Leppert MF - Search Results

1

Further evidence for the role of genes on chromosome 2 and chromosome 5 in the inheritance of pulmonary function.

Malhotra A, Peiffer AP, Ryujin DT, Elsner T, Kanner RE, Leppert MF, Hasstedt SJ. Malhotra A, et al. Among authors: leppert mf. Am J Respir Crit Care Med. 2003 Sep 1;168(5):556-61. doi: 10.1164/rccm.200303-410OC. Epub 2003 Jun 5. Am J Respir Crit Care Med. 2003. PMID: 12791583

2

The power to detect genetic linkage for quantitative traits in the Utah CEPH pedigrees.

Malhotra A, Cromer K, Leppert MF, Hasstedt SJ. Malhotra A, et al. Among authors: leppert mf. J Hum Genet. 2005;50(2):69-75. doi: 10.1007/s10038-004-0222-8. Epub 2005 Jan 29. J Hum Genet. 2005. PMID: 15682273

3

Recessive inheritance of obesity in familial non-insulin-dependent diabetes mellitus, and lack of linkage to nine candidate genes.

Hasstedt SJ, Hoffman M, Leppert MF, Elbein SC. Hasstedt SJ, et al. Among authors: leppert mf. Am J Hum Genet. 1997 Sep;61(3):668-77. doi: 10.1086/515509. Am J Hum Genet. 1997. PMID: 9326333 Free PMC article.

4

A primary genetic linkage map for human chromosome 12.

O'Connell P, Lathrop GM, Law M, Leppert M, Nakamura Y, Hoff M, Kumlin E, Thomas W, Elsner T, Ballard L, et al. O'Connell P, et al. Genomics. 1987 Sep;1(1):93-102. doi: 10.1016/0888-7543(87)90110-8. Genomics. 1987. PMID: 3478299

5

Intermediate inheritance of Tourette syndrome, assuming assortative mating.

Hasstedt SJ, Leppert M, Filloux F, van de Wetering BJ, McMahon WM. Hasstedt SJ, et al. Am J Hum Genet. 1995 Sep;57(3):682-9. Am J Hum Genet. 1995. PMID: 7668298 Free PMC article.

6

A locus for febrile seizures (FEB3) maps to chromosome 2q23-24.

Peiffer A, Thompson J, Charlier C, Otterud B, Varvil T, Pappas C, Barnitz C, Gruenthal K, Kuhn R, Leppert M. Peiffer A, et al. Ann Neurol. 1999 Oct;46(4):671-8. doi: 10.1002/1531-8249(199910)46:4<671::aid-ana20>3.0.co;2-5. Ann Neurol. 1999. PMID: 10514109

7

AGT genetic variation, plasma AGT, and blood pressure: An analysis of the Utah Genetic Reference Project pedigrees.

Watkins WS, Rohrwasser A, Peiffer A, Leppert MF, Lalouel JM, Jorde LB. Watkins WS, et al. Among authors: leppert mf. Am J Hypertens. 2010 Aug;23(8):917-23. doi: 10.1038/ajh.2010.83. Epub 2010 Apr 22. Am J Hypertens. 2010. PMID: 20414195

8

A novel form of juvenile recessive ALS maps to loci on 6p25 and 21q22.

Butterfield RJ, Ramachandran D, Hasstedt SJ, Otterud BE, Leppert MF, Swoboda KJ, Flanigan KM. Butterfield RJ, et al. Among authors: leppert mf. Neuromuscul Disord. 2009 Apr;19(4):279-87. doi: 10.1016/j.nmd.2009.02.006. Epub 2009 Mar 21. Neuromuscul Disord. 2009. PMID: 19318250

9

A genetic linkage map with 29 loci spanning human chromosome 13q.

Gerken S, Leppert M, O'Connell P, Cavenee W, James CD, Ballard L, Stauffer D, Elsner T, Plaetke R, Lalouel JM, et al. Gerken S, et al. Genomics. 1993 May;16(2):515-9. doi: 10.1006/geno.1993.1219. Genomics. 1993. PMID: 8100218

10

Do non-insulin-dependent diabetes mellitus (NIDDM) and insulin-dependent diabetes mellitus (IDDM) share genetic susceptibility loci? An analysis of putative IDDM susceptibility regions in familial NIDDM.

Elbein SC, Hoffman MD, Mayorga RA, Barrett KL, Leppert M, Hasstedt S. Elbein SC, et al. Metabolism. 1997 Jan;46(1):48-52. doi: 10.1016/s0026-0495(97)90166-9. Metabolism. 1997. PMID: 9005968

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