Pearce Wilcox

Maurice Wilkins Centre — New Zealand

Medicine · Health Sciences

49h-index6.2kcitations203works1.52yr avg
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Research Topics

Cystic Fibrosis Research Advances(58), Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis(52), Chronic Obstructive Pulmonary Disease (COPD) Research(35), Systemic Sclerosis and Related Diseases(34), Respiratory Support and Mechanisms(20)

Publications193 total

Melanoma leverages innate immune IRAK-M signaling to limit metastasis through PTPN22-Induced signaling repression
Cancer Letters·2025
Return of the huia? Why Māori worldviews must be part of the ‘de-extinction’ debate
2025Open Access
Rakeiora Genomics Platform: a pathfinder for genomic medicine research in Aotearoa New Zealand
Journal of the Royal Society of New Zealand·2025Open Access
The population-specific Thr44Met OCT3 coding variant affects metformin pharmacokinetics with subsequent effects on insulin sensitivity in C57Bl/6J mice
Diabetologia·2024· 2 citedOpen Access
Safety and Tolerability of SGLT-2 Inhibitors Following Lung Transplantation
2024
Brain AVM compactness score in children with hereditary hemorrhagic telangiectasia
Child s Nervous System·2024Open Access
De Novo Brain Vascular Malformations in Hereditary Hemorrhagic Telangiectasia
Pediatric Neurology·2024· 6 citedOpen Access
Impact of surgical lung biopsy on lung function and survival in patients with idiopathic pulmonary fibrosis in a multi‐centre registry cohort
Respirology·2024· 5 citedOpen Access
Characteristics and risk factors of interstitial pneumonia with autoimmune features
Respiratory Medicine·2023· 7 citedOpen Access
Predicting New-onset Exertional and Resting Hypoxemia in Fibrotic Interstitial Lung Disease
Annals of the American Thoracic Society·2023· 10 citedOpen Access
Circulating cytokine levels in systemic sclerosis related interstitial lung disease and idiopathic pulmonary fibrosis
Scientific Reports·2023· 19 citedOpen Access
An analysis of sex differences in pulmonary arteriovenous malformation presentation, complications and management in a large, multinational registry of patients with hereditary haemorrhagic telangiectasia
ERJ Open Research·2023· 2 citedOpen Access
Eligibility criteria from pharmaceutical randomised controlled trials of idiopathic pulmonary fibrosis: a registry-based study
European Respiratory Journal·2023· 19 cited
Pulmonary exacerbation inflammatory phenotypes in adults with cystic fibrosis
Journal of Cystic Fibrosis·2022· 11 cited
High-quality read-based phasing of cystic fibrosis cohort informs genetic understanding of disease modification
Human Genetics and Genomics Advances·2022· 7 citedOpen Access
Diagnostic agreement among experts assessing adults presenting with possible cystic fibrosis: need for improvement and implications for patient care
ERJ Open Research·2022· 2 citedOpen Access
Inhalational exposures in patients with fibrotic interstitial lung disease: Presentation, pulmonary function and survival in the <scp>Canadian Registry</scp> for <scp>Pulmonary Fibrosis</scp>
Respirology·2022· 27 citedOpen Access
Genetic evidence supports the development of SLC26A9 targeting therapies for the treatment of lung disease
npj Genomic Medicine·2022· 17 citedOpen Access
Association between elevated peripheral blood eosinophil count and respiratory outcomes in adults with cystic fibrosis
Journal of Cystic Fibrosis·2022· 5 citedOpen Access
High Quality Phasing Using Linked-Read Whole Genome Sequencing of Patient Cohorts Informs Genetic Understanding of Complex Traits
2022· 1 citedOpen Access
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Frequent Co-authors

Christopher J. Ryerson(14), Nasreen Khalil(8), Andreas Freitag(7), Richard L. Pardy(7), Nancy Morrison(6), Kerri A. Johannson(6), James V. Dunne(5), Elizabeth Tullis(5), A. George F. Davidson(5), Despina D. Frangolias(5), Martin Kolb(5), H. Manganas(5), Nathan Hambly(5), Charlene D. Fell(5), Harold R. Collard(4), Shawn D. Aaron(4), Katherine L. Vandemheen(4), David P. Speert(4), Pat G. Camp(4), Peter D. Paré(4)