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Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia.
Harold D, Connolly S, Riley BP, Kendler KS, McCarthy SE, McCombie WR, Richards A, Owen MJ, O'Donovan MC, Walters J; Wellcome Trust Case Control Consortium 2; Schizophrenia Working Group of the Psychiatric Genomics Consortium; Donohoe G, Gill M, Corvin A, Morris DW. Harold D, et al. Among authors: gill m. Am J Med Genet B Neuropsychiatr Genet. 2019 Apr;180(3):223-231. doi: 10.1002/ajmg.b.32716. Epub 2019 Feb 23. Am J Med Genet B Neuropsychiatr Genet. 2019. PMID: 30801977 Free PMC article.
Association of DRD4 in children with ADHD and comorbid conduct problems.
Holmes J, Payton A, Barrett J, Harrington R, McGuffin P, Owen M, Ollier W, Worthington J, Gill M, Kirley A, Hawi Z, Fitzgerald M, Asherson P, Curran S, Mill J, Gould A, Taylor E, Kent L, Craddock N, Thapar A. Holmes J, et al. Among authors: gill m. Am J Med Genet. 2002 Mar 8;114(2):150-3. doi: 10.1002/ajmg.10149. Am J Med Genet. 2002. PMID: 11857575
No association between allelic variants of HOXA1/HOXB1 and autism.
Gallagher L, Hawi Z, Kearney G, Fitzgerald M, Gill M. Gallagher L, et al. Among authors: gill m. Am J Med Genet B Neuropsychiatr Genet. 2004 Jan 1;124B(1):64-7. doi: 10.1002/ajmg.b.20094. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 14681917
Confirming RGS4 as a susceptibility gene for schizophrenia.
Morris DW, Rodgers A, McGhee KA, Schwaiger S, Scully P, Quinn J, Meagher D, Waddington JL, Gill M, Corvin AP. Morris DW, et al. Among authors: gill m. Am J Med Genet B Neuropsychiatr Genet. 2004 Feb 15;125B(1):50-3. doi: 10.1002/ajmg.b.20109. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 14755443
Familiality of symptom dimensions in depression.
Korszun A, Moskvina V, Brewster S, Craddock N, Ferrero F, Gill M, Jones IR, Jones LA, Maier W, Mors O, Owen MJ, Preisig M, Reich T, Rietschel M, Farmer A, McGuffin P. Korszun A, et al. Among authors: gill m. Arch Gen Psychiatry. 2004 May;61(5):468-74. doi: 10.1001/archpsyc.61.5.468. Arch Gen Psychiatry. 2004. PMID: 15123491
Association analysis of the monoamine oxidase A and B genes with attention deficit hyperactivity disorder (ADHD) in an Irish sample: preferential transmission of the MAO-A 941G allele to affected children.
Domschke K, Sheehan K, Lowe N, Kirley A, Mullins C, O'sullivan R, Freitag C, Becker T, Conroy J, Fitzgerald M, Gill M, Hawi Z. Domschke K, et al. Among authors: gill m. Am J Med Genet B Neuropsychiatr Genet. 2005 Apr 5;134B(1):110-4. doi: 10.1002/ajmg.b.30158. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15717295
Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q.
McQueen MB, Devlin B, Faraone SV, Nimgaonkar VL, Sklar P, Smoller JW, Abou Jamra R, Albus M, Bacanu SA, Baron M, Barrett TB, Berrettini W, Blacker D, Byerley W, Cichon S, Coryell W, Craddock N, Daly MJ, Depaulo JR, Edenberg HJ, Foroud T, Gill M, Gilliam TC, Hamshere M, Jones I, Jones L, Juo SH, Kelsoe JR, Lambert D, Lange C, Lerer B, Liu J, Maier W, Mackinnon JD, McInnis MG, McMahon FJ, Murphy DL, Nothen MM, Nurnberger JI, Pato CN, Pato MT, Potash JB, Propping P, Pulver AE, Rice JP, Rietschel M, Scheftner W, Schumacher J, Segurado R, Van Steen K, Xie W, Zandi PP, Laird NM. McQueen MB, et al. Among authors: gill m. Am J Hum Genet. 2005 Oct;77(4):582-95. doi: 10.1086/491603. Epub 2005 Aug 15. Am J Hum Genet. 2005. PMID: 16175504 Free PMC article.
2,607 results