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Literature DB >> 19675094

Neurexin 1 (NRXN1) deletions in schizophrenia.

George Kirov¹, Dan Rujescu, Andres Ingason, David A Collier, Michael C O'Donovan, Michael J Owen.

Abstract

Entities: Disease Gene

Mesh：

Year: 2009 PMID： 19675094 PMCID： PMC2728827 DOI： 10.1093/schbul/sbp079

Source DB: PubMed Journal: Schizophr Bull ISSN： 0586-7614 Impact factor: 9.306

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23 in total

1. High frequency of neurexin 1beta signal peptide structural variants in patients with autism.

Authors: Jinong Feng; Richard Schroer; Jin Yan; Wenjia Song; Chunmei Yang; Anke Bockholt; Edwin H Cook; Cindy Skinner; Charles E Schwartz; Steve S Sommer
Journal: Neurosci Lett Date: 2006-10-10 Impact factor: 3.046

2. Support for the involvement of large copy number variants in the pathogenesis of schizophrenia.

Authors: George Kirov; Detelina Grozeva; Nadine Norton; Dobril Ivanov; Kiran K Mantripragada; Peter Holmans; Nick Craddock; Michael J Owen; Michael C O'Donovan
Journal: Hum Mol Genet Date: 2009-01-29 Impact factor: 6.150

3. Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome.

Authors: B W M van Bon; H C Mefford; B Menten; D A Koolen; A J Sharp; W M Nillesen; J W Innis; T J L de Ravel; C L Mercer; M Fichera; H Stewart; L E Connell; K Ounap; K Lachlan; B Castle; N Van der Aa; C van Ravenswaaij; M A Nobrega; C Serra-Juhé; I Simonic; N de Leeuw; R Pfundt; E M Bongers; C Baker; P Finnemore; S Huang; V K Maloney; J A Crolla; M van Kalmthout; M Elia; G Vandeweyer; J P Fryns; S Janssens; N Foulds; S Reitano; K Smith; S Parkel; B Loeys; C G Woods; A Oostra; F Speleman; A C Pereira; A Kurg; L Willatt; S J L Knight; J R Vermeesch; C Romano; J C Barber; G Mortier; L A Pérez-Jurado; F Kooy; H G Brunner; E E Eichler; T Kleefstra; B B A de Vries
Journal: J Med Genet Date: 2009-04-15 Impact factor: 6.318

4. Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation.

Authors: J M Friedman; Agnes Baross; Allen D Delaney; Adrian Ally; Laura Arbour; Linlea Armstrong; Jennifer Asano; Dione K Bailey; Sarah Barber; Patricia Birch; Mabel Brown-John; Manqiu Cao; Susanna Chan; David L Charest; Noushin Farnoud; Nicole Fernandes; Stephane Flibotte; Anne Go; William T Gibson; Robert A Holt; Steven J M Jones; Giulia C Kennedy; Martin Krzywinski; Sylvie Langlois; Haiyan I Li; Barbara C McGillivray; Tarun Nayar; Trevor J Pugh; Evica Rajcan-Separovic; Jacqueline E Schein; Angelique Schnerch; Asim Siddiqui; Margot I Van Allen; Gary Wilson; Siu-Li Yong; Farah Zahir; Patrice Eydoux; Marco A Marra
Journal: Am J Hum Genet Date: 2006-07-25 Impact factor: 11.025

5. Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia.

Authors: George Kirov; Dilihan Gumus; Wei Chen; Nadine Norton; Lyudmila Georgieva; Murat Sari; Michael C O'Donovan; Fikret Erdogan; Michael J Owen; Hans-Hilger Ropers; Reinhard Ullmann
Journal: Hum Mol Genet Date: 2007-11-06 Impact factor: 6.150

6. Cartography of neurexins: more than 1000 isoforms generated by alternative splicing and expressed in distinct subsets of neurons.

Authors: B Ullrich; Y A Ushkaryov; T C Südhof
Journal: Neuron Date: 1995-03 Impact factor: 17.173

7. Disruption of neurexin 1 associated with autism spectrum disorder.

Authors: Hyung-Goo Kim; Shotaro Kishikawa; Anne W Higgins; Ihn-Sik Seong; Diana J Donovan; Yiping Shen; Eric Lally; Lauren A Weiss; Juliane Najm; Kerstin Kutsche; Maria Descartes; Lynn Holt; Stephen Braddock; Robin Troxell; Lee Kaplan; Fred Volkmar; Ami Klin; Katherine Tsatsanis; David J Harris; Ilse Noens; David L Pauls; Mark J Daly; Marcy E MacDonald; Cynthia C Morton; Bradley J Quade; James F Gusella
Journal: Am J Hum Genet Date: 2008-01 Impact factor: 11.025

Review 8. Genetics of autism spectrum disorders.

Authors: Ravinesh A Kumar; Susan L Christian
Journal: Curr Neurol Neurosci Rep Date: 2009-05 Impact factor: 5.081

Review 9. Schizophrenia genetics: advancing on two fronts.

Authors: Michael J Owen; Hywel J Williams; Michael C O'Donovan
Journal: Curr Opin Genet Dev Date: 2009-04-01 Impact factor: 5.578

10. Mapping autism risk loci using genetic linkage and chromosomal rearrangements.

Authors: Peter Szatmari; Andrew D Paterson; Lonnie Zwaigenbaum; Wendy Roberts; Jessica Brian; Xiao-Qing Liu; John B Vincent; Jennifer L Skaug; Ann P Thompson; Lili Senman; Lars Feuk; Cheng Qian; Susan E Bryson; Marshall B Jones; Christian R Marshall; Stephen W Scherer; Veronica J Vieland; Christopher Bartlett; La Vonne Mangin; Rhinda Goedken; Alberto Segre; Margaret A Pericak-Vance; Michael L Cuccaro; John R Gilbert; Harry H Wright; Ruth K Abramson; Catalina Betancur; Thomas Bourgeron; Christopher Gillberg; Marion Leboyer; Joseph D Buxbaum; Kenneth L Davis; Eric Hollander; Jeremy M Silverman; Joachim Hallmayer; Linda Lotspeich; James S Sutcliffe; Jonathan L Haines; Susan E Folstein; Joseph Piven; Thomas H Wassink; Val Sheffield; Daniel H Geschwind; Maja Bucan; W Ted Brown; Rita M Cantor; John N Constantino; T Conrad Gilliam; Martha Herbert; Clara Lajonchere; David H Ledbetter; Christa Lese-Martin; Janet Miller; Stan Nelson; Carol A Samango-Sprouse; Sarah Spence; Matthew State; Rudolph E Tanzi; Hilary Coon; Geraldine Dawson; Bernie Devlin; Annette Estes; Pamela Flodman; Lambertus Klei; William M McMahon; Nancy Minshew; Jeff Munson; Elena Korvatska; Patricia M Rodier; Gerard D Schellenberg; Moyra Smith; M Anne Spence; Chris Stodgell; Ping Guo Tepper; Ellen M Wijsman; Chang-En Yu; Bernadette Rogé; Carine Mantoulan; Kerstin Wittemeyer; Annemarie Poustka; Bärbel Felder; Sabine M Klauck; Claudia Schuster; Fritz Poustka; Sven Bölte; Sabine Feineis-Matthews; Evelyn Herbrecht; Gabi Schmötzer; John Tsiantis; Katerina Papanikolaou; Elena Maestrini; Elena Bacchelli; Francesca Blasi; Simona Carone; Claudio Toma; Herman Van Engeland; Maretha de Jonge; Chantal Kemner; Frederieke Koop; Frederike Koop; Marjolein Langemeijer; Marjolijn Langemeijer; Channa Hijmans; Channa Hijimans; Wouter G Staal; Gillian Baird; Patrick F Bolton; Michael L Rutter; Emma Weisblatt; Jonathan Green; Catherine Aldred; Julie-Anne Wilkinson; Andrew Pickles; Ann Le Couteur; Tom Berney; Helen McConachie; Anthony J Bailey; Kostas Francis; Gemma Honeyman; Aislinn Hutchinson; Jeremy R Parr; Simon Wallace; Anthony P Monaco; Gabrielle Barnby; Kazuhiro Kobayashi; Janine A Lamb; Ines Sousa; Nuala Sykes; Edwin H Cook; Stephen J Guter; Bennett L Leventhal; Jeff Salt; Catherine Lord; Christina Corsello; Vanessa Hus; Daniel E Weeks; Fred Volkmar; Maïté Tauber; Eric Fombonne; Andy Shih; Kacie J Meyer
Journal: Nat Genet Date: 2007-02-18 Impact factor: 38.330

96 in total

Review 1. The genetics of Tourette disorder.

Authors: Matthew W State
Journal: Curr Opin Genet Dev Date: 2011-01-27 Impact factor: 5.578

2. De novo mutation in schizophrenia.

Authors: Elliott Rees; George Kirov; Michael C O'Donovan; Michael J Owen
Journal: Schizophr Bull Date: 2012-03-26 Impact factor: 9.306

Review 3. Genomic copy number variation in disorders of cognitive development.

Authors: Eric M Morrow
Journal: J Am Acad Child Adolesc Psychiatry Date: 2010-11 Impact factor: 8.829

Review 4. Integrative Review of Genetic Factors Influencing Neurodevelopmental Outcomes in Preterm Infants.

Authors: Lisa M Blair; Rita H Pickler; Cindy Anderson
Journal: Biol Res Nurs Date: 2015-09-15 Impact factor: 2.522

Review 5. Will brain cells derived from induced pluripotent stem cells or directly converted from somatic cells (iNs) be useful for schizophrenia research?

Authors: Cheryl Filippich; Ernst J Wolvetang; Bryan J Mowry
Journal: Schizophr Bull Date: 2013-07-24 Impact factor: 9.306

6. Phenotype mining in CNV carriers from a population cohort.

Authors: Olli P H Pietiläinen; Karola Rehnström; Eveliina Jakkula; Susan K Service; Eliza Congdon; Carola Tilgmann; Anna-Liisa Hartikainen; Anja Taanila; Ulla Heikura; Tiina Paunio; Samuli Ripatti; Marjo-Riitta Jarvelin; Matti Isohanni; Chiara Sabatti; Aarno Palotie; Nelson B Freimer; Leena Peltonen
Journal: Hum Mol Genet Date: 2011-04-19 Impact factor: 6.150