Haines JL - Search Results

1

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis.

Kwiatkowski TJ Jr, Bosco DA, Leclerc AL, Tamrazian E, Vanderburg CR, Russ C, Davis A, Gilchrist J, Kasarskis EJ, Munsat T, Valdmanis P, Rouleau GA, Hosler BA, Cortelli P, de Jong PJ, Yoshinaga Y, Haines JL, Pericak-Vance MA, Yan J, Ticozzi N, Siddique T, McKenna-Yasek D, Sapp PC, Horvitz HR, Landers JE, Brown RH Jr. Kwiatkowski TJ Jr, et al. Among authors: haines jl. Science. 2009 Feb 27;323(5918):1205-8. doi: 10.1126/science.1166066. Science. 2009. PMID: 19251627

2

Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markers.

Rosen DR, Sapp P, O'Regan J, McKenna-Yasek D, Schlumpf KS, Haines JL, Gusella JF, Horvitz HR, Brown RH Jr. Rosen DR, et al. Among authors: haines jl. Am J Med Genet. 1994 May 15;51(1):61-9. doi: 10.1002/ajmg.1320510114. Am J Med Genet. 1994. PMID: 7913294

3

Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33.

Hosler BA, Sapp PC, Berger R, O'Neill G, Bejaoui K, Hamida MB, Hentati F, Chin W, McKenna-Yasek D, Haines JL, Patterson D, Horvitz HR, Brown RH Jr, Day CB. Hosler BA, et al. Among authors: haines jl. Neurogenetics. 1998 Dec;2(1):34-42. doi: 10.1007/s100480050049. Neurogenetics. 1998. PMID: 9933298

4

Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22.

Hosler BA, Siddique T, Sapp PC, Sailor W, Huang MC, Hossain A, Daube JR, Nance M, Fan C, Kaplan J, Hung WY, McKenna-Yasek D, Haines JL, Pericak-Vance MA, Horvitz HR, Brown RH Jr. Hosler BA, et al. Among authors: haines jl. JAMA. 2000 Oct 4;284(13):1664-9. doi: 10.1001/jama.284.13.1664. JAMA. 2000. PMID: 11015796

5

Gene linkage in familial amyotrophic lateral sclerosis: a progress report.

Brown RH Jr, Horvitz HR, Rouleau GA, McKenna-Yasek D, Beard C, Sapp P, Haines JL, Gusella JF, Figlewicz DA. Brown RH Jr, et al. Among authors: haines jl. Adv Neurol. 1991;56:215-26. Adv Neurol. 1991. PMID: 1853758 No abstract available.

6

Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity.

Siddique T, Figlewicz DA, Pericak-Vance MA, Haines JL, Rouleau G, Jeffers AJ, Sapp P, Hung WY, Bebout J, McKenna-Yasek D, et al. Siddique T, et al. Among authors: haines jl. N Engl J Med. 1991 May 16;324(20):1381-4. doi: 10.1056/NEJM199105163242001. N Engl J Med. 1991. PMID: 2020294 Free article.

7

Lack of association between apolipoprotein E genotype and sporadic amyotrophic lateral sclerosis.

Siddique T, Pericak-Vance MA, Caliendo J, Hong ST, Hung WY, Kaplan J, McKenna-Yasek D, Rimmler JB, Sapp P, Saunders AM, Scott WK, Siddique N, Haines JL, Brown RH. Siddique T, et al. Among authors: haines jl. Neurogenetics. 1998 Mar;1(3):213-6. doi: 10.1007/s100480050031. Neurogenetics. 1998. PMID: 10737125

8

Identification of flanking markers for the familial amyotrophic lateral sclerosis gene ALS1 on chromosome 21.

Figlewicz DA, McInnis MG, Goto J, Haines JL, Warren AC, Krizus A, Khodr N, Brown RH Jr, McKenna-Yasek D, Antonarakis SE, et al. Figlewicz DA, et al. Among authors: haines jl. J Neurol Sci. 1994 Jul;124 Suppl:90-5. doi: 10.1016/0022-510x(94)90190-2. J Neurol Sci. 1994. PMID: 7807155

9

The glycinamide ribonucleotide transformylase (GART) gene is not responsible for familial amyotrophic lateral sclerosis.

Goto J, Figlewicz DA, Haines JL, Brown RH Jr, Khodr N, Rouleau GA. Goto J, et al. Among authors: haines jl. Neuromuscul Disord. 1993 Mar;3(2):157-60. doi: 10.1016/0960-8966(93)90008-8. Neuromuscul Disord. 1993. PMID: 8358240

10

Temperature-sensitive mutations in the III-IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenita.

McClatchey AI, Van den Bergh P, Pericak-Vance MA, Raskind W, Verellen C, McKenna-Yasek D, Rao K, Haines JL, Bird T, Brown RH Jr, et al. McClatchey AI, et al. Among authors: haines jl. Cell. 1992 Feb 21;68(4):769-74. doi: 10.1016/0092-8674(92)90151-2. Cell. 1992. PMID: 1310898

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