Knowles JA - Search Results

1

A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus.

Aita VM, Liu J, Knowles JA, Terwilliger JD, Baltazar R, Grunn A, Loth JE, Kanyas K, Lerer B, Endicott J, Wang Z, Penchaszadeh G, Gilliam TC, Baron M. Aita VM, et al. Among authors: knowles ja. Am J Hum Genet. 1999 Jan;64(1):210-7. doi: 10.1086/302185. Am J Hum Genet. 1999. PMID: 9915960 Free PMC article.

2

Perils of gene mapping with microsatellite markers.

Knowles JA, Vieland VJ, Gilliam TC. Knowles JA, et al. Am J Hum Genet. 1992 Oct;51(4):905-9. Am J Hum Genet. 1992. PMID: 1415237 Free PMC article. No abstract available.

3

Genetic homogeneity between acute and chronic forms of spinal muscular atrophy.

Gilliam TC, Brzustowicz LM, Castilla LH, Lehner T, Penchaszadeh GK, Daniels RJ, Byth BC, Knowles J, Hislop JE, Shapira Y, et al. Gilliam TC, et al. Nature. 1990 Jun 28;345(6278):823-5. doi: 10.1038/345823a0. Nature. 1990. PMID: 1972783

4

Fine genetic mapping of a gene for autosomal recessive retinitis pigmentosa on chromosome 6p21.

Shugart YY, Banerjee P, Knowles JA, Lewis CA, Jacobson SG, Matise TC, Penchaszadeh G, Gilliam TC, Ott J. Shugart YY, et al. Among authors: knowles ja. Am J Hum Genet. 1995 Aug;57(2):499-502. Am J Hum Genet. 1995. PMID: 7668276 Free PMC article. No abstract available.

5

Identification of a locus, distinct from RDS-peripherin, for autosomal recessive retinitis pigmentosa on chromosome 6p.

Knowles JA, Shugart Y, Banerjee P, Gilliam TC, Lewis CA, Jacobson SG, Ott J. Knowles JA, et al. Hum Mol Genet. 1994 Aug;3(8):1401-3. doi: 10.1093/hmg/3.8.1401. Hum Mol Genet. 1994. PMID: 7987322

6

Refinement of the spinal muscular atrophy locus to the interval between D5S435 and MAP1B.

Soares VM, Brzustowicz LM, Kleyn PW, Knowles JA, Palmer DA, Asokan S, Penchaszadeh GK, Munsat TL, Gilliam TC. Soares VM, et al. Among authors: knowles ja. Genomics. 1993 Feb;15(2):365-71. doi: 10.1006/geno.1993.1069. Genomics. 1993. PMID: 8449502 Free article.

7

High-resolution mapping and transcript identification at the progressive epilepsy with mental retardation locus on chromosome 8p.

Ranta S, Lehesjoki AE, de Fatima Bonaldo M, Knowles JA, Hirvasniemi A, Ross B, de Jong PJ, Soares MB, de la Chapelle A, Gilliam TC. Ranta S, et al. Among authors: knowles ja. Genome Res. 1997 Sep;7(9):887-96. doi: 10.1101/gr.7.9.887. Genome Res. 1997. PMID: 9314494 Free article.

8

TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosa.

Banerjee P, Kleyn PW, Knowles JA, Lewis CA, Ross BM, Parano E, Kovats SG, Lee JJ, Penchaszadeh GK, Ott J, Jacobson SG, Gilliam TC. Banerjee P, et al. Among authors: knowles ja. Nat Genet. 1998 Feb;18(2):177-9. doi: 10.1038/ng0298-177. Nat Genet. 1998. PMID: 9462751

9

Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p21.3.

Banerjee P, Lewis CA, Kleyn PW, Shugart YY, Ross BM, Penchaszadeh GK, Ott J, Jacobson SG, Gilliam TC, Knowles JA. Banerjee P, et al. Among authors: knowles ja. Genomics. 1998 Mar 1;48(2):171-7. doi: 10.1006/geno.1997.5174. Genomics. 1998. PMID: 9521870 Free article.

10

No evidence for significant linkage between bipolar affective disorder and chromosome 18 pericentromeric markers in a large series of multiplex extended pedigrees.

Knowles JA, Rao PA, Cox-Matise T, Loth JE, de Jesus GM, Levine L, Das K, Penchaszadeh GK, Alexander JR, Lerer B, Endicott J, Ott J, Gilliam TC, Baron M. Knowles JA, et al. Am J Hum Genet. 1998 Apr;62(4):916-24. doi: 10.1086/301785. Am J Hum Genet. 1998. PMID: 9529343 Free PMC article.

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