J
James A. Knowles
Researcher at University of Southern California
Publications - 121
Citations - 26985
James A. Knowles is an academic researcher from University of Southern California. The author has contributed to research in topics: Genome-wide association study & Gene. The author has an hindex of 49, co-authored 111 publications receiving 22785 citations. Previous affiliations of James A. Knowles include Zilkha Neurogenetic Institute.
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Journal ArticleDOI
Genome-wide association study of Tourette's syndrome
Jeremiah M. Scharf,Jeremiah M. Scharf,Dongmei Yu,Carol A. Mathews,Benjamin M. Neale,Benjamin M. Neale,S. E. Stewart,S. E. Stewart,Jesen Fagerness,Patrick Evans,Eric R. Gamazon,Christopher K. Edlund,Anna Tikhomirov,Lisa Osiecki,Cornelia Illmann,Anna Pluzhnikov,Anuar Konkashbaev,Lea K. Davis,Buhm Han,Jacquelyn Crane,Priya Moorjani,Priya Moorjani,Andrew Crenshaw,Melissa Parkin,Victor I. Reus,Thomas L. Lowe,Martha Rangel-Lugo,Sylvain Chouinard,Yves Dion,Simon Girard,Danielle C. Cath,Danielle C. Cath,J.H. Smit,Robert A. King,Thomas V. Fernandez,James F. Leckman,Kenneth K. Kidd,J.R. Kidd,A.J. Pakstis,Matthew W. State,Luis Diego Herrera,Roxana Romero,Eduardo Fournier,Paul Sandor,Cathy L. Barr,N. Phan,Varda Gross-Tsur,Fortu Benarroch,Yehuda Pollak,Cathy L. Budman,Cathy L. Budman,Ruth D. Bruun,Ruth D. Bruun,Gerald Erenberg,Allan L. Naarden,P. C. Lee,Nicholas T. Weiss,Barbara Kremeyer,Barbara Kremeyer,Gabriel Bedoya Berrío,Desmond Campbell,Desmond Campbell,J. C. Cardona Silgado,William Cornejo Ochoa,S. C. Mesa Restrepo,H. Müller,A. V. Valencia Duarte,A. V. Valencia Duarte,Gholson J. Lyon,Gholson J. Lyon,Mark Leppert,Jubel Morgan,Robert B. Weiss,Marco A. Grados,K. Anderson,S. Davarya,Harvey S. Singer,John T. Walkup,Joseph Jankovic,Jay A. Tischfield,Gary A. Heiman,Donald L. Gilbert,Pieter J. Hoekstra,Pieter J. Hoekstra,Mary M. Robertson,Mary M. Robertson,R. Kurlan,Chunyu Liu,J. R. Gibbs,AB Singleton,John Hardy,Eric Strengman,Eric Strengman,Roel A. Ophoff,Roel A. Ophoff,Michael Wagner,Rainald Moessner,Daniel B. Mirel,Danielle Posthuma,Danielle Posthuma,Chiara Sabatti,Eskin E,David V. Conti,James A. Knowles,Andres Ruiz-Linares,Guy A. Rouleau,Shaun Purcell,Shaun Purcell,Shaun Purcell,Peter Heutink,Ben A. Oostra,William M. McMahon,Nelson B. Freimer,Nancy J. Cox,David L. Pauls +114 more
TL;DR: This study lays the groundwork for the eventual identification of common TS susceptibility variants in larger cohorts and helps to provide a more complete understanding of the full genetic architecture of this disorder.
Journal ArticleDOI
Evidence For Genetic Heterogeneity Between Clinical Subtypes of Bipolar Disorder
Alexander W. Charney,Douglas M. Ruderfer,Eli A. Stahl,Jennifer L. Moran,Kimberly Chambert,Richard A. Belliveau,Liz Forty,Katherine Gordon-Smith,A. Di Florio,A. Di Florio,Phil Lee,Phil Lee,Evelyn J. Bromet,Peter F. Buckley,Michael Escamilla,A. H. Fanous,A. H. Fanous,Laura J. Fochtmann,Douglas S. Lehrer,Dolores Malaspina,Stephen R. Marder,Christopher P. Morley,Humberto Nicolini,Diana O. Perkins,Jeffrey J. Rakofsky,Mark Hyman Rapaport,Helena Medeiros,Janet L. Sobell,Elaine K. Green,Lena Backlund,Sarah E. Bergen,Sarah E. Bergen,Anders Juréus,Martin Schalling,Paul Lichtenstein,Panos Roussos,James A. Knowles,Ian Jones,Lisa Jones,Christina M. Hultman,Christina M. Hultman,Roy H. Perlis,Shaun Purcell,Steven A. McCarroll,Steven A. McCarroll,Carlos N. Pato,M. T. Pato,Nicholas John Craddock,Mikael Landén,Mikael Landén,Jordan W. Smoller,Pamela Sklar +51 more
TL;DR: A large sample size allowed us to test the heritability and genetic correlation of BD subtypes and investigate their genetic overlap with schizophrenia and major depressive disorder, and results point to a partial difference in the genetic architecture ofBD subtypes as currently defined.
Journal ArticleDOI
Further development of YBOCS dimensions in the OCD Collaborative Genetics study: symptoms vs. categories.
Anthony Pinto,Benjamin D. Greenberg,Marco A. Grados,O. Joseph Bienvenu,Jack Samuels,Dennis L. Murphy,Gregor Hasler,Robert L. Stout,Scott L. Rauch,Yin Yao Shugart,David L. Pauls,James A. Knowles,Abby J. Fyer,James T. McCracken,John Piacentini,Ying Wang,Virginia L. Willour,Bernadette Cullen,Kung-Yee Liang,Rudolf Hoehn-Saric,Mark A. Riddle,Steven A. Rasmussen,Gerald Nestadt +22 more
TL;DR: In this paper, a five-factor structural model of OCD symptoms, including separate factor analyses employing individual symptoms and symptom categories, as well as sibling concordance, was presented.
Journal ArticleDOI
Hoarding in obsessive-compulsive disorder: clinical and genetic correlates.
Christine Lochner,Craig J. Kinnear,Sian M. J. Hemmings,Seller C,Dana J.H. Niehaus,James A. Knowles,Willie M. U. Daniels,Johanna C. Moolman-Smook,Soraya Seedat,Dan J. Stein +9 more
TL;DR: DNA extracted from venous blood in a Caucasian subset of the interviewed OCD patients was genotyped to investigate polymorphisms in genes involved in monoamine function and previously hypothesized to be relevant to OCD, consistent with the hypothesis that hoarding represents a unique symptom subtype in OCD with a distinctive clinical and psychobiological profile.
Journal ArticleDOI
Cross-disorder genome-wide analyses suggest a complex genetic relationship between tourette's syndrome and OCD
Dongmei Yu,Carol A. Mathews,Jeremiah M. Scharf,Benjamin M. Neale,Lea K. Davis,Eric R. Gamazon,Eske M. Derks,Patrick Evans,Christopher K. Edlund,Jacquelyn Crane,Jesen Fagerness,Lisa Osiecki,Patience J. Gallagher,Gloria Gerber,Stephen A. Haddad,Cornelia Illmann,Lauren M. McGrath,Catherine Mayerfeld,Sampath Arepalli,Cristina Barlassina,Cathy L. Barr,Laura Bellodi,Fortu Benarroch,Gabriel Bedoya Berrió,O. Joseph Bienvenu,Donald W. Black,Michael H. Bloch,Helena Brentani,Ruth D. Bruun,Ruth D. Bruun,Cathy L. Budman,Cathy L. Budman,Beatriz Camarena,Desmond Campbell,Carolina Cappi,Julio C. Cardona Silgado,Maria Cristina Cavallini,Denise A. Chavira,Sylvain Chouinard,Edwin H. Cook,M.R. Cookson,Vladimir Coric,Bernadette Cullen,Daniele Cusi,Richard Delorme,D. Denys,Yves Dion,Valsama Eapen,Karin Egberts,Peter Falkai,Thomas V. Fernandez,Eduardo Fournier,Helena Garrido,Daniel A. Geller,Donald L. Gilbert,Simon Girard,Hans Joergen Grabe,Marco A. Grados,Benjamin D. Greenberg,Varda Gross-Tsur,Edna Grünblatt,John Hardy,Gary A. Heiman,Sian M. J. Hemmings,Luis Diego Herrera,Dianne M. Hezel,Pieter J. Hoekstra,Joseph Jankovic,James L. Kennedy,Robert A. King,Anuar Konkashbaev,Barbara Kremeyer,R. Kurlan,Nuria Lanzagorta,Marion Leboyer,James F. Leckman,Leonhard Lennertz,Chunyu Liu,Christine Lochner,Thomas L. Lowe,Sara Lupoli,Fabio Macciardi,Wolfgang Maier,Paolo Manunta,Maurizio Marconi,James T. McCracken,Sandra Catalina Mesa Restrepo,Rainald Moessner,Priya Moorjani,Jubel Morgan,H. Müller,Dennis L. Murphy,Allan L. Naarden,Erika L. Nurmi,William Cornejo Ochoa,Roel A. Ophoff,Roel A. Ophoff,Andrew J. Pakstis,Michele T. Pato,Carlos N. Pato,John Piacentini,Christopher Pittenger,Yehuda Pollak,Scott L. Rauch,Tobias J. Renner,Victor I. Reus,Margaret A. Richter,Mark A. Riddle,Mary M. Robertson,Roxana Romero,Maria Conceição do Rosário,David R. Rosenberg,Stephan Ruhrmann,Chiara Sabatti,Erika Salvi,Aline S. Sampaio,Aline S. Sampaio,Jack Samuels,Paul Sandor,Brooke Sheppard,Harvey S. Singer,Jan Smit,Dan J. Stein,Eric Strengman,Jay A. Tischfield,Maurizio Turiel,Ana V. Valencia Duarte,Homero Vallada,Jeremy Veenstra-VanderWeele,Susanne Walitza,Susanne Walitza,Ying Wang,Michael E. Weale,Robert B. Weiss,Jens R. Wendland,H.G.M. Westenberg,Yin Yao Shugart,Ana Gabriela Hounie,Euripedes Constantino Miguel,Humberto Nicolini,Michael Wagner,Andres Ruiz-Linares,Danielle C. Cath,Danielle C. Cath,William M. McMahon,Danielle Posthuma,Danielle Posthuma,Ben A. Oostra,Gerald Nestadt,Guy A. Rouleau,Shaun Purcell,Shaun Purcell,Shaun Purcell,Michael A. Jenike,Peter Heutink,Peter Heutink,Gregory L. Hanna,David V. Conti,Paul D. Arnold,Nelson B. Freimer,S. Evelyn Stewart,S. Evelyn Stewart,James A. Knowles,Nancy J. Cox,David L. Pauls +164 more
TL;DR: The GWAS signals were enriched for SNPs strongly associated with variations in brain gene expression levels (expression quantitative loci, or eQTLs), suggesting the presence of true functional variants that contribute to risk of these disorders.