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

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.

2

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

3

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

4

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.

5

Association of angiotensin converting enzyme and plasminogen activator inhibitor-1 promoter gene polymorphisms with features of the insulin resistance syndrome in patients with premature coronary heart disease.

Viitanen L, Pihlajamäki J, Halonen P, Lehtonen M, Kareinen A, Lehto S, Laakso M. Viitanen L, et al. Atherosclerosis. 2001 Jul;157(1):57-64. doi: 10.1016/s0021-9150(00)00705-x. Atherosclerosis. 2001. PMID: 11427204

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

Apolipoprotein A-I/C-III/A-IV gene cluster in familial combined hyperlipidemia: effects on LDL-cholesterol and apolipoproteins B and C-III.

Dallinga-Thie GM, Bu XD, van Linde-Sibenius Trip M, Rotter JI, Lusis AJ, de Bruin TW. Dallinga-Thie GM, et al. J Lipid Res. 1996 Jan;37(1):136-47. J Lipid Res. 1996. PMID: 8820109 Free article.

8

Heritability of life span in the Old Order Amish.

Mitchell BD, Hsueh WC, King TM, Pollin TI, Sorkin J, Agarwala R, Schäffer AA, Shuldiner AR. Mitchell BD, et al. Am J Med Genet. 2001 Sep 1;102(4):346-52. doi: 10.1002/ajmg.1483. Am J Med Genet. 2001. PMID: 11503162

9

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

10

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

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