Linkage-Disequilibrium Mapping of Autistic Disorder, with 15q11-13 Markers

Cited by (368)

Items 101–200 of 368

  1. Neurodevelopmental disorders involving genomic imprinting at human chromosome 15q11–q13
    Stormy J. Chamberlain, Marc Lalande · 2010 · Neurobiology of Disease
  2. Pervasive developmental disorder and epilepsy due to maternally derived duplication of 15q11-q13
    Fiorella Gurrieri, Agatino Battaglia, L. Torrisi, Raffaella Tancredi, C. Cavallaro, Eugenio Sangiorgi, Giovanni Neri · 1999 · Neurology
  3. The Human Aminophospholipid-Transporting ATPase Gene ATP10C Maps Adjacent to UBE3A and Exhibits Similar Imprinted Expression
    Laura B. K. Herzing, Soo‐Jeong Kim, Edwin H. Cook, David H. Ledbetter · 2001 · The American Journal of Human Genetics
  4. A systematic review of molecular imaging (PET and SPECT) in autism spectrum disorder: Current state and future research opportunities
    Nicole R. Zürcher, Anisha Bhanot, Christopher J. McDougle, Jacob M. Hooker · 2015 · Neuroscience & Biobehavioral Reviews
  5. Genetic studies in autistic disorder and chromosome 15
    Meredyth P. Bass, Marisa M. Menold, Chantelle M. Wolpert, S. L. Donnelly, Sarah A. Ravan, Elizabeth R. Hauser, Lewis O. Maddox, Jeffery M. Vance, Ruth K. Abramson, H. H. Wright et al. · 2000 · Neurogenetics
  6. Evaluation of autism traits in Angelman syndrome: a resource to unfold autism genes
    Maria Teresa Bonati, Silvia Russo, Palma Finelli, Maria Rosa Valsecchi, Francesca Cogliati, Florinda Cavalleri, Wendy Roberts, Maurizio Elia, Lidia Larizza · 2007 · Neurogenetics
  7. Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: Efficient identification of known microduplications and identification of a novel microduplication in ASMT
    Guiqing Cai, Lisa J. Edelmann, Juliet Goldsmith, Ninette Cohen, Alisa Nakamine, Jennifer G. Reichert, Ellen J. Hoffman, Danielle Zurawiecki, Jeremy M. Silverman, Eric Hollander et al. · 2008 · BMC Medical Genomics
  8. Differences Between the Pattern of Developmental Abnormalities in Autism Associated With Duplications 15q11.2-q13 and Idiopathic Autism
    Jerzy Węgiel, N. Carolyn Schanen, Edwin H. Cook, Marian Sigman, William Ted Brown, Izabela Kuchna, Krzysztof Nowicki, Jarek Wegiel, Humi Imaki, Shuang Yong Ma et al. · 2012 · Journal of Neuropathology & Experimental Neurology
  9. 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
  10. 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
  11. Genome-wide Linkage Analyses of Quantitative and Categorical Autism Subphenotypes
    Xiao-Qing Liu, Andrew D. Paterson, Péter Szatmári · 2008 · Biological Psychiatry
  12. Analysis of the neuroligin 4Y gene in patients with autism
    Yan Jin, Jinong Feng, Richard J. Schroer, Wenyan Li, Cindy D. Skinner, Charles E. Schwartz, Edwin H. Cook, Steve S. Sommer · 2008 · Psychiatric Genetics
  13. Autism
    G. Robert DeLong · 1999 · Neurology
  14. The Human Genome Project and Its Impact on Psychiatry
    William Maxwell Cowan, Kathy L. Kopnisky, Steven E. Hyman · 2002 · Annual Review of Neuroscience
  15. Brain weight in autism: Normal in the majority of cases, megalencephalic in rare cases
    Eric Courchesne, Ralph‐Axel Müller, Osamu Saitoh · 1999 · Neurology
  16. Neural Hyperexcitability in Autism Spectrum Disorders
    Takarae, Yukari, Sweeney, John · 2017 · Brain Sciences
  17. A Third-Pass Genome Scan in Panic Disorder: Evidence for Multiple Susceptibility Loci
    Abby J. Fyer, Steven P. Hamilton, Martina Durner, Fatemeh G. Haghighi, Gary A. Heiman, Ramiro Costa, Oleg Vadimovich Evgrafov, Philip Adams, Ada Baisre de Leon, Nilda Taveras et al. · 2006 · Biological Psychiatry
  18. Clinical management of behavioral characteristics of Prader–Willi syndrome
    Anastasia Dimitropoulos · 2010 · Neuropsychiatric Disease and Treatment
  19. Evaluation of the GABAergic nervous system in autistic brain: 123I-iomazenil SPECT study
    Tatsuo Mori, Kenji Mori, Emiko Fujii, Yoshihiro Toda, Masahito Miyazaki, Masafumi Harada, Toshiaki Hashimoto, Shoji Kagami · 2011 · Brain and Development
  20. Etiopathogenesis of Catatonia
    Dirk Marcel Dhossche, Laura Stoppelbein, Ujjwal Kumar Rout · 2010 · Journal of Ect
  21. Autism and the pervasive developmental disorders
    Tony Charman · 1999 · Current Opinion in Neurology
  22. Relationship between clinical and genetic features in “inverted duplicated chromosome 15” patients
    Renato Borgatti, Paolo Piccinelli, Davide Passoni, Leda Dalprà, Monica Rosa Miozzo, Roberto Micheli, Chiara Gagliardi, Umberto Balottin · 2001 · Pediatric Neurology
  23. Dense linkage disequilibrium mapping in the 15q11–q13 maternal expression domain yields evidence for association in autism
    Erika L. Nurmi, Tarek Tawfik Amin, Lana M. Olson, Michelle M. Jacobs, Jacob L. McCauley, A Y Lam, Edward L. Organ, Susan E. Folstein, Jonathan L. Haines, James S. Sutcliffe · 2003 · Molecular Psychiatry
  24. Capillary electrophoresis of proteins for proteomic studies
    Takashi Manabe · 1999 · Electrophoresis
  25. Chapter 4. Personality Disorders and Relational Disorders: A Research Agenda for Addressing Crucial Gaps in DSM
    Michael B. First, Carl Compton Bell, Bruce C. Cuthbert, John Harrison Krystal, Robert T. Malison, David R. Offord, David Reiss, M. Tracie Shea, Tom Widiger, Katherine L. Wisner · 2002 · American Psychiatric Association Publishing eBooks
  26. Identifying Autism Susceptibility Genes
    Elena Maestrini, Alina Paul, Anthony P. Monaco, Anthony J. Bailey · 2000 · Neuron
  27. Linkage disequilibrium between GABRB3 gene and nonsyndromic familial cleft lip with or without cleft palate
    Luca Scapoli, Marcella Martinelli, Furio Pezzetti, Francesco Carinci, Maria Bodo, Mauro G. Tognon, Paolo Carinci · 2001 · Human Genetics
  28. Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders
    Patrick Bolton, Marijcke W. M. Veltman, Emma J. L. Weisblatt, Joanne R. Holmes, Nicholas Simon Thomas, Sheila A. Youings, Russell J. Thompson, Siân E. Roberts, Nicholas Robert Dennis, Caroline E. Browne et al. · 2004 · Psychiatric Genetics
  29. Neuronal nicotinic acetylcholine receptor subunits in autism: an immunohistochemical investigation in the thalamus
    M.A. Ray, A.J. Graham, Mee Hee Lee, Robert Henry Perry, JENNIFER A. COURT, Elaine King Perry · 2005 · Neurobiology of Disease
  30. Autism genetics – an overview
    Jiani Yin, Christian Patrick Schaaf · 2016 · Prenatal Diagnosis
  31. Mechanisms underlying the EEG biomarker in Dup15q syndrome
    Joel Frohlich, Lawrence T. Reiter, Vidya Saravanapandian, Charlotte DiStefano, Scott Huberty, Carly Hyde, Stormy J. Chamberlain, Carrie E. Bearden, Peyman Golshani, Andrei Irimia A et al. · 2019 · Molecular Autism
  32. Technical Report: The Pediatrician's Role in the Diagnosis and Management of Autistic Spectrum Disorder in Children
    2001 · PEDIATRICS
  33. The genetics of autism
    Sarah J. Spence · 2004 · Seminars in Pediatric Neurology
  34. Genes, language development, and language disorders
    Shelley D. Smith · 2007 · Mental Retardation and Developmental Disabilities Research Reviews
  35. 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
  36. Imprinted genes and mental dysfunction
    William Davies, Anthony R Isles, Lawrence S. Wilkinson · 2001 · Annals of Medicine
  37. Genetic analysis of GABRB3 as a candidate gene of autism spectrum disorders
    Chia‐Hsiang Chen, Chia-Chun Huang, Min-Chih Cheng, Yen‐Nan Chiu, Wen‐Che Tsai, Yu‐Yu Wu, Shih-Kai Liu, Susan Shur‐Fen Gau · 2014 · Molecular Autism
  38. The Oscillopathic Nature of Language Deficits in Autism: From Genes to Language Evolution
    Antonio Benítez‐Burraco, Elliot Murphy · 2016 · Frontiers in Human Neuroscience
  39. Chapter 2. Neuroscience Research Agenda to Guide Development of a Pathophysiologically Based Classification System
    Dennis S. Charney, David Harrison Barlow, Kelly N. Botteron, Jonathan D. Cohen, David A Goldman, Raquel E. Gur, Keh‐Ming Lin, Juan F. López, James H. Meador‐Woodruff, Steven O. Moldin et al. · 2002 · American Psychiatric Association Publishing eBooks
  40. Calcium and activity-dependent signaling in the developing cerebral cortex
    Arjun McKinney, Arpana, Petrova, Ralitsa, Panagiotakos, Georgia · 2022 · Development
  41. Neuron-specific impairment of inter-chromosomal pairing and transcription in a novel model of human 15q-duplication syndrome
    Makiko Meguro‐Horike, Dag H. Yasui, Weston T. Powell, Diane I. Schroeder, Mitsuo Oshimura, Janine M. LaSalle, Shin‐ichi Horike · 2011 · Human Molecular Genetics
  42. Association of GABRB3 Polymorphisms with Autism Spectrum Disorders in Korean Trios
    Soon Ae Kim, Jin‐Hee Kim, Mira Park, In Hee Cho, Hee Jeong Yoo · 2006 · Neuropsychobiology
  43. Neuroimaging genetics approaches to identify new biomarkers for the early diagnosis of autism spectrum disorder
    Sabah Nisar, Mohammad Haris · 2023 · Molecular Psychiatry
  44. Single Nucleotide Polymorphisms Predict Symptom Severity of Autism Spectrum Disorder
    Yun Jiao, Rong Chen, Xiaoyan Ke, Lü Cheng, Kangkang Chu, Zuhong Lu, Edward H. Herskovits · 2011 · Journal of Autism and Developmental Disorders
  45. Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q, 13q, 15q, 16p, 17q, 19q and 22q in Finnish multiplex families
    Mari Auranen, Taina Tuulikki Nieminen, S Majuri, Raija Vanhala, Leena Peltonen, Irma E. Järvelä · 2000 · Molecular Psychiatry
  46. A Paternally Inherited Duplication in the Prader-Willi/ Angelman Syndrome Critical Region: A Case and Family Study
    Marijcke W. M. Veltman, Russell J. Thompson, Ellen E. Craig, Nicholas Robert Dennis, Siân E. Roberts, Vanessa Moore, Josie A. Brown, Patrick Bolton · 2005 · Journal of Autism and Developmental Disorders
  47. A family with a grand‐maternally derived interstitial duplication of proximal 15q
    Fatih Z Boyar, MM Whitney, Amy C. Lossie, BA Gray, KL Keller, HJ Stalker, RT Zori, Gary R. Geffken, J Mutch, PJ Edge et al. · 2001 · Clinical Genetics
  48. Autism: Neuropathology, Alterations of the GABAergic System, and Animal Models
    Imke A. J. van Kooten, Patrick R. Hof, Hermán van Engeland, Harry W.M. Steinbusch, Paul H. Patterson, Christoph Schmitz · 2005 · International review of neurobiology
  49. Early Pharmacological Treatment of Autism: A Rationale for Developmental Treatment
    Terrence C. Bethea, Linmarie Sikich · 2007 · Biological Psychiatry
  50. The Genetics of Autism Spectrum Disorders
    Dorothy E. Grice, Joseph D. Buxbaum · 2006 · NeuroMolecular Medicine
  51. La génétique de l’autisme
    Stéphane Jamain, Catalina Betancur, Bruno Giros A, Marion Leboyer, Thomas Bourgeron · 2003 · médecine/sciences
  52. Genetic variation in GABRB3 is associated with Asperger syndrome and multiple endophenotypes relevant to autism
    Varun Warrier, Simon Baron‐Cohen, Bhismadev Chakrabarti · 2013 · Molecular Autism
  53. Chromosome 22 workshop report
    Sibylle G. Schwab, Dieter B. Wildenauer, David Andrew Collier, A. Ekelund, Pablo V. Gejman, Joachim Franz Hallmayer, John R. Kelsoe, A. von Gontard, D.B. Wildenauer · 1999 · American Journal of Medical Genetics
  54. Polymorphisms of candidate genes in Slovak autistic patients
    Kelemenova, Silvia, Schmidtova, Eva, Ficek, Andrej, Celec, Peter, Kubranska, Aneta, Ostatnikova, Daniela · 2010 · Psychiatric Genetics
  55. A question of balance: a proposal for new mouse models of autism
    Crystal L. Murcia, Forrest O. Gulden, Karl Herrup · 2004 · International Journal of Developmental Neuroscience
  56. Epigenetic Mechanisms in Autism Spectrum Disorder
    Adrian Zhubi, Edwin H. Cook, Alessandro Guidotti, Dennis R. Grayson · 2014 · International review of neurobiology
  57. Mutation screening of the UBE3A /E6-AP gene in autistic disorder
    Jeremy M. Veenstra-VanderWeele, David Gonen, BENNETT L. LEVENTHAL, EH Cook · 1999 · Molecular Psychiatry
  58. Stratification based on language‐related endophenotypes in autism: Attempt to replicate reported linkage
    Sarah J. Spence, Rita M. Cantor, Lien Chung, Sharon H. Kim, Daniel H. Geschwind, Maricela Alarcón · 2006 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
  59. An inversion inv(4)(p12–p15.3) in autistic siblings implicates the 4p GABA receptor gene cluster
    John B. Vincent, Shin‐ichi Horike, Sanaa Choufani, A D Paterson, W Roberts, Péter Szatmári, Rosanna Weksberg, B Fernandez, Stephen W. Scherer · 2006 · Journal of Medical Genetics
  60. Proton Magnetic Resonance Spectroscopy as a Probe into the Pathophysiology of A utism S pectrum D isorders ( ASD ): A Review
    Joshua M. Baruth, Christopher A. Wall, Marc C. Patterson, John D. Port · 2013 · Autism Research
  61. Epigenetic Factors and Autism Spectrum Disorders
    Bess M. Flashner, Mark E. Russo, Jenine E. Boileau, Derek W. Leong, G. Ian Gallicano · 2013 · NeuroMolecular Medicine
  62. The Autism Genome Project
    Diane Hu‐Lince, David Wesley Craig, Matthew J. Huentelman, Dietrich A. Stephan · 2005 · American Journal of PharmacoGenomics
  63. Early functional brain development in autism and the promise of sleep fMRI
    Pierce, Karen · 2011 · Brain Research
  64. Disease susceptibility genes for autism
    Irina N. Bespalova, Joseph D. Buxbaum · 2003 · Annals of Medicine
  65. Chromosomal Anomalies in Individuals with Autism
    Dries Castermans, Valérie Wilquet, Jean G. Steyaert, Wim Van de Ven, Jean‐Pierre Fryns, Koenraad Devriendt · 2004 · Autism
  66. Genetic clues to the biological basis of autism
    Martha Turner, Gabrielle Barnby, Anthony J. Bailey · 2000 · Molecular Medicine Today
  67. Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families
    Jun Z. Li, Holly K. Tabor, Loan Nguyen, Christopher Gleason, Linda J. Lotspeich, Donna Spiker, NEIL J. RISCH, R Myers · 2001 · American Journal of Medical Genetics
  68. Biopsychological correlates of repetitive and restricted behaviors in autism spectrum disorders
    Miguel Comparan‐Meza, Ivette Cruz, Fernando Jáuregui-Huerta, Rocío E. González-Castañeda, Óscar González-Pérez, Alma Y. Gálvez‐Contreras · 2021 · Brain and Behavior
  69. Array‐based comparative genomic hybridization analysis of recurrent chromosome 15q rearrangements
    Trilochan Sahoo, Chad A. Shaw, Andrew Young, Nathan L. Whitehouse, Richard J. Schroer, Roger E. Stevenson, Arthur L. Beaudet · 2005 · American Journal of Medical Genetics Part A
  70. Organization of the human superior olivary complex in 15q duplication syndromes and autism spectrum disorders
    Richard Lukose, K. Beebe, Randy Joseph Kulesza · 2014 · Neuroscience
  71. The role of GABAergic neural circuits in the pathogenesis of autism spectrum disorder
    Jing Di, Jian Li, Bruce F. O’Hara, Ian L. Alberts, Lei Xiong, Jijun Li, Xiaohong Li · 2020 · International Journal of Developmental Neuroscience
  72. Vitamin D receptor variants in 192 patients with schizophrenia and other psychiatric diseases
    Yan Jin, Jinong Feng, Nick J. Craddock, Ian Richard Jones, Edwin H. Cook, David A Goldman, Leonard L. Heston, Jiesheng Chen, Patricia Burkhart, Wenyan Li et al. · 2005 · Neuroscience Letters
  73. GABRB3 Gene Deficient Mice: A Potential Model of Autism Spectrum Disorder
    Timothy M. DeLorey · 2005 · International review of neurobiology
  74. Autism Spectrum Disorders: Phenotype and Diagnosis
    2006 · CRC Press eBooks
  75. Autism
    Anthony P. Monaco, Janine A. Lamb, Jeremy R Parr, Anthony J. Bailey · 2002 · NeuroMolecular Medicine
  76. Polymorphisms in SLC6A4, PAH, GABRB3, and MAOB and modification of psychotic disorder features
    Sarah E. Bergen, Ayman H. Fanous, Dermot Walsh, F. Anthony O’Neill, Kenneth S. Kendler · 2009 · Schizophrenia Research
  77. Using genetic findings in autism for the development of new pharmaceutical compounds
    Jacob A. S. Vorstman, Will P. J. M. Spooren, Antonio Maria Persico, David Andrew Collier, Stefan Aigner, Ravi Jagasia, Jeffrey Colm Glennon, Jan K. Buitelaar · 2013 · Psychopharmacology
  78. Meta-Analysis of the Association between GABA Receptor Polymorphisms and Autism Spectrum Disorder (ASD)
    Manijeh Mahdavi, Majid Kheirollahi, Roya Riahi, Fariborz Khorvash, Mehdi Khorrami, Maryam Mirsafaie · 2018 · Journal of Molecular Neuroscience
  79. Pharmacologic Treatment of Autism
    Mark T. Palermo, Paolo Curatolo · 2004 · Journal of Child Neurology
  80. The molecular genetics of autism
    Thomas H. Wassink, Joseph Piven · 2000 · Current Psychiatry Reports
  81. Autism
    Roberto F. Tuchman · 2003 · Neurologic Clinics
  82. The prevalence of epigenetic mechanisms in the regulation of cognitive functions and behaviour
    Tamara B. Franklin, Isabelle M. Mansuy · 2010 · Current Opinion in Neurobiology
  83. A Proton Magnetic Resonance Spectroscopic Study in Autism Spectrum Disorder Using a 3-Tesla Clinical Magnetic Resonance Imaging (MRI) System: The Anterior Cingulate Cortex and the Left Cerebellum
    Hiromichi Ito, Kenji Mori, Masafumi Harada, Sonoka Hisaoka, Yoshihiro Toda, Tatsuo Mori, Aya Goji, Yoko Abe, Masahito Miyazaki, Shoji Kagami · 2017 · Journal of Child Neurology
  84. Positron emission tomography imaging of the γ-aminobutyric acid system
    Jan D. Andersson, David Matuskey, Sjoerd J. Finnema · 2018 · Neuroscience Letters
  85. The Genetics of Childhood Psychiatric Disorders: A Decade of Progress
    Matthew W. State, Paul J. Lombroso, David L. Pauls, James Frederick Leckman · 2000 · Journal of the American Academy of Child & Adolescent Psychiatry
  86. Emerging drugs for the treatment of symptoms associated with autism spectrum disorders
    Wink, Logan K, Plawecki, Martin H, Erickson, Craig A, Stigler, Kimberly A, McDougle, Christopher J · 2010 · Expert Opinion on Emerging Drugs
  87. Autism - A Neurodevelopmental Journey from Genes to Behaviour
    Valsamma Eapen · 2011 · InTech eBooks
  88. Full-Genome Scans with Autistic Disorder: A Review
    Lise Gutknecht · 2001 · Behavior Genetics
  89. Ordered‐subset analysis of savant skills in autism for 15q11‐q13
    D.Q. Ma, James M Jaworski, Marisa M. Menold, S. L. Donnelly, Ruth K. Abramson, H.H. Wright, G. R. DeLong, John R. Gilbert, Margaret Ann Pericak‐Vance, Michael L. Cuccaro · 2005 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
  90. An association analysis of microsatellite markers across the Prader-Willi/Angelman critical region on chromosome 15 (q11-13) and autism spectrum disorder
    Sarah R Curran, Siân E. Roberts, Simon N. Thomas, Marijcke W. M. Veltman, Josie Browne, Emanuela Medda, Andrew R. Pickles, Pak Chung Sham, Patrick Bolton · 2005 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
  91. Chapter 6. Beyond the Funhouse Mirrors: Research Agenda on Culture and Psychiatric Diagnosis
    Renato D. Alarcón, Margarita M. Alegria, Carl Compton Bell, Cheryl Anne Boyce, Laurence J. Kirmayer, Keh-Ming Lin, Steven R. López, Bedirhan Üstün, Katherine L. Wisner · 2002 · American Psychiatric Association Publishing eBooks
  92. Shared Susceptibility Region On Chromosome 15 Between Autism And Catatonia
    Yvon C. Chagnon · 2006 · International review of neurobiology
  93. Case-Control Family Study of Lesser Variant Traits in Autism
    JAMES ALLEN WILCOX, Ming T. Tsuang, Thomas Schnurr, Nicolas Baida-Fragoso · 2003 · Neuropsychobiology
  94. Structural and Functional Aberrations of the Auditory Brainstem in Autism Spectrum Disorder
    Amanda Smith, Samantha Storti, Richard Lukose, Randy Joseph Kulesza · 2019 · Journal of Osteopathic Medicine
  95. Are Autistic and Catatonic Regression Related? A Few Working Hypotheses Involving Gaba, Purkinje Cell Survival, Neurogenesis, and ECT
    Dirk Marcel Dhossche, Ujjwal Kumar Rout · 2006 · International review of neurobiology
  96. Scanning of estrogen receptor α (ERα) and thyroid hormone receptor α (TRα) genes in patients with psychiatric diseases: Four missense mutations identified in ERα gene
    Jinong Feng, Yan Jin, Shawneen Michaud, Nick J. Craddock, Ian R. Jones, Edwin H. Cook, David A Goldman, Leonard L. Heston, Leena Peltonen, Lynn E. DeLisi et al. · 2001 · American Journal of Medical Genetics
  97. No evidence for linkage of liability to autism toHOXA1in a sample from the CPEA network
    Bernie Devlin, Pamela J. Bennett, Edwin H. Cook, Géraldine Dawson, David Gonen, Elena L. Grigorenko, William McMahon, David L. Pauls, Moyra Smith, M. Anne Spence et al. · 2002 · American Journal of Medical Genetics
  98. Toward the Language Oscillogenome
    Elliot Murphy, Antonio Benítez‐Burraco · 2018 · Frontiers in Psychology
  99. Array Comparative Genomic Hybridization Findings in a Cohort Referred for an Autism Evaluation
    Gerald Bradley Schaefer, Lois Janelle Starr, Dianne Pickering, Gwenn L. Skar, Kristi A. DeHaai, Warren G. Sanger · 2010 · Journal of Child Neurology
  100. Mutation screening and transmission disequilibrium study of ATP10C in autism
    Soo‐Jeong Kim, Laura B. K. Herzing, Jeremy M. Veenstra-VanderWeele, Catherine Lord, Rachel Yeung-Courchesne, BENNETT L. LEVENTHAL, David H. Ledbetter, Eric Courchesne, Edwin H. Cook · 2002 · American Journal of Medical Genetics