Mark J Hamilton (Mark Hamilton)

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2017-2020
Publications (10 Years): 4

Top Venues

European journal of human genetics : EJHG

Journal of medical genetics

PloS one

Neurology. Genetics

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

Publications

Jacob N Miller, Ellen van der Plas, Mark J Hamilton, Timothy R Koscik, Laurie Gutmann, Sarah A Cumming, Darren G Monckton, Peggy C Nopoulos
Variant repeats within the DMPK CTG expansion protect function in myotonic dystrophy type 1. Neurology. Genetics 6 (5) (2020)
Sarah A Cumming, Mark J Hamilton, Yvonne Robb, Helen Gregory, Catherine McWilliam, Anneli Cooper, Berit Adam, Josephine McGhie, Graham Hamilton, Pawel Herzyk, Michael R Tschannen, Elizabeth Worthey, Richard Petty, Bob Ballantyne, null null, Jon Warner, Maria Elena Farrugia, Cheryl Longman, Darren G Monckton
De novo repeat interruptions are associated with reduced somatic instability and mild or absent clinical features in myotonic dystrophy type 1. European journal of human genetics : EJHG 26 (11) (2018)
Mark J Hamilton, Yvonne Robb, Sarah Cumming, Helen Gregory, Alexis Duncan, Monika Rahman, Anne McKeown, Catherine McWilliam, John Dean, Alison Wilcox, Maria E Farrugia, Anneli Cooper, Josephine McGhie, Berit Adam, Richard Petty, null null, Cheryl Longman, Iain Findlay, Alan Japp, Darren G Monckton, Martin A Denvir
Elevated plasma levels of cardiac troponin-I predict left ventricular systolic dysfunction in patients with myotonic dystrophy type 1: A multicentre cohort follow-up study. PloS one 12 (3) (2017)
Mark J Hamilton, Richard C Caswell, Natalie Canham, Trevor Cole, Helen V Firth, Nicola Foulds, Ketil Heimdal, Emma Hobson, Gunnar Houge, Shelagh Joss, Dhavendra Kumar, Anne Katrin Lampe, Isabelle Maystadt, Victoria McKay, Kay Metcalfe, Ruth Newbury-Ecob, Soo-Mi Park, Leema Robert, Cecilie F Rustad, Emma Wakeling, Andrew O M Wilkie, The Deciphering Developmental Disorders Study, Stephen R F Twigg, Mohnish Suri
Heterozygous mutations affecting the protein kinase domain of CDK13 cause a syndromic form of developmental delay and intellectual disability. Journal of medical genetics 55 (1) (2017)

Mark J Hamilton.css-eqlu8i{font-size:small;padding-left:4px;} (Mark Hamilton)

Publication Activity (10 Years)

Top Topics

Top Venues

Mark J Hamilton (Mark Hamilton)