Adam S. Gordon - Northwestern University

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论文共 45 篇作者统计合作学者相似作者

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A Case of Non-Syndromic Congenital Cataracts Caused by a Novel MAF Variant in the C-Terminal DNA-Binding Domain—Case Report and Literature Review

Sharon H. Zhao,Kai Lee Yap,Valerie Allegretti,Andy Drackley,Alexander Ing,Adam Gordon,Andrew Skol,Patrick Mcmullen,Brenda L. Bohnsack,Sudhi P. Kurup,Hantamalala Ralay Ranaivo,Jennifer L. Rossen

GENESno. 6 (2024)

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Consideration of Disease Penetrance in the Selection of Secondary Findings Gene-Disease Pairs: A Policy Statement of the American College of Medical Genetics and Genomics (ACMG)

Adam S. Gordon,Kristy Lee,Noura S. Abul-Husn,Laura M. Amendola,Kyle Brothers,Wendy K. Chung,Michael H. Gollob,Steven M. Harrison,Ray E. Hershberger,C. Sue Richards,Douglas R. Stewart,Christa Lese Martin,David T. Miller

Genetics in Medicinepp.101142, (2024)

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Returning Integrated Genomic Risk and Clinical Recommendations: the Emerge Study

Jodell E. Linder,Aimee Allworth,Harris 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 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 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（2023）

引用17浏览0WOS引用

ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

David T Miller,Kristy Lee,Noura S Abul-Husn,Laura M Amendola,Kyle Brothers,Wendy K Chung,Michael H Gollob,Adam S Gordon,Steven M Harrison,Ray E Hershberger,Teri E Klein,C Sue Richards, Douglas R Stewart,Christa Lese Martin, ACMG Secondary Findings Working Group. Electronic address: documents@acmg.net

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

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Large-scale Genome-Wide Association Study of Coronary Artery Disease in Genetically Diverse Populations

Catherine Tcheandjieu,Xiang Zhu,Austin T. Hilliard,Shoa L. Clarke,Valerio Napolioni,Shining Ma,Kyung Min Lee,Huaying Fang,Fei Chen,Yingchang Lu,Noah L. Tsao,Sridharan Raghavan,Satoshi Koyama,Bryan R. Gorman,Marijana Vujkovic,Derek Klarin,Michael G. Levin,Nasa Sinnott-Armstrong,Genevieve L. Wojcik,Mary E. Plomondon,Thomas M. Maddox,Stephen W. Waldo,Alexander G. Bick,Saiju Pyarajan,Jie Huang,Rebecca Song,Yuk-Lam Ho,Steven Buyske,Charles Kooperberg,Jeffrey Haessler,Ruth J. F. Loos,Ron Do,Marie Verbanck,Kumardeep Chaudhary,Kari E. North,Christy L. Avery,Mariaelisa Graff,Christopher A. Haiman,Loïc Le Marchand,Lynne R. Wilkens,Joshua C. Bis,Hampton Leonard,Botong Shen,Leslie A. Lange,Ayush Giri,Ozan Dikilitas,Iftikhar J. Kullo,Ian B. Stanaway,Gail P. Jarvik,Adam S. Gordon,Scott Hebbring,Bahram Namjou,Kenneth M. Kaufman,Kaoru Ito,Kazuyoshi Ishigaki,Yoichiro Kamatani,Shefali S. Verma,Marylyn D. Ritchie,Rachel L. Kember, Aris Baras,Luca A. Lotta,Sekar Kathiresan,Elizabeth R. Hauser,Donald R. Miller,Jennifer S. Lee,Danish Saleheen,Peter D. Reaven,Kelly Cho,J. Michael Gaziano,Pradeep Natarajan,Jennifer E. Huffman,Benjamin F. Voight,Daniel J. Rader,Kyong-Mi Chang,Julie A. Lynch,Scott M. Damrauer,Peter W. F. Wilson,Hua Tang,Yan V. Sun,Philip S. Tsao,Christopher J. O’Donnell,Themistocles L. Assimes

Carolina Digital Repository (University of North Carolina at Chapel Hill)（2022）

引用126浏览0WOSNATURE引用

126

ACMG SF V3.1 List for Reporting of Secondary Findings in Clinical Exome and Genome Sequencing: A Policy Statement of the American College of Medical Genetics and Genomics (ACMG)

David T. Miller,Kristy Lee,Noura S. Abul-Husn,Laura M. Amendla,Kyle Brothers,Wendy K. Chung,Michael H. Gollob,Adam S. Gordon,Steven M. Harrison,Ray E. Hershberger,Teri E. Klein,Carolyn Sue Richards,Douglas R. Stewart,Christa Lese Martin

Genetics in medicine（2022）

引用85浏览0WOS引用

Response to McGurk Et Al

Michael H. Gollob,Ray E. Hershberger,Adam S. Gordon,Steven M. Harrison,Kristy Lee,Christa Lese Martin,David T. Miller

Genetics in medicine（2022）

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Anti-racist Strategies for Clinical and Translational Research: Design, Implementation, and Lessons Learned from a New Course

Nia J. Heard-Garris, Jen F. Brown,Uchenna C. Ewulonu,Mita S. Goel,Adam S. Gordon,Candace Henley,Sadiya S. Khan, Shawn M. Smith,Susanna A. McColley

Journal of clinical and translational science（2022）

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