Literature DB >> 12126600

Schizophrenia and genetics: new insights.

Anne S Bassett1, Eva W Chow, Rosanna Weksberg, Linda Brzustowicz.   

Abstract

There is consistent evidence that the principal etiology of schizophrenia involves predisposing genetic factors. Recent years have seen several new insights in the genetics of schizophrenia. Several chromosomal regions show significant evidence that they contain schizophrenia susceptibility genes. A clinically relevant genetic subtype of schizophrenia (22q deletion syndrome) has been identified. There is new evidence that spontaneous mutations may play a role. There are new recommendations for genetic counseling. The progress to date suggests that understanding of a neurodevelopmental pathway from genetic susceptibility to schizophrenia will soon be fundamentally altered by molecular genetic advances in this complex disease.

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Year:  2002        PMID: 12126600      PMCID: PMC3188303          DOI: 10.1007/s11920-996-0051-x

Source DB:  PubMed          Journal:  Curr Psychiatry Rep        ISSN: 1523-3812            Impact factor:   5.285


  62 in total

1.  Microdeletion 22q11.2: clinical data and deletion size.

Authors:  W S Kerstjens-Frederikse; H Kurahashi; D A Driscoll; M L Budarf; B S Emanuel; B Beatty; T Scheidl; J Siegel-Bartelt; K Henderson; C Cytrynbaum; G Nie; I Teshima
Journal:  J Med Genet       Date:  1999-09       Impact factor: 6.318

2.  Genome scan of European-American schizophrenia pedigrees: results of the NIMH Genetics Initiative and Millennium Consortium.

Authors:  S V Faraone; T Matise; D Svrakic; J Pepple; D Malaspina; B Suarez; C Hampe; C T Zambuto; K Schmitt; J Meyer; P Markel; H Lee; J Harkavy Friedman; C Kaufmann; C R Cloninger; M T Tsuang
Journal:  Am J Med Genet       Date:  1998-07-10

Review 3.  22q11 deletion syndrome: a genetic subtype of schizophrenia.

Authors:  A S Bassett; E W Chow
Journal:  Biol Psychiatry       Date:  1999-10-01       Impact factor: 13.382

4.  Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS.

Authors:  A Swillen; K Devriendt; E Legius; B Eyskens; M Dumoulin; M Gewillig; J P Fryns
Journal:  J Med Genet       Date:  1997-06       Impact factor: 6.318

Review 5.  Phenotype of adults with the 22q11 deletion syndrome: A review.

Authors:  E Cohen; E W Chow; R Weksberg; A S Bassett
Journal:  Am J Med Genet       Date:  1999-10-08

6.  A common molecular basis for rearrangement disorders on chromosome 22q11.

Authors:  L Edelmann; R K Pandita; E Spiteri; B Funke; R Goldberg; N Palanisamy; R S Chaganti; E Magenis; R J Shprintzen; B E Morrow
Journal:  Hum Mol Genet       Date:  1999-07       Impact factor: 6.150

7.  Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21.

Authors:  J L Blouin; B A Dombroski; S K Nath; V K Lasseter; P S Wolyniec; G Nestadt; M Thornquist; G Ullrich; J McGrath; L Kasch; M Lamacz; M G Thomas; C Gehrig; U Radhakrishna; S E Snyder; K G Balk; K Neufeld; K L Swartz; N DeMarchi; G N Papadimitriou; D G Dikeos; C N Stefanis; A Chakravarti; B Childs; D E Housman; H H Kazazian; S Antonarakis; A E Pulver
Journal:  Nat Genet       Date:  1998-09       Impact factor: 38.330

8.  Chromosome 22qII deletions. An under-recognised cause of idiopathic learning disability.

Authors:  K C Murphy; R G Jones; E Griffiths; P W Thompson; M J Owen
Journal:  Br J Psychiatry       Date:  1998-02       Impact factor: 9.319

9.  A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2.

Authors:  S D Detera-Wadleigh; J A Badner; W H Berrettini; T Yoshikawa; L R Goldin; G Turner; D Y Rollins; T Moses; A R Sanders; J D Karkera; L E Esterling; J Zeng; T N Ferraro; J J Guroff; D Kazuba; M E Maxwell; J I Nurnberger; E S Gershon
Journal:  Proc Natl Acad Sci U S A       Date:  1999-05-11       Impact factor: 11.205

10.  22q11 deletion syndrome in adults with schizophrenia.

Authors:  A S Bassett; K Hodgkinson; E W Chow; S Correia; L E Scutt; R Weksberg
Journal:  Am J Med Genet       Date:  1998-07-10
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  4 in total

1.  MiR-574-5P, miR-1827, and miR-4429 as Potential Biomarkers for Schizophrenia.

Authors:  Omran Davarinejad; Sajad Najafi; Hossein Zhaleh; Farzaneh Golmohammadi; Farnaz Radmehr; Mostafa Alikhani; Reza Heidari Moghadam; Yazdan Rahmati
Journal:  J Mol Neurosci       Date:  2021-11-22       Impact factor: 3.444

2.  Association of synapsin 2 with schizophrenia in families of Northern European ancestry.

Authors:  Viatcheslav Saviouk; Michael P Moreau; Irina V Tereshchenko; Linda M Brzustowicz
Journal:  Schizophr Res       Date:  2007-09-04       Impact factor: 4.939

3.  Tumor necrosis factor promoter haplotype associated with schizophrenia reveals a linked locus on 1q44.

Authors:  V Saviouk; E W C Chow; A S Bassett; L M Brzustowicz
Journal:  Mol Psychiatry       Date:  2005-04       Impact factor: 15.992

4.  Disruption of the neurexin 1 gene is associated with schizophrenia.

Authors:  Dan Rujescu; Andres Ingason; Sven Cichon; Olli P H Pietiläinen; Michael R Barnes; Timothea Toulopoulou; Marco Picchioni; Evangelos Vassos; Ulrich Ettinger; Elvira Bramon; Robin Murray; Mirella Ruggeri; Sarah Tosato; Chiara Bonetto; Stacy Steinberg; Engilbert Sigurdsson; Thordur Sigmundsson; Hannes Petursson; Arnaldur Gylfason; Pall I Olason; Gudmundur Hardarsson; Gudrun A Jonsdottir; Omar Gustafsson; Ragnheidur Fossdal; Ina Giegling; Hans-Jürgen Möller; Annette M Hartmann; Per Hoffmann; Caroline Crombie; Gillian Fraser; Nicholas Walker; Jouko Lonnqvist; Jaana Suvisaari; Annamari Tuulio-Henriksson; Srdjan Djurovic; Ingrid Melle; Ole A Andreassen; Thomas Hansen; Thomas Werge; Lambertus A Kiemeney; Barbara Franke; Joris Veltman; Jacobine E Buizer-Voskamp; Chiara Sabatti; Roel A Ophoff; Marcella Rietschel; Markus M Nöthen; Kari Stefansson; Leena Peltonen; David St Clair; Hreinn Stefansson; David A Collier
Journal:  Hum Mol Genet       Date:  2008-10-22       Impact factor: 6.150

  4 in total

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