Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients.

Curras-Freixes M, Inglada-Perez L, Mancikova V, Montero-Conde C, Leton R, Comino-Mendez I, Apellaniz-Ruiz M, Sanchez-Barroso L, Aguirre Sanchez-Covisa M, Alcazar V, Aller J, Alvarez-Escola C, Andia-Melero VM, Azriel-Mira S, Calatayud-Gutierrez M, Diaz JA, Diez-Hernandez A, Lamas-Oliveira C, Marazuela M, Matias-Guiu X, Meoro-Aviles A, Patino-Garcia A, Pedrinaci S, Riesco-Eizaguirre G, Sabado-Alvarez C, Saez-Villaverde R, Sainz de los Terreros A, Sanz Guadarrama O, Sastre-Marcos J, Scola-Yurrita B, Segura-Huerta A, Serrano-Corredor MS, Villar-Vicente MR, Rodriguez-Antona C, Korpershoek E, Cascon A, Robledo M.

J. Med. Genet. 2015; 52: 647-656. FI: 6.335 (Q1).

Incidence of Nodal Metastasis and Isolated Aortic Metastases in Patients With Surgically Staged Endometrioid Endometrial Cancer.

Ruiz R, Goiri K, Avila M, Januarena I, Lekuona A.

Int. J. Gynecol. Cancer. 2015; 25: 875-878. FI: 1.958 (Q2).

Deletion at 6q24.2-26 predicts longer survival of high-grade serous epithelial ovarian cancer patients.

Kamieniak MM, Rico D, Milne RL, Munoz-Repeto I, Ibanez K, Grillo MA, Domingo S, Borrego S, Cazorla A, Garcia-Bueno JM, Hernando S, Garcia-Donas J, Hernandez-Agudo E, Ramon y Cajal T, Robles-Diaz L, Marquez-Rodas I, Cusido M, Saez R, Lacambra-Calvet C, Osorio A, Urioste M, Cigudosa JC, Paz-Ares L, Palacios J, Benitez J, Garcia MJ.

Mol. Oncol. 2015; 9: 422-436. FI: 5.331 (Q1).

Hereditary hypophosphatemic rickets with hypercalciuria: a case report.

Areses-Trapote R, López-García JA, Ubetagoyena-Arrieta M, Eizaguirre A, Sáez-Villaverde R.

Nefrología. 2012; 32: 529-534. FI: 1.000 (Q4).

Next-generation sequencing used to discover novel genetic variants predisposing to heart disease.

Pérez-Cabornero L, Cantalapiedra D, Forteza A, Sáez-Villaverde R, Zumalde J, Fernández-Pedrosa V, Zuniga-Trejos S, Gil-Borja M, Lázaro M, Santillán S.

Cardiovasc. Res. 2012; 93: 11-0. FI: 6.064 (Q1).

Spectrum of Mutations in the Renin-Angiotensin System Genes in Autosomal Recessive Renal Tubular Dysgenesis.

Gribouval O, Moriniere V, Pawtowski A, Arrondel C, Sallinen SL, Saloranta C, Clericuzio C, Viot G, Tantau J, Blesson S, Cloarec S, Machet MC, Chitayat D, Thauvin C, Laurent N, Sampson JR, Bernstein JA, Clemenson A, Prieur, F, Laurent D, Levy-Mozziconacci A, Lachlan K, Alessandri JL, Cartault F, Riviere JP, Picard N, Baumann C, Delezoide AL, Belar Ortega, M, Chassaing N, Labrune P, Yu S, Firth H, Wellesley D, Bitzan M, Alfares A, Braverman N, Krogh L, Tolmie J, Gaspar H, Doray B, Majore S, Bonneau D, Triau S, Loirat, Chantal, David, Albert, Bartholdi D, Peleg, A, Brackman D, Stone R, DeBerardinis R, Corvol P, Michaud A, Antignac C, Gubler MC.

Hum. Mutat. 2012; 33: 316-326. FI: 5.686 (Q1).