Nuria Ruiz-Reig

7PUBLICATIONS
52CO-AUTHORS
Artificial life and complex adaptive systemsGene expression (incl. microarray and other genome-wide approaches)Evolutionary computationMedical infection agents (incl. prions)Polymerisation mechanisms
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Publications (7)

|Jul 01, 2026
Competing programs shape cortical sensorimotor-association axis development.

|Jan 13, 2026
Biallelic variants in CELSR1 cause brain malformations, neurodevelopmental disorders and epilepsy in humans.

Claudia M Bonardi, Rikke S Møller, Nuria Ruiz-Reig

|Jul 16, 2025
Competing Programs Shape Cortical Sensorimotor-Association Axis Development.

Jeremiah Tsyporin, Menglei Zhang, Cai Qi

|Nov 07, 2022
KIF2A deficiency causes early-onset neurodegeneration.

Nuria Ruiz-Reig, Georges Chehade, Janne Hakanen

|Apr 26, 2021
DIAPH3 deficiency links microtubules to mitotic errors, defective neurogenesis, and brain dysfunction.

Eva On-Chai Lau, Devid Damiani, Georges Chehade

|Dec 30, 2018
Developmental Requirement of Homeoprotein Otx2 for Specific Habenulo-Interpeduncular Subcircuits.

Nuria Ruiz-Reig, Malalaniaina Rakotobe, Ingrid Bethus

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Frequent Collaborators

5 joint publications

Fadel Tissir

2 joint publications

Akemi Shibata

2 joint publications

Daniel Z Doyle

2 joint publications

Nikkita Salla