Haines JL - Search Results

1

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

2

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.

3

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

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

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

6

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

7

Confirmation of linkage of type 1 hereditary sensory neuropathy to human chromosome 9q22.

Bejaoui K, McKenna-Yasek D, Hosler BA, Burns-Deater E, Deater LM, O'Neill G, Haines JL, Brown RH Jr. Bejaoui K, et al. Among authors: haines jl. Neurology. 1999 Feb;52(3):510-5. doi: 10.1212/wnl.52.3.510. Neurology. 1999. PMID: 10025779

8

Genetics of multiple sclerosis.

Haines JL, Pericak-Vance MA. Haines JL, et al. Curr Dir Autoimmun. 1999;1:273-88. doi: 10.1159/000060491. Curr Dir Autoimmun. 1999. PMID: 11791446 Review. No abstract available.

9

Flanking markers for the gene causing von Recklinghausen neurofibromatosis (NF1).

Seizinger BR, Farmer GE, Haines JL, Ozelius LJ, Anderson K, Korf BR, Parry DM, Pericak-Vance MA, Mulvihill JJ, Menon A, et al. Seizinger BR, et al. Among authors: haines jl. Am J Hum Genet. 1989 Jan;44(1):30-2. Am J Hum Genet. 1989. PMID: 2491778 Free PMC article.

10

A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group.

Haines JL, Ter-Minassian M, Bazyk A, Gusella JF, Kim DJ, Terwedow H, Pericak-Vance MA, Rimmler JB, Haynes CS, Roses AD, Lee A, Shaner B, Menold M, Seboun E, Fitoussi RP, Gartioux C, Reyes C, Ribierre F, Gyapay G, Weissenbach J, Hauser SL, Goodkin DE, Lincoln R, Usuku K, Oksenberg JR, et al. Haines JL, et al. Nat Genet. 1996 Aug;13(4):469-71. doi: 10.1038/ng0896-469. Nat Genet. 1996. PMID: 8696344

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