Antonei B. Csòka

Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome

Maria Eriksson, W. Ted Brown, Leslie B. Gordon et al. · Nature · 2003 · 2.2K citations · Full text

Medicine, Genetics, Molecular Genetics +5

Lamin A/C Expression Is a Marker of Mouse and Human Embryonic Stem Cell Differentiation

Dan Constantinescu, Heather Gray, Paul J. Sammak et al. · Stem Cells · 2005 · 353 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +12

Expression Analysis of Six Paralogous Human Hyaluronidase Genes Clustered on Chromosomes 3p21 and 7q31

Antonei B. Csòka, Stephen W. Scherer, Robert Stern · Genomics · 1999 · 258 citations

Life Sciences, Genetics, Molecular Genetics +5

Epigenetic side-effects of common pharmaceuticals: A potential new field in medicine and pharmacology

Antonei B. Csòka, Moshe Szyf · Medical Hypotheses · 2009 · 242 citations

Medicine, Molecular Medicine, Pharmacology +16

Genome‐scale expression profiling of Hutchinson–Gilford progeria syndrome reveals widespread transcriptional misregulation leading to mesodermal/mesenchymal defects and accelerated atherosclerosis

Antonei B. Csòka, Sangeeta B. English, Carl P. Simkevich et al. · Aging Cell · 2004 · 191 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17