William A. Gahl
William A. Gahl formerly served (2002 to 2019) as the Clinical Director of the National Human Genome Research Institute at the NIH main campus in Bethesda, MD.Gahl graduated with a BS degree from Massachusetts Institute of Technology in 1972. He earned his MD degree in 1976 and his PhD degree in 1981 degree from the University of Wisconsin, Madison. Gahl is board-certified in medical geneticist, biochemical genetics, and pediatrics.
Gahl conducts research on rare inborn errors of metabolism, focusing on the observation and treatment of patients in the clinic as well as carrying out biochemical, molecular biological, and cell biological investigations in the laboratory. His group focuses on a number of disorders, including cystinosis, Hermansky-Pudlak syndrome, alkaptonuria, and sialic acid diseases.
Gahl was the leader in creating the National Institutes of Health Undiagnosed Diseases Program (UDP). The UDP is a trans-National Institutes of Health (NIH) initiative that focuses on the most puzzling medical cases referred to the NIH Clinical Center in Bethesda, Md. The program's success led to the creation of the Undiagnosed Diseases Network, which eventually expanded the effort to encompass eleven additional clinical sites at academic medical centers across the US, along with a DNA sequencing core, a coordinating center, a metabolomics core, a central biorepository, and a model organisms screening center.
He was elected to the National Academy of Medicine in 2018. Provided by Wikipedia
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Patients with rare diseases: from therapeutic orphans to pioneers of personalized treatments by Christoph Klein, William A Gahl
Published 2017-11-01Get full text
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Calciphylaxis in POEMS syndrome: Case report by Danica Novacic, Thomas Uldrick, Alina Dulau-Florea, Colleen Evans Howe, Chyi-Chia R. Lee, Heidi H. Kong, William A. Gahl
Published 2024-01-01Get full text
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Investigating the Utility of Leukocyte Sialic Acid Measurements in Lysosomal Free Sialic Acid Storage Disorder by Marya S. Sabir, Laura Pollard, Lynne Wolfe, David R. Adams, Carla Ciccone, Petcharat Leoyklang, Frances M. Platt, Marjan Huizing, William A. Gahl, May Christine V. Malicdan
Published 2025-07-01Get full text
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Retrospective assessment of clinical global impression of severity and change in GM1 gangliosidosis: a tool to score natural history data in rare disease cohorts by Connor J. Lewis, Jean M. Johnston, Silvia Zaragoza Domingo, Gilbert Vezina, Precilla D’Souza, William A. Gahl, David A. Adams, Cynthia J. Tifft, Maria T. Acosta
Published 2025-03-01Get full text
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Generation and characterization of two iPSC lines derived from subjects with Free Sialic Acid Storage Disorder (FSASD) by Marya S. Sabir, Petcharat Leoyklang, Mary E. Hackbarth, Evgenia Pak, Amalia Dutra, Richard Tait, Laura Pollard, David R. Adams, William A. Gahl, Marjan Huizing, May Christine V. Malicdan
Published 2024-12-01Get full text
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Lysosomal free sialic acid storage disorder iPSC-derived neural cells display altered glycosphingolipid metabolism by Marya S. Sabir, Vukasin M. Jovanovic, Seungmi Ryu, Chaitali Sen, Pinar Ormanoglu, Laura Pollard, Richard Steet, William A. Gahl, Marjan Huizing, Carlos A. Tristan, Frances M. Platt, May Christine V. Malicdan
Published 2025-08-01Get full text
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An atypical presentation of infiltrative diffuse low-grade glioma in an adolescent: case report by Zoe Wolfenson, Daniel Benavides, Connor J. Lewis, Gilbert Vezina, Lynne Wolfe, Ellen Macnamara, John Yang, John D. Heiss, Kenneth Aldape, Chris Dampier, Sadhana Jackson, Robert Stone, David Korones, William A. Gahl, Maria T. Acosta
Published 2025-07-01Get full text
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A Case for Automated Segmentation of MRI Data in Neurodegenerative Diseases: Type II GM1 Gangliosidosis by Connor J. Lewis, Jean M. Johnston, Precilla D’Souza, Josephine Kolstad, Christopher Zoppo, Zeynep Vardar, Anna Luisa Kühn, Ahmet Peker, Zubir S. Rentiya, Muhammad H. Yousef, William A. Gahl, Mohammed Salman Shazeeb, Cynthia J. Tifft, Maria T. Acosta
Published 2025-04-01Get full text
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FOXR1 regulates stress response pathways and is necessary for proper brain development. by Andressa Mota, Hannah K Waxman, Rui Hong, Gavin D Lagani, Sheng-Yong Niu, Féodora L Bertherat, Lynne Wolfe, Christine May Malicdan, Thomas C Markello, David R Adams, William A Gahl, Christine S Cheng, Uwe Beffert, Angela Ho
Published 2021-11-01Get full text
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A murine model lacking Lyst recapitulates Chediak-Higashi syndrome with an earlier-onset neurodegenerative phenotype by Sunny Greene, Mackenzie L. Talbert, F. Graeme Frost, Patricia M. Zerfas, Danielle Springer, Audrey Noguchi, Marie Morimoto, Dawn Maynard, Lisa Garrett, Gene Elliot, Maria Traver, David Yarnell, Petcharat Leoyklang, John D. Burke, Elena-Raluca Nicoli, William A. Gahl, Wendy J. Introne, May Christine V. Malicdan
Published 2025-07-01Get full text
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Variants in WASHC3, a component of the WASH complex, cause short stature, variable neurodevelopmental abnormalities, and distinctive facial dysmorphism by Youn Hee Jee, Julian C. Lui, Dana Marafi, Zhi-Jie Xia, Ruchika Bhatia, Elaine Zhou, Isabella Herman, Adrian Temnycky, Philip Whalen, Gene Elliot, Ellen W. Leschek, Robin Wijngaard, Ronald van Beek, Annemarie de Vreugd, Maaike C. de Vries, Clara D.M. van Karnebeek, Machteld M. Oud, Thomas C. Markello, Kevin M. Barnes, Hadil Alrohaif, Hudson H. Freeze, William A. Gahl, May Christine V. Malicdan, Jennifer E. Posey, James R. Lupski, Jeffrey Baron
Published 2025-01-01Get full text
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A global survey about undiagnosed rare diseases: perspectives, challenges, and solutions by Simone Baldovino, Savino Sciascia, Claudio Carta, Marco Salvatore, Laura L. Cellai, Gianluca Ferrari, Aimé Lumaka, Stephen Groft, Yasemin Alanay, Maleeha Azam, Gareth Baynam, Helene Cederroth, Eva Maria Cutiongco-de la Paz, Vajira Harshadeva Weerabaddana Dissanayake, Roberto Giugliani, Claudia Gonzaga-Jauregui, Dineshani Hettiarachchi, Oleg Kvlividze, Guida Landoure, Prince Makay, Béla Melegh, Ugur Ozbek, Karaman Pagava, Ratna Dua Puri, Vaness I. Romero, Vinod Scaria, Saumya S. Jamuar, Vorasuk Shotelersuk, Dario Roccatello, William A. Gahl, Samuel A. Wiafe, Olaf Bodamer, Manuel Posada, Domenica Taruscio
Published 2025-02-01Get full text
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