Fulya Taylan

27PUBLICATIONS

201CO-AUTHORS

Medical molecular engineering of nucleic acids and proteinsNeurogeneticsMedical biotechnology not elsewhere classifiedPatient safetySolid tumours

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Publications (27)

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|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

|Apr 04, 2025

Precision Omics Initiative Sweden (PROMISE) will integrate research with healthcare.

Anders Kämpe, Sanna Gudmundsson, Colum P Walsh

|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 21, 2024

Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon.

Angelica Maria Delgado-Vega, Helene Cederroth, Fulya Taylan

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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

4 joint publications

Elizabeth Emma Palmer

Giedre Grigelioniene

Jessica Nordlund

Vasilios Zachariadis

Valtteri Wirta

Carolina Maya-González

Frequent Collaborators

15 joint publications

Ann Nordgren

6 joint publications

Anna Lindstrand

5 joint publications

Richard Rosenquist

5 joint publications

Kristina Lagerstedt-Robinson