William G. Wilson

Lyell McEwin Hospital — Australia

Agricultural and Biological Sciences · Life Sciences

50h-index10.2kcitations246works0.22yr avg
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Research Topics

Plant and animal studies(27), Ecology and Vegetation Dynamics Studies(23), Mathematical and Theoretical Epidemiology and Ecology Models(23), Evolution and Genetic Dynamics(23), Evolutionary Game Theory and Cooperation(17)

Publications244 total

A Digital Health Approach to Improve Compliance With Surveillance Colonoscopy Guidelines: The <scp>SCOPES</scp> Program
Cancer Medicine·2026Open Access
Patterns and Predictors of Steroid Use in a Real‐World Inflammatory Bowel Disease Cohort
JGH Open·2025Open Access
DOP015 Consistency and Quality of Inflammatory Bowel Disease care in Australasia; Towards Benchmarking, Crohn’s Colitis Cure Data Insight’s Program
Journal of Crohn s and Colitis·2025
P1225 A cross-sectional study of Inflammatory Bowel Disease in older people across Australasia, a Crohn’s Colitis Cure data insights program
Journal of Crohn s and Colitis·2025· 1 cited
P654 Assessing patient-perceived burden of disease in Ulcerative Colitis: a novel scoring approach in a real-world Australasian cohort
Journal of Crohn s and Colitis·2024Open Access
Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections
Genetics in Medicine·2023· 8 citedOpen Access
Clinical, biochemical and molecular characterization of 12 patients with pyruvate carboxylase deficiency treated with triheptanoin
Molecular Genetics and Metabolism·2023· 4 citedOpen Access
Loss-of-function variants in<i>MYCBP2</i>cause neurobehavioural phenotypes and corpus callosum defects
Brain·2022· 37 citedOpen Access
Highlighting the Dystonic Phenotype Related to <scp><i>GNAO1</i></scp>
Movement Disorders·2022· 58 citedOpen Access
eP188: Novel HECW2 variant presenting with tachypnea and multisystemic congenital malformations
Genetics in Medicine·2022
Ophthalmic Diagnosis and Novel Management of Infantile Refsum Disease with Combination Docosahexaenoic Acid and Cholic Acid
Case Reports in Ophthalmological Medicine·2021· 4 citedOpen Access
BDV Syndrome: an Emerging Syndrome With Profound Obesity and Neurodevelopmental Delay Resembling Prader-Willi Syndrome
The Journal of Clinical Endocrinology & Metabolism·2021· 19 citedOpen Access
Pathogenic <scp> <i>MAST3</i> </scp> Variants in the <scp>STK</scp> Domain Are Associated with Epilepsy
Annals of Neurology·2021· 18 citedOpen Access
Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature
The American Journal of Human Genetics·2021· 67 citedOpen Access
Pathogenic <i>MAST3</i> variants in the STK domain are associated with epilepsy
2021· 2 citedOpen Access
Location, location, location: protein truncating variants in different loci of SRCAP cause three distinct neurodevelopmental disorders, associated with distinctive DNA methylation signatures
2020
The broad phenotypic spectrum of PPP2R1A-related neurodevelopmental disorders correlates with the degree of biochemical dysfunction
Genetics in Medicine·2020· 48 citedOpen Access
Training the next generation of genomic medicine providers: trends in medical education and national assessment
Genetics in Medicine·2020· 13 cited
Defining the clinical phenotype of Saul–Wilson syndrome
Genetics in Medicine·2020· 19 citedOpen Access
Part II: Environmental Harms
2019
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Frequent Co-authors

André M. de Roos(5), Alan Hastings(4), William F. Morris(4), Lawrence D. Harder(4), Martin Morgan(3), Kim Cuddington(3), Raquel E. Gur(3), Edward McCauley(3), Judith L. Bronstein(3), Roger M. Nisbet(3), Francisca Millan(3), Tiffany M. Knight(2), James E. Byers(2), Jeffrey A. Crooks(2), Clive G. Jones(2), John Lambrinos(2), Theresa Sinicrope Talley(2), Vishwajit L. Nimgaonkar(2), Rodney C.P. Go(2), Robert Savage(2)