Lin JP - Search Results

1

Evidence for genetic heterogeneity in monilethrix.

Richard G, Itin P, Lin JP, Bon A, Bale SJ. Richard G, et al. Among authors: lin jp. J Invest Dermatol. 1996 Dec;107(6):812-4. doi: 10.1111/1523-1747.ep12330568. J Invest Dermatol. 1996. PMID: 8941666 Free article.

2

Linkage studies in erythrokeratodermias: fine mapping, genetic heterogeneity and analysis of candidate genes.

Richard G, Lin JP, Smith L, Whyte YM, Itin P, Wollina U, Epstein E Jr, Hohl D, Giroux JM, Charnas L, Bale SJ, DiGiovanna JJ. Richard G, et al. Among authors: lin jp. J Invest Dermatol. 1997 Nov;109(5):666-71. doi: 10.1111/1523-1747.ep12337713. J Invest Dermatol. 1997. PMID: 9347797 Free article.

3

Parental transmission and D18S37 allele sharing in bipolar affective disorder.

Lin JP, Bale SJ. Lin JP, et al. Genet Epidemiol. 1997;14(6):665-8. doi: 10.1002/(SICI)1098-2272(1997)14:6<665::AID-GEPI19>3.0.CO;2-O. Genet Epidemiol. 1997. PMID: 9433560 Clinical Trial.

4

Familial autoimmunity in pedigrees of idiopathic inflammatory myopathy patients suggests common genetic risk factors for many autoimmune diseases.

Ginn LR, Lin JP, Plotz PH, Bale SJ, Wilder RL, Mbauya A, Miller FW. Ginn LR, et al. Among authors: lin jp. Arthritis Rheum. 1998 Mar;41(3):400-5. doi: 10.1002/1529-0131(199803)41:3<400::AID-ART4>3.0.CO;2-5. Arthritis Rheum. 1998. PMID: 9506566

5

Familial clustering of rheumatoid arthritis with other autoimmune diseases.

Lin JP, Cash JM, Doyle SZ, Peden S, Kanik K, Amos CI, Bale SJ, Wilder RL. Lin JP, et al. Hum Genet. 1998 Oct;103(4):475-82. doi: 10.1007/s004390050853. Hum Genet. 1998. PMID: 9856493

6

Rheumatoid arthritis in the Pima Indians: the intersection of epidemiologic, demographic, and genealogic data.

Hirsch R, Lin JP, Scott WW Jr, Ma LD, Pillemer SR, Kastner DL, Jacobsson LT, Bloch DA, Knowler WC, Bennett PH, Bale SJ. Hirsch R, et al. Among authors: lin jp. Arthritis Rheum. 1998 Aug;41(8):1464-9. doi: 10.1002/1529-0131(199808)41:8<1464::AID-ART17>3.0.CO;2-X. Arthritis Rheum. 1998. PMID: 9704646

7

Genealogy construction in a historically isolated population: application to genetic studies of rheumatoid arthritis in the Pima Indian.

Lin JP, Hirsch R, Jacobsson LT, Scott WW, Ma LD, Pillemer SR, Knowler WC, Kastner DL, Bale SJ. Lin JP, et al. Genet Med. 1999 Jul-Aug;1(5):187-93. doi: 10.1097/00125817-199907000-00004. Genet Med. 1999. PMID: 11256671 Free article.

8

Genetic heterogeneity and spectrum of mutations of the PRKAR1A gene in patients with the carney complex.

Kirschner LS, Sandrini F, Monbo J, Lin JP, Carney JA, Stratakis CA. Kirschner LS, et al. Among authors: lin jp. Hum Mol Genet. 2000 Dec 12;9(20):3037-46. doi: 10.1093/hmg/9.20.3037. Hum Mol Genet. 2000. PMID: 11115848

9

Segregation of Allgrove (triple-A) syndrome in Puerto Rican kindreds with chromosome 12 (12q13) polymorphic markers.

Stratakis CA, Lin JP, Pras E, Rennert OM, Bourdony CJ, Chan WY. Stratakis CA, et al. Among authors: lin jp. Proc Assoc Am Physicians. 1997 Sep;109(5):478-82. Proc Assoc Am Physicians. 1997. PMID: 9285947

10

A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22).

Lafferty AR, Torpy DJ, Stowasser M, Taymans SE, Lin JP, Huggard P, Gordon RD, Stratakis CA. Lafferty AR, et al. Among authors: lin jp. J Med Genet. 2000 Nov;37(11):831-5. doi: 10.1136/jmg.37.11.831. J Med Genet. 2000. PMID: 11073536 Free PMC article.

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