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Items: 1 to 20 of 94


Mapping of a major locus that determines telomere length in humans.

Vasa-Nicotera M, Brouilette S, Mangino M, Thompson JR, Braund P, Clemitson JR, Mason A, Bodycote CL, Raleigh SM, Louis E, Samani NJ.

Am J Hum Genet. 2005 Jan;76(1):147-51. Epub 2004 Nov 1. Erratum in: Am J Hum Genet. 2005 Feb;76(2):373.


Mapping genetic loci that determine leukocyte telomere length in a large sample of unselected female sibling pairs.

Andrew T, Aviv A, Falchi M, Surdulescu GL, Gardner JP, Lu X, Kimura M, Kato BS, Valdes AM, Spector TD.

Am J Hum Genet. 2006 Mar;78(3):480-6. Epub 2006 Jan 6.


A regulatory SNP of the BICD1 gene contributes to telomere length variation in humans.

Mangino M, Brouilette S, Braund P, Tirmizi N, Vasa-Nicotera M, Thompson JR, Samani NJ.

Hum Mol Genet. 2008 Aug 15;17(16):2518-23. doi: 10.1093/hmg/ddn152. Epub 2008 May 16.


QTL mapping of leukocyte telomere length in American Indians: the Strong Heart Family Study.

Zhu Y, Voruganti VS, Lin J, Matsuguchi T, Blackburn E, Best LG, Lee ET, MacCluer JW, Cole SA, Zhao J.

Aging (Albany NY). 2013 Sep;5(9):704-16.


Quantitative trait loci for BMD identified by autosome-wide linkage scan to chromosomes 7q and 21q in men from the Amish Family Osteoporosis Study.

Streeten EA, McBride DJ, Pollin TI, Ryan K, Shapiro J, Ott S, Mitchell BD, Shuldiner AR, O'Connell JR.

J Bone Miner Res. 2006 Sep;21(9):1433-42.


White cell telomere length and risk of premature myocardial infarction.

Brouilette S, Singh RK, Thompson JR, Goodall AH, Samani NJ.

Arterioscler Thromb Vasc Biol. 2003 May 1;23(5):842-6. Epub 2003 Mar 20.


Lack of association between leukocyte telomere length and genetic variants in two ageing-related candidate genes.

Zhang F, Kato BS, Gardner JP, Kimura M, Spector TD, Ahmadi KR.

Mech Ageing Dev. 2007 Jul-Aug;128(7-8):415-22. Epub 2007 May 25.


Linkage and potential association of obesity-related phenotypes with two genes on chromosome 12q24 in a female dizygous twin cohort.

Wilson SG, Adam G, Langdown M, Reneland R, Braun A, Andrew T, Surdulescu GL, Norberg M, Dudbridge F, Reed PW, Sambrook PN, Kleyn PW, Spector TD.

Eur J Hum Genet. 2006 Mar;14(3):340-8.


Genome scan for adiposity in Dutch dyslipidemic families reveals novel quantitative trait loci for leptin, body mass index and soluble tumor necrosis factor receptor superfamily 1A.

van der Kallen CJ, Cantor RM, van Greevenbroek MM, Geurts JM, Bouwman FG, Aouizerat BE, Allayee H, Buurman WA, Lusis AJ, Rotter JI, de Bruin TW.

Int J Obes Relat Metab Disord. 2000 Nov;24(11):1381-91.


Insulin resistance, oxidative stress, hypertension, and leukocyte telomere length in men from the Framingham Heart Study.

Demissie S, Levy D, Benjamin EJ, Cupples LA, Gardner JP, Herbert A, Kimura M, Larson MG, Meigs JB, Keaney JF, Aviv A.

Aging Cell. 2006 Aug;5(4):325-30.


Telomere length is shorter in healthy offspring of subjects with coronary artery disease: support for the telomere hypothesis.

Brouilette SW, Whittaker A, Stevens SE, van der Harst P, Goodall AH, Samani NJ.

Heart. 2008 Apr;94(4):422-5. doi: 10.1136/hrt.2007.139675.


Putative susceptibility locus on chromosome 21q for lumbar disc disease (LDD) in the Finnish population.

Virtanen IM, Noponen N, Barral S, Karppinen J, Li H, Vuoristo M, Niinimäki J, Ott J, Ala-Kokko L, Männikkö M.

J Bone Miner Res. 2007 May;22(5):701-7.


QTL Mapping and Candidate Gene Analysis of Telomere Length Control Factors in Maize (Zea mays L.).

Brown AN, Lauter N, Vera DL, McLaughlin-Large KA, Steele TM, Fredette NC, Bass HW.

G3 (Bethesda). 2011 Nov;1(6):437-50. doi: 10.1534/g3.111.000703. Epub 2011 Nov 1.


Mapping quantitative trait loci affecting dairy conformation to chromosome 27 in two Holstein grandsire families.

Van Tassell CP, Sonstegard TS, Ashwell MS.

J Dairy Sci. 2004 Feb;87(2):450-7.


Genetic dissection of myopia: evidence for linkage of ocular axial length to chromosome 5q.

Zhu G, Hewitt AW, Ruddle JB, Kearns LS, Brown SA, Mackinnon JR, Chen CY, Hammond CJ, Craig JE, Montgomery GW, Martin NG, Mackey DA.

Ophthalmology. 2008 Jun;115(6):1053-1057.e2. Epub 2007 Oct 26.


A genome-wide scan for coronary heart disease suggests in Indo-Mauritians a susceptibility locus on chromosome 16p13 and replicates linkage with the metabolic syndrome on 3q27.

Francke S, Manraj M, Lacquemant C, Lecoeur C, Leprêtre F, Passa P, Hebe A, Corset L, Yan SL, Lahmidi S, Jankee S, Gunness TK, Ramjuttun US, Balgobin V, Dina C, Froguel P.

Hum Mol Genet. 2001 Nov 15;10(24):2751-65.


Genetic determination of telomere size in humans: a twin study of three age groups.

Slagboom PE, Droog S, Boomsma DI.

Am J Hum Genet. 1994 Nov;55(5):876-82.


Expanded genomewide scan implicates a novel locus at 3q28 among Caribbean hispanics with familial Alzheimer disease.

Lee JH, Cheng R, Santana V, Williamson J, Lantigua R, Medrano M, Arriaga A, Stern Y, Tycko B, Rogaeva E, Wakutani Y, Kawarai T, St George-Hyslop P, Mayeux R.

Arch Neurol. 2006 Nov;63(11):1591-8.


Mapping the major susceptibility loci for familial Graves' and Hashimoto's diseases: evidence for genetic heterogeneity and gene interactions.

Tomer Y, Barbesino G, Greenberg DA, Concepcion E, Davies TF.

J Clin Endocrinol Metab. 1999 Dec;84(12):4656-64.


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