Chantal Calis

Post-natal myogenic and adipogenic developmental

Nard Kubben, Jan Willem Voncken, Gonda Konings et al. · Nucleus · 2011 · 99 citations · Full text

Identification of differential protein interactors of lamin A and progerin

Nard Kubben, Jan Willem Voncken, Jeroen Demmers et al. · Nucleus · 2010 · 94 citations · Full text

Protein Assembly, Nuclear Lamina, Differential Protein Interactors +17

Whole Exome Sequencing Is the Preferred Strategy to Identify the Genetic Defect in Patients With a Probable or Possible Mitochondrial Cause

Tom E. J. Theunissen, Minh Nguyen, Rick Kamps et al. · Frontiers in Genetics · 2018 · 94 citations · Full text

Clinical Symptoms, Genetics, Genetic Epidemiology +20

Nonsense mutations in CABC1/ADCK3 cause progressive cerebellar ataxia and atrophy

Mike Gerards, Bianca van den Bosch, Chantal Calis et al. · Mitochondrion · 2010 · 72 citations

Neurodegenerative Diseases, Mendelian Disorder, Genetic Disorder +7

Defective complex I assembly due to <i>C20orf7</i> mutations as a new cause of Leigh syndrome

Mike Gerards, Wim J. Sluiter, B.J.C. van den Bosch et al. · Journal of Medical Genetics · 2009 · 68 citations · Full text