Christopher R McMaster

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 13

Top Topics

Tyrosine Kinase

Congenital Heart Disease

Top Venues

Nature genetics

Life science alliance

Brain : a journal of neurology

Nature communications

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

Publications

Gareth S Baynam, Daria Julkowska, Sarah Bowdin, Azure Hermes, Christopher R McMaster, Elissa Prichep, Étienne Richer, Francois Hendrikus van der Westhuizen, Gabriela M Repetto, Helen Louise Malherbe, Juergen K V Reichardt, Laura Arbour, Maui Hudson, Kelly du Plessis, Melissa A Haendel, Phillip Wilcox, Sally Ann Lynch, Shamir Rind, Simon Easteal, Xavier Estivil, Nadine Caron, Meck Chongo, Yarlalu Thomas, Mary Catherine V Letinturier, Barend Christiaan Vorster
Advancing diagnosis and research for rare genetic diseases in Indigenous peoples. Nature genetics 56 (2) (2024)
Gareth S Baynam, Daria Julkowska, Sarah Bowdin, Azure Hermes, Christopher R McMaster, Elissa Prichep, Étienne Richer, Francois Hendrikus van der Westhuizen, Gabriela M Repetto, Helen Louise Malherbe, Juergen K V Reichardt, Laura Arbour, Maui Hudson, Kelly du Plessis, Melissa A Haendel, Phillip Wilcox, Sally Ann Lynch, Shamir Rind, Simon Easteal, Xavier Estivil, Nadine Caron, Meck Chongo, Yarlalu Thomas, Mary Catherine V Letinturier, Barend Christiaan Vorster
Advancing diagnosis and research for rare genetic diseases in Indigenous peoples. Nature genetics 56 (2) (2024)
Mahtab Tavasoli, Christopher R McMaster
Defects in integrin complex formation promote CHKB -mediated muscular dystrophy. Life science alliance 7 (8) (2024)
Mahtab Tavasoli, Christopher R McMaster
Defects in integrin complex formation promote CHKB -mediated muscular dystrophy. Life science alliance 7 (8) (2024)
Gareth S Baynam, Daria Julkowska, Sarah Bowdin, Azure Hermes, Christopher R McMaster, Elissa Prichep, Étienne Richer, Francois Hendrikus van der Westhuizen, Gabriela M Repetto, Helen Louise Malherbe, Juergen K V Reichardt, Laura Arbour, Maui Hudson, Kelly du Plessis, Melissa A Haendel, Phillip Wilcox, Sally Ann Lynch, Shamir Rind, Simon Easteal, Xavier Estivil, Nadine Caron, Meck Chongo, Yarlalu Thomas, Mary Catherine V Letinturier, Barend Christiaan Vorster
Advancing diagnosis and research for rare genetic diseases in Indigenous peoples. Nature genetics 56 (2) (2024)
Mahtab Tavasoli, Christopher R McMaster
Defects in integrin complex formation promote CHKB -mediated muscular dystrophy. Life science alliance 7 (8) (2024)
Gareth S Baynam, Daria Julkowska, Sarah Bowdin, Azure Hermes, Christopher R McMaster, Elissa Prichep, Étienne Richer, Francois Hendrikus van der Westhuizen, Gabriela M Repetto, Helen Louise Malherbe, Juergen K V Reichardt, Laura Arbour, Maui Hudson, Kelly du Plessis, Melissa A Haendel, Phillip Wilcox, Sally Ann Lynch, Shamir Rind, Simon Easteal, Xavier Estivil, Nadine Caron, Meck Chongo, Yarlalu Thomas, Mary Catherine V Letinturier, Barend Christiaan Vorster
Advancing diagnosis and research for rare genetic diseases in Indigenous peoples. Nature genetics 56 (2) (2024)
Gareth S Baynam, Daria Julkowska, Sarah Bowdin, Azure Hermes, Christopher R McMaster, Elissa Prichep, Étienne Richer, Francois Hendrikus van der Westhuizen, Gabriela M Repetto, Helen Louise Malherbe, Juergen K V Reichardt, Laura Arbour, Maui Hudson, Kelly du Plessis, Melissa A Haendel, Phillip Wilcox, Sally Ann Lynch, Shamir Rind, Simon Easteal, Xavier Estivil, Nadine Caron, Meck Chongo, Yarlalu Thomas, Mary Catherine V Letinturier, Barend Christiaan Vorster
Advancing diagnosis and research for rare genetic diseases in Indigenous peoples. Nature genetics 56 (2) (2024)
Mahtab Tavasoli, Christopher R McMaster
Defects in integrin complex formation promote CHKB -mediated muscular dystrophy. Life science alliance 7 (8) (2024)
Gareth S Baynam, Daria Julkowska, Sarah Bowdin, Azure Hermes, Christopher R McMaster, Elissa Prichep, Étienne Richer, Francois Hendrikus van der Westhuizen, Gabriela M Repetto, Helen Louise Malherbe, Juergen K V Reichardt, Laura Arbour, Maui Hudson, Kelly du Plessis, Melissa A Haendel, Phillip Wilcox, Sally Ann Lynch, Shamir Rind, Simon Easteal, Xavier Estivil, Nadine Caron, Meck Chongo, Yarlalu Thomas, Mary Catherine V Letinturier, Barend Christiaan Vorster
Advancing diagnosis and research for rare genetic diseases in Indigenous peoples. Nature genetics (2024)
Chiara Klöckner, J Pedro Fernández-Murray, Mahtab Tavasoli, Heinrich Sticht, Gisela Stoltenburg-Didinger, Leila Motlagh Scholle, Somayeh Bakhtiari, Michael C Kruer, Hossein Darvish, Saghar Ghasemi Firouzabadi, Alex Pagnozzi, Anju Shukla, Katta Mohan Girisha, Dhanya Lakshmi Narayanan, Parneet Kaur, Reza Maroofian, Maha Saad Zaki, Mahmoud M Noureldeen, Andreas Merkenschlager, Janina Gburek-Augustat, Elisa Cali, Selina Banu, Kamrun Nahar, Stephanie Efthymiou, Henry Houlden, Rami Abou Jamra, Jason Williams, Christopher R McMaster, Konrad Platzer
Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephaly. Brain : a journal of neurology 145 (6) (2022)
Mahtab Tavasoli, Sarah Lahire, Stanislav Sokolenko, Robyn Novorolsky, Sarah Anne Reid, Abir Lefsay, Meredith O C Otley, Kitipong Uaesoontrachoon, Joyce Rowsell, Sadish Srinivassane, Molly Praest, Alexandra MacKinnon, Melissa Stella Mammoliti, Ashley Alyssa Maloney, Marina Moraca, J Pedro Fernandez-Murray, Meagan McKenna, Christopher J Sinal, Kanneboyina Nagaraju, George S Robertson, Eric P Hoffman, Christopher R McMaster
Mechanism of action and therapeutic route for a muscular dystrophy caused by a genetic defect in lipid metabolism. Nature communications 13 (1) (2022)
Katherine A Strynatka, Michelle C Gurrola-Gal, Jason N Berman, Christopher R McMaster
How Surrogate and Chemical Genetics in Model Organisms Can Suggest Therapies for Human Genetic Diseases. Genetics 208 (3) (2018)