Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 188

1.

Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia.

Grozeva D, Kirov G, Ivanov D, Jones IR, Jones L, Green EK, St Clair DM, Young AH, Ferrier N, Farmer AE, McGuffin P, Holmans PA, Owen MJ, O'Donovan MC, Craddock N; Wellcome Trust Case Control Consortium..

Arch Gen Psychiatry. 2010 Apr;67(4):318-27. doi: 10.1001/archgenpsychiatry.2010.25.

2.

Reduced burden of very large and rare CNVs in bipolar affective disorder.

Grozeva D, Kirov G, Conrad DF, Barnes CP, Hurles M, Owen MJ, O'Donovan MC, Craddock N.

Bipolar Disord. 2013 Dec;15(8):893-8. doi: 10.1111/bdi.12125.

PMID:
24127788
3.

High frequencies of de novo CNVs in bipolar disorder and schizophrenia.

Malhotra D, McCarthy S, Michaelson JJ, Vacic V, Burdick KE, Yoon S, Cichon S, Corvin A, Gary S, Gershon ES, Gill M, Karayiorgou M, Kelsoe JR, Krastoshevsky O, Krause V, Leibenluft E, Levy DL, Makarov V, Bhandari A, Malhotra AK, McMahon FJ, Nöthen MM, Potash JB, Rietschel M, Schulze TG, Sebat J.

Neuron. 2011 Dec 22;72(6):951-63. doi: 10.1016/j.neuron.2011.11.007.

4.

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.

5.

Copy number variation in schizophrenia in Sweden.

Szatkiewicz JP, O'Dushlaine C, Chen G, Chambert K, Moran JL, Neale BM, Fromer M, Ruderfer D, Akterin S, Bergen SE, Kähler A, Magnusson PK, Kim Y, Crowley JJ, Rees E, Kirov G, O'Donovan MC, Owen MJ, Walters J, Scolnick E, Sklar P, Purcell S, Hultman CM, McCarroll SA, Sullivan PF.

Mol Psychiatry. 2014 Jul;19(7):762-73. doi: 10.1038/mp.2014.40.

6.

Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.

Bergen SE, O'Dushlaine CT, Ripke S, Lee PH, Ruderfer DM, Akterin S, Moran JL, Chambert KD, Handsaker RE, Backlund L, Ösby U, McCarroll S, Landen M, Scolnick EM, Magnusson PK, Lichtenstein P, Hultman CM, Purcell SM, Sklar P, Sullivan PF.

Mol Psychiatry. 2012 Sep;17(9):880-6. doi: 10.1038/mp.2012.73.

7.

De novo CNVs in bipolar affective disorder and schizophrenia.

Georgieva L, Rees E, Moran JL, Chambert KD, Milanova V, Craddock N, Purcell S, Sklar P, McCarroll S, Holmans P, O'Donovan MC, Owen MJ, Kirov G.

Hum Mol Genet. 2014 Dec 15;23(24):6677-83. doi: 10.1093/hmg/ddu379.

8.

Expanding the range of ZNF804A variants conferring risk of psychosis.

Steinberg S, Mors O, Børglum AD, Gustafsson O, Werge T, Mortensen PB, Andreassen OA, Sigurdsson E, Thorgeirsson TE, Böttcher Y, Olason P, Ophoff RA, Cichon S, Gudjonsdottir IH, Pietiläinen OP, Nyegaard M, Tuulio-Henriksson A, Ingason A, Hansen T, Athanasiu L, Suvisaari J, Lonnqvist J, Paunio T, Hartmann A, Jürgens G, Nordentoft M, Hougaard D, Norgaard-Pedersen B, Breuer R, Möller HJ, Giegling I, Glenthøj B, Rasmussen HB, Mattheisen M, Bitter I, Réthelyi JM, Sigmundsson T, Fossdal R, Thorsteinsdottir U, Ruggeri M, Tosato S, Strengman E; Genetic Risk and Outcome in Psychosis., Kiemeney LA, Melle I, Djurovic S, Abramova L, Kaleda V, Walshe M, Bramon E, Vassos E, Li T, Fraser G, Walker N, Toulopoulou T, Yoon J, Freimer NB, Cantor RM, Murray R, Kong A, Golimbet V, Jönsson EG, Terenius L, Agartz I, Petursson H, Nöthen MM, Rietschel M, Peltonen L, Rujescu D, Collier DA, Stefansson H, St Clair D, Stefansson K.

Mol Psychiatry. 2011 Jan;16(1):59-66. doi: 10.1038/mp.2009.149.

9.

Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder.

Kember RL, Georgi B, Bailey-Wilson JE, Stambolian D, Paul SM, Bućan M.

BMC Genet. 2015 Mar 15;16:27. doi: 10.1186/s12863-015-0184-1.

10.

Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism.

Fernandez TV, Sanders SJ, Yurkiewicz IR, Ercan-Sencicek AG, Kim YS, Fishman DO, Raubeson MJ, Song Y, Yasuno K, Ho WS, Bilguvar K, Glessner J, Chu SH, Leckman JF, King RA, Gilbert DL, Heiman GA, Tischfield JA, Hoekstra PJ, Devlin B, Hakonarson H, Mane SM, Günel M, State MW.

Biol Psychiatry. 2012 Mar 1;71(5):392-402. doi: 10.1016/j.biopsych.2011.09.034.

11.

Copy number variation in schizophrenia in the Japanese population.

Ikeda M, Aleksic B, Kirov G, Kinoshita Y, Yamanouchi Y, Kitajima T, Kawashima K, Okochi T, Kishi T, Zaharieva I, Owen MJ, O'Donovan MC, Ozaki N, Iwata N.

Biol Psychiatry. 2010 Feb 1;67(3):283-6. doi: 10.1016/j.biopsych.2009.08.034.

PMID:
19880096
12.

Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sample.

McQuillin A, Bass N, Anjorin A, Lawrence J, Kandaswamy R, Lydall G, Moran J, Sklar P, Purcell S, Gurling H.

Eur J Hum Genet. 2011 May;19(5):588-92. doi: 10.1038/ejhg.2010.221.

13.

Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder.

Priebe L, Degenhardt FA, Herms S, Haenisch B, Mattheisen M, Nieratschker V, Weingarten M, Witt S, Breuer R, Paul T, Alblas M, Moebus S, Lathrop M, Leboyer M, Schreiber S, Grigoroiu-Serbanescu M, Maier W, Propping P, Rietschel M, Nöthen MM, Cichon S, Mühleisen TW.

Mol Psychiatry. 2012 Apr;17(4):421-32. doi: 10.1038/mp.2011.8.

PMID:
21358712
14.

De novo CNVs in bipolar disorder: recurrent themes or new directions?

Girirajan S, Eichler EE.

Neuron. 2011 Dec 22;72(6):885-7. doi: 10.1016/j.neuron.2011.12.008.

15.

Tourette syndrome is associated with recurrent exonic copy number variants.

Sundaram SK, Huq AM, Wilson BJ, Chugani HT.

Neurology. 2010 May 18;74(20):1583-90. doi: 10.1212/WNL.0b013e3181e0f147.

16.

Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia.

Grozeva D, Conrad DF, Barnes CP, Hurles M, Owen MJ, O'Donovan MC, Craddock N, Kirov G; WTCCC..

Schizophr Res. 2012 Mar;135(1-3):1-7. doi: 10.1016/j.schres.2011.11.004.

17.

Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder.

Jarick I, Volckmar AL, Pütter C, Pechlivanis S, Nguyen TT, Dauvermann MR, Beck S, Albayrak Ö, Scherag S, Gilsbach S, Cichon S, Hoffmann P, Degenhardt F, Nöthen MM, Schreiber S, Wichmann HE, Jöckel KH, Heinrich J, Tiesler CM, Faraone SV, Walitza S, Sinzig J, Freitag C, Meyer J, Herpertz-Dahlmann B, Lehmkuhl G, Renner TJ, Warnke A, Romanos M, Lesch KP, Reif A, Schimmelmann BG, Hebebrand J, Scherag A, Hinney A.

Mol Psychiatry. 2014 Jan;19(1):115-21. doi: 10.1038/mp.2012.161.

18.

Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?

Van Den Bossche MJ, Johnstone M, Strazisar M, Pickard BS, Goossens D, Lenaerts AS, De Zutter S, Nordin A, Norrback KF, Mendlewicz J, Souery D, De Rijk P, Sabbe BG, Adolfsson R, Blackwood D, Del-Favero J.

Am J Med Genet B Neuropsychiatr Genet. 2012 Oct;159B(7):812-22. doi: 10.1002/ajmg.b.32088.

PMID:
22911887
19.

Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample.

Szatkiewicz JP, Neale BM, O'Dushlaine C, Fromer M, Goldstein JI, Moran JL, Chambert K, Kähler A, Magnusson PK, Hultman CM, Sklar P, Purcell S, McCarroll SA, Sullivan PF.

Mol Psychiatry. 2013 Nov;18(11):1178-84. doi: 10.1038/mp.2013.98.

20.

After GWAS: searching for genetic risk for schizophrenia and bipolar disorder.

Gershon ES, Alliey-Rodriguez N, Liu C.

Am J Psychiatry. 2011 Mar;168(3):253-6. doi: 10.1176/appi.ajp.2010.10091340. Review.

PMID:
21285144
Items per page

Supplemental Content

Support Center