Inês Girão Meireles de Sousa


AuthID: R-000-MR3

Publicações a aguardar confirmação

1
TÍTULO: Ulcerative Colitis Is Under Dual (Mitochondrial and Nuclear) Genetic Control  Full Text
AUTORES: Alexandra Rosa; Patricia Abrantes; Ines Sousa; Vania Francisco; Patricia Santos; David Francisco; Joana M Xavier; Sofia A Oliveira;
PUBLICAÇÃO: 2016, FONTE: INFLAMMATORY BOWEL DISEASES, VOLUME: 22, NÚMERO: 4
INDEXADO EM: Scopus WOS CrossRef: 10
2
TÍTULO: Fourier modeling of the BOLD response to a breath-hold task: Optimization and reproducibility  Full Text
AUTORES: Joana Pinto; Joao Jorge; Ines Sousa; Pedro Vilela; Patricia Figueiredo;
PUBLICAÇÃO: 2016, FONTE: NEUROIMAGE, VOLUME: 135
INDEXADO EM: Scopus WOS CrossRef: 6
3
TÍTULO: Multicentric Genome-Wide Association Study for Primary Spontaneous Pneumothorax
AUTORES: Sousa, I; Abrantes, P; Francisco, V; Teixeira, G; Monteiro, M; Neves, J; Norte, A; Cordeiro, CR; Sa, JME; Reis, E; Santos, P; Oliveira, M; Sousa, S; Fradinho, M; Malheiro, F; Negrao, L; Feijo, S; Oliveira, SA;
PUBLICAÇÃO: 2016, FONTE: PLOS ONE, VOLUME: 11, NÚMERO: 5
INDEXADO EM: Scopus WOS CrossRef: 7 Handle
NO MEU: ORCID
4
5
TÍTULO: Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disorders  Full Text
AUTORES: Catarina T Correia; Ines C Conceicao; Barbara Oliveira; Joana Coelho; Ines Sousa; Ana F Sequeira; Joana Almeida; Catia Cafe; Frederico Duque; Susana Mouga; Wendy Roberts; Kun Gao; Jennifer K Lowe; Bhooma Thiruvahindrapuram; Susan Walker; Christian R Marshall; Dalila Pinto; John I Nurnberger; Stephen W Scherer; Daniel H Geschwind; Guiomar Oliveira; Astrid M Vicente; ...Mais
PUBLICAÇÃO: 2014, FONTE: MOLECULAR AUTISM, VOLUME: 5, NÚMERO: 1
INDEXADO EM: Scopus WOS CrossRef
6
TÍTULO: Pseudotumoral acute hemicerebellitis in a child  Full Text
AUTORES: Rita B Morais; Ines Sousa; Maria J Leiria; Conceicao Marques; Jose C Ferreira; Pedro Cabral;
PUBLICAÇÃO: 2013, FONTE: EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, VOLUME: 17, NÚMERO: 2
INDEXADO EM: Scopus WOS CrossRef
NO MEU: ORCID
7
TÍTULO: FUT2: Filling the gap between genes and environment in Behçet's disease?
AUTORES: Xavier, JM; Shahram, F; Sousa, I; Davatchi, F; Matos, M; Abdollahi, BS; Sobral, J; Nadji, A; Oliveira, M; Ghaderibarim, F; Shafiee, NM; Oliveira, SA;
PUBLICAÇÃO: 2013, FONTE: Annals of the Rheumatic Diseases, VOLUME: 74, NÚMERO: 3
INDEXADO EM: Scopus CrossRef
NO MEU: ORCID
8
TÍTULO: Individual common variants exert weak effects on the risk for autism spectrum disorderspi
AUTORES: Richard Anney; Lambertus Klei; Dalila Pinto; Joana Almeida; Elena Bacchelli; Gillian Baird; Nadia Bolshakova; Sven Boelte; Patrick F Bolton; Thomas Bourgeron; Sean Brennan; Jessica Brian; Jillian Casey; Judith Conroy; Catarina Correia; Christina Corsello; Emily L Crawford; Maretha de Jonge; Richard Delorme; Eftichia Duketis; Frederico Duque; Annette Estes; Penny Farrar; Bridget A Fernandez; Susan E Folstein; Eric Fombonne; John Gilbert; Christopher Gillberg; Joseph T Glessner; Andrew Green; Jonathan Green; Stephen J Guter; Elizabeth A Heron; Richard Holt; Jennifer L Howe; Gillian Hughes; Vanessa Hus; Roberta Igliozzi; Suma Jacob; Graham P Kenny; Cecilia Kim; Alexander Kolevzon; Vlad Kustanovich; Clara M Lajonchere; Janine A Lamb; Miriam Law Smith; Marion Leboyer; Ann Le Couteur; Bennett L Leventhal; Xiao Qing Liu; Frances Lombard; Catherine Lord; Linda Lotspeich; Sabata C Lund; Tiago R Magalhaes; Carine Mantoulan; Christopher J McDougle; Nadine M Melhem; Alison Merikangas; Nancy J Minshew; Ghazala K Mirza; Jeff Munson; Carolyn Noakes; Gudrun Nygren; Katerina Papanikolaou; Alistair T Pagnamenta; Barbara Parrini; Tara Paton; Andrew Pickles; David J Posey; Fritz Poustka; Jiannis Ragoussis; Regina Regan; Wendy Roberts; Kathryn Roeder; Bernadette Roge; Michael L Rutter; Sabine Schlitt; Naisha Shah; Val C Sheffield; Latha Soorya; Ines Sousa; Vera Stoppioni; Nuala Sykes; Raffaella Tancredi; Ann P Thompson; Susanne Thomson; Ana Tryfon; John Tsiantis; Herman Van Engeland; John B Vincent; Fred Volkmar; Vorstman, JAS; Simon Wallace; Kirsty Wing; Kerstin Wittemeyer; Shawn Wood; Danielle Zurawiecki; Lonnie Zwaigenbaum; Anthony J Bailey; Agatino Battaglia; Rita M Cantor; Hilary Coon; Michael L Cuccaro; Geraldine Dawson; Sean Ennis; Christine M Freitag; Daniel H Geschwind; Jonathan L Haines; Sabine M Klauck; William M McMahon; Elena Maestrini; Judith Miller; Anthony P Monaco; Stanley F Nelson; John I Nurnberger; Guiomar Oliveira; Jeremy R Parr; Margaret A Pericak Vance; Joseph Piven; Gerard D Schellenberg; StephenW. Scherer; Astrid M Vicente ; Thomas H Wassink; Ellen M Wijsman; Catalina Betancur; Joseph D Buxbaum; Edwin H Cook; Louise Gallagher; Michael Gill; Joachim Hallmayer; Andrew D Paterson; James S Sutcliffe; Peter Szatmari; Veronica J Vieland; Hakon Hakonarson; Bernie Devlin; ...Mais
PUBLICAÇÃO: 2012, FONTE: HUMAN MOLECULAR GENETICS, VOLUME: 21, NÚMERO: 21
INDEXADO EM: Scopus WOS CrossRef
NO MEU: ORCID
9
TÍTULO: A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder  Full Text
AUTORES: Jillian P Casey; Tiago Magalhaes; Judith M Conroy; Regina Regan; Naisha Shah; Richard Anney; Denis C Shields; Brett S Abrahams; Joana Almeida; Elena Bacchelli; Anthony J Bailey; Gillian Baird; Agatino Battaglia; Tom Berney; Nadia Bolshakova; Patrick F Bolton; Thomas Bourgeron; Sean Brennan; Phil Cali; Catarina Correia; Christina Corsello; Marc Coutanche; Geraldine Dawson; Maretha de Jonge; Richard Delorme; Eftichia Duketis; Frederico Duque; Annette Estes; Penny Farrar; Bridget A Fernandez; Susan E Folstein; Suzanne Foley; Eric Fombonne; Christine M Freitag; John Gilbert; Christopher Gillberg; Joseph T Glessner; Jonathan Green; Stephen J Guter; Hakon Hakonarson; Richard Holt; Gillian Hughes; Vanessa Hus; Roberta Igliozzi; Cecilia Kim; Sabine M Klauck; Alexander Kolevzon; Janine A Lamb; Marion Leboyer; Ann Le Couteur; Bennett L Leventhal; Catherine Lord; Sabata C Lund; Elena Maestrini; Carine Mantoulan; Christian R Marshall; Helen McConachie; Christopher J McDougle; Jane McGrath; William M McMahon; Alison Merikangas; Judith Miller; Fiorella Minopoli; Ghazala K Mirza; Jeff Munson; Stanley F Nelson; Gudrun Nygren; Guiomar Oliveira; Alistair T Pagnamenta; Katerina Papanikolaou; Jeremy R Parr; Barbara Parrini; Andrew Pickles; Dalila Pinto; Joseph Piven; David J Posey; Annemarie Poustka; Fritz Poustka; Jiannis Ragoussis; Bernadette Roge; Michael L Rutter; Ana F Sequeira; Latha Soorya; Ines Sousa; Nuala Sykes; Vera Stoppioni; Raffaella Tancredi; Maite Tauber; Ann P Thompson; Susanne Thomson; John Tsiantis; Herman Van Engeland; John B Vincent; Fred Volkmar; Jacob A S Vorstman; Simon Wallace; Kai Wang; Thomas H Wassink; Kathy White; Kirsty Wing; Kerstin Wittemeyer; Brian L Yaspan; Lonnie Zwaigenbaum; Catalina Betancur; Joseph D Buxbaum; Rita M Cantor; Edwin H Cook; Hilary Coon; Michael L Cuccaro; Daniel H Geschwind; Jonathan L Haines; Joachim Hallmayer; Anthony P Monaco; John I Nurnberger; Margaret A Pericak Vance; Gerard D Schellenberg; Stephen W Scherer; James S Sutcliffe; Peter Szatmari; Veronica J Vieland; Ellen M Wijsman; Andrew Green; Michael Gill; Louise Gallagher; Astrid Vicente ; Sean Ennis; ...Mais
PUBLICAÇÃO: 2012, FONTE: HUMAN GENETICS, VOLUME: 131, NÚMERO: 4
INDEXADO EM: Scopus WOS CrossRef
NO MEU: ORCID
10
TÍTULO: Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders  Full Text
AUTORES: Richard J L Anney; Elaine M Kenny; Colm O'Dushlaine; Brian L Yaspan; Elena Parkhomenka; Joseph D Buxbaum; James Sutcliffe; Michael Gill; Louise Gallagher; Anthony J Bailey§; Bridget A Fernandez; Peter Szatmari§; Stephen W Scherer§; Andrew Patterson§; Christian R Marshall; Dalila Pinto; John B Vincent; Eric Fombonne; Catalina Betancur§; Richard Delorme; Marion Leboyer; Thomas Bourgeron; Carine Mantoulan; Bernadette Roge; Maïté Tauber; Christine M Freitag§; Fritz Poustka; Eftichia Duketis; Sabine M Klauck§; Annemarie Poustka; Katerina Papanikolaou; John Tsiantis; Louise Gallagher§; Michael Gill§; Richard Anney; Nadia Bolshakova; Sean Brennan; Gillian Hughes; Jane McGrath; Alison Merikangas; Sean Ennis§; Andrew Green; Jillian P Casey; Judith M Conroy; Regina Regan; Naisha Shah; Elena Maestrini§; Elena Bacchelli; Fiorella Minopoli; Vera Stoppioni; Agatino Battaglia§; Roberta Igliozzi; Barbara Parrini; Raffaella Tancredi; Guiomar Oliveira§; Joana Almeida; Frederico Duque; Astrid Vicente§; Catarina Correia; Tiago R Magalhaes; Christopher Gillberg; Gudrun Nygren; Maretha de Jonge; Herman Van Engeland; Jacob AS Vorstman; Kerstin Wittemeyer; Gillian Baird; Patrick F Bolton; Michael L Rutter; Jonathan Green; Janine A Lamb; Andrew Pickles; Jeremy R Parr; Ann Le Couteur; Tom Berney; Helen McConachie; Simon Wallace; Marc Coutanche; Suzanne Foley; Kathy White; Anthony P Monaco§; Richard Holt; Penny Farrar; Alistair T Pagnamenta; Ghazala K Mirza; Jiannis Ragoussis; Inês Sousa; Nuala Sykes; Kirsty Wing; Joachim Hallmayer§; Rita M Cantor§; Stanley F Nelson; Daniel H Geschwind§; Brett S Abrahams; Fred Volkmar; Margaret A Pericak-Vance§; Michael L Cuccaro; John Gilbert; Edwin H Cook§; Stephen J Guter; Suma Jacob; John I Nurnberger Jr§; Christopher J McDougle; David J Posey; Catherine Lord; Christina Corsello; Vanessa Hus; Joseph D Buxbaum§; Alexander Kolevzon; Latha Soorya; Elena Parkhomenko; Bennett L Leventhal; Geraldine Dawson; Veronica J Vieland§; Hakon Hakonarson§; Joseph T Glessner; Cecilia Kim; Kai Wang; Gerard D Schellenberg§; Bernie Devlin§; Lamburtus Klei; Nancy Minshew; James S Sutcliffe§; Jonathan L Haines§; Sabata C Lund; Susanne Thomson; Brian L Yaspan; Hilary Coon§; Judith Miller; William M McMahon; Jeff Munson; Annette Estes; Ellen M Wijsman§; Joseph D Buxbaum; James Sutcliffe; Michael Gill; Louise Gallagher; ...Mais
PUBLICAÇÃO: 2011, FONTE: European Journal of Human Genetics, VOLUME: 19, NÚMERO: 10
INDEXADO EM: Scopus CrossRef
NO MEU: ORCID
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