David M. Markie

Dunedin, OTA, New Zealand

Last Updated: 09/26/2026

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Found 37 publications

A primary care pharmacogenetic precision medicine pilot based on specific Māori tribal ethical frameworks and principles.

A primary care pharmacogenetic precision medicine pilot based on specific Māori tribal ethical frameworks and principles.

Journal: Journal of community genetics

Published: May 19, 2026

Rakeiora Genomics Platform: a pathfinder for genomic medicine research in Aotearoa New Zealand.

Rakeiora Genomics Platform: a pathfinder for genomic medicine research in Aotearoa New Zealand.

Journal: Journal of the Royal Society of New Zealand

Published: August 04, 2025

Altered corpus callosum microstructure in people with non-syndromic congenital mirror movements (CMM).

Altered corpus callosum microstructure in people with non-syndromic congenital mirror movements (CMM).

Journal: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology

Published: March 30, 2025

Aberrant connectivity of the lateralized readiness system in non-syndromic congenital mirror movements.

Aberrant connectivity of the lateralized readiness system in non-syndromic congenital mirror movements.

Journal: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology

Published: May 05, 2024

Distinctive Brain Malformations in Zhu-Tokita-Takenouchi-Kim Syndrome.

Distinctive Brain Malformations in Zhu-Tokita-Takenouchi-Kim Syndrome.

Journal: AJNR. American journal of neuroradiology

Published: February 24, 2022

Author Correction: Mutations in PYCR1 cause cutis laxa with progeroid features.

Author Correction: Mutations in PYCR1 cause cutis laxa with progeroid features.

Journal: Nature genetics

Published: January 22, 2022

Tuberous sclerosis complex: a complex case.

Tuberous sclerosis complex: a complex case.

Journal: Cold Spring Harbor molecular case studies

Published: December 19, 2021

Intragenic Deletions in FLNB Are Part of the Mutational Spectrum Causing Spondylocarpotarsal Synostosis Syndrome.

Intragenic Deletions in FLNB Are Part of the Mutational Spectrum Causing Spondylocarpotarsal Synostosis Syndrome.

Journal: Genes

Published: March 10, 2021

Deletion of Exon 1 in AMER1 in Osteopathia Striata with Cranial Sclerosis.

Deletion of Exon 1 in AMER1 in Osteopathia Striata with Cranial Sclerosis.

Journal: Genes

Published: November 03, 2020

Correction to: Trans-ancestral dissection of urate- and gout-associated major loci SLC2A9 and ABCG2 reveals primate-specific regulatory effects.

Correction to: Trans-ancestral dissection of urate- and gout-associated major loci SLC2A9 and ABCG2 reveals primate-specific regulatory effects.

Journal: Journal of human genetics

Published: September 09, 2020

Trans-ancestral dissection of urate- and gout-associated major loci SLC2A9 and ABCG2 reveals primate-specific regulatory effects.

Trans-ancestral dissection of urate- and gout-associated major loci SLC2A9 and ABCG2 reveals primate-specific regulatory effects.

Journal: Journal of human genetics

Published: June 10, 2020

Wilms tumor in patients with osteopathia striata with cranial sclerosis.

Wilms tumor in patients with osteopathia striata with cranial sclerosis.

Journal: European journal of human genetics : EJHG

Published: June 02, 2020

Showing 1-12 of 37

Last Updated: 09/26/2026