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Employment (3)

The University of Manchester: Manchester, GB

Employment
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University of Manchester - PURE

University of Manchester: Manchester, Manchester, GB

2017-07-02 to 2017-07-02 | NIHR Academic Clinical Fellow
Employment
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JH McDermott

Central Manchester University Hospitals NHS Foundation Trust: Manchester, Manchester, GB

2015-07-01 to 2017-07-01
Employment
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JH McDermott

Education and qualifications (3)

The University of Manchester: Manchester, GB

Education
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University of Manchester - PURE

University of Manchester: Manchester, Manchester, GB

2009-07-01 to 2015-07-01 | MBChB (Hons) (Manchester Medical School)
Education
Source: Self-asserted source
JH McDermott

University of Manchester: Manchester, Manchester, GB

2011-07-01 to 2012-07-01 | Pathology BSc (Hons) (Manchester Medical School)
Education
Source: Self-asserted source
JH McDermott

Works (50 of 62)

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Page 1 of 2

Development and Validation of a Rapid Point-of-Care CYP2C19 Genotyping Platform.

The Journal of molecular diagnostics : JMD
2024-12 | Journal article
Contributors: Burke KA; O'Sullivan J; Godfrey N; Sharma V; Hilton S; Wright SJ; Greaves NS; Newman WG; McDermott JH
Source: Self-asserted source
JH McDermott via Europe PubMed Central
grade
Preferred source (of 2)‎

Pharmacogenomics: DPYD and Prevention of Toxicity.

Clinical oncology (Royal College of Radiologists (Great Britain))
2024-12 | Journal article
Contributors: Keen J; McDermott JH; Aguilar-Martinez E; Newman WG
Source: Self-asserted source
JH McDermott via Europe PubMed Central

Genedrive CYP2C19 ID Kit - Instructions for Use (IFU) V5.0

2024-11-07 | Report | Author
SOURCE-WORK-ID:

27619581

Contributors: JH McDermott; William Newman
Source: check_circle
figshare

A national survey of first line antibiotic use in neonatal units - and the potential scope for iatrogenic sensorineural hearing loss prevention.

Frontiers in pediatrics
2024-10 | Journal article
Contributors: Peterson J; Muddiman L; Groves F; Booth N; Newman WG; McDermott JH; Mahaveer A
Source: Self-asserted source
JH McDermott via Europe PubMed Central

CYP2C19 genetic testing for Mavacamten and ischaemic stroke treatment: What does the result mean for cardiovascular prescribers in the UK and Europe?

European heart journal. Cardiovascular pharmacotherapy
2024-10 | Journal article
Contributors: Magavern EF; McDermott JH; Caulfield MJ; Newman WG
Source: Self-asserted source
JH McDermott via Europe PubMed Central

Genetic Risk of Axonal Neuropathy Following Infection

2024-10 | Preprint
Contributors: Harkness JR; McDermott JH; Marsden S; Jamieson P; Metcalfe KA; Khan N; Macken WL; Pitceathly RD; Record CJ; Maroofian R et al.
Source: Self-asserted source
JH McDermott via Europe PubMed Central

Pre-Emptive Pharmacogenetic Testing in the Acute Hospital Setting: A Cross-Sectional Study.

QJM : monthly journal of the Association of Physicians
2024-10 | Journal article
Contributors: McDermott JH; Burke K; Fullerton N; O'Sullivan J; Alex A; Ingham A; Sharma V; Godfrey N; Odudu A; Syed T et al.
Source: Self-asserted source
JH McDermott via Europe PubMed Central
grade
Preferred source (of 2)‎

Understanding general practitioner and pharmacist preferences for pharmacogenetic testing in primary care: a discrete choice experiment.

The pharmacogenomics journal
2024-08 | Journal article
Contributors: McDermott JH; Sharma V; Beaman GM; Keen J; Newman WG; Wilson P; Payne K; Wright S
Source: Self-asserted source
JH McDermott via Europe PubMed Central
grade
Preferred source (of 2)‎

Pharmacogenetics Clinical Decision Support Systems for Primary Care in England: Co-Design Study.

Journal of medical Internet research
2024-07 | Journal article
Contributors: Sharma V; McDermott J; Keen J; Foster S; Whelan P; Newman W
Source: Self-asserted source
JH McDermott via Europe PubMed Central

Rapid point of care testing: the next frontier in pharmacogenomics.

Pharmacogenomics
2024-07 | Journal article
Contributors: Leach M; Newman WG; McDermott JH
Source: Self-asserted source
JH McDermott via Europe PubMed Central

A review of clopidogrel resistance in lower extremity arterial disease

JVS - Vascular Insights
2024-07-13 | Journal article | Author
SOURCE-WORK-ID:

f44f952c-8e44-45ba-b5d8-a677eb5faacd

Contributors: Kerry Burke; JH McDermott; Stuart Wright; William Newman; Nicholas Greaves
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University of Manchester - PURE

Public preferences for pharmacogenetic testing in the NHS: Embedding a discrete choice experiment within service design to better meet user needs

British Journal of Clinical Pharmacology
2024-07-01 | Journal article | Author
SOURCE-WORK-ID:

33fbbd2c-118e-4977-beb3-1899f1d9bb42

EID:

2-s2.0-85190799044

Contributors: JH McDermott; videha sharma; William Newman; Paul Wilson; Katherine Payne; Stuart Wright
Source: check_circle
University of Manchester - PURE
grade
Preferred source (of 2)‎

Genomics and insurance in the United Kingdom: increasing complexity and emerging challenges.

Health economics, policy, and law
2024-05 | Journal article
Contributors: Dixon P; Horton RH; Newman WG; McDermott JH; Lucassen A
Source: Self-asserted source
JH McDermott via Europe PubMed Central

A Prospective Observational Study to Assess the Impact of Pharmacogenetics on Outcomes in Vascular Surgery (PROSPER)

medRxiv
2024-05-24 | Working paper | Author
SOURCE-WORK-ID:

f25db320-75bb-459f-8f0c-931cb88da783

Contributors: Kerry A Burke; Selman Mirza; Stuart Wright; Nicholas S Greaves; William Newman; JH McDermott
Source: check_circle
University of Manchester - PURE

A metabolic signature for NADSYN1-dependent congenital NAD deficiency disorder.

The Journal of clinical investigation
2024-02 | Journal article
Contributors: Szot JO; Cuny H; Martin EM; Sheng DZ; Iyer K; Portelli S; Nguyen V; Gereis JM; Alankarage D; Chitayat D et al.
Source: Self-asserted source
JH McDermott via Europe PubMed Central

Educational animation for healthcare professionals enrolled in a study investigating preferences for a pharmacogenetic service in primary care in the NHS

2024-02-16 | Interactive resource | Author
SOURCE-WORK-ID:

25218194

Contributors: JH McDermott
Source: check_circle
figshare

P10.016.D Biallelic variants in RCC1 result in fever associated axonal neuropathy with encephalopathy

European Journal of Human Genetics
2024-01-08 | Other | Author
SOURCE-WORK-ID:

132d7f4f-1854-49ae-8492-f00853e4a93e

WOSUID:

001147414902357

Contributors: J. Robert Harkness; JH McDermott; K Metcalfe; W Macken; A Sabir; S Santra; J Urquhart; L Demain; R Maroofian; M Zamani et al.
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University of Manchester - PURE

Exploring NICU nurses' views of a novel genetic point-of-care test identifying neonates at risk of antibiotic-induced ototoxicity

Journal of Advanced Nursing
2024-01-07 | Journal article | Author
SOURCE-WORK-ID:

c83bd263-b97a-4ff1-9b60-504eaee3bb15

EID:

2-s2.0-85181681052

Contributors: Georgia Brown; Natalie Warrington; Fiona Ulph; Nicola Booth; Karen Harvey; Rachel L. James; Karen Tricker; Paul Wilson; William Newman; JH McDermott et al.
Source: check_circle
University of Manchester - PURE
grade
Preferred source (of 2)‎

MT-RNR1 Genotype Should Not Affect Childhood Vaccination-Unintended Consequences of Guidelines.

JAMA pediatrics
2023-11 | Journal article
Contributors: McDermott JH; Wolf J; Newman WG
Source: Self-asserted source
JH McDermott via Europe PubMed Central

Introduction to pharmacogenetics.

Drug and therapeutics bulletin
2023-10 | Journal article
Contributors: McDermott JH; Newman W
Source: Self-asserted source
JH McDermott via Europe PubMed Central

Educational animation for participants in a study investigating preferences for a pharmacogenetic service in primary care in the NHS

2023-10-31 | Interactive resource | Author
SOURCE-WORK-ID:

24460957

Contributors: JH McDermott
Source: check_circle
figshare

Development of a point-of-care genetic test for effective treatment of ischaemic stroke: an early model-based cost-effectiveness analysis [version 1; peer review: 1 approved, 2 approved with reservations]

Wellcome Open Research
2023-10-20 | Journal article | Author
SOURCE-WORK-ID:

0f32a1f7-8696-4f08-bdc4-4d28af2382d3

EID:

2-s2.0-85177472870

Contributors: Stuart Wright; JH McDermott; Dwaipayan Sen; Craig James Smith; William Newman; Katherine Payne
Source: check_circle
University of Manchester - PURE

The Implementation of Pharmacogenetics in the United Kingdom.

Handbook of experimental pharmacology
2023-06 | Journal article
Contributors: McDermott JH; Sharma V; Keen J; Newman WG; Pirmohamed M
Source: Self-asserted source
JH McDermott via Europe PubMed Central

Pharmacogenetics clinical decision support tools for primary care in England: a co-design study (Preprint)

2023-05-23 | Other | Author
SOURCE-WORK-ID:

b8a4f8f2-8f65-4e34-ae26-5e1b2205c7b3

Contributors: videha sharma; JH McDermott; Jessica Keen; Simon Foster; Pauline Whelan; William Newman
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University of Manchester - PURE

Letters to the Editor.

Journal of paediatrics and child health
2023-02 | Journal article
Contributors: McDermott JH; Newman WG
Source: Self-asserted source
JH McDermott via Europe PubMed Central

Exercise instructors are not consistently implementing the strength component of the UK chief medical officers' physical activity guidelines in their exercise prescription for older adults

2023-01 | Conference paper | Author
SOURCE-WORK-ID:

c935e21d-3722-4212-80cc-45a48452ef12

WOSUID:

001115283100008

EID:

2-s2.0-85178951579

Contributors: Ashley Gluchowski; Helena Bilsborough; JH McDermott; Helen Hawley-Hague; Chris Todd
Source: check_circle
University of Manchester - PURE

Patient and public involvement in hearing research

International Journal of Audiology
2022-12-26 | Journal article | Author
SOURCE-WORK-ID:

05c8d81b-e606-4886-9b19-7eb86531faf1

EID:

2-s2.0-85145391814

Contributors: Piers Dawes; Paolo Arru; Rachel Corry; JH McDermott; Julia Garlick; Hannah Guest; Emily Howlett; Iain Jackson; Rachel L. James; Annie Keane et al.
Source: check_circle
University of Manchester - PURE

Options for Detecting Risk of Aminoglycoside-Induced Ototoxicity in Neonates-Reply.

JAMA pediatrics
2022-08 | Journal article
Contributors: McDermott JH; Newman WG
Source: Self-asserted source
JH McDermott via Europe PubMed Central

The role of <i>CYP2C19</i> genotyping to guide antiplatelet therapy following ischemic stroke or transient ischemic attack.

Expert review of clinical pharmacology
2022-08 | Journal article
Contributors: McDermott JH; Leach M; Sen D; Smith CJ; Newman WG; Bath PM
Source: Self-asserted source
JH McDermott via Europe PubMed Central

Characterizing pharmacogenetic programs using the consolidated framework for implementation research: A structured scoping review

Frontiers in Medicine
2022-08-18 | Journal article | Author
SOURCE-WORK-ID:

20f9a99a-4592-4f4f-8160-7a31bb8ccc97

EID:

2-s2.0-85137714517

Contributors: JH McDermott; Stuart Wright; videha sharma; William Newman; Katherine Payne; Paul Wilson
Source: check_circle
University of Manchester - PURE

A blockchain-based framework to support pharmacogenetic data sharing.

The pharmacogenomics journal
2022-07 | Journal article
Contributors: Albalwy F; McDermott JH; Newman WG; Brass A; Davies A
Source: Self-asserted source
JH McDermott via Europe PubMed Central
grade
Preferred source (of 2)‎

First Genotype-Phenotype Study in TBX4 Syndrome: Gain-of-Function Mutations Causative for Lung Disease.

American journal of respiratory and critical care medicine
2022-07 | Journal article
Contributors: Prapa M; Lago-Docampo M; Swietlik EM; Montani D; Eyries M; Humbert M; Welch CCL; Chung W; Berger RMF; Bogaard HJ et al.
Source: Self-asserted source
JH McDermott via Europe PubMed Central

Rapid Point-of-Care Genotyping to Avoid Aminoglycoside-Induced Ototoxicity in Neonatal Intensive Care.

JAMA pediatrics
2022-03-21 | Journal article
Source: Self-asserted source
JH McDermott
grade
Preferred source (of 2)‎

Clinical Pharmacogenetics Implementation Consortium Guideline for the Use of Aminoglycosides Based on MT-RNR1 Genotype

Clinical Pharmacology and Therapeutics
2022-02-01 | Journal article | Author
SOURCE-WORK-ID:

58236dd7-7fac-43e2-9135-55e90d643d39

EID:

2-s2.0-85108551956

WOSUID:

000663667000001

Contributors: JH McDermott; Joshua Wolf; Keito Hoshitsuki; Rachel Huddart; Kelly E Caudle; Michelle Whirl-Carrillo; Peter S Steyger; Richard J H Smith; Neal Cody; Cristina Rodriguez-Antona et al.
Source: check_circle
University of Manchester - PURE
grade
Preferred source (of 2)‎

The diagnostic utility of clinical exome sequencing in 60 patients with hearing loss disorders

Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery
2021-10-12 | Journal article | Author
SOURCE-WORK-ID:

24d04414-ba64-4ae6-8c8c-f76756dc7d6e

EID:

2-s2.0-85116756258

WOSUID:

000669685900001

Contributors: Leslie P Molina-Ramírez; Emma Mm Burkitt-Wright; Haroon Saeed; JH McDermott; Claire Kyle; Ronnie Wright; Christopher Campbell; Sanjeev S Bhaskar; Algy Taylor; Laura Dutton et al.
Source: check_circle
University of Manchester - PURE

Pharmacogenomic testing to support prescribing in primary care: a structured review of implementation models

Pharmacogenomics
2021-08-01 | Journal article | Author
SOURCE-WORK-ID:

a8fd9cb6-a6c5-4db6-ac47-77331c5207ef

EID:

2-s2.0-85114556785

WOSUID:

000691686400001

Contributors: Judith Hayward; JH McDermott; Nadeem Qureshi; William Newman
Source: check_circle
University of Manchester - PURE

Pharmacogenetics to Avoid Loss of Hearing (PALOH) trial: a protocol for a prospective observational implementation trial.

BMJ open
2021-06 | Journal article
Contributors: McDermott JH; Mahood R; Stoddard D; Mahaveer A; Turner MA; Corry R; Garlick J; Miele G; Ainsworth S; Kemp L et al.
Source: Self-asserted source
JH McDermott via Europe PubMed Central
grade
Preferred source (of 2)‎

Genomic and healthcare dynamics of nosocomial SARS-CoV-2 transmission.

eLife
2021-03 | Journal article
Contributors: Ellingford JM; George R; McDermott JH; Ahmad S; Edgerley JJ; Gokhale D; Newman WG; Ball S; Machin N; Black GC
Source: Self-asserted source
JH McDermott via Europe PubMed Central
grade
Preferred source (of 2)‎

A Non-Adaptive Combinatorial Group Testing Strategy to Facilitate Healthcare Worker Screening During the Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) Outbreak.

The Journal of molecular diagnostics : JMD
2021-02 | Journal article
Contributors: McDermott JH; Stoddard D; Woolf PJ; Ellingford JM; Gokhale D; Taylor A; Demain L; Newman WG; Black G
Source: Self-asserted source
JH McDermott via Europe PubMed Central

The rise of point-of-care genetics: how the SARS-CoV-2 pandemic will accelerate adoption of genetic testing in the acute setting.

European journal of human genetics : EJHG
2021-02 | Journal article
Contributors: McDermott JH; Burn J; Donnai D; Newman WG
Source: Self-asserted source
JH McDermott via Europe PubMed Central

A diagnostic evaluation of single screen testing for malaria in the returning traveller - a large retrospective cohort study.

Academic emergency medicine : official journal of the Society for Academic Emergency Medicine
2021-01 | Journal article
Contributors: Reynard C; Geary K; Chiodini P; Brereton M; Burthem J; McDermott J; van den Berg P; Body R
Source: Self-asserted source
JH McDermott via Europe PubMed Central
grade
Preferred source (of 2)‎

Genomic Sequencing and Healthcare Dynamics Track Nosocomial SARS-CoV-2 Transmission

2020-12 | Preprint
OTHER-ID:

PPR254095

Contributors: Ellingford JM; George R; McDermott JH; Ahmed S; Edgerley JJ; Gokhale D; Newman WG; Ball S; Machin N; Black GC
Source: Self-asserted source
JH McDermott via Europe PubMed Central

Using a biomarker acutely to identify babies at risk of serious adverse effects from antibiotics: where is the 'Terrible Moral and Medical Dilemma'?

Journal of medical ethics
2020-12 | Journal article
Contributors: Lucassen AM; McDermott JH; Newman W
Source: Self-asserted source
JH McDermott via Europe PubMed Central
grade
Preferred source (of 2)‎

New insights into the clinical and molecular spectrum of the novel CYFIP2-related neurodevelopmental disorder and impairment of the WRC-mediated actin dynamics.

Genetics in medicine : official journal of the American College of Medical Genetics
2020-11 | Journal article
Contributors: Begemann A; Sticht H; Begtrup A; Vitobello A; Faivre L; Banka S; Alhaddad B; Asadollahi R; Becker J; Bierhals T et al.
Source: Self-asserted source
JH McDermott via Europe PubMed Central

Reply: Expanding the clinical and genetic spectrum of PCYT2-related disorders.

Brain : a journal of neurology
2020-09 | Journal article
Contributors: Vaz FM; McDermott JH; Engelen M; Banka S
Source: Self-asserted source
JH McDermott via Europe PubMed Central

A Non-Adaptive Combinatorial Group Testing Strategy to Facilitate Healthcare Worker Screening During the Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) Outbreak

2020-07 | Preprint
OTHER-ID:

PPR246576

Contributors: McDermott JH; Stoddard D; Woolf P; Ellingford JM; Gokhale D; Taylor A; Demain LA; Newman WG; Black G
Source: Self-asserted source
JH McDermott via Europe PubMed Central
grade
Preferred source (of 2)‎

Genetic testing in the acute setting: a round table discussion.

Journal of medical ethics
2020-07-10 | Journal article
Source: Self-asserted source
JH McDermott

Refusal of viral testing during the SARS-CoV-2 pandemic.

Clinical medicine (London, England)
2020-07-03 | Journal article
Source: Self-asserted source
JH McDermott
grade
Preferred source (of 2)‎

Utilising Point of Care Diagnostics to Minimise Nosocomial Infection in the 2019 Novel Coronavirus (SARS-CoV-2) Pandemic.

QJM : monthly journal of the Association of Physicians
2020-06-03 | Journal article
Source: Self-asserted source
JH McDermott

Mutations in PCYT2 disrupt etherlipid biosynthesis and cause a complex hereditary spastic paraplegia.

Brain : a journal of neurology
2019-10-22 | Journal article
Source: Self-asserted source
JH McDermott
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