Lehner T - Search Results

1

Failure to find a chromosome 18 pericentric linkage in families with schizophrenia.

DeLisi LE, Lofthouse R, Lehner T, Morganti C, Vita A, Shields G, Bass N, Ott J, Crow TJ. DeLisi LE, et al. Among authors: lehner t. Am J Med Genet. 1995 Dec 18;60(6):532-4. doi: 10.1002/ajmg.1320600609. Am J Med Genet. 1995. PMID: 8825890

2

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: lehner t. Schizophr Bull. 1989;15(3):441-52. doi: 10.1093/schbul/15.3.441. Schizophr Bull. 1989. PMID: 2814374

3

An examination of linkage of schizophrenia and schizoaffective disorder to the pseudoautosomal region (Xp22.3).

Crow TJ, Delisi LE, Lofthouse R, Poulter M, Lehner T, Bass N, Shah T, Walsh C, Boccio-Smith A, Shields G, et al. Crow TJ, et al. Among authors: lehner t. Br J Psychiatry. 1994 Feb;164(2):159-64. doi: 10.1192/bjp.164.2.159. Br J Psychiatry. 1994. PMID: 7818635

4

Measuring the inflation of the lod score due to its maximization over model parameter values in human linkage analysis.

Weeks DE, Lehner T, Squires-Wheeler E, Kaufmann C, Ott J. Weeks DE, et al. Among authors: lehner t. Genet Epidemiol. 1990;7(4):237-43. doi: 10.1002/gepi.1370070402. Genet Epidemiol. 1990. PMID: 2227370

5

Two new approaches toward linkage heterogeneity of FAD: two-locus models and age of onset as a discriminator.

Mérette C, Lehner T, Ott J. Mérette C, et al. Among authors: lehner t. Genet Epidemiol. 1993;10(6):455-9. doi: 10.1002/gepi.1370100621. Genet Epidemiol. 1993. PMID: 8314043

6

Preliminary ranking procedures for multilocus ordering based on radiation hybrid data.

Weeks DE, Lehner T, Ott J. Weeks DE, et al. Among authors: lehner t. Cytogenet Cell Genet. 1992;59(2-3):125-7. doi: 10.1159/000133222. Cytogenet Cell Genet. 1992. PMID: 1737477 No abstract available.

7

Interpreting nonsignificant outcomes of heterogeneity tests in gene mapping.

Mérette C, Lehner T, Ott J. Mérette C, et al. Among authors: lehner t. Am J Hum Genet. 1991 Dec;49(6):1381-4. Am J Hum Genet. 1991. PMID: 1746563 Free PMC article. No abstract available.

8

Short tandem repeat polymorphism linkage studies in a new family with X-linked mental retardation (MRX20).

Lazzarini A, Stenroos ES, Lehner T, McKoy V, Gold B, McCormack MK, Reid CS, Ott J, Johnson WG. Lazzarini A, et al. Among authors: lehner t. Am J Med Genet. 1995 Jul 17;57(4):552-7. doi: 10.1002/ajmg.1320570407. Am J Med Genet. 1995. PMID: 7573127

9

Spastic paraplegia with iron deposits in the basal ganglia: a new X-linked mental retardation syndrome.

Arena JF, Schwartz C, Stevenson R, Lawrence L, Carpenter A, Duara R, Ledbetter D, Huang T, Lehner T, Ott J, et al. Arena JF, et al. Among authors: lehner t. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):479-90. doi: 10.1002/ajmg.1320430172. Am J Med Genet. 1992. PMID: 1605230

10

Linkage analysis for a disease with a complex mode of inheritance in a simulated data set.

Lehner T, Sandkuyl LA, Ott J. Lehner T, et al. Prog Clin Biol Res. 1989;329:141-6. Prog Clin Biol Res. 1989. PMID: 2622943 No abstract available.

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