Isabel Hernández

Lack of Helios During Neural Development Induces Adult Schizophrenia-Like Behaviors Associated With Aberrant Levels of the TRIF-Recruiter Protein WDFY1

B. Arranz, A. Giralt, J. Alberch, 2020, Frontiers in Cellular Neuroscience.

Homozygous R136S mutation in PRNP gene causes recessive inherited early onset prion disease

J. Castilla, R. Sánchez-Valle, H. Eraña, 2021 .

Multiple organ involvement by alpha‐synuclein pathology in Lewy body disorders

E. Tolosa, F. Valldeoriola, M. Marti, 2014, Movement disorders : official journal of the Movement Disorder Society.

Crowdfunded whole-genome sequencing of the celebrity cat Lil BUB identifies causal mutations for her osteopetrosis and polydactyly

Bianca, A. Boyko, G. Barsh, 2019 .

Multi-omic analyses in Abyssinian cats with primary renal amyloid deposits

A. Boyko, G. Barsh, N. Pedersen, 2021, Scientific Reports.

Homozygous R136S mutation in PRNP gene causes inherited early onset prion disease

J. Castilla, R. Sánchez-Valle, H. Eraña, 2021, Alzheimer's research & therapy.

Complex Feline Disease Mapping Using a Dense Genotyping Array

A. Boyko, R. Todhunter, J. J. Hayward, 2021, bioRxiv.

A unique common ancestor introduced P301L mutation in MAPT gene in frontotemporal dementia patients from Barcelona (Baix Llobregat, Spain)

A. Brice, R. Sánchez-Valle, V. Redaelli, 2019, Neurobiology of Aging.

Multiple organ involvement by alpha‐synuclein pathology in Lewy body disorders

E. Tolosa, F. Valldeoriola, M. Marti, 2014, Movement disorders : official journal of the Movement Disorder Society.