Author

Marta Diñeiro

Observed names: Diñeiro, Marta, M. Diñeiro, Marta Diñeiro Soto, Marta Diñeiro Soto

ORCID: 0000-0002-4910-8675

Observed ORCID: 0000-0002-4910-8675

OpenAlex ID: A5089737441

Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients

2018 · Rubén Cabanillas, Marta Diñeiro, et al. · BMC Medical Genomics · 107

Comprehensive genomic diagnosis of inherited retinal and optical nerve disorders reveals hidden syndromes and personalized therapeutic options

2020 · Marta Diñeiro, Raquel Capín, et al. · Acta Ophthalmologica · 18

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Radixin modulates the function of outer hair cell stereocilia

2020 · Sonal Prasad, Barbara Vona, et al. · Communications Biology · 17

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Clinical Impact of Genetic Diagnosis of Sensorineural Hearing Loss in Adults

2022 · Patricia Corriols-Noval, Eugenia Carmela López Simón, et al. · Otology & Neurotology · 14

A novel molecular diagnostics platform for somatic and germline precision oncology

2017 · Rubén Cabanillas, Marta Diñeiro, et al. · Molecular Genetics & Genomic Medicine · 13

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CANVAS: A New Genetic Entity in the Otorhinolaryngologist’s Differential Diagnosis

2021 · María Costales, Rodrigo Casanueva, et al. · Otolaryngology · 7

Clinical utility of liquid biopsy and integrative genomic profiling in early-stage and oligometastatic cancer patients treated with radiotherapy

2022 · Guadalupe A. Cifuentes, Adrián Santiago, et al. · British Journal of Cancer · 6

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Association Study of MTHFR Polymorphisms with Nonarteritic Anterior Ischemic Optic Neuropathy in a Spanish Population

2020 · Beatriz Fernández-Vega, Lydia Álvarez, et al. · Biomedicine Hub · 5

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Utilidad clínica de la secuenciación de nueva generación en el diagnóstico etiológico de la hipoacusia neurosensorial en una Unidad de Hipoacusia Infantil

2019 · María Costales, Marta Diñeiro, et al. · Acta Otorrinolaringológica Española · 5

A Novel Recurrent 200 kb CRYL1 Deletion Underlies DFNB1A Hearing Loss in Patients from Northwestern Spain

2025 · Guadalupe A. Cifuentes, Marta Diñeiro, et al. · Genes · 4

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Clinical Utility of Next-generation Sequencing in the Aetiological Diagnosis of Sensorineural Hearing Loss in a Childhood Hearing Loss Unit

2020 · María Costales, Marta Diñeiro, et al. · Acta Otorrinolaringologica (English Edition) · 3

Sequencing results from multiple individuals of different ethnicities strongly question the existence of the KCNE1B pseudogene

2019 · Marta Diñeiro, Guadalupe A. Cifuentes, et al. · European Journal of Human Genetics · 1

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Effect of antioxidant supplementation with acetyl-L-carnitine and N-acetylcysteine on preimplantation embryo development: a prospective within-patient study.

2026 · Marta Diñeiro Soto

Enhanced Exome Sequencing Improves the Genetic Diagnosis of Deafblindness

2026 · Guadalupe A. Cifuentes, Marta Diñeiro, et al. · Genes

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72P Liquid biopsy biomarkers utility in radiation oncology

2022 · G.A. Cifuentes, L. Mendez, et al. · Annals of Oncology

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87P ctDNA analysis as a prognostic factor for early-stage and oligometastatic patients treated with radiotherapy

2022 · G. Alvarez Cifuentes, A. Santiago, et al. · Annals of Oncology

Secuenciación genómica para el diagnóstico etiológico de la hipoacusia del adulto

2019 · Patricia Corriols Noval, Maria Costales Marcos, et al. · Revista ORL

Additional file 9: of Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients