185 related articles for article (PubMed ID: 21855053)
1. De novo rates and selection of schizophrenia-associated copy number variants.
Rees E; Moskvina V; Owen MJ; O'Donovan MC; Kirov G
Biol Psychiatry; 2011 Dec; 70(12):1109-14. PubMed ID: 21855053
[TBL] [Abstract][Full Text] [Related]
2. De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.
Kirov G; Pocklington AJ; Holmans P; Ivanov D; Ikeda M; Ruderfer D; Moran J; Chambert K; Toncheva D; Georgieva L; Grozeva D; Fjodorova M; Wollerton R; Rees E; Nikolov I; van de Lagemaat LN; Bayés A; Fernandez E; Olason PI; Böttcher Y; Komiyama NH; Collins MO; Choudhary J; Stefansson K; Stefansson H; Grant SG; Purcell S; Sklar P; O'Donovan MC; Owen MJ
Mol Psychiatry; 2012 Feb; 17(2):142-53. PubMed ID: 22083728
[TBL] [Abstract][Full Text] [Related]
3. De novo rates and selection of large copy number variation.
Itsara A; Wu H; Smith JD; Nickerson DA; Romieu I; London SJ; Eichler EE
Genome Res; 2010 Nov; 20(11):1469-81. PubMed ID: 20841430
[TBL] [Abstract][Full Text] [Related]
4. De novo mutation in schizophrenia.
Rees E; Kirov G; O'Donovan MC; Owen MJ
Schizophr Bull; 2012 May; 38(3):377-81. PubMed ID: 22451492
[TBL] [Abstract][Full Text] [Related]
5. Assessment of de novo copy-number variations in Italian patients with schizophrenia: Detection of putative mutations involving regulatory enhancer elements.
Piluso G; Monteleone P; Galderisi S; Giugliano T; Bertolino A; Rocca P; Rossi A; Mucci A; Aguglia E; Andriola I; Bellomo A; Comparelli A; Gambi F; Fagiolini A; Marchesi C; Roncone R; Sacchetti E; Santonastaso P; Siracusano A; Stratta P; Tortorella A; Steardo L; Bucci P; Nigro V; Maj M;
World J Biol Psychiatry; 2019 Feb; 20(2):126-136. PubMed ID: 29069978
[TBL] [Abstract][Full Text] [Related]
6. 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; 23(24):6677-83. PubMed ID: 25055870
[TBL] [Abstract][Full Text] [Related]
7. Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data.
Glessner JT; Bick AG; Ito K; Homsy J; Rodriguez-Murillo L; Fromer M; Mazaika E; Vardarajan B; Italia M; Leipzig J; DePalma SR; Golhar R; Sanders SJ; Yamrom B; Ronemus M; Iossifov I; Willsey AJ; State MW; Kaltman JR; White PS; Shen Y; Warburton D; Brueckner M; Seidman C; Goldmuntz E; Gelb BD; Lifton R; Seidman J; Hakonarson H; Chung WK
Circ Res; 2014 Oct; 115(10):884-896. PubMed ID: 25205790
[TBL] [Abstract][Full Text] [Related]
8. Genomic copy number variations: A breakthrough in our knowledge on schizophrenia etiology?
Hosak L; Silhan P; Hosakova J
Neuro Endocrinol Lett; 2012; 33(2):183-90. PubMed ID: 22592199
[TBL] [Abstract][Full Text] [Related]
9. Increased de novo copy number variants in the offspring of older males.
Flatscher-Bader T; Foldi CJ; Chong S; Whitelaw E; Moser RJ; Burne TH; Eyles DW; McGrath JJ
Transl Psychiatry; 2011 Aug; 1(8):e34. PubMed ID: 22832608
[TBL] [Abstract][Full Text] [Related]
10. 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; 72(6):951-63. PubMed ID: 22196331
[TBL] [Abstract][Full Text] [Related]
11. Large-scale discovery of novel neurodevelopmental disorder-related genes through a unified analysis of single-nucleotide and copy number variants.
Hamanaka K; Miyake N; Mizuguchi T; Miyatake S; Uchiyama Y; Tsuchida N; Sekiguchi F; Mitsuhashi S; Tsurusaki Y; Nakashima M; Saitsu H; Yamada K; Sakamoto M; Fukuda H; Ohori S; Saida K; Itai T; Azuma Y; Koshimizu E; Fujita A; Erturk B; Hiraki Y; Ch'ng GS; Kato M; Okamoto N; Takata A; Matsumoto N
Genome Med; 2022 Apr; 14(1):40. PubMed ID: 35468861
[TBL] [Abstract][Full Text] [Related]
12. High-resolution copy number variation analysis of schizophrenia in Japan.
Kushima I; Aleksic B; Nakatochi M; Shimamura T; Shiino T; Yoshimi A; Kimura H; Takasaki Y; Wang C; Xing J; Ishizuka K; Oya-Ito T; Nakamura Y; Arioka Y; Maeda T; Yamamoto M; Yoshida M; Noma H; Hamada S; Morikawa M; Uno Y; Okada T; Iidaka T; Iritani S; Yamamoto T; Miyashita M; Kobori A; Arai M; Itokawa M; Cheng MC; Chuang YA; Chen CH; Suzuki M; Takahashi T; Hashimoto R; Yamamori H; Yasuda Y; Watanabe Y; Nunokawa A; Someya T; Ikeda M; Toyota T; Yoshikawa T; Numata S; Ohmori T; Kunimoto S; Mori D; Iwata N; Ozaki N
Mol Psychiatry; 2017 Mar; 22(3):430-440. PubMed ID: 27240532
[TBL] [Abstract][Full Text] [Related]
13. Rare CNVs in Suicide Attempt include Schizophrenia-Associated Loci and Neurodevelopmental Genes: A Pilot Genome-Wide and Family-Based Study.
Sokolowski M; Wasserman J; Wasserman D
PLoS One; 2016; 11(12):e0168531. PubMed ID: 28030616
[TBL] [Abstract][Full Text] [Related]
14. Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples.
Huguet G; Schramm C; Douard E; Jiang L; Labbe A; Tihy F; Mathonnet G; Nizard S; Lemyre E; Mathieu A; Poline JB; Loth E; Toro R; Schumann G; Conrod P; Pausova Z; Greenwood C; Paus T; Bourgeron T; Jacquemont S;
JAMA Psychiatry; 2018 May; 75(5):447-457. PubMed ID: 29562078
[TBL] [Abstract][Full Text] [Related]
15. miRNA and miRNA target genes in copy number variations occurring in individuals with intellectual disability.
Qiao Y; Badduke C; Mercier E; Lewis SM; Pavlidis P; Rajcan-Separovic E
BMC Genomics; 2013 Aug; 14():544. PubMed ID: 23937676
[TBL] [Abstract][Full Text] [Related]
16. The penetrance of copy number variations for schizophrenia and developmental delay.
Kirov G; Rees E; Walters JT; Escott-Price V; Georgieva L; Richards AL; Chambert KD; Davies G; Legge SE; Moran JL; McCarroll SA; O'Donovan MC; Owen MJ
Biol Psychiatry; 2014 Mar; 75(5):378-85. PubMed ID: 23992924
[TBL] [Abstract][Full Text] [Related]
17. 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; 71(5):392-402. PubMed ID: 22169095
[TBL] [Abstract][Full Text] [Related]
18. Rare variants and risk for schizophrenia: more support.
Rapoport J; Ahn K
Biol Psychiatry; 2011 Dec; 70(12):1102-3. PubMed ID: 22115410
[No Abstract] [Full Text] [Related]
19. Phenotypic features of patients with schizophrenia carrying de novo gene mutations: a pilot study.
Malherbe PJ; Roos JL; Ehlers R; Karayiorgou M; Roos JL
Psychiatry Res; 2015 Jan; 225(1-2):108-114. PubMed ID: 25467704
[TBL] [Abstract][Full Text] [Related]
20. Identification of novel candidate disease genes from de novo exonic copy number variants.
Gambin T; Yuan B; Bi W; Liu P; Rosenfeld JA; Coban-Akdemir Z; Pursley AN; Nagamani SCS; Marom R; Golla S; Dengle L; Petrie HG; Matalon R; Emrick L; Proud MB; Treadwell-Deering D; Chao HT; Koillinen H; Brown C; Urraca N; Mostafavi R; Bernes S; Roeder ER; Nugent KM; Bader PI; Bellus G; Cummings M; Northrup H; Ashfaq M; Westman R; Wildin R; Beck AE; Immken L; Elton L; Varghese S; Buchanan E; Faivre L; Lefebvre M; Schaaf CP; Walkiewicz M; Yang Y; Kang SL; Lalani SR; Bacino CA; Beaudet AL; Breman AM; Smith JL; Cheung SW; Lupski JR; Patel A; Shaw CA; Stankiewicz P
Genome Med; 2017 Sep; 9(1):83. PubMed ID: 28934986
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
