Author

Marta Fernandez

Biogipuzkoa Health Research Institute

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Bioengineering· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Assay:bulk RNA-seq· 1 Assay:ChIP-seq· 1 Approach:deep learning· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1

Frequent Co-Authors

Amaia CipitriaiD· 1 shared Ana Cristina RiestraiD· 1 shared Ana Legórburu· 1 shared Ariadna Bada-NavarroiD· 1 shared Beatriz BaladróniD· 1 shared Beatriz Martínez–DelgadoiD· 1 shared Bekim SadikovićiD· 1 shared Diana Sánchez-PonceiD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperBioengineering

Amaia CipitriaORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Matrix biophysical cues drive transient or prolonged breast cancer dormancy programmes

Unai Heras, José Miguel Pardo-Sánchez, Jone Berasain, Iune Toledo, Leire Iturriaga, Itxaso Calafel, Robert Aguirresarobe, Guillermo de Cárcer, Julio A. Aguirre‐Ghiso, E. Arizaga Batiz, Marta Fernandez, Rosa M Zubizarreta Susperregui, Ana Legórburu, Ana Cristina Riestra, Oihane Mitxelena‐Iribarren, Amaia Cipitria

This study shows that matrix stiffness influences breast cancer cell dormancy states, with soft matrices inducing transient dormancy and stiff matrices causing prolonged dormancy.

bioRxiv · Oct 29, 2026 · PreprintBioengineering

EHMT2 LOSS-OF-FUNCTION ALTERATIONS CAUSE A KLEEFSTRA-LIKE SYNDROME

Beatriz Martínez–Delgado, Estrella López Martín, Jennifer Kerkhof, Beatriz Baladrón, Lidia Mirela Mielu, Diana Sánchez-Ponce, Ariadna Bada-Navarro, Marina Herrero-Matesanz, Lidia López, Jessica Rzasa, Dmitrijs Rots, Marta Fernandez, Esther Hernández‐SanMiguel, Gema Gómez‐Mariano, Purificación Marín Reina, , María J. Barrero

The paper identifies a de novo EHMT2 mutation causing a Kleefstra-like syndrome by reducing enzyme activity and altering epigenetic profiles.

medRxiv · Jan 10, 2024 · PreprintGenetic & Genomic Medicine