María A Ramos-Arroyo (Maria A Ramos-Arroyo)

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 7

Top Topics

Bipolar Disorder

Top Venues

European journal of human genetics : EJHG

Orphanet journal of rare diseases

This page only lists publications with an associated author ORCID identifier.

Publications

Ainara Ruiz de Sabando, Marc Ciosi, Arkaitz Galbete, Sarah A Cumming, null null, Darren G Monckton, María A Ramos-Arroyo
Somatic CAG repeat instability in intermediate alleles of the HTT gene and its potential association with a clinical phenotype. European journal of human genetics : EJHG (2024)
Ainara Ruiz de Sabando, Marc Ciosi, Arkaitz Galbete, Sarah A Cumming, null null, Darren G Monckton, María A Ramos-Arroyo
Somatic CAG repeat instability in intermediate alleles of the HTT gene and its potential association with a clinical phenotype. European journal of human genetics : EJHG 32 (7) (2024)
Ainara Ruiz de Sabando, Marc Ciosi, Arkaitz Galbete, Sarah A Cumming, null null, Darren G Monckton, María A Ramos-Arroyo
Somatic CAG repeat instability in intermediate alleles of the HTT gene and its potential association with a clinical phenotype. European journal of human genetics : EJHG 32 (7) (2024)
Ainara Ruiz de Sabando, Marc Ciosi, Arkaitz Galbete, Sarah A Cumming, null null, Darren G Monckton, María A Ramos-Arroyo
Somatic CAG repeat instability in intermediate alleles of the HTT gene and its potential association with a clinical phenotype. European journal of human genetics : EJHG 32 (7) (2024)
Ainara Ruiz de Sabando, Marc Ciosi, Arkaitz Galbete, Sarah A Cumming, null null, Darren G Monckton, María A Ramos-Arroyo
Somatic CAG repeat instability in intermediate alleles of the HTT gene and its potential association with a clinical phenotype. European journal of human genetics : EJHG (2024)
Ainara Ruiz de Sabando, Marc Ciosi, Arkaitz Galbete, Sarah A Cumming, null null, Darren G Monckton, María A Ramos-Arroyo
Somatic CAG repeat instability in intermediate alleles of the HTT gene and its potential association with a clinical phenotype. European journal of human genetics : EJHG 32 (7) (2024)
Esther Vicente, Ainara Ruiz de Sabando, Fermín García, Itziar Gastón, Eva Ardanaz, María A Ramos-Arroyo
Validation of diagnostic codes and epidemiologic trends of Huntington disease: a population-based study in Navarre, Spain. Orphanet journal of rare diseases 16 (1) (2021)