1P41 RR03655/RR/NCRR NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1989	1
1995	2
1996	1
1997	2
1998	1
1999	4
2000	2
2001	3
2002	2
2003	2
2004	1
2008	1
2024	0

1

Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins.

Sultana R, Yu CE, Yu J, Munson J, Chen D, Hua W, Estes A, Cortes F, de la Barra F, Yu D, Haider ST, Trask BJ, Green ED, Raskind WH, Disteche CM, Wijsman E, Dawson G, Storm DR, Schellenberg GD, Villacres EC. Sultana R, et al. Genomics. 2002 Aug;80(2):129-34. doi: 10.1006/geno.2002.6810. Genomics. 2002. PMID: 12160723

2

Segregation analysis of quantitative traits in nuclear families: comparison of three program packages.

Konigsberg LW, Kammerer CM, MacCluer JW. Konigsberg LW, et al. Genet Epidemiol. 1989;6(6):713-26. doi: 10.1002/gepi.1370060608. Genet Epidemiol. 1989. PMID: 2606342

3

Dense mapping of chromosome 12q13.12-q23.3 and linkage to asthma and atopy.

Barnes KC, Freidhoff LR, Nickel R, Chiu YF, Juo SH, Hizawa N, Naidu RP, Ehrlich E, Duffy DL, Schou C, Levett PN, Marsh DG, Beaty TH. Barnes KC, et al. J Allergy Clin Immunol. 1999 Aug;104(2 Pt 1):485-91. doi: 10.1016/s0091-6749(99)70398-2. J Allergy Clin Immunol. 1999. PMID: 10452776 Free article.

4

Genetic segregation analysis of alcohol and other substance-use disorders in families with recurrent, early-onset major depression.

Maher BS, Marazita ML, Zubenko WN, Kaplan BB, Zubenko GS. Maher BS, et al. Am J Drug Alcohol Abuse. 2002 Nov;28(4):711-31. doi: 10.1081/ada-120015878. Am J Drug Alcohol Abuse. 2002. PMID: 12492266

5

Complex segregation analysis of families ascertained through Gilles de la Tourette syndrome.

Seuchter SA, Hebebrand J, Klug B, Knapp M, Lehmkuhl G, Poustka F, Schmidt M, Remschmidt H, Baur MP. Seuchter SA, et al. Genet Epidemiol. 2000 Jan;18(1):33-47. doi: 10.1002/(SICI)1098-2272(200001)18:1<33::AID-GEPI3>3.0.CO;2-2. Genet Epidemiol. 2000. PMID: 10603457

6

Complex genetic contribution of the Apo AI-CIII-AIV gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypes.

Dallinga-Thie GM, van Linde-Sibenius Trip M, Rotter JI, Cantor RM, Bu X, Lusis AJ, de Bruin TW. Dallinga-Thie GM, et al. J Clin Invest. 1997 Mar 1;99(5):953-61. doi: 10.1172/JCI119260. J Clin Invest. 1997. PMID: 9062353 Free PMC article.

7

Increased platelet aggregability associated with platelet GPIIIa PlA2 polymorphism: the Framingham Offspring Study.

Feng D, Lindpaintner K, Larson MG, Rao VS, O'Donnell CJ, Lipinska I, Schmitz C, Sutherland PA, Silbershatz H, D'Agostino RB, Muller JE, Myers RH, Levy D, Tofler GH. Feng D, et al. Arterioscler Thromb Vasc Biol. 1999 Apr;19(4):1142-7. doi: 10.1161/01.atv.19.4.1142. Arterioscler Thromb Vasc Biol. 1999. PMID: 10195947

8

An autosomal genomic scan for loci linked to type II diabetes mellitus and body-mass index in Pima Indians.

Hanson RL, Ehm MG, Pettitt DJ, Prochazka M, Thompson DB, Timberlake D, Foroud T, Kobes S, Baier L, Burns DK, Almasy L, Blangero J, Garvey WT, Bennett PH, Knowler WC. Hanson RL, et al. Am J Hum Genet. 1998 Oct;63(4):1130-8. doi: 10.1086/302061. Am J Hum Genet. 1998. PMID: 9758619 Free PMC article.

9

Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses.

Deffenbacher KE, Kenyon JB, Hoover DM, Olson RK, Pennington BF, DeFries JC, Smith SD. Deffenbacher KE, et al. Hum Genet. 2004 Jul;115(2):128-38. doi: 10.1007/s00439-004-1126-6. Epub 2004 May 11. Hum Genet. 2004. PMID: 15138886

10

Statistical modeling of interlocus interactions in a complex disease: rejection of the multiplicative model of epistasis in type 1 diabetes.

Cordell HJ, Todd JA, Hill NJ, Lord CJ, Lyons PA, Peterson LB, Wicker LS, Clayton DG. Cordell HJ, et al. Genetics. 2001 May;158(1):357-67. doi: 10.1093/genetics/158.1.357. Genetics. 2001. PMID: 11333244 Free PMC article.

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