A Genomewide Screen for Autism: Strong Evidence for Linkage to Chromosomes 2q, 7q, and 16p

*·2001·The American Journal of Human Genetics

Cited by (453)

Items 101–200 of 453

  1. Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11
    Ogdie, Matthew N., Fisher, Simon E., Yang, May, Ishii, Janeen, Francks, Clyde, Loo, Sandra K., Cantor, Rita M., McCracken, James T., McGough, James J., Smalley, Susan L. et al. · 2004 · The American Journal of Human Genetics
  2. Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects
    Lamb, J A, Barnby, G, Bonora, E, Sykes, N, Bacchelli, E, Blasi, F, Maestrini, E, Broxholme, J, Tzenova, J, Weeks, D et al. · 2005 · Journal of Medical Genetics
  3. Evidence for multiple loci from a genome scan of autism kindreds
    Schellenberg, G D, Dawson, G, Sung, Y J, Estes, A, Munson, J, Rosenthal, E, Rothstein, J, Flodman, P, Smith, M, Coon, H et al. · 2006 · Molecular Psychiatry
  4. Networking in Autism: Leveraging Genetic, Biomarker and Model System Findings in the Search for New Treatments
    Veenstra-VanderWeele, Jeremy, Blakely, Randy D · 2012 · Neuropsychopharmacology
  5. A Genomewide Scan for Intelligence Identifies Quantitative Trait Loci on 2q and 6p
    Daniëlle Posthuma, Michelle Luciano A, Eco J. C. de Geus, Margaret J. Wright, P. Eline Slagboom, Grant W. Montgomery, Dorret Irene Boomsma, Nicholas G. Martin · 2005 · The American Journal of Human Genetics
  6. The Functional Impact of SLC6 Transporter Genetic Variation
    Maureen K. Hahn, Randy Blakely · 2006 · The Annual Review of Pharmacology and Toxicology
  7. Regulation of neuronal migration, an emerging topic in autism spectrum disorders
    Orly Reiner, Eyal Karzbrun, Aditya Kshirsagar, Kozo Kaibuchi · 2015 · Journal of Neurochemistry
  8. Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs
    María Guadalupe Carmona Alarcón, Amanda L. Yonan, T. Conrad Gilliam, Rita M. Cantor, Daniel H. Geschwind · 2005 · Molecular Psychiatry
  9. Serotonin as a link between the gut-brain-microbiome axis in autism spectrum disorders
    Israelyan, Narek, Margolis, Kara Gross · 2018 · Pharmacological Research
  10. How to diagnose autism
    C. J Dover, Ann S. Le Couteur · 2007 · Archives of Disease in Childhood
  11. Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene
    Bacchelli, E, Blasi, F, Biondolillo, M, Lamb, J A, Bonora, E, Barnby, G, Parr, J, Beyer, K S, Klauck, S M, Poustka, A et al. · 2003 · Molecular Psychiatry
  12. A review of neuropsychological and neuroimaging research in autistic spectrum disorders: Attention, inhibition and cognitive flexibility
    Jane Sanders, Katherine A. Johnson, Hugh Garavan, Michael Gill, Louise Gallagher · 2007 · Research in Autism
  13. Social timing, clock genes and autism: a new hypothesis
    D. Wimpory, Bradley Nicholas, S. Nash · 2002 · Journal of Intellectual Disability Research
  14. A review of gene linkage, association and expression studies in autism and an assessment of convergent evidence
    Mao Sheng Yang, Michael Gill · 2006 · International Journal of Developmental Neuroscience
  15. Autism: An Emerging Public Health Problem
    Craig J. Newschaffer, Laura Kresch Curran · 2003 · Public Health Reports
  16. Association of Specific Language Impairment (SLI) to the Region of 7q31
    Erin K. O’Brien, Xuyang Zhang, Carla J. Nishimura, J. Bruce Tomblin, Jeffrey Clark Murray · 2003 · The American Journal of Human Genetics
  17. Lack of evidence for an association between WNT2 and RELN polymorphisms and autism
    Jun Z. Li, Loan Nguyen, Christopher Gleason, Linda J. Lotspeich, Donna Spiker, NEIL J. RISCH, R Myers · 2003 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
  18. Mercury Exposure in Children With Autistic Spectrum Disorder: Case-Control Study
    Patrick Ip, Virginia Chun Nei Wong, M. Ho, Joseph Jonathan Lee, Wilfred Hing Sang Wong · 2004 · Journal of Child Neurology
  19. Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability
    Alistair T. Pagnamenta, Hameed Khan, Susan Walker, Dianne Gerrelli, Kirsty Wing, María Clara Bonaglia, Roberto Giorda, Tom P. Berney, Elisa Mani, Massimo Molteni et al. · 2010 · Journal of Medical Genetics
  20. Genetic testing in autism: how much is enough?
    Gail E. Herman, Nathan Henninger, Karen L. Ratliff-Schaub, Matthew Pastore, Sara M. Fitzgerald‐Butt, Kim L. McBride · 2007 · Genetics in Medicine
  21. Autism spectrum disorders: The quest for genetic syndromes
    D. Zafeiriou, A. Ververi, V. Dafoulis, E. Kalyva, E. Vargiami · 2013 · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
  22. Current Developments in the Genetics of Autism: From Phenome to Genome
    Molly C. Losh, Patrick F. Sullivan, Dimitri G. Trembath, Joseph Piven · 2008 · Journal of Neuropathology & Experimental Neurology
  23. Serotonin transporter gene and autism: a haplotype analysis in an Irish autistic population
    Jennifer Conroy, Eleanor Meally, Geraldine Kearney, Michael Fitzgerald, Michael Gill, Louise Gallagher · 2004 · Molecular Psychiatry
  24. Absence of association between a polymorphic GGC repeat in the 5′ untranslated region of the reelin gene and autism
    M. Krebs, C. Betancur, S. Leroy, M. Bourdel, C. Gillberg, M. Leboyer · 2002 · Molecular Psychiatry
  25. The proneural determinant MASH1 regulates forebrainDlx1/2expression through the I12b intergenic enhancer
    Luc Poitras, Noël Ghanem, Gary Hatch, Marc Ekker · 2007 · Development
  26. Genetics of autism spectrum disorder
    Sabine M. Klauck · 2006 · European Journal of Human Genetics
  27. Bivariate linkage scan for reading disability and attention‐deficit/hyperactivity disorder localizes pleiotropic loci
    Javier Gayán, Erik G. Willcutt, Simon E. Fisher, Clyde Francks, Lon R. Cardon, Richard K. Olson, Bruce F. Pennington, S. D. Smith, Anthony P. Monaco, J. C. DeFries · 2005 · Journal of Child Psychology and Psychiatry
  28. Essential role of the nuclear isoform of RBFOX1, a candidate gene for autism spectrum disorders, in the brain development
    Hamada, Nanako, Ito, Hidenori, Nishijo, Takuma, Iwamoto, Ikuko, Morishita, Rika, Tabata, Hidenori, Momiyama, Toshihiko, Nagata, Koh-Ichi · 2016 · Scientific Reports
  29. Examination of Potential Overlap in Autism and Language Loci on Chromosomes 2, 7, and 13 in Two Independent Samples Ascertained for Specific Language Impairment
    Christopher W. Bartlett, Judy F. Flax, Mark W. Logue, Brett J. Smith, Veronica J. Vieland, Paula Anne Tallal, Linda M. Brzustowicz · 2004 · Human Heredity
  30. Genetic Influences and Autism
    Michael L. Rutter · 2005 · Wiley eBooks
  31. Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regression
    Cynthia A. Molloy, Mehdi A. Keddache, Lisa Joy Martin · 2005 · Molecular Psychiatry
  32. On the twin risk in autism.
    J. Hallmayer, E. Glasson, C. Bower, B. Petterson, L. Croen, J. Grether, N. Risch · 2002 · American Journal of Human Genetics
  33. Absence of coding mutations in the X‐linked genes neuroligin 3 and neuroligin 4 in individuals with autism from the IMGSAC collection
    Francesca Blasi, Elena Bacchelli, Giulia Pesaresi, Simona Carone, Anthony J. Bailey, Elena Maestrini · 2006 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
  34. Confirmation of Association Between Autism and the Mitochondrial Aspartate/Glutamate Carrier SLC25A12 Gene on Chromosome 2q31
    Ricardo Segurado, Judith Conroy, Eleanor Meally, Michael Fitzgerald, Michael Gill, Louise Gallagher · 2005 · American Journal of Psychiatry
  35. Genomic and genetic aspects of autism spectrum disorder
    Xiaoxi Liu, Toru Takumi · 2014 · Biochemical and Biophysical Research Communications
  36. Social Interaction Behaviors Discriminate Young Children With Autism and Williams Syndrome
    Alan J. Lincoln, Yvonne M. Searcy, WENDY JONES, Catherine Lord · 2007 · Journal of the American Academy of Child & Adolescent Psychiatry
  37. A girl with neurofibromatosis type 1, atypical autism and mosaic ring chromosome 17
    Markéta Havlovičová, Drahuše Novotná, Eduard Kočárek, Kamila Novotna, Šárka Bendová, Borivoj Petrak, Michal Hrdlička, Zdeněk Sedláček · 2006 · American Journal of Medical Genetics Part A
  38. The DLX1and DLX2 genes and susceptibility to autism spectrum disorders
    Xudong Liu, Natalia Novosedlik, Ami Wang, Melissa L. Hudson, Ira L. Cohen, Albert E. Chudley, Cynthia Forster‐Gibson, M. E. Suzanne Lewis, Jeanette J. A. Holden · 2008 · European Journal of Human Genetics
  39. RELN Mutations in Autism Spectrum Disorder
    Dawn B. Lammert, Brian W. Howell · 2016 · Frontiers in Cellular Neuroscience
  40. Trophoblast Inclusions Are Significantly Increased in the Placentas of Children in Families at Risk for Autism
    Cheryl K. Walker, Kaitlin W. Anderson, Kristin M. Milano, Saier Ye, Daniel Joseph Tancredi, Isaac N. Pessah, Irva Hertz‐Picciotto, Harvey J. Kliman · 2013 · Biological Psychiatry
  41. Constitutional Downregulation of SEMA5A Expression in Autism
    Malin Melin, Birgit Carlsson, Henrik Söderström Anckarsäter, Maria Råstam, Catalina Betancur, Anders Isaksson, Christopher Gillberg, Niklas Dahl · 2006 · Neuropsychobiology
  42. Genome-wide scan for loci of Asperger syndrome
    Tero Ylisaukko‐oja, Taina Nieminen‐von Wendt, Elli Kempas, Susan Sarenius, Teppo Varilo, L. von Wendt, Leena Peltonen, Irma E. Järvelä · 2004 · Molecular Psychiatry
  43. The search for autism disease genes
    Wassink, Thomas H, Brzustowicz, Linda M, Bartlett, Christopher W, Szatmari, Peter · 2004 · Mental Retardation and Developmental Disabilities Research Reviews
  44. MET and autism susceptibility: family and case-control studies
    I. Sousa, T. Clark, C. Toma, Kazuhiro Kobayashi, Maja Choma, R. Holt, Nuala H. Sykes, J. Lamb, A. Bailey, A. Battaglia et al. · 2008 · European Journal of Human Genetics
  45. Genome-wide Linkage Analyses of Quantitative and Categorical Autism Subphenotypes
    Xiao-Qing Liu, Andrew D. Paterson, Péter Szatmári · 2008 · Biological Psychiatry
  46. Reprint of: Serotonin as a link between the gut-brain-microbiome axis in autism spectrum disorders
    Narek Israelyan, Kara Gross Margolis · 2019 · Pharmacological Research
  47. Mutation analysis of the coding sequence of the MECP2 gene in infantile autism
    Kim S. Beyer, Francesca Blasi, Elena Bacchelli, Sabine M. Klauck, Elena Maestrini, Annemarie Poustka, International Molecular Genetic Study of Autism Consortium · 2002 · Human Genetics
  48. Genomic imprinting in the development and evolution of psychotic spectrum conditions
    Bernard J. Crespi · 2008 · Biological reviews/Biological reviews of the Cambridge Philosophical Society
  49. Asperger syndrome
    Marc Woodbury‐Smith, Fred R. Volkmar · 2008 · European Child & Adolescent Psychiatry
  50. Linkage and candidate gene studies of autism spectrum disorders in European populations
    Richard Holt, Gabrielle Barnby, Elena Maestrini, Elena Bacchelli, Denise Brocklebank, Inês Sousa, Erik J. Mulder, Katri Kantojärvi, Irma E. Järvelä, Sabine M. Klauck et al. · 2010 · European Journal of Human Genetics
  51. Examination of association of genes in the serotonin system to autism
    Bernard M. Anderson, Nathalie C. Schnetz‐Boutaud, J. Bartlett, A. M. Wotawa, H. H. Wright, Ruth K. Abramson, Michael L. Cuccaro, John R. Gilbert, Margaret Ann Pericak‐Vance, Jonathan L. Haines · 2009 · Neurogenetics
  52. Excess of Twins among Affected Sibling Pairs with Autism: Implications for the Etiology of Autism
    David A. Greenberg, Susan E. Hodge, Janice Sowinski, Doug Nicoll · 2001 · The American Journal of Human Genetics
  53. The Human Genome Project and Its Impact on Psychiatry
    William Maxwell Cowan, Kathy L. Kopnisky, Steven E. Hyman · 2002 · Annual Review of Neuroscience
  54. Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network
    Bernie Devlin, Pamela J. Bennett, Géraldine Dawson, Denise A. Figlewicz, Elena L. Grigorenko, William McMahon, Nancy J. Minshew, David L. Pauls, Moyra Smith, M. Anne Spence et al. · 2004 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
  55. A genome-wide search for alleles and haplotypes associated with autism and related pervasive developmental disorders on the Faroe Islands
    Lauritsen, M B, Als, T D, Dahl, H A, Flint, T J, Wang, A G, Vang, M, Kruse, T A, Ewald, H, Mors, O · 2006 · Molecular Psychiatry
  56. Mutation screening and association analysis of six candidate genes for autism on chromosome 7q
    Elena Bonora, Janine A. Lamb, Gabrielle Barnby, Nuala Sykes, Thomas Moberly, Kim S. Beyer, Sabine M. Klauck, F. Poustka, Elena Bacchelli, Francesca Blasi et al. · 2004 · European Journal of Human Genetics
  57. The Swedish Version of the Diagnostic Interview for Social and Communication Disorders (DISCO-10). Psychometric Properties
    Gudrun Nygren, Bibbi S. Hagberg, Eva Billstedt, Åsa Skoglund, Christopher Gillberg, Maria Johansson · 2009 · Journal of Autism and Developmental Disorders
  58. A new imprinted cluster on the human chromosome 7q21-q31, identified by human-mouse monochromosomal hybrids
    Chiga Okita, Makiko Meguro, Hidetoshi Hoshiya, Masayuki Haruta, Yuki Sakamoto, Mitsuo Oshimura · 2003 · Genomics
  59. Improved Diagnostic Validity of the ADOS Revised Algorithms: A Replication Study in an Independent Sample
    Oosterling, Iris, Roos, Sascha, de Bildt, Annelies, Rommelse, Nanda, de Jonge, Maretha, Visser, Janne, Lappenschaar, Martijn, Swinkels, Sophie, van der Gaag, Rutger Jan, Buitelaar, Jan · 2010 · Journal of Autism and Developmental Disorders
  60. Is synesthesia more common in patients with Asperger syndrome?
    Janina Neufeld, Mandy Roy, Antonia Zapf, Christopher Sinke, Hinderk Meiners Emrich, Vanessa Prox-Vagedes, Wolfgang Dillo, Markus Zedler · 2013 · Frontiers in Human Neuroscience
  61. Association of tryptophan 2,3 dioxygenase gene polymorphism with autism
    Rafiqun Nabi, Fatema Serajee, Diane C. Chugani, Hailang Zhong, A.H.M. Mahbubul Huq · 2003 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
  62. A high-density SNP genome-wide linkage scan in a large autism extended pedigree
    Allen-Brady, K, Miller, J, Matsunami, N, Stevens, J, Block, H, Farley, M, Krasny, L, Pingree, C, Lainhart, J, Leppert, M et al. · 2009 · Molecular Psychiatry
  63. Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism
    Anne Philippi, Elke Roschmann, Frédéric Torès, Pierre Lindenbaum, Abdel Benajou, L Germain-Leclerc, Charles Marcaillou, Karine Fontaine, Maud Vanpeene, Sudipta Singha Roy et al. · 2005 · Molecular Psychiatry
  64. NYAP: a phosphoprotein family that links PI3K to WAVE1 signalling in neurons
    Yokoyama, Kazumasa, Tezuka, Tohru, Kotani, Masaharu, Nakazawa, Takanobu, Hoshina, Naosuke, Shimoda, Yasushi, Kakuta, Shigeru, Sudo, Katsuko, Watanabe, Kazutada, Iwakura, Yoichiro et al. · 2011 · The EMBO Journal
  65. Genetics of Childhood Disorders: XLVI. Autism, Part 5: Genetics of Autism
    Jeremy M. Veenstra-VanderWeele, Edwin H. Cook · 2003 · Journal of the American Academy of Child & Adolescent Psychiatry
  66. Three autism candidate genes: a synthesis of human genetic analysis with other disciplines
    Christopher W. Bartlett, Neda Gharani, James H. Millonig, Linda M. Brzustowicz · 2004 · International Journal of Developmental Neuroscience
  67. Molecular genetic aspects of attention-deficit/hyperactivity disorder
    Philip Heiser, Susann Friedel, Astrid Dempfle, Kerstin Konrad, J SMIDT, Justyna Grabarkiewicz, Beate Herpertz‐Dahlmann, Helmut Remschmidt, Johannes Hebebrand · 2004 · Neuroscience & Biobehavioral Reviews
  68. Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort
    Guo, Hui, Peng, Yu, Hu, Zhengmao, Li, Ying, Xun, Guanglei, Ou, Jianjun, Sun, Liangdan, Xiong, Zhimin, Liu, Yanling, Wang, Tianyun et al. · 2017 · Scientific Reports
  69. Genetic aspects in attention-deficit/hyperactivity disorder
    Özgür Albayrak, Susann Friedel, BENNO GRAF SCHIMMELMANN, Anke Hinney, Johannes Hebebrand · 2008 · Journal of Neural Transmission
  70. Analysis of four DLX homeobox genes in autistic probands
    Steven P. Hamilton, Jonathan M. Woo, Elaine J. Carlson, Noël Ghanem, Marc Ekker, John L.R. Rubenstein · 2005 · BMC Genetics
  71. The association analysis of RELN and GRM8 genes with autistic spectrum disorder in chinese han population
    Hui Li, Yun Li, Jie Shao, Rong Li, Yufeng Qin, Chunhong Xie, Zhengyan Zhao · 2007 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
  72. Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection
    Nuala Sykes, Claudio Toma A, Natalie Wilson, Emanuela Valeria Volpi, Inês Sousa, Alistair T. Pagnamenta, Raffaella Tancredi, Agatino Battaglia, Elena Maestrini, Anthony J. Bailey et al. · 2009 · European Journal of Human Genetics
  73. Association between the neurofibromatosis‐1 (NF1) locus and autism in the Japanese population
    Tetsuya Marui, Ohiko Hashimoto, Eiji Nanba, Chieko Kato, Mamoru Tochigi, Tadashi Umekage, Michiko Ishijima, Kazuhisa Kohda, Nobumasa Kato, Tsukasa Sasaki · 2004 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
  74. Genome-wide association study identifies ITGB3 as a QTL for whole blood serotonin
    Lauren A. Weiss, Jeremy M. Veenstra-VanderWeele, Dina L. Newman, Soo‐Jeong Kim, Harvey E. Dytch, Mary Sara McPeek, Suzanne Cheng, Carole Ober, Edwin H. Cook, Mark Abney · 2004 · European Journal of Human Genetics
  75. Toward localizing genes underlying cerebral asymmetry and mental health
    Susan L. Smalley, Sandra K. Loo, MAY H. YANG, Rita M. Cantor · 2005 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
  76. Cognitive and verbal abilities of 24- to 36-month-old siblings of children with autism
    Yirmiya, Nurit, Gamliel, Ifat, Shaked, Michal, Sigman, Marian · 2007 · Journal of Autism and Developmental Disorders
  77. Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry
    Inês Sousa, Taane Gregory Clark, Richard Holt, Alistair T. Pagnamenta, Erik J. Mulder, Ruud B. Minderaa, Anthony J. Bailey, Agatino Battaglia, Sabine M. Klauck, Fritz Poustka et al. · 2010 · Molecular Autism
  78. Autism spectrum disorders: Molecular genetic advances
    Elena Bacchelli, Elena Maestrini · 2006 · American Journal of Medical Genetics Part C Seminars in Medical Genetics
  79. Identification of Rare Recurrent Copy Number Variants in High-Risk Autism Families and Their Prevalence in a Large ASD Population
    Nori Matsunami, Dexter Hadley, Charles H. Hensel, G. Bryce Christensen, Cecilia Kim, Edward C. Frackelton, Kelly Thomas, Renata Pellegrino da Silva, Jeff Stevens, Lisa Morrison Baird et al. · 2013 · PLoS ONE
  80. The Nonkinase Phorbol Ester Receptor α1-Chimerin Binds the NMDA Receptor NR2A Subunit and Regulates Dendritic Spine Density
    Thomas Van de Ven, Hendrika M. A. VanDongen, Antonius M.J. VanDongen · 2005 · Journal of Neuroscience
  81. Review of animal models for autism: implication of thyroid hormone
    Miyuki Sadamatsu, Hirohiko Kanai, Xiaobin Xu, Ying Liu, Nobumasa Kato · 2006 · Congenital Anomalies
  82. Familial associations of intense preoccupations, an empirical factor of the restricted, repetitive behaviors and interests domain of autism
    Christopher J. Smith, Colleen M. Lang, Lauren A. Kryzak, Abraham Reichenberg, Eric Hollander, Jeremy M. Silverman · 2009 · Journal of Child Psychology and Psychiatry
  83. Genes, language development, and language disorders
    Shelley D. Smith · 2007 · Mental Retardation and Developmental Disabilities Research Reviews
  84. Lack of Evidence for Association of the Serotonin Transporter Gene SLC6A4 with Autism
    Nicolás Ramoz, Jennifer G. Reichert, Thomas E. Corwin, Christopher J. Smith, Jeremy M. Silverman, Eric Hollander, Joseph D. Buxbaum · 2006 · Biological Psychiatry
  85. Presence of Large Deletions in Kindreds with Autism
    Chang‐En Yu, Géraldine Dawson, JEFFREY A. MUNSON, Ian D’Souza, Julie Osterling, Annette Mercer Estes, Anne‐Louise Leutenegger, Pamela L. Flodman, Moyra Smith, Wendy H. Raskind et al. · 2002 · The American Journal of Human Genetics
  86. Novel aspects of enteric serotonergic signaling in health and brain-gut disease
    Andrew Del Colle, Narek Israelyan, Kara Gross Margolis · 2019 · American Journal of Physiology-Gastrointestinal and Liver Physiology
  87. High density SNP association study of a major autism linkage region on chromosome 17
    Jennifer L. Stone, Barry Merriman, Rita M. Cantor, Daniel H. Geschwind, Stanley F. Nelson · 2007 · Human Molecular Genetics
  88. Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes
    Nicola H. Chapman, Alejandro Q. Nato, Raphael Bernier, Katy Ankenman, Harkirat K. Sohi, JEFFREY A. MUNSON, Ashok Patowary, Marilyn Archer, Elizabeth Blue, Sara Jane Webb et al. · 2015 · Human Genetics
  89. Bioinformatic analysis of autism positional candidate genes using biological databases and computational gene network prediction
    Amanda L. Yonan, Abraham A. Palmer, Kenneth C. Smith, Igor Feldman, H. K. Lee, J. Yonan, S G Fischer, Paul Pavlidis, T. Conrad Gilliam · 2003 · Genes Brain & Behavior
  90. Association analysis of the NrCAM gene in autism and in subsets of families with severe obsessive–compulsive or self-stimulatory behaviors
    Takeshi Sakurai, Nicolás Ramoz, Jennifer G. Reichert, Thomas E. Corwin, Lauren A. Kryzak, Christopher J. Smith, Jeremy M. Silverman, Eric Hollander, Joseph D. Buxbaum · 2006 · Psychiatric Genetics
  91. Genetic and Neurodevelopmental Influences in Autistic Disorder
    R. Nicolson, P. Szatmari · 2003 · Canadian journal of psychiatry. Revue canadienne de psychiatrie
  92. Serotonin transporter intron 2 polymorphism associated with rigid‐compulsive behaviors in Dutch individuals with pervasive developmental disorder
    Erik J. Mulder, George M. Anderson, Ido P. Kema, Astrid M. Brugman, Cees E.J. Ketelaars, Annelies A. de Bildt, Natasja D.J. van Lang, Johan A. den Boer, Ruud B. Minderaa · 2005 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
  93. Role of the cytoplasmic isoform of RBFOX1/A2BP1 in establishing the architecture of the developing cerebral cortex
    Hamada, Nanako, Ito, Hidenori, Iwamoto, Ikuko, Morishita, Rika, Tabata, Hidenori, Nagata, Koh-ichi · 2015 · Molecular Autism
  94. Etiologic yield of autistic spectrum disorders: A prospective study
    Agatino Battaglia, John C. Carey · 2006 · American Journal of Medical Genetics Part C Seminars in Medical Genetics
  95. MMPI-2 Personality Profiles of High-Functioning Adults With Autism Spectrum Disorders
    Sally J. Ozonoff, Nicanor Garcia, Elaine Clark, Janet E. Lainhart · 2005 · Assessment
  96. Autism and pervasive developmental disorders
    Carlos A. Gadia, Roberto F. Tuchman, Newra Tellechea Rotta · 2004 · Jornal de Pediatria
  97. Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees
    Hilary H Coon, Michele Villalobos, Reid J. Robison, Nicola J. Camp, Dale S. Cannon, Kristina Allen‐Brady, Judith S. Miller, William M. McMahon · 2010 · Molecular Autism
  98. Association of INPP1, PIK3CG, and TSC2 gene variants with autistic disorder: implications for phosphatidylinositol signalling in autism
    Fatema Serajee, R Nabi, H Zhong, A H M Mahbubul Huq · 2003 · Journal of Medical Genetics
  99. FMR1 and Autism, an Intriguing Connection Revisited
    William Fyke, Milen T. Velinov · 2021 · Genes
  100. Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population
    Xiaoping Li, Zhengmao Hu, Yiqun He, Zhimin Xiong, Zhigao Long, Yu Peng, Fengxiao Bu, Jie Ling, Guanglei Xun, Xiaoyun Mo et al. · 2010 · Psychiatric Genetics