Andrew G L Douglas (Andrew Gl Douglas)

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 7

Top Topics

Amyotrophic Lateral Sclerosis

Tyrosine Kinase

Top Venues

Journal of medical genetics

European journal of human genetics : EJHG

Life science alliance

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

Publications

Andrew G L Douglas, Diana Baralle
Reduced penetrance of gene variants causing amyotrophic lateral sclerosis. Journal of medical genetics 61 (3) (2024)
Andrew G L Douglas, Diana Baralle
Reduced penetrance of gene variants causing amyotrophic lateral sclerosis. Journal of medical genetics 61 (3) (2024)
Andrew G L Douglas, Diana Baralle
Reduced penetrance of gene variants causing amyotrophic lateral sclerosis. Journal of medical genetics (2024)
Andrew G L Douglas, Diana Baralle
Reduced penetrance of gene variants causing amyotrophic lateral sclerosis. Journal of medical genetics (2023)
Kelsey A Nolden, John M Egner, Jack J Collier, Oliver M Russell, Charlotte L Alston, Megan C Harwig, Michael E Widlansky, Souphatta Sasorith, Inês A Barbosa, Andrew G L Douglas, Júlia Baptista, Mark Walker, Deirdre E Donnelly, Andrew A Morris, Hui Jeen Tan, Manju A Kurian, Kathleen Gorman, Santosh Mordekar, Charu Deshpande, Rajib Samanta, Robert McFarland, R Blake Hill, Robert W Taylor, Monika Oláhová
Novel <i>DNM1L</i> variants impair mitochondrial dynamics through divergent mechanisms. Life science alliance 5 (12) (2022)
Lauren M Cairns, Julia Rankin, Asma Hamad, Nicola Cooper, Katrina Merrifield, Vani Jain, Elisabeth Rosser, Megan Rogers, Sarah Buston, Cheryl Stopford, Gabriela Jones, Henrietta Lefroy, Andrea H Németh, Simon Holden, Andrew G L Douglas
Genetic testing in motor neuron disease and frontotemporal dementia: a 5-year multicentre evaluation. Journal of medical genetics (2021)
Alexander J M Blakes, Emily Gaul, Wayne Lam, Nora Shannon, Karen M Knapp, Louise S Bicknell, Meremaihi R Jackson, Emma M Wade, Stephen P Robertson, Susan M White, Raoul Heller, Andrew Chase, Diana Baralle, Andrew G L Douglas
Pathogenic variants causing ABL1 malformation syndrome cluster in a myristoyl-binding pocket and increase tyrosine kinase activity. European journal of human genetics : EJHG 29 (4) (2020)