Leveraging base-pair mammalian constraint to understand genetic variation and human disease | Zendy

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Leveraging base-pair mammalian constraint to understand genetic variation and human disease

Author(s) -

Patrick F. Sullivan,

Jennifer R. S. Meadows,

Steven Gazal,

BaDoi N. Phan,

Xue Li,

Diane P. Genereux,

Michael X. Dong,

Matteo Bianchi,

Gregory Andrews,

Sharadha Sakthikumar,

Jessika Nordin,

Ananya Roy,

Matthew J. Christmas,

Voichita D. Marinescu,

Chao Wang,

Ola Wallerman,

James R. Xue,

Shuyang Yao,

Quan Sun,

Jin Szatkiewicz,

Jia Wen,

Laura M. Huckins,

Alyssa J. Lawler,

Kathleen C. Keough,

Zhili Zheng,

Jian Zeng,

Naomi R. Wray,

Yun Li,

Jessica Johnson,

Jiawen Chen,

Benedict Paten,

Steven K. Reilly,

Graham M. Hughes,

Zhiping Weng,

Katherine S. Pollard,

Andreas R. Pfenning,

Karin ForsbergNilsson,

Elinor K. Karlsson,

Kerstin LindbladToh,

Joel Armstrong,

Susan J. Birren,

Kevin R. Bredemeyer,

Ana M. Breit,

Hiram Clawson,

Joana Damas,

Federica Di Palma,

Mark Diekhans,

Eduardo Eizirik,

Kaili Fan,

Cornelia Fanter,

Nicole M. Foley,

Carlos J. Garcia,

John Gatesy,

Linda Goodman,

Jenna Grimshaw,

Michaela K. Halsey,

Andrew J. Harris,

Glenn Hickey,

Michael Hiller,

Allyson G. Hindle,

Robert Hubley,

Jeremy Johnson,

David Juan,

Irene M. Kaplow,

Bogdan Kirilenko,

KlausPeter Koepfli,

Jennifer M. Korstian,

Amanda Kowalczyk,

Sergey V. Kozyrev,

Colleen Lawless,

Thomas Lehmann,

Danielle L. Levesque,

Harris A. Lewin,

Abigail Lind,

Ava Mackay-Smith,

Tomás MarquèsBonet,

Victor C. Mason,

Wynn K. Meyer,

Jill E. Moore,

Lucas R. Moreira,

Diana D. Moreno-Santillán,

Kathleen M. Morrill,

Gerard Muntané,

William J. Murphy,

Arcadi Navarro,

Martin Nweeia,

Sylvia Ortmann,

Austin Osmanski,

Nicole S. Paulat,

Henry Pratt,

David A. Ray,

Jeb Rosen,

Irina Ruf,

Louise Ryan,

Oliver A. Ryder,

Pardis C. Sabeti,

Daniel E. Schäffer,

Aitor Serres,

Beth Shapiro,

Arian F. A. Smit,

Mark S. Springer,

Chaitanya Srinivasan,

Cynthia Steiner,

Jessica M. Storer,

Kevin A. Sullivan,

Elisabeth Sundström,

Megan A. Supple,

Ross Swofford,

Joy-El Talbot,

Emma C. Teeling,

Jason Turner-Maier,

Alejandro Valenzuela,

Franziska Wagner,

Juehan Wang,

Aryn P. Wilder,

Morgan Wirthlin,

Xiaomeng Zhang

Publication year - 2023

Publication title -

science

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 12.556

H-Index - 1186

eISSN - 1095-9203

pISSN - 0036-8075

DOI - 10.1126/science.abn2937

Subject(s) - human genome , biology , genome , annotation , human genetic variation , disease , computational biology , genetics , heritability , mechanism (biology) , human disease , constraint (computer aided design) , genetic variation , genomics , human genetics , copy number variation , function (biology) , genome wide association study , evolutionary biology , gene , single nucleotide polymorphism , medicine , genotype , mechanical engineering , philosophy , epistemology , pathology , engineering

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