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Items: 1 to 20 of 118

1.

Association of genetic loci with sleep apnea in European Americans and African-Americans: the Candidate Gene Association Resource (CARe).

Patel SR, Goodloe R, De G, Kowgier M, Weng J, Buxbaum SG, Cade B, Fulop T, Gharib SA, Gottlieb DJ, Hillman D, Larkin EK, Lauderdale DS, Li L, Mukherjee S, Palmer L, Zee P, Zhu X, Redline S.

PLoS One. 2012;7(11):e48836. doi: 10.1371/journal.pone.0048836. Epub 2012 Nov 14.

2.

A candidate gene study of obstructive sleep apnea in European Americans and African Americans.

Larkin EK, Patel SR, Goodloe RJ, Li Y, Zhu X, Gray-McGuire C, Adams MD, Redline S.

Am J Respir Crit Care Med. 2010 Oct 1;182(7):947-53. doi: 10.1164/rccm.201002-0192OC. Epub 2010 Jun 10.

3.

Whole genome scan for obstructive sleep apnea and obesity in African-American families.

Palmer LJ, Buxbaum SG, Larkin EK, Patel SR, Elston RC, Tishler PV, Redline S.

Am J Respir Crit Care Med. 2004 Jun 15;169(12):1314-21. Epub 2004 Apr 7.

PMID:
15070816
4.

Variants in C-reactive protein and IL-6 genes and susceptibility to obstructive sleep apnea in children: a candidate-gene association study in European American and Southeast European populations.

Kaditis AG, Gozal D, Khalyfa A, Kheirandish-Gozal L, Capdevila OS, Gourgoulianis K, Alexopoulos EI, Chaidas K, Bhattacharjee R, Kim J, Rodopoulou P, Zintzaras E.

Sleep Med. 2014 Feb;15(2):228-35. doi: 10.1016/j.sleep.2013.08.795. Epub 2013 Dec 4.

5.

The relationship between craniofacial morphology and obstructive sleep apnea in whites and in African-Americans.

Cakirer B, Hans MG, Graham G, Aylor J, Tishler PV, Redline S.

Am J Respir Crit Care Med. 2001 Mar;163(4):947-50.

PMID:
11282771
6.

Heritability of craniofacial structures in normal subjects and patients with sleep apnea.

Chi L, Comyn FL, Keenan BT, Cater J, Maislin G, Pack AI, Schwab RJ.

Sleep. 2014 Oct 1;37(10):1689-98. doi: 10.5665/sleep.4082.

7.

Polymorphisms in nitric oxide synthase and endothelin genes among children with obstructive sleep apnea.

Chatsuriyawong S, Gozal D, Kheirandish-Gozal L, Bhattacharjee R, Khalyfa AA, Wang Y, Sukhumsirichart W, Khalyfa A.

BMC Med Genomics. 2013 Sep 6;6:29. doi: 10.1186/1755-8794-6-29.

8.

Genome-wide association study of cardiac structure and systolic function in African Americans: the Candidate Gene Association Resource (CARe) study.

Fox ER, Musani SK, Barbalic M, Lin H, Yu B, Ogunyankin KO, Smith NL, Kutlar A, Glazer NL, Post WS, Paltoo DN, Dries DL, Farlow DN, Duarte CW, Kardia SL, Meyers KJ, Sun YV, Arnett DK, Patki AA, Sha J, Cui X, Samdarshi TE, Penman AD, Bibbins-Domingo K, Bůžková P, Benjamin EJ, Bluemke DA, Morrison AC, Heiss G, Carr JJ, Tracy RP, Mosley TH, Taylor HA, Psaty BM, Heckbert SR, Cappola TP, Vasan RS.

Circ Cardiovasc Genet. 2013 Feb;6(1):37-46. doi: 10.1161/CIRCGENETICS.111.962365. Epub 2012 Dec 28.

9.
10.

Genetic loci for serum magnesium among African-Americans and gene-environment interaction at MUC1 and TRPM6 in European-Americans: the Atherosclerosis Risk in Communities (ARIC) study.

Tin A, Köttgen A, Folsom AR, Maruthur NM, Tajuddin SM, Nalls MA, Evans MK, Zonderman AB, Friedrich CA, Boerwinkle E, Coresh J, Kao WH.

BMC Genet. 2015 May 29;16:56. doi: 10.1186/s12863-015-0219-7.

11.

Large-scale candidate gene analysis in whites and African Americans identifies IL6R polymorphism in relation to atrial fibrillation: the National Heart, Lung, and Blood Institute's Candidate Gene Association Resource (CARe) project.

Schnabel RB, Kerr KF, Lubitz SA, Alkylbekova EL, Marcus GM, Sinner MF, Magnani JW, Wolf PA, Deo R, Lloyd-Jones DM, Lunetta KL, Mehra R, Levy D, Fox ER, Arking DE, Mosley TH, Müller-Nurasyid M, Young TR, Wichmann HE, Seshadri S, Farlow DN, Rotter JI, Soliman EZ, Glazer NL, Wilson JG, Breteler MM, Sotoodehnia N, Newton-Cheh C, Kääb S, Ellinor PT, Alonso A, Benjamin EJ, Heckbert SR; Candidate Gene Association Resource (CARe) Atrial Fibrillation/Electrocardiography Working Group.

Circ Cardiovasc Genet. 2011 Oct;4(5):557-64. doi: 10.1161/CIRCGENETICS.110.959197. Epub 2011 Aug 16.

12.

Comparison of BMI, AHI, and apolipoprotein E ε4 (APOE-ε4) alleles among sleep apnea patients with different skeletal classifications.

Roedig JJ, Phillips BA, Morford LA, Van Sickels JE, Falcao-Alencar G, Fardo DW, Hartsfield JK Jr, Ding X, Kluemper GT.

J Clin Sleep Med. 2014 Apr 15;10(4):397-402. doi: 10.5664/jcsm.3614.

13.

Relationship between zinc finger protein 36 (ZFP36) gene polymorphisms and obstructive sleep apnea.

Zhang Y, Li NF, Abulikemu S, Zhang DL, Wang YC, Kong JQ, Nuer GL, Yan ZT, Li HJ, Zhang JH, Zhang XY.

Genet Mol Res. 2015 Jun 18;14(2):6733-43. doi: 10.4238/2015.June.18.17.

14.

Genome-wide association study for serum urate concentrations and gout among African Americans identifies genomic risk loci and a novel URAT1 loss-of-function allele.

Tin A, Woodward OM, Kao WH, Liu CT, Lu X, Nalls MA, Shriner D, Semmo M, Akylbekova EL, Wyatt SB, Hwang SJ, Yang Q, Zonderman AB, Adeyemo AA, Palmer C, Meng Y, Reilly M, Shlipak MG, Siscovick D, Evans MK, Rotimi CN, Flessner MF, Köttgen M, Cupples LA, Fox CS, Köttgen A; CARe and CHARGE Consortia.

Hum Mol Genet. 2011 Oct 15;20(20):4056-68. doi: 10.1093/hmg/ddr307. Epub 2011 Jul 18.

15.

Reciprocal interactions of obstructive sleep apnea and hypertension associated with ACE I/D polymorphism in males.

Koyama RG, Drager LF, Lorenzi-Filho G, Cintra FD, Pereira AC, Poyares D, Krieger JE, Castro RM, Tufik S, de Mello MT, Pedrazzoli M.

Sleep Med. 2009 Dec;10(10):1107-11. doi: 10.1016/j.sleep.2008.12.012. Epub 2009 May 23.

PMID:
19482546
16.

Serotonin-2A and 2C receptor gene polymorphisms in Japanese patients with obstructive sleep apnea.

Sakai K, Takada T, Nakayama H, Kubota Y, Nakamata M, Satoh M, Suzuki E, Akazawa K, Gejyo F.

Intern Med. 2005 Sep;44(9):928-33.

17.

Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe).

Wassel CL, Lange LA, Keating BJ, Taylor KC, Johnson AD, Palmer C, Ho LA, Smith NL, Lange EM, Li Y, Yang Q, Delaney JA, Tang W, Tofler G, Redline S, Taylor HA Jr, Wilson JG, Tracy RP, Jacobs DR Jr, Folsom AR, Green D, O'Donnell CJ, Reiner AP.

Blood. 2011 Jan 6;117(1):268-75. doi: 10.1182/blood-2010-06-289546. Epub 2010 Oct 26.

18.

Fine-mapping in African Americans of 8 recently discovered genetic loci for plasma lipids: the Jackson Heart Study.

Keebler ME, Deo RC, Surti A, Konieczkowski D, Guiducci C, Burtt N, Buxbaum SG, Sarpong DF, Steffes MW, Wilson JG, Taylor HA, Kathiresan S.

Circ Cardiovasc Genet. 2010 Aug;3(4):358-64. doi: 10.1161/CIRCGENETICS.109.914267. Epub 2010 Jun 22.

19.

Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe project.

Musunuru K, Romaine SP, Lettre G, Wilson JG, Volcik KA, Tsai MY, Taylor HA Jr, Schreiner PJ, Rotter JI, Rich SS, Redline S, Psaty BM, Papanicolaou GJ, Ordovas JM, Liu K, Krauss RM, Glazer NL, Gabriel SB, Fornage M, Cupples LA, Buxbaum SG, Boerwinkle E, Ballantyne CM, Kathiresan S, Rader DJ.

PLoS One. 2012;7(5):e36473. doi: 10.1371/journal.pone.0036473. Epub 2012 May 21.

20.

[The association between polymorphism of the serotonin 2A, 2C receptor genes and obstructive sleep apnea-hypopnea syndrome in Han population].

Zhu JY, Hu K, Ma ZS, Liu D.

Zhonghua Jie He He Hu Xi Za Zhi. 2007 Dec;30(12):912-7. Chinese.

PMID:
18336767

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