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Science Advances|April 4, 2015
Myosin-binding protein C corrects an intrinsic inhomogeneity in cardiac excitation-contraction couplingMichael J Previs, Benjamin L Prosser, Ji Young Mun, et al.
BMC Medical Genetics|April 3, 2016
Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility lociHamid Reza Saadati, Michael Wittig, Ingo Helbig, et al.
Neurology|April 14, 2025
Deciphering the Natural History of <i>SCN8A</i>-Related DisordersJan H Magielski, Stacey Cohen, Michael C Kaufman, et al.
Neuromolecular Medicine|June 25, 2010
Association study of TRPC4 as a candidate gene for generalized epilepsy with photosensitivitySarah von Spiczak, Hiltrud Muhle, Ingo Helbig, et al.
Medrxiv : the Preprint Server for Health Sciences|May 7, 2024
The clinical and genetic spectrum of paediatric speech and language disorders in 52,143 individualsJan Magielski, Sarah M Ruggiero, Julie Xian, et al.
Epilepsia|January 12, 2011
A retrospective study of the relation between vaccination and occurrence of seizures in Dravet syndromeBlanca Tro-Baumann, Sarah von Spiczak, Jan Lotte, et al.
The Journal of Biological Chemistry|December 20, 2007
S100A1 binds to the calmodulin-binding site of ryanodine receptor and modulates skeletal muscle excitation-contraction couplingBenjamin L Prosser, Nathan T Wright, Erick O Hernãndez-Ochoa, et al.
Circulation Research|February 7, 2024
Integrated Stress Response Potentiates Ponatinib-Induced CardiotoxicityGege Yan, Zhenbo Han, Youjeong Kwon, et al.
Annals of Neurology|February 22, 2018
Mutations in SCN3A cause early infantile epileptic encephalopathyTariq Zaman, Ingo Helbig, Ivana Babić Božović, et al.
Plos One|August 6, 2025
DNA methylation differences stratified by normalized fetal/placental weight ratios suggest neurodevelopmental deficits in neonates with congenital heart diseaseMarin Jacobwitz, Michael Xie, Jamie Catalano, et al.
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