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Diana Gonzaga
ResearcherPublications, citations & collaboration network
Diana Gonzaga is a researcher indexed in ScholarIQ from OpenAlex & ORCID. ScholarIQ records 12 works, 39 citations, an h-index of 3 and an i10-index of 2.
12
Works
39
Citations
3
h-index
2
i10-index
IDs:OpenAlex
How has Diana Gonzaga's publication output changed over time?
ScholarIQpublication output · 2012–2024
Output declined50% over the shown period — from 2 works in 2012 to 1 in 2024.
2
2
1
2
2
1
201220162019202220232024
What are the most-cited papers on Diana Gonzaga?
ScholarIQmost cited works
New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset
María del Mar O’Callaghan, Sonia Emperador, Ester López‐Gallardo, Cristina Jou, Núria Bujan, Raquel Montero, Àngels García‐Cazorla, Diana Gonzaga, Isidró Ferrer, Paz Briones, Eduardo Ruiz‐Pesini, Mercè Pineda, Rafael Artuch, Julio Montoya
S185726200. 201224 Citations
El papel de los cannabinoides en los trastornos del neurodesarrollo de niños y adolescentes
Francisca Freitas, Sofia Pimenta, Sara Soares, Diana Gonzaga, Inês Vaz Matos, C. Prior
Revista de Neurología. 202211 CitationsOPEN ACCESS
Refining the Clinical Spectrum of the 17p13.3 Microduplication Syndrome: Case-Report of a Familial Small Microduplication
Jorge Diogo Da Silva, Diana Gonzaga, Ana Barreta, Hildeberto Correia, Ana María Fortuna, Ana Rita Soares, Natáliya Tkachenko
Biomedicines. 20223 CitationsOPEN ACCESS
Co-occurrence of neurofibromatosis type 1, caused by Alu insertion, and 16p13.11 microduplication
Rita Quental, Diana Pinho, Natália Tkachenko, Diana Gonzaga, Maria do Céu Mota, Cristina Garrido, Carla Carmona, Sofia Quental, Ana Maria Fortuna, Claudio Lopes Soares
S3034796422. 20241 CitationsOPEN ACCESS
Infeção do trato urinário - agentes etiológicos e padrão de resistência local
Hernâni Brito, Diana Gonzaga, Paulo Pereira, Liliana Rocha, Paula Matos
S4306402433. 20120 CitationsOPEN ACCESS
Related on ScholarIQ
Hospital de Santo António
Institution
New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset
Paper
El papel de los cannabinoides en los trastornos del neurodesarrollo de niños y adolescentes
Paper
Refining the Clinical Spectrum of the 17p13.3 Microduplication Syndrome: Case-Report of a Familial Small Microduplication
Paper
Co-occurrence of neurofibromatosis type 1, caused by Alu insertion, and 16p13.11 microduplication
Paper
Infeção do trato urinário - agentes etiológicos e padrão de resistência local
Paper