Lin JP - Search Results

1

Effects of covariates: a summary of Group 5 contributions.

Hauser ER, Hsu FC, Daley D, Olson JM, Rampersaud E, Lin JP, Paterson AD, Poisson LM, Chase GA, Dahmen G, Ziegler A. Hauser ER, et al. Among authors: lin jp. Genet Epidemiol. 2003;25 Suppl 1:S43-9. doi: 10.1002/gepi.10283. Genet Epidemiol. 2003. PMID: 14635168

2

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.

3

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

4

Familial hyperaldosteronism type II: description of a large kindred and exclusion of the aldosterone synthase (CYP11B2) gene.

Torpy DJ, Gordon RD, Lin JP, Huggard PR, Taymans SE, Stowasser M, Chrousos GP, Stratakis CA. Torpy DJ, et al. Among authors: lin jp. J Clin Endocrinol Metab. 1998 Sep;83(9):3214-8. doi: 10.1210/jcem.83.9.5086. J Clin Endocrinol Metab. 1998. PMID: 9745430

5

Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2.

Stratakis CA, Carney JA, Lin JP, Papanicolaou DA, Karl M, Kastner DL, Pras E, Chrousos GP. Stratakis CA, et al. Among authors: lin jp. J Clin Invest. 1996 Feb 1;97(3):699-705. doi: 10.1172/JCI118467. J Clin Invest. 1996. PMID: 8609225 Free PMC article.

6

Description of a large kindred with autosomal dominant inheritance of branchial arch anomalies, hearing loss, and ear pits, and exclusion of the branchio-oto-renal (BOR) syndrome gene locus (chromosome 8q13.3).

Stratakis CA, Lin JP, Rennert OM. Stratakis CA, et al. Among authors: lin jp. Am J Med Genet. 1998 Sep 23;79(3):209-14. Am J Med Genet. 1998. PMID: 9788564

7

Clinical heterogeneity in autosomal dominant optic atrophy in two 3q28-qter linked central Illinois families.

Chen AS, Kovach MJ, Herman K, Avakian A, Frank W, Forrester S, Lin JP, Kimonis V. Chen AS, et al. Among authors: lin jp. Genet Med. 2000 Sep-Oct;2(5):283-9. doi: 10.1097/00125817-200009000-00003. Genet Med. 2000. PMID: 11399209 Free article.

8

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.

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 unique point mutation in the PMP22 gene is associated with Charcot-Marie-Tooth disease and deafness.

Kovach MJ, Lin JP, Boyadjiev S, Campbell K, Mazzeo L, Herman K, Rimer LA, Frank W, Llewellyn B, Jabs EW, Gelber D, Kimonis VE. Kovach MJ, et al. Among authors: lin jp. Am J Hum Genet. 1999 Jun;64(6):1580-93. doi: 10.1086/302420. Am J Hum Genet. 1999. PMID: 10330345 Free PMC article.

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