Barmada MM - Search Results

1

Hereditary lymphedema: evidence for linkage and genetic heterogeneity.

Ferrell RE, Levinson KL, Esman JH, Kimak MA, Lawrence EC, Barmada MM, Finegold DN. Ferrell RE, et al. Among authors: barmada mm. Hum Mol Genet. 1998 Dec;7(13):2073-8. doi: 10.1093/hmg/7.13.2073. Hum Mol Genet. 1998. PMID: 9817924

2

The SPINK1 N34S mutation is not associated with Type 2 diabetes mellitus in a population of the USA.

Schneider A, Lawrence EC, Barmada MM, Norris JM, Hamman RF, Marshall JA, Ferrell RE, Whitcomb DC. Schneider A, et al. Among authors: barmada mm. Diabet Med. 2005 Jun;22(6):744-8. doi: 10.1111/j.1464-5491.2005.01513.x. Diabet Med. 2005. PMID: 15910626

3

Linkage and association between inflammatory bowel disease and a locus on chromosome 12.

Duerr RH, Barmada MM, Zhang L, Davis S, Preston RA, Chensny LJ, Brown JL, Ehrlich GD, Weeks DE, Aston CE. Duerr RH, et al. Among authors: barmada mm. Am J Hum Genet. 1998 Jul;63(1):95-100. doi: 10.1086/301929. Am J Hum Genet. 1998. PMID: 9634527 Free PMC article.

4

High-density genome scan in Crohn disease shows confirmed linkage to chromosome 14q11-12.

Duerr RH, Barmada MM, Zhang L, Pfützer R, Weeks DE. Duerr RH, et al. Among authors: barmada mm. Am J Hum Genet. 2000 Jun;66(6):1857-62. doi: 10.1086/302947. Epub 2000 Apr 3. Am J Hum Genet. 2000. PMID: 10747815 Free PMC article.

5

The IBD2 locus shows linkage heterogeneity between ulcerative colitis and Crohn disease.

Parkes M, Barmada MM, Satsangi J, Weeks DE, Jewell DP, Duerr RH. Parkes M, et al. Among authors: barmada mm. Am J Hum Genet. 2000 Dec;67(6):1605-10. doi: 10.1086/316905. Epub 2000 Nov 10. Am J Hum Genet. 2000. PMID: 11078482 Free PMC article.

6

Model-free linkage analysis: performance under real-world conditions.

Barmada MM, O'Connell JR. Barmada MM, et al. Genet Epidemiol. 2001;21 Suppl 1:S498-503. doi: 10.1002/gepi.2001.21.s1.s498. Genet Epidemiol. 2001. PMID: 11793726

7

The peroxisome proliferator-activated receptor gamma coactivator-1 alpha gene (PGC-1alpha) is not associated with type 2 diabetes mellitus or body mass index among Hispanic and non Hispanic Whites from Colorado.

Nelson TL, Fingerlin TE, Moss L, Barmada MM, Ferrell RE, Norris JM. Nelson TL, et al. Among authors: barmada mm. Exp Clin Endocrinol Diabetes. 2007 Apr;115(4):268-75. doi: 10.1055/s-2007-960495. Exp Clin Endocrinol Diabetes. 2007. PMID: 17479445

8

Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy.

Hart TC, Gorry MC, Hart PS, Woodard AS, Shihabi Z, Sandhu J, Shirts B, Xu L, Zhu H, Barmada MM, Bleyer AJ. Hart TC, et al. Among authors: barmada mm. J Med Genet. 2002 Dec;39(12):882-92. doi: 10.1136/jmg.39.12.882. J Med Genet. 2002. PMID: 12471200 Free PMC article.

9

Genome-wide association analysis of age-at-onset in Alzheimer's disease.

Kamboh MI, Barmada MM, Demirci FY, Minster RL, Carrasquillo MM, Pankratz VS, Younkin SG, Saykin AJ; Alzheimer's Disease Neuroimaging Initiative; Sweet RA, Feingold E, DeKosky ST, Lopez OL. Kamboh MI, et al. Among authors: barmada mm. Mol Psychiatry. 2012 Dec;17(12):1340-6. doi: 10.1038/mp.2011.135. Epub 2011 Oct 18. Mol Psychiatry. 2012. PMID: 22005931 Free PMC article.

10

Genetic variants associated with susceptibility to psychosis in late-onset Alzheimer's disease families.

Barral S, Vardarajan BN, Reyes-Dumeyer D, Faber KM, Bird TD, Tsuang D, Bennett DA, Rosenberg R, Boeve BF, Graff-Radford NR, Goate AM, Farlow M, Lantigua R, Medrano MZ, Wang X, Kamboh MI, Barmada MM, Schaid DJ, Foroud TM, Weamer EA, Ottman R, Sweet RA, Mayeux R; NIA-LOAD/NCRAD Family Study Group. Barral S, et al. Among authors: barmada mm. Neurobiol Aging. 2015 Nov;36(11):3116.e9-3116.e16. doi: 10.1016/j.neurobiolaging.2015.08.006. Epub 2015 Aug 15. Neurobiol Aging. 2015. PMID: 26359528 Free PMC article.

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