C
Chantal Kemner
Researcher at Utrecht University
Publications - 165
Citations - 9769
Chantal Kemner is an academic researcher from Utrecht University. The author has contributed to research in topics: Autism & Pervasive developmental disorder. The author has an hindex of 50, co-authored 162 publications receiving 9040 citations. Previous affiliations of Chantal Kemner include Maastricht University & University of Michigan.
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Journal ArticleDOI
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Peter Szatmari,Andrew D. Paterson,Lonnie Zwaigenbaum,Wendy Roberts,Jessica Brian,Xiao-Qing Liu,John B. Vincent,Jennifer 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 W. Bartlett,La Vonne Mangin,Rhinda Goedken,Alberto M. 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 C. Sheffield,Daniel H. Geschwind,Maja Bucan,W. Ted Brown,Rita M. Cantor,John N. Constantino,T. Conrad Gilliam,Martha R. Herbert,Clara Lajonchere,David H. Ledbetter,Christa Lese-Martin,Janet Miller,Stan F. Nelson,Carol A. Samango-Sprouse,Sarah J. Spence,Matthew W. State,Rudolph E. Tanzi,Hilary Coon,Geraldine Dawson,Bernie Devlin,Annette Estes,Pamela Flodman,Lambertus Klei,William M. McMahon,Nancy J. Minshew,Jeff Munson,Elena Korvatska,Elena Korvatska,Patricia M. Rodier,Gerard D. Schellenberg,Gerard D. Schellenberg,Moyra Smith,M. Anne Spence,Christopher J. Stodgell,Ping Guo Tepper,Ellen M. Wijsman,Chang En Yu,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,Frederike Koop,Marjolijn Langemeijer,Channa Hijimans,Wouter G. Staal,Gillian Baird,Patrick Bolton,Michael 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,Inês Sousa,Nuala Sykes,Edwin H. Cook,Stephen J. Guter,Bennett L. Leventhal,Jeff Salt,Catherine Lord,Christina Corsello,Vanessa Hus,Daniel E. Weeks,Fred R. Volkmar,Maïté Tauber,Eric Fombonne,Andy Shih +139 more
TL;DR: Linkage and copy number variation analyses implicate chromosome 11p12–p13 and neurexins, respectively, among other candidate loci, highlighting glutamate-related genes as promising candidates for contributing to ASDs.
Journal ArticleDOI
A full genome screen for autism with evidence for linkage to a region on chromosome 7q International Molecular Genetic Study of Autism Consortium
Anthony J. Bailey,Amaia Hervas,Nicola Matthews,Sarah Palferman,Simon Wallace,Anne Aubin,Janine Michelotti,Catherine Wainhouse,Katerina Papanikolaou,Michael Rutter,Elena Maestrini,Angela J. Marlow,Daniel E. Weeks,Daniel E. Weeks,Janine A. Lamb,Clyde Francks,Georgina Kearsley,Pat Scudder,Anthony P. Monaco,Gillian Baird,Anthony Cox,Helen Cockerill,Fleming Nuffield,Ann Le Couteur,Tom Berney,Hayley Cooper,Thomas Kelly,Jonathan Green,Jane Whittaker,Anne Gilchrist,Patrick Bolton,Anne Schönewald,Michael G. Daker,Caroline Mackie Ogilvie,Zoe Docherty,Zandra Deans,Bryan Bolton,Ros Packer,Fritz Poustka,Dorothea Rühl,Gabriele Schmötzer,Sven Bölte,Sabine M. Klauck,Anja Spieler,Annemarie Poustka,Herman van Engeland,Chantal Kemner,Maretha de Jonge,Ineke Den Hartog,Catherine Lord,Edwin H. Cook,Bennett L. Leventhal,Fred Volkmar,David Pauls,Ami Klin,Susan L. Smalley,Eric Fombonne,Bernadette Rogé,Maïté Tauber,Evelyne Arti-Vartayan,Jeanne Fremolle-Kruck,Lennart Pederson,Demetrious Haracopos,Karen Brøndum-Nielsen,Rodney M. J. Cotterill +64 more
TL;DR: A two-stage genome search for susceptibility loci in autism was performed on 87 affected sib pairs plus 12 non-sib affected relative-pairs, from a total of 99 families identified by an international consortium, and a region on chromosome 7q was the most significant.
Journal ArticleDOI
A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q and 16p
Le, Couteur, A,Thomas Kelly,T Berney,Helen McConachie,Jeremy R. Parr,Sarah Palferman,Nicola Matthews,Martha Turner,Janette Moore,Amaia Hervas,Anne Aubin,Simon Wallace,Janine Michelotti,Catherine Wainhouse,Alina Paul,Emily J. Thompson,Ramyani Gupta,Claire Garner,Marianne Murin,Christine M. Freitag,Nuala Ryder,E Cottington,Andrew Pickles,Michael Rutter,Anthony J. Bailey,Gabrielle Barnby,Janine A. Lamb,Angela J. Marlow,Pat Scudder,Anthony P. Monaco,Gillian Baird,Antony Cox,Zoe Docherty,Pamela Warburton,Elizabeth P. Green,Stephen Abbs,De, Vries, Pj,Patrick Bolton,Jonathan Green,Anne Gilchrist,Jane Whittacker,Bryan Bolton,Ros Packer,Elena Maestrini,Francesca Blasi,Van, Engeland, H,De, Jonge, Mv,Chantal Kemner,Sabine M. Klauck,Kim S. Beyer,Sabine Epp,Annemarie Poustka,Axel Benner,JW Goethe,Fritz Poustka,Dorothea Rühl,Gabriele Schmötzer,S Boolte,Sabine Feineis-Matthews,Eric Fombonne,B Rogee,Jeanne Fremolle-Kruck,Catherine Pienkowski,Maïté Tauber,Lennart Pedersen,KB Nielsen,Gunna Eriksen,Demetrious Haracopos,Rmj Cotterill,John Tsiantis,Katerina Papanikolaou,Catherine Lord,Christina Corsello,Stephen J. Guter,Bennett L. Leventhal,Edwin H. Cook,Susan L. Smalley,Julia Bailey,James J. McGough,Jennifer G. Levitt,David Pauls,Fred R. Volkmar,Daniel E. Weeks,Int, Mol, Genetic, Study, Autism, Cons +83 more
TL;DR: The addition of new families and markers provides further support for previous reports of linkages on chromosomes 7q and 16p and two new regions of linkage have also been identified on chromosomes 2q and 17q.
Journal ArticleDOI
Gaze behavior of children with pervasive developmental disorder toward human faces: a fixation time study.
TL;DR: Results plead against the notion that the abnormal gaze behavior in everyday life is due to the presence of facial stimuli per se, and show that autistic children have the same fixation behavior as normal children for upright faces, with or without an emotional expression.
Journal ArticleDOI
Spatial Frequency Training Modulates Neural Face Processing : Learning Transfers from Low- to High-Level Visual Features
TL;DR: It is shown that training-induced increased sensitivity to a low-level feature, namely low spatial frequency (LSF), alters neural processing of this feature in high-level visual stimuli and suggests that SF discrimination learning transfers from simple stimuli to complex objects.