169 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. 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]
7. 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]
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. 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]
14. 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]
15. 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]
16. 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]
17. Genome-wide search for replicable risk gene regions in alcohol and nicotine co-dependence.
Zuo L; Zhang F; Zhang H; Zhang XY; Wang F; Li CS; Lu L; Hong J; Lu L; Krystal J; Deng HW; Luo X
Am J Med Genet B Neuropsychiatr Genet; 2012 Jun; 159B(4):437-44. PubMed ID: 22488850
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Association between common alcohol dehydrogenase gene (ADH) variants and schizophrenia and autism.
Zuo L; Wang K; Zhang XY; Pan X; Wang G; Tan Y; Zhong C; Krystal JH; State M; Zhang H; Luo X
Hum Genet; 2013 Jul; 132(7):735-43. PubMed ID: 23468174
[TBL] [Abstract][Full Text] [Related]
20. Genetic Variants in HSD17B3, SMAD3, and IPO11 Impact Circulating Lipids in Response to Fenofibrate in Individuals With Type 2 Diabetes.
Rotroff DM; Pijut SS; Marvel SW; Jack JR; Havener TM; Pujol A; Schluter A; Graf GA; Ginsberg HN; Shah HS; Gao H; Morieri ML; Doria A; Mychaleckyi JC; McLeod HL; Buse JB; Wagner MJ; Motsinger-Reif AA;
Clin Pharmacol Ther; 2018 Apr; 103(4):712-721. PubMed ID: 28736931
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
