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NTNG1 mutations are a rare cause of Rett syndrome

American journal of medical genetics. Part A, 2006-04, Vol.140A (7), p.691-694

2006

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Early onset seizures and Rett-like features associated with mutations in CDKL5

European journal of human genetics : EJHG, 2005-10, Vol.13 (10), p.1113-1120

2005

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p.R270X MECP2 mutation and mortality in Rett syndrome

European journal of human genetics : EJHG, 2005-11, Vol.13 (11), p.1235-1238

2005

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Variation in exon 1 coding region and promoter of MECP2 in Rett syndrome and controls

European journal of human genetics : EJHG, 2005-01, Vol.13 (1), p.124-126

2005

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CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patients

Journal of medical genetics, 2006-09, Vol.43 (9), p.729-734

2006

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ST6GAL1‐mediated aberrant sialylation promotes prostate cancer progression

The Journal of pathology, 2023-09, Vol.261 (1), p.71-84

2023

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Upregulation of GALNT7 in prostate cancer modifies O-glycosylation and promotes tumour growth

Oncogene, 2023-03, Vol.42 (12), p.926-937

2023

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Mutations of CDKL5 Cause a Severe Neurodevelopmental Disorder with Infantile Spasms and Mental Retardation

American journal of human genetics, 2004-12, Vol.75 (6), p.1079-1093

2004

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Factors Associated With Coronary Angiography Performed Within 6 Months of Randomization to the Conservative Strategy in the ISCHEMIA Trial

Circulation. Cardiovascular interventions, 2024-06, Vol.17 (6), p.e013435

2024

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Dietary antioxidants and risk of Barrett's esophagus and adenocarcinoma of the esophagus in an Australian population

International journal of cancer, 2013-07, Vol.133 (1), p.214-224

2013

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Association of Helicobacter pylori Infection With Reduced Risk for Esophageal Cancer Is Independent of Environmental and Genetic Modifiers

Gastroenterology (New York, N.Y. 1943), 2010-07, Vol.139 (1), p.73-83

2010

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Correlation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X-chromosome inactivation

Journal of medical genetics, 2007-02, Vol.44 (2), p.148-152

2007

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Aspirin, Nonsteroidal Anti-inflammatory Drugs, and the Risks of Cancers of the Esophagus

Cancer epidemiology, biomarkers & prevention, 2008-05, Vol.17 (5), p.1169-1178

2008

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Dietary patterns and risk of oesophageal cancers: a population-based case–control study

British journal of nutrition, 2012-04, Vol.107 (8), p.1207-1216

2012

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Prevalence and determinants of frequent gastroesophageal reflux symptoms in the Australian community

Diseases of the esophagus, 2012-09, Vol.25 (7), p.573-583

2012

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Eating habits and risk of esophageal cancers: a population-based case-control study

Cancer causes & control, 2010-09, Vol.21 (9), p.1475-1484

2010

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Prevalence and determinants of frequent gastroesophageal reflux symptoms in the Australian community

Diseases of the esophagus, 2012-09, Vol.25 (7), p.573-583

2012

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NTNG1 mutations are a rare cause of Rett syndrome

Early onset seizures and Rett-like features associated with mutations in CDKL5

p.R270X MECP2 mutation and mortality in Rett syndrome

Variation in exon 1 coding region and promoter of MECP2 in Rett syndrome and controls

CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patients

ST6GAL1‐mediated aberrant sialylation promotes prostate cancer progression

Upregulation of GALNT7 in prostate cancer modifies O-glycosylation and promotes tumour growth

Preclinical development of an oral anti- Wolbachia macrolide drug for the treatment of lymphatic filariasis and onchocerciasis

Mutations of CDKL5 Cause a Severe Neurodevelopmental Disorder with Infantile Spasms and Mental Retardation

Factors Associated With Coronary Angiography Performed Within 6 Months of Randomization to the Conservative Strategy in the ISCHEMIA Trial

Dietary antioxidants and risk of Barrett's esophagus and adenocarcinoma of the esophagus in an Australian population

Association of Helicobacter pylori Infection With Reduced Risk for Esophageal Cancer Is Independent of Environmental and Genetic Modifiers

Correlation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X-chromosome inactivation

Aspirin, Nonsteroidal Anti-inflammatory Drugs, and the Risks of Cancers of the Esophagus

Dietary patterns and risk of oesophageal cancers: a population-based case–control study

Prevalence and determinants of frequent gastroesophageal reflux symptoms in the Australian community

Eating habits and risk of esophageal cancers: a population-based case-control study

Prevalence and determinants of frequent gastroesophageal reflux symptoms in the Australian community

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