Julian Ik-Tsen Heng (Julian I-T Heng, Julian I T Heng)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2022
Publications (10 Years): 7

Top Venues

Molecular genetics & genomic medicine

Human mutation

Journal of neurochemistry

Clinical genetics

Curtin University

Florey Institute of Neuroscience and Mental Health (PHD)

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

Affiliation History

Curtin University Mar 13 2017

Australia

Associate Professor :: Curtin Health Innovation Research Institute

Harry Perkins Institute of Medical Research - Mar 10 2017

Australia

Associate Professor and Group Leader

Australian Regenerative Medicine Institute

Australia

Senior Research Fellow and Group Leader

Florey Institute of Neuroscience and Mental Health

Australia

Postdoctoral Fellow

National Institute for Medical Research

United Kingdom

Research Fellow :: Molecular Neurobiology

Florey Institute of Neuroscience and Mental Health

Australia

Postdoctoral Scientist

Education History

Florey Institute of Neuroscience and Mental Health

Australia

PHD

University of Western Australia

Australia

BSC

Publications

Cathryn Poulton, Gareth Baynam, Kye Pugh, Michael Mason, Catherine Kiraly-Borri, Dylan Gration, Lauren Dreyer, Leon Viti, Mark Agostino, Julian Ik-Tsen Heng
Further evidence for distinct traits associated with RBM10 missense variants. Clinical genetics 102 (2) (2022)
Mark Agostino, Fiona McKenzie, Chloe Buck, Karen J Woodward, Vanessa J Atkinson, Dimitar N Azmanov, Julian Ik-Tsen Heng
Studying Disease-Associated UBE3A Missense Variants Using Enhanced Sampling Molecular Simulations. ACS omega 7 (29) (2022)
Julian Ik-Tsen Heng, Leon Viti, Kye Pugh, Owen J Marshall, Mark Agostino
Understanding the impact of ZBTB18 missense variation on transcription factor function in neurodevelopment and disease. Journal of neurochemistry 161 (3) (2022)
Isabel A Hemming, Steven Blake, Mark Agostino, Julian Ik-Tsen Heng
General population ZBTB18 missense variants influence DNA binding and transcriptional regulation. Human mutation 41 (9) (2020)
Isabel A Hemming, Olivier Clément, Ivan E Gladwyn-Ng, Hayley D Cullen, Han Leng Ng, Heng B See, Linh Ngo, Daniela Ulgiati, Kevin D G Pfleger, Mark Agostino, Julian Ik-Tsen Heng
Disease-associated missense variants in ZBTB18 disrupt DNA binding and impair the development of neurons within the embryonic cerebral cortex. Human mutation 40 (10) (2019)
Karen J Woodward, Julie Stampalia, Hannah Vanyai, Hashika Rijhumal, Kim Potts, Fiona Taylor, Joanne Peverall, Tanya Grumball, Soruba Sivamoorthy, Hamid Alinejad-Rokny, John Wray, Andrew Whitehouse, Lakshmi Nagarajan, Jacqueline Scurlock, Sabine Afchani, Matthew Edwards, Ashleigh Murch, John Beilby, Gareth Baynam, Cathy Kiraly-Borri, Fiona McKenzie, Julian Ik-Tsen Heng
Atypical nested 22q11.2 duplications between LCR22B and LCR22D are associated with neurodevelopmental phenotypes including autism spectrum disorder with incomplete penetrance. Molecular genetics & genomic medicine 7 (2) (2019)
Cathryn Poulton, Gareth Baynam, Clarissa Yates, Hamid Alinejad-Rokny, Simon Williams, Helen Wright, Karen J Woodward, Soruba Sivamoorthy, Joanne Peverall, Peter Shipman, David Ravine, John Beilby, Julian Ik-Tsen Heng
A review of structural brain abnormalities in Pallister-Killian syndrome. Molecular genetics & genomic medicine 6 (1) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Julian Ik-Tsen Heng (Julian I-T Heng, Julian I T Heng)