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Carlos Alberto Reyes-Silva

Observed names: Carlos Alberto Reyes, Carlos Reyes-Silva
ORCID: 0000-0002-1141-3279
Observed ORCID: 0000-0002-1141-3279
OpenAlex ID: A5045883670
Genetic Testing to Inform Epilepsy Treatment Management From an International Study of Clinical Practice
2022 · Dianalee McKnight, Ana Morales, et al. · JAMA Neurology · 95
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A snapshot of current genetic testing practice in Lynch syndrome: The results of a representative survey of 33 Latin American existing centres/registries
2019 · Adriana Della Valle, Benedito Mauro Rossi, et al. · European Journal of Cancer · 32
Case Report: Misdiagnosis of Maturity-Onset Diabetes of the Young as type 1, type 2 or gestational diabetes: insights from a Latin American tertiary center
2025 · Rossana Ruiz-Urbaez, David Males-Maldonado, et al. · Frontiers in Medicine · 6
Characterization of Screening Strategies for Lynch Syndrome in Latin America
2025 · Anthony Vladimir Campos-Segura, Karin Alvarez, et al. · Clinical Gastroenterology and Hepatology · 5
Dyggve–Melchior–Clausen Syndrome in Ecuador: Expanding Knowledge on a Rare Genetic Disorder
2025 · Carlos Reyes-Silva, Joseline Gallardo-Vizuete, et al. · Genes · 4
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Diabetic Nephropathy, Retinopathy, and Functional Hypogonadism in a Patient with MODY10: A Case Report
2024 · Rossana Ruiz-Urbaez, Mariela Viviana Villagómez-Estrada, et al. · Medicina · 4
Case Report: CYLD cutaneous syndrome with malignant transformation to spiradenocarcinoma: cooperative effects of CYLD truncation and an MSH2 clamp-domain variant in an Ecuadorian patient
2026 · Carlos Reyes-Silva, Gabriela Jaramillo-Koupermann, et al. · Frontiers in Medicine · 1
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Thiamine-responsive megaloblastic anemia syndrome with novel compound heterozygous SLC19A2 mutations and thrombotic events: a case report
2026 · Francisco Xavier Jiménez, Carlos Rojas, et al. · Journal of Medical Case Reports
Pseudoacondroplasia: desafío diagnóstico y abordaje multidisciplinario en una paciente con escoliosis congénita y talla baja
2025 · Joffre Andres Calvopiña Rea, Carlos Alberto Reyes, et al. · Revista Colombiana de Endocrinología Diabetes & Metabolismo
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Germline structural variant as the cause of Lynch Syndrome in a family from Ecuador
2025 · Gemma Llargués-Sistac, Laia Bonjoch, et al. · npj Genomic Medicine
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Case Report: Craniofacial deafness hand syndrome with unusual cardiovascular symptoms and lack of holistic care
2025 · Samantha Saenz Hinojosa, Carlos Reyes-Silva, et al. · Frontiers in Genetics
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Síndrome de quilomicronemia familiar, deficiencia del factor de maduración de lipasa
2023 · Joffre Andrés Calvopiña-Rea, Carlos Alberto Reyes-Silva, et al. · Revista Colombiana de Endocrinología Diabetes & Metabolismo
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Works count: 12
Citation count: 147
H-index: 4
I10-index: 2
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