Lehner T - Search Results

1

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

2

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

3

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: lehner t. Hum Hered. 1993 Nov-Dec;43(6):380-7. doi: 10.1159/000154164. Hum Hered. 1993. PMID: 7904586

4

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.

5

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: lehner t. Schizophr Bull. 1990;16(4):673-86. doi: 10.1093/schbul/16.4.673. Schizophr Bull. 1990. PMID: 2077644

6

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.

7

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

8

Late onset autosomal dominant cerebellar ataxia. A family description and linkage analysis with the HLA system.

Arruda WO, Petzl-Erler ML, Cardoso MA, Lehner T, Ott J. Arruda WO, et al. Among authors: lehner t. Arq Neuropsiquiatr. 1991 Sep;49(3):285-91. doi: 10.1590/s0004-282x1991000300009. Arq Neuropsiquiatr. 1991. PMID: 1807228

9

Linkage analysis of spinal muscular atrophy.

Daniels RJ, Thomas NH, MacKinnon RN, Lehner T, Ott J, Flint TJ, Dubowitz V, Ignatius J, Donner M, Zerres K, et al. Daniels RJ, et al. Among authors: lehner t. Genomics. 1992 Feb;12(2):335-9. doi: 10.1016/0888-7543(92)90382-3. Genomics. 1992. PMID: 1346777

10

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.

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