Core Programs

Publications

Amyotropic Lateral Sclerosis (ALS)

Li YJ, Pericak-Vance MA, Haines JL, Siddique N, McKenna-Yasek D, Hung WY, Sapp P, Allen CI, Chen W, Hosler B, Saunders AM, Dellefave LM, Brown RH Jr, Siddique T. Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis. Neurogenetics 5(4):209-13, 2004.

Sapp PC, Hosler BA, McKenna-Yasek D, Chin W, Gann A, Genise H, Gorenstein J, Huang M, Sailer W, Scheffler M, Valesky M, Haines JL, Pericak-Vance M, Siddique T, Horvitz HR, Brown, Jr. RH. Identification of Two Novel Loci for Dominantly Inherited Familial Amyotrophic Lateral Sclerosis. Am J Hum Genet 73:397-403, 2003.

Yang Y, Hentati A, Deng HX, Dabbagh O, Sasaki T, Hirano M, Hung WY, Ouahchi K, Yan J, Azim AC, Cole N, Gascon G, Yagmour A, Ben-Hamida M, Hentati F, Siddique T. The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis. Nature Genetics 29(2): 160-165, 2001.

Hosler BA, Siddique T, Sapp PC, Sailor W, Huang MC, Hossain A, Rimmler JB, Daube JR, Nance M, Fan C, Kaplan J, Hung W-Y, Haines JL, Pericak-Vance MA, Horvitz HR, and Brown RH Jr. Linkage of familial amyotrophic lateral sclerosis with fronto-temporal dementia (ALS-FTD) to chromosome 9q21-q22. JAMA, 284(13): 1664-1669, 2000.

Hentati A, Ouahchi K, Pericak-Vance MA, Nijhawan D, Ahmad A, Yang Y, Rimmler J, Hung W, Schlotter B, Ahmed A, Ben Hamida M, Hentati F, Siddique T. Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers. Neurogenetics 2(1):55-60, 1998.

Juneja T, Pericak-Vance MA, Laing NG, Dave S, Siddique T. Prognosis in familial amyotrophic lateral sclerosis: progression and survival in patients with glu100gly and ala4val mutations in Cu, Zn superoxide dismutase. Neurology 48(1):55-7, 1997.

Hentati A, Bejaoui K, Pericak-Vance MA, Hentati F, Speer MC, Hung WY, Figlewicz DA, Haines J, Rimmler J, Ben Hamida C et al. Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35. Nat Genet 7(3):425-8, 1994.

Eubanks JH, Puranam RS, Kleckner NW, Bettler B, Heinemann SF, McNamara JO. The gene encoding the glutamate receptor subunit GluR5 is located on human chromosome 21q21.1-22.1 in the vicinity of the gene for familial amyotrophic lateral sclerosis. Proc Natl Acad Sci USA 1:90(1):178-82, 1993.

Siddique T, Pericak-Vance MA, Brooks BR, Antel J, Roos RP, Munsat T, Phillips K, Warner K, Bias W, Siddique N, Hung W Y, and Roses AD. Exclusion mapping in familial amyotrophic lateral sclerosis (ALS). Neurology 38(1):270, 1988.

Siddique T, Pericak-Vance MA, Brooks BR, Bias W, Walker N, Siddique T, Hung W Y, and Roses AD. Linkage in familial amyotrophic lateral sclerosis (ALS). Cytogenet Cell Genet 46:692, 1987.

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