Celia Badenas

foglalkozás: kutató

Series

There is nothing here

Create a new serie

Works

There is nothing here

Create a new work

Articles 108

Date

Title

Authors

2019-02-27

POT1 germline mutations but not TERT promoter mutations are implicated in melanoma susceptibility in a large cohort of Spanish melanoma families

Miriam Potrony, Paula Aguilera, Cristina Carrera, Celia Badenas, Susana Puig, Maria Teresa Landi, Joan Anton Puig-Butille
2018-03-02

Acquired erythropoietic uroporphyria secondary to myelodysplastic syndrome with chromosome 3 alterations: a case report

Andrea Combalia, Sebastian Podlipnik, Celia Badenas, Paula Aguilera
2018-04-30

Genome-wide linkage analysis in Spanish melanoma-prone families identifies a new familial melanoma susceptibility locus at 11q

Miriam Potrony, Celia Badenas, Gemma Tell-Martí, Paula Aguilera, Cristina Carrera
2017-12-22

Novel clinical and molecular findings in Spanish patients with naevoid basal cell carcinoma syndrome

N Alonso, Irene Palacios-Álvarez, Celia Badenas, Alicia Barreiro-Capurro
2017-10-17

Melanocortin 1 receptor (MC1R) polymorphisms' influence on size and dermoscopic features of nevi

Susana Puig, María Gabriela Vallone, Gemma Tell-Martí, Miriam Potrony, Celia Badenas, Pol Gimenez Xavier, Cristina Carrera, Josep Malvehy, Joan Anton Puig-Butille
2017-11-22

Amelanotic melanoma in oculocutaneous albinism: a genetic, dermoscopic and reflectance confocal microscopy study

Simone Ribero, Cristina Carrera, Gemma Tell-Martí, Celia Badenas
2017-12-03

A Common Variant in the MC1R Gene (p.V92M) is associated with Alzheimer's Disease Risk.

Daniel A. Alcolea, Rubén Fernández-Santiago, Gemma Tell-Martí, Miriam Potrony, Celia Badenas, Anna Antonell, Raquel Sanchez-Valle, José Luis Molinuevo
2017-10-05

Parental Origin of the Retained X Chromosome in Monosomy X Miscarriages and Ongoing Pregnancies.

Celia Badenas, Antoni Borrell
2017-02-06

IRF4 rs12203592 functional variant and melanoma survival

Miriam Potrony, Pol Gimenez Xavier, Gemma Tell-Martí, Celia Badenas, Cristina Carrera
2017-02-07

AURKA Overexpression Is Driven by FOXM1 and MAPK/ERK Activation in Melanoma Cells Harboring BRAF or NRAS Mutations: Impact on Melanoma Prognosis and Therapy.

Paula Aguilera, Eduard Cabré, Gemma Tell-Martí, Francesca Mateo, Celia Badenas, Josep M Piulats
2016-08-11

Late-onset cutaneous porphyria in a patient heterozygous for a uroporphyrinogen III synthase gene mutation

Paula Aguilera, Celia Badenas
2016-10-01

Association Between Confocal Morphologic Classification and Clinical Phenotypes of Multiple Primary and Familial Melanomas

Thais C Grazziotin, Cristina Carrera, Miriam Potrony, Paula Aguilera, Celia Badenas, Josep Malvehy, Susana Puig, Joan Anton Puig-Butille, Johanna Brito, Ivette Alarcon, Llucìa Alos
2016-08-31

Genetic susceptibility to cutaneous melanoma in southern Switzerland: role of CDKN2A, MC1R and MITF

Susana Puig, Miriam Potrony, Celia Badenas
2016-12-06

The p. R151C Polymorphism in MC1R Gene Modifies the Age of Onset in Spanish Huntington's Disease Patients

Gemma Tell-Martí, Pol Gimenez Xavier, Miriam Potrony, Celia Badenas
2016-10-28

Association between dermoscopic and reflectance confocal microscopy features of cutaneous melanoma with BRAF mutational status.

Susana Puig, Giuseppe Argenziano, Caterina Longo, Simone Ribero, Celia Badenas, Cristina Carrera, Josep Malvehy, Joan Anton Puig-Butille
2016-09-22

A 92,XXXY Miscarriage Consecutive to a Digynic Triploid Pregnancy

Celia Badenas, Ester Margarit Torrent, Irene Madrigal, Aurora Sanchez Diaz
2016-11-02

Genomic Microarray in Fetuses with Early Growth Restriction: A Multicenter Study

Antoni Borrell, Celia Badenas
2016-11-01

Time and tumor type (primary or metastatic) do not influence the detection of BRAF/NRAS mutations in formalin fixed paraffin embedded samples from melanomas

Susana Puig, Miriam Potrony, Celia Badenas, Paula Aguilera, Gemma Tell-Martí, Cristina Carrera, Josep Malvehy, Joan Anton Puig-Butille, Llucìa Alos
2016-06-16

Discrepant mutational status between naevi and melanomas in naevus-associated melanomas: about mutation-specific immunohistochemistry: reply from the authors

Gemma Tell-Martí, Celia Badenas, Cristina Carrera, Josep Malvehy, Susana Puig, Joan Anton Puig-Butille
2015-09

Update in genetic susceptibility in melanoma

Miriam Potrony, Celia Badenas, Paula Aguilera, Cristina Carrera, Josep Malvehy, Susana Puig, Joan Anton Puig-Butille
2015-06-19

Mutational status of naevus-associated melanomas

Gemma Tell-Martí, Celia Badenas, Cristina Carrera, Josep Malvehy, Susana Puig, Joan Anton Puig-Butille
2015-12-17

Characterization of individuals at high risk of developing melanoma in Latin America: bases for genetic counseling in melanoma

Susana Puig, Miriam Potrony, Cristina Carrera, Paula Aguilera, Eduardo Nagore, Rajiv Kumar, Gilles Landman, Luciana Facure, Maria Isabel Achatz, João Pedreira Duprat Neto, Thais C Grazziotin, Clara Latorre, Josep Malvehy, Celia Badenas, Patricia Ashton-Prolla, Roberto Giugliani, Dirce Carraro, Bianca Costa Soares de Sá, Joan Anton Puig-Butille, Celia Requena, Renato Marchiori Bakos, Horacio Cabo, Blanca Carlos-Ortega
2015-12-09

Prevalence of MITF p.E318K in Patients With Melanoma Independent of the Presence of CDKN2A Causative Mutations

Susana Puig, Miriam Potrony, Paula Aguilera, Celia Badenas, Gemma Tell-Martí, Cristina Carrera, Josep Malvehy, Joan Anton Puig-Butille
2015-05-01

Multiple BRAF Wild-Type Melanomas During Dabrafenib Treatment for Metastatic BRAF-Mutant Melanoma

Susana Puig, Cristina Carrera, Gemma Tell-Martí, Celia Badenas, Josep Malvehy, Llucìa Alos, Joan Anton Puig-Butille
2015-08-05

Atypical Clinical Presentation of Xeroderma Pigmentosum in a Patient Harboring a Novel Missense Mutation in the XPC Gene: The Importance of Clinical Suspicion

Susana Puig, Marion Chavez-Bourgeois, Celia Badenas, Paula Aguilera, Josep Malvehy, Cristina Carrera, Llucìa Alos, Antoni Bennássar
2015-03-13

The MC1R melanoma risk variant p.R160W is associated with Parkinson disease

Rubén Fernández-Santiago, Susana Puig, Gemma Tell-Martí, Miriam Potrony, Celia Badenas, Montserrat Milà, Josep Malvehy, Mario Ezquerra, Joan Anton Puig-Butille
2015-11-27

Skewed X Inactivation in Women Carrying the FMR1 Premutation and Its Relation with Fragile-X-Associated Tremor/Ataxia Syndrome.

Maria Isabel Alvarez-Mora, Celia Badenas, Irene Madrigal, Montserrat Milà
2015-12-02

Erratum: Corrigendum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

Lorenza Pastorino, Corine Bertolotto, Robert Ballotti, Philippe Bahadoran, Eve Maubec, Fabienne Lesueur, Irwin Davidson, Pierre Vabres, Florence Demenais, Nicolas Dupin, Bin Tean Teh, Pilar Galan, Celia Badenas, Mark Lathrop, Bernard Escudier, Diana Zelenika, Brigitte Bressac-de Paillerets, Marie-Françoise Avril, Paola Ghiorzo, Christian Ingvar, Hamida Mohamdi, Sandy Giuliano, Thomas Strub, Mahaut de Lichy, Karine Bille, Philippe Dessen, Benoit d'Hayer, Audrey Remenieras, Arnaud de la Fouchardiere, Vincent Molinie, Stéphane Dalle, Nicolas Poulalhon, Luc Thomas, Pascale Andry-Benzaquen, Françoise Boitier, Annick Rossi, Jean Luc Perrot, Bruno Labeille, Laurence Brugières, Simon Saule, Betty Gardie, Jérôme Couturier, Etienne Rouleau, Rosette Lidereau, Philippe Vielh, Hélène Blanché, Valérie Chaudru, Susana Puig
2015-12-12

Reply

Gemma Tell-Martí, Miriam Potrony, Celia Badenas, Montserrat Milà, Josep Malvehy, Mario Ezquerra, Rubén Fernández-Santiago, Susana Puig, Joan Anton Puig-Butille
2014-09-04

[Acute intermittent porphyria: Long-term follow up of 35 patients]

Celia Badenas, Paula Aguilera
2014-10

TERT gene amplification is associated with poor outcome in acral lentiginous melanoma

Cristina Carrera, Celia Badenas, Josep Malvehy, Susana Puig, Joan Anton Puig-Butille, Adriana Garcia-Herrera, Llucìa Alos
2014-03-01

Capturing the biological impact of CDKN2A and MC1R genes as an early predisposing event in melanoma and non melanoma skin cancer

María José Escámez, Gemma Tell-Martí, Lucia Martinez, Celia Badenas, Paula Aguilera, Susana Puig, Joaquín Dopazo

Human - wd:Q56435755

Welcome to Inventaire

the library of your friends and communities

learn more