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Results: 1 to 20 of 117

1.

Integrated genome-wide association study findings: identification of a neurodevelopmental network for attention deficit hyperactivity disorder.

Poelmans G, Pauls DL, Buitelaar JK, Franke B.

Am J Psychiatry. 2011 Apr;168(4):365-77. doi: 10.1176/appi.ajp.2010.10070948. Epub 2011 Feb 15. Review.

PMID:
21324949
[PubMed - indexed for MEDLINE]
2.

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. doi: 10.1038/mp.2010.29. Epub 2010 Mar 23.

PMID:
20308990
[PubMed - indexed for MEDLINE]
3.

Analysis of GWAS top hits in ADHD suggests association to two polymorphisms located in genes expressed in the cerebellum.

Lantieri F, Glessner JT, Hakonarson H, Elia J, Devoto M.

Am J Med Genet B Neuropsychiatr Genet. 2010 Sep;153B(6):1127-33. doi: 10.1002/ajmg.b.31110.

PMID:
20607790
[PubMed - indexed for MEDLINE]
4.

A high-density single-nucleotide polymorphism screen of 23 candidate genes in attention deficit hyperactivity disorder: suggesting multiple susceptibility genes among Chinese Han population.

Guan L, Wang B, Chen Y, Yang L, Li J, Qian Q, Wang Z, Faraone SV, Wang Y.

Mol Psychiatry. 2009 May;14(5):546-54. doi: 10.1038/sj.mp.4002139. Epub 2008 Jan 8.

PMID:
18180757
[PubMed - indexed for MEDLINE]
5.

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. doi: 10.1016/j.jpsychires.2013.08.006. Epub 2013 Aug 30.

PMID:
24041656
[PubMed - indexed for MEDLINE]
6.

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 23;376(9750):1401-8. doi: 10.1016/S0140-6736(10)61109-9. Epub 2010 Sep 29.

PMID:
20888040
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Case-control study of six genes asymmetrically expressed in the two cerebral hemispheres: association of BAIAP2 with attention-deficit/hyperactivity disorder.

Ribasés M, Bosch R, Hervás A, Ramos-Quiroga JA, Sánchez-Mora C, Bielsa A, Gastaminza X, Guijarro-Domingo S, Nogueira M, Gómez-Barros N, Kreiker S, Gross-Lesch S, Jacob CP, Lesch KP, Reif A, Johansson S, Plessen KJ, Knappskog PM, Haavik J, Estivill X, Casas M, Bayés M, Cormand B.

Biol Psychiatry. 2009 Nov 15;66(10):926-34. doi: 10.1016/j.biopsych.2009.06.024. Epub 2009 Sep 5.

PMID:
19733838
[PubMed - indexed for MEDLINE]
8.

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 4;44(1):78-84. doi: 10.1038/ng.1013.

PMID:
22138692
[PubMed - indexed for MEDLINE]
9.

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. doi: 10.1586/ern.13.30. Review.

PMID:
23545057
[PubMed - indexed for MEDLINE]
10.

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. doi: 10.1038/mp.2009.57. Epub 2009 Jun 23. Erratum in: Mol Psychiatry. 2010 Nov;15(11):1122.

PMID:
19546859
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

The genetics of attention-deficit/hyperactivity disorder.

Coghill D, Banaschewski T.

Expert Rev Neurother. 2009 Oct;9(10):1547-65. doi: 10.1586/ern.09.78. Review.

PMID:
19831843
[PubMed - indexed for MEDLINE]
12.

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; Psychiatric GWAS Consortium: ADHD Subgroup, Doyle AE, Reif A, Rothenberger A, Franke B, Sonuga-Barke EJ, Steinhausen HC, Buitelaar JK, Kuntsi J, Biederman J, Lesch KP, Kent L, Asherson P, Oades RD, Loo SK, Nelson SF, Faraone SV, Smalley SL, Banaschewski T, Arias Vasquez A, Todorov A, Charach A, Miranda A, Warnke A, Thapar A, Neale BM, Cormand B, Freitag C, Mick E, Mulas F, Middleton F, HakonarsonHakonarson H, Palmason H, Schäfer H, Roeyers H, McGough JJ, Romanos J, Crosbie J, Meyer J, Ramos-Quiroga JA, Sergeant J, Elia J, Langely K, Nisenbaum L, Romanos M, Daly MJ, Ribasés M, Gill M, O'Donovan M, Owen M, Casas M, Bayés M, Lambregts-Rommelse N, Williams N, Holmans P, Anney RJ, Ebstein RP, Schachar R, Medland SE, Ripke S, Walitza S, Nguyen TT, Renner TJ, Hu X.

Am J Med Genet B Neuropsychiatr Genet. 2013 Jul;162B(5):419-30. doi: 10.1002/ajmg.b.32169. Epub 2013 May 31.

PMID:
23728934
[PubMed - indexed for MEDLINE]
13.

Candidate genes involved in neural plasticity and the risk for attention-deficit hyperactivity disorder: a meta-analysis of 8 common variants.

Forero DA, Arboleda GH, Vasquez R, Arboleda H.

J Psychiatry Neurosci. 2009 Sep;34(5):361-6.

PMID:
19721846
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Candidate gene analysis in an on-going genome-wide association study of attention-deficit hyperactivity disorder: suggestive association signals in ADRA1A.

Elia J, Capasso M, Zaheer Z, Lantieri F, Ambrosini P, Berrettini W, Devoto M, Hakonarson H.

Psychiatr Genet. 2009 Jun;19(3):134-41. doi: 10.1097/YPG.0b013e32832a5043.

PMID:
19352218
[PubMed - indexed for MEDLINE]
15.

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.

PMID:
22420048
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Structural variations in attention-deficit hyperactivity disorder.

Elia J, Gai X, Hakonarson H, White PS.

Lancet. 2011 Jan 29;377(9763):377-8; author reply 378. doi: 10.1016/S0140-6736(11)60120-7. No abstract available.

PMID:
21277432
[PubMed - indexed for MEDLINE]
17.

Genome-wide association study in German patients with attention deficit/hyperactivity disorder.

Hinney A, Scherag A, Jarick I, Albayrak Ö, Pütter C, Pechlivanis S, Dauvermann MR, Beck S, Weber H, Scherag S, Nguyen TT, Volckmar AL, Knoll N, Faraone SV, Neale BM, Franke B, Cichon S, Hoffmann P, Nöthen MM, Schreiber S, Jöckel KH, Wichmann HE, Freitag C, Lempp T, Meyer J, Gilsbach S, Herpertz-Dahlmann B, Sinzig J, Lehmkuhl G, Renner TJ, Warnke A, Romanos M, Lesch KP, Reif A, Schimmelmann BG, Hebebrand J; Psychiatric GWAS Consortium: ADHD subgroup.

Am J Med Genet B Neuropsychiatr Genet. 2011 Dec;156B(8):888-97. doi: 10.1002/ajmg.b.31246. Epub 2011 Oct 19.

PMID:
22012869
[PubMed - indexed for MEDLINE]
18.

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 10;3(95):95ra75. doi: 10.1126/scitranslmed.3002464.

PMID:
21832240
[PubMed - indexed for MEDLINE]
Free Article
19.

Genome-wide association study of motor coordination problems in ADHD identifies genes for brain and muscle function.

Fliers EA, Vasquez AA, Poelmans G, Rommelse N, Altink M, Buschgens C, Asherson P, Banaschewski T, Ebstein R, Gill M, Miranda A, Mulas F, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Sonuga-Barke E, Steinhausen HC, Faraone SV, Buitelaar JK, Franke B.

World J Biol Psychiatry. 2012 Mar;13(3):211-22. doi: 10.3109/15622975.2011.560279. Epub 2011 Apr 7.

PMID:
21473668
[PubMed - indexed for MEDLINE]
20.

Replication of an association of a promoter polymorphism of the dopamine transporter gene and Attention Deficit Hyperactivity Disorder.

Doyle C, Brookes K, Simpson J, Park J, Scott S, Coghill DR, Hawi Z, Kirley A, Gill M, Kent L.

Neurosci Lett. 2009 Sep 22;462(2):179-81. doi: 10.1016/j.neulet.2009.06.084. Epub 2009 Jul 2.

PMID:
19576958
[PubMed - indexed for MEDLINE]

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