Edmund Cauley

Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy

Daniel P. S. Osborn, Heather L. Pond, Neda Mazaheri et al. · The American Journal of Human Genetics · 2017 · 66 citations · Full text

Inpp5k Cause, Rare Diseases, Mendelian Disorder +7

Chronic activation of hypothalamic oxytocin neurons improves cardiac function during left ventricular hypertrophy-induced heart failure

Kara Garrott, Jhansi Dyavanapalli, Edmund Cauley et al. · Cardiovascular Research · 2017 · 63 citations · Full text

Neurotransmission to parasympathetic cardiac vagal neurons in the brain stem is altered with left ventricular hypertrophy-induced heart failure

Edmund Cauley, Xin Wang, Jhansi Dyavanapalli et al. · American Journal of Physiology-Heart and Circulatory Physiology · 2015 · 39 citations · Full text

Cardiac Muscle, Heart Failure, Synaptic Transmission +19

De novo and biallelic DEAF1 variants cause a phenotypic spectrum

Maria João Nabais Sá, Philip J. Jensik, Stacey McGee et al. · Genetics in Medicine · 2019 · 33 citations · Full text

Allelic Variant, Developmental Biology, Genetic Disorder +10

Overlap of polymicrogyria, hydrocephalus, and Joubert syndrome in a family with novel truncating mutations in ADGRG1/GPR56 and KIAA0556

Edmund Cauley, Ahlam A. Hamed, Inaam N. Mohamed et al. · Neurogenetics · 2019 · 26 citations

Mendelian Disorder, Genetic Disorder, Genetics +6