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Items: 1 to 20 of 76

1.

A loss-of-function mutation in tryptophan hydroxylase 2 segregating with attention-deficit/hyperactivity disorder.

McKinney J, Johansson S, Halm√ły A, Dramsdahl M, Winge I, Knappskog PM, Haavik J.

Mol Psychiatry. 2008 Apr;13(4):365-7. doi: 10.1038/sj.mp.4002152. No abstract available.

PMID:
18347598
2.

Family-based association study of tryptophan hydroxylase 2 and serotonin 1A receptor genes in attention deficit hyperactivity disorder.

Hsu CD, Tzang RF, Liou YJ, Hong CJ, Tsai SJ.

Psychiatr Genet. 2013 Feb;23(1):38. doi: 10.1097/YPG.0b013e3283586378. No abstract available.

PMID:
23247084
3.

What are the key directions in the genetics of attention deficit hyperactivity disorder?

Martin N, McDougall M, Hay DA.

Curr Opin Psychiatry. 2008 Jul;21(4):356-61. doi: 10.1097/YCO.0b013e328303ba54. Review.

PMID:
18520740
4.

Response to Zhang et al (2005): loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major Depression. Neuron 45, 11-16.

Van Den Bogaert A, De Zutter S, Heyrman L, Mendlewicz J, Adolfsson R, Van Broeckhoven C, Del-Favero J.

Neuron. 2005 Dec 8;48(5):704; author reply 705-6. No abstract available.

PMID:
16337903
5.

Response to Zhang et al. (2005): loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major depression. Neuron 45, 11-16.

Glatt CE, Carlson E, Taylor TR, Risch N, Reus VI, Schaefer CA.

Neuron. 2005 Dec 8;48(5):704-5; author reply 705-6. No abstract available.

6.

Response to Zhang et al. (2005): loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major depression. Neuron 45, 11-16.

Zhou Z, Peters EJ, Hamilton SP, McMahon F, Thomas C, McGrath PJ, Rush J, Trivedi MH, Charney DS, Roy A, Wisniewski S, Lipsky R, Goldman D.

Neuron. 2005 Dec 8;48(5):702-3; author reply 705-6. No abstract available.

7.

Functional properties of missense variants of human tryptophan hydroxylase 2.

McKinney JA, Turel B, Winge I, Knappskog PM, Haavik J.

Hum Mutat. 2009 May;30(5):787-94. doi: 10.1002/humu.20956.

PMID:
19319927
8.

Lack of potassium current in W309R mutant KCNQ3 channel causing benign familial neonatal convulsions (BFNC).

Sugiura Y, Nakatsu F, Hiroyasu K, Ishii A, Hirose S, Okada M, Jibiki I, Ohno H, Kaneko S, Ugawa Y.

Epilepsy Res. 2009 Mar;84(1):82-5. doi: 10.1016/j.eplepsyres.2008.12.003. Epub 2009 Jan 23.

PMID:
19167866
9.

Arginine vasopressin receptor gene-based single-nucleotide polymorphism analysis in attention deficit hyperactivity disorder.

van West D, Del-Favero J, Deboutte D, Van Broeckhoven C, Claes S.

Psychiatr Genet. 2009 Apr;19(2):102-3. doi: 10.1097/YPG.0b013e32832a0b2b. No abstract available.

PMID:
19668115
10.

Mutation screening in the DHCR7 gene of patients with attention deficit and hyperactivity disorder.

Witsch-Baumgartner M, Loeffler J, Menzel HJ, Utermann G, Neuhaus C.

Am J Med Genet. 2001 Jul 22;102(1):106-7. No abstract available.

PMID:
11471183
11.

Attention deficit hyperactivity disorder in obese melanocortin-4-receptor (MC4R) deficient subjects: a newly described expression of MC4R deficiency.

Agranat-Meged A, Ghanadri Y, Eisenberg I, Ben Neriah Z, Kieselstein-Gross E, Mitrani-Rosenbaum S.

Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1547-53. doi: 10.1002/ajmg.b.30842.

PMID:
18777518
12.

Does connection to primary care matter for children with attention-deficit/hyperactivity disorder?

Toomey SL, Finkelstein J, Kuhlthau K.

Pediatrics. 2008 Aug;122(2):368-74. doi: 10.1542/peds.2007-2794.

PMID:
18676555
13.

Converging methods in studying attention-deficit/hyperactivity disorder: what can we learn from neuroimaging and genetics?

Durston S.

Dev Psychopathol. 2008 Fall;20(4):1133-43. doi: 10.1017/S0954579408000539. Review.

PMID:
18838034
14.

Candidate gene studies of ADHD: a meta-analytic review.

Gizer IR, Ficks C, Waldman ID.

Hum Genet. 2009 Jul;126(1):51-90. doi: 10.1007/s00439-009-0694-x. Epub 2009 Jun 9. Review.

PMID:
19506906
15.

Attention-deficit/hyperactivity disorder: how much responsibility are pediatricians taking?

Stein RE, Horwitz SM, Storfer-Isser A, Heneghan AM, Hoagwood KE, Kelleher KJ, O'Connor KG, Olson L.

Pediatrics. 2009 Jan;123(1):248-55. doi: 10.1542/peds.2007-3198.

PMID:
19117889
16.

Overweight in children and adolescents in relation to attention-deficit/hyperactivity disorder: results from a national sample.

Waring ME, Lapane KL.

Pediatrics. 2008 Jul;122(1):e1-6. doi: 10.1542/peds.2007-1955.

PMID:
18595954
17.

Attention deficit hyperactivity disorder in a multigenerational pedigree.

Faraone SV, Biederman J, Mick E, Wozniak J, Kiely K, Guite J, Ablon JS, Warburton R, Reed E.

Biol Psychiatry. 1996 May 15;39(10):906-8. No abstract available.

PMID:
8860195
18.

High proportion of single CYP2D6 gene deletion in Chinese attention-deficit-hyperactivity disorder children and its risk in oppositional defiant disorder.

Tzeng RF, Liu SI, Wu LS, Chen ST, Yu YH, Li PC, Chern SR, Lee PY, Lan TH, Loh el-W.

Psychiatry Clin Neurosci. 2008 Dec;62(6):749. doi: 10.1111/j.1440-1819.2008.01885.x. No abstract available.

19.

Association between the alpha-2C-adrenergic receptor gene and attention deficit hyperactivity disorder in a Korean sample.

Cho SC, Kim JW, Kim BN, Hwang JW, Shin MS, Park M, Kim SA, Cho DY, Yoo HJ, Chung US, Son JW, Park TW.

Neurosci Lett. 2008 Dec 3;446(2-3):108-11. doi: 10.1016/j.neulet.2008.09.058.

PMID:
18835330
20.

Monoamine oxidase deficiency: a cause of flushing and attention-deficit/ hyperactivity disorder?

Cheung NW, Earl J.

Arch Intern Med. 2001 Nov 12;161(20):2503-4. No abstract available.

PMID:
11700166

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