Inês Girão Meireles de Sousa. É Investigador Auxiliar na Universidade de Lisboa. Publicou 14 artigos em revistas especializadas. Possui 6 itens de produção técnica. Recebeu 5 prémios e/ou homenagens. Nas suas actividades profissionais interagiu com 591 colaboradores em co-autorias de trabalhos científicos.
Endereço de acesso a este CV: http://www.degois.pt/visualizador/curriculum.jsp?key=9774980969541909

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

2006-2011	Doutoramento Phd
Genética Molecular Humana (4 anos » years) . University of Oxford, Reino Unido. Com o tipo » With the type: Reconhecimento » Acknowledgement.

2000-2005	Licenciatura Licentiate degree
Biologia Microbiana e Genética (5 anos » years) . Universidade de Lisboa, Portugal.

2010-2011	Pós-Doutoramento Postdoctorate
Instituto Nacional de Saúde Doutor Ricardo Jorge, Portugal.

2004-2005	Outros Others
Genetics of Autism. Universidade de Lisboa, Portugal.

2001-2002	Outros Others
Biologia Vegetal. Universidade de Lisboa, Portugal.

Universidade de Lisboa

Abr/2011-Actual

Investigador Auxiliar

Instituto Nacional de Saúde Doutor Ricardo Jorge

Jul/2010-Fev/2011

Investigador Auxiliar

Compreende Understandig	Português (Bem), Inglês (Bem).
Fala Speaking	Português (Bem), Inglês (Bem).
Lê Reading	Português (Bem), Inglês (Bem).
Escreve Writing	Português (Bem), Inglês (Bem).

2012	L'Oreal/UNESCO/FCT For Women in Science, L'Oreal/UNESCO/FCT.
2011	National Fellowship Award, European Society of Human Genetics.
2010	Prémio de Investigação Clínica, Sociedade Portuguesa de Genética Humana.
2005	Excellency Award for the best student of the year (university level), PT Multimédia.
2008	Prize scholarship 2008/2009 for graduate students with the highest distinction, Merton College, University of Oxford.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

13.	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.

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).

Produção científica Scientific production

Produção técnica Technical production

Total

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

Total

Produção técnica Technical production

6

Outros tipos de produção técnica Other technical production

6

	Frederico de Oliveira Duque
	Guiomar Gonçalves de Oliveira
	Peter Jordan