Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Díez, Orland
Osorio, Ana
Durán, Mercedes
Martinez-Ferrandis, José Ignacio
Hoya, Miguel de la
Salazar, Raquel
Vega, Ana
Campos, Berta
Rodríguez-López, Raquel
Velasco, Eladio
Chaves, Javier
Díaz-Rubio, Eduardo
Jesús Cruz, Juan
Torres, María
Esteban, Eva
Cervantes, Andrés
Alonso, Carmen
San Román, Juan Manuel
González-Sarmiento, Rogelio
Miner, Cristina
Carracedo, Angel
Eugenia Armengod, María
Caldés, Trinidad
Benítez, Javier
and
Baiget, Montserrat
2003.
Analysis ofBRCA1andBRCA2genes in Spanish breast/ovarian cancer patients: A high proportion of mutations unique to Spain and evidence of founder effects.
Human Mutation,
Vol. 22,
Issue. 4,
p.
301.
Osorio, Ana
Rodríguez‐López, Raquel
Díez, Orland
de la Hoya, Miguel
Ignacio Martínez, José
Vega, Ana
Esteban‐Cardeñosa, Eva
Alonso, Carmen
Caldés, Trinidad
and
Benítez, Javier
2004.
The breast cancer low‐penetrance allele 1100delC in the CHEK2 gene is not present in Spanish familial breast cancer population.
International Journal of Cancer,
Vol. 108,
Issue. 1,
p.
54.
Campos, Berta
Díez, Orland
Álvarez, Carolina
Palma, Lorena
Domènech, Montserrat
Balmaña, Judith
Sanz, Judit
Ramírez, Amaya
Alonso, Carmen
Carvallo, Pilar
and
Baiget, Montserrat
2004.
Análisis del haplotipo en portadores de la mutación 6857delAA en el gen BRCA2 en 4 familias con cáncer de mama u ovario hereditario.
Medicina Clínica,
Vol. 123,
Issue. 14,
p.
543.
Filippini, Sandra
Blanco, Ana
Fernández-Marmiesse, Ana
Álvarez-Iglesias, Vanesa
Ruíz-Ponte, Clara
Carracedo, Ángel
and
Vega, Ana
2007.
Multiplex SNaPshot for detection of BRCA1/2 common mutations in Spanish and Spanish related breast/ovarian cancer families.
BMC Medical Genetics,
Vol. 8,
Issue. 1,
Milne, Roger L.
Osorio, Ana
Cajal, Teresa Ramón y
Vega, Ana
Llort, Gemma
de la Hoya, Miguel
Díez, Orland
Alonso, M. Carmen
Lazaro, Conxi
Blanco, Ignacio
Sánchez-de-Abajo, Ana
Caldés, Trinidad
Blanco, Ana
Graña, Begoña
Durán, Mercedes
Velasco, Eladio
Chirivella, Isabel
Cardeñosa, Eva Esteban
Tejada, María-Isabel
Beristain, Elena
Miramar, María-Dolores
Calvo, María-Teresa
Martínez, Eduardo
Guillén, Carmen
Salazar, Raquel
San Román, Carlos
Antoniou, Antonis C.
Urioste, Miguel
and
Benítez, Javier
2008.
The Average Cumulative Risks of Breast and Ovarian Cancer for Carriers of Mutations in BRCA1 and BRCA2 Attending Genetic Counseling Units in Spain.
Clinical Cancer Research,
Vol. 14,
Issue. 9,
p.
2861.
Marroni, F.
Cipollini, G.
Peissel, B.
D'Andrea, E.
Pensabene, M.
Radice, P.
Caligo, M. A.
Presciuttini, S.
and
Bevilacqua, G.
2008.
Reconstructing the Genealogy of a BRCA1 Founder Mutation by Phylogenetic Analysis.
Annals of Human Genetics,
Vol. 72,
Issue. 3,
p.
310.
Gómez-Fernández, Nuria
Castellví-Bel, Sergi
Fernández-Rozadilla, Ceres
Balaguer, Francesc
Muñoz, Jenifer
Madrigal, Irene
Milà, Montserrat
Graña, Begoña
Vega, Ana
Castells, Antoni
Carracedo, Ángel
and
Ruiz-Ponte, Clara
2009.
Molecular analysis of the APC and MUTYH genes in Galician and Catalonian FAP families: a different spectrum of mutations?.
BMC Medical Genetics,
Vol. 10,
Issue. 1,
Diez, Orland
Gutiérrez-Enríquez, Sara
and
Balmaña, Judith
2010.
Heterogeneous prevalence of recurrent BRCA1 and BRCA2 mutations in Spain according to the geographical area: implications for genetic testing.
Familial Cancer,
Vol. 9,
Issue. 2,
p.
187.
Salgado, Josefa
Aramendía, José M.
Gutierrez, Cristina
Gil, Carmen
Robles, Maitane
and
García-Foncillas, Jesús
2010.
A novel BRCA2 mutation that segregates with breast and prostate cancer in a Spanish family.
Breast Cancer Research and Treatment,
Vol. 121,
Issue. 1,
p.
219.
Janavičius, Ramūnas
2010.
Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control.
EPMA Journal,
Vol. 1,
Issue. 3,
p.
397.
Fachal, Laura
Gómez‐Caamaño, Antonio
Celeiro‐Muñoz, Catuxa
Peleteiro, Paula
Blanco, Ana
Carballo, Ana
Forteza, Jerónimo
Carracedo, Ángel
and
Vega, Ana
2011.
BRCA1 mutations do not increase prostate cancer risk: Results from a meta‐analysis including new data.
The Prostate,
Vol. 71,
Issue. 16,
p.
1768.
Rodríguez‐Pazos, L.
Ginarte, M.
Fachal, L.
Toribio, J.
Carracedo, A.
and
Vega, A.
2011.
Analysis of
TGM1, ALOX12B, ALOXE3, NIPAL4
and
CYP4F22
in autosomal recessive congenital ichthyosis from Galicia (NW Spain): evidence of founder effects
.
British Journal of Dermatology,
Vol. 165,
Issue. 4,
p.
906.
Jiang, Xuejuan
Castelao, Jose Esteban
Chavez-Uribe, Elisabet
Rodriguez, Beatriz Fernandez
Muñoz, Catuxa Celeiro
Redondo, Carmen M.
Fernandez, Maite Peña
Dominguez, Alejandro Novo
Pereira, Carina Doris
Martínez, María Elena
García-Caballero, Tomás
Rodriguez, Máximo Fraga
Antúnez, José
Carracedo, Angel
Forteza-Vila, Jerónimo
Gago-Dominguez, Manuela
and
Aziz, Syed A.
2012.
Family History and Breast Cancer Hormone Receptor Status in a Spanish Cohort.
PLoS ONE,
Vol. 7,
Issue. 1,
p.
e29459.
Redondo, Carmen M.
Gago-Domínguez, Manuela
Ponte, Sara Miranda
Castelo, Manuel Enguix
Jiang, Xuejuan
García, Ana Alonso
Fernández, Maite Peña
Tomé, María Ausencia
Fraga, Máximo
Gude, Francisco
Martínez, María Elena
Garzón, Víctor Muñoz
Carracedo, Ángel
Castelao, J. Esteban
and
Toland, Amanda Ewart
2012.
Breast Feeding, Parity and Breast Cancer Subtypes in a Spanish Cohort.
PLoS ONE,
Vol. 7,
Issue. 7,
p.
e40543.
Infante, M.
Duran, M.
Acedo, A.
Sanchez-Tapia, E. M.
Diez-Gomez, B.
Barroso, A.
Garcia-Gonzalez, M.
Feliubadalo, L.
Lasa, A.
de la Hoya, M.
Esteban-Cardenosa, E.
Diez, O.
Martinez-Bouzas, C.
Godino, J.
Teule, A.
Osorio, A.
Lastra, E.
Gonzalez-Sarmiento, R.
Miner, C.
and
Velasco, E. A.
2013.
The highly prevalent BRCA2 mutation c.2808_2811del (3036delACAA) is located in a mutational hotspot and has multiple origins.
Carcinogenesis,
Vol. 34,
Issue. 11,
p.
2505.
Fachal, L.
Santamariña, M.
Blanco, A.
Carracedo, Á.
and
Vega, A.
2013.
CHEK2 c.1100delC mutation among non-BRCA1/2 Spanish hereditary breast cancer families.
Clinical and Translational Oncology,
Vol. 15,
Issue. 2,
p.
164.
Blay, Pilar
Santamaría, Iñigo
Pitiot, Ana S
Luque, María
Alvarado, Marta G
Lastra, Ana
Fernández, Yolanda
Paredes, Ángeles
Freije, José MP
and
Balbín, Milagros
2013.
Mutational analysis of BRCA1 and BRCA2 in hereditary breast and ovarian cancer families from Asturias (Northern Spain).
BMC Cancer,
Vol. 13,
Issue. 1,
Fachal, Laura
Blanco, Ana
Santamariña, Marta
Carracedo, Angel
Vega, Ana
and
Toland, Amanda Ewart
2014.
Large Genomic Rearrangements of BRCA1 and BRCA2 among Patients Referred for Genetic Analysis in Galicia (NW Spain): Delimitation and Mechanism of Three Novel BRCA1 Rearrangements.
PLoS ONE,
Vol. 9,
Issue. 3,
p.
e93306.
de Juan, Inmaculada
Palanca, Sarai
Domenech, Asunción
Feliubadaló, Lidia
Segura, Ángel
Osorio, Ana
Chirivella, Isabel
de la Hoya, Miguel
Sánchez, Ana Beatriz
Infante, Mar
Tena, Isabel
Díez, Orland
Garcia-Casado, Zaida
Vega, Ana
Teulé, Àlex
Barroso, Alicia
Pérez, Pedro
Durán, Mercedes
Carrasco, Estela
Juan-Fita, Mª José
Murria, Rosa
Llop, Marta
Barragan, Eva
Izquierdo, Ángel
Benítez, Javier
Caldés, Trinidad
Salas, Dolores
and
Bolufer, Pascual
2015.
BRCA1 and BRCA2 mutations in males with familial breast and ovarian cancer syndrome. Results of a Spanish multicenter study.
Familial Cancer,
Vol. 14,
Issue. 4,
p.
505.
Pajares, Bella
Porta, Javier
Porta, Jose María
Sousa, Cristina Fernández-de
Moreno, Ignacio
Porta, Daniel
Durán, Gema
Vega, Tamara
Ortiz, Inmaculada
Muriel, Carolina
Alba, Emilio
and
Márquez, Antonia
2018.
Hereditary breast and ovarian cancer in Andalusian families: a genetic population study.
BMC Cancer,
Vol. 18,
Issue. 1,