R01-HG00376/HG/NHGRI NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1995	1
1996	1
1998	1
1999	2
2000	1
2001	1
2002	1
2003	1
2024	0

1

A tobit variance-component method for linkage analysis of censored trait data.

Epstein MP, Lin X, Boehnke M. Epstein MP, et al. Am J Hum Genet. 2003 Mar;72(3):611-20. doi: 10.1086/367924. Epub 2003 Feb 13. Am J Hum Genet. 2003. PMID: 12587095 Free PMC article.

2

Probability of detection of genotyping errors and mutations as inheritance inconsistencies in nuclear-family data.

Douglas JA, Skol AD, Boehnke M. Douglas JA, et al. Am J Hum Genet. 2002 Feb;70(2):487-95. doi: 10.1086/338919. Epub 2002 Jan 8. Am J Hum Genet. 2002. PMID: 11791214 Free PMC article.

3

Experimentally-derived haplotypes substantially increase the efficiency of linkage disequilibrium studies.

Douglas JA, Boehnke M, Gillanders E, Trent JM, Gruber SB. Douglas JA, et al. Nat Genet. 2001 Aug;28(4):361-4. doi: 10.1038/ng582. Nat Genet. 2001. PMID: 11443299

4

A multipoint method for detecting genotyping errors and mutations in sibling-pair linkage data.

Douglas JA, Boehnke M, Lange K. Douglas JA, et al. Am J Hum Genet. 2000 Apr;66(4):1287-97. doi: 10.1086/302861. Epub 2000 Mar 28. Am J Hum Genet. 2000. PMID: 10739757 Free PMC article.

5

The W64R variant of the beta3-adrenergic receptor is not associated with type II diabetes or obesity in a large Finnish sample.

Ghosh S, Langefeld CD, Ally D, Watanabe RM, Hauser ER, Magnuson VL, Nylund SJ, Valle T, Eriksson J, Bergman RN, Tuomilehto J, Collins FS, Boehnke M. Ghosh S, et al. Diabetologia. 1999 Feb;42(2):238-44. doi: 10.1007/s001250051144. Diabetologia. 1999. PMID: 10064105 Free article.

6

Type 2 diabetes: evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs.

Ghosh S, Watanabe RM, Hauser ER, Valle T, Magnuson VL, Erdos MR, Langefeld CD, Balow J Jr, Ally DS, Kohtamaki K, Chines P, Birznieks G, Kaleta HS, Musick A, Te C, Tannenbaum J, Eldridge W, Shapiro S, Martin C, Witt A, So A, Chang J, Shurtleff B, Porter R, Kudelko K, Unni A, Segal L, Sharaf R, Blaschak-Harvan J, Eriksson J, Tenkula T, Vidgren G, Ehnholm C, Tuomilehto-Wolf E, Hagopian W, Buchanan TA, Tuomilehto J, Bergman RN, Collins FS, Boehnke M. Ghosh S, et al. Proc Natl Acad Sci U S A. 1999 Mar 2;96(5):2198-203. doi: 10.1073/pnas.96.5.2198. Proc Natl Acad Sci U S A. 1999. PMID: 10051618 Free PMC article.

7

Mapping genes for NIDDM. Design of the Finland-United States Investigation of NIDDM Genetics (FUSION) Study.

Valle T, Tuomilehto J, Bergman RN, Ghosh S, Hauser ER, Eriksson J, Nylund SJ, Kohtamäki K, Toivanen L, Vidgren G, Tuomilehto-Wolf E, Ehnholm C, Blaschak J, Langefeld CD, Watanabe RM, Magnuson V, Ally DS, Hagopian WA, Ross E, Buchanan TA, Collins F, Boehnke M. Valle T, et al. Diabetes Care. 1998 Jun;21(6):949-58. doi: 10.2337/diacare.21.6.949. Diabetes Care. 1998. PMID: 9614613

8

Lod score curves for phase-unknown matings.

Hulbert-Shearon T, Boehnke M, Lange K. Hulbert-Shearon T, et al. Hum Hered. 1996 Jan-Feb;46(1):55-7. doi: 10.1159/000154326. Hum Hered. 1996. PMID: 8825464

9

Recombination fraction estimate of zero in the presence of apparent recombinants: effects of incomplete penetrance and sporadic cases.

Boehnke M, Hulbert-Shearon T. Boehnke M, et al. Genet Epidemiol. 1995;12(5):509-13. doi: 10.1002/gepi.1370120508. Genet Epidemiol. 1995. PMID: 8557183 Free article.

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