Z
Zoe Docherty
Researcher at Guy's Hospital
Publications - 16
Citations - 1536
Zoe Docherty is an academic researcher from Guy's Hospital. The author has contributed to research in topics: Heritability of autism & Autism. The author has an hindex of 13, co-authored 16 publications receiving 1514 citations.
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Journal ArticleDOI
A full genome screen for autism with evidence for linkage to a region on chromosome 7q International Molecular Genetic Study of Autism Consortium
Anthony J. Bailey,Amaia Hervas,Nicola Matthews,Sarah Palferman,Simon Wallace,Anne Aubin,Janine Michelotti,Catherine Wainhouse,Katerina Papanikolaou,Michael Rutter,Elena Maestrini,Angela J. Marlow,Daniel E. Weeks,Daniel E. Weeks,Janine A. Lamb,Clyde Francks,Georgina Kearsley,Pat Scudder,Anthony P. Monaco,Gillian Baird,Anthony Cox,Helen Cockerill,Fleming Nuffield,Ann Le Couteur,Tom Berney,Hayley Cooper,Thomas Kelly,Jonathan Green,Jane Whittaker,Anne Gilchrist,Patrick Bolton,Anne Schönewald,Michael G. Daker,Caroline Mackie Ogilvie,Zoe Docherty,Zandra Deans,Bryan Bolton,Ros Packer,Fritz Poustka,Dorothea Rühl,Gabriele Schmötzer,Sven Bölte,Sabine M. Klauck,Anja Spieler,Annemarie Poustka,Herman van Engeland,Chantal Kemner,Maretha de Jonge,Ineke Den Hartog,Catherine Lord,Edwin H. Cook,Bennett L. Leventhal,Fred Volkmar,David Pauls,Ami Klin,Susan L. Smalley,Eric Fombonne,Bernadette Rogé,Maïté Tauber,Evelyne Arti-Vartayan,Jeanne Fremolle-Kruck,Lennart Pederson,Demetrious Haracopos,Karen Brøndum-Nielsen,Rodney M. J. Cotterill +64 more
TL;DR: A two-stage genome search for susceptibility loci in autism was performed on 87 affected sib pairs plus 12 non-sib affected relative-pairs, from a total of 99 families identified by an international consortium, and a region on chromosome 7q was the most significant.
Journal ArticleDOI
A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q and 16p
Le, Couteur, A,Thomas Kelly,T Berney,Helen McConachie,Jeremy R. Parr,Sarah Palferman,Nicola Matthews,Martha Turner,Janette Moore,Amaia Hervas,Anne Aubin,Simon Wallace,Janine Michelotti,Catherine Wainhouse,Alina Paul,Emily J. Thompson,Ramyani Gupta,Claire Garner,Marianne Murin,Christine M. Freitag,Nuala Ryder,E Cottington,Andrew Pickles,Michael Rutter,Anthony J. Bailey,Gabrielle Barnby,Janine A. Lamb,Angela J. Marlow,Pat Scudder,Anthony P. Monaco,Gillian Baird,Antony Cox,Zoe Docherty,Pamela Warburton,Elizabeth P. Green,Stephen Abbs,De, Vries, Pj,Patrick Bolton,Jonathan Green,Anne Gilchrist,Jane Whittacker,Bryan Bolton,Ros Packer,Elena Maestrini,Francesca Blasi,Van, Engeland, H,De, Jonge, Mv,Chantal Kemner,Sabine M. Klauck,Kim S. Beyer,Sabine Epp,Annemarie Poustka,Axel Benner,JW Goethe,Fritz Poustka,Dorothea Rühl,Gabriele Schmötzer,S Boolte,Sabine Feineis-Matthews,Eric Fombonne,B Rogee,Jeanne Fremolle-Kruck,Catherine Pienkowski,Maïté Tauber,Lennart Pedersen,KB Nielsen,Gunna Eriksen,Demetrious Haracopos,Rmj Cotterill,John Tsiantis,Katerina Papanikolaou,Catherine Lord,Christina Corsello,Stephen J. Guter,Bennett L. Leventhal,Edwin H. Cook,Susan L. Smalley,Julia Bailey,James J. McGough,Jennifer G. Levitt,David Pauls,Fred R. Volkmar,Daniel E. Weeks,Int, Mol, Genetic, Study, Autism, Cons +83 more
TL;DR: The addition of new families and markers provides further support for previous reports of linkages on chromosomes 7q and 16p and two new regions of linkage have also been identified on chromosomes 2q and 17q.
Journal ArticleDOI
Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q
Sarah Palferman,Nicola Matthews,Martha Turner,Janette Moore,Amaia Hervas,Anne Aubin,Simon Wallace,Janine Michelotti,Catherine Wainhouse,Alina Paul,Elaine Thompson,Marianne Murin,Ramyani Gupta,Claire Garner,Andrew Pickles,Michael Rutter,Anthony J. Bailey,Anthony J. Bailey,Janine A. Lamb,Angela J. Marlow,Pat Scudder,Gabrielle Barnby,Anthony P. Monaco,Gillian Baird,Anthony Cox,Zoe Docherty,Pamela Warburton,Elizabeth P. Green,Stephen Abbs,Ann Le Couteur,Helen McConachie,Tom Berney,Thomas Kelly,Petrus J. de Vries,Patrick Bolton,Jonathan Green,Anne Gilchrist,Jane Whittacker,Bryan Bolton,Ros Packer,Elena Maestrini,Herman van Engeland,Maretha de Jonge,Chantal Kemner,Sabine M. Klauck,Kim S. Beyer,Sabine Epp,Annemarie Poustka,Axel Benner,Fritz Poustka,Dorothea Rühl,Gabriele Schmötzer,Sven Bölte,Sabine Feineis-Matthews,Eric Fombonne,Bernadette Rogé,Jeanne Fremolle-Kruck,Catherine Pienkowski,Marie Thérèse Tauber,Lennart Pedersen,Karen Brøndum-Nielsen,Gunna Eriksen,Demetrious Haracopos,Rodney M. J. Cotterill,John Tsiantis,Katerina Papanikolaou,Catherine Lord,Christina Corsello,Stephen J. Guter,Bennett L. Leventhal,Edwin H. Cook,Susan L. Smalley,Julia Bailey,Amy Liu,Martha Dedricks,Lisa Chrzanowski,Jennifer G. Levitt,David L. Pauls,Fred R. Volkmar,Daniel E. Weeks +79 more
TL;DR: The most significant susceptibility region in the first whole genome screen of multiplex families was on chromosome 7q, although this linkage was evident only in UK IMGSAC families.
Journal ArticleDOI
Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31.
Pamela Warburton,Gillian Baird,Wai Chen,Kathleen Morris,Brian W. Jacobs,Shirley Hodgson,Zoe Docherty +6 more
TL;DR: Two individuals are presented with different, apparently balanced chromosome rearrangements involving a breakpoint at 7q31, and the findings may be of interest and relevance to the genetic aetiology of autism, and helpful in the search for susceptibility loci for SDDSL and autism.
Journal ArticleDOI
Validation and implementation of array comparative genomic hybridisation as a first line test in place of postnatal karyotyping for genome imbalance
Joo Wook Ahn,Kathy Mann,Sally Walsh,Marwa Shehab,Sarah Hoang,Zoe Docherty,Shehla Mohammed,Caroline Mackie Ogilvie +7 more
TL;DR: Array CGH can be used in a diagnostic service setting in place of G-banded chromosome analysis, providing a more comprehensive and objective test for patients with suspected genome imbalance and alleviating the burden of further clinical investigations.