Fulya Taylan

28PUBLICATIONS
204CO-AUTHORS
Predictive and prognostic markersMedical molecular engineering of nucleic acids and proteinsNeurogeneticsMedical biotechnology not elsewhere classifiedSolid tumours
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Publications (28)

|Jul 30, 2026
Cumulative microscopy reveals cellular states in fibroblasts from patients with genetic disorders.

|Jul 07, 2026
Genomic Medicine Sweden: Advancing precision medicine at the national level.

|Mar 30, 2026
Biallelic variants in RNU2-2 cause a remarkably frequent developmental and epileptic encephalopathy.

Adam Jackson, Alexander J M Blakes, Bader Alhaddad

|Jul 22, 2025
Undiagnosed Hackathon Ends Diagnostic Odyssey in a Patient With DNA2 -Related Rothmund-Thomson Syndrome.

Beril Ay, Ozlem Akgun-Dogan, Fulya Taylan

|Dec 29, 2024
Pediatric Soft Tissue Sarcoma in Limb-Girdle Muscular Dystrophy: Molecular Findings and Clinical Implications.

Carolina Maya-González, Teresita Díaz De Ståhl, Sandra Wessman

|Oct 11, 2024
Smart variant filtering - A blueprint solution for massively parallel sequencing-based variant analysis.

Orlinda Brahimllari, Sandra Eloranta, Patrik Georgii-Hemming

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Frequent Collaborators

15 joint publications

Ann Nordgren

6 joint publications

Anna Lindstrand

5 joint publications

Richard Rosenquist

5 joint publications

Kristina Lagerstedt-Robinson