Fulya Taylan

Karolinska Institutet Science Park
Stockholm, AB, Sweden

Last Updated: 09/26/2026

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Found 64 publications

Genomic Medicine Sweden: Advancing precision medicine at the national level.

Genomic Medicine Sweden: Advancing precision medicine at the national level.

Journal: Journal of internal medicine
Published: July 07, 2026

Phenotypic and transcriptomic characterization of biallelic RNU2-2 developmental and epileptic encephalopathy.

Phenotypic and transcriptomic characterization of biallelic RNU2-2 developmental and epileptic encephalopathy.

Journal: Epilepsia
Published: February 25, 2026

Cumulative microscopy reveals cellular states in fibroblasts from patients with genetic disorders.

Cumulative microscopy reveals cellular states in fibroblasts from patients with genetic disorders.

Journal: EMBO reports
Published: January 27, 2026

Seasonal variation in childhood acute lymphoblastic leukemia, but not in acute myeloid leukemia, or brain tumors - A Swedish population-based study.

Seasonal variation in childhood acute lymphoblastic leukemia, but not in acute myeloid leukemia, or brain tumors - A Swedish population-based study.

Journal: Cancer epidemiology
Published: January 02, 2026

Cancer Risk in Marfan Syndrome: A Swedish Population-Based Cohort Study.

Cancer Risk in Marfan Syndrome: A Swedish Population-Based Cohort Study.

Journal: International journal of cancer
Published: December 07, 2025

Implementing electronic informed consent in rare disease genomics.

Implementing electronic informed consent in rare disease genomics.

Journal: Scientific reports
Published: October 20, 2025

Biallelic variants in RNU2-2 cause a remarkably frequent developmental and epileptic encephalopathy.

Biallelic variants in RNU2-2 cause a remarkably frequent developmental and epileptic encephalopathy.

Journal: Nature genetics
Published: September 02, 2025

Genetic heterogeneity in childhood leukemia/lymphoma: a Turkish cohort with strong predisposition.

Genetic heterogeneity in childhood leukemia/lymphoma: a Turkish cohort with strong predisposition.

Journal: Frontiers in genetics
Published: May 07, 2025

Risk of malignant melanoma and colorectal cancer in Birt-Hogg-Dubé syndrome - a matched cohort study.

Risk of malignant melanoma and colorectal cancer in Birt-Hogg-Dubé syndrome - a matched cohort study.

Journal: British journal of cancer
Published: April 24, 2025

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

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

Journal: Nature medicine
Published: April 04, 2025

Undiagnosed Hackathon Ends Diagnostic Odyssey in a Patient With DNA2 -Related Rothmund-Thomson Syndrome.

Undiagnosed Hackathon Ends Diagnostic Odyssey in a Patient With DNA2 -Related Rothmund-Thomson Syndrome.

Journal: American journal of medical genetics. Part A
Published: March 24, 2025

Pediatric Soft Tissue Sarcoma in Limb-Girdle Muscular Dystrophy: Molecular Findings and Clinical Implications.

Pediatric Soft Tissue Sarcoma in Limb-Girdle Muscular Dystrophy: Molecular Findings and Clinical Implications.

Journal: The American journal of case reports
Published: December 29, 2024
Showing 1-12 of 64

Last Updated: 09/26/2026