Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

17 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Comprehensive genomic diagnosis of inherited retinal and optical nerve disorders reveals hidden syndromes and personalized therapeutic options.
Diñeiro M, Capín R, Cifuentes GÁ, Fernández-Vega B, Villota E, Otero A, Santiago A, Pruneda PC, Castillo D, Viejo-Díaz M, Hernando I, Durán NS, Álvarez R, Lago CG, Ordóñez GR, Fernández-Vega Á, Cabanillas R, Cadiñanos J. Diñeiro M, et al. Among authors: capin r. Acta Ophthalmol. 2020 Dec;98(8):e1034-e1048. doi: 10.1111/aos.14479. Epub 2020 Jun 1. Acta Ophthalmol. 2020. PMID: 32483926 Free PMC article.
Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients.
Cabanillas R, Diñeiro M, Cifuentes GA, Castillo D, Pruneda PC, Álvarez R, Sánchez-Durán N, Capín R, Plasencia A, Viejo-Díaz M, García-González N, Hernando I, Llorente JL, Repáraz-Andrade A, Torreira-Banzas C, Rosell J, Govea N, Gómez-Martínez JR, Núñez-Batalla F, Garrote JA, Mazón-Gutiérrez Á, Costales M, Isidoro-García M, García-Berrocal B, Ordóñez GR, Cadiñanos J. Cabanillas R, et al. Among authors: capin r. BMC Med Genomics. 2018 Jul 9;11(1):58. doi: 10.1186/s12920-018-0375-5. BMC Med Genomics. 2018. PMID: 29986705 Free PMC article.
Sequencing results from multiple individuals of different ethnicities strongly question the existence of the KCNE1B pseudogene.
Diñeiro M, Cifuentes GA, Capín R, Santiago A, Otero A, Castillo D, Pruneda PC, Ordóñez GR, Cabanillas R, Cadiñanos J. Diñeiro M, et al. Among authors: capin r. Eur J Hum Genet. 2020 Apr;28(4):401-402. doi: 10.1038/s41431-019-0502-6. Epub 2019 Sep 16. Eur J Hum Genet. 2020. PMID: 31527855 Free PMC article. No abstract available.
Clinical utility of next-generation sequencing in the aetiological diagnosis of sensorineural hearing loss in a Childhood Hearing Loss Unit.
Costales M, Diñeiro M, Cifuentes GA, Capín R, Otero A, Viejo-Díaz M, Plasencia A, Núñez F, Gómez JR, Llorente JL, Cadiñanos J, Cabanillas R. Costales M, et al. Among authors: capin r. Acta Otorrinolaringol Esp (Engl Ed). 2020 May-Jun;71(3):166-174. doi: 10.1016/j.otorri.2019.05.005. Epub 2019 Nov 6. Acta Otorrinolaringol Esp (Engl Ed). 2020. PMID: 31706454 English, Spanish.
Clinical Impact of Genetic Diagnosis of Sensorineural Hearing Loss in Adults.
Corriols-Noval P, López Simón EC, Cadiñanos J, Diñeiro M, Capín R, González Aguado R, Costales Marcos M, Morales Angulo C, Cabanillas Farpón R. Corriols-Noval P, et al. Among authors: capin r. Otol Neurotol. 2022 Dec 1;43(10):1125-1136. doi: 10.1097/MAO.0000000000003706. Epub 2022 Oct 3. Otol Neurotol. 2022. PMID: 36190904
Clinical utility of liquid biopsy and integrative genomic profiling in early-stage and oligometastatic cancer patients treated with radiotherapy.
Cifuentes GA, Santiago A, Méndez Blanco L, Fueyo M, López Martínez E, Soria R, Martín López I, Cucarella Beltrán P, Pardo-Coto P, Rodriguez-Rubi D, Urquilla K, Durán NS, Álvarez R, Lago CG, Otero A, Diñeiro M, Capín R, Cadiñanos J, Cabanillas R. Cifuentes GA, et al. Among authors: capin r. Br J Cancer. 2023 Mar;128(5):857-876. doi: 10.1038/s41416-022-02102-z. Epub 2022 Dec 22. Br J Cancer. 2023. PMID: 36550207 Free PMC article.
17 results