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Results: 1 to 20 of 58

References for PMC Articles for PubMed (Select 21334180)

1.

Covariance modeling of MRI brain volumes in memory circuitry in schizophrenia: Sex differences are critical.

Abbs B, Liang L, Makris N, Tsuang M, Seidman LJ, Goldstein JM.

Neuroimage. 2011 Jun 15;56(4):1865-74. doi: 10.1016/j.neuroimage.2011.03.079. Epub 2011 Apr 8.

2.

Epigenetic studies of psychosis: current findings, methodological approaches, and implications for postmortem research.

Pidsley R, Mill J.

Biol Psychiatry. 2011 Jan 15;69(2):146-56. doi: 10.1016/j.biopsych.2010.03.029. Epub 2010 May 26. Review.

PMID:
20510393
3.

Specificity of familial transmission of schizophrenia psychosis spectrum and affective psychoses in the New England family study's high-risk design.

Goldstein JM, Buka SL, Seidman LJ, Tsuang MT.

Arch Gen Psychiatry. 2010 May;67(5):458-67. doi: 10.1001/archgenpsychiatry.2010.38.

4.

Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease.

Bassett AS, Scherer SW, Brzustowicz LM.

Am J Psychiatry. 2010 Aug;167(8):899-914. doi: 10.1176/appi.ajp.2009.09071016. Epub 2010 May 3. Review.

5.

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.

Wellcome Trust Case Control Consortium, Craddock N, Hurles ME, Cardin N, Pearson RD, Plagnol V, Robson S, Vukcevic D, Barnes C, Conrad DF, Giannoulatou E, Holmes C, Marchini JL, Stirrups K, Tobin MD, Wain LV, Yau C, Aerts J, Ahmad T, Andrews TD, Arbury H, Attwood A, Auton A, Ball SG, Balmforth AJ, Barrett JC, Barroso I, Barton A, Bennett AJ, Bhaskar S, Blaszczyk K, Bowes J, Brand OJ, Braund PS, Bredin F, Breen G, Brown MJ, Bruce IN, Bull J, Burren OS, Burton J, Byrnes J, Caesar S, Clee CM, Coffey AJ, Connell JM, Cooper JD, Dominiczak AF, Downes K, Drummond HE, Dudakia D, Dunham A, Ebbs B, Eccles D, Edkins S, Edwards C, Elliot A, Emery P, Evans DM, Evans G, Eyre S, Farmer A, Ferrier IN, Feuk L, Fitzgerald T, Flynn E, Forbes A, Forty L, Franklyn JA, Freathy RM, Gibbs P, Gilbert P, Gokumen O, Gordon-Smith K, Gray E, Green E, Groves CJ, Grozeva D, Gwilliam R, Hall A, Hammond N, Hardy M, Harrison P, Hassanali N, Hebaishi H, Hines S, Hinks A, Hitman GA, Hocking L, Howard E, Howard P, Howson JM, Hughes D, Hunt S, Isaacs JD, Jain M, Jewell DP, Johnson T, Jolley JD, Jones IR, Jones LA, Kirov G, Langford CF, Lango-Allen H, Lathrop GM, Lee J, Lee KL, Lees C, Lewis K, Lindgren CM, Maisuria-Armer M, Maller J, Mansfield J, Martin P, Massey DC, McArdle WL, McGuffin P, McLay KE, Mentzer A, Mimmack ML, Morgan AE, Morris AP, Mowat C, Myers S, Newman W, Nimmo ER, O'Donovan MC, Onipinla A, Onyiah I, Ovington NR, Owen MJ, Palin K, Parnell K, Pernet D, Perry JR, Phillips A, Pinto D, Prescott NJ, Prokopenko I, Quail MA, Rafelt S, Rayner NW, Redon R, Reid DM, Renwick, Ring SM, Robertson N, Russell E, St Clair D, Sambrook JG, Sanderson JD, Schuilenburg H, Scott CE, Scott R, Seal S, Shaw-Hawkins S, Shields BM, Simmonds MJ, Smyth DJ, Somaskantharajah E, Spanova K, Steer S, Stephens J, Stevens HE, Stone MA, Su Z, Symmons DP, Thompson JR, Thomson W, Travers ME, Turnbull C, Valsesia A, Walker M, Walker NM, Wallace C, Warren-Perry M, Watkins NA, Webster J, Weedon MN, Wilson AG, Woodburn M, Wordsworth BP, Young AH, Zeggini E, Carter NP, Frayling TM, Lee C, McVean G, Munroe PB, Palotie A, Sawcer SJ, Scherer SW, Strachan DP, Tyler-Smith C, Brown MA, Burton PR, Caulfield MJ, Compston A, Farrall M, Gough SC, Hall AS, Hattersley AT, Hill AV, Mathew CG, Pembrey M, Satsangi J, Stratton MR, Worthington J, Deloukas P, Duncanson A, Kwiatkowski DP, McCarthy MI, Ouwehand W, Parkes M, Rahman N, Todd JA, Samani NJ, Donnelly P.

Nature. 2010 Apr 1;464(7289):713-20. doi: 10.1038/nature08979.

6.

Turner syndrome and schizophrenia: a further hint for the role of the X-chromosome in the pathogenesis of schizophrenic disorders.

Roser P, Kawohl W.

World J Biol Psychiatry. 2010 Mar;11(2 Pt 2):239-42. doi: 10.3109/15622970701599060.

PMID:
20218787
7.

Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders.

Sebat J, Levy DL, McCarthy SE.

Trends Genet. 2009 Dec;25(12):528-35. doi: 10.1016/j.tig.2009.10.004. Epub 2009 Oct 31. Review.

8.

Searching genetic risk factors for schizophrenia and bipolar disorder: learn from the past and back to the future.

Alaerts M, Del-Favero J.

Hum Mutat. 2009 Aug;30(8):1139-52. doi: 10.1002/humu.21042. Review.

PMID:
19626716
9.

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.

International Schizophrenia Consortium, Purcell SM, Wray NR, Stone JL, Visscher PM, O'Donovan MC, Sullivan PF, Sklar P.

Nature. 2009 Aug 6;460(7256):748-52. doi: 10.1038/nature08185. Epub 2009 Jul 1.

10.

Common variants on chromosome 6p22.1 are associated with schizophrenia.

Shi J, Levinson DF, Duan J, Sanders AR, Zheng Y, Pe'er I, Dudbridge F, Holmans PA, Whittemore AS, Mowry BJ, Olincy A, Amin F, Cloninger CR, Silverman JM, Buccola NG, Byerley WF, Black DW, Crowe RR, Oksenberg JR, Mirel DB, Kendler KS, Freedman R, Gejman PV.

Nature. 2009 Aug 6;460(7256):753-7. doi: 10.1038/nature08192. Epub 2009 Jul 1.

11.

Common variants conferring risk of schizophrenia.

Stefansson H, Ophoff RA, Steinberg S, Andreassen OA, Cichon S, Rujescu D, Werge T, Pietiläinen OP, Mors O, Mortensen PB, Sigurdsson E, Gustafsson O, Nyegaard M, Tuulio-Henriksson A, Ingason A, Hansen T, Suvisaari J, Lonnqvist J, Paunio T, Børglum AD, Hartmann A, Fink-Jensen A, Nordentoft M, Hougaard D, Norgaard-Pedersen B, Böttcher Y, Olesen J, Breuer R, Möller HJ, Giegling I, Rasmussen HB, Timm S, Mattheisen M, Bitter I, Réthelyi JM, Magnusdottir BB, Sigmundsson T, Olason P, Masson G, Gulcher JR, Haraldsson M, Fossdal R, Thorgeirsson TE, Thorsteinsdottir U, Ruggeri M, Tosato S, Franke B, Strengman E, Kiemeney LA; Genetic Risk and Outcome in Psychosis (GROUP), Melle I, Djurovic S, Abramova L, Kaleda V, Sanjuan J, de Frutos R, Bramon E, Vassos E, Fraser G, Ettinger U, Picchioni M, Walker N, Toulopoulou T, Need AC, Ge D, Yoon JL, Shianna KV, Freimer NB, Cantor RM, Murray R, Kong A, Golimbet V, Carracedo A, Arango C, Costas J, Jönsson EG, Terenius L, Agartz I, Petursson H, Nöthen MM, Rietschel M, Matthews PM, Muglia P, Peltonen L, St Clair D, Goldstein DB, Stefansson K, Collier DA.

Nature. 2009 Aug 6;460(7256):744-7. doi: 10.1038/nature08186. Epub 2009 Jul 1.

12.

Evidence for X-chromosomal schizophrenia associated with microRNA alterations.

Feng J, Sun G, Yan J, Noltner K, Li W, Buzin CH, Longmate J, Heston LL, Rossi J, Sommer SS.

PLoS One. 2009 Jul 1;4(7):e6121. doi: 10.1371/journal.pone.0006121.

13.

Transcriptome analysis of male-female differences in prefrontal cortical development.

Weickert CS, Elashoff M, Richards AB, Sinclair D, Bahn S, Paabo S, Khaitovich P, Webster MJ.

Mol Psychiatry. 2009 Jun;14(6):558-61. doi: 10.1038/mp.2009.5. No abstract available.

PMID:
19455171
14.

A longer duration of schizophrenic illness has sex-specific associations within the working memory neural network in schizophrenia.

Elsabagh S, Premkumar P, Anilkumar AP, Kumari V.

Behav Brain Res. 2009 Jul 19;201(1):41-7. doi: 10.1016/j.bbr.2009.01.026. Epub 2009 Jan 29.

PMID:
19428614
15.

Polymorphisms in SLC6A4, PAH, GABRB3, and MAOB and modification of psychotic disorder features.

Bergen SE, Fanous AH, Walsh D, O'Neill FA, Kendler KS.

Schizophr Res. 2009 Apr;109(1-3):94-7. doi: 10.1016/j.schres.2009.02.009. Epub 2009 Mar 5.

16.

Genome scan in sibling pairs with juvenile-onset mood disorders: Evidence for linkage to 13q and Xq.

Wigg K, Feng Y, Gomez L, Kiss E, Kapornai K, Tamás Z, Mayer L, Baji I, Daróczi G, Benák I, Osváth VK, Dombovári E, Kaczvinszk E, Besnyõ M, Gádoros J, King N, Székely J, Kovacs M, Vetró A, Kennedy JL, Barr CL.

Am J Med Genet B Neuropsychiatr Genet. 2009 Jul 5;150B(5):638-46. doi: 10.1002/ajmg.b.30883.

PMID:
19035515
17.

Recent adaptive selection at MAOB and ancestral susceptibility to schizophrenia.

Carrera N, Sanjuán J, Moltó MD, Carracedo A, Costas J.

Am J Med Genet B Neuropsychiatr Genet. 2009 Apr 5;150B(3):369-74. doi: 10.1002/ajmg.b.30823.

PMID:
18553363
18.

The influence of sex chromosome aneuploidy on brain asymmetry.

Rezaie R, Daly EM, Cutter WJ, Murphy DG, Robertson DM, DeLisi LE, Mackay CE, Barrick TR, Crow TJ, Roberts N.

Am J Med Genet B Neuropsychiatr Genet. 2009 Jan 5;150B(1):74-85. doi: 10.1002/ajmg.b.30772.

PMID:
18454450
19.

Craddock & Owen vs Kraepelin: 85 years late, mesmerised by "polygenes".

Crow TJ.

Schizophr Res. 2008 Aug;103(1-3):156-60. doi: 10.1016/j.schres.2008.03.001. Epub 2008 Apr 22.

PMID:
18434093
20.

Differential methylation of the X-chromosome is a possible source of discordance for bipolar disorder female monozygotic twins.

Rosa A, Picchioni MM, Kalidindi S, Loat CS, Knight J, Toulopoulou T, Vonk R, van der Schot AC, Nolen W, Kahn RS, McGuffin P, Murray RM, Craig IW.

Am J Med Genet B Neuropsychiatr Genet. 2008 Jun 5;147B(4):459-62.

PMID:
17955481
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