Lindsay B. Henderson

Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis

Lei Sun, Johanna M. Rommens, Harriet Corvol et al. · Nature Genetics · 2012 · 208 citations · Full text

Physiology, Gastroenterology, Pathology +4

Monogenic variants in dystonia: an exome-wide sequencing study

Michael Zech, Robert Jech, Sylvia Boesch et al. · The Lancet Neurology · 2020 · 206 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +3

Functional Dysregulation of CDC42 Causes Diverse Developmental Phenotypes

Simone Martinelli, Oliver H.F. Krumbach, Francesca Pantaleoni et al. · The American Journal of Human Genetics · 2018 · 181 citations · Full text

Signal Transduction, Signaling Pathway, Cell Regulation +5

A Mild PUM1 Mutation Is Associated with Adult-Onset Ataxia, whereas Haploinsufficiency Causes Developmental Delay and Seizures

Vincenzo A. Gennarino, Elizabeth E. Palmer, Laura M. McDonell et al. · Cell · 2018 · 144 citations · Full text

Identification of IFRD1 as a modifier gene for cystic fibrosis lung disease

Yuanyuan Gu, Isaac T. W. Harley, Lindsay B. Henderson et al. · Nature · 2009 · 131 citations · Full text

Fibrosis, Medicine, Genetics +8