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Gastroenterologia Y Hepatologia|March 23, 2011
[Advances in the molecular diagnosis of Wilson's disease]Celia Badenas OrquinMedicina Clinica|September 8, 2014
[Acute intermittent porphyria: Long-term follow up of 35 patients]Carmen Herrero, Celia Badenas, Paula Aguilera, et al.European Journal of Human Genetics : EJHG|March 16, 2006
A novel mutation in JARID1C gene associated with mental retardationCristina Santos, Laia Rodriguez-Revenga, Irene Madrigal, et al.Menopause (New York, N.Y.)|April 18, 2009
Premature ovarian failure and fragile X female premutation carriers: no evidence for a skewed X-chromosome inactivation patternLaia Rodriguez-Revenga, Irene Madrigal, Celia Badenas, et al.Dermatologic Therapy|October 11, 2012
Genetic counseling in melanomaCelia Badenas, Paula Aguilera, Joan A Puig-Butillé, et al.Neuro-Degenerative Diseases|November 27, 2015
Skewed X Inactivation in Women Carrying the FMR1 Premutation and Its Relation with Fragile-X-Associated Tremor/Ataxia SyndromeMaria Isabel Alvarez-Mora, Laia Rodriguez-Revenga, Aina Feliu, et al.Prenatal Diagnosis|June 21, 2005
46,XY,18q+/46,XY,18q- mosaicism in a fragile X prenatal diagnosisLaia Rodriguez-Revenga, Celia Badenas, Irene Madrigal, et al.Medicine|June 3, 2010
Familial and sporadic porphyria cutanea tarda: clinical and biochemical features and risk factors in 152 patientsCarlos Muñoz-Santos, Antonio Guilabert, Nemesio Moreno, et al.Journal of the American Academy of Dermatology|July 28, 2014
Increased prevalence of lung, breast, and pancreatic cancers in addition to melanoma risk in families bearing the cyclin-dependent kinase inhibitor 2A mutation: implications for genetic counselingMiriam Potrony, Joan Anton Puig-Butillé, Paula Aguilera, et al.Annals of Translational Medicine|October 22, 2015
Update in genetic susceptibility in melanomaMiriam Potrony, Celia Badenas, Paula Aguilera, et al.Pageof 7