Ainara Ruiz de Sabando

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 10

Top Topics

Bipolar Disorder

Top Venues

European journal of human genetics : EJHG

Human molecular genetics

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)
Ainara Ruiz de Sabando, Edurne Urrutia Lafuente, Arkaitz Galbete, Marc Ciosi, Fermín García Amigot, Virginia García Solaesa, null null, Darren G Monckton, Maria A Ramos-Arroyo
Spanish HTT gene study reveals haplotype and allelic diversity with possible implications for germline expansion dynamics in Huntington disease. Human molecular genetics (2022)
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)
Ainara Ruiz de Sabando, Edurne Urrutia Lafuente, Fermín García-Amigot, Angel Alonso Sánchez, Lourdes Morales Garofalo, Sira Moreno, Eva Ardanaz, Maria A Ramos-Arroyo
Genetic and clinical characterization of BRCA-associated hereditary breast and ovarian cancer in Navarra (Spain). BMC cancer 19 (1) (2019)
Julie Kim, Chao Wang, Ainara Ruiz de Sabando, Hannah L Cole, Timothy J Huang, Jie Yang, Thomas D Bannister, Vincent W Yang, Agnieszka B Bialkowska
The Novel Small-Molecule SR18662 Efficiently Inhibits the Growth of Colorectal Cancer In Vitro and In Vivo. Molecular cancer therapeutics 18 (11) (2019)