H
Homero Vallada
Researcher at University of São Paulo
Publications - 196
Citations - 9178
Homero Vallada is an academic researcher from University of São Paulo. The author has contributed to research in topics: Population & Allele. The author has an hindex of 47, co-authored 188 publications receiving 8477 citations. Previous affiliations of Homero Vallada include King's College London.
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Journal ArticleDOI
The genome sequence of the plant pathogen Xylella fastidiosa
Andrew J. G. Simpson,Fernando C. Reinach,Paulo Arruda,F. A. Abreu,Marcio Luis Acencio,R. Alvarenga,Lucia Maria Carareto Alves,Jorge E. Araya,Gilson S. Baia,C. S. Baptista,Mario H. Barros,Eric D. Bonaccorsi,Silvana Bordin,Joseph M. Bové,Marcelo R.S. Briones,M. R.P. Bueno,Anamaria A. Camargo,Luis Eduardo Aranha Camargo,Dirce Maria Carraro,Helaine Carrer,N. B. Colauto,Carlos Augusto Colombo,Fernando Ferreira Costa,M. C. R. Costa,Claudio M. Costa-Neto,Luiz Lehmann Coutinho,M. Cristofani,Emmanuel Dias-Neto,C. Docena,Hamza El-Dorry,Agda Paula Facincani,Ari J. S. Ferreira,V. C.A. Ferreira,Jesus Aparecido Ferro,Jane Silveira Fraga,Suzelei C. França,Marília Caixeta Franco,Marcus Frohme,Luiz Roberto Furlan,M. Garnier,Gustavo H. Goldman,Maria Helena S. Goldman,Suely Lopes Gomes,Arthur Gruber,Paulo L. Ho,Joerg Hoheisel,M.L. Junqueira,Edson L. Kemper,João Paulo Kitajima,José Eduardo Krieger,Eiko E. Kuramae,F. Laigret,Marcio Rodrigues Lambais,Luciana C. C. Leite,Eliana Gertrudes de Macedo Lemos,Manoel Victor Franco Lemos,Silvio A. Lopes,Catalina Romero Lopes,J. A. Machado,Marco Antonio Machado,Alda Maria Backx Noronha Madeira,Humberto Maciel França Madeira,Humberto Maciel França Madeira,Celso Luis Marino,Marilis V. Marques,Elizabeth A. L. Martins,E. M.F. Martins,Adriana Yamaguti Matsukuma,Carlos Frederico Martins Menck,E. C. Miracca,Cristina Yumi Miyaki,Claudia Barros Monteiro-Vitorello,D. H. Moon,Maria Aparecida Nagai,Ana L. T. O. Nascimento,Luis Eduardo Soares Netto,A. Nhani,Francisco G. Nobrega,Francisco G. Nobrega,Luiz R. Nunes,Marcos Antonio de Oliveira,M. C. de Oliveira,R. C. de Oliveira,Darío Abel Palmieri,A. Paris,B. R. Peixoto,Gonçalo A.G. Pereira,H. A. Pereira,João Bosco Pesquero,Ronaldo Bento Quaggio,Patrícia G. Roberto,Vanderlei Rodrigues,Artur J.M. Rosa,V. E. de Rosa,R. G. de Sá,Roberto Vicente Santelli,H. E. Sawasaki,A.C.R. da Silva,A M da Silva,F. R. da Silva,Wilson A. Silva,J. F. da Silveira,M. L.Z. Silvestri,Walter José Siqueira,A. A. de Souza,A. P. de Souza,M. F. Terenzi,Daniela Truffi,Siu Mui Tsai,M. H. Tsuhako,Homero Vallada,M. A. Van Sluys,Sergio Verjovski-Almeida,André Luiz Vettore,Marco Antônio Zago,Mayana Zatz,João Meidanis,João C. Setubal +117 more
TL;DR: The complete genome sequence of X. fastidiosa clone 9a5c is reported, providing direct evidence of phage-mediated horizontal gene transfer and indicating that the molecular basis for bacterial pathogenicity is both conserved and independent of host.
Journal Article
A novel functional polymorphism within the promoter of the serotonin transporter gene: possible role in susceptibility to affective disorders
David A. Collier,Gerald Stöber,Tao Li,Armin Heils,Marco Catalano,D. Di Bella,Maria Arranz,Robin M. Murray,Homero Vallada,D. Bengel,Clemens R. Müller,G.W. Roberts,Enrico Smeraldi,George Kirov,Pak C. Sham,Klaus-Peter Lesch +15 more
TL;DR: It is suggested that 5-HTTLPR-dependent variation in functional 5- HTT expression is a potential genetic susceptibility factor for affective disorders.
Journal ArticleDOI
Revealing the complex genetic architecture of obsessive-compulsive disorder using meta-analysis
Paul D. Arnold,Kathleen D. Askland,Cristina Barlassina,Laura Bellodi,Oscar J. Bienvenu,Donald W. Black,Michael H. Bloch,Helena Brentani,Christie L. Burton,Beatriz Camarena,Carolina Cappi,Danielle C. Cath,Maria Cristina Cavallini,David V. Conti,Edwin H. Cook,Vladimir Coric,Bernadette Cullen,Danielle Cusi,Lea K. Davis,Richard Delorme,Damiaan Denys,Eske M. Derks,Valsamma Eapen,Christopher K. Edlund,Lauren Erdman,Peter Falkai,Martijn Figee,Abigail J. Fyer,Daniel A. Geller,Fernando S. Goes,Hans J. Grabe,M. A. Grados,Benjamin D. Greenberg,Edna Grünblatt,Wei Guo,Gregory L. Hanna,Sian M. J. Hemmings,Ana Gabriela Hounie,Michael Jenicke,Clare L. Keenan,James L. Kennedy,Ekaterina A. Khramtsova,Anuar Konkashbaev,James A. Knowles,Janice Krasnow,Cristophe Lange,Nuria Lanzagorta,Marion Leboyer,Leonhard Lennertz,Bingbin Li,K. Y. Liang,Christine Lochner,Fabio Macciardi,Brion S. Maher,Wolfgang Maier,Maurizio Marconi,Carol A. Mathews,Manuel Matthesien,James T. McCracken,Nicole C.R. McLaughlin,Euripedes Constantino Miguel,Rainald Moessner,Dennis L. Murphy,Benjamin M. Neale,Gerald Nestadt,Paul S. Nestadt,Humberto Nicolini,Ericka Nurmi,Lisa Osiecki,David L. Pauls,John Piacentini,Danielle Posthuma,Ann E. Pulver,H. D. Qin,Steven A. Rasmussen,Scott L. Rauch,Margaret A. Richter,Mark A. Riddle,Stephan Ripke,Stephan Ruhrmann,Aline S. Sampaio,Jack Samuels,Jeremiah M. Scharf,Yin Yao Shugart,Jan Smit,Dan J. Stein,S. Evelyn Stewart,Maurizio Turiel,Homero Vallada,Jeremy Veenstra-VanderWeele,Michael Wagner,Susanne Walitza,Yi Wang,Jens R. Wendland,Nienke Vulink,Dongmei Yu,Gwyneth Zai +96 more
TL;DR: A meta-analysis from two independent OCD consortia, investigating a total of 2688 individuals of European ancestry with OCD and 7037 genomically matched controls, concludes that the largest single OCD genome-wide study to date represents a major integrative step in elucidating the genetic causes of OCD.
Journal ArticleDOI
Partitioning the heritability of tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture
Lea K. Davis,Dongmei Yu,Clare L. Keenan,Eric R. Gamazon,Anuar Konkashbaev,Eske M. Derks,Benjamin M. Neale,Jian Yang,S. Hong Lee,Patrick Evans,Cathy L. Barr,Laura Bellodi,Fortu Benarroch,Gabriel Bedoya Berrío,Oscar J. Bienvenu,Michael H. Bloch,Rianne M. Blom,Ruth D. Bruun,Cathy L. Budman,Beatriz Camarena,Desmond Campbell,Carolina Cappi,Julio C. Cardona Silgado,Danielle C. Cath,Maria Cristina Cavallini,Denise A. Chavira,Sylvain Chouinard,David V. Conti,Edwin H. Cook,Vladimir Coric,Bernadette Cullen,Dieter Deforce,Richard Delorme,Yves Dion,Christopher K. Edlund,Karin Egberts,Peter Falkai,Thomas V. Fernandez,Patience J. Gallagher,Helena Garrido,Daniel A. Geller,Simon Girard,Hans J. Grabe,Marco A. Grados,Benjamin D. Greenberg,Varda Gross-Tsur,Stephen A. Haddad,Gary A. Heiman,Sian M. J. Hemmings,Ana Gabriela Hounie,Cornelia Illmann,Joseph Jankovic,Michael A. Jenike,James L. Kennedy,Robert A. King,Barbara Kremeyer,R. Kurlan,Nuria Lanzagorta,Marion Leboyer,James F. Leckman,Leonhard Lennertz,Chunyu Liu,Christine Lochner,Thomas L. Lowe,Fabio Macciardi,James T. McCracken,Lauren M. McGrath,Sandra Catalina Mesa Restrepo,Rainald Moessner,Jubel Morgan,H. Müller,Dennis L. Murphy,Allan L. Naarden,William Cornejo Ochoa,Roel A. Ophoff,Lisa Osiecki,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,Guy A. Rouleau,Stephan Ruhrmann,Andres Ruiz-Linares,Aline S. Sampaio,Jack Samuels,Paul Sandor,Brooke Sheppard,Harvey S. Singer,Jan Smit,Dan J. Stein,Eric Strengman,Jay A. Tischfield,Ana V. Valencia Duarte,Homero Vallada,Filip Van Nieuwerburgh,Jeremy Veenstra-VanderWeele,Susanne Walitza,Ying Wang,Jens R. Wendland,H.G.M. Westenberg,Yin Yao Shugart,Euripedes Constantino Miguel,William M. McMahon,Michael Wagner,Humberto Nicolini,Danielle Posthuma,Gregory L. Hanna,Peter Heutink,Damiaan Denys,Paul D. Arnold,Ben A. Oostra,Gerald Nestadt,Nelson B. Freimer,David L. Pauls,Naomi R. Wray,S. Evelyn Stewart,Carol A. Mathews,James A. Knowles,Nancy J. Cox,Jeremiah M. Scharf +130 more
TL;DR: The results indicate that there is some genetic overlap between these two phenotypically-related neuropsychiatric disorders, but suggest that the two disorders have distinct genetic architectures.
Journal ArticleDOI
Genome-wide association study of obsessive-compulsive disorder.
S. E. Stewart,Dongmei Yu,Jeremiah M. Scharf,Benjamin M. Neale,Jesen Fagerness,Carol A. Mathews,Paul D. Arnold,Patrick Evans,Eric R. Gamazon,Lisa Osiecki,Lauren M. McGrath,Stephen A. Haddad,Jacquelyn Crane,Dianne M. Hezel,C. Illman,C. Mayerfeld,Anuar Konkashbaev,Chunyu Liu,Anna Pluzhnikov,Anna Tikhomirov,Christopher K. Edlund,Scott L. Rauch,Rainald Moessner,Peter Falkai,W. Maier,Stephan Ruhrmann,Hans-Jörgen Grabe,Leonhard Lennertz,Michael Wagner,Laura Bellodi,Maria Cristina Cavallini,Margaret A. Richter,Edwin H. Cook,James L. Kennedy,D. Rosenberg,Dan J. Stein,Sian M. J. Hemmings,Christine Lochner,Amin Azzam,Denise A. Chavira,Eduardo Fournier,Helena Garrido,Brooke Sheppard,Paula Umaña,D. L. Murphy,Jens R. Wendland,Jeremy Veenstra-VanderWeele,Damiaan Denys,Rianne M. Blom,Dieter Deforce,F. Van Nieuwerburgh,H.G.M. Westenberg,Susanne Walitza,Karin Egberts,Tobias J. Renner,Euripedes Constantino Miguel,Carolina Cappi,Ana Gabriela Hounie,M Conceição do Rosário,Aline S. Sampaio,Homero Vallada,Humberto Nicolini,Nuria Lanzagorta,Beatriz Camarena,Richard Delorme,Marion Leboyer,Carlos N. Pato,Michele T. Pato,E. Voyiaziakis,Peter Heutink,Danielle C. Cath,Danielle Posthuma,J.H. Smit,Jack Samuels,Oscar J. Bienvenu,Bernadette Cullen,Abby J. Fyer,Marco A. Grados,Benjamin D. Greenberg,James T. McCracken,Mark A. Riddle,Youfa Wang,Vladimir Coric,James F. Leckman,Michael H. Bloch,Christopher Pittenger,Valsamma Eapen,Donald W. Black,Roel A. Ophoff,Eric Strengman,Daniele Cusi,Maurizio Turiel,Francesca Frau,Fabio Macciardi,J. R. Gibbs,Mark R. Cookson,Andrew B. Singleton,S. Arepalli,Allissa Dillman,L. Ferrucci,D. G. Hernandez,R. Johnson,Dan L. Longo,M. A. Nalls,Richard O'Brien,Bryan J. Traynor,Juan C. Troncoso,M. Van Der Brug,H. R. Zielke,Alan B. Zonderman,John Hardy,Andrew Crenshaw,Melissa Parkin,Daniel B. Mirel,David V. Conti,Shaun Purcell,Gerald Nestadt,Gregory L. Hanna,Michael A. Jenike,James A. Knowles,Nancy J. Cox,David L. Pauls,John Hardy,Mina Ryten,Colin Smith,Daniah Trabzuni,Robert Walker,Michael E. Weale +127 more
TL;DR: Although no SNPs were identified to be associated with OCD at a genome-wide significant level in the combined trio–case–control sample, a significant enrichment of methylation QTLs and frontal lobe expression quantitative trait loci (eQTLs) was observed within the top-ranked SNPs, suggesting these top signals may have a broad role in gene expression in the brain, and possibly in the etiology of OCD.