Inês Girão Meireles de Sousa
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Data da última atualização
»Last update
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26/02/2012 |
Dados pessoais (Personal data)
Nome completo
Full name |
Inês Girão Meireles de Sousa |
Nome em citações bibliográficas
Quoting name |
Sousa, I |
Categoria profissional
Position |
Investigador Auxiliar |
Endereço profissional
Professional address |
Universidade de Lisboa Faculdade de Medicina Instituto de Medicina Molecular - IMM Av. Prof. Egas Moniz, Edf. Egas Moniz Lisboa 1649-028 Lisboa Portugal Telefone: (+351)217999411Extensão: 47149 Fax: (+351)217951780 Correio electrónico: ines.meireles.sousa@gmail.com |
Sexo
Gender |
Feminino»Female |
Graus Académicos
(Academic Degrees)
2006-2011 |
Doutoramento Phd |
Genética Molecular Humana
(4 anos » years)
.
University of Oxford,
Reino Unido. Com o tipo » With the type:
Reconhecimento » Acknowledgement.
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2000-2005 |
Licenciatura Licentiate degree |
Biologia Microbiana e Genética
(5 anos » years)
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Universidade de Lisboa,
Portugal.
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Formação complementar ( studies)
2010-2011 |
Pós-Doutoramento Postdoctorate |
Instituto Nacional de Saúde Doutor Ricardo Jorge,
Portugal.
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2004-2005 |
Outros Others |
Genetics of Autism. Universidade de Lisboa,
Portugal.
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2001-2002 |
Outros Others |
Biologia Vegetal. Universidade de Lisboa,
Portugal.
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Vínculos profissionais
(Professional Positions)
Abr/2011-Actual |
Investigador Auxiliar |
Instituto Nacional de Saúde Doutor Ricardo Jorge |
Jul/2010-Fev/2011 |
Investigador Auxiliar |
Línguas (Languages)
Compreende Understandig |
Português (Bem), Inglês (Bem). |
Fala Speaking |
Português (Bem), Inglês (Bem). |
Lê Reading |
Português (Bem), Inglês (Bem). |
Escreve Writing |
Português (Bem), Inglês (Bem). |
Prémios e títulos (Awards Prizes, and Honours)
2012 |
L'Oreal/UNESCO/FCT For Women in Science,
L'Oreal/UNESCO/FCT.
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2011 |
National Fellowship Award,
European Society of Human Genetics.
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2010 |
Prémio de Investigação Clínica,
Sociedade Portuguesa de Genética Humana.
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2005 |
Excellency Award for the best student of the year (university level),
PT Multimédia.
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2008 |
Prize scholarship 2008/2009 for graduate students with the highest distinction,
Merton College, University of Oxford.
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Produção científica, técnica e artística/cultural
(Scientific, technical and artistical/cultural
production)
Capítulos de livros publicados Published book chapters |
1. |
De Sousa, I; Holt, Richard; Pagnamenta, Alistair; Monaco, Anthony; Roth, Ilona; Rezaie, Payam. 2011. Book chapter II - Unravelling the genetics of autism spectrum disorders. In Researching the Autism Spectrum, ed. Ilona RothPayam Rezaie, 53 - 111. ISBN: 9780511973918. Cambridge: Cambridge University Press.
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Artigos em revistas sem arbitragem científica Papers in periodics without scientific refereeing |
1. |
Anney, Richard J. L; Kenny, Elaine M; O'Dushlaine, Colm; Parkhomenka, Elena; Bailey§, Anthony J; Fernandez, Bridget A; Szatmari§, Peter; Scherer§, Stephen W; Patterson§, Andrew; Marshall, Christian R; Pinto, Dalila; Vincent, John B; Fombonne, Eric; Betancur§, Catalina; Delorme, Richard; Leboyer, Marion; Bourgeron, Thomas; Mantoulan, Carine; Roge, Bernadette; Tauber, Maïté; Freitag§, Christine M; Poustka, Fritz; Duketis, Eftichia; Klauck§, Sabine M; Poustka, Annemarie; Papanikolaou, Katerina; Tsiantis, John; Gallagher§, Louise; Gill§, Michael; Anney, Richard; Bolshakova, Nadia; Brennan, Sean; Hughes, Gillian; McGrath, Jane; Merikangas, Alison; Ennis§, Sean; Green, Andrew; Casey, Jillian P; Conroy, Judith M; Regan, Regina; Shah, Naisha; Maestrini§, Elena; Bacchelli, Elena; Minopoli, Fiorella; Stoppioni, Vera; Battaglia§, Agatino; Igliozzi, Roberta; Parrini, Barbara; Tancredi, Raffaella; Oliveira§, Guiomar; Almeida, Joana; Duque, Frederico; Vicente§, Astrid; Correia, Catarina; Magalhaes, Tiago R; Gillberg, Christopher; Nygren, Gudrun; Jonge, Maretha; Van Engeland, H; Vorstman, Jacob A; Wittemeyer, Kerstin; Baird, Gillian; Bolton, Patrick F; Rutter, Michael L; Green, Jonathan; Lamb, Janine A; Pickles, Andrew; Parr, Jeremy R; Couteur, Ann L; Berney, Tom; McConachie, Helen; Wallace, Simon; Coutanche, Marc; Foley, Suzanne; White, Kathy; Monaco§, Anthony P; Holt, Richard; Farrar, Penny; Pagnamenta, Alistair T; Mirza, Ghazala K; Ragoussis, Jiannis; Sousa, Inês; Sykes, Nuala; Wing, Kirsty; Hallmayer§, Joachim; Cantor§, Rita M; Nelson, Stanley F; Geschwind§, Daniel H; Abrahams, Brett S; Volkmar, Fred; Pericak-Vance§, Margaret A; Cuccaro, Michael L; Gilbert, John; Cook§, Edwin H; Guter, Stephen J; Jacob, Suma; Nurnberger Jr§, J. I; McDougle, Christopher J; Posey, David J; Lord, Catherine; Corsello, Christina; Hus, Vanessa; Buxbaum§, Joseph D; Kolevzon, Alexander; Soorya, Latha; Parkhomenko, Elena; Leventhal, Bennett L; Dawson, Geraldine; Vieland§, Veronica J; Hakonarson§, Hakon; Glessner, Joseph T; Kim, Cecilia; Wang, Kai; Schellenberg§, Gerard D; Devlin§, Bernie; Klei, Lamburtus; Minshew, Nancy; Sutcliffe§, James S; Haines§, Jonathan L; Lund, Sabata C; Thomson, Susanne; Yaspan, Brian L; Coon§, Hilary; Miller, Judith; McMahon, William M; Munson, Jeff; Estes, Annette; Wijsman§, Ellen M; Buxbaum, Joseph D; Sutcliffe, James; Gill, Michael; Gallagher, Louise. 2011. "Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for
autism spectrum disorders", European Journal of Human Genetics 19, 10: 1082 - 1089.
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2. |
Mendes, Ana I; Mascarenhas, Mário R; Matos, Sónia; Sousa, Inês; Ferreira, Joana; Barbosa, Ana P; Bicho, Manuel; Jordan, Peter. 2011. "A WNK4 gene variant relates to osteoporosis and not to hypertension in the Portuguese population", Molecular Genetics and Metabolism 102, 4: 465 - 469.
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3. |
Anney, R.; Klei, L.; Pinto, D.; Regan, R.; Conroy, J.; Magalhaes, T. R; Correia, C.; Abrahams, B. S; Sykes, N.; Pagnamenta, A. T; Almeida, J.; Bacchelli, E.; Bailey, A. J; Baird, G.; Battaglia, A.; Berney, T.; Bolshakova, N.; Bolte, S.; Bolton, P. F; Bourgeron, T.; Brennan, S.; Brian, J.; Carson, A. R; Casallo, G.; Casey, J.; Chu, S. H; Cochrane, L.; Corsello, C.; Crawford, E. L; Crossett, A.; Dawson, G.; de Jonge, M; Delorme, R.; Drmic, I.; Duketis, E.; Duque, F.; Estes, A.; Farrar, P.; Fernandez, B. A; Folstein, S. E; Fombonne, E.; Freitag, C. M; Gilbert, J.; Gillberg, C.; Glessner, J. T; Goldberg, J.; Green, J.; Guter, S. J; Hakonarson, H.; Heron, E. A; Hill, M.; Holt, R.; Howe, J. L; Hughes, G.; Hus, V.; Igliozzi, R.; Kim, C.; Klauck, S. M; Kolevzon, A.; Korvatska, O.; Kustanovich, V.; Lajonchere, C. M; Lamb, J. A; Laskawiec, M.; Leboyer, M.; Le Couteur, A; Leventhal, B. L; Lionel, A. C; Liu, X.-Q.; Lord, C.; Lotspeich, L.; Lund, S. C; Maestrini, E.; Mahoney, W.; Mantoulan, C.; Marshall, C. R; McConachie, H.; McDougle, C. J; McGrath, J.; McMahon, W. M; Melhem, N. M; Merikangas, A.; Migita, O.; Minshew, N. J; Mirza, G. K; Munson, J.; Nelson, S. F; Noakes, C.; Noor, A.; Nygren, G.; Oliveira, G.; Papanikolaou, K.; Parr, J. R; Parrini, B.; Paton, T.; Pickles, A.; Piven, J.; Posey, D. J; Poustka, A.; Poustka, F.; Prasad, A.; Ragoussis, J.; Renshaw, K.; Rickaby, J.; Roberts, W.; Roeder, K.; Roge, B.; Rutter, M. L; Bierut, L. J; Rice, J. P; Salt, J.; Sansom, K.; Sato, D.; Segurado, R.; Senman, L.; Shah, N.; Sheffield, V. C; Soorya, L.; Sousa, I.; Stoppioni, V.; Strawbridge, C.; Tancredi, R.; Tansey, K.; Thiruvahindrapduram, B.; Thompson, A. P; Thomson, S.; Tryfon, A.; Tsiantis, J.; Van Engeland, H; Vincent, J. B; Volkmar, F.; Wallace, S.; Wang, K.; Wang, Z.; Wassink, T. H; Wing, K.; Wittemeyer, K.; Wood, S.; Yaspan, B. L; Zurawiecki, D.; Zwaigenbaum, L.; Betancur, C.; Buxbaum, J. D; Cantor, R. M; Cook, E. H; Coon, H.; Cuccaro, M. L; Gallagher, L.; Geschwind, D. H; Gill, M.; Haines, J. L; Miller, J.; Monaco, A. P; Nurnberger, J. I; Paterson, A. D; Pericak-Vance, M. A; Schellenberg, G. D; Scherer, S. W; Sutcliffe, J. S; Szatmari, P.; Vicente, A. M; Vieland, V. J; Wijsman, E. M; Devlin, B.; Ennis, S.; Hallmayer, J.. 2010. "A genome-wide scan for common alleles affecting risk for autism", Human Molecular Genetics 19, 20: 4072 - 4082.
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4. |
Correia, C. T; Coutinho, A. M; Sequeira, A. F; Sousa, I. G; Lourenço Venda, L; Almeida, J. P; Abreu, R. L; Lobo, C.; Miguel, T. S; Conroy, J.; Cochrane, L.; Gallagher, L.; Gill, M.; Ennis, S.; Oliveira, G. G; Vicente, A. M. 2010. "Increased BDNF levels and NTRK2 gene association suggest a disruption of BDNF/TrkB signaling in autism", Genes, Brain and Behavior 9, 7: 841 - 848.
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5. |
Holt, Richard; Barnby, Gabrielle; Maestrini, Elena; Bacchelli, Elena; Brocklebank, Denise; Sousa, Inês; Mulder, Erik J; Kantojärvi, Katri; Järvelä, Irma; Klauck, Sabine M; Poustka, Fritz; Bailey, Anthony J; Monaco, Anthony P. 2010. "Linkage and candidate gene studies of autism spectrum disorders in European populations", European Journal of Human Genetics 18, 9: 1013 - 1019.
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6. |
Pinto, Dalila; Pagnamenta, Alistair T; Klei, Lambertus; Anney, Richard; Merico, Daniele; Regan, Regina; Conroy, Judith; Magalhaes, Tiago R; Correia, Catarina; Abrahams, Brett S; Almeida, Joana; Bacchelli, Elena; Bader, Gary D; Bailey, Anthony J; Baird, Gillian; Battaglia, Agatino; Berney, Tom; Bolshakova, Nadia; Bölte, Sven; Bolton, Patrick F; Bourgeron, Thomas; Brennan, Sean; Brian, Jessica; Bryson, Susan E; Carson, Andrew R; Casallo, Guillermo; Casey, Jillian; Chung, Brian H; Cochrane, Lynne; Corsello, Christina; Crawford, Emily L; Crossett, Andrew; Cytrynbaum, Cheryl; Dawson, Geraldine; de Jonge, M; Delorme, Richard; Drmic, Irene; Duketis, Eftichia; Duque, Frederico; Estes, Annette; Farrar, Penny; Fernandez, Bridget A; Folstein, Susan E; Fombonne, Eric; Freitag, Christine M; Gilbert, John; Gillberg, Christopher; Glessner, Joseph T; Goldberg, Jeremy; Green, Andrew; Green, Jonathan; Guter, Stephen J; Hakonarson, Hakon; Heron, Elizabeth A; Hill, Matthew; Holt, Richard; Howe, Jennifer L; Hughes, Gillian; Hus, Vanessa; Igliozzi, Roberta; Kim, Cecilia; Klauck, Sabine M; Kolevzon, Alexander; Korvatska, Olena; Kustanovich, Vlad; Lajonchere, Clara M; Lamb, Janine A; Laskawiec, Magdalena; Leboyer, Marion; Le Couteur, A; Leventhal, Bennett L; Lionel, Anath C; Liu, Xiao-Qing; Lord, Catherine; Lotspeich, Linda; Lund, Sabata C; Maestrini, Elena; Mahoney, William; Mantoulan, Carine; Marshall, Christian R; McConachie, Helen; McDougle, Christopher J; McGrath, Jane; McMahon, William M; Merikangas, Alison; Migita, Ohsuke; Minshew, Nancy J; Mirza, Ghazala K; Munson, Jeff; Nelson, Stanley F; Noakes, Carolyn; Noor, Abdul; Nygren, Gudrun; Oliveira, Guiomar; Papanikolaou, Katerina; Parr, Jeremy R; Parrini, Barbara; Paton, Tara; Pickles, Andrew; Pilorge, Marion; Piven, Joseph; Ponting, Chris P; Posey, David J; Poustka, Annemarie; Poustka, Fritz; Prasad, Aparna; Ragoussis, Jiannis; Renshaw, Katy; Rickaby, Jessica; Roberts, Wendy; Roeder, Kathryn; Roge, Bernadette; Rutter, Michael L; Bierut, Laura J; Rice, John P; Salt, Jeff; Sansom, Katherine; Sato, Daisuke; Segurado, Ricardo; Sequeira, Ana F; Senman, Lili; Shah, Naisha; Sheffield, Val C; Soorya, Latha; Sousa, Inês; Stein, Olaf; Sykes, Nuala; Stoppioni, Vera; Strawbridge, Christina; Tancredi, Raffaella; Tansey, Katherine; Thiruvahindrapduram, Bhooma; Thompson, Ann P; Thomson, Susanne; Tryfon, Ana; Tsiantis, John; Van Engeland, H; Vincent, John B; Volkmar, Fred; Wallace, Simon; Wang, Kai; Wang, Zhouzhi; Wassink, Thomas H; Webber, Caleb; Weksberg, Rosanna; Wing, Kirsty; Wittemeyer, Kerstin; Wood, Shawn; Wu, Jing; Yaspan, Brian L; Zurawiecki, Danielle; Zwaigenbaum, Lonnie; Buxbaum, Joseph D; Cantor, Rita M; Cook, Edwin H; Coon, Hilary; Cuccaro, Michael L; Devlin, Bernie; Ennis, Sean; Gallagher, Louise; Geschwind, Daniel H; Gill, Michael; Haines, Jonathan L; Hallmayer, Joachim; Miller, Judith; Monaco, Anthony P; Nurnberger Jr, J. I; Paterson, Andrew D; Pericak-Vance, Margaret A; Schellenberg, Gerard D; Szatmari, Peter; Vicente, Astrid M; Vieland, Veronica J; Wijsman, Ellen M; Scherer, Stephen W; Sutcliffe, James S; Betancur, Catalina. 2010. "Functional impact of global rare copy number variation in autism spectrum disorders", Nature 466, 7304: 368 - 372.
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7. |
Maestrini, E; Pagnamenta, A T; Lamb, J A; Bacchelli, E; Sykes, N H; Sousa, I; Toma, C; Barnby, G; Butler, H; Winchester, L; Scerri, T S; Minopoli, F; Reichert, J; Cai, G; Buxbaum, J D; Korvatska, O; Schellenberg, G D; Dawson, G; Bildt, A; Minderaa, R B; Mulder, E J; Morris, A P; Bailey, A J; Monaco, A P. 2009. "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", Molecular Psychiatry 15, 9: 954 - 968.
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8. |
Sykes, Nuala H; Toma, Claudio; Wilson, Natalie; Volpi, Emanuela V; Sousa, Inês; Pagnamenta, Alistair T; Tancredi, Raffaella; Battaglia, Agatino; Maestrini, Elena; Bailey, Anthony J; Monaco, Anthony P. 2009. "Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection", European Journal of Human Genetics 17, 10: 1347 - 1353.
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9. |
Sousa, Inês; Clark, Taane G; Toma, Claudio; Kobayashi, Kazuhiro; Choma, Maja; Holt, Richard; Sykes, Nuala H; Lamb, Janine A; Bailey, Anthony J; Battaglia, Agatino; Maestrini, Elena; Monaco, Anthony P. 2008. "MET and autism susceptibility: family and case–control studies", European Journal of Human Genetics 17, 6: 749 - 758.
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10. |
Toma, C; Rossi, M; Sousa, I; Blasi, F; Bacchelli, E; Alen, R; Vanhala, R; Monaco, A P; Järvelä, I; Maestrini, E. 2007. "Is ASMT a susceptibility gene for autism spectrum disorders? A replication study in European populations", Molecular Psychiatry 12, 11: 977 - 979.
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11. |
Coutinho, Ana M; Sousa, Inês; Martins, Madalena; Correia, Catarina; Morgadinho, Teresa; Bento, Celeste; Marques, Carla; Ataíde, Assunção; Miguel, Teresa S; Moore, Jason H; Oliveira, Guiomar; Vicente, Astrid M. 2007. "Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels", Human Genetics 121, 2: 243 - 256.
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12. |
Szatmari, Peter; Paterson, Andrew D; Zwaigenbaum, Lonnie; Roberts, Wendy; Brian, Jessica; Liu, Xiao-Qing; Vincent, John B; Skaug, Jennifer L; Thompson, Ann P; Senman, Lili; Feuk, Lars; Qian, Cheng; Bryson, Susan E; Jones, Marshall B; Marshall, Christian R; Scherer, Stephen W; Vieland, Veronica J; Bartlett, Christopher; Mangin, La V; Goedken, Rhinda; Segre, Alberto; Pericak-Vance, Margaret A; Cuccaro, Michael L; Gilbert, John R; Wright, Harry H; Abramson, Ruth K; Betancur, Catalina; Bourgeron, Thomas; Gillberg, Christopher; Leboyer, Marion; Buxbaum, Joseph D; Davis, Kenneth L; Hollander, Eric; Silverman, Jeremy M; Hallmayer, Joachim; Lotspeich, Linda; Sutcliffe, James S; Haines, Jonathan L; Folstein, Susan E; Piven, Joseph; Wassink, Thomas H; Sheffield, Val; Geschwind, Daniel H; Bucan, Maja; Brown, W T; Cantor, Rita M; Constantino, John N; Gilliam, T C; Herbert, Martha; LaJonchere, Clara; Ledbetter, David H; Lese-Martin, Christa; Miller, Janet; Nelson, Stan; Samango-Sprouse, Carol A; Spence, Sarah; State, Matthew; Tanzi, Rudolph E; Coon, Hilary; Dawson, Geraldine; Devlin, Bernie; Estes, Annette; Flodman, Pamela; Klei, Lambertus; McMahon, William M; Minshew, Nancy; Munson, Jeff; Korvatska, Elena; Rodier, Patricia M; Schellenberg, Gerard D; Smith, Moyra; Spence, M A; Stodgell, Chris; Tepper, Ping G; Wijsman, Ellen M; Yu, Chang-En; Rogé, Bernadette; Mantoulan, Carine; Wittemeyer, Kerstin; Poustka, Annemarie; Felder, Bärbel; Klauck, Sabine M; Schuster, Claudia; Poustka, Fritz; Bölte, Sven; Feineis-Matthews, Sabine; Herbrecht, Evelyn; Schmötzer, Gabi; Tsiantis, John; Papanikolaou, Katerina; Maestrini, Elena; Bacchelli, Elena; Blasi, Francesca; Carone, Simona; Toma, Claudio; Van Engeland, H; de Jonge, M; Kemner, Chantal; Koop, Frederike; Langemeijer, Marjolijn; Hijimans, Channa; Staal, Wouter G; Baird, Gillian; Bolton, Patrick F; Rutter, Michael L; Weisblatt, Emma; Green, Jonathan; Aldred, Catherine; Wilkinson, Julie-Anne; Pickles, Andrew; Le Couteur, A; Berney, Tom; McConachie, Helen; Bailey, Anthony J; Francis, Kostas; Honeyman, Gemma; Hutchinson, Aislinn; Parr, Jeremy R; Wallace, Simon; Monaco, Anthony P; Barnby, Gabrielle; Kobayashi, Kazuhiro; Lamb, Janine A; Sousa, Ines; Sykes, Nuala; Cook, Edwin H; Guter, Stephen J; Leventhal, Bennett L; Salt, Jeff; Lord, Catherine; Corsello, Christina; Hus, Vanessa; Weeks, Daniel E; Volkmar, Fred; Tauber, Maïté; Fombonne, Eric; Shih, Andy. 2007. "Mapping autism risk loci using genetic linkage and chromosomal rearrangements", Nature Genetics 39, 3: 319 - 328.
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Ferreira, Nicolau J; Meireles de S. I. G; Luís, Tiago C; Currais, António J. M; Figueiredo, Ana C; Costa, Monya M; Lima, A. S. B; Santos, Pedro A. G; Barroso, José G; Pedro, Luis G; Scheffer, Johannes J. C. 2007. "Pittosporum undulatum Vent. grown in Portugal: secretory structures, seasonal variation and enantiomeric composition of its
essential oil", Flavour and Fragrance Journal 22, 1: 1 - 9.
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Apresentação oral de trabalho Oral work presentation |
1. |
Sousa, I. Whole-Genome CNV analysis identifies rare ANXA1 duplications in autism spectrum disorders,14th meeting of Sociedade Portuguesa de Genética Humana,Coimbra,2010 (Conferência ou palestra). |
2. |
Sousa, I; Clark, T.G.; Holt, R.; Pagnamenta, A. T; Sykes, N.; Mulder, E J; Bailey, A. J; Battaglia, A.; Klauck, S.M.; Poustka, A.; Monaco, A. P; Kim, Cecilia. Leucine rich repeat gene polymorphisms are associated with autism spectrum disorder susceptibility in populations of European
ancestry ,The American Society for Human Genetics 59th Annual Meeting,Honolulu,2009 (Poster). |
3. |
Holt, R.; Sousa, I; Bacchelli, E; Brocklebank, Denise; Maestrini, E; Barnby, G; Bailey, A. J; Monaco, A. P; Consortium, EU A. M. Association Studies of Autism Spectrum Disorders in Populations of European Ancestry,The American Society for Human Genetics 59th Annual Meeting,Honolulu,2009 (Poster). |
4. |
Pagnamenta, A. T; Maestrini, E; Lamb, J. A; Sykes, N.; Sousa, I; Toma, C; Bacchelli, E; Morris, A P; Monaco, A. P; Kim, Cecilia. High-density SNP association and CNV analysis of two Autism Susceptibility Loci,The American Society for Human Genetics 58th Annual Meeting,Philadelphia,2008 (Poster). |
5. |
Correia, C.; Sousa, I; Peixeiro, I.; Lourenço, L.; Almeida, J.; Lontro, R.; Galllagher, L.; Gill, M.; Ennis, S.; Oliveira, G.; Vicente, A. M. The BDNF receptor gene NTRK2 is a susceptibility gene for autism,2008 (Poster). |
6. |
Sousa, I; Sykes, N.; Clark, T.G.; Allan, C.; Lamb, J. A; Kobayashi, Kazuhiro; Holt, R.; Pagnamenta, A. T; Bailey, A. J; Monaco, A. P; Kim, Cecilia. Association of MET gene variants with autism susceptibility,The American Society for Human Genetics 57th Annual Meeting,San Diego,2007 (Poster). |
Indicadores de produção
(Production indicators)
Produção científica
Scientific production |
Produção técnica
Technical production |
Produção científica Scientific production |
14 |
Livros e capítulos Books and book chapters |
1 |
Capítulos de livros publicados Published book chapters |
1 |
Artigos científicos em revistas Papers in periodics |
13 |
Sem arbitragem científica Without scientific refereeing |
13 |
Produção técnica Technical production |
6 |
Outros tipos de produção técnica Other technical production |
6 |
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