Mark Hamilton

De novo repeat interruptions are associated with reduced somatic instability and mild or absent clinical features in myotonic dystrophy type 1

Sarah A. Cumming, Mark Hamilton, Yvonne Robb et al. · European Journal of Human Genetics · 2018 · 100 citations · Full text

Rare Diseases, Mendelian Disorder, Genetic Disorder +9

Rubinstein–Taybi syndrome type 2: report of nine new cases that extend the phenotypic and genotypic spectrum

Mark Hamilton, Ruth Newbury‐Ecob, Muriel Holder‐Espinasse et al. · Clinical Dysmorphology · 2016 · 73 citations

Prevalence, correlates, and self-management of HIV-related depressive symptoms

Lucille Sanzero Eller, Eli Haugen Bunch, Dean Wantland et al. · AIDS Care · 2010 · 52 citations

Psychological Co-morbidities, Mental Health, Social Sciences +16

Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants

Sayaka Kayumi, Luis A. Pérez‐Jurado, María Palomares‐Bralo et al. · Genetics in Medicine · 2022 · 48 citations · Full text

Heterozygous mutations affecting the protein kinase domain of <i>CDK13</i> cause a syndromic form of developmental delay and intellectual disability

Mark Hamilton, Richard Caswell, Natalie Canham et al. · Journal of Medical Genetics · 2017 · 45 citations · Full text