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Maria João Santos is a superior laboratory technician, since June 2007, at Laboratory of Mitochondrial BioMedicine and Theranostics (LBioMiT), Center for Neurosciences and Cell Biology, University of Coimbra, which is recognized as an entity certified since 2011 by NP EN ISO 9001: 2008, with registration number 2011 / CEP.3971 (entity certifying APCER). She performs genetic analyzes, integrated in the diagnostic tests of mitochondrial cytopathies, using up-to-date techniques, such as Next Generation Sequence. She has a degree in Biochemistry and a master's degree in Cellular and Molecular Biology, both in the University of Coimbra. She is a PhD student of the Doctoral Program in Health Sciences, at the Faculty of Medicine, University of Coimbra. In May 2009, she did a scientific internship abroad, to learn how to perform the quantification analysis of the mitochondrial genome, at the Medical Genetics Laboratories, Baylor College of Medicine, Houston, Texas, USA. Then, she implemented this technique at the LBioMiT, allowing the identification of a syndrome characterized by a decrease of the mitochondrial DNA copy number, the depletion syndrome. She is particularly interested in this syndrome, especially in the genetic causes associated with it, many of which are still unknown. In February 2015 she took part in the Global Action Against Dementia European Young Leaders in London, where she represented Portugal. Since 2017 she has been working in her PhD projet entitled "Unravelling the mitochondrial genomics, proteomics and metabolomics impairments occurring in Leber's Hereditary Optic Neuropathy". Maria João Santos is co-author of 10 publications in peer reviewed journals and 34 papers in conference proceedings. She has 140 scientific communications, 101 of which are posters and 39 are oral presentations. In the last few years she has also participated in 3 research projects approved by the Foundation for Science and Technology and other 6 projects. h-index: 6; Citations: 125. [(Scopus) - 05/03/2022].
Identificação

Identificação pessoal

Nome completo
Maria João Ferreira Canas dos Santos

Nomes de citação

  • Santos, Maria João
  • Santos, M.J.

Identificadores de autor

Ciência ID
B411-7F7F-AE32
ORCID iD
0000-0002-4018-8787

Domínios de atuação

  • Ciências Médicas e da Saúde - Biotecnologia Médica - Diagnóstico e Terapias de Base Genética
  • Ciências Naturais - Ciências Biológicas - Biologia Molecular

Idiomas

Idioma Conversação Leitura Escrita Compreensão Peer-review
Inglês Utilizador proficiente (C1) Utilizador proficiente (C1) Utilizador proficiente (C1) Utilizador proficiente (C1)
Francês Utilizador elementar (A1) Utilizador elementar (A1) Utilizador elementar (A1) Utilizador elementar (A1)
Formação
Grau Classificação
2014/09 - 2023
Em curso
Doctoral Program in Health Sciences (Doutoramento)
Especialização em Biomedical Sciences
Universidade de Coimbra Faculdade de Medicina, Portugal
"Unraveling the mitochondrial impairments and organelle stress occurring in Leber’s Hereditary Optic Neuropathy" (TESE/DISSERTAÇÃO)
2006/10 - 2010/06/24
Concluído
Master's degree in Cellular and Molecular Biology (Mestrado)
Universidade de Coimbra Faculdade de Ciencias e Tecnologia, Portugal
"Monitoring Kidney Transplantation using Real-Time PCR for Relative Gene Expression Analysis" (TESE/DISSERTAÇÃO)
Very Good
2001/09 - 2006/07
Concluído
Biochemistry (Licenciatura)
Universidade de Coimbra Faculdade de Ciencias e Tecnologia, Portugal
"Monitoring Kidney Transplantation using Real-Time PCR for Relative Gene Expression Analysis" (TESE/DISSERTAÇÃO)
14 (out of 20)
Percurso profissional

Outros

Categoria Profissional
Instituição de acolhimento
Empregador
2007/06/01 - Atual Superior Research Technician CNC - Center for neuroscience and cell biology, University of Coimbra, Portugal
CNC - Center for neuroscience and cell biology, University of Coimbra, Portugal
2009/05/25 - 2009/06/10 Training in mtDNA copy number quantification by real-time PCR Baylor College of Medicine, Estados Unidos
2006/11/01 - 2007/05/31 Scholarship technician CNC - Center for neuroscience and cell biology, University of Coimbra, Portugal
2006/08/01 - 2006/10/31 Volunteer Hospitais da Universidade de Coimbra Centro de Histocompatibilidade do Centro, Portugal
Hospitais da Universidade de Coimbra Centro de Histocompatibilidade do Centro, Portugal
Projetos

Projeto

Designação Financiadores
2017 - Atual From obesity to adisopathy: role of mitochondria. Epigenetic study.
NA
Investigador
Universidade de Coimbra Centro de Neurociências e Biologia Celular, Portugal
2022 - 2023/03/18 MitONOFF - malfunctions of the energy factory
fbr_oc2_01_universidade de coimbra
Outra
Universidade de Coimbra, Portugal
EEA Grants
2018 - 2022/05/31 Providing free of charge complete genetic tests to all Portuguese patients with a clinical and instrumental diagnosis of Optic Nerve Atrophy
NA
Investigador
Universidade de Coimbra Centro de Neurociências e Biologia Celular, Portugal
Santhera Pharmaceuticals Schweiz AG
Em curso
2020 - 2021/12/31 Analysis of biomarkers, bioenergy and psychological evaluation of well-being in Clown Doctor intervention
POISE-03-4639-FSE-000427
Investigador
Universidade de Coimbra Centro de Neurociências e Biologia Celular, Portugal
2015 - 2016/03/31 Unveiling intracellular organelle interaction with mitochondria in Leber Hereditary Optic Neuropathy: functional genomics approach.
SPDM Grant 2014
Investigador
CNC - Center for neuroscience and cell biology, University of Coimbra, Portugal
2013 - 2015/08/31 Translational Bigenomics Investigation in Leber´s Hereditary Optic Neuropathy: Genotype-Phenotype Correlation
PTDC/DTP-EPI/0929/2012
Investigador
Universidade de Coimbra Centro de Neurociências e Biologia Celular, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2012 - 2015/06/30 Neuropsychological Assessment and Dual Genome Investigation in Frontotemporal Dementia
PTDC/SAUEPI/121811/2010
Investigador
Universidade de Coimbra Centro de Neurociências e Biologia Celular, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2010 - 2013/02/04 Analysis of transcription deregulation in brain and peripheral Huntington’s disease models - influence of modulating histone deacetylases
PTDC/SAU-FCF/108056/2008
Investigador
Universidade de Coimbra Centro de Neurociências e Biologia Celular, Portugal
Fundação para a Ciência e a Tecnologia
Concluído
2007 - 2008/01/04 Research of changes in MTND1 gene in Frontotemporal Dementia / Investigação de alterações no gene MTND1 na demência frontotemporal
Projecto GAI nº 19/07
Investigador
Universidade de Coimbra Faculdade de Medicina, Portugal
Universidade de Coimbra
Concluído
Produções

Publicações

Artigo em revista
  1. Jacinto, Sandra; Guerreiro, Patrícia; de Oliveira, Rita Machado; Cunha-Oliveira, Teresa; Santos, Maria João; Grazina, Manuela; Rego, Ana Cristina; Outeiro, Tiago F.. "MPV17 Mutations Are Associated With a Quiescent Energetic Metabolic Profile". Frontiers in Cellular Neuroscience 15 641264 (2021): http://dx.doi.org/10.3389/fncel.2021.641264.
    Publicado • 10.3389/fncel.2021.641264
  2. Bacalhau, M.; Simões, M.; Rocha, M.C.; Hardy, S.A.; Vincent, A.E.; Durães, J.; Macário, M.C.; et al. "Disclosing the functional changes of two genetic alterations in a patient with Chronic Progressive External Ophthalmoplegia: Report of the novel mtDNA m.7486G>A variant". Neuromuscular Disorders 28 4 (2018): 350-360. http://www.scopus.com/inward/record.url?eid=2-s2.0-85041560601&partnerID=MN8TOARS.
    Publicado • 10.1016/j.nmd.2017.11.006
  3. Santos, D.; Santos, M.J.; Alves-Ferreira, M.; Coelho, T.; Sequeiros, J.; Alonso, I.; Oliveira, P.; et al. "MtDNA copy number associated with age of onset in familial amyloid polyneuropathy". Journal of Neurology, Neurosurgery and Psychiatry 89 3 (2018): 300-304. http://www.scopus.com/inward/record.url?eid=2-s2.0-85042883375&partnerID=MN8TOARS.
    Publicado • 10.1136/jnnp-2017-316657
  4. Bacalhau, M.; Pratas, J.; Simões, M.; Mendes, C.; Ribeiro, C.; Santos, M.J.; Diogo, L.; Macário, M.C.; Grazina, M.. "Response to "In silico prediction is insufficient to assess pathogenicity of mtDNA variants"". European Journal of Medical Genetics (2017): http://www.scopus.com/inward/record.url?eid=2-s2.0-85027531111&partnerID=MN8TOARS.
    Publicado • 10.1016/j.ejmg.2017.08.008
  5. Bacalhau, M.; Pratas, J.; Simões, M.; Mendes, C.; Ribeiro, C.; Santos, M.J.; Diogo, L.; Macário, M.C.; Grazina, M.. "In silico analysis for predicting pathogenicity of five unclassified mitochondrial DNA mutations associated with mitochondrial cytopathies' phenotypes". European Journal of Medical Genetics 60 3 (2017): 172-177. http://www.scopus.com/inward/record.url?eid=2-s2.0-85008450521&partnerID=MN8TOARS.
    Publicado • 10.1016/j.ejmg.2016.12.009
  6. Ribeiro, C.; do Carmo Macário, M.; Viegas, A.T.; Pratas, J.; Santos, M.J.; Simões, M.; Mendes, C.; et al. "Identification of a novel deletion in SURF1 gene: Heterogeneity in Leigh syndrome with COX deficiency". Mitochondrion 31 (2016): 84-88. http://www.scopus.com/inward/record.url?eid=2-s2.0-84994711178&partnerID=MN8TOARS.
    Publicado • 10.1016/j.mito.2016.10.004
  7. Gaspar, R.; Santana, I.; Mendes, C.; Fernandes, A.S.; Duro, D.; Simões, M.; Luís, D.; Santos, M.J.; Grazina, M.. "Genetic variation of MT-ND genes in frontotemporal lobar degeneration: Biochemical phenotype-genotype correlation". Neurodegenerative Diseases 15 2 (2015): 70-80. http://www.scopus.com/inward/record.url?eid=2-s2.0-84928938610&partnerID=MN8TOARS.
    Publicado • 10.1159/000380766
  8. Montero, Raquel; Grazina, Manuela; López-Gallardo, Ester; Montoya, Julio; Briones, Paz; Navarro-Sastre, Aleix; Land, John M.; et al. "Coenzyme Q10 deficiency in mitochondrial DNA depletion syndromes". Mitochondrion 13 4 (2013): 337-341. http://dx.doi.org/10.1016/j.mito.2013.04.001.
    Publicado • 10.1016/j.mito.2013.04.001
  9. Tavares, M.V.; Santos, M.J.; Domingues, A.P.; Pratas, J.; Mendes, C.; Simões, M.; Moura, P.; Diogo, L.; Grazina, M.. "Antenatal manifestations of mitochondrial disorders". Journal of Inherited Metabolic Disease 36 5 (2013): 805-811. http://www.scopus.com/inward/record.url?eid=2-s2.0-84884350140&partnerID=MN8TOARS.
    Publicado • 10.1007/s10545-012-9567-x
  10. Ferreira, I.L.; Nascimento, M.V.; Ribeiro, M.; Almeida, S.; Cardoso, S.M.; Grazina, M.; Pratas, J.; et al. "Mitochondrial-dependent apoptosis in Huntington's disease human cybrids". Experimental Neurology 222 2 (2010): 243-255. http://www.scopus.com/inward/record.url?eid=2-s2.0-77549084450&partnerID=MN8TOARS.
    Publicado • 10.1016/j.expneurol.2010.01.002
Poster em conferência
  1. Santos, Maria João. "Mitochondrial protein import genes involvement in Leber’s hereditary optic neuropathy (LHON)". Trabalho apresentado em 15th International Symposium of the Portuguese Society for Metabolic Disorders (SPDM), 2019.
  2. Simões, M.; Bacalhau, Mafalda; Fonseca, M.I.; Ribeiro, C.; Santos, Maria João; Macário, M.C.; Diogo, L.; Grazina, M. "Assembly of OXPHOS system in patients with respiratory chain disease". Trabalho apresentado em 15th International Symposium of the Portuguese Society for Metabolic Disorders (SPDM), 2019.
  3. "A 24h screening test for TOP-3 LHON pathogenic sequence variants to be used in clinical setting and treatment assessment". Trabalho apresentado em CIBB meeting, 2019.
  4. Bacalhau, Mafalda; Simões, M.; Pratas, J.; Diogo, L.; Garcia, P.; Vaz, M.; Santos, Maria João; et al. "Mitochondrial dysfunction in a lysosomal storage disorder: a case of spinocerebellar ataxia". Trabalho apresentado em International Symposium MitoPorto: advances in mitochondrial research, 2017.
  5. Fonseca, M.I.; Bacalhau, Mafalda; Ribeiro, C.; Santos, Maria João; Macário, M.C.; Fonseca, P.; Diogo, L.; Simões, M.; Grazina, M. "Investigation of OXPHOS complexes' assembly in four LHON patients: Heterogeneity of genetic background". Trabalho apresentado em 20th Annual Meeting of the Portuguese Society of Human Genetics (SPGH – Sociedade Portuguesa de Genética Humana), 2016.
  6. Santos, D.; Santos, Maria João; Coelho, T.; Alves-Ferreira, M.; Sequeiros, J.; Alonso, I.; Sousa, A.; Grazina, M; Lemos, C.. "Mitochondrial DNA copy number and new insights on biological mechanisms of Familial Amyloid Polyneuropathy". Trabalho apresentado em XV International Symposium on Amyloidosis, 2016.
  7. Gomes, C.A.; Simões, M.; Ribeiro, C.; Macário, M.C.; Mendes, C.; Pratas, J.; Santos, Maria João; et al. "Investigation of TFAM gene involvement in LHON-plus: the phantom deletion story". Trabalho apresentado em XII International Symposium of the Portuguese Society for Metabolic Disorders (SPDM), 2016.
  8. Ramos, A.; Ribeiro, C.; Simões, M.; Santos, Maria João; Grazina, M. "The challenges of bioinformatics for NGS genetic data analysis and Sanger sequencing remaining: laboratory implications and clinical significance of mutations". Trabalho apresentado em XII International Symposium of the Portuguese Society for Metabolic Disorders (SPDM), 2016.
  9. Ribeiro, C.; Pratas, J.; Santos, Maria João; Simões, M.; Mendes, C.; Macario, M.C.; Diogo, L.; et al. "Leber Hereditary Optic Neuropathy: biochemical and genetic investigation in 10 portuguese patients.". Trabalho apresentado em XI International Symposium of the Portuguese Society for Metabolic Disorders (SPDM), 2015.
  10. Barreto, P.; Pratas, J.; Mendes, C.; Santos, Maria João; Simões, M.; Martins, C.; Duarte, J.; et al. "Hearing loss: mitochondrial genetics etiology and implications in aminoglycosids use". Trabalho apresentado em 4th In4med - Congresso médico-científico organizado pelo núcleo de estudantes de Medicina da Associação Académica de Coimbra (NEM/AAC) - "Viver (d)a Medicina", 2015.
  11. Gomes, C.A.; Ribeiro, C.; Simões, M.; Mendes, C.; Pratas, J.; Santos, Maria João; Silva, E.; et al. "Genetic investigation of mitochondrial transcription factor a (TFAM) in an unusual Leber's hereditary optic neuropathy (LHON-plus case)". Trabalho apresentado em XII CNC Annual Meeting, 2014.
  12. Domingues, A.P.; Ribeiro, C.; Santos, Maria João; Pratas, J.; Belo, A.; Moura, P.; Grazina, M. "The role of DEFB1 polymorphisms in premature rupture of membranes before 34 weeks". Trabalho apresentado em XII CNC Annual Meeting, 2014.
  13. Bacalhau, Mafalda; Pratas, J.; Santos, Maria João; Vaz, M.; Simões, M.; Mendes, C.; Rego, C.; et al. "Establishing the pathogenicity of mitochondrial DNA mutations: a cell and molecular biology approach". Trabalho apresentado em XII CNC Annual Meeting, 2014.
  14. Monteiro, N.; Ribeiro, J.C.; Santos, Maria João; Grazina, M; Pereira, P.; Girao, Henrique; Silva, E.; Silva, F.. "MYO7A transcript analysis in an Usher syndrome type 1 patient with heterozygous compound mutations". Trabalho apresentado em VI Annual Meeting of IBILI, 2014.
  15. Simões, M.; Mendes, C.; Pratas, J.; Ribeiro, C.; Veríssimo, C.; Santos, Maria João; Diogo, L.; et al. "Biochemical genetics heterogeneity in Leigh Syndrome: a case series of 40 patients". Trabalho apresentado em X International Symposium of the Portuguese Society for Metabolic Disorders (SPDM), 2014.
  16. Guiomar, P.; Vaz, M.; Bacalhau, Mafalda; Mendes, C.; Simões, M.; Pratas, J.; Santos, Maria João; et al. "Functional genomics analysis of an unusual LHON case - preliminary results". Trabalho apresentado em X International Symposium of the Portuguese Society for Metabolic Disorders (SPDM), 2014.
  17. Bacalhau, Mafalda; Pratas, J.; Santos, Maria João; Ribeiro, C.; Vaz, M.; Mendes, C.; Simões, M.; et al. "Establishing the pathogenecity of a novel mitochondrial DNA mutation". Trabalho apresentado em X International Symposium of the Portuguese Society for Metabolic Disorders (SPDM), 2014.
    10.1063/1.4904621
Resumo em conferência
  1. Grazina, M; Simões, M.; Bacalhau, M.; Ribeiro, C.; Santos, Maria João; Macário, M.C.; Diogo, L.; et al. "Functional genomics' studies are mandatory for clarifying pathogenicity of novel genetic variants detected by NGS in OXPHOS disorders.". Trabalho apresentado em 52nd European Society of Human Genetics (ESHG) Conference, Gothenburg, 2018.
    Publicado
  2. Domingues, A.P.; Ribeiro, C.; Santos, Maria João; Pratas, J.; Belo, A.; Moura, P.; Grazina, M. "The role of DEFB1 polymorphisms in premature rupture of membranes before 34 weeks". Trabalho apresentado em Journal of Perinatal Medicine, 2015.
    Publicado
  3. Ribeiro, C.; Pratas, J.; Santos, Maria João; Simões, M.; Mendes, C.; Macário, M.C.; Diogo, L.; et al. "Dual genome investigation in Leber Hereditary Optic Neuropathy". Trabalho apresentado em European Journal of Human Genetics, 2015.
    Publicado
  4. Tavares, R.; Santana, I.; Gaspar, R.; Santos, Maria João; Mendes, C.; Duro, D.; Simões, M.; Luís, D.; Grazina, M. "MT-RNRs genes sequencing: genotype correlation with biochemical and clinical phenotypes.". Trabalho apresentado em Sinapse, 2015.
    Publicado
  5. Ribeiro, C.; Guiomar, P.; Pratas, J.; Bacalhau, M.; Vaz, M.; Simões, M.; Mendes, C.; et al. "Leber hereditary optic neuropathy plus - more than just a mitochondrial DNA mutation". Trabalho apresentado em Sinapse, 2015.
    Publicado
  6. Gaspar, R.; Santana, I.; Abrantes, J.; Mendes, C.; Monteiro, R.; Santos, Maria João; Duro, D.; et al. "Complex V investigation in frontotemporal lobar degeneration: molecular and biochemical analysis". Trabalho apresentado em J Inherit Metab Dis, 2014.
    Publicado
  7. Guiomar, P.; Vaz, M.; Bacalhau, Mafalda; Mendes, C.; Simões, M.; Pratas, J.; Santos, Maria João; et al. "Molecular and cellular analysis in an unusual LHON case". Trabalho apresentado em J Inherit Metab Dis, 2014.
    Publicado
  8. Macario, M.C.; Duque, C.; Topuz, S.; Tomas, J.; Gouveia, A.R.; Rebelo, O.; Ribeiro, C.; et al. "Mitochondrial disorders associated with mitochondrial DNA polymerase gamma mutations in a neurologic adult population.". Trabalho apresentado em J Inherit Metab Dis, 2014.
    Publicado
  9. Oliveira, I.; Santana, I.; Santos, Maria João; Duro, D.; Gaspar, R.; Luís, D.; Grazina, M. "Mitochondrial genome encoding tRNAs sequence in Frontotemporal Lobar Degeneration". Trabalho apresentado em European Journal of Human Genetics, 2014.
    Publicado
  10. Gaspar, R.; Santana, I.; Abrantes, J.; Mendes, C.; Santos, Maria João; Duro, D.; Simões, M.; Luís, D.; Grazina, M.. "Mitochondrial DNA variants coding for Complex V contributing to frontotemporal lobar degeneration". Trabalho apresentado em Sinapse, 2014.
    Publicado
Tese / Dissertação
  1. Santos, Maria João. "Monitoring Kidney Transplantation using Real-Time PCR for Relative Gene Expression Analysis". Mestrado, Universidade de Coimbra Faculdade de Ciencias e Tecnologia, 2010.
  2. Santos, Maria João. "Monitoring Kidney Transplantation using Real-Time PCR for Relative Gene Expression Analysis". Licenciatura, Universidade de Coimbra Faculdade de Ciencias e Tecnologia, 2006.
Atividades

Apresentação oral de trabalho

Título da apresentação Nome do evento
Anfitrião (Local do evento)
2021/02/28 Rare Energies: See Beyond / Energias Raras: Ver Mais Além Rare Energies: See Beyond / Energias Raras: Ver Mais Além
Laboratory of Mitochondrial BioMedicine and Theranostics, Center for Neuroscience and Cell Biology (CNC) (Coimbra, Portugal)
2020/11/06 Challenges in LHON diagnostics / Desafios no diagnóstico genético de LHON VIII Neurogenetics Meeting: Mitochondrial Diseases: and when power fails?
IBMC Institute for Molecular and Cell Biology (Online, Portugal)
2019/03/16 Mitochondrial protein import genes involvement in Leber’s hereditary optic neuropathy (LHON) XV International Symposium of the Portuguese Society for Metabolic Disorders (SPDM)
SPDM (Coimbra, Portugal)
2019/03/16 Assembly of OXPHOS system in patients with respiratory chain disease. XV International Symposium of the Portuguese Society for Metabolic Disorders (SPDM)
SPDM (Coimbra, Portugal)
2018/10/22 Mitochondrial DNA: When the Circle Goes Bad MEETING MITOCHONDRIAL DNA AND DERIVED PEPTIDES IN HEALTH AND DISEASE
(Coimbra, Portugal)
2018/09/26 Advanced Functional Genomics Studies: a step forward in genetics. 5th meeting of users of NGS ILLUMINA platforms
ILC (Coimbra, Portugal)
2017/10/03 Challenges of NGS implementation for genetic screening of MRC disorders. 4th meeting of users of NGS ILLUMINA platforms
ILC (Porto, Portugal)
2017/06/08 Investigation of OPA1 gene in Leber’s Hereditary Optic Neuropathy XLI Jornadas Portuguesas de Genética
(Aveiro, Portugal)
2017/03/17 Report of a novel mitochondrial ATP8 gene mutation in a patient with severe optic neuropathy: functional demonstration of pathogenicity XIII International Symposium of the Portuguese Society for Metabolic Disorders (SPDM)
SPDM (Évora, Portugal)
2016/03/18 Investigation of TFAM gene involvement in LHON-plus: the phantom deletion story XII International Symposium of the Portuguese Society for Metabolic Disorders (SPDM)
SPDM (Coimbra, Portugal)
2016/03/18 Evaluation of m.7486G>A pathogenicity using a functional genomics’ approach. XII International Symposium of the Portuguese Society for Metabolic Disorders (SPDM)
SPDM (Coimbra, Portugal)
2015/12/18 Functional genomics analysis to gathering evidence for m.7486G>A mutation pathogenicity XIII CNC Annual Meeting
CNC (Coimbra, Portugal)
2015/05/30 MT-RNRs genes sequencing: genotype correlation with biochemical and clinical phenotypes 29ª Reunião do Grupo de Estudo de Envelhecimento Cerebral e Demências (GEECD)
GEECD (Aveiro, Portugal)
2015/05/21 Leber hereditary optic neuropathy plus - more than just a mitochondrial DNA mutation Fórum de Neurologia
(Aveiro, Portugal)
2015/04/19 Genética e Doença Cardiovascular - Quando é útil o teste genético para o diagnóstico e estratificação de risco? XXXVI Congresso Português de Cardiologia
Sociedade Portuguesa de Caridologia (Albufeira, Portugal)
2015/03/20 Mitochondrial diseases linked to mutations of the POLG gene XI International Symposium of the Portuguese Society for Metabolic Disorders (SPDM)
SPDM (Porto, Portugal)
2015/01/22 Establishing the pathogenicity of mitochondrial DNA mutations: a cell and molecular biology approach Annual Meeting PhD Program in Health Sciences
Faculdade de Medicina da Universidade de Coimbra (Coimbra, Portugal)
2014/06/27 Analysis of MTRNR genes in Frontotemporal Lobar Degeneration 28ª Reunião do Grupo de Estudo de Envelhecimento Cerebral e Demências (GEECD)
GEECD (Aveiro, Portugal)
2014/06/27 Mitochondrial genome variants influencing protein translation in frontotemporal lobar degeneration 28ª Reunião do Grupo de Estudo de Envelhecimento Cerebral e Demências (GEECD)
GEECD (Aveiro, Portugal)
2014/05/15 Mitochondrial DNA variants coding for Complex V contributing to frontotemporal lobar degeneration Fórum de Neurologia
(Coimbra, Portugal)
2014/03/20 Identification of a novel SURF1 gene mutation in Leigh syndrome X International Symposium of the Portuguese Society for Metabolic Disorders (SPDM)
SPDM (Cascais, Portugal)

Organização de evento

Nome do evento
Tipo de evento (Tipo de participação)
Instituição / Organização
2021/02/28 - 2021/02/28 Rare Energies: See Beyond / Energias Raras: Ver Mais Além (2021/02/28 - 2021/02/28)
Conferência (Membro da Comissão Organizadora)
CNC - Center for neuroscience and cell biology, University of Coimbra, Portugal
2020/10/11 - 2020/10/11 The blindness of a composer and the vision of science in rare disease / A cegueira de um compositor e a visão na ciência de uma doença rara (2020/10/11 - 2020/10/11)
Conferência (Membro da Comissão Organizadora)
CNC - Center for neuroscience and cell biology, University of Coimbra, Portugal

Participação em evento

Descrição da atividade
Tipo de evento
Nome do evento
Instituição / Organização
2021/12/20 - 2021/12/20 CIBB Meeting 2021
Encontro
CIBB Meeting 2021
Universidade de Coimbra Centro de Neurociências e Biologia Celular, Portugal
2021/12/09 - 2021/12/09 LHON Forum 2021
Seminário
LHON Forum 2021
Chiesi España SA, Espanha
2021/11/17 - 2021/11/18 MAD Retreat
Encontro
Science Out of the Box - MAD (Metabolism, aging and Disease) Group Retreat 2021
Universidade de Coimbra Centro de Neurociências e Biologia Celular, Portugal
2021/08/28 - 2021/08/31 European Human Genetics Virtual Conference 2021
Congresso
European Human Genetics Virtual Conference 2021
European Society of Human Genetics, Áustria
2021/07/02 - 2021/07/23 VIII Cell Culture and Tissue Training Course 2021
Outro
VIII Cell Culture and Tissue Training Course 2021
Universidade de Coimbra Faculdade de Medicina, Portugal
2020/06/06 - 2020/06/09 European Human Genetics Conference 2020 (Online event)
Congresso
European Human Genetics Conference 2020
2019/12/19 - 2019/12/20 CIBB Meeting 2019
Congresso
CIBB Meeting 2019
Center for Innovative Biomedicine and Biotechnology, Portugal
2019/11/08 - 2019/11/08 NGS/WES – Genomic revolution in the clinical practice
Oficina (workshop)
NGS/WES – Genomic revolution in the clinical practice
2019/10/09 - 2019/10/09 6ª Reunião de Utilizadores de Plataformas NGS / 6th meeting of users of NGS ILLUMINA platforms
Encontro
6th meeting of users of NGS ILLUMINA platforms
2019/05/21 - 2019/05/21 EU General Data Protection Regulation (GDPR/RGPD) - training session
Seminário
EU General Data Protection Regulation (GDPR/RGPD) - training session
Universidade de Coimbra Centro de Neurociências e Biologia Celular, Portugal
2019/03/20 - 2019/03/22 S5 System training
Oficina (workshop)
S5 System training
Universidade de Coimbra Faculdade de Medicina, Portugal
2019/03/14 - 2019/03/16 XV International Symposium of the Portuguese Society for Metabolic Disorders (SPDM)
Congresso
XV International Symposium of the Portuguese Society for Metabolic Disorders (SPDM)
2018/10/12 - 2018/10/12 How to write a winning abstract
Oficina (workshop)
How to write a winning abstract
Santhera Pharmaceuticals Schweiz AG, Suiça
2018/09/27 - 2018/09/27 Genomics Day
Encontro
Genomics Day
2018/09/26 - 2018/09/27 5ª Reunião de Utilizadores de Plataformas NGS / 5th meeting of users of NGS ILLUMINA platforms
Encontro
5th meeting of users of NGS ILLUMINA platforms
2018/05/22 - 2018/05/22 Gestão de Resíduos Hospitalares Perigosos - Triagem e Acondicionamento / Management of Hazardous Hospital Waste - Sorting and Packaging
Seminário
Management of Hazardous Hospital Waste - Sorting and Packaging
2017/12/21 - 2017/12/21 2nd Meeting on Biomedical Research @UC
Encontro
2nd Meeting on Biomedical Research @UC
Universidade de Coimbra Centro de Neurociências e Biologia Celular, Portugal
2017/09/20 - 2017/12/13 Plataforma de Gestão da Qualidade UeBe.Q / Quality Management Platform UeBe.Q
Oficina (workshop)
Quality Management Platform UeBe.Q
2017/10/02 - 2017/10/03 4ª Reunião de Utilizadores de Plataformas NGS / 4th meeting of users of NGS ILLUMINA platforms
Encontro
4th meeting of users of NGS ILLUMINA platforms
2017/09/27 - 2017/09/27 Ação de Formação sobre Gestão Integrada de Resíduos Hospitalares / Training on Integrated Management of Hospital Waste
Seminário
Training on Integrated Management of Hospital Waste
2017/09/21 - 2017/09/22 Bring Your Own Data To Link Rare Disease Registries
Oficina (workshop)
Bring Your Own Data To Link Rare Disease Registries
2017/09/18 - 2017/09/20 5th International Summer School on Rare Disease and Orphan Drug Registries
Oficina (workshop)
5th International Summer School on Rare Disease and Orphan Drug Registries
2017/04/28 - 2017/04/29 I Congresso de Investigação em Medicina da Escolas Médicas Portuguesas / I Congress of the Portuguese Medical Schools
Congresso
I Congress of the Portuguese Medical Schools
Universidade de Coimbra, Portugal
2016/12/19 - 2016/12/20 1st Meeting on Biomedical Research @UC
Encontro
1st Meeting on Biomedical Research @UC
Universidade de Coimbra Centro de Neurociências e Biologia Celular, Portugal
2016/11/29 - 2016/11/30 3ª Reunião de utilizadores Illumina / 3rd meeting of users of NGS ILLUMINA platforms
Encontro
3rd meeting of users of NGS ILLUMINA platforms
2016/06/14 - 2016/06/14 Formação para a realização de ensaios de NGS / Training to perform NGS tests
Oficina (workshop)
Training to perform NGS tests
2016/06/07 - 2016/06/07 Simpósio sobre genética e proteção de dados pessoais / Symposium on genetics and personal data protection
Simpósio
Symposium on genetics and personal data protection
2016/04/21 - 2016/05/10 Requisitos da Norma NP EN ISO 9001:2015 / Requirements of NP EN ISO 9001:2015 Standard
Seminário
Requirements of NP EN ISO 9001:2015 Standard
Universidade de Coimbra Centro de Neurociências e Biologia Celular, Portugal
2016/04/07 - 2016/04/07 Let's talk about CRISP
Seminário
Let's talk about CRISP
2016/03/17 - 2016/03/18 XII International Symposium of the Portuguese Society for Metabolic Disorders (SPDM)
Congresso
XII International Symposium of the Portuguese Society for Metabolic Disorders (SPDM)
2015/12/17 - 2015/12/18 XIII CNC Annual Meeting
Encontro
XIII CNC Annual Meeting
Universidade de Coimbra Centro de Neurociências e Biologia Celular, Portugal
2015/10/23 - 2015/10/23 Formação de Saúde e Segurança no trabalho (SST) / Health and Safety Training
Seminário
Health and Safety Training
2014/12/15 - 2014/12/16 XII CNC Annual Meeting
Encontro
XII CNC Annual Meeting
2014/11/20 - 2014/11/20 Info Day Nacional – Oportunidades e Desafios à Investigação & Inovação em Saúde, Alterações Demográficas e Bem-estar
Simpósio
Info Day Nacional – Oportunidades e Desafios à Investigação & Inovação em Saúde, Alterações Demográficas e Bem-estar
2014/05/31 - 2014/06/03 European Human Genetics Conference 2014
Congresso
European Human Genetics Conference 2014
2013/12/17 - 2013/12/17 Neuropatia Ótica Hereditária de Leber - update / Leber hereditary optic neuropathy - update
Seminário
Leber hereditary optic neuropathy - update

Tutoria

Tópico Nome do aluno
2018/09/03 - 2018/09/28 Mentoring of LORE student (4 weeks long Research Exchange of Med Student) Emilijia Welker
2018/07/02 - 2018/07/27 Mentoring of LORE student (4 weeks long Research Exchange of Med Student) Mireia Santamaría Sáez-Torres
2017/07/03 - 2017/07/28 Mentoring of LORE student (4 weeks long Research Exchange of Med Student) Julia Armengol
2017/07/03 - 2017/07/28 Mentoring of LORE student (4 weeks long Research Exchange of Med Student) Andrea Castillo
2016/09/05 - 2016/09/30 Mentoring of LORE student (4 weeks long Research Exchange of Med Student) Christina Noceti
2016/07/04 - 2016/07/27 Mentoring of LORE student (4 weeks long Research Exchange of Med Student) Man Wong