Katherine G. Johnson

Newcastle Upon Tyne, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 32 publications

A cry for kelp: Evidence for polyphenolic inhibition of Oxford Nanopore sequencing of brown algae.

A cry for kelp: Evidence for polyphenolic inhibition of Oxford Nanopore sequencing of brown algae.

Journal: Journal of phycology

Published: June 26, 2024

Standards of Care for the Health of Transgender and Gender Diverse People, Version 8.

Standards of Care for the Health of Transgender and Gender Diverse People, Version 8.

Journal: International journal of transgender health

Published: October 14, 2022

Impact of nitrogen (N) and phosphorus (P) enrichment and skewed N:P stoichiometry on the skeletal formation and microstructure of symbiotic reef corals.

Impact of nitrogen (N) and phosphorus (P) enrichment and skewed N:P stoichiometry on the skeletal formation and microstructure of symbiotic reef corals.

Journal: Coral reefs (Online)

Published: August 02, 2021

Increased serum miR-193a-5p during non-alcoholic fatty liver disease progression: Diagnostic and mechanistic relevance.

Increased serum miR-193a-5p during non-alcoholic fatty liver disease progression: Diagnostic and mechanistic relevance.

Journal: JHEP reports : innovation in hepatology

Published: June 10, 2021

Publisher Correction: Characterization of three TRAPPC11 variants suggests a critical role for the extreme carboxy terminus of the protein.

Publisher Correction: Characterization of three TRAPPC11 variants suggests a critical role for the extreme carboxy terminus of the protein.

Journal: Scientific reports

Published: November 11, 2020

The clinical-phenotype continuum in DYNC1H1-related disorders-genomic profiling and proposal for a novel classification.

The clinical-phenotype continuum in DYNC1H1-related disorders-genomic profiling and proposal for a novel classification.

Journal: Journal of human genetics

Published: February 25, 2020

Improved Criteria for the Classification of Titin Variants in Inherited Skeletal Myopathies.

Improved Criteria for the Classification of Titin Variants in Inherited Skeletal Myopathies.

Journal: Journal of neuromuscular diseases

Published: February 11, 2020

First clinical and myopathological description of a myofibrillar myopathy with congenital onset and homozygous mutation in FLNC.

First clinical and myopathological description of a myofibrillar myopathy with congenital onset and homozygous mutation in FLNC.

Journal: Human mutation

Published: December 21, 2019

Transcriptomic profiling across the nonalcoholic fatty liver disease spectrum reveals gene signatures for steatohepatitis and fibrosis.

Transcriptomic profiling across the nonalcoholic fatty liver disease spectrum reveals gene signatures for steatohepatitis and fibrosis.

Journal: Science translational medicine

Published: December 04, 2019

Phenotypic and genetic spectrum of patients with limb-girdle muscular dystrophy type 2A from Serbia.

Phenotypic and genetic spectrum of patients with limb-girdle muscular dystrophy type 2A from Serbia.

Journal: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology

Published: December 03, 2019

Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness.

Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: November 25, 2019

POGLUT1 biallelic mutations cause myopathy with reduced satellite cells, α-dystroglycan hypoglycosylation and a distinctive radiological pattern.

POGLUT1 biallelic mutations cause myopathy with reduced satellite cells, α-dystroglycan hypoglycosylation and a distinctive radiological pattern.

Journal: Acta neuropathologica

Published: September 19, 2019

Showing 1-12 of 32

Last Updated: 09/26/2026