203 related articles for article (PubMed ID: 33671795)
1. 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]
2. 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]
3. Deep learning prediction of attention-deficit hyperactivity disorder in African Americans by copy number variation.
Liu Y; Qu HQ; Chang X; Nguyen K; Qu J; Tian L; Glessner J; Sleiman PM; Hakonarson H
Exp Biol Med (Maywood); 2021 Nov; 246(21):2317-2323. PubMed ID: 34233526
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis.
Williams NM; Zaharieva I; Martin A; Langley K; Mantripragada K; Fossdal R; Stefansson H; Stefansson K; Magnusson P; Gudmundsson OO; Gustafsson O; Holmans P; Owen MJ; O'Donovan M; Thapar A
Lancet; 2010 Oct; 376(9750):1401-8. PubMed ID: 20888040
[TBL] [Abstract][Full Text] [Related]
6. Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes.
Elia J; Gai X; Xie HM; Perin JC; Geiger E; Glessner JT; D'arcy M; deBerardinis R; Frackelton E; Kim C; Lantieri F; Muganga BM; Wang L; Takeda T; Rappaport EF; Grant SF; Berrettini W; Devoto M; Shaikh TH; Hakonarson H; White PS
Mol Psychiatry; 2010 Jun; 15(6):637-46. PubMed ID: 19546859
[TBL] [Abstract][Full Text] [Related]
7. A Protective Role of Low Polygenic Risk Score in Healthy Individuals Carrying Attention-Deficit/Hyperactivity Disorder-Associated Copy Number Variations.
Chang X; Qu H; Liu Y; Glessner J; Hakonarson H
Biol Psychiatry; 2024 May; 95(9):881-887. PubMed ID: 37865391
[TBL] [Abstract][Full Text] [Related]
8. Recent developments in the genetics of attention-deficit hyperactivity disorder.
Grimm O; Kittel-Schneider S; Reif A
Psychiatry Clin Neurosci; 2018 Sep; 72(9):654-672. PubMed ID: 29722101
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Genome-wide copy number variation analysis in adult attention-deficit and hyperactivity disorder.
Ramos-Quiroga JA; Sánchez-Mora C; Casas M; Garcia-Martínez I; Bosch R; Nogueira M; Corrales M; Palomar G; Vidal R; Coll-Tané M; Bayés M; Cormand B; Ribasés M
J Psychiatr Res; 2014 Feb; 49():60-7. PubMed ID: 24269040
[TBL] [Abstract][Full Text] [Related]
11. Novel Loci Associated With Attention-Deficit/Hyperactivity Disorder Are Revealed by Leveraging Polygenic Overlap With Educational Attainment.
Shadrin AA; Smeland OB; Zayats T; Schork AJ; Frei O; Bettella F; Witoelar A; Li W; Eriksen JA; Krull F; Djurovic S; Faraone SV; Reichborn-Kjennerud T; Thompson WK; Johansson S; Haavik J; Dale AM; Wang Y; Andreassen OA
J Am Acad Child Adolesc Psychiatry; 2018 Feb; 57(2):86-95. PubMed ID: 29413154
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder.
Elia J; Glessner JT; Wang K; Takahashi N; Shtir CJ; Hadley D; Sleiman PM; Zhang H; Kim CE; Robison R; Lyon GJ; Flory JH; Bradfield JP; Imielinski M; Hou C; Frackelton EC; Chiavacci RM; Sakurai T; Rabin C; Middleton FA; Thomas KA; Garris M; Mentch F; Freitag CM; Steinhausen HC; Todorov AA; Reif A; Rothenberger A; Franke B; Mick EO; Roeyers H; Buitelaar J; Lesch KP; Banaschewski T; Ebstein RP; Mulas F; Oades RD; Sergeant J; Sonuga-Barke E; Renner TJ; Romanos M; Romanos J; Warnke A; Walitza S; Meyer J; Pálmason H; Seitz C; Loo SK; Smalley SL; Biederman J; Kent L; Asherson P; Anney RJ; Gaynor JW; Shaw P; Devoto M; White PS; Grant SF; Buxbaum JD; Rapoport JL; Williams NM; Nelson SF; Faraone SV; Hakonarson H
Nat Genet; 2011 Dec; 44(1):78-84. PubMed ID: 22138692
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Common variants in the TPH1 and TPH2 regions are not associated with persistent ADHD in a combined sample of 1,636 adult cases and 1,923 controls from four European populations.
Johansson S; Halmøy A; Mavroconstanti T; Jacobsen KK; Landaas ET; Reif A; Jacob C; Boreatti-Hümmer A; Kreiker S; Lesch KP; Kan CC; Kooij JJ; Kiemeney LA; Buitelaar JK; Franke B; Ribasés M; Bosch R; Bayés M; Casas M; Ramos-Quiroga JA; Cormand B; Knappskog P; Haavik J
Am J Med Genet B Neuropsychiatr Genet; 2010 Jul; 153B(5):1008-15. PubMed ID: 20213726
[TBL] [Abstract][Full Text] [Related]
16. Brief Report: Whole-Exome Sequencing to Identify Rare Variants and Gene Networks That Increase Susceptibility to Scleroderma in African Americans.
Gourh P; Remmers EF; Boyden SE; Alexander T; Morgan ND; Shah AA; Mayes MD; Doumatey A; Bentley AR; Shriner D; Domsic RT; Medsger TA; Steen VD; Ramos PS; Silver RM; Korman B; Varga J; Schiopu E; Khanna D; Hsu V; Gordon JK; Saketkoo LA; Gladue H; Kron B; Criswell LA; Derk CT; Bridges SL; Shanmugam VK; Kolstad KD; Chung L; Jan R; Bernstein EJ; Goldberg A; Trojanowski M; Kafaja S; Maksimowicz-McKinnon KM; Mullikin JC; Adeyemo A; Rotimi C; Boin F; Kastner DL; Wigley FM
Arthritis Rheumatol; 2018 Oct; 70(10):1654-1660. PubMed ID: 29732714
[TBL] [Abstract][Full Text] [Related]
17. Glioma risk associated with extent of estimated European genetic ancestry in African Americans and Hispanics.
Ostrom QT; Egan KM; Nabors LB; Gerke T; Thompson RC; Olson JJ; LaRocca R; Chowdhary S; Eckel-Passow JE; Armstrong G; Wiencke JK; Bernstein JL; Claus EB; Il'yasova D; Johansen C; Lachance DH; Lai RK; Merrell RT; Olson SH; Sadetzki S; Schildkraut JM; Shete S; Houlston RS; Jenkins RB; Wrensch MR; Melin B; Amos CI; Huse JT; Barnholtz-Sloan JS; Bondy ML
Int J Cancer; 2020 Feb; 146(3):739-748. PubMed ID: 30963577
[TBL] [Abstract][Full Text] [Related]
18. An association study of sequence variants in the forkhead box P2 (FOXP2) gene and adulthood attention-deficit/hyperactivity disorder in two European samples.
Ribasés M; Sánchez-Mora C; Ramos-Quiroga JA; Bosch R; Gómez N; Nogueira M; Corrales M; Palomar G; Jacob CP; Gross-Lesch S; Kreiker S; Reif A; Lesch KP; Cormand B; Casas M; Bayés M
Psychiatr Genet; 2012 Aug; 22(4):155-60. PubMed ID: 22504457
[TBL] [Abstract][Full Text] [Related]
19. Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.
Williams NM; Franke B; Mick E; Anney RJ; Freitag CM; Gill M; Thapar A; O'Donovan MC; Owen MJ; Holmans P; Kent L; Middleton F; Zhang-James Y; Liu L; Meyer J; Nguyen TT; Romanos J; Romanos M; Seitz C; Renner TJ; Walitza S; Warnke A; Palmason H; Buitelaar J; Rommelse N; Vasquez AA; Hawi Z; Langley K; Sergeant J; Steinhausen HC; Roeyers H; Biederman J; Zaharieva I; Hakonarson H; Elia J; Lionel AC; Crosbie J; Marshall CR; Schachar R; Scherer SW; Todorov A; Smalley SL; Loo S; Nelson S; Shtir C; Asherson P; Reif A; Lesch KP; Faraone SV
Am J Psychiatry; 2012 Feb; 169(2):195-204. PubMed ID: 22420048
[TBL] [Abstract][Full Text] [Related]
20. Copy-number variations are enriched for neurodevelopmental genes in children with developmental coordination disorder.
Mosca SJ; Langevin LM; Dewey D; Innes AM; Lionel AC; Marshall CC; Scherer SW; Parboosingh JS; Bernier FP
J Med Genet; 2016 Dec; 53(12):812-819. PubMed ID: 27489308
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
