177 related articles for article (PubMed ID: 34233526)
1. 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]
2. 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]
3. Application of deep learning algorithm on whole genome sequencing data uncovers structural variants associated with multiple mental disorders in African American patients.
Liu Y; Qu HQ; Mentch FD; Qu J; Chang X; Nguyen K; Tian L; Glessner J; Sleiman PMA; Hakonarson H
Mol Psychiatry; 2022 Mar; 27(3):1469-1478. PubMed ID: 34997195
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Glutamatergic copy number variants and their role in attention-deficit/hyperactivity disorder.
Akutagava-Martins GC; Salatino-Oliveira A; Genro JP; Contini V; Polanczyk G; Zeni C; Chazan R; Kieling C; Anselmi L; Menezes AM; Grevet EH; Bau CH; Rohde LA; Hutz MH
Am J Med Genet B Neuropsychiatr Genet; 2014 Sep; 165B(6):502-9. PubMed ID: 24985920
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. The molecular genetic architecture of attention deficit hyperactivity disorder.
Hawi Z; Cummins TD; Tong J; Johnson B; Lau R; Samarrai W; Bellgrove MA
Mol Psychiatry; 2015 Mar; 20(3):289-97. PubMed ID: 25600112
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.
Lionel AC; Crosbie J; Barbosa N; Goodale T; Thiruvahindrapuram B; Rickaby J; Gazzellone M; Carson AR; Howe JL; Wang Z; Wei J; Stewart AF; Roberts R; McPherson R; Fiebig A; Franke A; Schreiber S; Zwaigenbaum L; Fernandez BA; Roberts W; Arnold PD; Szatmari P; Marshall CR; Schachar R; Scherer SW
Sci Transl Med; 2011 Aug; 3(95):95ra75. PubMed ID: 21832240
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Duplications in ADHD patients harbour neurobehavioural genes that are co-expressed with genes associated with hyperactivity in the mouse.
Taylor A; Steinberg J; Webber C
Am J Med Genet B Neuropsychiatr Genet; 2015 Mar; 168B(2):97-107. PubMed ID: 25656289
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Genetics of attention-deficit/hyperactivity disorder: current findings and future directions.
Akutagava-Martins GC; Salatino-Oliveira A; Kieling CC; Rohde LA; Hutz MH
Expert Rev Neurother; 2013 Apr; 13(4):435-45. PubMed ID: 23545057
[TBL] [Abstract][Full Text] [Related]
18. Association between copy number variation losses and alcohol dependence across African American and European American ethnic groups.
Ulloa AE; Chen J; Vergara VM; Calhoun V; Liu J
Alcohol Clin Exp Res; 2014 May; 38(5):1266-74. PubMed ID: 24512105
[TBL] [Abstract][Full Text] [Related]
19. Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree.
Lesch KP; Selch S; Renner TJ; Jacob C; Nguyen TT; Hahn T; Romanos M; Walitza S; Shoichet S; Dempfle A; Heine M; Boreatti-Hümmer A; Romanos J; Gross-Lesch S; Zerlaut H; Wultsch T; Heinzel S; Fassnacht M; Fallgatter A; Allolio B; Schäfer H; Warnke A; Reif A; Ropers HH; Ullmann R
Mol Psychiatry; 2011 May; 16(5):491-503. PubMed ID: 20308990
[TBL] [Abstract][Full Text] [Related]
20. From Rare Copy Number Variants to Biological Processes in ADHD.
Harich B; van der Voet M; Klein M; Čížek P; Fenckova M; Schenck A; Franke B
Am J Psychiatry; 2020 Sep; 177(9):855-866. PubMed ID: 32600152
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
