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722 results

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Page 1
Huntington disease: no evidence for locus heterogeneity.
Conneally PM, Haines JL, Tanzi RE, Wexler NS, Penchaszadeh GK, Harper PS, Folstein SE, Cassiman JJ, Myers RH, Young AB, et al. Conneally PM, et al. Among authors: haines jl. Genomics. 1989 Aug;5(2):304-8. doi: 10.1016/0888-7543(89)90062-1. Genomics. 1989. PMID: 2571579 Free article.
An autosomal genomic screen for autism. Collaborative linkage study of autism.
Barrett S, Beck JC, Bernier R, Bisson E, Braun TA, Casavant TL, Childress D, Folstein SE, Garcia M, Gardiner MB, Gilman S, Haines JL, Hopkins K, Landa R, Meyer NH, Mullane JA, Nishimura DY, Palmer P, Piven J, Purdy J, Santangelo SL, Searby C, Sheffield V, Singleton J, Slager S, et al. Barrett S, et al. Among authors: haines jl. Am J Med Genet. 1999 Dec 15;88(6):609-15. doi: 10.1002/(sici)1096-8628(19991215)88:6<609::aid-ajmg7>3.3.co;2-c. Am J Med Genet. 1999. Corrected and republished in: Am J Med Genet. 2001 Dec 8;105(8):609-15. PMID: 10581478 Corrected and republished.
Evidence supporting WNT2 as an autism susceptibility gene.
Wassink TH, Piven J, Vieland VJ, Huang J, Swiderski RE, Pietila J, Braun T, Beck G, Folstein SE, Haines JL, Sheffield VC. Wassink TH, et al. Among authors: haines jl. Am J Med Genet. 2001 Jul 8;105(5):406-13. doi: 10.1002/ajmg.1401. Am J Med Genet. 2001. PMID: 11449391
Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families.
Nurmi EL, Bradford Y, Chen Y, Hall J, Arnone B, Gardiner MB, Hutcheson HB, Gilbert JR, Pericak-Vance MA, Copeland-Yates SA, Michaelis RC, Wassink TH, Santangelo SL, Sheffield VC, Piven J, Folstein SE, Haines JL, Sutcliffe JS. Nurmi EL, et al. Among authors: haines jl. Genomics. 2001 Sep;77(1-2):105-13. doi: 10.1006/geno.2001.6617. Genomics. 2001. PMID: 11543639
Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease.
Martin ER, Scott WK, Nance MA, Watts RL, Hubble JP, Koller WC, Lyons K, Pahwa R, Stern MB, Colcher A, Hiner BC, Jankovic J, Ondo WG, Allen FH Jr, Goetz CG, Small GW, Masterman D, Mastaglia F, Laing NG, Stajich JM, Ribble RC, Booze MW, Rogala A, Hauser MA, Zhang F, Gibson RA, Middleton LT, Roses AD, Haines JL, Scott BL, Pericak-Vance MA, Vance JM. Martin ER, et al. Among authors: haines jl. JAMA. 2001 Nov 14;286(18):2245-50. doi: 10.1001/jama.286.18.2245. JAMA. 2001. PMID: 11710889 Free PMC article.
Linkage and association analysis of chromosome 19q13 in multiple sclerosis.
Pericak-Vance MA, Rimmler JB, Martin ER, Haines JL, Garcia ME, Oksenberg JR, Barcellos LF, Lincoln R, Goodkin DE, Hauser SL. Pericak-Vance MA, et al. Among authors: haines jl. Neurogenetics. 2001 Oct;3(4):195-201. doi: 10.1007/s100480100119. Neurogenetics. 2001. PMID: 11714099
722 results