Searching journal content for Heidi Rehm in author.

Displaying results 1-4 of 4
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  1. Resource: A harmonized public resource of deeply sequenced diverse human genomes
    • Zan Koenig,
    • Mary T. Yohannes,
    • Lethukuthula L. Nkambule,
    • Xuefang Zhao,
    • Julia K. Goodrich,
    • Heesu Ally Kim,
    • Michael W. Wilson,
    • Grace Tiao,
    • Stephanie P. Hao,
    • Nareh Sahakian,
    • Katherine R. Chao,
    • Mark A. Walker,
    • Yunfei Lyu,
    • gnomAD Project Consortium,
    • Heidi L. Rehm,
    • Benjamin M. Neale,
    • Michael E. Talkowski,
    • Mark J. Daly,
    • Harrison Brand,
    • Konrad J. Karczewski,
    • Elizabeth G. Atkinson,
    • and Alicia R. Martin
    Genome Res. May 2024 34: 796-809; Published in Advance May 15, 2024, doi:10.1101/gr.278378.123
  2. Resource: Discordant calls across genotype discovery approaches elucidate variants with systematic errors
    • Elizabeth G. Atkinson,
    • Mykyta Artomov,
    • Alexander A. Loboda,
    • Heidi L. Rehm,
    • Daniel G. MacArthur,
    • Konrad J. Karczewski,
    • Benjamin M. Neale,
    • and Mark J. Daly
    Genome Res. May 30, 2023 ; Published in Advance May 30, 2023, doi:10.1101/gr.277908.123
  3. Resource: Mitochondrial DNA variation across 56,434 individuals in gnomAD
    • Kristen M. Laricchia,
    • Nicole J. Lake,
    • Nicholas A. Watts,
    • Megan Shand,
    • Andrea Haessly,
    • Laura Gauthier,
    • David Benjamin,
    • Eric Banks,
    • Jose Soto,
    • Kiran Garimella,
    • James Emery,
    • Genome Aggregation Database Consortium,
    • Heidi L. Rehm,
    • Daniel G. MacArthur,
    • Grace Tiao,
    • Monkol Lek,
    • Vamsi K. Mootha,
    • and Sarah E. Calvo
    Genome Res. March 2022 32: 569-582; Published in Advance January 24, 2022, doi:10.1101/gr.276013.121
    OPEN ACCESS ARTICLE
  4. Research: Actionable exomic incidental findings in 6503 participants: challenges of variant classification
    • Laura M. Amendola,
    • Michael O. Dorschner,
    • Peggy D. Robertson,
    • Joseph S. Salama,
    • Ragan Hart,
    • Brian H. Shirts,
    • Mitzi L. Murray,
    • Mari J. Tokita,
    • Carlos J. Gallego,
    • Daniel Seung Kim,
    • James T. Bennett,
    • David R. Crosslin,
    • Jane Ranchalis,
    • Kelly L. Jones,
    • Elisabeth A. Rosenthal,
    • Ella R. Jarvik,
    • Andy Itsara,
    • Emily H. Turner,
    • Daniel S. Herman,
    • Jennifer Schleit,
    • Amber Burt,
    • Seema M. Jamal,
    • Jenica L. Abrudan,
    • Andrew D. Johnson,
    • Laura K. Conlin,
    • Matthew C. Dulik,
    • Avni Santani,
    • Danielle R. Metterville,
    • Melissa Kelly,
    • Ann Katherine M. Foreman,
    • Kristy Lee,
    • Kent D. Taylor,
    • Xiuqing Guo,
    • Kristy Crooks,
    • Lesli A. Kiedrowski,
    • Leslie J. Raffel,
    • Ora Gordon,
    • Kalotina Machini,
    • Robert J. Desnick,
    • Leslie G. Biesecker,
    • Steven A. Lubitz,
    • Surabhi Mulchandani,
    • Greg M. Cooper,
    • Steven Joffe,
    • C. Sue Richards,
    • Yaoping Yang,
    • Jerome I. Rotter,
    • Stephen S. Rich,
    • Christopher J. O’Donnell,
    • Jonathan S. Berg,
    • Nancy B. Spinner,
    • James P. Evans,
    • Stephanie M. Fullerton,
    • Kathleen A. Leppig,
    • Robin L. Bennett,
    • Thomas Bird,
    • Virginia P. Sybert,
    • William M. Grady,
    • Holly K. Tabor,
    • Jerry H. Kim,
    • Michael J. Bamshad,
    • Benjamin Wilfond,
    • Arno G. Motulsky,
    • C. Ronald Scott,
    • Colin C. Pritchard,
    • Tom D. Walsh,
    • Wylie Burke,
    • Wendy H. Raskind,
    • Peter Byers,
    • Fuki M. Hisama,
    • Heidi Rehm,
    • Debbie A. Nickerson,
    • and Gail P. Jarvik
    Genome Res. March 2015 25: 305-315; Published in Advance January 30, 2015, doi:10.1101/gr.183483.114
    OPEN ACCESS ARTICLE
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