Isabella Fogh

De Crespigny Park
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 31 publications

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

Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data.

Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data.

Journal: Cell genomics

Published: April 01, 2024

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

The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases.

The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases.

Journal: Neurobiology of disease

Published: October 15, 2022

Association of the risk factor UNC13A with survival and upper motor neuron involvement in amyotrophic lateral sclerosis.

Association of the risk factor UNC13A with survival and upper motor neuron involvement in amyotrophic lateral sclerosis.

Journal: Frontiers in aging neuroscience

Published: October 12, 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

TMEM106B Acts as a Modifier of Cognitive and Motor Functions in Amyotrophic Lateral Sclerosis.

TMEM106B Acts as a Modifier of Cognitive and Motor Functions in Amyotrophic Lateral Sclerosis.

Journal: International journal of molecular sciences

Published: July 20, 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

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

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: March 12, 2021

SCFD1 expression quantitative trait loci in amyotrophic lateral sclerosis are differentially expressed.

SCFD1 expression quantitative trait loci in amyotrophic lateral sclerosis are differentially expressed.

Journal: Brain communications

Published: February 27, 2021

Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis.

Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis.

Journal: NPJ genomic medicine

Published: December 15, 2020

Showing 1-12 of 31

Last Updated: 09/26/2026