Boehnke M - Search Results

1

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

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

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

4

Association of an apolipoprotein CII allele with familial dementia of the Alzheimer type.

Schellenberg GD, Deeb SS, Boehnke M, Bryant EM, Martin GM, Lampe TH, Bird TD. Schellenberg GD, et al. Among authors: boehnke m. J Neurogenet. 1987 Apr;4(2-3):97-108. J Neurogenet. 1987. PMID: 2885403

5

Family with dominantly inherited ataxia, amyotrophy, and peripheral sensory loss. Spinopontine atrophy or Machado-Joseph Azorean disease in another non-Portuguese family?

Eto K, Sumi SM, Bird TD, McEvoy-Bush T, Boehnke M, Schellenberg G. Eto K, et al. Among authors: boehnke m. Arch Neurol. 1990 Sep;47(9):968-74. doi: 10.1001/archneur.1990.00530090038011. Arch Neurol. 1990. PMID: 2396938

6

The use of apolipoprotein CII as a genetic marker for myotonic dystrophy.

Bird TD, Boehnke M, Schellenberg GD, Deeb SS, Lipe HP. Bird TD, et al. Among authors: boehnke m. Arch Neurol. 1987 Mar;44(3):273-5. doi: 10.1001/archneur.1987.00520150029015. Arch Neurol. 1987. PMID: 2881531

7

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.

8

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

9

Modest evidence for linkage and possible confirmation of association between NOTCH4 and schizophrenia in a large Veterans Affairs Cooperative Study sample.

Skol AD, Young KA, Tsuang DW, Faraone SV, Haverstock SL, Bingham S, Prabhudesai S, Mena F, Menon AS, Yu CE, Rundell P, Pepple J, Sauter F, Baldwin C, Weiss D, Collins J, Keith T, Boehnke M, Schellenberg GD, Tsuang MT. Skol AD, et al. Among authors: boehnke m. Am J Med Genet B Neuropsychiatr Genet. 2003 Apr 1;118B(1):8-15. doi: 10.1002/ajmg.b.10055. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12627457

10

Genome scan of schizophrenia families in a large Veterans Affairs Cooperative Study sample: evidence for linkage to 18p11.32 and for racial heterogeneity on chromosomes 6 and 14.

Faraone SV, Skol AD, Tsuang DW, Young KA, Haverstock SL, Prabhudesai S, Mena F, Menon AS, Leong L, Sautter F, Baldwin C, Bingham S, Weiss D, Collins J, Keith T, Vanden Eng JL, Boehnke M, Tsuang MT, Schellenberg GD. Faraone SV, et al. Among authors: boehnke m. Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 5;139B(1):91-100. doi: 10.1002/ajmg.b.30213. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 16152571

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