Boehnke M - Search Results

1

The apolipoprotein E/CI/CII gene cluster and late-onset Alzheimer disease.

Yu CE, Payami H, Olson JM, Boehnke M, Wijsman EM, Orr HT, Kukull WA, Goddard KA, Nemens E, White JA, et al. Yu CE, et al. Among authors: boehnke m. Am J Hum Genet. 1994 Apr;54(4):631-42. Am J Hum Genet. 1994. PMID: 8128960 Free PMC article.

2

Genetic association and linkage analysis of the apolipoprotein CII locus and familial Alzheimer's disease.

Schellenberg GD, Boehnke M, Wijsman EM, Moore DK, Martin GM, Bird TD. Schellenberg GD, et al. Among authors: boehnke m. Ann Neurol. 1992 Feb;31(2):223-7. doi: 10.1002/ana.410310214. Ann Neurol. 1992. PMID: 1349467

3

Monte Carlo comparison of preliminary methods for ordering multiple genetic loci.

Olson JM, Boehnke M. Olson JM, et al. Among authors: boehnke m. Am J Hum Genet. 1990 Sep;47(3):470-82. Am J Hum Genet. 1990. PMID: 2393021 Free PMC article.

4

Absence of linkage of chromosome 21q21 markers to familial Alzheimer's disease.

Schellenberg GD, Bird TD, Wijsman EM, Moore DK, Boehnke M, Bryant EM, Lampe TH, Nochlin D, Sumi SM, Deeb SS, et al. Schellenberg GD, et al. Among authors: boehnke m. Science. 1988 Sep 16;241(4872):1507-10. doi: 10.1126/science.3420406. Science. 1988. PMID: 3420406

5

Integrated mapping analysis of the Werner syndrome region of chromosome 8.

Oshima J, Yu CE, Boehnke M, Weber JL, Edelhoff S, Wagner MJ, Wells DE, Wood S, Disteche CM, Martin GM, et al. Oshima J, et al. Among authors: boehnke m. Genomics. 1994 Sep 1;23(1):100-13. doi: 10.1006/geno.1994.1464. Genomics. 1994. PMID: 7829057 Free article.

6

Fine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotype.

Cerosaletti KM, Lange E, Stringham HM, Weemaes CM, Smeets D, Sölder B, Belohradsky BH, Taylor AM, Karnes P, Elliott A, Komatsu K, Gatti RA, Boehnke M, Concannon P. Cerosaletti KM, et al. Among authors: boehnke m. Am J Hum Genet. 1998 Jul;63(1):125-34. doi: 10.1086/301927. Am J Hum Genet. 1998. PMID: 9634525 Free PMC article.

7

Examination of genetic linkage of chromosome 15 to schizophrenia in a large Veterans Affairs Cooperative Study sample.

Tsuang DW, Skol AD, Faraone SV, Bingham S, Young KA, Prabhudesai S, Haverstock SL, Mena F, Menon AS, Bisset D, Pepple J, Sauter F, Baldwin C, Weiss D, Collins J, Boehnke M, Schellenberg GD, Tsuang MT; Veterans Affairs Cooperative Study. Tsuang DW, et al. Among authors: boehnke m. Am J Med Genet. 2001 Dec 8;105(8):662-8. Am J Med Genet. 2001. PMID: 11803512

8

Alternative genetic models for the inheritance of the phenylthiocarbamide taste deficiency.

Olson JM, Boehnke M, Neiswanger K, Roche AF, Siervogel RM. Olson JM, et al. Among authors: boehnke m. Genet Epidemiol. 1989;6(3):423-34. doi: 10.1002/gepi.1370060305. Genet Epidemiol. 1989. PMID: 2753352 Free article.

9

The frequency of C4B variants of complement in familial and sporadic Alzheimer disease.

Bird TD, Boehnke M, Anderson J, Lampe TH, Schellenberg G, Larson EB. Bird TD, et al. Among authors: boehnke m. Alzheimer Dis Assoc Disord. 1987;1(4):251-5. doi: 10.1097/00002093-198701040-00004. Alzheimer Dis Assoc Disord. 1987. PMID: 3502596

10

Mapping of a gene for autosomal dominant juvenile-onset open-angle glaucoma to chromosome Iq.

Richards JE, Lichter PR, Boehnke M, Uro JL, Torrez D, Wong D, Johnson AT. Richards JE, et al. Among authors: boehnke m. Am J Hum Genet. 1994 Jan;54(1):62-70. Am J Hum Genet. 1994. PMID: 8279471 Free PMC article.

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