J
Jacobine E. Buizer-Voskamp
Researcher at Utrecht University
Publications - 29
Citations - 3859
Jacobine E. Buizer-Voskamp is an academic researcher from Utrecht University. The author has contributed to research in topics: Population & Copy-number variation. The author has an hindex of 19, co-authored 29 publications receiving 3636 citations. Previous affiliations of Jacobine E. Buizer-Voskamp include University of Groningen & University Medical Center Utrecht.
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Large recurrent microdeletions associated with schizophrenia
Hreinn Stefansson,Dan Rujescu,Sven Cichon,Olli Pietiläinen,Andres Ingason,Stacy Steinberg,Ragnheidur Fossdal,Engilbert Sigurdsson,Thordur Sigmundsson,Jacobine E. Buizer-Voskamp,Thomas Hansen,Thomas Hansen,Klaus D. Jakobsen,Klaus D. Jakobsen,Pierandrea Muglia,Clyde Francks,Paul M. Matthews,Arnaldur Gylfason,Bjarni V. Halldorsson,Daniel F. Gudbjartsson,Thorgeir E. Thorgeirsson,Asgeir Sigurdsson,Adalbjorg Jonasdottir,Aslaug Jonasdottir,Asgeir Björnsson,Sigurborg Mattiasdottir,Thorarinn Blondal,Magnús Haraldsson,Brynja B. Magnusdottir,Ina Giegling,Hans-Jürgen Möller,Annette M. Hartmann,Kevin V. Shianna,Dongliang Ge,Anna C. Need,Caroline Crombie,Gillian Fraser,Nicholas Walker,Jouko Lönnqvist,Jaana Suvisaari,Annamarie Tuulio-Henriksson,Tiina Paunio,T. Toulopoulou,Elvira Bramon,Marta Di Forti,Robin M. Murray,Mirella Ruggeri,Evangelos Vassos,Sarah Tosato,Muriel Walshe,Tao Li,Tao Li,Catalina Vasilescu,Thomas W. Mühleisen,August G. Wang,Henrik Ullum,Srdjan Djurovic,Ingrid Melle,Jes Olesen,Lambertus A. Kiemeney,Barbara Franke,Chiara Sabatti,Nelson B. Freimer,Jeffrey R. Gulcher,Unnur Thorsteinsdottir,Augustine Kong,Ole A. Andreassen,Roel A. Ophoff,Roel A. Ophoff,Alexander Georgi,Marcella Rietschel,Thomas Werge,Hannes Petursson,David Goldstein,Markus M. Nöthen,Leena Peltonen,Leena Peltonen,David A. Collier,David A. Collier,David St Clair,Kari Stefansson,Kari Stefansson +81 more
TL;DR: In a genome-wide search for CNVs associating with schizophrenia, a population-based sample was used to identify de novo CNVs by analysing 9,878 transmissions from parents to offspring and three deletions significantly associate with schizophrenia and related psychoses in the combined sample.
Journal ArticleDOI
Disruption of the neurexin 1 gene is associated with schizophrenia
Dan Rujescu,Andres Ingason,Andres Ingason,Sven Cichon,Olli Pietiläinen,Michael R. Barnes,Timothea Toulopoulou,Marco Picchioni,Evangelos Vassos,Ulrich Ettinger,Elvira Bramon,Robin M. 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 Lönnqvist,Jaana Suvisaari,Annamari Tuulio-Henriksson,Srdjan Djurovic,Ingrid Melle,Ole A. Andreassen,Thomas Hansen,Thomas Werge,Lambertus A. Kiemeney,Barbara Franke,Joris A. Veltman,Jacobine E. Buizer-Voskamp,Chiara Sabatti,Roel A. Ophoff,Marcella Rietschel,Markus M. Nöthen,K. Stefansson,Leena Peltonen,David St Clair,Hreinn Stefansson,David A. Collier +52 more
TL;DR: It is concluded that NRXN1 deletions affecting exons confer risk of schizophrenia.
Journal ArticleDOI
Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients
Terry Vrijenhoek,Jacobine E. Buizer-Voskamp,Inge van der Stelt,Eric Strengman,Chiara Sabatti,Ad Geurts van Kessel,Han G. Brunner,Roel A. Ophoff,Roel A. Ophoff,Joris A. Veltman +9 more
TL;DR: A role for rare CNVs in schizophrenia susceptibility is supported and at least three candidate genes for this complex disorder are identified.
Journal ArticleDOI
Copy number variations of chromosome 16p13.1 region associated with schizophrenia
Andres Ingason,Andres Ingason,Dan Rujescu,Sven Cichon,Engilbert Sigurdsson,Thordur Sigmundsson,Olli Pietiläinen,Jacobine E. Buizer-Voskamp,Eric Strengman,Clyde Francks,Pierandrea Muglia,Arnaldur Gylfason,Omar Gustafsson,Pall I. Olason,Stacy Steinberg,Thomas Hansen,K.D. Jakobsen,Henrik B. Rasmussen,Ina Giegling,H.-J. Möller,Annette M. Hartmann,Caroline Crombie,Gillian Fraser,Neil Walker,Jan-Erik Lönnqvist,Jaana Suvisaari,Annamari Tuulio-Henriksson,Elvira Bramon,Lambertus A. Kiemeney,Barbara Franke,Robin M. Murray,Evangelos Vassos,Timothea Toulopoulou,Thomas W. Mühleisen,Sarah Tosato,Mirella Ruggeri,Srdjan Djurovic,Ole A. Andreassen,Zhongyang Zhang,Thomas Werge,Roel A. Ophoff,Roel A. Ophoff,M. Rietschel,Markus M. Nöthen,H. Petursson,Hreinn Stefansson,Leena Peltonen,Leena Peltonen,David A. Collier,Kari Stefansson,D. St Clair +50 more
TL;DR: It is concluded that duplications and perhaps also deletions of chromosome 16p13.1, previously reported to be associated with autism and MR, also confer risk of schizophrenia.
Journal ArticleDOI
Gene-network analysis identifies susceptibility genes related to glycobiology in autism.
Bert van der Zwaag,Lude Franke,Lude Franke,Martin Poot,Ron Hochstenbach,Henk A. Spierenburg,Jacob A. S. Vorstman,Emma van Daalen,Maretha de Jonge,Nienke E. Verbeek,Eva H. Brilstra,Ruben van 't Slot,Roel A. Ophoff,Michael A. van Es,Hylke M. Blauw,Jan H. Veldink,Jacobine E. Buizer-Voskamp,Frits A. Beemer,Leonard H. van den Berg,Cisca Wijmenga,Cisca Wijmenga,Hans Kristian Ploos van Amstel,Herman van Engeland,J. Peter H. Burbach,Wouter G. Staal +24 more
TL;DR: It is suggested that the occurrence of genomic gains and losses of genes associated with glycobiology are important contributors to the development of ASD.