173 related articles for article (PubMed ID: 26079129)
1. Significant association between rare IPO11-HTR1A variants and attention deficit hyperactivity disorder in Caucasians.
Zuo L; Saba L; Lin X; Tan Y; Wang K; Krystal JH; Tabakoff B; Luo X
Am J Med Genet B Neuropsychiatr Genet; 2015 Oct; 168(7):544-56. PubMed ID: 26079129
[TBL] [Abstract][Full Text] [Related]
2. Genome-wide significant association signals in IPO11-HTR1A region specific for alcohol and nicotine codependence.
Zuo L; Zhang XY; Wang F; Li CS; Lu L; Ye L; Zhang H; Krystal JH; Deng HW; Luo X
Alcohol Clin Exp Res; 2013 May; 37(5):730-9. PubMed ID: 23216389
[TBL] [Abstract][Full Text] [Related]
3. Rare SERINC2 variants are specific for alcohol dependence in individuals of European descent.
Zuo L; Wang KS; Zhang XY; Li CS; Zhang F; Wang X; Chen W; Gao G; Zhang H; Krystal JH; Luo X
Pharmacogenet Genomics; 2013 Aug; 23(8):395-402. PubMed ID: 23778322
[TBL] [Abstract][Full Text] [Related]
4. Rare ADH variant constellations are specific for alcohol dependence.
Zuo L; Zhang H; Malison RT; Li CS; Zhang XY; Wang F; Lu L; Lu L; Wang X; Krystal JH; Zhang F; Deng HW; Luo X
Alcohol Alcohol; 2013; 48(1):9-14. PubMed ID: 23019235
[TBL] [Abstract][Full Text] [Related]
5. A case-control association study of serotonin 1A receptor gene and tryptophan hydroxylase 2 gene in attention deficit hyperactivity disorder.
Shim SH; Hwangbo Y; Kwon YJ; Jeong HY; Lee BH; Hwang JA; Kim YK
Prog Neuropsychopharmacol Biol Psychiatry; 2010 Aug; 34(6):974-9. PubMed ID: 20470849
[TBL] [Abstract][Full Text] [Related]
6. Association between HTR1A gene polymorphisms and attention deficit hyperactivity disorder in Korean children.
Park YH; Lee KK; Kwon HJ; Ha M; Kim EJ; Yoo SJ; Paik KC; Lim MH
Genet Test Mol Biomarkers; 2013 Mar; 17(3):178-82. PubMed ID: 23308375
[TBL] [Abstract][Full Text] [Related]
7. Rare Recurrent Variants in Noncoding Regions Impact Attention-Deficit Hyperactivity Disorder (ADHD) Gene Networks in Children of both African American and European American Ancestry.
Liu Y; Chang X; Qu HQ; Tian L; Glessner J; Qu J; Li D; Qiu H; Sleiman P; Hakonarson H
Genes (Basel); 2021 Feb; 12(2):. PubMed ID: 33671795
[TBL] [Abstract][Full Text] [Related]
8. Non-coding structural variation differentially impacts attention-deficit hyperactivity disorder (ADHD) gene networks in African American vs Caucasian children.
Liu Y; Chang X; Qu H; Glessner J; Tian L; Li D; Qiu H; Sleiman PMA; Hakonarson H
Sci Rep; 2020 Sep; 10(1):15252. PubMed ID: 32943653
[TBL] [Abstract][Full Text] [Related]
9. KTN1 variants and risk for attention deficit hyperactivity disorder.
Luo X; Guo X; Tan Y; Zhang Y; Garcia-Milian R; Wang Z; Shi J; Yu T; Ji J; Wang X; Xu J; Zhang H; Zuo L; Lu L; Wang K; Li CR
Am J Med Genet B Neuropsychiatr Genet; 2020 Jun; 183(4):234-244. PubMed ID: 32190980
[TBL] [Abstract][Full Text] [Related]
10. A gene-environment investigation on personality traits in two independent clinical sets of adult patients with personality disorder and attention deficit/hyperactive disorder.
Jacob CP; Nguyen TT; Dempfle A; Heine M; Windemuth-Kieselbach C; Baumann K; Jacob F; Prechtl J; Wittlich M; Herrmann MJ; Gross-Lesch S; Lesch KP; Reif A
Eur Arch Psychiatry Clin Neurosci; 2010 Jun; 260(4):317-26. PubMed ID: 19894072
[TBL] [Abstract][Full Text] [Related]
11. Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder.
Jarick I; Volckmar AL; Pütter C; Pechlivanis S; Nguyen TT; Dauvermann MR; Beck S; Albayrak Ö; Scherag S; Gilsbach S; Cichon S; Hoffmann P; Degenhardt F; Nöthen MM; Schreiber S; Wichmann HE; Jöckel KH; Heinrich J; Tiesler CM; Faraone SV; Walitza S; Sinzig J; Freitag C; Meyer J; Herpertz-Dahlmann B; Lehmkuhl G; Renner TJ; Warnke A; Romanos M; Lesch KP; Reif A; Schimmelmann BG; Hebebrand J; Scherag A; Hinney A
Mol Psychiatry; 2014 Jan; 19(1):115-21. PubMed ID: 23164820
[TBL] [Abstract][Full Text] [Related]
12. Investigating regions of shared genetic variation in attention deficit/hyperactivity disorder and major depressive disorder: a GWAS meta-analysis.
Powell V; Martin J; Thapar A; Rice F; Anney RJL
Sci Rep; 2021 Apr; 11(1):7353. PubMed ID: 33795730
[TBL] [Abstract][Full Text] [Related]
13. Rare, low frequency and common coding variants in CHRNA5 and their contribution to nicotine dependence in European and African Americans.
Olfson E; Saccone NL; Johnson EO; Chen LS; Culverhouse R; Doheny K; Foltz SM; Fox L; Gogarten SM; Hartz S; Hetrick K; Laurie CC; Marosy B; Amin N; Arnett D; Barr RG; Bartz TM; Bertelsen S; Borecki IB; Brown MR; Chasman DI; van Duijn CM; Feitosa MF; Fox ER; Franceschini N; Franco OH; Grove ML; Guo X; Hofman A; Kardia SL; Morrison AC; Musani SK; Psaty BM; Rao DC; Reiner AP; Rice K; Ridker PM; Rose LM; Schick UM; Schwander K; Uitterlinden AG; Vojinovic D; Wang JC; Ware EB; Wilson G; Yao J; Zhao W; Breslau N; Hatsukami D; Stitzel JA; Rice J; Goate A; Bierut LJ
Mol Psychiatry; 2016 May; 21(5):601-7. PubMed ID: 26239294
[TBL] [Abstract][Full Text] [Related]
14. Expression quantitative trait locus fine mapping of the 17q12-21 asthma locus in African American children: a genetic association and gene expression study.
Ober C; McKennan CG; Magnaye KM; Altman MC; Washington C; Stanhope C; Naughton KA; Rosasco MG; Bacharier LB; Billheimer D; Gold DR; Gress L; Hartert T; Havstad S; Khurana Hershey GK; Hallmark B; Hogarth DK; Jackson DJ; Johnson CC; Kattan M; Lemanske RF; Lynch SV; Mendonca EA; Miller RL; Naureckas ET; O'Connor GT; Seroogy CM; Wegienka G; White SR; Wood RA; Wright AL; Zoratti EM; Martinez FD; Ownby D; Nicolae DL; Levin AM; Gern JE;
Lancet Respir Med; 2020 May; 8(5):482-492. PubMed ID: 32380068
[TBL] [Abstract][Full Text] [Related]
15. Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants.
Yang L; Neale BM; Liu L; Lee SH; Wray NR; Ji N; Li H; Qian Q; Wang D; Li J; Faraone SV; Wang Y;
Am J Med Genet B Neuropsychiatr Genet; 2013 Jul; 162B(5):419-430. PubMed ID: 23728934
[TBL] [Abstract][Full Text] [Related]
16. Association of Serotonin Receptors with Attention Deficit Hyperactivity Disorder: A Systematic Review and Meta-analysis.
Hou YW; Xiong P; Gu X; Huang X; Wang M; Wu J
Curr Med Sci; 2018 Jun; 38(3):538-551. PubMed ID: 30074224
[TBL] [Abstract][Full Text] [Related]
17. Acetylcholine-metabolizing butyrylcholinesterase (BCHE) copy number and single nucleotide polymorphisms and their role in attention-deficit/hyperactivity syndrome.
Jacob CP; Weber H; Retz W; Kittel-Schneider S; Heupel J; Renner T; Lesch KP; Reif A
J Psychiatr Res; 2013 Dec; 47(12):1902-8. PubMed ID: 24041656
[TBL] [Abstract][Full Text] [Related]
18. A New Genomewide Association Meta-Analysis of Alcohol Dependence.
Zuo L; Tan Y; Zhang X; Wang X; Krystal J; Tabakoff B; Zhong C; Luo X
Alcohol Clin Exp Res; 2015 Aug; 39(8):1388-95. PubMed ID: 26173551
[TBL] [Abstract][Full Text] [Related]
19. Serotonin 1A receptor gene, schizophrenia and bipolar disorder: an association study and meta-analysis.
Kishi T; Okochi T; Tsunoka T; Okumura T; Kitajima T; Kawashima K; Yamanouchi Y; Kinoshita Y; Naitoh H; Inada T; Kunugi H; Kato T; Yoshikawa T; Ujike H; Ozaki N; Iwata N
Psychiatry Res; 2011 Jan; 185(1-2):20-6. PubMed ID: 20594600
[TBL] [Abstract][Full Text] [Related]
20. Mapping the 17q12-21.1 Locus for Variants Associated with Early-Onset Asthma in African Americans.
Gui H; Levin AM; Hu D; Sleiman P; Xiao S; Mak ACY; Yang M; Barczak AJ; Huntsman S; Eng C; Hochstadt S; Zhang E; Whitehouse K; Simons S; Cabral W; Takriti S; Abecasis G; Blackwell TW; Kang HM; Nickerson DA; Germer S; Lanfear DE; Gilliland F; Gauderman WJ; Kumar R; Erle DJ; Martinez FD; Hakonarson H; Burchard EG; Williams LK
Am J Respir Crit Care Med; 2021 Feb; 203(4):424-436. PubMed ID: 32966749
[No Abstract] [Full Text] [Related]
[Next] [New Search]
