Kent L - Search Results

1

Evidence that genetic variation in the oxytocin receptor (OXTR) gene influences social cognition in ADHD.

Park J, Willmott M, Vetuz G, Toye C, Kirley A, Hawi Z, Brookes KJ, Gill M, Kent L. Park J, et al. Among authors: kent l. Prog Neuropsychopharmacol Biol Psychiatry. 2010 May 30;34(4):697-702. doi: 10.1016/j.pnpbp.2010.03.029. Epub 2010 Mar 27. Prog Neuropsychopharmacol Biol Psychiatry. 2010. PMID: 20347913

2

Association of the steroid sulfatase (STS) gene with attention deficit hyperactivity disorder.

Brookes KJ, Hawi Z, Kirley A, Barry E, Gill M, Kent L. Brookes KJ, et al. Among authors: kent l. Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1531-5. doi: 10.1002/ajmg.b.30873. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18937300

3

Polymorphisms of the steroid sulfatase (STS) gene are associated with attention deficit hyperactivity disorder and influence brain tissue mRNA expression.

Brookes KJ, Hawi Z, Park J, Scott S, Gill M, Kent L. Brookes KJ, et al. Among authors: kent l. Am J Med Genet B Neuropsychiatr Genet. 2010 Dec 5;153B(8):1417-24. doi: 10.1002/ajmg.b.31120. Epub 2010 Sep 22. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 20862695 Free PMC article.

4

Evidence that variation at the serotonin transporter gene influences susceptibility to attention deficit hyperactivity disorder (ADHD): analysis and pooled analysis.

Kent L, Doerry U, Hardy E, Parmar R, Gingell K, Hawi Z, Kirley A, Lowe N, Fitzgerald M, Gill M, Craddock N. Kent L, et al. Mol Psychiatry. 2002;7(8):908-12. doi: 10.1038/sj.mp.4001100. Mol Psychiatry. 2002. PMID: 12232786

5

Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD.

Kent L, Green E, Hawi Z, Kirley A, Dudbridge F, Lowe N, Raybould R, Langley K, Bray N, Fitzgerald M, Owen MJ, O'Donovan MC, Gill M, Thapar A, Craddock N. Kent L, et al. Mol Psychiatry. 2005 Oct;10(10):939-43. doi: 10.1038/sj.mp.4001696. Mol Psychiatry. 2005. PMID: 15940292

6

Rare DNA variants in the brain-derived neurotrophic factor gene increase risk for attention-deficit hyperactivity disorder: a next-generation sequencing study.

Hawi Z, Cummins TD, Tong J, Arcos-Burgos M, Zhao Q, Matthews N, Newman DP, Johnson B, Vance A, Heussler HS, Levy F, Easteal S, Wray NR, Kenny E, Morris D, Kent L, Gill M, Bellgrove MA. Hawi Z, et al. Among authors: kent l. Mol Psychiatry. 2017 Apr;22(4):580-584. doi: 10.1038/mp.2016.117. Epub 2016 Jul 26. Mol Psychiatry. 2017. PMID: 27457811

7

Serotonergic system and attention deficit hyperactivity disorder (ADHD): a potential susceptibility locus at the 5-HT(1B) receptor gene in 273 nuclear families from a multi-centre sample.

Hawi Z, Dring M, Kirley A, Foley D, Kent L, Craddock N, Asherson P, Curran S, Gould A, Richards S, Lawson D, Pay H, Turic D, Langley K, Owen M, O'Donovan M, Thapar A, Fitzgerald M, Gill M. Hawi Z, et al. Among authors: kent l. Mol Psychiatry. 2002;7(7):718-25. doi: 10.1038/sj.mp.4001048. Mol Psychiatry. 2002. PMID: 12192616

8

Nicotinic acetylcholine receptor alpha4 subunit gene polymorphism and attention deficit hyperactivity disorder.

Kent L, Middle F, Hawi Z, Fitzgerald M, Gill M, Feehan C, Craddock N. Kent L, et al. Psychiatr Genet. 2001 Mar;11(1):37-40. doi: 10.1097/00041444-200103000-00007. Psychiatr Genet. 2001. PMID: 11409698

9

ADHD and DAT1: further evidence of paternal over-transmission of risk alleles and haplotype.

Hawi Z, Kent L, Hill M, Anney RJ, Brookes KJ, Barry E, Franke B, Banaschewski T, Buitelaar J, Ebstein R, Miranda A, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Sonuga-Barke E, Steinhausen HC, Faraone SV, Asherson P, Gill M. Hawi Z, et al. Among authors: kent l. Am J Med Genet B Neuropsychiatr Genet. 2010 Jan 5;153B(1):97-102. doi: 10.1002/ajmg.b.30960. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19388000

10

No association between CHRNA7 microsatellite markers and attention-deficit hyperactivity disorder.

Kent L, Green E, Holmes J, Thapar A, Gill M, Hawi Z, Fitzgerald M, Asherson P, Curran S, Mills J, Payton A, Craddock N. Kent L, et al. Am J Med Genet. 2001 Dec 8;105(8):686-9. doi: 10.1002/ajmg.1553. Am J Med Genet. 2001. PMID: 11803515

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