Katie I. Johnson

Nottingham, ENG NG51PB, United Kingdom

Last Updated: 09/26/2026

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Found 26 publications

Palindrome-mediated 16p13.3 triplications cause a recognizable neurodegenerative disorder with ataxia.

Palindrome-mediated 16p13.3 triplications cause a recognizable neurodegenerative disorder with ataxia.

Journal: American journal of human genetics
Published: July 28, 2025

Challenges in the imaging and diagnosis of chronic non-bacterial osteomyelitis (CNO).

Challenges in the imaging and diagnosis of chronic non-bacterial osteomyelitis (CNO).

Journal: Clinical radiology
Published: May 15, 2024

Large-scale evaluation of outcomes after a genetic diagnosis in children with severe developmental disorders.

Large-scale evaluation of outcomes after a genetic diagnosis in children with severe developmental disorders.

Journal: Genetics in medicine open
Published: November 14, 2023

Patient and parent perspectives on paediatric cancer multidisciplinary team working and national advisory panels in the UK: a qualitative research study.

Patient and parent perspectives on paediatric cancer multidisciplinary team working and national advisory panels in the UK: a qualitative research study.

Journal: Archives of disease in childhood
Published: November 09, 2023

Decision-support tools to build climate resilience against emerging infectious diseases in Europe and beyond.

Decision-support tools to build climate resilience against emerging infectious diseases in Europe and beyond.

Journal: The Lancet regional health. Europe
Published: May 03, 2023

Publisher Correction: Characterising within-hospital SARS-CoV-2 transmission events using epidemiological and viral genomic data across two pandemic waves.

Publisher Correction: Characterising within-hospital SARS-CoV-2 transmission events using epidemiological and viral genomic data across two pandemic waves.

Journal: Nature communications
Published: February 18, 2022

Clinical utility of vinblastine therapeutic drug monitoring for the treatment of infantile myofibroma patients: A case series.

Clinical utility of vinblastine therapeutic drug monitoring for the treatment of infantile myofibroma patients: A case series.

Journal: Pediatric blood & cancer
Published: February 15, 2022

Traboulsi syndrome caused by mutations in ASPH: An autosomal recessive disorder with overlapping features of Marfan syndrome.

Traboulsi syndrome caused by mutations in ASPH: An autosomal recessive disorder with overlapping features of Marfan syndrome.

Journal: European journal of medical genetics
Published: February 11, 2022

Re: value of additional lateral radiographs in paediatric skeletal surveys for suspected physical abuse.

Re: value of additional lateral radiographs in paediatric skeletal surveys for suspected physical abuse.

Journal: Clinical radiology
Published: February 02, 2022

Characterising within-hospitalSARS-CoV-2 transmission events using epidemiological and viral genomic data across two pandemic waves.

Characterising within-hospitalSARS-CoV-2 transmission events using epidemiological and viral genomic data across two pandemic waves.

Journal: Nature communications
Published: October 28, 2021

Altered subgenomic RNA abundance provides unique insight into SARS-CoV-2 B.1.1.7/Alpha variant infections.

Altered subgenomic RNA abundance provides unique insight into SARS-CoV-2 B.1.1.7/Alpha variant infections.

Journal: Communications biology
Published: September 07, 2021

Four-year experience of paediatric penetrating injuries: findings from a paediatric major trauma centre in the UK.

Four-year experience of paediatric penetrating injuries: findings from a paediatric major trauma centre in the UK.

Journal: Clinical radiology
Published: February 02, 2021
Showing 1-12 of 26

Last Updated: 09/26/2026