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William A Gahl, M.D., Ph.D.

Clinical Director, National Human Genome Research Institute
Senior Investigator, Medical Genetics Branch
Head, Section on Human Biochemical Genetics

Selected Publications

Papers

Phornphutkul C., Introne W.J., Perry M.B., Bernardini I., Murphey M.D., Fitzpatrick D.L., Anderson P.D., Huizing M., Anikster Y., Gerber L.H., Gahl W.A. Natural history of alkaptonuria. N Engl J Med, 347:2111-2121. 2002. [PubMed]

Gahl W.A., Thoene J.G., Schneider J.A. Cystinosis. N Engl J Med, 347:111-121. 2002. [PubMed]

Kleta R., Romeo E., Ristic Z., Ohura T., Stuart C., Arcos-Burgos M., Dave M.H., Wagner C.A., Camargo S.R.M., Inoue S., Matsuura N., Helip-Wooley A., Bockenhauer D., Warth R., Bernardini I., Visser G., Eggermann T., Lee P., Chairoungdua A., Jutabha P., Babu E., Nilwarangkoon S., Anzai N., Kanai Y., Verrey F., Gahl W.A., Koizumi A. Mutations in SLC6A19, encoding BoAT1, cause Hartnup disorder. Nature Genet, 36(9):999-1002. 2004. [PubMed]

Gunay-Aygun, M., Huizing, M,, Gahl, W.A. Molecular defects that affect platelet dense granules. Thromb Haemostasis, 30(5):537-47. 2004. [PubMed]

Sonies, B.C., Almajid, P., Kleta, R., Bernardini, I., Gahl, W.A. Swallowing dysfunction in 101 patients with nephropathic cystinosis: Benefit of long-term cysteamine therapy. Medicine, 84:137-146, 2005. [PubMed]

Suwannarat, P., O'Brien, K., Perry, M.B., Sebring, N., Bernardini, I., Kaiser-Kupfer, M.I., Rubin, B.I., Tsilou, E., Gerber, L.H., Gahl, W.A. Use of nitisinone in patients with alkaptonuria. Metabolism Clin Exptl, 54:719-728, 2005.

Helip-Wooley, A., Westbroek, W., Dorward, H., Mommaas, M., Boissy, R., Gahl, W.A., Huizing, M. Hermansky-Pudlak syndrome type-3 protein interacts with clathrin and traffics lysosome-related organelles. BMC Cell Biology, 6:33, 2005. [PubMed]

Ueda, M., O'Brien, K., Rosing, D.R., Ling, A., Kleta, R., MacAreavey, D., Bernardini, I., Gahl, W.A. Coronary artery and other vascular calcifications in cystinosis patients after kidney transplantation. Clin J Am Soc Nephrol, 1:555-562, 2006.

Helip-Wooley, A., Boissy, R.E., Westbroek, W., Dorward, H., Koshoffer, A., Huizing, M., Gahl, W.A. Improper trafficking of melanocyte-specific proteins in Hermansky-Pudlak syndrome type-5. J Invest Dermatol, 127:1471-1478. 2007. [PubMed]

Galeano, B., Klootwijk, R., Manoli, I., Sun, M-S., Ciccone, C., Darvish, D., Starost M.F., Zerfas, P.M., Hoffmann, V.J., Hoogstraten-Miller, S., Krasnewich, D.M., Gahl, W.A., Huizing M. Mutation in the key enzyme of sialic acid biosynthesis causes severe glomerular proteinuria and is rescued by N-acetylmannosamine. J Clin Invest, 117:1585-1594. 2007. [PubMed]

Book Chapters

Gahl W.A., Thoene J., Schneider J.A. Cystinosis: A Disorder of Lysosomal Membrane Transport. In: Scriver CR, Beaudet AL, Sly WS, Valle D, Childs B, Kinzler KW, Vogelstein B. The Metabolic and Molecular Basis of Inherited Disease. McGraw-Hill Companies, Inc., Eighth Edition, pp. 5085-5108. 2001.

Aula P., Gahl W.A. Sialic Acid Storage Diseases. In: Scriver CR, Beaudet AL, Sly WS, Valle D, Childs B, Kinzler KW, Vogelstein B. The Metabolic and Molecular Basis of Inherited Disease. McGraw-Hill Companies, Inc., Eighth Edition, pp. 5109-5120. 2001.

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Last Reviewed: April 29, 2009