Rahul Phadke

Publication Activity (10 Years)

Years Active: 2019-2022
Publications (10 Years): 4

Top Topics

Skeletal Muscle

Mitochondrial Dna

Metabolic Syndrome

Top Venues

Neuropathology and applied neurobiology

JCSM rapid communications

Genetics in medicine : official journal of the American College of Medical Genetics

Journal of the American Heart Association

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

Publications

Enrico Bugiardini, Andreia M Nunes, Ariany Oliveira-Santos, Marisela Dagda, Tatiana M Fontelonga, Pamela Barraza-Flores, Alan M Pittman, Jasper M Morrow, Matthew Parton, Henry Houlden, Perry Mark Elliott, Petros Syrris, Roderick P P W M Maas, Mohammed Majid Akhtar, Benno Küsters, Joost Raaphorst, Meyke Schouten, Erik-Jan Kamsteeg, Baziel G M van Engelen, Michael G Hanna, Rahul Phadke, Luis Rocha Lopes, Emma Matthews, Dean J Burkin
Integrin α7 Mutations Are Associated With Adult-Onset Cardiac Dysfunction in Humans and Mice. Journal of the American Heart Association 11 (23) (2022)
Pinki Munot, Nadine McCrea, Silvia Torelli, Adnan Manzur, Caroline Sewry, Darren Chambers, Lucy Feng, Pierpaolo Ala, Irina Zaharieva, Nicola Ragge, Helen Roper, Tamas Marton, Phil Cox, Miroslav P Milev, Wen-Chen Liang, Shinsuke Maruyama, Ichizo Nishino, Michael Sacher, Rahul Phadke, Francesco Muntoni
TRAPPC11-related muscular dystrophy with hypoglycosylation of alpha-dystroglycan in skeletal muscle and brain. Neuropathology and applied neurobiology (2021)
Karen J Suetterlin, S Veronica Tan, Roope Mannikko, Rahul Phadke, Michael Orford, Simon Eaton, Avan A Sayer, Miranda D Grounds, Emma Matthews, Linda Greensmith, Michael G Hanna
Ageing contributes to phenotype transition in a mouse model of periodic paralysis. JCSM rapid communications 4 (2) (2021)
Nandaki Keshavan, Jose Abdenur, Glenn Anderson, Zahra Assouline, Giulia Barcia, Lamia Bouhikbar, Anupam Chakrapani, Maureen Cleary, Marta C Cohen, François Feillet, Carl Fratter, Natalie S Hauser, Tom Jacques, Amanda Lam, Helen McCullagh, Rahul Phadke, Agnès Rötig, Mark Sharrard, Mariella T Simon, Conrad Smith, Ewen W Sommerville, Robert W Taylor, Wyatt W Yue, Shamima Rahman
The natural history of infantile mitochondrial DNA depletion syndrome due to RRM2B deficiency. Genetics in medicine : official journal of the American College of Medical Genetics 22 (1) (2019)