Morgan K - Search Results

1

Lack of association between bipolar disorder and tyrosine hydroxylase: a meta-analysis.

Turecki G, Rouleau GA, Mari J, Joober R, Morgan K. Turecki G, et al. Among authors: morgan k. Am J Med Genet. 1997 Jul 25;74(4):348-52. doi: 10.1002/(sici)1096-8628(19970725)74:4<348::aid-ajmg2>3.0.co;2-l. Am J Med Genet. 1997. PMID: 9259367

2

A systematic evaluation of linkage studies in bipolar disorder.

Turecki G, Rouleau GA, Mari JJ, Morgan K. Turecki G, et al. Among authors: morgan k. Acta Psychiatr Scand. 1996 May;93(5):317-26. doi: 10.1111/j.1600-0447.1996.tb10655.x. Acta Psychiatr Scand. 1996. PMID: 8792900 Review.

3

Schizophrenia and chromosome 6p.

Turecki G, Rouleau GA, Joober R, Mari J, Morgan K. Turecki G, et al. Among authors: morgan k. Am J Med Genet. 1997 Apr 18;74(2):195-8. Am J Med Genet. 1997. PMID: 9129723 Review.

4

Modeling the phenotype in parametric linkage analysis of bipolar disorder.

Turecki G, Rouleau G, Morgan K. Turecki G, et al. Among authors: morgan k. Genet Epidemiol. 1997;14(6):687-91. doi: 10.1002/(SICI)1098-2272(1997)14:6<687::AID-GEPI23>3.0.CO;2-L. Genet Epidemiol. 1997. PMID: 9433564

5

Analysis of 14 CAG repeat-containing genes in schizophrenia.

Joober R, Benkelfat C, Toulouse A, Lafrenière RG, Lal S, Ajroud S, Turecki G, Bloom D, Labelle A, Lalonde P, Alda M, Morgan K, Palmour R, Rouleau GA. Joober R, et al. Among authors: morgan k. Am J Med Genet. 1999 Dec 15;88(6):694-9. Am J Med Genet. 1999. PMID: 10581491

6

Genetic mapping of the breast-ovarian cancer syndrome to a small interval on chromosome 17q12-21: exclusion of candidate genes EDH17B2 and RARA.

Simard J, Feunteun J, Lenoir G, Tonin P, Normand T, Luu The V, Vivier A, Lasko D, Morgan K, Rouleau GA, et al. Simard J, et al. Among authors: morgan k. Hum Mol Genet. 1993 Aug;2(8):1193-9. doi: 10.1093/hmg/2.8.1193. Hum Mol Genet. 1993. PMID: 8401501

7

Identification of deletion and triple alpha-globin gene haplotypes in the Montreal beta-thalassemia screening program: implications for genetic medicine.

Akerman BR, Fujiwara TM, Lancaster GA, Morgan K, Scriver CR. Akerman BR, et al. Among authors: morgan k. Am J Med Genet. 1990 May;36(1):76-84. doi: 10.1002/ajmg.1320360115. Am J Med Genet. 1990. PMID: 2333910

8

Cystic fibrosis mutations in French Canadians: three CFTR mutations are relatively frequent in a Quebec population with an elevated incidence of cystic fibrosis.

Rozen R, De Braekeleer M, Daigneault J, Ferreira-Rajabi L, Gerdes M, Lamoureux L, Aubin G, Simard F, Fujiwara TM, Morgan K. Rozen R, et al. Among authors: morgan k. Am J Med Genet. 1992 Feb 1;42(3):360-4. doi: 10.1002/ajmg.1320420322. Am J Med Genet. 1992. PMID: 1536179

9

The impact of transmission-ratio distortion on allele sharing in affected sibling pairs.

Greenwood CM, Morgan K. Greenwood CM, et al. Among authors: morgan k. Am J Hum Genet. 2000 Jun;66(6):2001-4. doi: 10.1086/302918. Epub 2000 Apr 20. Am J Hum Genet. 2000. PMID: 10775526 Free PMC article.

10

Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22-and identification of a shared haplotype.

Bétard C, Rasquin-Weber A, Brewer C, Drouin E, Clark S, Verner A, Darmond-Zwaig C, Fortin J, Mercier J, Chagnon P, Fujiwara TM, Morgan K, Richter A, Hudson TJ, Mitchell GA. Bétard C, et al. Among authors: morgan k. Am J Hum Genet. 2000 Jul;67(1):222-8. doi: 10.1086/302993. Epub 2000 May 11. Am J Hum Genet. 2000. PMID: 10820129 Free PMC article.

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