Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q

Autor: Angela J. Marlow, Anthony Cox, Andrew Pickles, Patrick Bolton, Elaine Thompson, Lisa Chrzanowski, Pat Scudder, Kim S. Beyer, Jeanne Fremolle-Kruck, Ros Packer, Anthony P. Monaco, Annemarie Poustka, Janine Michelotti, Axel Benner, Karen Brøndum-Nielsen, Michael Rutter, Christina Corsello, Elizabeth P. Green, Tom Berney, Jane Whittacker, Fred R. Volkmar, Bennett L. Leventhal, Catherine Wainhouse, Simon Wallace, Maretha de Jonge, Elena Maestrini, Sabine M. Klauck, Claire Garner, Catherine Pienkowski, Ramyani Gupta, Alina Paul, David L. Pauls, Chantal Kemner, Edwin H. Cook, Katerina Papanikolaou, Marie Thérèse Tauber, Eric Fombonne, Pamela Warburton, Catherine Lord, Lennart Pedersen, Jonathan Green, Thomas Kelly, Amaia Hervas, Bernadette Rogé, Helen McConachie, Sabine Feineis-Matthews, Sabine Epp, Gillian Baird, Anne Aubin, Rodney M. J. Cotterill, Fritz Poustka, Janette Moore, Amy Liu, Martha Turner, Daniel E. Weeks, Janine A. Lamb, Julia Bailey, Martha Dedricks, John Tsiantis, Sven Bölte, Jennifer G. Levitt, Sarah Palferman, Gabriele Schmötzer, Nicola Matthews, Zoe Docherty, Gabrielle Barnby, Stephen Abbs, Susan L. Smalley, Bryan Bolton, Ann Le Couteur, Marianne Murin, Herman van Engeland, Dorothea Rühl, Petrus J. de Vries, Stephen J. Guter, Anthony J. Bailey, Demetrious Haracopos, Gunna Eriksen, Anne Gilchrist

Publikováno v: ResearcherID

Autism is a neurodevelopmental disorder that usually arises on the basis of a complex genetic predisposition. The most significant susceptibility region in the first whole genome screen of multiplex families was on chromosome 7q, although this linkag

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9330fb92598bb1503b0d3a73b77d092
https://ora.ox.ac.uk/objects/uuid:8de04b5a-0fd5-41d3-8f2e-0319b44f97aa

Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31

Autor: Brian W. Jacobs, Kathleen Morris, Zoe Docherty, Shirley Hodgson, Pamela Warburton, Gillian Baird, Wai Chen

Publikováno v: American Journal of Medical Genetics. 96:228-234

Childhood autism is characterised by impairments in communication and reciprocal social interaction together with restricted/stereotyped interests, which are evident before 3 years of age. Specific developmental disorders of speech and language (SDDS

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c86cace4a860b8eef61071c9f990449
https://doi.org/10.1002/(sici)1096-8628(20000403)96:2<228::aid-ajmg20>3.0.co

A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p

Autor: Elizabeth P. Green, David Pauls, Katerina Papanikolaou, Amaia Hervas, Alina Paul, De, Vries, Pj, Lennart Pedersen, Axel Benner, Catherine Lord, Fred R. Volkmar, Sabine Feineis-Matthews, Jennifer G. Levitt, Angela J. Marlow, Helen McConachie, Emily J. Thompson, Claire Garner, Catherine Pienkowski, Janette Moore, Gabriele Schmötzer, Nicola Matthews, Nuala Ryder, Anne Gilchrist, De, Jonge, Mv, Van, Engeland, H, Anne Aubin, Christine M. Freitag, Stephen Abbs, Ros Packer, Catherine Wainhouse, Antony Cox, KB Nielsen, Susan L. Smalley, Daniel E. Weeks, Bryan Bolton, Eric Fombonne, S Boolte, Francesca Blasi, Sabine M. Klauck, Rmj Cotterill, Andrew Pickles, Kim S. Beyer, Gillian Baird, Annemarie Poustka, Marianne Murin, Christina Corsello, Int, Mol, Genetic, Study, Autism, Cons, Elena Maestrini, Simon Wallace, Anthony P. Monaco, Julia Bailey, Janine Michelotti, Thomas Kelly, Le, Couteur, A, Stephen J. Guter, Anthony J. Bailey, B Rogee, Sarah Palferman, Demetrious Haracopos, Gunna Eriksen, James J. McGough, Zoe Docherty, Maïté Tauber, E Cottington, Patrick Bolton, Martha Turner, Fritz Poustka, Jeanne Fremolle-Kruck, Gabrielle Barnby, Dorothea Rühl, John Tsiantis, Pat Scudder, Bennett L. Leventhal, T Berney, Michael Rutter, Jeremy R. Parr, Edwin H. Cook, Pamela Warburton, Chantal Kemner, Jane Whittacker, Ramyani Gupta, Sabine Epp, JW Goethe, Jonathan Green, Janine A. Lamb

Publikováno v: ResearcherID

Autism is characterized by impairments in reciprocal communication and social interaction and by repetitive and stereotyped patterns of activities and interests. Evidence for a strong underlying genetic predisposition comes from twin and family studi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcf34322e3855df0fcd67fdd968afc76
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000170271400009&KeyUID=WOS:000170271400009