R
Rhinda Goedken
Researcher at University of Iowa
Publications - 15
Citations - 2008
Rhinda Goedken is an academic researcher from University of Iowa. The author has contributed to research in topics: Autism & Heritability of autism. The author has an hindex of 11, co-authored 15 publications receiving 1934 citations. Previous affiliations of Rhinda Goedken include Roy J. and Lucille A. Carver College of Medicine.
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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
Examination of AVPR1a as an autism susceptibility gene
Thomas H. Wassink,Joseph Piven,Veronica J. Vieland,Jennifer Pietila,Rhinda Goedken,Susan E. Folstein,Val C. Sheffield +6 more
TL;DR: Though the AVPR1a gene was tested by screening its exons in 125 independent autistic probands and genotyping two promoter polymorphisms in 65 autism affected sibling pair (ASP) families, there was no nonconservative coding sequence changes and evidence of linkage and of linkage disequilibrium was identified.
Journal ArticleDOI
Genomewide survey of panic disorder.
Raymond R. Crowe,Rhinda Goedken,Steve Samuelson,Ricky Wilson,Jeffrey J. Nelson,Russell Noyes +5 more
TL;DR: The maximum evidence of linkage from two genome scans of panic disorder lies within a small region of chromosome 7p, which lies within the D7S2846 locus, located at 57.8 cM on chromosome 7 according to the Marshfield Clinic map.
Journal ArticleDOI
Evaluation of FOXP2 as an autism susceptibility gene
Thomas H. Wassink,Joseph Piven,Veronica J. Vieland,Jennifer Pietila,Rhinda Goedken,Susan E. Folstein,Val C. Sheffield +6 more
TL;DR: It is concluded that FOXP2 is unlikely to contribute significantly to autism susceptibility and should not be considered a risk factor for autism.
Journal ArticleDOI
Cancer risk in children and adolescents with birth defects: a population-based cohort study
Lorenzo D. Botto,Timothy J. Flood,Julian Little,Mark Fluchel,Sergey Krikov,Marcia L. Feldkamp,Yuan Wu,Rhinda Goedken,Soman Puzhankara,Paul A. Romitti +9 more
TL;DR: Children with some structural, non-chromosomal birth defects, but not others, have a moderately increased risk for childhood cancer, but the excess risk varied markedly by type of birth defect.