Literature DB >> 14699434

22q11 deletion syndrome in childhood onset schizophrenia: an update.

A Sporn, A Addington, A L Reiss, M Dean, N Gogtay, U Potocnik, D Greenstein, J Hallmayer, P Gochman, M Lenane, N Baker, J Tossell, J L Rapoport.   

Abstract

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Year:  2004        PMID： 14699434     DOI： 10.1038/sj.mp.4001477

Source DB:  PubMed          Journal:  Mol Psychiatry        ISSN： 1359-4184            Impact factor:   15.992


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  30 in total

Review 1.  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

2.  Prevalence of 22q11.2 deletions in 311 Dutch patients with schizophrenia.

Authors:  Mechteld L C Hoogendoorn; Jacob A S Vorstman; Gholam R Jalali; Jean-Paul Selten; Richard J Sinke; Beverly S Emanuel; René S Kahn
Journal:  Schizophr Res       Date:  2007-10-26       Impact factor: 4.939

3.  Autism spectrum disorders and childhood-onset schizophrenia: clinical and biological contributions to a relation revisited.

Authors:  Judith Rapoport; Alex Chavez; Deanna Greenstein; Anjene Addington; Nitin Gogtay
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  2009-01       Impact factor: 8.829

4.  Sex chromosome anomalies in childhood onset schizophrenia: an update.

Authors:  K Eckstrand; A M Addington; T Stromberg; B Merriman; R Miller; P Gochman; R Long; A Dutra; Z Chen; P Meltzer; S F Nelson; J L Rapoport
Journal:  Mol Psychiatry       Date:  2008-10       Impact factor: 15.992

Review 5.  Trajectories of anatomic brain development as a phenotype.

Authors:  Jay N Giedd; Rhoshel K Lenroot; Philip Shaw; Francois Lalonde; Mark Celano; Samantha White; Julia Tossell; Anjene Addington; Nitin Gogtay
Journal:  Novartis Found Symp       Date:  2008

Review 6.  Genomic structural variation and schizophrenia.

Authors:  Jennifer Gladys Mulle
Journal:  Curr Psychiatry Rep       Date:  2008-04       Impact factor: 5.285

Review 7.  Comprehensive neurocognitive endophenotyping strategies for mouse models of genetic disorders.

Authors:  Michael R Hunsaker
Journal:  Prog Neurobiol       Date:  2012-01-13       Impact factor: 11.685

Review 8.  Clinical perspectives on the genetics of schizophrenia: a bottom-up orientation.

Authors:  Willem M A Verhoeven; Siegfried Tuinier
Journal:  Neurotox Res       Date:  2008-10       Impact factor: 3.911

9.  Psychotic features as the first manifestation of 22q11.2 deletion syndrome.

Authors:  So Dahm Kook; Suk Kyoon An; Kyung Ran Kim; Woo Jung Kim; Eun Lee; Kee Namkoong
Journal:  Psychiatry Investig       Date:  2010-02-19       Impact factor: 2.505

10.  Defining new guidelines for screening the 22q11.2 deletion based on a clinical and dysmorphologic evaluation of 194 individuals and review of the literature.

Authors:  Fabíola P Monteiro; Társis P Vieira; Ilária C Sgardioli; Miriam C Molck; Ana Paula Damiano; Josiane Souza; Isabella L Monlleó; Marshall I B Fontes; Agnes C Fett-Conte; Têmis M Félix; Gabriela F Leal; Erlane M Ribeiro; Claudio E M Banzato; Clarissa de R Dantas; Iscia Lopes-Cendes; Vera Lúcia Gil-da-Silva-Lopes
Journal:  Eur J Pediatr       Date:  2013-02-26       Impact factor: 3.183
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