Sullivan University of North Carolina at Chapel Hill
Martin R. Pollak
Martin R. Pollak Beth Israel Deaconess Medical Center
Mark J. Daly
Mark J. Daly Massachusetts General Hospital
Shaun Purcell
Shaun Purcell Harvard Medical School
Alkes L. Price
Alkes L. Price Harvard University
Menachem Fromer
Menachem Fromer Broad Institute
Tonu Esko
Tonu Esko University of Tartu
Aarno Palotie
Aarno Palotie University of Helsinki

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