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论文共 10 篇作者统计合作学者相似作者

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The Impact of Clinical Genome Sequencing in a Global Population with Suspected Rare Genetic Disease

Erin Thorpe, Taylor Williams,Chad Shaw, Evgenii Chekalin,Julia Ortega,Keisha Robinson, Jason Button,Marilyn C. Jones,Miguel del Campo,Donald Basel,Julie McCarrier,Laura Davis Keppen,Erin Royer, Romina Foster-Bonds,Milagros M. Duenas-Roque,Nora Urraca,Kerri Bosfield,Chester W. Brown, Holly Lydigsen,Henry J. Mroczkowski,Jewell Ward,Fabio Sirchia,Elisa Giorgio,Keith Vaux, Hildegard Pena Salguero,Aime Lumaka,Gerrye Mubungu,Prince Makay,Mamy Ngole,Prosper Tshilobo Lukusa,Adeline Vanderver,Kayla Muirhead,Omar Sherbini,Melissa D. Lah,Katelynn Anderson,Jeny Bazalar-Montoya,Richard S. Rodriguez,Mario Cornejo-Olivas,Karina Milla-Neyra,Marwan Shinawi,Pilar Magoulas,Duncan Henry, Kate Gibson,Samuel Wiafe,Parul Jayakar,Daria Salyakina,Diane Masser-Frye,Arturo Serize,Jorge E. Perez,Alan Taylor,Shruti Shenbagam,Ahmad Abou Tayoun,Alka Malhotra,Maren Bennett,Vani Rajan,James Avecilla, Andrew Warren, Max Arseneault,Tasha Kalista,Ali Crawford,Subramanian S. Ajay,Denise L. Perry,John Belmont,Ryan J. Taft

AMERICAN JOURNAL OF HUMAN GENETICSno. 7 (2024)

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A Validated PCR-free Clinical Whole Genome Sequencing System for the Detection of Germline Variants

Christine Glidewell-Kenney,Vitor Onuchic, Konstantin Sabourov, Noah Dukler, Mike Mehan,Joyce Lee, Francesca Fiocco,Nafeesa Khan, Jing Su, Ying Liu, Jairus Kleinert, Ramya Akula Suresh Babu, Adrian Leelin, Laura Rivas Yepes, Krizelle Minde, Christian Abaya, Sruja Iyer, Devina Naidu, Carrie Ludman, Tram Nguyen, Mitch Bekritsky, Victoria Corey, Daniel Andrews, Derek Blythe, Paul Wenz, Kelechi Eluwa,Ali Crawford,Ryan Taft

EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 640-641

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Variants in ZFX Are Associated with an X-linked Neurodevelopmental Disorder with Recurrent Facial Gestalt