Literature DB >> 15812168

Computer-assisted phenotype characterization for genetic research in psychiatry.

Heiner Fangerau1, Stephanie Ohlraun, Ralf O Granath, Markus M Nöthen, Marcella Rietschel, Thomas G Schulze.   

Abstract

Psychiatric disorders differ from other complex phenotypes in their lack of objectively assessable biological markers that contribute to the establishment of a research diagnosis for genetic studies. To nevertheless allow for the delineation of genetically meaningful diagnostic entities for psychiatric genetic research, comprehensive phenotype characterization procedures are required. It is widely agreed that these should include the standardized assessment of life-time clinical symptomatology, sociodemographic, and environmental factors. Data should be based on several sources, i.e. diagnostic interviews with probands and their relatives as well as a thorough review of medical records, and final assignment of diagnosis should follow robust algorithms (i.e. best-estimate procedures, consensus diagnosis). Here, we outline a practical implementation of such a phenotype characterization strategy, including patient recruitment, study enrolment procedures, comprehensive diagnostic assessment, and data management. We argue that successful psychiatric phenotype characterization requires flexible tools. For this purpose, we have developed a computer-assisted phenotype characterization inventory, built around the backbone of a relational database. It allows for the straightforward assessment of symptoms, automated error checks and diagnostic assignment, easily manageable data storage and handling, and flexible data transfer between various research centers even across language barriers, while at the same time keeping up with the highest standards for the protection of sensitive patient data. Copyright 2004 S. Karger AG, Basel.

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Year:  2004        PMID: 15812168     DOI: 10.1159/000083538

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  15 in total

1.  Molecular genetic overlap in bipolar disorder, schizophrenia, and major depressive disorder.

Authors:  Thomas G Schulze; Nirmala Akula; René Breuer; Jo Steele; Michael A Nalls; Andrew B Singleton; Franziska A Degenhardt; Markus M Nöthen; Sven Cichon; Marcella Rietschel; Francis J McMahon
Journal:  World J Biol Psychiatry       Date:  2012-03-09       Impact factor: 4.132

2.  Genomewide scan and fine-mapping linkage studies in four European samples with bipolar affective disorder suggest a new susceptibility locus on chromosome 1p35-p36 and provides further evidence of loci on chromosome 4q31 and 6q24.

Authors:  Johannes Schumacher; Radka Kaneva; Rami Abou Jamra; Guillermo Orozco Diaz; Stephanie Ohlraun; Vihra Milanova; Young-Ae Lee; Fabio Rivas; Fermin Mayoral; Robert Fuerst; Antonia Flaquer; Christine Windemuth; Eudoxia Gay; Sebastian Sanz; Maria José González; Susana Gil; Francisco Cabaleiro; Francisco del Rio; Fermin Perez; Jesus Haro; Christian Kostov; Vesselin Chorbov; Amelia Nikolova-Hill; Vessela Stoyanova; George Onchev; Ivo Kremensky; Konstantin Strauch; Thomas G Schulze; Peter Nürnberg; Wolfgang Gaebel; Ansgar Klimke; Georg Auburger; Thomas F Wienker; Luba Kalaydjieva; Peter Propping; Sven Cichon; Assen Jablensky; Marcella Rietschel; Markus M Nöthen
Journal:  Am J Hum Genet       Date:  2005-11-02       Impact factor: 11.025

3.  Brief report: no association between premorbid adjustment in adult-onset schizophrenia and genetic variation in Dysbindin.

Authors:  Frederike Schirmbeck; Alexander Georgi; Jana Strohmaier; Christine Schmael; Katja V Boesshenz; Thomas W Mühleisen; Stefan Herms; Per Hoffmann; Rami Abou Jamra; Johannes Schumacher; Wolfgang Maier; Peter Propping; Markus M Nöthen; Sven Cichon; Marcella Rietschel; Thomas G Schulze
Journal:  J Autism Dev Disord       Date:  2008-05-13

4.  The 1000 Genomes Project: deep genomic sequencing waiting for deep psychiatric phenotyping.

Authors:  Ridha Joober
Journal:  J Psychiatry Neurosci       Date:  2011-05       Impact factor: 6.186

5.  Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder.

Authors:  Sven Cichon; Thomas W Mühleisen; Franziska A Degenhardt; Manuel Mattheisen; Xavier Miró; Jana Strohmaier; Michael Steffens; Christian Meesters; Stefan Herms; Moritz Weingarten; Lutz Priebe; Britta Haenisch; Michael Alexander; Jennifer Vollmer; René Breuer; Christine Schmäl; Peter Tessmann; Susanne Moebus; H-Erich Wichmann; Stefan Schreiber; Bertram Müller-Myhsok; Susanne Lucae; Stéphane Jamain; Marion Leboyer; Frank Bellivier; Bruno Etain; Chantal Henry; Jean-Pierre Kahn; Simon Heath; Marian Hamshere; Michael C O'Donovan; Michael J Owen; Nick Craddock; Markus Schwarz; Helmut Vedder; Jutta Kammerer-Ciernioch; Andreas Reif; Johanna Sasse; Michael Bauer; Martin Hautzinger; Adam Wright; Philip B Mitchell; Peter R Schofield; Grant W Montgomery; Sarah E Medland; Scott D Gordon; Nicholas G Martin; Omar Gustafsson; Ole Andreassen; Srdjan Djurovic; Engilbert Sigurdsson; Stacy Steinberg; Hreinn Stefansson; Kari Stefansson; Lejla Kapur-Pojskic; Liliana Oruc; Fabio Rivas; Fermín Mayoral; Alexander Chuchalin; Gulja Babadjanova; Alexander S Tiganov; Galina Pantelejeva; Lilia I Abramova; Maria Grigoroiu-Serbanescu; Carmen C Diaconu; Piotr M Czerski; Joanna Hauser; Andreas Zimmer; Mark Lathrop; Thomas G Schulze; Thomas F Wienker; Johannes Schumacher; Wolfgang Maier; Peter Propping; Marcella Rietschel; Markus M Nöthen
Journal:  Am J Hum Genet       Date:  2011-02-25       Impact factor: 11.025

Review 6.  Genetic research into bipolar disorder: the need for a research framework that integrates sophisticated molecular biology and clinically informed phenotype characterization.

Authors:  Thomas G Schulze
Journal:  Psychiatr Clin North Am       Date:  2010-03

7.  A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case-control and family-based sample of German ancestry.

Authors:  Jana Strohmaier; Josef Frank; Jens R Wendland; Johannes Schumacher; Rami Abou Jamra; Jens Treutlein; Vanessa Nieratschker; René Breuer; Manuel Mattheisen; Stefan Herms; Thomas W Mühleisen; Wolfgang Maier; Markus M Nöthen; Sven Cichon; Marcella Rietschel; Thomas G Schulze
Journal:  Schizophr Res       Date:  2010-01-18       Impact factor: 4.939

8.  Psychiatric comorbidity and functional impairment in a clinically referred sample of adults with attention-deficit/hyperactivity disorder (ADHD).

Authors:  Esther Sobanski; Daniel Brüggemann; Barbara Alm; Sebastian Kern; Monika Deschner; Thomas Schubert; Alexandra Philipsen; Marcella Rietschel
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  2007-10       Impact factor: 5.270

9.  The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations.

Authors:  Johannes Schumacher; Gonzalo Laje; Rami Abou Jamra; Tim Becker; Thomas W Mühleisen; Catalina Vasilescu; Manuel Mattheisen; Stefan Herms; Per Hoffmann; Axel M Hillmer; Alexander Georgi; Christine Herold; Thomas G Schulze; Peter Propping; Marcella Rietschel; Francis J McMahon; Markus M Nöthen; Sven Cichon
Journal:  Hum Mol Genet       Date:  2009-05-04       Impact factor: 6.150

10.  Genome-wide association analysis of age at onset and psychotic symptoms in bipolar disorder.

Authors:  Pamela Belmonte Mahon; Mehdi Pirooznia; Fernando S Goes; Fayaz Seifuddin; Jo Steele; Phil Hyoun Lee; Jie Huang; Marian L Hamshere; J Raymond Depaulo; John R Kelsoe; Marcella Rietschel; Markus Nöthen; Sven Cichon; Hugh Gurling; Shaun Purcell; Jordan W Smoller; Nick Craddock; Thomas G Schulze; Francis J McMahon; James B Potash; Peter P Zandi
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2011-02-08       Impact factor: 3.568

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