Nigel M Williams

Nigel M Williams

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Nigel M Williams

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The genetic and clinico-pathological profile of early-onset progressive supranuclear palsy.

Mov Disord 2019 Jul 12. Epub 2019 Jul 12.

Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, United Kingdom.

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http://dx.doi.org/10.1002/mds.27786DOI Listing
July 2019

Association of Genetic Risk for Rheumatoid Arthritis With Cognitive and Psychiatric Phenotypes Across Childhood and Adolescence.

JAMA Netw Open 2019 Jun 5;2(6):e196118. Epub 2019 Jun 5.

Division of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, United Kingdom.

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http://dx.doi.org/10.1001/jamanetworkopen.2019.6118DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593640PMC
June 2019

Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2.

Neurology 2018 06 11;90(23):e2059-e2067. Epub 2018 May 11.

From The Dalglish Family 22q Clinic for Adults and Department of Psychiatry (E.B., A.M.F., A.S.B.), Toronto General Research Institute (A.S.B.), and Division of Cardiology, Department of Medicine (A.S.B.), University Health Network, Toronto, Canada; De Hartekamp Groep (E.B.), Centre for People with Intellectual Disability, Haarlem; Department of Nuclear Medicine (E.B., J.B.), Academic Medical Center, Amsterdam, the Netherlands; Clinical Genetics Research Program and Campbell Family Mental Health Research Institute (N.J.B., A.M.F., A.S.B.), Centre for Addiction and Mental Health, Toronto; Institute of Medical Science (N.J.B., M.M., A.E.L., A.S.B.), Division of Neurology, Department of Medicine (C.M., M.M., A.E.L.), and Department of Psychiatry (A.S.B.), University of Toronto; Deer Lodge Movement Disorders Centre (S.U.); Section of Neurology (S.U.), Division of Internal Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg; Morton and Gloria Shulman Movement Disorders Centre and the Edmond J. Safra Program in Parkinson's Disease Research (C.M., A.E.L.), Toronto Western Hospital and University of Toronto, Canada; Department of Molecular Neuroscience (K.Y.M., N.W.W.), UCL Institute of Neurology, London, UK; Department of Neurology (S.K.), Kansai Medical University, Osaka, Japan; Department of Neurology (M.J.B.), University of Virginia School of Medicine, Charlottesville; Medical Genetics Unit (P.P.), Perugia University Hospital, Italy; Department of Neurology (B.D.B.), University of Colorado Anschutz Medical Campus, Aurora; Neurology Section (B.D.B.), VA Eastern Colorado Health Care System, Denver; Cognitive & Movement Disorders Clinic and Hurvitz Brain Sciences Research Program (M.M.), Sunnybrook Health Sciences Centre, Toronto, Canada; Departments of Clinical Neurosciences (Movement Disorders) (B.D.) and Genetics (Neurogenetics) (K.N.), Timone University Hospital (AP-HM), Provence-Alpes-Côte d'Azur; Aix-Marseille University (B.D., K.N.), Marseille; Department of Genetics (Neurogenetics) (P.C., A.J.), Pitié-Salpêtrière University Hospital; Sorbonne University (P.C., A.J.), Paris; Department of Neurosciences (Movement Disorders) (E.M.), Lille University Hospital; Lille University (E.M.); Department of Neurology (Movement Disorders) (T.D.), Pierre Wertheimer University Hospital, Lyon; Marc Jeannerod Center for Cognitive Neurosciences (T.D.), Lyon-1 University; Department of Neurology (Movement Disorders) and Clinical Investigation Center (Clinical and Experimental Neurosciences) (O.C.), Poitiers University Hospital; Department of Neurology (Movement Disorders) (S.D.), Rennes University Hospital; Rennes-1 University (S.D.); Department of Clinical Neurosciences (Movement Disorders) (M.B.), Nice University Hospital, France; Department of Psychiatry (A.M.F.), Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, the Netherlands; Center for Human Genetics (E.V., A.S., A.V.), University Hospital Leuven; Department of Human Genetics (A.S.), KU Leuven, Belgium; Department of Neurology (A.P.), University of Munich, Germany; Scientific and Technological Coordination Unit of the ANLIS Directorate (C.P.), National Administration of Laboratories and Institutes of Health, Argentina; Department of Neurodegenerative Diseases (T.G.), Center of Neurology and Hertie-Institute for Clinical Brain Research, University of Tübingen; German Center for Neurodegenerative Diseases (DZNE) (T.G.); Department of Neurology (K.C.), AZ Turnhout, Antwerp, Belgium; Neurology Unit and Stroke Center (F.B.), Hôpital Foch, Suresnes, France; Movement Disorder Division (K.M.), Johns Hopkins University, Baltimore, MD; and Psychological Medicine and Clinical Neurosciences (N.M.W.), MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff University, UK.

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http://dx.doi.org/10.1212/WNL.0000000000005660DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5993183PMC
June 2018

Establishing the role of rare coding variants in known Parkinson's disease risk loci.

Neurobiol Aging 2017 11 2;59:220.e11-220.e18. Epub 2017 Aug 2.

Centre for Genetic Epidemiology, Institute for Clinical Epidemiology and Applied Biometry, University of Tübingen, Tübingen, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2017.07.009DOI Listing
November 2017

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.

Authors:
Christian R Marshall Daniel P Howrigan Daniele Merico Bhooma Thiruvahindrapuram Wenting Wu Douglas S Greer Danny Antaki Aniket Shetty Peter A Holmans Dalila Pinto Madhusudan Gujral William M Brandler Dheeraj Malhotra Zhouzhi Wang Karin V Fuentes Fajarado Michelle S Maile Stephan Ripke Ingrid Agartz Margot Albus Madeline Alexander Farooq Amin Joshua Atkins Silviu A Bacanu Richard A Belliveau Sarah E Bergen Marcelo Bertalan Elizabeth Bevilacqua Tim B Bigdeli Donald W Black Richard Bruggeman Nancy G Buccola Randy L Buckner Brendan Bulik-Sullivan William Byerley Wiepke Cahn Guiqing Cai Murray J Cairns Dominique Campion Rita M Cantor Vaughan J Carr Noa Carrera Stanley V Catts Kimberley D Chambert Wei Cheng C Robert Cloninger David Cohen Paul Cormican Nick Craddock Benedicto Crespo-Facorro James J Crowley David Curtis Michael Davidson Kenneth L Davis Franziska Degenhardt Jurgen Del Favero Lynn E DeLisi Dimitris Dikeos Timothy Dinan Srdjan Djurovic Gary Donohoe Elodie Drapeau Jubao Duan Frank Dudbridge Peter Eichhammer Johan Eriksson Valentina Escott-Price Laurent Essioux Ayman H Fanous Kai-How Farh Martilias S Farrell Josef Frank Lude Franke Robert Freedman Nelson B Freimer Joseph I Friedman Andreas J Forstner Menachem Fromer Giulio Genovese Lyudmila Georgieva Elliot S Gershon Ina Giegling Paola Giusti-Rodríguez Stephanie Godard Jacqueline I Goldstein Jacob Gratten Lieuwe de Haan Marian L Hamshere Mark Hansen Thomas Hansen Vahram Haroutunian Annette M Hartmann Frans A Henskens Stefan Herms Joel N Hirschhorn Per Hoffmann Andrea Hofman Hailiang Huang Masashi Ikeda Inge Joa Anna K Kähler René S Kahn Luba Kalaydjieva Juha Karjalainen David Kavanagh Matthew C Keller Brian J Kelly James L Kennedy Yunjung Kim James A Knowles Bettina Konte Claudine Laurent Phil Lee S Hong Lee Sophie E Legge Bernard Lerer Deborah L Levy Kung-Yee Liang Jeffrey Lieberman Jouko Lönnqvist Carmel M Loughland Patrik K E Magnusson Brion S Maher Wolfgang Maier Jacques Mallet Manuel Mattheisen Morten Mattingsdal Robert W McCarley Colm McDonald Andrew M McIntosh Sandra Meier Carin J Meijer Ingrid Melle Raquelle I Mesholam-Gately Andres Metspalu Patricia T Michie Lili Milani Vihra Milanova Younes Mokrab Derek W Morris Bertram Müller-Myhsok Kieran C Murphy Robin M Murray Inez Myin-Germeys Igor Nenadic Deborah A Nertney Gerald Nestadt Kristin K Nicodemus Laura Nisenbaum Annelie Nordin Eadbhard O'Callaghan Colm O'Dushlaine Sang-Yun Oh Ann Olincy Line Olsen F Anthony O'Neill Jim Van Os Christos Pantelis George N Papadimitriou Elena Parkhomenko Michele T Pato Tiina Paunio Diana O Perkins Tune H Pers Olli Pietiläinen Jonathan Pimm Andrew J Pocklington John Powell Alkes Price Ann E Pulver Shaun M Purcell Digby Quested Henrik B Rasmussen Abraham Reichenberg Mark A Reimers Alexander L Richards Joshua L Roffman Panos Roussos Douglas M Ruderfer Veikko Salomaa Alan R Sanders Adam Savitz Ulrich Schall Thomas G Schulze Sibylle G Schwab Edward M Scolnick Rodney J Scott Larry J Seidman Jianxin Shi Jeremy M Silverman Jordan W Smoller Erik Söderman Chris C A Spencer Eli A Stahl Eric Strengman Jana Strohmaier T Scott Stroup Jaana Suvisaari Dragan M Svrakic Jin P Szatkiewicz Srinivas Thirumalai Paul A Tooney Juha Veijola Peter M Visscher John Waddington Dermot Walsh Bradley T Webb Mark Weiser Dieter B Wildenauer Nigel M Williams Stephanie Williams Stephanie H Witt Aaron R Wolen Brandon K Wormley Naomi R Wray Jing Qin Wu Clement C Zai Rolf Adolfsson Ole A Andreassen Douglas H R Blackwood Elvira Bramon Joseph D Buxbaum Sven Cichon David A Collier Aiden Corvin Mark J Daly Ariel Darvasi Enrico Domenici Tõnu Esko Pablo V Gejman Michael Gill Hugh Gurling Christina M Hultman Nakao Iwata Assen V Jablensky Erik G Jönsson Kenneth S Kendler George Kirov Jo Knight Douglas F Levinson Qingqin S Li Steven A McCarroll Andrew McQuillin Jennifer L Moran Bryan J Mowry Markus M Nöthen Roel A Ophoff Michael J Owen Aarno Palotie Carlos N Pato Tracey L Petryshen Danielle Posthuma Marcella Rietschel Brien P Riley Dan Rujescu Pamela Sklar David St Clair James T R Walters Thomas Werge Patrick F Sullivan Michael C O'Donovan Stephen W Scherer Benjamin M Neale Jonathan Sebat

Nat Genet 2017 01 21;49(1):27-35. Epub 2016 Nov 21.

Beyster Center for Psychiatric Genomics, University of California, San Diego, La Jolla, California, USA.

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http://dx.doi.org/10.1038/ng.3725DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5737772PMC
January 2017

Is the MC1R variant p.R160W associated with Parkinson's?

Ann Neurol 2016 Jan 12;79(1):159-61. Epub 2015 Dec 12.

Department of Clinical Neuroscience, Institute of Neurology, University College London, London, United Kingdom.

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http://dx.doi.org/10.1002/ana.24527DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4738170PMC
January 2016

Genetic risk and age in Parkinson's disease: Continuum not stratum.

Mov Disord 2015 May 17;30(6):850-4. Epub 2015 Mar 17.

Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.

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http://dx.doi.org/10.1002/mds.26192DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5217457PMC
May 2015

Polygenic risk of Parkinson disease is correlated with disease age at onset.

Ann Neurol 2015 Apr 13;77(4):582-91. Epub 2015 Mar 13.

Institute of Psychological Medicine and Clinical Neurosciences, Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Department of Psychological Medicine and Neurology, Cardiff University School of Medicine, Cardiff, United Kingdom.

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http://dx.doi.org/10.1002/ana.24335DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737223PMC
April 2015

Genome-wide association analysis identifies 13 new risk loci for schizophrenia.

Authors:
Stephan Ripke Colm O'Dushlaine Kimberly Chambert Jennifer L Moran Anna K Kähler Susanne Akterin Sarah E Bergen Ann L Collins James J Crowley Menachem Fromer Yunjung Kim Sang Hong Lee Patrik K E Magnusson Nick Sanchez Eli A Stahl Stephanie Williams Naomi R Wray Kai Xia Francesco Bettella Anders D Borglum Brendan K Bulik-Sullivan Paul Cormican Nick Craddock Christiaan de Leeuw Naser Durmishi Michael Gill Vera Golimbet Marian L Hamshere Peter Holmans David M Hougaard Kenneth S Kendler Kuang Lin Derek W Morris Ole Mors Preben B Mortensen Benjamin M Neale Francis A O'Neill Michael J Owen Milica Pejovic Milovancevic Danielle Posthuma John Powell Alexander L Richards Brien P Riley Douglas Ruderfer Dan Rujescu Engilbert Sigurdsson Teimuraz Silagadze August B Smit Hreinn Stefansson Stacy Steinberg Jaana Suvisaari Sarah Tosato Matthijs Verhage James T Walters Douglas F Levinson Pablo V Gejman Kenneth S Kendler Claudine Laurent Bryan J Mowry Michael C O'Donovan Michael J Owen Ann E Pulver Brien P Riley Sibylle G Schwab Dieter B Wildenauer Frank Dudbridge Peter Holmans Jianxin Shi Margot Albus Madeline Alexander Dominique Campion David Cohen Dimitris Dikeos Jubao Duan Peter Eichhammer Stephanie Godard Mark Hansen F Bernard Lerer Kung-Yee Liang Wolfgang Maier Jacques Mallet Deborah A Nertney Gerald Nestadt Nadine Norton Francis A O'Neill George N Papadimitriou Robert Ribble Alan R Sanders Jeremy M Silverman Dermot Walsh Nigel M Williams Brandon Wormley Maria J Arranz Steven Bakker Stephan Bender Elvira Bramon David Collier Benedicto Crespo-Facorro Jeremy Hall Conrad Iyegbe Assen Jablensky Rene S Kahn Luba Kalaydjieva Stephen Lawrie Cathryn M Lewis Kuang Lin Don H Linszen Ignacio Mata Andrew McIntosh Robin M Murray Roel A Ophoff John Powell Dan Rujescu Jim Van Os Muriel Walshe Matthias Weisbrod Durk Wiersma Peter Donnelly Ines Barroso Jenefer M Blackwell Elvira Bramon Matthew A Brown Juan P Casas Aiden P Corvin Panos Deloukas Audrey Duncanson Janusz Jankowski Hugh S Markus Christopher G Mathew Colin N A Palmer Robert Plomin Anna Rautanen Stephen J Sawcer Richard C Trembath Ananth C Viswanathan Nicholas W Wood Chris C A Spencer Gavin Band Céline Bellenguez Colin Freeman Garrett Hellenthal Eleni Giannoulatou Matti Pirinen Richard D Pearson Amy Strange Zhan Su Damjan Vukcevic Peter Donnelly Cordelia Langford Sarah E Hunt Sarah Edkins Rhian Gwilliam Hannah Blackburn Suzannah J Bumpstead Serge Dronov Matthew Gillman Emma Gray Naomi Hammond Alagurevathi Jayakumar Owen T McCann Jennifer Liddle Simon C Potter Radhi Ravindrarajah Michelle Ricketts Avazeh Tashakkori-Ghanbaria Matthew J Waller Paul Weston Sara Widaa Pamela Whittaker Ines Barroso Panos Deloukas Christopher G Mathew Jenefer M Blackwell Matthew A Brown Aiden P Corvin Mark I McCarthy Chris C A Spencer Elvira Bramon Aiden P Corvin Michael C O'Donovan Kari Stefansson Edward Scolnick Shaun Purcell Steven A McCarroll Pamela Sklar Christina M Hultman Patrick F Sullivan

Nat Genet 2013 Oct 25;45(10):1150-9. Epub 2013 Aug 25.

1] Analytical and Translational Genetics Unit, Massachusetts General Hospital, Boston, Massachusetts, USA. [2] Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA. [3].

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http://dx.doi.org/10.1038/ng.2742DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3827979PMC
October 2013

Recent advances in the genetics of the ALS-FTLD complex.

Curr Neurol Neurosci Rep 2012 Jun;12(3):243-50

MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff CF14 4XN, UK.

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http://dx.doi.org/10.1007/s11910-012-0268-5DOI Listing
June 2012

Phenotype evaluation and genomewide linkage study of clinical variables in schizophrenia.

Am J Med Genet B Neuropsychiatr Genet 2011 Dec 29;156B(8):929-40. Epub 2011 Sep 29.

MRC Centre for Neuropsychiatric Genetics and Genomics, Department of Psychological Medicine and Neurology, School of Medicine, Cardiff University, Heath Park, Cardiff, UK.

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http://dx.doi.org/10.1002/ajmg.b.31240DOI Listing
December 2011

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.

Neuron 2011 Oct 21;72(2):257-68. Epub 2011 Sep 21.

Neuromuscular Diseases Research Unit, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1016/j.neuron.2011.09.010DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200438PMC
October 2011

Molecular mechanisms in 22q11 deletion syndrome.

Authors:
Nigel M Williams

Schizophr Bull 2011 Sep;37(5):882-9

Department of Psychological Medicine and Neurology, MRC Centre in Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff, UK.

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http://dx.doi.org/10.1093/schbul/sbr095DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3160222PMC
September 2011

Experimental approaches for identifying schizophrenia risk genes.

Curr Top Behav Neurosci 2010 ;4:587-610

Department of Psychological Medicine and Neurology, MRC Centre in Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff, UK.

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March 2011

The genetic aetiology of late-onset chronic progressive cerebellar ataxia. A population-based study.

J Neurol 2009 Mar 6;256(3):343-8. Epub 2009 Mar 6.

Dept. of Neurology, Ophthalmology and Audiological Medicine, School of Medicine, Cardiff University, Heath Park, Cardiff, CF14 4XN, UK.

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http://link.springer.com/10.1007/s00415-009-0015-2
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http://dx.doi.org/10.1007/s00415-009-0015-2DOI Listing
March 2009

Analysis of copy number variation using quantitative interspecies competitive PCR.

Nucleic Acids Res 2008 Oct 12;36(17):e112. Epub 2008 Aug 12.

Department of Psychological Medicine, Wales School of Medicine, Cardiff University, Heath Park, Cardiff CF14 4XN, UK.

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http://nar.oxfordjournals.org/content/36/17/e112.full-text-l
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http://nar.oxfordjournals.org/lookup/doi/10.1093/nar/gkn495
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http://dx.doi.org/10.1093/nar/gkn495DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2553599PMC
October 2008

Support for neuregulin 1 as a susceptibility gene for bipolar disorder and schizophrenia.

Biol Psychiatry 2008 Sep 7;64(5):419-27. Epub 2008 May 7.

Department of Psychological Medicine, School of Medicine, Cardiff University, Heath Park, Cardiff CF14 4XN, United Kingdom.

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http://dx.doi.org/10.1016/j.biopsych.2008.03.025DOI Listing
September 2008

Gene copy number variation in schizophrenia.

Am J Med Genet B Neuropsychiatr Genet 2008 Jul;147B(5):606-11

Department of Psychological Medicine, School of Medicine, Cardiff University, Cardiff, UK.

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http://dx.doi.org/10.1002/ajmg.b.30645DOI Listing
July 2008

Cis- and trans- loci influence expression of the schizophrenia susceptibility gene DTNBP1.

Hum Mol Genet 2008 Apr 8;17(8):1169-74. Epub 2008 Jan 8.

Department of Psychological Medicine, School of Medicine, Cardiff University, Heath Park, Cardiff CF14 4XN, UK.

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https://academic.oup.com/hmg/article-lookup/doi/10.1093/hmg/
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http://dx.doi.org/10.1093/hmg/ddn006DOI Listing
April 2008

Strong evidence that GNB1L is associated with schizophrenia.

Hum Mol Genet 2008 Feb 13;17(4):555-66. Epub 2007 Nov 13.

Department of Psychological Medicine, Wales School of Medicine, Cardiff University, Heath Park, Cardiff CF14 4XN, UK.

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http://dx.doi.org/10.1093/hmg/ddm330DOI Listing
February 2008

Gene copy number variation in schizophrenia.

Schizophr Res 2007 Nov 7;96(1-3):93-9. Epub 2007 Sep 7.

Department of Psychological Medicine, School of Medicine, Cardiff University, Cardiff, CF14 4XN, UK.

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http://linkinghub.elsevier.com/retrieve/pii/S092099640700330
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http://dx.doi.org/10.1016/j.schres.2007.07.029DOI Listing
November 2007

Association analysis of AKT1 and schizophrenia in a UK case control sample.

Schizophr Res 2007 Jul 26;93(1-3):58-65. Epub 2007 Mar 26.

Department of Psychological Medicine, Wales School of Medicine, Henry Wellcome Building, Cardiff University, Heath Park, Cardiff CF14 4XN, UK.

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http://dx.doi.org/10.1016/j.schres.2007.02.006DOI Listing
July 2007

Chromosome 22 deletion syndrome and schizophrenia.

Int Rev Neurobiol 2006 ;73:1-27

Department of Psychological Medicine, Henry Wellcome Building for Biomedical Research, College of Medicine, Cardiff University, Cardiff, United Kingdom.

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http://dx.doi.org/10.1016/S0074-7742(06)73001-XDOI Listing
August 2006

Is the dysbindin gene (DTNBP1) a susceptibility gene for schizophrenia?

Schizophr Bull 2005 Oct 15;31(4):800-5. Epub 2005 Sep 15.

Department of Psychological Medicine, Cardiff University, UK.

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http://dx.doi.org/10.1093/schbul/sbi061DOI Listing
October 2005

No association between schizophrenia and polymorphisms in COMT in two large samples.

Am J Psychiatry 2005 Sep;162(9):1736-8

Department of Psychological Medicine, Henry Wellcome Building for Biomedical Research, Cardiff University, Heath Park, Cardiff, CF14 4XN, UK.

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http://dx.doi.org/10.1176/appi.ajp.162.9.1736DOI Listing
September 2005

Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression.

Hum Mol Genet 2005 Jul 25;14(14):1947-54. Epub 2005 May 25.

Department of Psychological Medicine, School of Medicine, Cardiff University, Heath Park, UK.

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http://academic.oup.com/hmg/article/14/14/1947/608349/Haplot
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http://dx.doi.org/10.1093/hmg/ddi199DOI Listing
July 2005

No evidence for association between polymorphisms in GRM3 and schizophrenia.

BMC Psychiatry 2005 May 13;5:23. Epub 2005 May 13.

Department of Psychological Medicine, Wales School of Medicine, Henry Wellcome Building, Cardiff University, Heath Park, Cardiff, UK.

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http://dx.doi.org/10.1186/1471-244X-5-23DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1142331PMC
May 2005

DNA pooling as a tool for large-scale association studies in complex traits.

Ann Med 2004 ;36(2):146-52

Department of Psychological Medicine, University of Wales College of Medicine, Cardiff, UK.

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August 2004

Genetic abnormalities of chromosome 22 and the development of psychosis.

Curr Psychiatry Rep 2004 Jun;6(3):176-82

Department of Psychological Medicine, Henry Wellcome Building for Biomedical Research, University of Wales College of Medicine, Cardiff CF14 4XN, Wales, UK.

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June 2004

Identification and analysis of the promoter region of the human hyaluronan synthase 2 gene.

J Biol Chem 2004 May 25;279(20):20576-81. Epub 2004 Feb 25.

Institute of Nephrology, University of Wales College of Medicine, Heath Park, Cardiff CF14 4XN, Wales, UK.

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http://dx.doi.org/10.1074/jbc.M312666200DOI Listing
May 2004

Dysbindin-1 and schizophrenia: from genetics to neuropathology.

J Clin Invest 2004 May;113(9):1255-7

Department of Psychological Medicine, University of Wales College of Medicine, Cardiff, United Kingdom.

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http://www.jci.org/articles/view/21470
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http://dx.doi.org/10.1172/JCI21470DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC398436PMC
May 2004

Recent advances in the genetics of schizophrenia.

Hum Mol Genet 2003 Oct 2;12 Spec No 2:R125-33. Epub 2003 Sep 2.

Department of Psychological Medicine, University of Wales College of Medicine, Cardiff,

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http://dx.doi.org/10.1093/hmg/ddg302DOI Listing
October 2003

The human hyaluronan synthase genes: genomic structures, proximal promoters and polymorphic microsatellite markers.

Int J Biochem Cell Biol 2003 Aug;35(8):1272-83

Institute of Nephrology, University of Wales College of Medicine, Heath Park, Cardiff CF14 4XN, UK.

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August 2003

A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain.

Am J Hum Genet 2003 Jul 11;73(1):152-61. Epub 2003 Jun 11.

Department of Psychological Medicine, University of Wales College of Medicine, Cardiff, CF14 4XN, Wales, UK.

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http://linkinghub.elsevier.com/retrieve/pii/S000292970763901
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1180576PMC
http://dx.doi.org/10.1086/376578DOI Listing
July 2003

Schizophrenia and functional polymorphisms in the MAOA and COMT genes: no evidence for association or epistasis.

Am J Med Genet 2002 Jul;114(5):491-6

Department of Psychological Medicine, University of Wales College of Medicine, Heath Park, Cardiff CF4 4XN, UK.

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http://doi.wiley.com/10.1002/ajmg.10517
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http://dx.doi.org/10.1002/ajmg.10517DOI Listing
July 2002

Genome scans and microarrays: converging on genes for schizophrenia?

Genome Biol 2002 27;3(4):REVIEWS1011. Epub 2002 Mar 27.

Department of Psychological Medicine, Neuropsychiatric Genetics Unit, University of Wales College of Medicine, Cardiff, CF14 4XN, UK.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC139350PMC
http://dx.doi.org/10.1186/gb-2002-3-4-reviews1011DOI Listing
June 2002

Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools.

Hum Genet 2002 May 23;110(5):471-8. Epub 2002 Mar 23.

Department of Psychological Medicine, University of Wales College of Medicine, Heath Park, Cardiff CF14 4XN, UK.

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http://dx.doi.org/10.1007/s00439-002-0706-6DOI Listing
May 2002