Inês Girão Meireles de Sousa


AuthID: R-000-MR3

Publicações a aguardar confirmação

11
TÍTULO: A genome-wide scan for common alleles affecting risk for autism
AUTORES: Richard Anney; Lambertus Klei; Dalila Pinto; Regina Regan; Judith Conroy; Tiago R Magalhaes; Catarina Correia; Brett S Abrahams; Nuala Sykes; Alistair T Pagnamenta; Joana Almeida; Elena Bacchelli; Anthony J Bailey; Gillian Baird; Agatino Battaglia; Tom Berney; Nadia Bolshakova; Sven Boelte; Patrick F Bolton; Thomas Bourgeron; Sean Brennan; Jessica Brian; Andrew R Carson; Guillermo Casallo; Jillian Casey; Su H Chu; Lynne Cochrane; Christina Corsello; Emily L Crawford; Andrew Crossett; Geraldine Dawson; Maretha de Jonge; Richard Delorme; Irene Drmic; Eftichia Duketis; Frederico Duque; Annette Estes; Penny Farrar; Bridget A Fernandez; Susan E Folstein; Eric Fombonne; Christine M Freitag; John Gilbert; Christopher Gillberg; Joseph T Glessner; Jeremy Goldberg; Jonathan Green; Stephen J Guter; Hakon Hakonarson; Elizabeth A Heron; Matthew Hill; Richard Holt; Jennifer L Howe; Gillian Hughes; Vanessa Hus; Roberta Igliozzi; Cecilia Kim; Sabine M Klauck; Alexander Kolevzon; Olena Korvatska; Vlad Kustanovich; Clara M Lajonchere; Janine A Lamb; Magdalena Laskawiec; Marion Leboyer; Ann Le Couteur; Bennett L Leventhal; Anath C Lionel; Xiao Qing Liu; Catherine Lord; Linda Lotspeich; Sabata C Lund; Elena Maestrini; William Mahoney; Carine Mantoulan; Christian R Marshall; Helen McConachie; Christopher J McDougle; Jane McGrath; William M McMahon; Nadine M Melhem; Alison Merikangas; Ohsuke Migita; Nancy J Minshew; Ghazala K Mirza; Jeff Munson; Stanley F Nelson; Carolyn Noakes; Abdul Noor; Gudrun Nygren; Guiomar Oliveira; Katerina Papanikolaou; Jeremy R Parr; Barbara Parrini; Tara Paton; Andrew Pickles; Joseph Piven; David J osey; Annemarie Poustka; Fritz Poustka; Aparna Prasad; Jiannis Ragoussis; Katy Renshaw; Jessica Rickaby; Wendy Roberts; Kathryn Roeder; Bernadette Roge; Michael L Rutter; Laura J Bierut; John P Rice; Jeff Salt; Katherine Sansom; Daisuke Sato; Ricardo Segurado; Lili Senman; Naisha Shah; Val C Sheffield; Latha Soorya; Ines Sousa; Vera Stoppioni; Christina Strawbridge; Raffaella Tancredi; Katherine Tansey; Bhooma Thiruvahindrapduram; Ann P Thompson; Susanne Thomson; Ana Tryfon; John Tsiantis; Herman Van Engeland; John B Vincent; Fred Volkmar; Simon Wallace; Kai Wang; Zhouzhi Z Wang; Thomas H Wassink; Kirsty Wing; Kerstin Wittemeyer; Shawn Wood; Brian L Yaspan; Danielle Zurawiecki; Lonnie Zwaigenbaum; Catalina Betancur; Joseph D Buxbaum; Rita M Cantor; Edwin H Cook; Hilary Coon; Michael L Cuccaro; Louise Gallagher; Daniel H Geschwind; Michael Gill; Jonathan L Haines; Judith Miller; Anthony P Monaco; John I Nurnberger; Andrew D Paterson; Margaret A Pericak Vance; Gerard D Schellenberg; Stephen W Scherer; James S Sutcliffe; Peter Szatmari; Astrid M Vicente ; Veronica J Vieland; Ellen M Wijsman; Bernie Devlin; Sean Ennis; Joachim Hallmayer; ...Mais
PUBLICAÇÃO: 2010, FONTE: HUMAN MOLECULAR GENETICS, VOLUME: 19, NÚMERO: 20
INDEXADO EM: Scopus WOS CrossRef
NO MEU: ORCID
12
TÍTULO: Increased BDNF levels and NTRK2 gene association suggest a disruption of BDNF/TrkB signaling in autism  Full Text
AUTORES: Correia, CT; Coutinho, AM; Sequeira, AF; Sousa, IG; Lourenco L O Venda; Almeida, JP; Abreu, RL; Lobo, C; Miguel, TS; Conroy, J; Cochrane, L; Gallagher, L; Gill, M; Ennis, S; Oliveira, GG ; Vicente, AM ;
PUBLICAÇÃO: 2010, FONTE: GENES BRAIN AND BEHAVIOR, VOLUME: 9, NÚMERO: 7
INDEXADO EM: Scopus WOS CrossRef: 82
NO MEU: ORCID
13
TÍTULO: Functional impact of global rare copy number variation in autism spectrum disorders  Full Text
AUTORES: Dalila Pinto; Alistair T Pagnamenta; Lambertus Klei; Richard Anney; Daniele Merico; Regina Regan; Judith Conroy; Tiago R Magalhaes; Catarina Correia; Brett S Abrahams; Joana Almeida; Elena Bacchelli; Gary D Bader; Anthony J Bailey; Gillian Baird; Agatino Battaglia; Tom Berney; Nadia Bolshakova; Sven Boelte; Patrick F Bolton; Thomas Bourgeron; Sean Brennan; Jessica Brian; Susan E Bryson; Andrew R Carson; Guillermo Casallo; Jillian Casey; Brian H Y Chung; Lynne Cochrane; Christina Corsello; Emily L Crawford; Andrew Crossett; Cheryl Cytrynbaum; Geraldine Dawson; Maretha de Jonge; Richard Delorme; Irene Drmic; Eftichia Duketis; Frederico Duque; Annette Estes; Penny Farrar; Bridget A Fernandez; Susan E Folstein; Eric Fombonne; Christine M Freitag; John Gilbert; Christopher Gillberg; Joseph T Glessner; Jeremy Goldberg; Andrew Green; Jonathan Green; Stephen J Guter; Hakon Hakonarson; Elizabeth A Heron; Matthew Hill; Richard Holt; Jennifer L Howe; Gillian Hughes; Vanessa Hus; Roberta Igliozzi; Cecilia Kim; Sabine M Klauck; Alexander Kolevzon; Olena Korvatska; Vlad Kustanovich; Clara M Lajonchere; Janine A Lamb; Magdalena Laskawiec; Marion Leboyer; Ann Le Couteur; Bennett L Leventhal; Anath C Lionel; Xiao Qing Liu; Catherine Lord; Linda Lotspeich; Sabata C Lund; Elena Maestrini; William Mahoney; Carine Mantoulan; Christian R Marshall; Helen McConachie; Christopher J McDougle; Jane McGrath; William M McMahon; Alison Merikangas; Ohsuke Migita; Nancy J Minshew; Ghazala K Mirza; Jeff Munson; Stanley F Nelson; Carolyn Noakes; Abdul Noor; Gudrun Nygren; Guiomar Oliveira; Katerina Papanikolaou; Jeremy R Parr; Barbara Parrini; Tara Paton; Andrew Pickles; Marion Pilorge; Joseph Piven; Chris P Ponting; David J Posey; Annemarie Poustka; Fritz Poustka; Aparna Prasad; Jiannis Ragoussis; Katy Renshaw; Jessica Rickaby; Wendy Roberts; Kathryn Roeder; Bernadette Roge; Michael L Rutter; Laura J Bierut; John P Rice; Jeff Salt; Katherine Sansom; Daisuke Sato; Ricardo Segurado; Ana F Sequeira; Lili Senman; Naisha Shah; Val C Sheffield; Latha Soorya; Ines Sousa; Olaf Stein; Nuala Sykes; Vera Stoppioni; Christina Strawbridge; Raffaella Tancredi; Katherine Tansey; Bhooma Thiruvahindrapduram; Ann P Thompson; Susanne Thomson; Ana Tryfon; John Tsiantis; Herman Van Engeland; John B Vincent; Fred Volkmar; Simon Wallace; Kai Wang; Zhouzhi Z Wang; Thomas H Wassink; Caleb Webber; Rosanna Weksberg; Kirsty Wing; Kerstin Wittemeyer; Shawn Wood; Jing Wu; Brian L Yaspan; Danielle Zurawiecki; Lonnie Zwaigenbaum; Joseph D Buxbaum; Rita M Cantor; Edwin H Cook; Hilary Coon; Michael L Cuccaro; Bernie Devlin; Sean Ennis; Louise Gallagher; Daniel H Geschwind; Michael Gill; Jonathan L Haines; Joachim Hallmayer; Judith Miller; Anthony P Monaco; John I Nurnberger; Andrew D Paterson; Margaret A Pericak Vance; Gerard D Schellenberg; Peter Szatmari; Astrid M Vicente ; Veronica J Vieland; Ellen M Wijsman; Stephen W Scherer; James S Sutcliffe; Catalina Betancur; ...Mais
PUBLICAÇÃO: 2010, FONTE: NATURE, VOLUME: 466, NÚMERO: 7304
INDEXADO EM: Scopus WOS CrossRef
NO MEU: ORCID
14
TÍTULO: Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry  Full Text
AUTORES: Sousa, I; Clark, T; Holt, R; Pagnamenta, A; Mulder, E; Minderaa, R; Bailey, A; Battaglia, A; Klauck, S; Poustka, F; Monaco, A;
PUBLICAÇÃO: 2010, FONTE: Molecular Autism, VOLUME: 1, NÚMERO: 1
INDEXADO EM: Scopus CrossRef
NO MEU: ORCID
15
TÍTULO: Linkage and candidate gene studies of autism spectrum disorders in European populations  Full Text
AUTORES: Holt, R; Barnby, G; Maestrini, E; Bacchelli, E; Brocklebank, D; Sousa, I; Mulder, EJ; Kantojarvi, K; Jarvela, I; Klauck, SM; Poustka, F; Bailey, AJ; Monaco, AP;
PUBLICAÇÃO: 2010, FONTE: European Journal of Human Genetics, VOLUME: 18, NÚMERO: 9
INDEXADO EM: Scopus CrossRef
NO MEU: ORCID
16
TÍTULO: High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility  Full Text
AUTORES: Maestrini, E; Pagnamenta, AT; Lamb, JA; Bacchelli, E; Sykes, NH; Sousa, I; Toma, C; Barnby, G; Butler, H; Winchester, L; Scerri, TS; Minopoli, F; Reichert, J; Cai, G; Buxbaum, JD; Korvatska, O; Schellenberg, GD; Dawson, G; Bildt, AD; Minderaa, RB; Mulder, EJ; Morris, AP; Bailey, AJ; Monaco, AP; ...Mais
PUBLICAÇÃO: 2010, FONTE: Molecular Psychiatry, VOLUME: 15, NÚMERO: 9
INDEXADO EM: Scopus CrossRef
NO MEU: ORCID
17
TÍTULO: Erratum: Linkage and candidate gene studies of autism spectrum disorders in European populations (European Journal of Human Genetics (2010) 18 (1013-10190) DOI: 10.1038/ejhg.2010.69)
AUTORES: Holt, R; Barnby, G; Maestrini, E; Bacchelli, E; Brocklebank, D; Sousa, I; Mulder, EJ; Kantojarvi, K; Jarvela, I; Klauck, SM; Poustka, F; Bailey, AJ; Monaco, AP;
PUBLICAÇÃO: 2010, FONTE: European Journal of Human Genetics, VOLUME: 18, NÚMERO: 9
INDEXADO EM: Scopus
18
TÍTULO: Corrigendum to: Linkage and candidate gene studies of autism spectrum disorders in European populations  Full Text
AUTORES: Richard Holt; Gabrielle Barnby; Elena Maestrini; Elena Bacchelli; Denise Brocklebank; Inês Sousa; Erik J Mulder; Katri Kantojärvi; Irma Järvelä; Sabine M Klauck; Fritz Poustka; Anthony J Bailey; Anthony P Monaco;
PUBLICAÇÃO: 2010, FONTE: Eur J Hum Genet - European Journal of Human Genetics, VOLUME: 18, NÚMERO: 9
INDEXADO EM: CrossRef
NO MEU: ORCID
19
TÍTULO: MET and autism susceptibility: Family and case-control studies  Full Text
AUTORES: Sousa, I; Clark, TG; Toma, C; Kobayashi, K; Choma, M; Holt, R; Sykes, NH; Lamb, JA; Bailey, AJ; Battaglia, A; Maestrini, E; Monaco, AP;
PUBLICAÇÃO: 2009, FONTE: European Journal of Human Genetics, VOLUME: 17, NÚMERO: 6
INDEXADO EM: Scopus CrossRef
NO MEU: ORCID
20
TÍTULO: Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection  Full Text
AUTORES: Sykes, NH; Toma, C; Wilson, N; Volpi, EV; Sousa, I; Pagnamenta, AT; Tancredi, R; Battaglia, A; Maestrini, E; Bailey, AJ; Monaco, AP;
PUBLICAÇÃO: 2009, FONTE: European Journal of Human Genetics, VOLUME: 17, NÚMERO: 10
INDEXADO EM: Scopus CrossRef
NO MEU: ORCID
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