T. Ylisaukko‐oja, M. Alarcón, R. Cantor, M. Auranen, R. Vanhala, E. Kempas, L. Wendt, I. Järvelä, D. Geschwind, L. Peltonen (2006)
Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish familiesAnnals of Neurology, 59
A. Bailey, A. Couteur, I. Gottesman, P. Bolton, E. Simonoff, E. Yuzda, M. Rutter (1995)
Autism as a strongly genetic disorder: evidence from a British twin studyPsychological Medicine, 25
A. Midei, J. Licinio (2004)
General SummaryMolecular Psychiatry, 9
P. Szatmari, A. Paterson, L. Zwaigenbaum, W. Roberts, J. Brian, Xiao-qing Liu, J. Vincent, J. Skaug, A. Thompson, Lili Senman, L. Feuk, Cheng Qian, S. Bryson, Marshall Jones, C. Marshall, S. Scherer, V. Vieland, Christopher Bartlett, L. Mangin, R. Goedken, Alberto Segre, M. Pericak-Vance, M. Cuccaro, J. Gilbert, H. Wright, R. Abramson, C. Betancur, T. Bourgeron, C. Gillberg, M. Leboyer, J. Buxbaum, K. Davis, E. Hollander, J. Silverman, Joachim Hallmayer, L. Lotspeich, J. Sutcliffe, J. Haines, S. Folstein, J. Piven, T. Wassink, V. Sheffield, D. Geschwind, M. Bucan, W. Brown, R. Cantor, J. Constantino, T. Gilliam, M. Herbert, C. Lajonchere, D. Ledbetter, Christa Lese-Martin, Janet Miller, S. Nelson, C. Samango-Sprouse, S. Spence, M. State, R. Tanzi, H. Coon, G. Dawson, B. Devlin, A. Estes, P. Flodman, L. Klei, W. McMahon, N. Minshew, J. Munson, E. Korvatska, P. Rodier, G. Schellenberg, Moyra Smith, M. Spence, C. Stodgell, P. Tepper, E. Wijsman, Chang-En Yu, B. Rogé, Carine Mantoulan, Kerstin Wittemeyer, A. Poustka, B. Felder, S. Klauck, C. Schuster, F. Poustka, S. Bölte, Sabine Feineis-Matthews, Evelyn Herbrecht, G. Schmötzer, J. Tsiantis, K. Papanikolaou, E. Maestrini, E. Bacchelli, F. Blasi, Simona Carone, Claudio Toma, H. Engeland, M. Jonge, C. Kemner, F. Koop, M. Langemeijer, Channa Hijmans, W. Staal, G. Baird, P. Bolton, M. Rutter, E. Weisblatt, Jonathan Green, C. Aldred, J. Wilkinson, A. Pickles, A. Couteur, T. Berney, H. McConachie, A. Bailey, Kostas Francis, Gemma Honeyman, A. Hutchinson, J. Parr, S. Wallace, A. Monaco, G. Barnby, Kazuhiro Kobayashi, J. Lamb, I. Sousa, N. Sykes, E. Cook, Stephen Guter, B. Leventhal, Jeff Salt, C. Lord, Christina Corsello, Vanessa Hus, D. Weeks, F. Volkmar, M. Tauber, E. Fombonne, A. Shih, Kacie Meyer (2007)
Mapping autism risk loci using genetic linkage and chromosomal rearrangementsNature Genetics, 39
S. Yu, M. Pritchard, E. Kremer, M. Lynch, J. Nancarrow, E. Baker, K. Holman, J. Mulley, S. Warren, D. Schlessinger, al. et (1991)
Fragile X genotype characterized by an unstable region of DNAScience, 252
C. Lord, M. Rutter, A. Couteur (1994)
Autism Diagnostic Interview-Revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disordersJournal of Autism and Developmental Disorders, 24
(1999)
Ann Stat
(2005)
Natl Vital Stat Rep
David Skuse (1999)
Genomic imprinting of the X chromosome: a novel mechanism for the evolution of sexual dimorphism.The Journal of laboratory and clinical medicine, 133 1
A. Verkerk, M. Pieretti, J. Sutcliffe, Ying-Hui Fu, D. Kuhl, A. Pizzuti, O. Reiner, S. Richards, Maureen Victoria, Fuping Zhang, Bert Eussen, G. Ommen, L. Blonden, G. Riggins, J. Chastain, Catherine Kunst, H. Galjaard, C. Caskey, D. Nelson, B. Oostra, S. Warren (1991)
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromeCell, 65
A. Reichenberg, R. Gross, M. Weiser, M. Bresnahan, J. Silverman, S. Harlap, J. Rabinowitz, C. Shulman, D. Malaspina, G. Lubin, H. Knobler, M. Davidson, E. Susser (2006)
Advancing paternal age and autism.Archives of general psychiatry, 63 9
G. Wood (1999)
Binomial mixtures: geometric estimation of the mixing distributionAnnals of Statistics, 27
I. Oberle, François Rousseau, D. Heitz, C. Kretz, D. Devys, A. Hanauer, J. Boué, M. Bertheas, J. Mandel (1991)
Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndromeScience, 252
M. Jacquemont, D. Sanlaville, R. Redon, O. Raoul, V. Cormier-Daire, S. Lyonnet, J. Amiel, M. Merrer, D. Heron, M. Blois, M. Prieur, M. Vekemans, N. Carter, A. Munnich, L. Colleaux, A. Philippe (2006)
Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disordersJournal of Medical Genetics, 43
R. Amir, I. Veyver, Mimi Wan, Charles Tran, U. Francke, H. Zoghbi (1999)
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2Nature Genetics, 23
(1999)
Nat Genet
H. Rj (1996)
The Society for Neuroscience 1995 annual meeting.Molecular Psychiatry, 1
(1995)
Psychol Med
(2006)
Mol Psychiatry
(2006)
Ann Neurol
(1999)
J Lab Clin Med
B. Lindsay (1995)
Mixture models : theory, geometry, and applications
S. Baron-Cohen, Rebecca Knickmeyer, M. Belmonte (2005)
Sex Differences in the Brain: Implications for Explaining AutismScience, 310
(2007)
MMWR Surveill Summ
L. Lovász (1999)
Hit-and-run mixes fastMathematical Programming, 86
D. Geschwind, Janice Sowinski, C. Lord, P. Iversen, Jonathan Shestack, P. Jones, L. Ducat, S. Spence (2001)
The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions.American journal of human genetics, 69 2
(1994)
J Autism Dev Disord
This work was supported by a grant from the Simons Foundation
Ted Brown (Institute for Basic Research in Developmental Disabilities
N. Risch, D. Spiker, L. Lotspeich, N. Nouri, David Hinds, Joachim Hallmayer, L. Kalaydjieva, Patty McCague, S. Dimiceli, Tawna Pitts, Loan Nguyen, Joan Yang, Courtney Harper, Danielle Thorpe, Saritha Vermeer, Helena Young, J. Hebert, A. Lin, Joan Ferguson, Carla Chiotti, Susan Wiese-Slater, Tamara Rogers, B. Salmon, P. Nicholas, P. Petersen, C. Pingree, W. McMahon, Dona Wong, L. Cavalli-Sforza, H. Kraemer, R. Myers (1999)
A genomic screen of autism: evidence for a multilocus etiology.American journal of human genetics, 65 2
M. Auranen, R. Vanhala, T. Varilo, K. Ayers, E. Kempas, T. Ylisaukko‐oja, J. Sinsheimer, L. Peltonen, I. Järvelä (2002)
A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27.American journal of human genetics, 71 4
J. Sebat, B. Lakshmi, D. Malhotra, J. Troge, Christa Lese-Martin, T. Walsh, B. Yamrom, Seungtai Yoon, A. Krasnitz, J. Kendall, A. Leotta, D. Pai, Ray Zhang, Yoon-ha Lee, J. Hicks, S. Spence, Annette Lee, K. Puura, T. Lehtimäki, D. Ledbetter, P. Gregersen, J. Bregman, J. Sutcliffe, V. Jobanputra, W. Chung, D. Warburton, M. King, D. Skuse, D. Geschwind, T. Gilliam, Kenny Ye, M. Wigler (2007)
Strong Association of De Novo Copy Number Mutations with AutismScience, 316
S. Palferman, N. Matthews, M. Turner, Janette Moore, A. Hervás, Anne Aubin, S. Wallace, J. Michelotti, Catherine Wainhouse, A. Paul, E. Thompson, Ramyani Gupta, C. Garner, Marianna Murin, C. Freitag, N. Ryder, E. Cottington, J. Parr, A. Pickles, M. Rutter, A. Bailey, G. Barnby, J. Lamb, A. Marlow, Pat Scudder, A. Monaco, G. Baird, A. Cox, Z. Docherty, P. Warburton, Elizabeth Green, S. Abbs, A. Couteur, H. McConachie, T. Berney, T. Kelly, P. Vries, P. Bolton, Jonathan Green, A. Gilchrist, J. Whittacker, Bryan Bolton, R. Packer, E. Maestrini, F. Blasi, H. Engeland, M. Jonge, C. Kemner, S. Klauck, K. Beyer, Sabine Epp, A. Poustka, A. Benner, Jw Goethe, F. Poustka, D. Rühl, Gabriele Schmötzer, S. Boolte, Sabine Feineis-Matthews, E. Fombonne, B. Rogee, Jeanne Fremolle-Kruck, C. Pienkowski, M. Tauber, Lennart Pedersen, Kb Nielsen, G. Eriksen, D. Haracopos, R. Cotterill, J. Tsiantis, K. Papanikolaou, C. Lord, Christina Corsello, Stephen Guter, B. Leventhal, E. Cook, S. Smalley, J. Bailey, J. McGough, J. Levitt, D. Pauls, F. Volkmar, D. Weeks (2001)
A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.American journal of human genetics, 69 3
Amanda Yonan, M. Alarcón, R. Cheng, P. Magnusson, S. Spence, A. Palmer, A. Grunn, Suh-Hang Juo, J. Terwilliger, Jianjun Liu, R. Cantor, D. Geschwind, T. Gilliam (2003)
A genomewide screen of 345 families for autism-susceptibility loci.American journal of human genetics, 73 4
(2003)
Am J Hum Genet
T. Mathews, B. Hamilton (2005)
Trend analysis of the sex ratio at birth in the United States.National vital statistics reports : from the Centers for Disease Control and Prevention, National Center for Health Statistics, National Vital Statistics System, 53 20
Jianjun Liu, D. Nyholt, P. Magnussen, E. Parano, P. Pavone, D. Geschwind, C. Lord, P. Iversen, J. Hoh, the Consortium, J. Ott, T. Gilliam (2001)
A genomewide screen for autism susceptibility loci.American journal of human genetics, 69 2
(1999)
Math Prog
(2005)
Hum Mol Genet 14 Spec No 1 : R 27 – R 32
C. Lord, M. Rutter, S. Goode, Jacquelyn Heemsbergen, H. Jordan, Lynn Mawhood, E. Schopler (1989)
Austism diagnostic observation schedule: A standardized observation of communicative and social behaviorJournal of Autism and Developmental Disorders, 19
(1993)
The European Chromosome 16 Tuberous Sclerosis Consortium
(1991)
Science
M. Storozhuk (2006)
[Retrograde signaling in the GABA- and glutamatergic synapses of the brain].Fiziolohichnyi zhurnal, 52 3
Cure Autism Now and is supported
(2006)
Neuron 52:103–121
M. Nellist, B. Janssen, P. Brook-Carter, A. Hesseling-Janssen, M. Maheshwar, S. Verhoef, Ans Ouweland, D. Lindhout, B. Eussen, I. Cordeiro, H. Santos, D. Halley, J. Sampson, C. Ward, B. Peral, S. Thomas, J. Hughes, P. Harris, J. Roelfsema, J. Saris, L. Spruit, D. Peters, J. Dauwerse, M. Bruening (1993)
Identification and characterization of the tuberous sclerosis gene on chromosome 16Cell, 75
Proceedings of the National Academy of Sciences – Unpaywall
Published: Jul 26, 2007
Access the full text.
Sign up today, get DeepDyve free for 14 days.