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Items: 1 to 20 of 64

1.

Multigene interactions and the prediction of depression in the Wisconsin Longitudinal Study.

Roetker NS, Yonker JA, Lee C, Chang V, Basson JJ, Roan CL, Hauser TS, Hauser RM, Atwood CS.

BMJ Open. 2012 Jul 2;2(4). pii: e000944. doi: 10.1136/bmjopen-2012-000944. Print 2012.

2.

Single nucleotide polymorphisms in ANKK1 and the dopamine D2 receptor gene affect cognitive outcome shortly after traumatic brain injury: a replication and extension study.

McAllister TW, Flashman LA, Harker Rhodes C, Tyler AL, Moore JH, Saykin AJ, McDonald BC, Tosteson TD, Tsongalis GJ.

Brain Inj. 2008 Aug;22(9):705-14. doi: 10.1080/02699050802263019.

3.

Assessment of genetic and nongenetic interactions for the prediction of depressive symptomatology: an analysis of the Wisconsin Longitudinal Study using machine learning algorithms.

Roetker NS, Page CD, Yonker JA, Chang V, Roan CL, Herd P, Hauser TS, Hauser RM, Atwood CS.

Am J Public Health. 2013 Oct;103 Suppl 1:S136-44. doi: 10.2105/AJPH.2012.301141. Epub 2013 Aug 8.

4.

Significant association of ANKK1 and detection of a functional polymorphism with nicotine dependence in an African-American sample.

Huang W, Payne TJ, Ma JZ, Beuten J, Dupont RT, Inohara N, Li MD.

Neuropsychopharmacology. 2009 Jan;34(2):319-30. doi: 10.1038/npp.2008.37. Epub 2008 Mar 19.

5.

Endometrial vezatin and its association with endometriosis risk.

Holdsworth-Carson SJ, Fung JN, Luong HT, Sapkota Y, Bowdler LM, Wallace L, Teh WT, Powell JE, Girling JE, Healey M, Montgomery GW, Rogers PA.

Hum Reprod. 2016 May;31(5):999-1013. doi: 10.1093/humrep/dew047. Epub 2016 Mar 22.

PMID:
27005890
6.

Genetic variation and human longevity.

Soerensen M.

Dan Med J. 2012 May;59(5):B4454.

PMID:
22549493
7.

Association between ANKK1 (rs1800497) polymorphism of DRD2 gene and attention deficit hyperactivity disorder: a meta-analysis.

Pan YQ, Qiao L, Xue XD, Fu JH.

Neurosci Lett. 2015 Mar 17;590:101-5. doi: 10.1016/j.neulet.2015.01.076. Epub 2015 Jan 29.

PMID:
25641135
8.

A genetic schizophrenia-susceptibility region located between the ANKK1 and DRD2 genes.

Dubertret C, Bardel C, Ramoz N, Martin PM, Deybach JC, Adès J, Gorwood P, Gouya L.

Prog Neuropsychopharmacol Biol Psychiatry. 2010 Apr 16;34(3):492-9. doi: 10.1016/j.pnpbp.2010.02.003. Epub 2010 Feb 6.

PMID:
20138949
9.

Family-based association analyses of alcohol dependence phenotypes across DRD2 and neighboring gene ANKK1.

Dick DM, Wang JC, Plunkett J, Aliev F, Hinrichs A, Bertelsen S, Budde JP, Goldstein EL, Kaplan D, Edenberg HJ, Nurnberger J Jr, Hesselbrock V, Schuckit M, Kuperman S, Tischfield J, Porjesz B, Begleiter H, Bierut LJ, Goate A.

Alcohol Clin Exp Res. 2007 Oct;31(10):1645-53.

PMID:
17850642
10.

Assessing SNP-SNP interactions among DNA repair, modification and metabolism related pathway genes in breast cancer susceptibility.

Sapkota Y, Mackey JR, Lai R, Franco-Villalobos C, Lupichuk S, Robson PJ, Kopciuk K, Cass CE, Yasui Y, Damaraju S.

PLoS One. 2013 Jun 3;8(6):e64896. doi: 10.1371/journal.pone.0064896. Print 2014.

11.

Genetic variants altering dopamine D2 receptor expression or function modulate the risk of opiate addiction and the dosage requirements of methadone substitution.

Doehring A, Hentig Nv, Graff J, Salamat S, Schmidt M, Geisslinger G, Harder S, Lötsch J.

Pharmacogenet Genomics. 2009 Jun;19(6):407-14. doi: 10.1097/FPC.0b013e328320a3fd.

PMID:
19373123
12.

Association of DRD2 and DRD3 polymorphisms with Parkinson's disease in a multiethnic consortium.

McGuire V, Van Den Eeden SK, Tanner CM, Kamel F, Umbach DM, Marder K, Mayeux R, Ritz B, Ross GW, Petrovitch H, Topol B, Popat RA, Costello S, Manthripragada AD, Southwick A, Myers RM, Nelson LM.

J Neurol Sci. 2011 Aug 15;307(1-2):22-9. doi: 10.1016/j.jns.2011.05.031. Epub 2011 Jun 12.

13.

Association study of the SLC6A3 VNTR (DAT) and DRD2/ANKK1 Taq1A polymorphisms with alcohol dependence in a population from northeastern Brazil.

Vasconcelos AC, Neto Ede S, Pinto GR, Yoshioka FK, Motta FJ, Vasconcelos DF, Canalle R.

Alcohol Clin Exp Res. 2015 Feb;39(2):205-11. doi: 10.1111/acer.12625.

PMID:
25684044
14.

Evaluating the ability of tree-based methods and logistic regression for the detection of SNP-SNP interaction.

García-Magariños M, López-de-Ullibarri I, Cao R, Salas A.

Ann Hum Genet. 2009 May;73(Pt 3):360-9. doi: 10.1111/j.1469-1809.2009.00511.x. Epub 2009 Mar 8.

15.

Prediction of susceptibility to major depression by a model of interactions of multiple functional genetic variants and environmental factors.

Wong ML, Dong C, Andreev V, Arcos-Burgos M, Licinio J.

Mol Psychiatry. 2012 Jun;17(6):624-33. doi: 10.1038/mp.2012.13. Epub 2012 Mar 27.

16.

Shared genetic factors for age at natural menopause in Iranian and European women.

Rahmani M, Earp MA, Ramezani Tehrani F, Ataee M, Wu J, Treml M, Nudischer R, P-Behnami S; ReproGen Consortium, Perry JR, Murabito JM, Azizi F, Brooks-Wilson A.

Hum Reprod. 2013 Jul;28(7):1987-94. doi: 10.1093/humrep/det106. Epub 2013 Apr 16.

PMID:
23592221
17.

Impulsivity and genetic variants in DRD2 and ANKK1 moderate longitudinal associations between sleep problems and overweight from ages 5 to 11.

Chan TW, Bates JE, Lansford JE, Dodge KA, Pettit GS, Dick DM, Latendresse SJ.

Int J Obes (Lond). 2014 Mar;38(3):404-10. doi: 10.1038/ijo.2013.123. Epub 2013 Jul 5.

18.
20.

Periodic leg movements during sleep are associated with polymorphisms in BTBD9, TOX3/BC034767, MEIS1, MAP2K5/SKOR1, and PTPRD.

Moore H 4th, Winkelmann J, Lin L, Finn L, Peppard P, Mignot E.

Sleep. 2014 Sep 1;37(9):1535-42. doi: 10.5665/sleep.4006.

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