Oriola J - Search Results

1

Novel truncating germline variant reinforces TINF2 as a susceptibility gene for familial non-medullary thyroid cancer.

Oriola J, Díez O, Mora M, Halperin I, Martínez S, Masas M, Tenes A, Bernal A, Duran R, Orois A. Oriola J, et al. J Med Genet. 2024 Sep 24;61(10):939-942. doi: 10.1136/jmg-2024-110185. J Med Genet. 2024. PMID: 39103207

2

NOP53 as A Candidate Modifier Locus for Familial Non-Medullary Thyroid Cancer.

Orois A, Gara SK, Mora M, Halperin I, Martínez S, Alfayate R, Kebebew E, Oriola J. Orois A, et al. Among authors: oriola j. Genes (Basel). 2019 Nov 7;10(11):899. doi: 10.3390/genes10110899. Genes (Basel). 2019. PMID: 31703244 Free PMC article.

3

Lack of Mutations in POT1 Gene in Selected Families with Familial Non-Medullary Thyroid Cancer.

Orois A, Badenas C, Reverter JL, López V, Potrony M, Mora M, Halperin I, Oriola J. Orois A, et al. Among authors: oriola j. Horm Cancer. 2020 Apr;11(2):111-116. doi: 10.1007/s12672-020-00383-5. Epub 2020 Mar 14. Horm Cancer. 2020. PMID: 32172474 Free PMC article.

4

Familial non medullary thyroid carcinoma: Beyond the syndromic forms.

Orois A, Mora M, Halperin I, Oriola J. Orois A, et al. Among authors: oriola j. Endocrinol Diabetes Nutr (Engl Ed). 2021 Apr;68(4):260-269. doi: 10.1016/j.endinu.2020.08.002. Epub 2020 Nov 13. Endocrinol Diabetes Nutr (Engl Ed). 2021. PMID: 33191196 Review. English, Spanish.

5

Familial non medullary thyroid carcinoma: Beyond the syndromic forms.

Orois A, Mora M, Halperin I, Oriola J. Orois A, et al. Among authors: oriola j. Endocrinol Diabetes Nutr (Engl Ed). 2021 Apr;68(4):260-269. doi: 10.1016/j.endien.2020.08.013. Epub 2021 Jul 8. Endocrinol Diabetes Nutr (Engl Ed). 2021. PMID: 34266638 Review.

6

Novel point mutation in exon 10 of the RET proto-oncogene in a family with medullary thyroid carcinoma.

Oriola J, Páramo C, Halperin I, García-Mayor RV, Rivera-Fillat F. Oriola J, et al. Am J Med Genet. 1998 Jul 7;78(3):271-3. doi: 10.1002/(sici)1096-8628(19980707)78:3<271::aid-ajmg13>3.0.co;2-c. Am J Med Genet. 1998. PMID: 9677065

7

The finding of a somaticdeletion in RET exon 15 clarified the sporadic nature of amedullary thyroid carcinoma suspected to be familial.

Oriola J, Halperin I, Rivera-Fillat F, Donis-Keller H. Oriola J, et al. J Endocrinol Invest. 2002 Jan;25(1):25-31. doi: 10.1007/BF03343957. J Endocrinol Invest. 2002. PMID: 11883863

8

Screening of selected genomic areas potentially involved in thyroid neoplasms.

Oriola J, Halperin I, Mallofré C, Muntané J, Angel M, Rivera-Fillat F. Oriola J, et al. Eur J Cancer. 2001 Dec;37(18):2470-4. doi: 10.1016/s0959-8049(01)00302-1. Eur J Cancer. 2001. PMID: 11720845

9

Identification of four novel mutations in the thyroid hormone receptor-β gene in 164 Spanish and 2 Greek patients with resistance to thyroid hormone.

Amor AJ, Halperin I, Alfayate R, Borrás VM, Escribano A, González C, Gutirrez A, Mauri M, Pérez P, Picό A, Vourliotaki I, Oriola J. Amor AJ, et al. Among authors: oriola j. Hormones (Athens). 2014 Jan-Mar;13(1):74-8. doi: 10.1007/BF03401322. Hormones (Athens). 2014. PMID: 24722129 Free article.

10

Aging phenotype and its relationship with IGF-I gene promoter polymorphisms in elderly people living in Catalonia.

Mora M, Perales MJ, Serra-Prat M, Palomera E, Buquet X, Oriola J, Puig-Domingo M; Mataró Ageing Study Group. Mora M, et al. Among authors: oriola j. Growth Horm IGF Res. 2011 Jun;21(3):174-80. doi: 10.1016/j.ghir.2011.03.007. Growth Horm IGF Res. 2011. PMID: 21658593

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