João Pedro Marques (João P Marques)

ResearcherID Ciência ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 40

Top Topics

Medical Education

Optical Coherence Tomography

Diabetic Retinopathy

Top Venues

Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie

Eye (London, England)

BMC ophthalmology

This page only lists publications with an associated author ORCID identifier.

Publications

Telmo Cortinhal, Cristina Santos, Sara Vaz-Pereira, Ana Ambrósio Marta, Lilianne Duarte, Vítor Miranda, José F Costa, Ana-Berta Sousa, Virginie G Peter, Karolina Kaminska, Carlo Rivolta, Ana Luísa Carvalho, Jorge Saraiva, Célia Azevedo Soares, Rufino Silva, Joaquim Murta, Luísa Coutinho Santos, João Pedro Marques
Genetic profile of syndromic retinitis pigmentosa in Portugal. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 262 (6) (2024)
Telmo Cortinhal, Cristina Santos, Sara Vaz-Pereira, Ana Ambrósio Marta, Lilianne Duarte, Vítor Miranda, José F Costa, Ana-Berta Sousa, Virginie G Peter, Karolina Kaminska, Carlo Rivolta, Ana Luísa Carvalho, Jorge Saraiva, Célia Azevedo Soares, Rufino Silva, Joaquim Murta, Luísa Coutinho Santos, João Pedro Marques
Genetic profile of syndromic retinitis pigmentosa in Portugal. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 262 (6) (2024)
Telmo Cortinhal, Cristina Santos, Sara Vaz-Pereira, Ana Ambrósio Marta, Lilianne Duarte, Vítor Miranda, José F Costa, Ana-Berta Sousa, Virginie G Peter, Karolina Kaminska, Carlo Rivolta, Ana Luísa Carvalho, Jorge Saraiva, Célia Azevedo Soares, Rufino Silva, Joaquim Murta, Luísa Coutinho Santos, João Pedro Marques
Genetic profile of syndromic retinitis pigmentosa in Portugal. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 262 (6) (2024)
Raquel Félix, Nuno Gouveia, João Bernardes, Rufino Silva, Joaquim Murta, João Pedro Marques
Prognostic impact of hyperreflective foci in nonsyndromic retinitis pigmentosa. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie (2024)
Miriam Bauwens, Vincent De Man, Isabelle Audo, Irina Balikova, Wadih M Zein, Vasily Smirnov, Sebastian Held, Sascha Vermeer, Elke Loos, Julie Jacob, Ingele Casteels, Julie Désir, Fanny Depasse, Stijn Van de Sompele, Mattias Van Heetvelde, Marieke De Bruyne, Camille Andrieu, Christel Condroyer, Aline Antonio, Robert Hufnagel, Ana Luísa Carvalho, João Pedro Marques, Christina Zeitz, Elfride De Baere, Markus Damme
Expanding the genetic landscape of Usher syndrome type IV caused by pathogenic ARSG variants. Clinical genetics (2024)
Nuno Gouveia, Oluji Chukwunalu, Carolina Oliveira, Celso Henrique Alves, Rufino Silva, Joaquim Murta, João Pedro Marques
Exploring self-reported visual function and vision-related anxiety in patients with RPGR-associated retinal degeneration. Scientific reports 14 (1) (2024)
Margarida Queirós Dias, Nuno Gouveia, Raquel Félix, Sérgio Estrela-Silva, Diogo Cabral, Ana Luísa Carvalho, Joaquim Murta, Rufino Silva, João Pedro Marques
Mutational spectrum and deep phenotyping in Pseudoxanthoma Elasticum: Findings from a Portuguese cohort. European journal of ophthalmology (2024)
Nuno Gouveia, Oluji Chukwunalu, Carolina Oliveira, Celso Henrique Alves, Rufino Silva, Joaquim Murta, João Pedro Marques
Exploring self-reported visual function and vision-related anxiety in patients with RPGR-associated retinal degeneration. Scientific reports 14 (1) (2024)
Nuno Gouveia, Oluji Chukwunalu, Carolina Oliveira, Celso Henrique Alves, Rufino Silva, Joaquim Murta, João Pedro Marques
Exploring self-reported visual function and vision-related anxiety in patients with RPGR-associated retinal degeneration. Scientific reports 14 (1) (2024)
Telmo Cortinhal, Cristina Santos, Sara Vaz-Pereira, Ana Ambrósio Marta, Lilianne Duarte, Vítor Miranda, José F Costa, Ana-Berta Sousa, Virginie G Peter, Karolina Kaminska, Carlo Rivolta, Ana Luísa Carvalho, Jorge Saraiva, Célia Azevedo Soares, Rufino Silva, Joaquim Murta, Luísa Coutinho Santos, João Pedro Marques
Genetic profile of syndromic retinitis pigmentosa in Portugal. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 262 (6) (2024)
Bruno Magalhães Teixeira, Inês Figueiredo, Miguel Raimundo, Hugo Quental, Ana Luísa Carvalho, Rufino Silva, Joaquim Murta, João Pedro Marques
Expanding the mutational and phenotypical spectrum of FHONDA syndrome. European journal of ophthalmology (2024)
Telmo Cortinhal, Cristina Santos, Sara Vaz-Pereira, Ana Ambrósio Marta, Lilianne Duarte, Vítor Miranda, José F Costa, Ana-Berta Sousa, Virginie G Peter, Karolina Kaminska, Carlo Rivolta, Ana Luísa Carvalho, Jorge Saraiva, Célia Azevedo Soares, Rufino Silva, Joaquim Murta, Luísa Coutinho Santos, João Pedro Marques
Genetic profile of syndromic retinitis pigmentosa in Portugal. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie (2024)
João Pedro Marques, Ricardo Machado Soares, Sílvia Simão, Rebhi Abuzaitoun, Chris Andrews, C Henrique Alves, António Francisco Ambrósio, Joaquim Murta, Rufino Silva, Maria Fernanda Abalem, K Thiran Jayasundera
Self-reported visual function and psychosocial impact of visual loss in EYS -associated retinal degeneration in a Portuguese population. Ophthalmic genetics (2023)
Sara Geada, Francisco Teixeira-Marques, Bruno Teixeira, Ana Luísa Carvalho, Nuno Lousan, Jorge Saraiva, Joaquim Murta, Rufino Silva, Xavier Zanlonghi, Sabine Defoort-Dhellemmes, Vasily M Smirnov, Claire-Marie Dhaenens, Catherine Blanchet, Isabelle Meunier, João Pedro Marques
Mutational Spectrum, Ocular and Olfactory Phenotypes of CNGB1 -Related RP-Olfactory Dysfunction Syndrome in a Multiethnic Cohort. Genes 14 (4) (2023)
Sara Geada, Francisco Teixeira-Marques, Bruno Teixeira, Ana Luísa Carvalho, Nuno Lousan, Jorge Saraiva, Joaquim Murta, Rufino Silva, Xavier Zanlonghi, Sabine Defoort-Dhellemmes, Vasily M Smirnov, Claire-Marie Dhaenens, Catherine Blanchet, Isabelle Meunier, João Pedro Marques
Mutational Spectrum, Ocular and Olfactory Phenotypes of CNGB1 -Related RP-Olfactory Dysfunction Syndrome in a Multiethnic Cohort. Genes 14 (4) (2023)
Sara Geada, Francisco Teixeira-Marques, Bruno Teixeira, Ana Luísa Carvalho, Nuno Lousan, Jorge Saraiva, Joaquim Murta, Rufino Silva, Xavier Zanlonghi, Sabine Defoort-Dhellemmes, Vasily M Smirnov, Claire-Marie Dhaenens, Catherine Blanchet, Isabelle Meunier, João Pedro Marques
Mutational Spectrum, Ocular and Olfactory Phenotypes of CNGB1 -Related RP-Olfactory Dysfunction Syndrome in a Multiethnic Cohort. Genes 14 (4) (2023)
Emmanuel Rebelo Neves, Ana Luísa Carvalho, Teresa Mesquita, Catarina Paiva, Mário Alfaiate, João Figueira, Joaquim Murta, João Pedro Marques
Bilateral functional worsening following voretigene neparvovec therapy. Eye (London, England) (2023)
Joana Silva Fernandes, Pedro Prata Gomes, Pedro Neves, João Pedro Marques
Idiopathic acute exudative polymorphous vitelliform maculopathy: the importance of multimodal imaging, systemic workup and genetic testing. BMJ case reports 16 (6) (2023)
Joana Silva Fernandes, Pedro Prata Gomes, Pedro Neves, João Pedro Marques
Idiopathic acute exudative polymorphous vitelliform maculopathy: the importance of multimodal imaging, systemic workup and genetic testing. BMJ case reports 16 (6) (2023)
Sara Geada, Francisco Teixeira-Marques, Bruno Teixeira, Ana Luísa Carvalho, Nuno Lousan, Jorge Saraiva, Joaquim Murta, Rufino Silva, Xavier Zanlonghi, Sabine Defoort-Dhellemmes, Vasily M Smirnov, Claire-Marie Dhaenens, Catherine Blanchet, Isabelle Meunier, João Pedro Marques
Mutational Spectrum, Ocular and Olfactory Phenotypes of CNGB1 -Related RP-Olfactory Dysfunction Syndrome in a Multiethnic Cohort. Genes 14 (4) (2023)
Obaid Imtiyazul Haque, Anbukayalvizhi Chandrasekaran, Faisal Nabi, Owais Ahmad, João Pedro Marques, Tanweer Ahmad
A novel compound heterozygous BEST1 gene mutation in two siblings causing autosomal recessive bestrophinopathy. BMC ophthalmology 22 (1) (2022)
João Pedro Marques, Emmanuel Neves, Sara Geada, Ana Luísa Carvalho, Joaquim Murta, Jorge Saraiva, Rufino Silva
Frequency of cystoid macular edema and vitreomacular interface disorders in genetically solved syndromic and non-syndromic retinitis pigmentosa. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 260 (9) (2022)
João Pedro Marques, Sara Vaz-Pereira, José Costa, Ana Marta, José Henriques, Rufino Silva
Challenges, facilitators and barriers to the adoption and use of a web-based national IRD registry: lessons learned from the IRD-PT registry. Orphanet journal of rare diseases 17 (1) (2022)
João Pedro Marques, Rosa Pinheiro, Ana Luísa Carvalho, Miguel Raimundo, Mário Soares, Pedro Melo, Joaquim Murta, Jorge Saraiva, Rufino Silva
Genetic spectrum, retinal phenotype, and peripapillary RNFL thickness in RPGR heterozygotes. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie (2022)
Obaid Imtiyazul Haque, Anbukayalvizhi Chandrasekaran, Faisal Nabi, Owais Ahmad, João Pedro Marques, Tanweer Ahmad
A novel compound heterozygous BEST1 gene mutation in two siblings causing autosomal recessive bestrophinopathy. BMC ophthalmology 22 (1) (2022)
João Pedro Marques, Luís Bernardes, Carolina Oliveira, Gabriela Fonseca, João Quadrado Gil, Luciana Sotero, Ana Paula Relvas, Joaquim Murta, Rufino Silva, Gabrielle Davis Lacy, Maria Fernanda Abalem, Kanishka T Jayasundera
Portuguese translation and linguistic validation of the Michigan Retinal Degeneration Questionnaire and the Michigan Vision-Related Anxiety Questionnaire in a cohort with inherited retinal degenerations. Ophthalmic genetics 43 (1) (2022)
Obaid Imtiyazul Haque, Anbukayalvizhi Chandrasekaran, Faisal Nabi, Owais Ahmad, João Pedro Marques, Tanweer Ahmad
A novel compound heterozygous BEST1 gene mutation in two siblings causing autosomal recessive bestrophinopathy. BMC ophthalmology 22 (1) (2022)
Obaid Imtiyazul Haque, Anbukayalvizhi Chandrasekaran, Faisal Nabi, Owais Ahmad, João Pedro Marques, Tanweer Ahmad
A novel compound heterozygous BEST1 gene mutation in two siblings causing autosomal recessive bestrophinopathy. BMC ophthalmology 22 (1) (2022)
João Pedro Marques, Pedro Pereira
Gyrate atrophy of the choroid and retina. Postgraduate medical journal (2021)
João Pedro Marques
Instagram as a vehicle to promote disease awareness and medical education in #retinaldystrophies. Postgraduate medical journal (2021)
João Pedro Marques, Fernanda Belga Ottoni Porto, Ana Luísa Carvalho, Emmanuel Neves, Rui Chen, Shirley Aparecida Madureira Sampaio, Joaquim Murta, Jorge Saraiva, Rufino Silva
EYS-Associated Sector Retinitis Pigmentosa. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie (2021)
Tiago M Rodrigues, João Pedro Marques, Rufino Silva
Response to 'Comment on: Macular OCT-angiography parameters to predict the clinical stage of nonproliferative diabetic retinopathy: an exploratory analysis'. Eye (London, England) 34 (12) (2020)
João Pedro Marques, Ana Luísa Carvalho, José Henriques, Joaquim Neto Murta, Jorge Saraiva, Rufino Silva
Design, development and deployment of a web-based interoperable registry for inherited retinal dystrophies in Portugal: the IRD-PT. Orphanet journal of rare diseases 15 (1) (2020)
Cláudia Farinha, Maria Luz Cachulo, Rita Coimbra, Dalila Alves, Sandrina Nunes, Isabel Pires, João Pedro Marques, José Costa, Amélia Martins, Isa Sobral, Patrícia Barreto, Ines Lains, João Figueira, Luisa Ribeiro, José Cunha-Vaz, Rufino Silva
Age-Related Macular Degeneration Staging by Color Fundus Photography vs. Multimodal Imaging-Epidemiological Implications (The Coimbra Eye Study-Report 6). Journal of clinical medicine 9 (5) (2020)
João Pedro Marques, João Bernardes, Sara Geada, Mário Soares, Dora Teixeira, Cláudia Farinha, Isabel Pires, Maria Luz Cachulo, Rufino Silva
Non-exudative macular neovascularization in pseudoxanthoma elasticum. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 259 (4) (2020)
Mariana A Oliveira, Cláudia Farinha, Tiago M Rodrigues, Amélia Martins, Maria da Luz Cachulo, João Pedro Marques, Isabel Pires, Rufino Silva
Macular atrophy development in neovascular age-related macular degeneration during first year of treatment: Incidence and risk factors. European journal of ophthalmology 31 (2) (2020)
Tiago M Rodrigues, João Pedro Marques, Mário Soares, Sílvia Simão, Pedro Melo, Amélia Martins, João Figueira, Joaquim N Murta, Rufino Silva
Macular OCT-angiography parameters to predict the clinical stage of nonproliferative diabetic retinopathy: an exploratory analysis. Eye (London, England) 33 (8) (2019)
João Pedro Marques, João Pires, Jorge Simão, Marco Marques, João Q Gil, Inês Laíns, Dalila Alves, Sandrina Nunes, Maria Luz Cachulo, John B Miller, Demetrios G Vavvas, Joan W Miller, Deeba Husain, Rufino Silva
Validation of RetmarkerAMD as a semiautomatic grading software for AMD. Eye (London, England) 34 (3) (2019)
Joana Providência, Tiago M Rodrigues, Mariana Oliveira, João Bernardes, João Pedro Marques, Joaquim Murta, Rufino Silva
Real-World Results of Aflibercept versus Ranibizumab for the Treatment of Exudative AMD Using a Fixed Regimen. BioMed research international 2018 (2018)
João Pedro Marques, Cláudia Farinha, Miguel Ângelo Costa, Ângela Ferrão, Sandrina Nunes, Rufino Silva
Protocol for a randomised, double-masked, sham-controlled phase 4 study on the efficacy, safety and tolerability of intravitreal aflibercept monotherapy compared with aflibercept with adjunctive photodynamic therapy in polypoidal choroidal vasculopathy: the ATLANTIC study. BMJ open 7 (8) (2017)