David M Markie (David Markie, D M Markie)

Publication Activity (10 Years)

Years Active: 2019-2022
Publications (10 Years): 5

Top Topics

Genome Wide Association Study

Cancer Stem Cells

Extracellular Matrix

Top Venues

European journal of human genetics : EJHG

Journal of human genetics

AJNR. American journal of neuroradiology

This page only lists publications with an associated author ORCID identifier.

Publications

Benjamin J Halliday, G Baynam, L Ewans, L Greenhalgh, Richard J Leventer, D T Pilz, R Sachdev, Ingrid Eileen Scheffer, David M Markie, George McGillivray, Stephen P Robertson, Simone A Mandelstam
Distinctive Brain Malformations in Zhu-Tokita-Takenouchi-Kim Syndrome. AJNR. American journal of neuroradiology 43 (11) (2022)
Riku Takei, Murray Cadzow, David M Markie, Matt Bixley, Amanda Phipps-Green, Tanya J Major, Changgui Li, Hyon K Choi, Zhi-Qiang Li, Wen-Hua Wei, null null, Hui Guo, Meian He, Yong-Yong Shi, Lisa K Stamp, Nicola Dalbeth, Tony Raymond Merriman, Wen-Hua Wei
Correction to: Trans-ancestral dissection of urate- and gout-associated major loci SLC2A9 and ABCG2 reveals primate-specific regulatory effects. Journal of human genetics (2020)
Riku Takei, Murray Cadzow, David M Markie, Matt Bixley, Amanda Phipps-Green, Tanya J Major, Changgui Li, Hyon K Choi, Zhi-Qiang Li, Hua Hu, null null, Hui Guo, Meian He, Yong-Yong Shi, Lisa K Stamp, Nicola Dalbeth, Tony Raymond Merriman, Wen-Hua Wei
Trans-ancestral dissection of urate- and gout-associated major loci SLC2A9 and ABCG2 reveals primate-specific regulatory effects. Journal of human genetics 66 (2) (2020)
Alicia Bach, Jingyi Mi, Matthew Hunter, Benjamin J Halliday, Sixto García-Miñaúr, Francesca Sperotto, Eva Trevisson, David M Markie, Ian M Morison, Marwan S Shinawi, Daniel N Willis, Stephen P Robertson
Wilms tumor in patients with osteopathia striata with cranial sclerosis. European journal of human genetics : EJHG 29 (3) (2020)
Sean G W Driver, Meremaihi R Jackson, Konrad Richter, Paul Tomlinson, Ben Brockway, Benjamin J Halliday, David M Markie, Stephen P Robertson, Emma M Wade
Biallelic variants in EFEMP1 in a man with a pronounced connective tissue phenotype. European journal of human genetics : EJHG 28 (4) (2019)