Returning integrated genomic risk and clinical recommendations: The eMERGE study.

Jodell E Linder,Aimee Allworth,Sarah T Bland,Pedro J Caraballo,Rex L Chisholm,Ellen Wright Clayton,David R Crosslin,Ozan Dikilitas, Alanna DiVietro,Edward D Esplin, Sophie Forman,Robert R Freimuth,Adam S Gordon,Richard Green,Maegan V Harden,Ingrid A Holm,Gail P Jarvik,Elizabeth W Karlson, Sofia Labrecque,Niall J Lennon,Nita A Limdi,Kathleen F Mittendorf,Shawn N Murphy,Lori Orlando,Cynthia A Prows,Luke V Rasmussen,Laura Rasmussen-Torvik,Robb Rowley,Konrad Teodor Sawicki,Tara Schmidlen,Shannon Terek,David Veenstra,Digna R Velez Edwards,Devin Absher,Noura S Abul-Husn, Jorge Alsip,Hana Bangash,Mark Beasley,Jennifer E Below,Eta S Berner,James Booth,Wendy K Chung,James J Cimino,John Connolly, Patrick Davis,Beth Devine,Stephanie M Fullerton,Candace Guiducci,Melissa L Habrat,Heather Hain,Hakon Hakonarson,Margaret Harr,Eden Haverfield,Valentina Hernandez,Christin Hoell,Martha Horike-Pyne,George Hripcsak,Marguerite R Irvin, Christopher Kachulis,Dean Karavite,Eimear E Kenny,Atlas Khan,Krzysztof Kiryluk,Bruce Korf,Leah Kottyan,Iftikhar J Kullo, Katie Larkin,Cong Liu,Edyta Malolepsza,Teri A Manolio,Thomas May,Elizabeth M McNally,Frank Mentch,Alexandra Miller,Sean D Mooney,Priyanka Murali, Brenda Mutai,Naveen Muthu,Bahram Namjou,Emma F Perez,Megan J Puckelwartz,Tejinder Rakhra-Burris,Dan M Roden,Elisabeth A Rosenthal,Seyedmohammad Saadatagah,Maya Sabatello,Dan J Schaid, Baergen Schultz, Lynn Seabolt,Gabriel Q Shaibi,Richard R Sharp,Brian Shirts,Maureen E Smith,Jordan W Smoller, Rene Sterling,Sabrina A Suckiel,Jeritt Thayer,Hemant K Tiwari,Susan B Trinidad,Theresa Walunas,Wei-Qi Wei,Quinn S Wells,Chunhua Weng,Georgia L Wiesner,Ken Wiley,Josh F Peterson

Genetics in medicine : official journal of the American College of Medical Genetics（2023）

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摘要

Return of a novel report for communicating monogenic, polygenic, and family history-based risk factors will inform the benefits of integrated genetic risk assessment for routine health care.

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关键词

Common variants,Family history,Genotyping,Monogenic risks,Polygenic risk scores

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