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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 5
2003 5
2004 2
2005 6
2006 6
2007 4
2008 6
2009 7
2010 13
2011 8
2012 8
2013 13
2014 11
2015 7
2016 8
2017 8
2018 2
2019 7
2020 8
2021 9
2022 5
2023 8
2024 5

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142 results

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Page 1
Epigenetic Mechanisms in Hirschsprung Disease.
Torroglosa A, Villalba-Benito L, Luzón-Toro B, Fernández RM, Antiñolo G, Borrego S. Torroglosa A, et al. Among authors: antinolo g. Int J Mol Sci. 2019 Jun 26;20(13):3123. doi: 10.3390/ijms20133123. Int J Mol Sci. 2019. PMID: 31247956 Free PMC article. Review.
CIBERER: Spanish national network for research on rare diseases: A highly productive collaborative initiative.
Luque J, Mendes I, Gómez B, Morte B, López de Heredia M, Herreras E, Corrochano V, Bueren J, Gallano P, Artuch R, Fillat C, Pérez-Jurado LA, Montoliu L, Carracedo Á, Millán JM, Webb SM, Palau F; CIBERER Network; Lapunzina P. Luque J, et al. Clin Genet. 2022 May;101(5-6):481-493. doi: 10.1111/cge.14113. Epub 2022 Feb 4. Clin Genet. 2022. PMID: 35060122 Free PMC article. Review.
What is new about the genetic background of Hirschsprung disease?
Luzón-Toro B, Villalba-Benito L, Torroglosa A, Fernández RM, Antiñolo G, Borrego S. Luzón-Toro B, et al. Among authors: antinolo g. Clin Genet. 2020 Jan;97(1):114-124. doi: 10.1111/cge.13615. Epub 2019 Aug 5. Clin Genet. 2020. PMID: 31355911 Review.
Influencers on Thyroid Cancer Onset: Molecular Genetic Basis.
Luzón-Toro B, Fernández RM, Villalba-Benito L, Torroglosa A, Antiñolo G, Borrego S. Luzón-Toro B, et al. Among authors: antinolo g. Genes (Basel). 2019 Nov 8;10(11):913. doi: 10.3390/genes10110913. Genes (Basel). 2019. PMID: 31717449 Free PMC article. Review.
A crowdsourcing database for the copy-number variation of the Spanish population.
López-López D, Roldán G, Fernández-Rueda JL, Bostelmann G, Carmona R, Aquino V, Perez-Florido J, Ortuño F, Pita G, Núñez-Torres R, González-Neira A; CSVS Crowdsourcing Group; Peña-Chilet M, Dopazo J. López-López D, et al. Hum Genomics. 2023 Mar 9;17(1):20. doi: 10.1186/s40246-023-00466-8. Hum Genomics. 2023. PMID: 36894999 Free PMC article.
ESR2 Gene and Medullary Thyroid Carcinoma.
Ruiz-Ferrer M, Fernández RM, Navarro E, Antiñolo G, Borrego S. Ruiz-Ferrer M, et al. Among authors: antinolo g. Thyroid. 2017 Nov;27(11):1456-1457. doi: 10.1089/thy.2017.0171. Epub 2017 Oct 11. Thyroid. 2017. PMID: 28891392 No abstract available.
Unusual clinical phenotype of Stargardt disease.
Molina-Solana P, Morillo-Sánchez MJ, Méndez-Vidal C, Ramos-Jiménez M, Domínguez-Serrano B, Antiñolo G, Rodríguez-de-la-Rúa-Franch E. Molina-Solana P, et al. Among authors: antinolo g. Arq Bras Oftalmol. 2021 Jul-Aug;84(4):391-394. doi: 10.5935/0004-2749.20210064. Arq Bras Oftalmol. 2021. PMID: 34008801 Free article.
Hirschsprung's disease as a model of complex genetic etiology.
Borrego S, Ruiz-Ferrer M, Fernández RM, Antiñolo G. Borrego S, et al. Among authors: antinolo g. Histol Histopathol. 2013 Sep;28(9):1117-36. doi: 10.14670/HH-28.1117. Epub 2013 Apr 19. Histol Histopathol. 2013. PMID: 23605783 Review.
Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications.
Perea-Romero I, Gordo G, Iancu IF, Del Pozo-Valero M, Almoguera B, Blanco-Kelly F, Carreño E, Jimenez-Rolando B, Lopez-Rodriguez R, Lorda-Sanchez I, Martin-Merida I, Pérez de Ayala L, Riveiro-Alvarez R, Rodriguez-Pinilla E, Tahsin-Swafiri S, Trujillo-Tiebas MJ; ESRETNET Study Group; ERDC Study Group; Associated Clinical Study Group; Garcia-Sandoval B, Minguez P, Avila-Fernandez A, Corton M, Ayuso C. Perea-Romero I, et al. Sci Rep. 2021 Jan 15;11(1):1526. doi: 10.1038/s41598-021-81093-y. Sci Rep. 2021. PMID: 33452396 Free PMC article.
142 results