Matthew State

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Neonatal Tbr1 Dosage Controls Cortical Layer 6 Connectivity.

Neuron 2018 11 11;100(4):831-845.e7. Epub 2018 Oct 11.

Nina Ireland Laboratory of Developmental Neurobiology, Department of Psychiatry, and Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA 94143, USA; Department of Psychiatry, Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA 94143, USA. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S08966273183082
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http://dx.doi.org/10.1016/j.neuron.2018.09.027DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6250594PMC
November 2018

Lost in Translation: Traversing the Complex Path from Genomics to Therapeutics in Autism Spectrum Disorder.

Neuron 2018 10;100(2):406-423

Department of Psychiatry, Langley Porter Psychiatric Institute, Quantitative Biosciences Institute, Institute for Human Genetics, and Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA 94143, USA. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S08966273183090
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http://dx.doi.org/10.1016/j.neuron.2018.10.015DOI Listing
October 2018

Tourette disorder and other tic disorders.

Handb Clin Neurol 2018 ;147:343-354

Child Study Center, Yale School of Medicine, New Haven, CT, United States; Department of Psychiatry, Yale University, New Haven, CT, United States. Electronic address:

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http://dx.doi.org/10.1016/B978-0-444-63233-3.00023-3DOI Listing
July 2018

The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders.

Cell 2018 07;174(3):505-520

Quantitative Biosciences Institute (QBI), University of California, San Francisco, San Francisco, CA 94143, USA; Gladstone Institutes, San Francisco, CA 94158, USA; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA 94143, USA; Helen Diller Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA 94143, USA. Electronic address:

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http://dx.doi.org/10.1016/j.cell.2018.06.016DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6247911PMC
July 2018

De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.

Authors:
Sébastien Küry Geeske M van Woerden Thomas Besnard Martina Proietti Onori Xénia Latypova Meghan C Towne Megan T Cho Trine E Prescott Melissa A Ploeg Stephan Sanders Holly A F Stessman Aurora Pujol Ben Distel Laurie A Robak Jonathan A Bernstein Anne-Sophie Denommé-Pichon Gaëtan Lesca Elizabeth A Sellars Jonathan Berg Wilfrid Carré Øyvind Løvold Busk Bregje W M van Bon Jeff L Waugh Matthew Deardorff George E Hoganson Katherine B Bosanko Diana S Johnson Tabib Dabir Øystein Lunde Holla Ajoy Sarkar Kristian Tveten Julitta de Bellescize Geir J Braathen Paulien A Terhal Dorothy K Grange Arie van Haeringen Christina Lam Ghayda Mirzaa Jennifer Burton Elizabeth J Bhoj Jessica Douglas Avni B Santani Addie I Nesbitt Katherine L Helbig Marisa V Andrews Amber Begtrup Sha Tang Koen L I van Gassen Jane Juusola Kimberly Foss Gregory M Enns Ute Moog Katrin Hinderhofer Nagarajan Paramasivam Sharyn Lincoln Brandon H Kusako Pierre Lindenbaum Eric Charpentier Catherine B Nowak Elouan Cherot Thomas Simonet Claudia A L Ruivenkamp Sihoun Hahn Catherine A Brownstein Fan Xia Sébastien Schmitt Wallid Deb Dominique Bonneau Mathilde Nizon Delphine Quinquis Jamel Chelly Gabrielle Rudolf Damien Sanlaville Philippe Parent Brigitte Gilbert-Dussardier Annick Toutain Vernon R Sutton Jenny Thies Lisenka E L M Peart-Vissers Pierre Boisseau Marie Vincent Andreas M Grabrucker Christèle Dubourg Wen-Hann Tan Nienke E Verbeek Martin Granzow Gijs W E Santen Jay Shendure Bertrand Isidor Laurent Pasquier Richard Redon Yaping Yang Matthew W State Tjitske Kleefstra Benjamin Cogné Slavé Petrovski Kyle Retterer Evan E Eichler Jill A Rosenfeld Pankaj B Agrawal Stéphane Bézieau Sylvie Odent Ype Elgersma Sandra Mercier

Am J Hum Genet 2017 Nov;101(5):768-788

CHU Nantes, Service de Génétique Médicale, 9 quai Moncousu, 44093 Nantes Cedex 1, France.

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http://dx.doi.org/10.1016/j.ajhg.2017.10.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5673671PMC
November 2017

The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery.

Front Neurosci 2016 3;10:351. Epub 2016 Aug 3.

Department of Molecular Biology and Genetics, Democritus University of Thrace Alexandroupoli, Greece.

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http://dx.doi.org/10.3389/fnins.2016.00351DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4971013PMC
August 2016

Constance E. Lieber, Theodore R. Stanley, and the Enduring Impact of Philanthropy on Psychiatry Research.

Biol Psychiatry 2016 07;80(2):84-86

Department of Psychiatry, University Neuropsychiatric Institute, University of Utah Health Sciences Center, Salt Lake City, Utah.

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http://dx.doi.org/10.1016/j.biopsych.2016.05.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150945PMC
July 2016

The PsychENCODE project.

Nat Neurosci 2015 Dec;18(12):1707-12

Yale University, New Haven, Connecticut, USA.

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http://dx.doi.org/10.1038/nn.4156DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4675669PMC
December 2015

Gene hunting in autism spectrum disorder: on the path to precision medicine.

Lancet Neurol 2015 Nov 16;14(11):1109-20. Epub 2015 Apr 16.

Department of Psychiatry, Langley Porter Psychiatric Institute, University of California, San Francisco, CA, USA.

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http://dx.doi.org/10.1016/S1474-4422(15)00044-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4694565PMC
November 2015

Loss of δ-catenin function in severe autism.

Nature 2015 Apr 25;520(7545):51-6. Epub 2015 Mar 25.

1] Center for Complex Disease Genomics, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA [2] National Institute of Mental Health (NIMH) Autism Centers of Excellence (ACE) Genetics Consortium at the University of California, Los Angeles, Los Angeles, California 90095, USA.

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http://dx.doi.org/10.1038/nature14186DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4383723PMC
April 2015

The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment.

Nat Commun 2015 Mar 10;6:6404. Epub 2015 Mar 10.

1] Department of Genetics, Yale School of Medicine, 333 Cedar Street, New Haven, Connecticut 06510, USA [2] Kavli Institute for Neuroscience, Yale School of Medicine, PO Box 208001, New Haven, Connecticut 06520, USA.

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http://dx.doi.org/10.1038/ncomms7404DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4355952PMC
March 2015

The Tourette International Collaborative Genetics (TIC Genetics) study, finding the genes causing Tourette syndrome: objectives and methods.

Eur Child Adolesc Psychiatry 2015 Feb 26;24(2):141-51. Epub 2014 Apr 26.

Department of Psychiatry, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

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http://dx.doi.org/10.1007/s00787-014-0543-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4209328PMC
February 2015

Autism spectrum disorders: from genes to neurobiology.

Curr Opin Neurobiol 2015 Feb 28;30:92-9. Epub 2014 Nov 28.

Department of Psychiatry, University of California, San Francisco, San Francisco, California 94158, United States; Institute for Human Genetics, University of California, San Francisco, San Francisco, California 94143, United States. Electronic address:

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http://dx.doi.org/10.1016/j.conb.2014.10.015DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4586254PMC
February 2015

Leveraging genetics and genomics to define the causes of mental illness.

Biol Psychiatry 2015 Jan;77(1):3-5

UCLA Center for Autism Research and Treatment, University of California, Los Angeles, Los Angeles, California.. Electronic address:

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http://dx.doi.org/10.1016/j.biopsych.2014.11.003DOI Listing
January 2015

No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins.

PLoS Genet 2015 Jan 26;11(1):e1004852. Epub 2015 Jan 26.

Yale University Department of Genetics, New Haven, Connecticut, United States of America; Yale University Child Study Center, New Haven, Connecticut, United States of America; University of California, San Francisco, Department of Psychiatry, San Francisco, California, United States of America.

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http://dx.doi.org/10.1371/journal.pgen.1004852DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306541PMC
January 2015

Synaptic, transcriptional and chromatin genes disrupted in autism.

The Inheritance of Tourette Disorder: A review.

J Obsessive Compuls Relat Disord 2014 Oct;3(4):380-385

Department of Psychiatry, Harvard Medical School, Psychiatric and Neurodevelopmental Genetics Unit, Center for Human Genetic Research, Massachusetts General Hospital, Boston, MA 02114 ; Department of Neurology, Harvard Medical School, Psychiatric and Neurodevelopmental Genetics Unit, Center for Human Genetic Research, Massachusetts General Hospital, Boston, MA 02114.

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http://dx.doi.org/10.1016/j.jocrd.2014.06.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4260404PMC
October 2014

The developmental transcriptome of the human brain: implications for neurodevelopmental disorders.

Curr Opin Neurol 2014 Apr;27(2):149-56

aDepartment of Neurobiology and Kavli Institute for Neuroscience bDepartment of Genetics, Yale School of Medicine, New Haven, Connecticut, cDepartment of Psychiatry, University of California, San Francisco, San Francisco, California, USA.

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http://dx.doi.org/10.1097/WCO.0000000000000069DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4038354PMC
April 2014

Recent challenges to the psychiatric diagnostic nosology: a focus on the genetics and genomics of neurodevelopmental disorders.

Int J Epidemiol 2014 Apr 11;43(2):465-75. Epub 2014 Mar 11.

Yale Child Study Center, Yale University School of Medicine, New Haven, CT, USA, Nathan Kline Institute for Psychiatric Research, Orangeburg, New York, USA, Department of Psychiatry, Yonsei University College of Medicine, Seoul, South Korea and Department of Psychiatry, University of California, San Francisco, CA, USA.

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http://dx.doi.org/10.1093/ije/dyu037DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4047292PMC
April 2014

Psychiatric disorders: diagnosis to therapy.

Cell 2014 Mar;157(1):201-14

Department of Psychiatry and Langley Porter Psychiatric Institute, University of California, San Francisco, San Francisco, CA 94143, USA. Electronic address:

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http://dx.doi.org/10.1016/j.cell.2014.02.042DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4104191PMC
March 2014

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.

Authors:
S Hong Lee Stephan Ripke Benjamin M Neale Stephen V Faraone Shaun M Purcell Roy H Perlis Bryan J Mowry Anita Thapar Michael E Goddard John S Witte Devin Absher Ingrid Agartz Huda Akil Farooq Amin Ole A Andreassen Adebayo Anjorin Richard Anney Verneri Anttila Dan E Arking Philip Asherson Maria H Azevedo Lena Backlund Judith A Badner Anthony J Bailey Tobias Banaschewski Jack D Barchas Michael R Barnes Thomas B Barrett Nicholas Bass Agatino Battaglia Michael Bauer Mònica Bayés Frank Bellivier Sarah E Bergen Wade Berrettini Catalina Betancur Thomas Bettecken Joseph Biederman Elisabeth B Binder Donald W Black Douglas H R Blackwood Cinnamon S Bloss Michael Boehnke Dorret I Boomsma Gerome Breen René Breuer Richard Bruggeman Paul Cormican Nancy G Buccola Jan K Buitelaar William E Bunney Joseph D Buxbaum William F Byerley Enda M Byrne Sian Caesar Wiepke Cahn Rita M Cantor Miguel Casas Aravinda Chakravarti Kimberly Chambert Khalid Choudhury Sven Cichon C Robert Cloninger David A Collier Edwin H Cook Hilary Coon Bru Cormand Aiden Corvin William H Coryell David W Craig Ian W Craig Jennifer Crosbie Michael L Cuccaro David Curtis Darina Czamara Susmita Datta Geraldine Dawson Richard Day Eco J De Geus Franziska Degenhardt Srdjan Djurovic Gary J Donohoe Alysa E Doyle Jubao Duan Frank Dudbridge Eftichia Duketis Richard P Ebstein Howard J Edenberg Josephine Elia Sean Ennis Bruno Etain Ayman Fanous Anne E Farmer I Nicol Ferrier Matthew Flickinger Eric Fombonne Tatiana Foroud Josef Frank Barbara Franke Christine Fraser Robert Freedman Nelson B Freimer Christine M Freitag Marion Friedl Louise Frisén Louise Gallagher Pablo V Gejman Lyudmila Georgieva Elliot S Gershon Daniel H Geschwind Ina Giegling Michael Gill Scott D Gordon Katherine Gordon-Smith Elaine K Green Tiffany A Greenwood Dorothy E Grice Magdalena Gross Detelina Grozeva Weihua Guan Hugh Gurling Lieuwe De Haan Jonathan L Haines Hakon Hakonarson Joachim Hallmayer Steven P Hamilton Marian L Hamshere Thomas F Hansen Annette M Hartmann Martin Hautzinger Andrew C Heath Anjali K Henders Stefan Herms Ian B Hickie Maria Hipolito Susanne Hoefels Peter A Holmans Florian Holsboer Witte J Hoogendijk Jouke-Jan Hottenga Christina M Hultman Vanessa Hus Andrés Ingason Marcus Ising Stéphane Jamain Edward G Jones Ian Jones Lisa Jones Jung-Ying Tzeng Anna K Kähler René S Kahn Radhika Kandaswamy Matthew C Keller James L Kennedy Elaine Kenny Lindsey Kent Yunjung Kim George K Kirov Sabine M Klauck Lambertus Klei James A Knowles Martin A Kohli Daniel L Koller Bettina Konte Ania Korszun Lydia Krabbendam Robert Krasucki Jonna Kuntsi Phoenix Kwan Mikael Landén Niklas Långström Mark Lathrop Jacob Lawrence William B Lawson Marion Leboyer David H Ledbetter Phil H Lee Todd Lencz Klaus-Peter Lesch Douglas F Levinson Cathryn M Lewis Jun Li Paul Lichtenstein Jeffrey A Lieberman Dan-Yu Lin Don H Linszen Chunyu Liu Falk W Lohoff Sandra K Loo Catherine Lord Jennifer K Lowe Susanne Lucae Donald J MacIntyre Pamela A F Madden Elena Maestrini Patrik K E Magnusson Pamela B Mahon Wolfgang Maier Anil K Malhotra Shrikant M Mane Christa L Martin Nicholas G Martin Manuel Mattheisen Keith Matthews Morten Mattingsdal Steven A McCarroll Kevin A McGhee James J McGough Patrick J McGrath Peter McGuffin Melvin G McInnis Andrew McIntosh Rebecca McKinney Alan W McLean Francis J McMahon William M McMahon Andrew McQuillin Helena Medeiros Sarah E Medland Sandra Meier Ingrid Melle Fan Meng Jobst Meyer Christel M Middeldorp Lefkos Middleton Vihra Milanova Ana Miranda Anthony P Monaco Grant W Montgomery Jennifer L Moran Daniel Moreno-De-Luca Gunnar Morken Derek W Morris Eric M Morrow Valentina Moskvina Pierandrea Muglia Thomas W Mühleisen Walter J Muir Bertram Müller-Myhsok Michael Murtha Richard M Myers Inez Myin-Germeys Michael C Neale Stan F Nelson Caroline M Nievergelt Ivan Nikolov Vishwajit Nimgaonkar Willem A Nolen Markus M Nöthen John I Nurnberger Evaristus A Nwulia Dale R Nyholt Colm O'Dushlaine Robert D Oades Ann Olincy Guiomar Oliveira Line Olsen Roel A Ophoff Urban Osby Michael J Owen Aarno Palotie Jeremy R Parr Andrew D Paterson Carlos N Pato Michele T Pato Brenda W Penninx Michele L Pergadia Margaret A Pericak-Vance Benjamin S Pickard Jonathan Pimm Joseph Piven Danielle Posthuma James B Potash Fritz Poustka Peter Propping Vinay Puri Digby J Quested Emma M Quinn Josep Antoni Ramos-Quiroga Henrik B Rasmussen Soumya Raychaudhuri Karola Rehnström Andreas Reif Marta Ribasés John P Rice Marcella Rietschel Kathryn Roeder Herbert Roeyers Lizzy Rossin Aribert Rothenberger Guy Rouleau Douglas Ruderfer Dan Rujescu Alan R Sanders Stephan J Sanders Susan L Santangelo Joseph A Sergeant Russell Schachar Martin Schalling Alan F Schatzberg William A Scheftner Gerard D Schellenberg Stephen W Scherer Nicholas J Schork Thomas G Schulze Johannes Schumacher Markus Schwarz Edward Scolnick Laura J Scott Jianxin Shi Paul D Shilling Stanley I Shyn Jeremy M Silverman Susan L Slager Susan L Smalley Johannes H Smit Erin N Smith Edmund J S Sonuga-Barke David St Clair Matthew State Michael Steffens Hans-Christoph Steinhausen John S Strauss Jana Strohmaier T Scott Stroup James S Sutcliffe Peter Szatmari Szabocls Szelinger Srinivasa Thirumalai Robert C Thompson Alexandre A Todorov Federica Tozzi Jens Treutlein Manfred Uhr Edwin J C G van den Oord Gerard Van Grootheest Jim Van Os Astrid M Vicente Veronica J Vieland John B Vincent Peter M Visscher Christopher A Walsh Thomas H Wassink Stanley J Watson Myrna M Weissman Thomas Werge Thomas F Wienker Ellen M Wijsman Gonneke Willemsen Nigel Williams A Jeremy Willsey Stephanie H Witt Wei Xu Allan H Young Timothy W Yu Stanley Zammit Peter P Zandi Peng Zhang Frans G Zitman Sebastian Zöllner Bernie Devlin John R Kelsoe Pamela Sklar Mark J Daly Michael C O'Donovan Nicholas Craddock Patrick F Sullivan Jordan W Smoller Kenneth S Kendler Naomi R Wray

Nat Genet 2013 Sep 11;45(9):984-94. Epub 2013 Aug 11.

The University of Queensland, Queensland Brain Institute, Brisbane, Queensland, Australia.

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http://dx.doi.org/10.1038/ng.2711DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3800159PMC
September 2013

Mutations in DSTYK and dominant urinary tract malformations.

N Engl J Med 2013 Aug 17;369(7):621-9. Epub 2013 Jul 17.

Divisions of Nephrology (S.S.-C., R.V.S., N.P., K.E.B., S.N.N., B.J.P., P.L.W., M.V., F.L., R.S., N.P., N.K., K.K., Q.A.-A., A.G.G.) and Pediatric Nephrology (P.L.W.) and the Department of Pathology (V.D.D.), Columbia University, and the Department of Medicine, St. Luke's-Roosevelt Hospital Center (S.S.-C.), New York; the Department of Genetics, Howard Hughes Medical Institute, and Yale Center for Mendelian Genomics, Yale University, New Haven, CT (M.C., M.S., R.P.L.); the Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, South Korea (M.C.); the Division of Nephrology, Dialysis, and Transplantation (M.B., F.L., G.C., A.C., M.D., C.M., G.P., G.M.G.) and Laboratory of Molecular Genetics (G.S., R.R.), Istituto Giannina Gaslini, the Division of Nephrology, Department of Internal Medicine (M.B.), and Dipartimento di Neuroscienze, Riabilitazione, Oftalmologia, Genetica e Scienze Materno Infantili (R.R.), University of Genoa, and IRCCS San Martino-IST (M.B.), Genoa; Cattedra di Nefrologia, Università di Brescia, Seconda Divisione di Nefrologia Azienda Ospedaliera Spedali Civili di Brescia Presidio di Montichiari, Brescia (C.I., F.S.); the Department of Clinical Medicine, Nephrology, and Health Sciences, Unit of Nephrology, University of Parma, Parma (B.B., S.G., L.A.); the Department of Medical and Surgical Sciences, University of Foggia, Foggia (M.G.); the Department of Emergency and Organ Transplantation, University of Bari, Bari (L.G.); and the Division of Nephrology and Dialysis, Hospital of Alghero, Alghero (D.C.) - all in Italy; the Nephrology Division, Massachusetts General Hospital (Y.L., I.A.D.), and Department of Genetics, Harvard Medical School (I.A.D.), Charlestown, MA; University Children's Hospital, Medical School of Skopje, Skopje, Macedonia (V.J.L., N.R.-B., Z.G., V.T.); the Department of Medical Genetics, Poznan University of Medical Sciences, Poznan, Poland (A.M.-K., A.L.-B.); and the Department of Pediatrics, University Hospital of Split (D.K.V., M.S.), and the Department of Anatomy, Histology, and Embryology (K.V., M.S.-B.), School of Medicine (M.S.), University of Split, Split, Croatia.

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http://dx.doi.org/10.1056/NEJMoa1214479DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846391PMC
August 2013

Intellectual disability is associated with increased runs of homozygosity in simplex autism.

Am J Hum Genet 2013 Jul 3;93(1):103-9. Epub 2013 Jul 3.

Laboratory for Molecular Medicine, Department of Molecular Biology, Cell Biology, and Biochemistry, Brown University, 70 Ship Street, Providence, RI 02912, USA.

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http://dx.doi.org/10.1016/j.ajhg.2013.06.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3710760PMC
July 2013

Recent developments in the genetics of autism spectrum disorders.

Curr Opin Genet Dev 2013 Jun 25;23(3):310-5. Epub 2013 Mar 25.

Department of Genetics, Yale University School of Medicine, New Haven, CT 06510, United States.

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http://dx.doi.org/10.1016/j.gde.2013.02.003DOI Listing
June 2013

The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders.

Neuron 2012 Dec;76(6):1052-6

Seaver Autism Center, Departments of Psychiatry, Neuroscience, and Genetics and Genomic Sciences, and the Friedman Brain Institute, Mount Sinai School of Medicine, New York, NY 10029, USA.

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http://dx.doi.org/10.1016/j.neuron.2012.12.008DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3863639PMC
December 2012

Neuroscience. The emerging biology of autism spectrum disorders.

Science 2012 Sep;337(6100):1301-3

Child Study Center and Department of Psychiatry, Yale University School of Medicine, New Haven, CT 06510, USA.

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http://dx.doi.org/10.1126/science.1224989DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3657753PMC
September 2012

A complex chromosomal rearrangement involving chromosomes 2, 5, and X in autism spectrum disorder.

Am J Med Genet B Neuropsychiatr Genet 2012 Jul 16;159B(5):529-36. Epub 2012 May 16.

Departamento de Genética e Biologia Evolutiva, Centro de Estudos do Genoma Humano, Instituto de Biociências, Universidade de São Paulo, São Paulo, Brazil.

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http://dx.doi.org/10.1002/ajmg.b.32059DOI Listing
July 2012

The conundrums of understanding genetic risks for autism spectrum disorders.

Nat Neurosci 2011 Oct 30;14(12):1499-506. Epub 2011 Oct 30.

Program on Neurogenetics, Departments of Child Psychiatry, Psychiatry and Genetics, Yale University School of Medicine, New Haven, Connecticut, USA.

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http://dx.doi.org/10.1038/nn.2924DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3940335PMC
October 2011

The genetics of Tourette disorder.

Authors:
Matthew W State

Curr Opin Genet Dev 2011 Jun 27;21(3):302-9. Epub 2011 Jan 27.

Department of Child Psychiatry, Yale University School of Medicine, New Haven, CT 06520, United States.

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http://dx.doi.org/10.1016/j.gde.2011.01.007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3102152PMC
June 2011

Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.

Neuron 2011 Jun;70(5):863-85

Program on Neurogenetics, Yale University School of Medicine, 230 South Frontage Road, New Haven, CT 06520, USA.

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http://dx.doi.org/10.1016/j.neuron.2011.05.002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3939065PMC
June 2011

High levels of histidine decarboxylase in the striatum of mice and rats.

Neurosci Lett 2011 May 1;495(2):110-4. Epub 2011 Apr 1.

Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.

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http://dx.doi.org/10.1016/j.neulet.2011.03.050DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3081964PMC
May 2011

The erosion of phenotypic specificity in psychiatric genetics: emerging lessons from CNTNAP2.

Authors:
Matthew W State

Biol Psychiatry 2011 May;69(9):816-7

Department of Psychiatry, Yale University School of Medicine, New Haven, Connecticut 06520, USA.

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http://dx.doi.org/10.1016/j.biopsych.2011.03.021DOI Listing
May 2011

Recent advances in Tourette syndrome.

Curr Opin Neurol 2011 Apr;24(2):119-25

Department of Psychiatry and the Child Study Center, Yale University School of Medicine, New Haven, Connecticut, USA.

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http://dx.doi.org/10.1097/WCO.0b013e328344648cDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4065550PMC
April 2011

The genetics of child psychiatric disorders: focus on autism and Tourette syndrome.

Authors:
Matthew W State

Neuron 2010 Oct;68(2):254-69

Department of Child Psychiatry, Yale University School of Medicine, New Haven, CT 06510, USA.

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http://linkinghub.elsevier.com/retrieve/pii/S089662731000828
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http://dx.doi.org/10.1016/j.neuron.2010.10.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3292208PMC
October 2010

Progress in cytogenetics: implications for child psychopathology.

J Am Acad Child Adolesc Psychiatry 2010 Aug 26;49(8):736-51; quiz 856-7. Epub 2010 May 26.

Program on Neurogenetics, Child Study Center, and Yale University School of Medicine, New Haven, CT 06520-7900, USA.

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http://dx.doi.org/10.1016/j.jaac.2010.03.016DOI Listing
August 2010

Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophy.

Neurogenetics 2010 Jul 15;11(3):319-25. Epub 2010 Jan 15.

Department of Neurosurgery, Neurobiology, Program on Neurogenetics Yale University School of Medicine, New Haven, CT, USA.

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http://dx.doi.org/10.1007/s10048-009-0232-yDOI Listing
July 2010

Another piece of the autism puzzle.

Authors:
Matthew W State

Nat Genet 2010 Jun;42(6):478-9

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http://dx.doi.org/10.1038/ng0610-478DOI Listing
June 2010

The genetics of autism: key issues, recent findings, and clinical implications.

Psychiatr Clin North Am 2010 Mar;33(1):83-105

Child Study Center, Yale University School of Medicine, New Haven, CT 06520, USA.

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http://dx.doi.org/10.1016/j.psc.2009.12.002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2841771PMC
March 2010

Autism and autism spectrum disorders: diagnostic issues for the coming decade.

J Child Psychol Psychiatry 2009 Jan;50(1-2):108-15

Child Study Center, Yale University, New Haven, CT 06520-7900, USA.

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http://dx.doi.org/10.1111/j.1469-7610.2008.02010.xDOI Listing
January 2009

Haplotype evolution of SLITRK1, a candidate gene for Gilles de la Tourette syndrome.

Am J Med Genet B Neuropsychiatr Genet 2008 Jun;147B(4):463-6

Department of Genetics, Yale University School of Medicine, New Haven, CT 06520-8005, USA.

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http://dx.doi.org/10.1002/ajmg.b.30641DOI Listing
June 2008

Autism genetics: strategies, challenges, and opportunities.

Autism Res 2008 Feb;1(1):4-17

Department of Genetics, Yale University School of Medicine, New Haven, Connecticut 06520, USA.

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http://dx.doi.org/10.1002/aur.3DOI Listing
February 2008

Mapping autism risk loci using genetic linkage and chromosomal rearrangements.

Authors:
Peter Szatmari Andrew D Paterson Lonnie Zwaigenbaum Wendy Roberts Jessica Brian Xiao-Qing Liu John B Vincent Jennifer L Skaug Ann P Thompson Lili Senman Lars Feuk Cheng Qian Susan E Bryson Marshall B Jones Christian R Marshall Stephen W Scherer Veronica J Vieland Christopher Bartlett La Vonne Mangin Rhinda Goedken Alberto Segre Margaret A Pericak-Vance Michael L Cuccaro John R Gilbert Harry H Wright Ruth K Abramson Catalina Betancur Thomas Bourgeron Christopher Gillberg Marion Leboyer Joseph D Buxbaum Kenneth L Davis Eric Hollander Jeremy M Silverman Joachim Hallmayer Linda Lotspeich James S Sutcliffe Jonathan L Haines Susan E Folstein Joseph Piven Thomas H Wassink Val Sheffield Daniel H Geschwind Maja Bucan W Ted Brown Rita M Cantor John N Constantino T Conrad Gilliam Martha Herbert Clara Lajonchere David H Ledbetter Christa Lese-Martin Janet Miller Stan Nelson Carol A Samango-Sprouse Sarah Spence Matthew State Rudolph E Tanzi Hilary Coon Geraldine Dawson Bernie Devlin Annette Estes Pamela Flodman Lambertus Klei William M McMahon Nancy Minshew Jeff Munson Elena Korvatska Patricia M Rodier Gerard D Schellenberg Moyra Smith M Anne Spence Chris Stodgell Ping Guo Tepper Ellen M Wijsman Chang-En Yu Bernadette Rogé Carine Mantoulan Kerstin Wittemeyer Annemarie Poustka Bärbel Felder Sabine M Klauck Claudia Schuster Fritz Poustka Sven Bölte Sabine Feineis-Matthews Evelyn Herbrecht Gabi Schmötzer John Tsiantis Katerina Papanikolaou Elena Maestrini Elena Bacchelli Francesca Blasi Simona Carone Claudio Toma Herman Van Engeland Maretha de Jonge Chantal Kemner Frederieke Koop Frederike Koop Marjolein Langemeijer Marjolijn Langemeijer Channa Hijmans Channa Hijimans Wouter G Staal Gillian Baird Patrick F Bolton Michael L Rutter Emma Weisblatt Jonathan Green Catherine Aldred Julie-Anne Wilkinson Andrew Pickles Ann Le Couteur Tom Berney Helen McConachie Anthony J Bailey Kostas Francis Gemma Honeyman Aislinn Hutchinson Jeremy R Parr Simon Wallace Anthony P Monaco Gabrielle Barnby Kazuhiro Kobayashi Janine A Lamb Ines Sousa Nuala Sykes Edwin H Cook Stephen J Guter Bennett L Leventhal Jeff Salt Catherine Lord Christina Corsello Vanessa Hus Daniel E Weeks Fred Volkmar Maïté Tauber Eric Fombonne Andy Shih Kacie J Meyer

Nat Genet 2007 Mar 18;39(3):319-28. Epub 2007 Feb 18.

Department of Psychiatry and Behavioural Neurosciences, McMaster University, Hamilton, Ontario L8N 3Z5, Canada.

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http://dx.doi.org/10.1038/ng1985DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867008PMC
March 2007

Recent advances in the genetics of autism.

Biol Psychiatry 2007 Feb 25;61(4):429-37. Epub 2006 Sep 25.

Child Study Center, Yale University School of Medicine, New Haven, Connecticut, USA.

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http://dx.doi.org/10.1016/j.biopsych.2006.06.020DOI Listing
February 2007

A surprising METamorphosis: autism genetics finds a common functional variant.

Authors:
Matthew W State

Proc Natl Acad Sci U S A 2006 Nov 30;103(45):16621-2. Epub 2006 Oct 30.

Program on Neurogenetics, Departments of Child Psychiatry and Genetics, Yale University School of Medicine, 230 South Frontage Road, New Haven, CT 06520, USA.

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http://dx.doi.org/10.1073/pnas.0608027103DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1636504PMC
November 2006

[Autism: genetics].

Braz J Psychiatry 2006 May 12;28 Suppl 1:S29-38. Epub 2006 Jun 12.

Child Study Center, Yale University School of Medicine, New Haven, CT 06520, USA.

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http://dx.doi.org//S1516-44462006000500005DOI Listing
May 2006