Nazli A. Basak

Kirac, Turkey

Last Updated: 09/26/2026

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Found 27 publications

Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis.

Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis.

Journal: Nature genetics
Published: August 15, 2025

Exosome Proteomics of SOD1D90A Mutation Suggest Early Disease Mechanisms, and FN1 as a Biomarker.

Exosome Proteomics of SOD1D90A Mutation Suggest Early Disease Mechanisms, and FN1 as a Biomarker.

Journal: Annals of clinical and translational neurology
Published: May 27, 2025

Sex-specific DNA methylation differences in Amyotrophic lateral sclerosis.

Sex-specific DNA methylation differences in Amyotrophic lateral sclerosis.

Journal: bioRxiv : the preprint server for biology
Published: December 09, 2024

Author Correction: The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration.

Author Correction: The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration.

Journal: Nature communications
Published: July 02, 2024

The GENESIS database and tools: A decade of discovery in Mendelian genomics.

The GENESIS database and tools: A decade of discovery in Mendelian genomics.

Journal: Experimental neurology
Published: May 25, 2024

Mutations in the tail and rod domains of the neurofilament heavy-chain gene increase the risk of ALS.

Mutations in the tail and rod domains of the neurofilament heavy-chain gene increase the risk of ALS.

Journal: Annals of clinical and translational neurology
Published: January 29, 2024

Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease.

Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease.

Journal: Brain : a journal of neurology
Published: October 06, 2023

Large-scale analyses of CAV1 and CAV2 suggest their expression is higher in post-mortem ALS brain tissue and affects survival.

Large-scale analyses of CAV1 and CAV2 suggest their expression is higher in post-mortem ALS brain tissue and affects survival.

Journal: Frontiers in cellular neuroscience
Published: November 30, 2022

Genetic variability in sporadic amyotrophic lateral sclerosis.

Genetic variability in sporadic amyotrophic lateral sclerosis.

Journal: Brain : a journal of neurology
Published: November 16, 2022

Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence data.

Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence data.

Journal: Frontiers in cellular neuroscience
Published: September 21, 2022

Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.

Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.

Journal: Nature genetics
Published: February 01, 2022

The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration.

The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration.

Journal: Nature communications
Published: February 01, 2022
Showing 1-12 of 27

Last Updated: 09/26/2026