All papers authored by Giulio Genovese
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James Nemesh,
Melissa Goldman,
Nolan Kamitaki ,
Nora Reed,
Robert E. Handsaker ,
Giulio Genovese ,
Jonathan S. Vogelgsang,
Sherif Gerges,
Seva Kashin,
Sulagna Ghosh ,
John M. Esposito,
Kiely Morris,
Daniel Meyer ,
Alyssa Lutservitz
and 8 other authors
A concerted neuron–astrocyte program declines in ageing and schizophrenia
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Olli Pietiläinen ,
Mykyta Artomov ,
Matthew Tegtmeyer,
Vera Valakh,
Leevi Lehtonen,
Christina Bell,
Tarjinder Singh ,
Aditi Trehan,
John Sherwood,
Danielle Manning,
Emily Peirent ,
Rhea Malik,
Ellen J. Guss ,
Derek Hawes
and 30 other authors
The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia
Download from www.nature.com
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Rachel E. Rodin,
Giulio Genovese ,
Caroline Dias ,
Alison R. Barton ,
Ronen E. Mukamel,
Bonnie Berger,
Peter J. Park ,
Christopher A. Walsh ,
Po-Ru Loh
Large mosaic copy number variations confer autism risk
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Chia-Ho Cheng,
Y. Ann Chen,
Hsin-An Hou ,
Björn Nilsson,
Giulio Genovese ,
Thomas Cluzeau,
Andrea Pellagatti ,
Bartlomiej P. Przychodzen,
Mar Mallo,
Leonor Arenillas ,
Azim Mohamedali,
Lionel Adès,
David A. Sallman,
Eric Padron
and 12 other authors
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Robert E. Handsaker,
Hilary K. Finucane,
Yakir A. Reshef,
Pier Francesco Palamara,
Brenda M. Birmann ,
Michael E. Talkowski,
Samuel F. Bakhoum,
Steven A. McCarroll,
Alkes L. Price
Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterations
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Mark J. Daly
Mosaic mutations in blood DNA sequence are associated with solid tumor cancers
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Menachem Fromer,
Eli A. Stahl,
Douglas M. Ruderfer,
Kimberly Chambert,
Mikael Landén,
Jennifer L. Moran,
Shaun M. Purcell,
Pamela Sklar,
Patrick F. Sullivan ,
Christina M. Hultman,
Steven A. McCarroll
Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia
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Giulio Genovese ,
Daniel P. Howrigan,
Andrea Byrnes,
Mitja I. Kurki,
Seyedeh M. Zekavat,
Christopher W. Whelan,
Mart Kals,
Michel G. Nivard ,
Alex Bloemendal,
Jonathan M. Bloom,
Jacqueline I. Goldstein,
Timothy Poterba,
Cotton Seed,
Robert E. Handsaker
and 20 other authors
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Anna K. Kähler,
Robert E. Handsaker,
Johan Lindberg,
Samuel A. Rose,
Samuel F. Bakhoum,
Kimberly Chambert,
Eran Mick,
Oscar Svantesson,
Shaun M. Purcell,
Benjamin M. Neale,
Menachem Fromer,
Mikael Landén,
Martin Höglund ,
Patrick F. Sullivan
and 9 other authors
Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence
Download from www.researchgate.net
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Robert E. Handsaker,
Heng Li,
Eimear E. Kenny,
Steven A. McCarroll
Mapping the Human Reference Genome’s Missing Sequence by Three-Way Admixture in Latino Genomes
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David J. Friedman,
Martin R. Pollak
APOL1 variants and kidney disease in people of recent African ancestry
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Robert E. Handsaker,
Heng Li,
Nicolas Altemose,
Amelia M. Lindgren,
Kimberly Chambert,
Bogdan Pasaniuc,
Alkes L. Price,
David Reich,
Cynthia C. Morton,
Martin R. Pollak,
James G. Wilson,
Steven A. McCarroll
Using population admixture to help complete maps of the human genome
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Stephen J. Tonna,
Andrea Uscinski Knob,
Gerald B. Appel,
Avi Katz,
Andrea J. Bernhardy,
Alexander W. Needham,
Ross Lazarus,
Martin R. Pollak,
M. Klein
Download from www.ncbi.nlm.nih.gov
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David J. Friedman,
Michael D. Ross,
Laurence Lecordier,
Pierrick Uzureau,
Barry I. Freedman,
Donald W. Bowden,
Carl D. Langefeld,
Taras K. Oleksyk,
Andrea Uscinski Knob,
Andrea L. Uscinski Knob,
Andrea J. Bernhardy,
Pamela J. Hicks,
George W. Nelson,
Benoit Vanhollebeke
and 4 other authors
Association of Trypanolytic ApoL1 Variants with Kidney Disease in African-Americans
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Gregory Leibon,
Martin R. Pollak,
Daniel N. Rockmore
Improved IBD detection using incomplete haplotype information
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