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Items: 1 to 20 of 61

1.

Cervical dystonia and genetic common variation in the dopamine pathway.

Groen JL, Simón-Sánchez J, Ritz K, Bochdanovits Z, Fang Y, van Hilten JJ, Aramideh M, van de Warrenburg BP, Boon AJ, Baas F, Heutink P, Tijssen MA.

Parkinsonism Relat Disord. 2013 Mar;19(3):346-9. doi: 10.1016/j.parkreldis.2012.08.016. Epub 2012 Sep 14.

PMID:
22981186
2.

Two-stage case-control association study of dopamine-related genes and migraine.

Corominas R, Ribases M, Camiña M, Cuenca-León E, Pardo J, Boronat S, Sobrido MJ, Cormand B, Macaya A.

BMC Med Genet. 2009 Sep 21;10:95. doi: 10.1186/1471-2350-10-95.

3.

Association of tagging single nucleotide polymorphisms on 8 candidate genes in dopaminergic pathway with schizophrenia in Croatian population.

Pal P, Mihanović M, Molnar S, Xi H, Sun G, Guha S, Jeran N, Tomljenović A, Malnar A, Missoni S, Deka R, Rudan P.

Croat Med J. 2009 Aug;50(4):361-9.

4.

Common polymorphisms in dystonia-linked genes and susceptibility to the sporadic primary dystonias.

Newman JR, Sutherland GT, Boyle RS, Limberg N, Blum S, O'Sullivan JD, Silburn PA, Mellick GD.

Parkinsonism Relat Disord. 2012 May;18(4):351-7. doi: 10.1016/j.parkreldis.2011.11.024. Epub 2011 Dec 14.

PMID:
22172551
5.

Common variation in EMSY and risk of breast and ovarian cancer: a case-control study using HapMap tagging SNPs.

Benusiglio PR, Lesueur F, Luccarini C, McIntosh J, Luben RN, Smith P, Dunning A, Easton DF, Ponder BA, Pharoah PD.

BMC Cancer. 2005 Jul 19;5:81.

6.

Role of polymorphisms in dopamine synthesis and metabolism genes and association of DBH haplotypes with Parkinson's disease among North Indians.

Punia S, Das M, Behari M, Mishra BK, Sahani AK, Govindappa ST, Jayaram S, Muthane UB, K TB, Juyal RC.

Pharmacogenet Genomics. 2010 Jul;20(7):435-41. doi: 10.1097/FPC.0b013e32833ad3bb.

PMID:
20498626
7.

Role of the dopamine D5 receptor (DRD5) as a susceptibility gene for cervical dystonia.

Brancati F, Valente EM, Castori M, Vanacore N, Sessa M, Galardi G, Berardelli A, Bentivoglio AR, Defazio G, Girlanda P, Abbruzzese G, Albanese A, Dallapiccola B; Italian Movement Disorder Study Group.

J Neurol Neurosurg Psychiatry. 2003 May;74(5):665-6.

8.

Role of functional dopaminergic gene polymorphisms in the etiology of idiopathic intellectual disability.

Bhowmik AD, Chaudhury S, Dutta S, Shaw J, Chatterjee A, Choudhury A, Saha A, Sadhukhan D, Kar T, Sinha S, Mukhopadhyay K.

Prog Neuropsychopharmacol Biol Psychiatry. 2011 Aug 15;35(7):1714-22. doi: 10.1016/j.pnpbp.2011.05.005. Epub 2011 May 13.

PMID:
21609749
9.

Genetic variations in the dopamine system and facial expression recognition in healthy chinese college students.

Zhu B, Chen C, Moyzis RK, Dong Q, Chen C, He Q, Stern HS, Li H, Li J, Li J, Lessard J, Lin C.

Neuropsychobiology. 2012;65(2):83-9. doi: 10.1159/000329555. Epub 2012 Jan 5.

10.

Smoking, genes encoding dopamine pathway and risk for Parkinson's disease.

Gu Z, Feng X, Dong X, Chan P.

Neurosci Lett. 2010 Sep 20;482(1):31-4. doi: 10.1016/j.neulet.2010.06.085. Epub 2010 Jul 14.

PMID:
20603187
11.

Association of BDNF Met66Met polymorphism with arm tremor in cervical dystonia.

Groen JL, Ritz K, Velseboer DC, Aramideh M, van Hilten JJ, Boon AJ, van de Warrenburg BP, Baas F, Tijssen MA.

Mov Disord. 2012 May;27(6):796-7. doi: 10.1002/mds.24922. Epub 2012 Jan 30. No abstract available.

PMID:
22290778
12.

Association analysis of TOR1A polymorphisms rs2296793 and rs3842225 in a Chinese population with cervical dystonia.

Zhou Q, Chen Y, Yang J, Cao B, Wei Q, Ou R, Song W, Zhao B, Wu Y, Shang H.

Neurosci Lett. 2016 Jan 26;612:185-188. doi: 10.1016/j.neulet.2015.12.030. Epub 2015 Dec 15.

PMID:
26704435
13.

Is TOR1A a risk factor in adult-onset primary torsion dystonia?

Groen JL, Ritz K, Tanck MW, van de Warrenburg BP, van Hilten JJ, Aramideh M, Baas F, Tijssen MA.

Mov Disord. 2013 Jun;28(6):827-31. doi: 10.1002/mds.25381. Epub 2013 Mar 4.

PMID:
23460578
14.

Comprehensive association testing of common genetic variation in DNA repair pathway genes in relationship with breast cancer risk in multiple populations.

Haiman CA, Hsu C, de Bakker PI, Frasco M, Sheng X, Van Den Berg D, Casagrande JT, Kolonel LN, Le Marchand L, Hankinson SE, Han J, Dunning AM, Pooley KA, Freedman ML, Hunter DJ, Wu AH, Stram DO, Henderson BE.

Hum Mol Genet. 2008 Mar 15;17(6):825-34. Epub 2007 Dec 3.

PMID:
18056155
15.

Aggressive behavior, related conduct problems, and variation in genes affecting dopamine turnover.

Grigorenko EL, De Young CG, Eastman M, Getchell M, Haeffel GJ, Klinteberg Ba, Koposov RA, Oreland L, Pakstis AJ, Ponomarev OA, Ruchkin VV, Singh JP, Yrigollen CM.

Aggress Behav. 2010 May-Jun;36(3):158-76. doi: 10.1002/ab.20339.

PMID:
20127808
16.

Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel.

Mok KY, Schneider SA, Trabzuni D, Stamelou M, Edwards M, Kasperaviciute D, Pickering-Brown S, Silverdale M, Hardy J, Bhatia KP.

Mov Disord. 2014 Feb;29(2):245-51. doi: 10.1002/mds.25732. Epub 2013 Nov 13.

17.

Dopaminergic pathway gene polymorphisms and genetic susceptibility to schizophrenia among north Indians.

Srivastava V, Deshpande SN, Thelma BK.

Neuropsychobiology. 2010;61(2):64-70. doi: 10.1159/000265131. Epub 2009 Dec 12.

PMID:
20016224
18.

Impact of five SNPs in dopamine-related genes on executive function.

Mitaki S, Isomura M, Maniwa K, Yamasaki M, Nagai A, Nabika T, Yamaguchi S.

Acta Neurol Scand. 2013 Jan;127(1):70-6. doi: 10.1111/j.1600-0404.2012.01673.x. Epub 2012 Apr 25.

PMID:
22530780
19.

Association study of dopamine transporter gene and schizophrenia in Korean population using multiple single nucleotide polymorphism markers.

Jeong SH, Joo EJ, Ahn YM, Kim YS.

Prog Neuropsychopharmacol Biol Psychiatry. 2004 Sep;28(6):975-83.

PMID:
15380858
20.

Genetic association study of synphilin-1 in idiopathic Parkinson's disease.

Myhre R, Klungland H, Farrer MJ, Aasly JO.

BMC Med Genet. 2008 Mar 21;9:19. doi: 10.1186/1471-2350-9-19.

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