Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Inês C. Conceição"'
Autor:
Marina Fuertes, Inês C Conceição, J. L. Gonçalves, Anabela Faria, Francisco Dionisio, Pedro Lopes-dos-Santos
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
CIÊNCIAVITAE
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
CIÊNCIAVITAE
Submitted by Francisco Dionísio (fadionisio@fc.ul.pt) on 2021-12-09T18:47:20Z No. of bitstreams: 1 Fuertes et al_corrected.pdf: 526351 bytes, checksum: 6302806b45baa910cacfa4760636fc0f (MD5) Approved for entry into archive by Margarida Matos (mmmato
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3167ba463e8802bea5bbc7b649900fd
Publikováno v:
PLoS ONE, Vol 6, Iss 8, p e23778 (2011)
BACKGROUND: Analysis of genomic sequence allows characterization of genome content and organization, and access beyond gene-coding regions for identification of functional elements. BAC libraries, where relatively large genomic regions are made readi
Externí odkaz:
https://doaj.org/article/3f9b6312d90741779d78615de7b99a9f
Autor:
Inês C Conceição, Montserrat Aguadé
Publikováno v:
PLoS ONE, Vol 5, Iss 10, p e13389 (2010)
BACKGROUND: In insects, like in most invertebrates, olfaction is the principal sensory modality, which provides animals with essential information for survival and reproduction. Odorant receptors are involved in this response, mediating interactions
Externí odkaz:
https://doaj.org/article/6a733946164248d4a3b29884696cab21
Autor:
Maria M. Rama, Frederico Duque, Susana Mouga, Cátia Café, Joana Almeida, Bárbara Oliveira, Astrid M. Vicente, Inês C. Conceição, Guiomar Oliveira
Publikováno v:
Psychiatric Genetics. 27:54-61
Objective: The PARK2 gene encodes Parkin, a component of a multiprotein E3 ubiquitin ligase complex that targets substrate proteins for proteasomal degradation. PARK2 mutations are frequently associated with Parkinson’s disease, but structural alte
Autor:
Geraldine Dawson, Sven Sandin, Frederico Duque, Peter Holmans, Marion Leboyer, Aarno Palotie, Fritz Poustka, Richard Delorme, Stephen Sanders, Alistair T. Pagnamenta, Lonnie Zwaigenbaum, Bridget A. Fernandez, A. Jeremy Willsey, Christine M. Freitag, Christa Lese Martin, Elena Maestrini, Elena Bacchelli, Guiomar Oliveira, Jeremy R. Parr, Guy A. Rouleau, Jonas Bybjerg-Grauholm, Joseph Piven, Latha Soorya, Lauren A. Weiss, Jonathan Green, Carsten Bøcker Pedersen, Louise Gallagher, Regina Regan, Stephan Ripke, Thomas Werge, Pat Levitt, Aravinda Chakravarti, Joana Almeida, Kathryn Roeder, Catalina Betancur, Bernie Devlin, Benjamin M. Neale, Gillian Baird, Jakob Grove, Thomas Bourgeron, David H. Ledbetter, Eftichia Duketis, Karola Rehnström, Gerard D. Schellenberg, Jillian P. Casey, Preben Bo Mortensen, Patrick Bolton, Igor Martsenkovsky, Elise Robinson, Hakon Hakonarson, Vanessa H. Bal, Stacy Steinberg, Christopher Gillberg, Kathryn Tsang, Jacob A. S. Vorstman, Verneri Anttila, Suma Jacob, Judith Conroy, J. Haines, William M. McMahon, Edwin H. Cook, Ann P. Thompson, Inês C. Conceição, Mark J. Daly, Arthur P. Goldberg, Sarah E. Medland, Milica Pejovic-Milovancevic, David M. Hougaard, Shrikant Mane, Christina M. Hultman, Susana Mouga, Hreinn Stefansson, Ellen M. Wijsman, Andreas G. Chiocchetti, Ole Mors, Phil Lee, Richard Anney, Astrid M. Vicente, Veronica J. Vieland, K. Stefansson, Stephen W. Scherer, Teimuraz Silagadze, Pall Magnusson, Donna M. Martin, Merete Nordentoft, Peter Szatmari, Patrícia B. S. Celestino-Soper, Ann S Le-Couteur, Cátia Café, Arthur L. Beaudet, Kerstin Wittemeyer, Anders D. Børglum, Joel S. Bader, Christopher S. Poultney, Hailiang Huang, Alexander Kolevzon, Margaret A. Pericak-Vance, Joachim Hallmayer, Rita M. Cantor, Eric Fombonne, Andrew Green, Dan E. Arking, M. Daniele Fallin, Matthew W. State, Christine Ladd-Acosta, Silvia Derubeis, Raphael Bernier, Regina Waltes, David G. Amaral, Manuel Mattheisen, Abraham Reichenberg, Lambertus Klei, Daniel Moreno-De-Luca, Marie Bækvad-Hansen, Maretha V. Dejonge, Susan G. McGrew, Joseph D. Buxbaum, Hilary Coon, Jennifer Reichert, Michael Gill, Herman Vanengeland, Christine Søholm Hansen, Anthony P. Monaco, Nadia Bolshakova, John I. Nurnberger, Nancy J. Minshew, Michael T. Murtha, Thomas H. Wassink, Evald Saemundsen, Simon Wallace, Sean Brennan, Sean Ennis, A. Gulhan Ercan-Sencicek, Sven Bölte, Oscar Svantesson, Susan L. Santangelo, Andrew D. Paterson, Robert L. Hendren, Timothy W. Yu, Dalila Pinto, D.E. Grice, Alison Merikangas, Stephen J. Guter, Anthony J. Bailey, Bernadette Rogé, Christopher A. Walsh, Susan E. Folstein, Wendy Roberts, Sabine M. Klauck, Marianne Giørtz Pedersen, Tiago R. Magalhaes, John R. Gilbert, Irva Hertz-Picciotto, James S. Sutcliffe, Evdokia Anagnostou, Catarina Correia, Eric M. Morrow, Daniel H. Geschwind, Jennifer K. Lowe, Agatino Battaglia, Bozenna Iliadou, Michael L. Cuccaro, Catherine Lord
Publikováno v:
Molecular Autism
Molecular Autism, BioMed Central, 2017, 8, pp.21. ⟨10.1186/s13229-017-0137-9⟩
Anney, R J L, Ripke, S, Anttila, V, Grove, J, Holmans, P, Huang, H, Klei, L, Lee, P H, Medland, S E, Neale, B, Robinson, E, Weiss, L A, Zwaigenbaum, L, Yu, T W, Wittemeyer, K, Willsey, A J, Wijsman, E M, Werge, T, Wassink, T H, Waltes, R, Walsh, C A, Wallace, S, Vorstman, J A S, Vieland, V J, Vicente, A M, Vanengeland, H, Tsang, K, Thompson, A P, Szatmari, P, Svantesson, O, Steinberg, S, Stefansson, K, Stefansson, H, State, M W, Soorya, L, Silagadze, T, Scherer, S W, Schellenberg, G D, Sandin, S, Sanders, S J, Saemundsen, E, Rouleau, G A, Rogé, B, Roeder, K, Roberts, W, Reichert, J, Reichenberg, A, Rehnström, K, Regan, R, Poustka, F, Poultney, C S, Piven, J, Pinto, D, Pericak-Vance, M A, Pejovic-Milovancevic, M, Pedersen, M G, Pedersen, C B, Paterson, A D, Parr, J R, Pagnamenta, A T, Oliveira, G, Nurnberger, J I, Nordentoft, M, Murtha, M T, Mouga, S, Mortensen, P B, Mors, O, Morrow, E M, Moreno-De-Luca, D, Monaco, A P, Minshew, N, Merikangas, A, McMahon, W M, McGrew, S G, Mattheisen, M, Martsenkovsky, I, Martin, D M, Mane, S M, Magnusson, P, Magalhaes, T, Maestrini, E, Lowe, J K, Lord, C, Levitt, P, Martin, C L, Ledbetter, D H, Leboyer, M, Lecouteur, A S, Ladd-Acosta, C, Kolevzon, A, Klauck, S M, Jacob, S, Iliadou, B, Hultman, C M, Hougaard, D M, Hertz-Picciotto, I, Hendren, R, Hansen, C S, Haines, J L, Guter, S J, Grice, D E, Green, J M, Green, A, Goldberg, A P, Gillberg, C, Gilbert, J, Gallagher, L, Freitag, C M, Fombonne, E, Folstein, S E, Fernandez, B, Fallin, M D, Ercan-Sencicek, A G, Ennis, S, Duque, F, Duketis, E, Delorme, R, Derubeis, S, Dejonge, M V, Dawson, G, Cuccaro, M L, Correia, C T, Conroy, J, Conceição, I C, Chiocchetti, A G, Celestino-Soper, P B S, Casey, J, Cantor, R M, Café, C, Bybjerg-Grauholm, J, Brennan, S, Bourgeron, T, Bolton, P F, Bölte, S, Bolshakova, N, Betancur, C, Bernier, R, Beaudet, A L, Battaglia, A, Bal, V H, Baird, G, Bailey, A J, Bækvad-Hansen, M, Bader, J S, Bacchelli, E, Anagnostou, E, Amaral, D, Almeida, J, Børglum, A D, Buxbaum, J D, Chakravarti, A, Cook, E H, Coon, H, Geschwind, D H, Gill, M, Hakonarson, H, Hallmayer, J, Palotie, A, Santangelo, S, Sutcliffe, J S, Arking, D E, Devlin, B & Daly, M J 2017, ' Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia ', Molecular Autism, vol. 8, 21 . https://doi.org/10.1186/s13229-017-0137-9
Molecular Autism, 2017, 8, pp.21. ⟨10.1186/s13229-017-0137-9⟩
Bolton, P F 2017, ' Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia ', Molecular Autism, vol. 8, pp. 21 . https://doi.org/10.1186/s13229-017-0137-9
Molecular Autism, Vol 8, Iss 1, Pp 1-17 (2017)
Molecular autism, vol 8, iss 1
The Autism Spectrum Disorders Working Group of the Psychiatric Genomics Consortium 2017, ' Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia ', Autism, vol. 8, no. 21, 21 . https://doi.org/10.1186/s13229-017-0137-9
Molecular Autism, BioMed Central, 2017, 8, pp.21. ⟨10.1186/s13229-017-0137-9⟩
Anney, R J L, Ripke, S, Anttila, V, Grove, J, Holmans, P, Huang, H, Klei, L, Lee, P H, Medland, S E, Neale, B, Robinson, E, Weiss, L A, Zwaigenbaum, L, Yu, T W, Wittemeyer, K, Willsey, A J, Wijsman, E M, Werge, T, Wassink, T H, Waltes, R, Walsh, C A, Wallace, S, Vorstman, J A S, Vieland, V J, Vicente, A M, Vanengeland, H, Tsang, K, Thompson, A P, Szatmari, P, Svantesson, O, Steinberg, S, Stefansson, K, Stefansson, H, State, M W, Soorya, L, Silagadze, T, Scherer, S W, Schellenberg, G D, Sandin, S, Sanders, S J, Saemundsen, E, Rouleau, G A, Rogé, B, Roeder, K, Roberts, W, Reichert, J, Reichenberg, A, Rehnström, K, Regan, R, Poustka, F, Poultney, C S, Piven, J, Pinto, D, Pericak-Vance, M A, Pejovic-Milovancevic, M, Pedersen, M G, Pedersen, C B, Paterson, A D, Parr, J R, Pagnamenta, A T, Oliveira, G, Nurnberger, J I, Nordentoft, M, Murtha, M T, Mouga, S, Mortensen, P B, Mors, O, Morrow, E M, Moreno-De-Luca, D, Monaco, A P, Minshew, N, Merikangas, A, McMahon, W M, McGrew, S G, Mattheisen, M, Martsenkovsky, I, Martin, D M, Mane, S M, Magnusson, P, Magalhaes, T, Maestrini, E, Lowe, J K, Lord, C, Levitt, P, Martin, C L, Ledbetter, D H, Leboyer, M, Lecouteur, A S, Ladd-Acosta, C, Kolevzon, A, Klauck, S M, Jacob, S, Iliadou, B, Hultman, C M, Hougaard, D M, Hertz-Picciotto, I, Hendren, R, Hansen, C S, Haines, J L, Guter, S J, Grice, D E, Green, J M, Green, A, Goldberg, A P, Gillberg, C, Gilbert, J, Gallagher, L, Freitag, C M, Fombonne, E, Folstein, S E, Fernandez, B, Fallin, M D, Ercan-Sencicek, A G, Ennis, S, Duque, F, Duketis, E, Delorme, R, Derubeis, S, Dejonge, M V, Dawson, G, Cuccaro, M L, Correia, C T, Conroy, J, Conceição, I C, Chiocchetti, A G, Celestino-Soper, P B S, Casey, J, Cantor, R M, Café, C, Bybjerg-Grauholm, J, Brennan, S, Bourgeron, T, Bolton, P F, Bölte, S, Bolshakova, N, Betancur, C, Bernier, R, Beaudet, A L, Battaglia, A, Bal, V H, Baird, G, Bailey, A J, Bækvad-Hansen, M, Bader, J S, Bacchelli, E, Anagnostou, E, Amaral, D, Almeida, J, Børglum, A D, Buxbaum, J D, Chakravarti, A, Cook, E H, Coon, H, Geschwind, D H, Gill, M, Hakonarson, H, Hallmayer, J, Palotie, A, Santangelo, S, Sutcliffe, J S, Arking, D E, Devlin, B & Daly, M J 2017, ' Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia ', Molecular Autism, vol. 8, 21 . https://doi.org/10.1186/s13229-017-0137-9
Molecular Autism, 2017, 8, pp.21. ⟨10.1186/s13229-017-0137-9⟩
Bolton, P F 2017, ' Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia ', Molecular Autism, vol. 8, pp. 21 . https://doi.org/10.1186/s13229-017-0137-9
Molecular Autism, Vol 8, Iss 1, Pp 1-17 (2017)
Molecular autism, vol 8, iss 1
The Autism Spectrum Disorders Working Group of the Psychiatric Genomics Consortium 2017, ' Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia ', Autism, vol. 8, no. 21, 21 . https://doi.org/10.1186/s13229-017-0137-9
Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium - Collaborators (162): Anney RJL, Ripke S, Anttila V, Grove J, Holmans P, Huang H, Klei L, Lee PH, Medland SE, Neale B, Robinson E, Weiss LA, Zwaigenbaum L, Yu TW, Witteme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1efa92826829f7f870799b08a5c31e5
https://www.hal.inserm.fr/inserm-01535717
https://www.hal.inserm.fr/inserm-01535717
Autor:
Greg Pasco, Ewa Pisula, Sue Fletcher-Watson, Frédérique Bonnet-Brilhault, Teresa Farroni, Anett Kaale, Joëlle Malvy, Anneli Kylliäinen, Jérémy Lefort-Besnard, Silvana Markovska-Simoska, Przemyslaw Tomalski, Sara Manso de Dios, Fabio Apicella, Kenneth Larsen, Synnve Schjølberg, Ricardo Canal-Bedia, Bonnie Auyeung, Marie Gomot, Stepanka Beranova, Inbal Millo, Rafał Kawa, Erica Salomone, Tony Charman, Astrid M. Vicente, Kim Davies, Emily J.H. Jones, Katarzyna Kapica, Nurit Yirmiya, Marija Raleva, Inês C. Conceição, Natasha Chericoni, Natércia Miranda, Bernadette Rogé
Publikováno v:
Fletcher-Watson, S, Apicella, F, Auyeung, B, Beranová, Š, Bonnet-Brilhault, F, Canal-Bedia, R, Charman, T, Chericoni, N, Conceição, I C, Davies, K, Farroni, T, Gomot, M, Jones, E, Kaale, A, Kapica, K, Kawa, R, Kylliainen, A, Larsen, K, Lefort-Besnard, J, Malvy, J, Manso de Dios, S, Markovska-Simoska, S, Millo, I, Miranda, N, Pasco, G, Pisula, E, Raleva, M, Rogé, B, Salomone, E, Schjolberg, S, Tomalski, P, Vicente, A & Yirmiya, N 2016, ' Attitudes of the autism community to early autism research ', Autism . https://doi.org/10.1177/1362361315626577
Fletcher-Watson, S, Apicella, F, Auyeung, B, Beranova, S, Bonnet-Brilhault, F, Canal-Bedia, R, Charman, T, Chericoni, N, Conceição, I C, Davies, K, Farroni, T, Gomot, M, Jones, E, Kaale, A, Kapica, K, Kawa, R, Kylliäinen, A, Larsen, K, Lefort-Besnard, J, Malvy, J, Manso De Dios, S, Markovska-Simoska, S, Millo, I, Miranda, N, Pasco, G, Pisula, E, Raleva, M, Rogé, B, Salomone, E, Schjolberg, S, Tomalski, P, Vicente, A M & Yirmiya, N 2017, ' Attitudes of the autism community to early autism research ', Autism, vol. 21, no. 1, pp. 61-74 . https://doi.org/10.1177/1362361315626577
Fletcher-Watson, S, Apicella, F, Auyeung, B, Beranova, S, Bonnet-Brilhault, F, Canal-Bedia, R, Charman, T, Chericoni, N, Conceição, I C, Davies, K, Farroni, T, Gomot, M, Jones, E, Kaale, A, Kapica, K, Kawa, R, Kylliäinen, A, Larsen, K, Lefort-Besnard, J, Malvy, J, Manso De Dios, S, Markovska-Simoska, S, Millo, I, Miranda, N, Pasco, G, Pisula, E, Raleva, M, Rogé, B, Salomone, E, Schjolberg, S, Tomalski, P, Vicente, A M & Yirmiya, N 2017, ' Attitudes of the autism community to early autism research ', Autism, vol. 21, no. 1, pp. 61-74 . https://doi.org/10.1177/1362361315626577
Investigation into the earliest signs of autism in infants has become a significant sub-field of autism research. This work invokes specific ethical concerns such as use of 'at-risk' language, communicating study findings to parents and the future pe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::300909aeb6f01cf912292de9a668010a
http://hdl.handle.net/2318/1653734
http://hdl.handle.net/2318/1653734
Autor:
Inês C. Conceição, Montserrat Aguadé
Publikováno v:
Journal of Molecular Evolution. 66:325-332
In insects, the odorant receptor (Or) multigene family is an intermediate-sized family with genes present in all chromosomes, indicating that duplication followed by interchromosomal transposition played an important role in the early stages of the f
Publikováno v:
PLoS ONE, Vol 6, Iss 8, p e23778 (2011)
Conceicao, Ines C.; Long, Anthony D.; Gruber, Jonathan D.; & Beldade, Patricia. (2011). Genomic Sequence around Butterfly Wing Development Genes: Annotation and Comparative Analysis. PLoS ONE, 6(8), e23778. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/25p8w6sw
PLoS ONE
Conceicao, Ines C.; Long, Anthony D.; Gruber, Jonathan D.; & Beldade, Patricia. (2011). Genomic Sequence around Butterfly Wing Development Genes: Annotation and Comparative Analysis. PLoS ONE, 6(8), e23778. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/25p8w6sw
PLoS ONE
BACKGROUND: Analysis of genomic sequence allows characterization of genome content and organization, and access beyond gene-coding regions for identification of functional elements. BAC libraries, where relatively large genomic regions are made readi
Autor:
Ana Filipa Sequeira, Guiomar Oliveira, Cátia Café, Joana E. Coelho, Catarina Correia, Stephen W. Scherer, Bárbara Oliveira, Dalila Pinto, Inês Sousa, Joana Almeida, Inês C. Conceição, Kun Gao, Christian R. Marshall, Frederico Duque, Susan Walker, Wendy Roberts, Astrid M. Vicente, Daniel H. Geschwind, Jennifer K. Lowe, John I. Nurnberger, Bhooma Thiruvahindrapuram, Susana Mouga
Publikováno v:
Molecular Autism
Molecular autism, vol 5, iss 1
Molecular autism, vol 5, iss 1
Background Validating the potential pathogenicity of copy number variants (CNVs) identified in genome-wide studies of autism spectrum disorders (ASD) requires detailed assessment of case/control frequencies, inheritance patterns, clinical correlation