Erik Madsen

Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling

Lot Snijders Blok, Erik Madsen, Jane Juusola et al. · The American Journal of Human Genetics · 2015 · 324 citations · Full text

Unexplained Intellectual Disability, Gender-specific Effects, Mendelian Disorder +10

<i>In vivo</i> correction of a Menkes disease model using antisense oligonucleotides

Erik Madsen, Paul A. Morcos, Bryce A. Mendelsohn et al. · Proceedings of the National Academy of Sciences · 2008 · 51 citations · Full text

In Vivo Gene Therapy, Molecular Regulation, Genetics +20

Zebrafish Mutants calamity and catastrophe Define Critical Pathways of Gene–Nutrient Interactions in Developmental Copper Metabolism

Erik Madsen, Jonathan D. Gitlin · PLoS Genetics · 2008 · 49 citations · Full text

Developmental Copper Metabolism, Genetics, Nutrient Availability +19

Mutations in the Endothelin Receptor Type A Cause Mandibulofacial Dysostosis with Alopecia

Christopher T. Gordon, K. Nicole Weaver, Roseli Maria Zechi‐Ceide et al. · The American Journal of Human Genetics · 2015 · 47 citations · Full text

Medicine, Dermatology, Scleroderma

Essential role for fibrillin‐2 in zebrafish notochord and vascular morphogenesis

John M. Gansner, Erik Madsen, Robert P. Mecham et al. · Developmental Dynamics · 2008 · 46 citations · Full text