A Genomewide Screen for Autism: Strong Evidence for Linkage to Chromosomes 2q, 7q, and 16p
*·2001·The American Journal of Human Genetics
DOI 10.1086/323264
Cited by (453)
Items 301–400 of 453
- L’autisme : surestimation des origines génétiquesBrigitte Chamak · 2010 · médecine/sciences
- Common genetic variation in the GAD1 gene and the entire family of DLX homeobox genes and autism spectrum disordersShun‐Chiao Chang, David L. Pauls, Christoph Lange, Roksana Sasanfar, Susan L. Santangelo · 2010 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
- Brief Report: A Case of Autism Associated with del(2)(q32.1q32.2) or (q32.2q32.3)Louise Gallagher, Kristin Becker, Geraldine Kearney, Adam Dunlop, Ray L. Stallings, Andrew Green, Michael Fitzgerald, Michael Gill · 2003 · Journal of Autism and Developmental Disorders
- Autismo: genéticaAbha R. Gupta, Matthew W. State · 2006 · Brazilian Journal of Psychiatry
- Imprinted Anomalies in Fetal and Childhood Growth Disorders: The Model of Russell-Silver and Beckwith-Wiedemann SyndromesIrène Netchine, Sylvie Rossignol, Salah Azzi, Frédéric Brioude, Yves Le Bouc · 2012 · Endocrine development
- Triggers for Autism: Genetic and Environmental FactorsHideo Matsuzaki, Keiko Iwata, Takayuki Manabe, Norio Mori · 2012 · Journal of Central Nervous System Disease
- Polymorphisms of coding trinucleotide repeats of homeogenes in neurodevelopmental psychiatric disordersFabrice Laroche, Nicolás Ramoz, Sophie Leroy, Célia Fortin, Bérangère Rousselot‐Pailley, Anne Philippe, Laurence Colleaux, Jean‐Louis Bresson, Agnès Mogenet, Bernard Golse et al. · 2008 · Psychiatric Genetics
- Genética do autismoGianna Maria Griz Carvalheira, Naja Vergani, Décio Brunoni · 2004 · Brazilian Journal of Psychiatry
- Molecular genetics of speech and language disordersDianne F. Newbury, Anthony P. Monaco · 2002 · Current Opinion in Pediatrics
- Sib‐pairs in multifactorial disorders: the sib‐similarity problemJH Edwards · 2002 · Clinical Genetics
- Current perspectives on the genetic analysis of autismHilary H Coon · 2006 · American Journal of Medical Genetics Part C Seminars in Medical Genetics
- The refinement of the critical region for the 2q31.2q32.3 deletion syndrome indicates candidate genes for mental retardation and speech impairmentAlessandro Cocchella, Michela Malacarne, Francesca Forzano, Carmela Marciano, Mauro Pierluigi, L Perroni, Francesca Faravelli, Emilio Di Maria · 2010 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
- A Novel Stratification Method in Linkage Studies to Address Inter- and Intra-Family Heterogeneity in AutismZohreh Talebizadeh, Dan E. Arking, Valerie Wailin Hu · 2013 · PLoS ONE
- Independent replication and initial fine mapping of 3p21–24 in Asperger syndromeKarola Rehnström, T Ylisaukko-oja, T Nieminen-von Wendt, S Sarenius, T Källman, E Kempas, L von Wendt, Leena Peltonen, Irma E. Järvelä · 2006 · Journal of Medical Genetics
- Conducting Genetic Epidemiology Studies of Autism Spectrum Disorders: Issues in MatchingP. Szatmari, L. Zwaigenbaum, S. Bryson · 2004 · Journal of Autism and Developmental Disorders
- The genetic basis of hair whorl, handedness, and other phenotypesJeff S. Hatfield · 2005 · Medical Hypotheses
- Genetik autistischer StörungenChristine Margarete Freitag · 2008 · Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie
- Using Sibling Designs to Understand Neurodevelopmental Disorders: From Genes and Environments to Prevention ProgrammingMark Wade, Heather Prime, Sheri Madigan · 2015 · BioMed Research International
- No association between the APOE gene and autismKimberly L. Raiford, Yujan Shao, Irving C. Allen, Eden R. Martin, Marisa M. Menold, H.H. Wright, Ruth K. Abramson, Gordon Worley, G. R. DeLong, Jeffery M. Vance et al. · 2003 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
- Trisomy 15q25.2‐qter in an autistic child: Genotype–phenotype correlationsMaria Teresa Bonati, Palma Finelli, Daniela L. Giardino, Giulietta Gottardi, Wendy Roberts, Lidia Larizza · 2005 · American Journal of Medical Genetics Part A
- The yield of subtelomeric FISH analysis in the evaluation of autistic spectrum disordersAgatino Battaglia, María Clara Bonaglia · 2006 · American Journal of Medical Genetics Part C Seminars in Medical Genetics
- The NeuroDevNet Autism Spectrum Disorders Demonstration ProjectLonnie Zwaigenbaum, Stephen W. Scherer, Péter Szatmári, Eric J Fombonne, Susan E. Bryson, Krista L. Hyde, Evdokia Anognostou, Jessica A. Brian, Alan Charles Evans, Geoff B. C. Hall et al. · 2011 · Seminars in Pediatric Neurology
- Genetic Basis of AutismElena Bonora, Anthony P. Monaco, Janine A. Lamb, Anthony J. Bailey, Gabrielle Barnby · 2006 · CRC Press eBooks
- New Interview and Observation Measures of the Broader Autism Phenotype: Description of Strategy and Reliability Findings for the Interview MeasuresJeremy R Parr, Maretha V. de Jonge, Simon Wallace, Andrew R. Pickles, Michael L. Rutter, Ann S. Le Couteur, Hermán van Engeland, Kerstin Wittemeyer, HELEN R. McCONACHIE, Bernadette Rogé et al. · 2015 · Autism Research
- Autism Spectrum Disorders: The Role of Genetics in Diagnosis and TreatmentStephen I. Deutsch · 2011 · InTech eBooks
- Identifying Loci for the Overlap Between Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder Using a Genome-wide QTL Linkage ApproachJudith S. Nijmeijer, Alejandro Arias Vásquez, Nanda N. J. Rommelse, Marieke E. Altink, Richard Anney, Philip J. Asherson, Tobias Banaschewski, Cathelijne J.M. Buschgens, Ellen A. Fliers, Michael Gill et al. · 2010 · Journal of the American Academy of Child & Adolescent Psychiatry
- Response to paper by Molloy et al.: Linkage on 21q and 7q in autism subset with regressionJeremy R Parr, Janine A. Lamb, Anthony J. Bailey, Anthony P. Monaco · 2006 · Molecular Psychiatry
- Autism Spectrum DisordersGéraldine Dawson, Karen Toth · 2015 · Wiley eBooks
- Fine mapping and association studies in a candidate region for autism on chromosome 2q31–q32Judith Conroy, Lynne E. Cochrane, Richard Anney, James S. Sutcliffe, Paula Carthy, Adam Dunlop, Marice Mullarkey, Bronagh O’Hici, Andrew Green, Sean Ennis et al. · 2008 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
- Examination of tetrahydrobiopterin pathway genes in autismNathalie C. Schnetz‐Boutaud, Bernard M. Anderson, K. D. Brown, H. H. Wright, Ruth K. Abramson, Michael L. Cuccaro, John R. Gilbert, Margaret Ann Pericak‐Vance, Jonathan L. Haines · 2009 · Genes Brain & Behavior
- A population-based association study of glutamate decarboxylase 1 as a candidate gene for autismHenriette N. Buttenschøn, Marlene Briciet Lauritsen, Agata El Daoud, Mads V. Hollegaard, Meta Jørgensen, Kristine Tvedegaard, DAVID MICHAEL HOUGAARD, Anders Dupont Børglum, Poul Thorsen, Ole N Mors · 2009 · Journal of Neural Transmission
- Association Between Peroxisomal Biogenesis Factor 7 and Autism Spectrum Disorders in a Korean PopulationMyungJa Ro, JungWon Park, Min Nam, Hee Jung Bang, Jae-Won Yang, Kyung-Sik Choi, Su Kang Kim, Joo‐Ho Chung, KyuBum Kwack · 2012 · Journal of Child Neurology
- Les facteurs génétiques dans les troubles spécifiques du langage oralDominique Bonneau, Christophe Verny, Joël Uzé · 2004 · Archives de Pédiatrie
- A critical review of the impact of candidate copy number variants on autism spectrum disorderSeyedeh Sedigheh Abedini, Shiva Akhavantabasi, Yuheng Liang, Julian Ik‐Tsen Heng, Roohallah Alizadehsani, Abdollah Dehzangi, Denis C. Bauer, Hamid Alinejad‐Rokny · 2024 · Mutation Research/Reviews in Mutation Research
- RELN gene polymorphisms and susceptibility to autism in Chinese Han populationPeichao Tian · 2012 · Neurology India
- Brief Report: Acrocallosal Syndrome and AutismCarlos Eduardo Steiner, Marilisa M. Guerreiro, Antonia Paula Marques‐de‐Faria · 2004 · Journal of Autism and Developmental Disorders
- SINESTESIA E O TRANSTORNO DO ESPECTRO DO AUTISMO (TEA)Maria Cecília Tomasi, Jaciara Muller Brandes, Juliana Lopes, Henrique Sartori, Luiz Arthur Rangel Cyrino · 2018 · Revista de Atenção à Saúde
- High-resolution chromosomal microarray analysis for copy-number variations in high-functioning autism reveals large aberration typical for intellectual disabilityAnna Maria Werling, Edna Grünblatt, Beatrice Oneda, Elise Bobrowski, Ronnie Gundelfinger, Regina Taurines, Marcel Romanos, Anita M. Rauch, Susanne Walitza · 2019 · Journal of Neural Transmission
- Copy Number Variants: A New Molecular Frontier in Clinical PsychiatryDaniel Moreno‐De‐Luca, Joseph F. Cubells · 2011 · Current Psychiatry Reports
- Gene Organization and Polymorphisms of Monoamine Transporters: Relationship to Psychiatric and Other Complex DiseasesMaureen K. Hahn, Randy Blakely · 2003 · Humana Press eBooks
- Mapping the structure of biomarkers in autism spectrum disorder: a review of the most influential studiesFang Jin, Zhidan Wang · 2024 · Frontiers in Neuroscience
- Transtorno do espectro autista: descobertas, perspectivas e Autism PlusVinícius Magalhães Borges, Lília Maria de Azevedo Moreira · 2018 · Revista de Ciências Médicas e Biológicas
- Antioxidant Behavioural Phenotype in the Immp2l Gene Knock-Out MouseAdam J. Lawther, Jerzy Zieba, Zhiming Fang, Teri M. Furlong, Illya Conn, Hemna Govindaraju, Laura L. Y. Choong, Nigel A. Turner, Khawar Sohail Siddiqui, Wallace John Bridge et al. · 2023 · Genes
- Transmission disequilibrium study of an oligodendrocyte and myelin glycoprotein gene allele in 431 families with an autistic probandIsabelle Poizot Martin, Julie Gauthier, Marcello D’Amelio, Sylviane Védrine, Patrick Vourc’h, Guy Armand Rouleau, Antonio Maria Persico, Christian Robert Andres · 2007 · Neuroscience Research
- Genetic landmarks through philately – autism spectrum disorders: a genetic updateA. Chudley · 2004 · Clinical Genetics
- An investigation into sub‐telomeric deletions of chromosome 22 and pervasive developmental disordersKumudini Nair‐Miranda, Ashleigh R. Murch, Beverly Petterson, W. Leonard Hill, Amelia Nikolova‐Hill, Linda D. Bradley, Sandy Jackson, Joachim Franz Hallmayer · 2003 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
- Can Asperger Syndrome Be Diagnosed at 26 Months Old? A Genetic High-Risk Single-Case StudySimon Baron‐Cohen, Fiona Gullon-Scott, Sally J Wheelwright, Mark Henry Johnson, Dheraj Bisarya, Atman Mukesh Desai, J. S. Ahluwalia · 2006 · Journal of Child Neurology
- Sequencing and Analyzing the t(1;7) Reciprocal Translocation Breakpoints Associated with a Case of Childhood-onset Schizophrenia/Autistic DisorderJacquelyn R. Idol, Anjene Musick Addington, Robert T. L. Long, Judith L. Rapoport, Eric D. Green · 2007 · Journal of Autism and Developmental Disorders
- Common Genetic Variants in Autism Spectrum DisordersRichard Anney · 2012 · Elsevier eBooks
- Lack of association between markers in the ITGA3, ITGAV, ITGA6 and ITGB3 and autism in an Irish sampleLynne E. Cochrane, Katherine E. Tansey, Michael Gill, Louise Gallagher, Richard Anney · 2010 · Autism Research
- LRRTM4 Terminal Exon Duplicated in Family with Tourette Syndrome, Autism and ADHDRaymond A. Clarke, Valsamma Eapen · 2021 · Genes
- Contribución genética, ambiental y epigenética en la susceptibilidad a los trastornos del espectro autistaAdriana Díaz‐Anzaldúa, Alejandro Díaz Martínez · 2013 · Revista de Neurología
- Association and gene–gene interactions study of reelin signaling pathway related genes with autism in the H an C hinese populationYidong Shen, Guanglei Xun, Hui Guo, Yiqun He, Jianjun Ou, Huixi Dong, Kun Xia, Jingping Zhao · 2015 · Autism Research
- Genetics of Psychiatric DisordersJohn I. Nürnberger, Wade H. Berrettini, Alexander B. Niculescu · 2008 · Humana Press eBooks
- Turning strains into strengths for understanding psychiatric disordersShannon J. Moore, Geoffrey G. Murphy, Victor A. Cazares · 2020 · Molecular Psychiatry
- Autism Spectrum DisordersSabine M. Klauck · 2008 · Nucleic acids and molecular biology
- Shared Chromosomal Susceptibility Regions Between Autism and Other Mental DisordersYvon C. Chagnon · 2005 · International review of neurobiology
- Neuropsychological Perspectives on Developmental PsychopathologySally J. Ozonoff, Bruce F. Pennington, Marjorie Solomon · 2015 · Wiley eBooks
- DSM ‐5 based algorithms for the Autism Diagnostic Interview‐Revised for children ages 4–17 yearsLinnea A. Lampinen, Shuting Zheng, Lindsay Olson, Vanessa Hus Bal, Audrey E. Thurm, Amy Esler, Stephen M. Kanne, So Hyun Kim, Catherine Lord, China I. Parenteau et al. · 2025 · Journal of Child Psychology and Psychiatry
- Deletion 2q37 syndrome: Cognitive‐behavioral trajectories and autistic features related to breakpoint and deletion sizeGene S. Fisch, Rena Ellen Falk, John C. Carey, Jaime Imitola, Maria C. Sederberg, Karen S. Caravalho, Sarah T. South · 2016 · American Journal of Medical Genetics Part A
- On the origins and diagnosis of asperger syndrome : a clinical, neuroimaging and genetic studyTaina Nieminen‐von Wendt · 2004
- Comments on the genetic control of forebrain developmentJohn L.R. Rubenstein · 2006 · Clinical Neuroscience Research
- A Girl with Pervasive Developmental Disorder and Complex Chromosome Rearrangement Involving 8p and 10pLonnie Zwaigenbaum, Lyn Kathryn Sonnenberg, Timothy W. Heshka, S. Eastwood, J. Xu · 2005 · Journal of Autism and Developmental Disorders
- Analysis of transmission of novel polymorphisms in the somatostatin receptor 5 (SSTR5) gene in patients with autismMarlene Briciet Lauritsen, Mette Nyegaard, Catalina Betancur, Catherine Colineaux, Trine L. Josiassen, Torben Arvid Kruse, Marion Leboyer, H. Ewald · 2003 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
- Clinical and genetic evaluation of a family showing both autism and epilepsyRomina Combi, Serena Redaelli, Massimiliano Beghi, Massimo Clerici, C Cornaggia, Leda Dalprà · 2010 · Brain Research Bulletin
- Unravelling the genetics of autism spectrum disordersInês Sousa, Richard Holt, Alistair T. Pagnamenta, Anthony P. Monaco · 2011 · Cambridge University Press eBooks
- Genome wide analysis in a family with sensorineural hearing loss, autism and mental retardationMohamed Ali Mosrati, Isabelle Schrauwen, Hassen Kamoun, Ilhem Charfeddine, Erik Fransén, Abdelmonem Ghorbel, Guy Van Camp, Saber Masmoudi · 2012 · Gene
- Clinical Presentation and Microarray Analysis of Peruvian Children with Atypical Development and/or Aberrant BehaviorMerlin G. Butler, Kelly Usrey, Jennifer Roberts, Stephen R. Schroeder, Ann M. Manzardo · 2014 · Genetics Research International
- Association between the g.296596G > A genetic variant of RELN gene and susceptibility to autism in a Chinese Han populationXiaoyan Fu, Zhu Mei, Lixin Sun · 2013 · Genetics and Molecular Biology
- Early assessment and diagnosis of childrenAnn S. Le Couteur · 2011 · Cambridge University Press eBooks
- Autism Spectrum DisordersChris Plauché Johnson, Scott M. Myers · 2008 · Elsevier eBooks
- Syndromes and epistemology II: Is autism a polygenic disorder?Gene S. Fisch · 2008 · American Journal of Medical Genetics Part A
- Programa de educación sanitaria para personas con trastornos del espectro autistaCarmen Nieto, R. Ventoso Roncero, A. Covaleda Rodrigo, D. Andériz Cebrián, E. de Oro Villora · 2008 · Anales de Pediatría
- Systematic genotype–phenotype analysis of autism susceptibility loci implicates additional symptoms to co-occur with autismJacobine E. Buizer‐Voskamp, Lude Franke, Wouter Staal, Emma van Daalen, Chantal Kemner, Roel A. Ophoff, Jacob A. S. Vorstman, Hermán van Engeland, Cisca Wijmenga · 2009 · European Journal of Human Genetics
- Determination of genetic changes in etiology of autism spectrum disorder in twins by whole-exome sequencingCeyda Hayretdağ, Pınar Algedik, Cumhur Gökhan Ekmekçi, Ozlem Bozdagi-Gunal, Umut Ağyüz, Halime Yıldırım, Ender Mehmet Coşkunpınar · 2020 · Gene Reports
- The Genetics of Autism Spectrum DisordersJohn J.M., Hakon Hakonarso · 2011 · InTech eBooks
- Genetic advances in autism hinge on the method of measuring symptomsRichard D. Todd · 2005 · Current Psychiatry Reports
- Protein kinase C-beta 1 gene variants are not associated with autism in the Irish populationMao Sheng Yang, Lynne E. Cochrane, Judith Conroy, Ziarih Hawi, Michael Fitzgerald, Louise Gallagher, Michael Gill · 2006 · Psychiatric Genetics
- Analysis of RBFOX1 gene expression in lymphoblastoid cell lines of Italian discordant autism spectrum disorders sib-pairsPaola Prandini, Chiara Zusi, Giovanni Malerba, ITAN, Pier Franco Pignatti, Elisabetta Trabetti · 2014 · Molecular and Cellular Probes
- Genes for reading and spellingTimothy Charles Bates · 2006 · London Review of Education
- Genetics of Psychiatric DisordersJohn I. Nürnberger, Wade Berrettini, Alexander B. Niculescu · 2016 · Springer eBooks
- Genetische Analysen zur Identifizierung molekularer Mechanismen bei Autismus-Spektrum-StörungenAndreas G. Chiocchetti, Sabine M. Klauck · 2011 · Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie
- Genetic pathways to autism spectrum disordersSunil Mehta, Erika L. Nurmi · 2013 · Neuropsychiatry
- Advances and Challenges in the Genetics of AutismDaniel B. Campbell · 2010 · FOCUS The Journal of Lifelong Learning in Psychiatry
- Autistic regression in a child with Silver–Russell Syndrome and maternal UPD 7Orna Vardi, Michael Davidovitch, Chana Vinkler, Marina Michelson, Tally Lerman‐Sagie, Dorit Lev · 2011 · European Journal of Paediatric Neurology
- Early Diagnostic AssessmentSarah Kuriakose, Rebecca A. Shalev · 2016 · Evidence-based practices in behavioral health
- Autism and autism spectrum disordersDaniel H. Geschwind, Maricela Alarcón · 2012 · Cambridge University Press eBooks
- The Human Secretin Gene in Children With Autistic Spectrum Disorder: Screening for Polymorphisms and MutationsSamuel S. Ng, Bkc Chow, Virginia Chun Nei Wong · 2005 · Journal of Child Neurology
- Autistic DisorderGeorge M. Realmuto, Muhammad Waqar Azeem · 2008 · Humana Press eBooks
- Gene Organization and Polymorphisms of Monoamine TransportersMaureen K. Hahn, Randy Blakely · 2002 · Humana Press eBooks
- Correction: Defining the Contribution of CNTNAP2 to Autism SusceptibilitySrirangan Sampath, Shambu Bhat, Simone Gupta, Ashley O’Connor, Andrew B. West, Dan E. Arking, Aravinda Chakravarti · 2013 · PLoS ONE
- Autistic Spectrum DisordersDeborah G. Hirtz, Ann Wagner, Pauline A. Filipek, Elliott H. Sherr · 2017 · Elsevier eBooks
- If genetic variation could talk: What genomic data may teach us about the importance of gene expression regulation in the genetics of autismErika Yeh, Lauren A. Weiss · 2016 · Molecular and Cellular Probes
- Autism: A Different VisionGolder N. Wilson, Vijay S. Tonk · 2018 · Open Journal of Psychiatry
- Exploring key genes and pathways associated with sex differences in autism spectrum disorder: integrated bioinformatic analysisHimani Nautiyal, Akanksha Jaiswar, Prabhash Kumar Jha, Shubham Dwivedi · 2024 · Mammalian Genome
- Identification of Chromosomal Regions Linked to Autism-Spectrum Disorders: A Meta-Analysis of Genome-Wide Linkage ScansIoanna Mpoulimari, Elias Zintzaras · 2022 · Genetic Testing and Molecular Biomarkers
- Effects of secretin on extracellular GABA and other amino acid concentrations in the rat hippocampusHans‐Willi Clement, Alexander Pschibul, Eberhard Schulz · 2005 · International review of neurobiology
- Autism Spectrum DisordersSunil Mehta, Daniel H. Geschwind · 2013 · Elsevier eBooks
- The Genetics of AutismDeborah K. Sokol, Debomoy K. Lahiri · 2011 · Springer eBooks
- The hyperserotonemia of autism spectrum disordersErik J. Mulder · 2006 · University of Groningen research database (University of Groningen / Centre for Information Technology)