Suchergebnisse - Ingrid A. Holm
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A clinician's guide to X-linked hypophosphatemia von Thomas O. Carpenter, Erik A. Imel, Ingrid A. Holm, Suzanne M. Jan de Beur, Karl Insogna
Veröffentlicht 2011Revisão -
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Pediatric clinical exome/genome sequencing and the engagement process: encouraging active conversation with the older child and adolescent: points to consider—a statement of the Am... von Lynn Wein Bush, Louis Bartoshesky, Karen L. David, Benjamin S. Wilfond, Janet L. Williams, Ingrid A. Holm
Veröffentlicht 2018Artigo -
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Guidelines for return of research results from pediatric genomic studies: deliberations of the Boston Children’s Hospital Gene Partnership Informed Cohort Oversight Board von Ingrid A. Holm, Sarah Savage, Robert C. Green, Eric T. Juengst, Amy L. McGuire, Susan Kornetsky, Stephanie J. Brewster, Steven Joffe, Patrick Taylor
Veröffentlicht 2014Artigo -
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The beliefs, motivations, and expectations of parents who have enrolled their children in a genetic biorepository von Erin D. Harris, Sonja I. Ziniel, Jonathan G. Amatruda, Catherine Clinton, Sarah Savage, Patrick L. Taylor, Noelle Huntington, Robert C. Green, Ingrid A. Holm
Veröffentlicht 2012Artigo -
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Hypervitaminosis D Associated with Drinking Milk von Claire H. Jacobus, Michael F. Holick, Qing Shao, Tai C. Chen, Ingrid A. Holm, Jonathan M. Kolodny, Ghada El‐Hajj Fuleihan, Ellen W. Seely
Veröffentlicht 1992Artigo -
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A systematic literature review of individuals’ perspectives on broad consent and data sharing in the United States von Nanibaa’ A. Garrison, Nila A Sathe, Armand H. Matheny Antommaria, Ingrid A. Holm, Saskia C. Sanderson, Maureen E. Smith, Melissa L McPheeters, Ellen Wright Clayton
Veröffentlicht 2015Artigo -
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Rethinking the “open future” argument against predictive genetic testing of children von Jeremy R. Garrett, John D. Lantos, Leslie G. Biesecker, Janet E. Childerhose, Wendy K. Chung, Ingrid A. Holm, Barbara A. Koenig, Jean E. McEwen, Benjamin S. Wilfond, Kyle B. Brothers
Veröffentlicht 2019Artigo -
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Perceived Benefits, Risks, and Utility of Newborn Genomic Sequencing in the BabySeq Project von Stacey Pereira, Jill O. Robinson, Amanda M. Gutierrez, Devan Petersen, Rebecca L. Hsu, Caroline H. Lee, Talia S. Schwartz, Ingrid A. Holm, Alan H. Beggs, Robert C. Green, Amy L. McGuire
Veröffentlicht 2019Artigo -
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A curated gene list for reporting results of newborn genomic sequencing von Ozge Ceyhan‐Birsoy, Kalotina Machini, Matthew S. Lebo, Timothy W. Yu, Pankaj B. Agrawal, Richard B. Parad, Ingrid A. Holm, Amy L. McGuire, Robert C. Green, Alan H. Beggs, Heidi L. Rehm
Veröffentlicht 2017Artigo -
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Patient re-contact after revision of genomic test results: points to consider—a statement of the American College of Medical Genetics and Genomics (ACMG) von Karen L. David, Robert G. Best, Leslie Manace Brenman, Lynn Wein Bush, Joshua L. Deignan, David B. Flannery, Jodi D. Hoffman, Ingrid A. Holm, David T. Miller, James O’Leary, Reed E. Pyeritz
Veröffentlicht 2018Artigo -
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Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents von Jeffrey R. Botkin, John W. Belmont, Jonathan S. Berg, Benjamin E. Berkman, Yvonne Bombard, Ingrid A. Holm, Howard P. Levy, Kelly E. Ormond, Howard M. Saal, Nancy B. Spinner, Benjamin S. Wilfond, Joseph D. McInerney
Veröffentlicht 2015Revisão -
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Genetic Determinants of Sudden Unexpected Death in Pediatrics von Hyun Yong Koh, Alireza Haghighi, Christine Keywan, Sanda Alexandrescu, Erin Plews-Ogan, Elisabeth A. Haas, Catherine A. Brownstein, Sara O. Vargas, Robin L. Haynes, Gerard T. Berry, Ingrid A. Holm, Annapurna Poduri, Richard D. Goldstein
Veröffentlicht 2022Artigo -
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Mutational Analysis of PHEX Gene in X-Linked Hypophosphatemia1 von Peter H. Dixon, Paul T. Christie, C Wooding, Dorothy Trump, Marvin Grieff, Ingrid A. Holm, Joseph M. Gertner, Jörg Schmidtke, Binita Shah, Nicholas Shaw, Colin Smith, Christina Tau, David Schlessinger, Michael P. Whyte, Rajesh V. Thakker
Veröffentlicht 1998Artigo -
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EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children von Bahram Namjou, Mehdi Keddache, Keith Marsolo, Michael Wagner, Todd Lingren, Beth L. Cobb, Cassandra Perry, Stephanie Kennebeck, Ingrid A. Holm, Rongling Li, Nancy A. Crimmins, Lisa J. Martin, Imre Solti, Isaac S. Kohane, John B. Harley
Veröffentlicht 2013Artigo -
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Mutations in the Gene Encoding the Calcium-Permeable Ion Channel TRPV4 Produce Spondylometaphyseal Dysplasia, Kozlowski Type and Metatropic Dysplasia von Deborah Krakow, Joris Vriens, Natalia Camacho, Phi Luong, Hannah Deixler, Tara Funari, Carlos A. Bacino, Mira Irons, Ingrid A. Holm, Laurie S. Sadler, Ericka Okenfuss, Annelies Janssens, Thomas Voets, David L. Rimoin, Ralph S. Lachman, Bernd Nilius, Daniel H. Cohn
Veröffentlicht 2009Artigo
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Exome sequencing
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