検索結果 - Flavia Chen
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The role of exome sequencing in newborn screening for inborn errors of metabolism 著者: Aashish N. Adhikari, Renata C. Gallagher, Yaqiong Wang, Robert J. Currier, George S. Amatuni, Laia Bassaganyas, Flavia Chen, Kunal Kundu, Mark Kvale, Sean D. Mooney, Robert L. Nussbaum, Savanna S. Randi, Jeremy R. Sanford, Joseph T.C. Shieh, Rajgopal Srinivasan, Uma Sunderam, Hao Tang, Dedeepya Vaka, Yangyun Zou, Barbara A. Koenig, Pui‐Yan Kwok, Neil Risch, Jennifer M. Puck, Steven E. Brenner
出版事項 2020Artigo -
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Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population 著者: Anne Slavotinek, Shannon Rego, Nuriye Sahin‐Hodoglugil, Mark Kvale, Billie R. Lianoglou, Tiffany Yip, Hannah Hoban, Simon Outram, Beatrice Anguiano, Flavia Chen, Jeremy Michelson, Roberta Cilio, Cynthia J. Curry, Renata C. Gallagher, Marisa Gardner, Rachel Kuperman, Bryce A. Mendelsohn, Elliott H. Sherr, Joseph T.C. Shieh, Jonathan B. Strober, Allison Tam, Jessica Tenney, William A. Weiss, Amy Whittle, Garrett Chin, Amanda Faubel, Hannah Prasad, Yusuph Mavura, Jessica Van Ziffle, W. Patrick Devine, Uğur Hodoğlugil, Pierre‐Marie Martin, Teresa N. Sparks, Barbara A. Koenig, Sara Ackerman, Neil Risch, Pui‐Yan Kwok, Mary E. Norton
出版事項 2023Artigo -
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Newborn Sequencing in Genomic Medicine and Public Health 著者: Jonathan S. Berg, Pankaj B. Agrawal, Donald B. Bailey, Alan H. Beggs, Steven E. Brenner, Amy Brower, Julie A. Cakici, Ozge Ceyhan‐Birsoy, Kee Chan, Flavia Chen, Robert J. Currier, Dmitry Dukhovny, Robert C. Green, Julie Harris-Wai, Ingrid A. Holm, Brenda Iglesias, Galen Joseph, Stephen F. Kingsmore, Barbara A. Koenig, Pui‐Yan Kwok, John D. Lantos, Steven J. Leeder, Megan A. Lewis, Amy L. McGuire, Laura V. Milko, Sean D. Mooney, Richard B. Parad, Stacey Pereira, Joshua E. Petrikin, Bradford C. Powell, Cynthia M. Powell, Jennifer M. Puck, Heidi L. Rehm, Neil Risch, Myra I. Roche, Joseph T.C. Shieh, Narayanan Veeraraghavan, Michael S. Watson, Laurel K. Willig, Timothy W. Yu, Tiina K. Urv, Anastasia L. Wise
出版事項 2017Artigo
関連主題
Medicine
Biology
Gene
Genetics
Newborn screening
Pediatrics
Computational biology
Exome sequencing
Genome
Mutation
Pathology
Personalized medicine
Psychiatry
Psychology
Public health
Social psychology
Whole genome sequencing
Alternative medicine
Bioinformatics
Business
Cognition
Cohort
DNA sequencing
Endocrinology
Epistemology
Exome
Family medicine
Fetus
Focus group
Genomic medicine