CALIDAD PUBLICACIONES

En nuestro área el 56% de las publicaciones realizadas son de un Q1, mientras que el 21% son Q2, el 10% son Q3 y el 13% Q4.

TÍTULO:               From pseudohypoparathyroidism to inactivating PTH/PTHrP signalling disorder (iPPSD), a novel classification proposed by the EuroPHP network

RESUMEN:         Thiele, S., Mantovani, G., Barlier, A., Boldrin, V., Bordogna, P., De Sanctis, L., Elli, F.M., Freson, K., Garin, I., Grybek, V., Hanna, P., Izzi, B., Hiort, O., Lecumberri, B., Pereda, A., Saraff, V., Silve, C., Turan, S., Usardi, A., Werner, R., De Nanclares, G.P., Linglart, A.. From pseudohypoparathyroidism to inactivating PTH/PTHrP signalling disorder (iPPSD), a novel classification proposed by the EuroPHP network. Eur J Endocrinol. 2016; 175: 1-17. FI: 3,892(Q2). DOI: 10.1530/EJE-16-0107.

TIPO:     Article         FI:   3,89       CUARTIL:  1

TÍTULO:  Genome-wide DNA methylation analysis of pseudohypoparathyroidism patients with GNAS imprinting defects

RESUMEN:         Rochtus, A., Martin-Trujillo, A., Izzi, B., Elli, F., Garin, I., Linglart, A., Mantovani, G., Perez de Nanclares, G., Thiele, S., Decallonne, B., Van Geet, C., Monk, D., Freson, K.. Genome-wide DNA methylation analysis of pseudohypoparathyroidism patients with GNAS imprinting defects. Clinical Epigenetics. 2016; 8: 10-0. FI: (Q). DOI: 10.1186/s13148-016-0175-8.

TIPO:     Article         FI:   4,33       CUARTIL:  1

TÍTULO:  Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci (vol 7, 123, 2015)

RESUMEN:         Eggermann, Thomas, Perez de Nanclares, Guiomar, Maher, Eamonn R., Temple, I. Karen, Tumer, Zeynep, Monk, David, Mackay, Deborah J. G., Gronskov, Karen, Riccio, Andrea, Linglart, Agnes, Netchine, Irene. Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci (vol 7, 123, 2015). Clin. Epigenetics. 2016; . FI: 4,327(Q1). DOI: 10.1186/s13148-016-0194-5.

TIPO:     Article         FI:   4,33       CUARTIL:  1

TÍTULO:  The Prevalence of GNAS Deficiency-Related Diseases in a Large Cohort of Patients Characterized by the EuroPHP Network

RESUMEN: Elli, F.M., Linglart, A., Garin, I., De Sanctis, L., Bordogna, P., Grybek, V., Pereda, A., Giachero, F., Verrua, E., Hanna, P., Mantovani, G., De Nanclares, G.P.. The Prevalence of GNAS Deficiency-Related Diseases in a Large Cohort of Patients Characterized by the EuroPHP Network. J. Clin. Endocrinol. Metab.. 2016; 101: 3657-3668. FI: 5,531(Q1). DOI: 10.1210/jc.2015-4310.

TIPO:     Article         FI:   5,53       CUARTIL:  1

TÍTULO:  Luminal B breast cancer subtype displays a dicotomic epigenetic pattern

RESUMEN: Bediaga, Naiara G., Beristain, Elena, Calvo, Borja, Viguri, Maria A., Gutierrez-Corres, Borja, Rezola, Ricardo, Ruiz-Diaz, Irune, Guerra, Isabel, de Pancorbo, Marian M.. Luminal B breast cancer subtype displays a dicotomic epigenetic pattern. Springerplus. 2016; 5: 623-0. FI: (Q2). DOI: 10.1186/s40064-016-2235-0.

TIPO:     Article         FI:   0,98       CUARTIL:  2

TÍTULO: Clinical and molecular analyses of Beckwith-Wiedemann syndrome: Comparison between spontaneous conception and assisted reproduction techniques

RESUMEN: Tenorio, J., Romanelli, V., Martin-Trujillo, A., Fernández, G.-M., Segovia, M., Perandones, C., Pérez Jurado, L.A., Esteller, M., Fraga, M., Arias, P., Gordo, G., Dapía, I., Mena, R., Palomares, M., Pérez de Nanclares, G., Nevado, J., García-Miñaur, S., Santos-Simarro, F., Martinez-Glez, V., Vallespín, E., The SOGRI Consortium, Monk, D., Lapunzina, P.. Clinical and molecular analyses of Beckwith-Wiedemann syndrome: Comparison between spontaneous conception and assisted reproduction techniques. Am J Med Genet A. 2016; 170: 2740-2749. FI: 2,082(Q3). DOI: 10.1002/ajmg.a.37852.

TIPO:     Article         FI:   2,08       CUARTIL:  3