Gilliam TC - Search Results

1

Physical mapping, linkage analysis of a putative schizophrenia locus on chromosome 5q.

Kaufmann CA, DeLisi LE, Lehner T, Gilliam TC. Kaufmann CA, et al. Among authors: gilliam tc. Schizophr Bull. 1989;15(3):441-52. doi: 10.1093/schbul/15.3.441. Schizophr Bull. 1989. PMID: 2814374

2

Report of a workshop on genetic linkage studies in schizophrenia.

Weeks DE, Brzustowicz L, Squires-Wheeler E, Cornblatt B, Lehner T, Stefanovich M, Bassett A, Gilliam TC, Ott J, Erlenmeyer-Kimling L. Weeks DE, et al. Among authors: gilliam tc. Schizophr Bull. 1990;16(4):673-86. doi: 10.1093/schbul/16.4.673. Schizophr Bull. 1990. PMID: 2077644

3

Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophrenia.

Gilliam TC, Freimer NB, Kaufmann CA, Powchik PP, Bassett AS, Bengtsson U, Wasmuth JJ. Gilliam TC, et al. Genomics. 1989 Nov;5(4):940-4. doi: 10.1016/0888-7543(89)90138-9. Genomics. 1989. PMID: 2591972 Free PMC article.

4

Molecular triangulation: bridging linkage and molecular-network information for identifying candidate genes in Alzheimer's disease.

Krauthammer M, Kaufmann CA, Gilliam TC, Rzhetsky A. Krauthammer M, et al. Among authors: gilliam tc. Proc Natl Acad Sci U S A. 2004 Oct 19;101(42):15148-53. doi: 10.1073/pnas.0404315101. Epub 2004 Oct 7. Proc Natl Acad Sci U S A. 2004. PMID: 15471992 Free PMC article.

5

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

6

Assessment of nonallelic genetic heterogeneity of chronic (type II and III) spinal muscular atrophy.

Brzustowicz LM, Mérette C, Kleyn PW, Lehner T, Castilla LH, Penchaszadeh GK, Das K, Munsat TL, Ott J, Gilliam TC. Brzustowicz LM, et al. Among authors: gilliam tc. Hum Hered. 1993 Nov-Dec;43(6):380-7. doi: 10.1159/000154164. Hum Hered. 1993. PMID: 7904586

7

Bipolar disorder and linkage to Xq28.

Baron M, Straub RE, Lehner T, Endicott J, Ott J, Gilliam TC, Lerer B. Baron M, et al. Among authors: gilliam tc. Nat Genet. 1994 Aug;7(4):461-2. doi: 10.1038/ng0894-461a. Nat Genet. 1994. PMID: 7951314 No abstract available.

8

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: gilliam tc. Am J Hum Genet. 1999 Jan;64(1):210-7. doi: 10.1086/302185. Am J Hum Genet. 1999. PMID: 9915960 Free PMC article.

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: gilliam tc. Genomics. 1998 Mar 1;48(2):171-7. doi: 10.1006/geno.1997.5174. Genomics. 1998. PMID: 9521870 Free article.

10

A microsatellite genetic linkage map of human chromosome 13.

Petrukhin KE, Speer MC, Cayanis E, Bonaldo MF, Tantravahi U, Soares MB, Fischer SG, Warburton D, Gilliam TC, Ott J. Petrukhin KE, et al. Among authors: gilliam tc. Genomics. 1993 Jan;15(1):76-85. doi: 10.1006/geno.1993.1012. Genomics. 1993. PMID: 8432553

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