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New functional and structural insights from updated mutational databases for complement factor H, Factor I, membrane cofactor protein and C3

Bioscience reports, 2014-10, Vol.34 (5), p.e00146

2014

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Heterozygote advantage at MHC DRB may influence response to infectious disease epizootics

Molecular ecology, 2015-04, Vol.24 (7), p.1419-1432

2015

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A Final Frontier in Environment-Genome Interactions? Integrated, Multi-Omic Approaches to Predictions of Non-Communicable Disease Risk

Frontiers in genetics, 2022-02, Vol.13, p.831866

2022

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A validation of Illumina EPIC array system with bisulfite-based amplicon sequencing

PeerJ (San Francisco, CA), 2021-02, Vol.9, p.e10762-e10762, Article e10762

2021

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Multivariate canonical correlation analysis identifies additional genetic variants for chronic kidney disease

NPJ systems biology and applications, 2024-03, Vol.10 (1), p.28-28, Article 28

2024

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Examining the role of components of Slc11a1 (Nramp1) in the susceptibility of New Zealand sea lions (Phocarctos hookeri) to disease

PloS one, 2015-04, Vol.10 (4), p.e0122703-e0122703

2015

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Prenatal cannabis exposure is associated with alterations in offspring DNA methylation at genes involved in neurodevelopment, across the life course

Molecular psychiatry, 2024-09

2024

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Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy

The Journal of immunology (1950), 2018-04, Vol.200 (7), p.2464-2478

2018

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Longitudinal research in Aotearoa New Zealand

Journal of the Royal Society of New Zealand, 2022-05, Vol.52 (3), p.213-215

2022

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Two distinct conformations of factor H regulate discrete complement-binding functions in the fluid phase and at cell surfaces

The Journal of biological chemistry, 2018-11, Vol.293 (44), p.17166-17187

2018

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Natural History and Clinicopathological Associations of TRPC6-Associated Podocytopathy

Journal of the American Society of Nephrology, 2024-10

2024

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Genome-wide DNA methylation analysis of heavy cannabis exposure in a New Zealand longitudinal cohort

Translational psychiatry, 2020-04, Vol.10 (1), p.114, Article 114

2020

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What have we learned from longitudinal studies in Aotearoa New Zealand?

Journal of the Royal Society of New Zealand, 2023-08, Vol.53 (4), p.425-428

2023

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DNA methylation analysis using bisulphite-based amplicon sequencing of individuals exposed to maternal tobacco use during pregnancy, and offspring conduct problems in childhood and adolescence

Reproduction fertility and development, 2022-04, Vol.34 (7), p.540-548

2022

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Genetic Evidence of a Population Bottleneck and Inbreeding in the Endangered New Zealand Sea Lion, Phocarctos hookeri

The Journal of heredity, 2016-09, Vol.107 (5), p.392-402

2016

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A ‘phenotypic hangover’: the predictive adaptive response and multigenerational effects of altered nutrition on the transcriptome of Drosophila melanogaster

Environmental epigenetics, 2017-10, Vol.3 (4), p.dvx019-dvx019

2017

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Database of Complement Gene Variants: A comprehensive database providing insights on function, structure and allele frequency for genetic variants identified in complement-mediated diseases

Immunobiology (1979), 2016-10, Vol.221 (10), p.1223-1223

2016

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Development of a predicted physical map of microsatellite locus positions for pinnipeds, with wider applicability to the Carnivora

Molecular ecology resources, 2011-05, Vol.11 (3), p.503-513

2011

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Complete Genome Sequences of Two Geographically Distinct Legionella micdadei Clinical Isolates

Genome announcements (Washington, DC), 2017-06, Vol.5 (22)

2017

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Canonical Correlation Analysis to Identify Single Nucleotide Polymorphisms in CKD: FR-PO302

Journal of the American Society of Nephrology, 2022-11, Vol.33 (11S), p.407-407

2022

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A Multivariate Analysis of Genome-Wide Association (GWAS) Data to Identify Genes Associated with CKD: PO1330

Journal of the American Society of Nephrology, 2021-10, Vol.32 (10S), p.425-425

2021

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Examining the Role of Components of Slc11a1 to Disease

PloS one, 2015-04, Vol.10 (4)

2015

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Heterozygote advantage at MHCDRB may influence response to infectious disease epizootics

Molecular ecology, 2015-04, Vol.24 (7), p.1419

2015

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Statistical validation of rare complement variants provides insights on the molecular basis of atypical haemolytic uraemic syndrome and C3 glomerulopathy

The Journal of immunology (1950), 2018-03, Vol.200 (7), p.2464-2478

2018

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Examining the Role of Components of Slc11a1 (Nramp1) in the Susceptibility of New Zealand Sea Lions (Phocarctos hookeri) to Disease: e0122703

PloS one, 2015-04, Vol.10 (4)

2015

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New functional and structural insights from updated mutational databases for complement factor H, Factor I, membrane cofactor protein and C3

Heterozygote advantage at MHC DRB may influence response to infectious disease epizootics

A Final Frontier in Environment-Genome Interactions? Integrated, Multi-Omic Approaches to Predictions of Non-Communicable Disease Risk

A validation of Illumina EPIC array system with bisulfite-based amplicon sequencing

Multivariate canonical correlation analysis identifies additional genetic variants for chronic kidney disease

Examining the role of components of Slc11a1 (Nramp1) in the susceptibility of New Zealand sea lions (Phocarctos hookeri) to disease

Prenatal cannabis exposure is associated with alterations in offspring DNA methylation at genes involved in neurodevelopment, across the life course

Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy

Longitudinal research in Aotearoa New Zealand

Two distinct conformations of factor H regulate discrete complement-binding functions in the fluid phase and at cell surfaces

Natural History and Clinicopathological Associations of TRPC6-Associated Podocytopathy

Genome-wide DNA methylation analysis of heavy cannabis exposure in a New Zealand longitudinal cohort

What have we learned from longitudinal studies in Aotearoa New Zealand?

DNA methylation analysis using bisulphite-based amplicon sequencing of individuals exposed to maternal tobacco use during pregnancy, and offspring conduct problems in childhood and adolescence

Genetic Evidence of a Population Bottleneck and Inbreeding in the Endangered New Zealand Sea Lion, Phocarctos hookeri

A ‘phenotypic hangover’: the predictive adaptive response and multigenerational effects of altered nutrition on the transcriptome of Drosophila melanogaster

Database of Complement Gene Variants: A comprehensive database providing insights on function, structure and allele frequency for genetic variants identified in complement-mediated diseases

Development of a predicted physical map of microsatellite locus positions for pinnipeds, with wider applicability to the Carnivora

Complete Genome Sequences of Two Geographically Distinct Legionella micdadei Clinical Isolates

Canonical Correlation Analysis to Identify Single Nucleotide Polymorphisms in CKD: FR-PO302

A Multivariate Analysis of Genome-Wide Association (GWAS) Data to Identify Genes Associated with CKD: PO1330

Examining the Role of Components of Slc11a1 to Disease

Heterozygote advantage at MHCDRB may influence response to infectious disease epizootics

Statistical validation of rare complement variants provides insights on the molecular basis of atypical haemolytic uraemic syndrome and C3 glomerulopathy

Examining the Role of Components of Slc11a1 (Nramp1) in the Susceptibility of New Zealand Sea Lions (Phocarctos hookeri) to Disease: e0122703

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