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Items: 1 to 20 of 147

1.

A new approach to chromosome-wide analysis of X-linked markers identifies new associations in Asian and European case-parent triads of orofacial clefts.

Skare Ø, Gjessing HK, Gjerdevik M, Haaland ØA, Romanowska J, Lie RT, Jugessur A.

PLoS One. 2017 Sep 6;12(9):e0183772. doi: 10.1371/journal.pone.0183772. eCollection 2017.

2.

Rationale and Design of a Genetic Study on Cardiometabolic Risk Factors: Protocol for the Tehran Cardiometabolic Genetic Study (TCGS).

Daneshpour MS, Fallah MS, Sedaghati-Khayat B, Guity K, Khalili D, Hedayati M, Ebrahimi A, Hajsheikholeslami F, Mirmiran P, Ramezani Tehrani F, Momenan AA, Ghanbarian A, Amouzegar A, Amiri P, Azizi F.

JMIR Res Protoc. 2017 Feb 23;6(2):e28. doi: 10.2196/resprot.6050.

3.

Polymorphisms in stearoyl coa desaturase and sterol regulatory element binding protein interact with N-3 polyunsaturated fatty acid intake to modify associations with anthropometric variables and metabolic phenotypes in Yup'ik people.

Lemas DJ, Klimentidis YC, Aslibekyan S, Wiener HW, O'Brien DM, Hopkins SE, Stanhope KL, Havel PJ, Allison DB, Fernandez JR, Tiwari HK, Boyer BB.

Mol Nutr Food Res. 2016 Dec;60(12):2642-2653. doi: 10.1002/mnfr.201600170. Epub 2016 Sep 15.

4.

Orexin-A is Associated with Increases in Cerebrospinal Fluid Phosphorylated-Tau in Cognitively Normal Elderly Subjects.

Osorio RS, Ducca EL, Wohlleber ME, Tanzi EB, Gumb T, Twumasi A, Tweardy S, Lewis C, Fischer E, Koushyk V, Cuartero-Toledo M, Sheikh MO, Pirraglia E, Zetterberg H, Blennow K, Lu SE, Mosconi L, Glodzik L, Schuetz S, Varga AW, Ayappa I, Rapoport DM, de Leon MJ.

Sleep. 2016 Jun 1;39(6):1253-60. doi: 10.5665/sleep.5846.

5.

Sequencing of the TBX6 Gene in Families with Familial Idiopathic Scoliosis.

Baschal EE, Swindle K, Justice CM, Baschal RM, Perera A, Wethey CI, Poole A, Pourquié O, Tassy O, Miller NH.

Spine Deform. 2015 Jul;3(4):288-296.

6.

A multi-SNP association test for complex diseases incorporating an optimal P-value threshold algorithm in nuclear families.

Wang YT, Sung PY, Lin PL, Yu YW, Chung RH.

BMC Genomics. 2015 May 15;16:381. doi: 10.1186/s12864-015-1620-3.

7.

ACN9 and alcohol dependence: family-based association analysis in multiplex alcohol dependence families.

Hill SY, Jones BL, Zezza N, Stiffler S.

Am J Med Genet B Neuropsychiatr Genet. 2015 Apr;168B(3):179-87. doi: 10.1002/ajmg.b.32295.

8.

Ethnic-specific genetic association of variants in the corticotropin-releasing hormone receptor 1 gene with nicotine dependence.

Tang X, Zhan S, Yang L, Cui W, Ma JZ, Payne TJ, Li MD.

Biomed Res Int. 2015;2015:263864. doi: 10.1155/2015/263864. Epub 2015 Feb 22.

9.

Replication of 13q31.1 association in nonsyndromic cleft lip with cleft palate in Europeans.

Jia Z, Leslie EJ, Cooper ME, Butali A, Standley J, Rigdon J, Suzuki S, Gongorjav A, Shonkhuuz TE, Natsume N, Shi B, Marazita ML, Murray JC.

Am J Med Genet A. 2015 May;167A(5):1054-1060. doi: 10.1002/ajmg.a.36912. Epub 2015 Mar 18.

10.
11.

Vitamin D-binding protein haplotype is associated with hospitalization for RSV bronchiolitis.

Randolph AG, Yip WK, Falkenstein-Hagander K, Weiss ST, Janssen R, Keisling S, Bont L.

Clin Exp Allergy. 2014 Feb;44(2):231-7. doi: 10.1111/cea.12247.

12.

Alpha-tryptase gene variation is associated with levels of circulating IgE and lung function in asthma.

Abdelmotelb AM, Rose-Zerilli MJ, Barton SJ, Holgate ST, Walls AF, Holloway JW.

Clin Exp Allergy. 2014 Jun;44(6):822-30. doi: 10.1111/cea.12259.

13.

Significant associations of CHRNA2 and CHRNA6 with nicotine dependence in European American and African American populations.

Wang S, D van der Vaart A, Xu Q, Seneviratne C, Pomerleau OF, Pomerleau CS, Payne TJ, Ma JZ, Li MD.

Hum Genet. 2014 May;133(5):575-86. doi: 10.1007/s00439-013-1398-9. Epub 2013 Nov 20.

14.

Family-based study of AVPR1B association and interaction with stressful life events on depression and anxiety in suicide attempts.

Ben-Efraim YJ, Wasserman D, Wasserman J, Sokolowski M.

Neuropsychopharmacology. 2013 Jul;38(8):1504-11. doi: 10.1038/npp.2013.49. Epub 2013 Feb 19.

15.

Serotonin transporter and receptor genes significantly impact nicotine dependence through genetic interactions in both European American and African American smokers.

Yang Z, Seneviratne C, Wang S, Ma JZ, Payne TJ, Wang J, Li MD.

Drug Alcohol Depend. 2013 May 1;129(3):217-25. doi: 10.1016/j.drugalcdep.2012.12.007. Epub 2013 Jan 4.

16.

Intra-familial tests of association between familial idiopathic scoliosis and linked regions on 9q31.3-q34.3 and 16p12.3-q22.2.

Miller NH, Justice CM, Marosy B, Swindle K, Kim Y, Roy-Gagnon MH, Sung H, Behneman D, Doheny KF, Pugh E, Wilson AF.

Hum Hered. 2012;74(1):36-44. doi: 10.1159/000343751. Epub 2012 Nov 13.

17.

A family-based association study identified CYP17 as a candidate gene for obesity susceptibility in Caucasians.

Yan H, Guo Y, Yang TL, Zhao LJ, Deng HW.

Genet Mol Res. 2012 Aug 6;11(3):1967-74. doi: 10.4238/2012.May.22.1.

18.

The PPAR alpha gene is associated with triglyceride, low-density cholesterol and inflammation marker response to fenofibrate intervention: the GOLDN study.

Frazier-Wood AC, Ordovas JM, Straka RJ, Hixson JE, Borecki IB, Tiwari HK, Arnett DK.

Pharmacogenomics J. 2013 Aug;13(4):312-7. doi: 10.1038/tpj.2012.9. Epub 2012 May 1.

19.

A genome-wide search for linkage to allergic rhinitis in Danish sib-pair families.

Kruse LV, Nyegaard M, Christensen U, Møller-Larsen S, Haagerup A, Deleuran M, Hansen LG, Venø SK, Goossens D, Del-Favero J, Børglum AD.

Eur J Hum Genet. 2012 Sep;20(9):965-72. doi: 10.1038/ejhg.2012.46. Epub 2012 Mar 14.

20.

Evidence of gene-environment interaction for the RUNX2 gene and environmental tobacco smoke in controlling the risk of cleft lip with/without cleft palate.

Wu T, Fallin MD, Shi M, Ruczinski I, Liang KY, Hetmanski JB, Wang H, Ingersoll RG, Huang S, Ye X, Wu-Chou YH, Chen PK, Jabs EW, Shi B, Redett R, Scott AF, Murray JC, Marazita ML, Munger RG, Beaty TH.

Birth Defects Res A Clin Mol Teratol. 2012 Feb;94(2):76-83. doi: 10.1002/bdra.22885. Epub 2012 Jan 12.

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