J. Genovés

Plasma idebenone monitoring in Friedreich's ataxia patients during a long-term follow-up.

H. Colom, D. Cuadras, R. Artuch, 2021, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

Four sisters compound heterozygotes for the pre- and full mutation in fragile X syndrome and a complete inactivation of X-functional chromosome: implications for genetic counseling

L. Martorell, A. Nascimento, J. Genovés, 2011, Journal of Human Genetics.

Predisposition to epilepsy in fragile X syndrome: Does the Val66Met polymorphism in the BDNF gene play a role?

L. Martorell, P. Póo, M. Tondo, 2011, Epilepsy & Behavior.

AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission

F. Tassone, E. Berry-Kravis, B. Durbin-Johnson, 2014, Journal of Neurodevelopmental Disorders.

Human papillomavirus detection and p16INK4a expression in cervical lesions: a comparative study.

Beatriz Bellosillo, B. Lloveras, L. Serrano, 2014, Human pathology.

Usefulness of p16INK4a staining for managing histological high-grade squamous intraepithelial cervical lesions

Beatriz Bellosillo, B. Lloveras, B. Bellosillo, 2017, Modern Pathology.

Screening for the presence of FMR1 premutation alleles in a Spanish population with fibromyalgia

C. Alegre, J. Gámez, L. Martorell, 2012, Clinical Rheumatology.