Emad Muhammad

Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenase

Aviva Levitas, Emad Muhammad, Gali Harel et al. · European Journal of Human Genetics · 2010 · 111 citations · Full text

Medicine, Genetics, Molecular Genetics +14

<i>PLEKHM2</i>mutation leads to abnormal localization of lysosomes, impaired autophagy flux and associates with recessive dilated cardiomyopathy and left ventricular noncompaction

Emad Muhammad, Aviva Levitas, Sonia R. Singh et al. · Human Molecular Genetics · 2015 · 75 citations · Full text

Life Sciences, Cardiology, Genetics +17

Congenital myopathy is caused by mutation of HACD1

Emad Muhammad, Orit Reish, Yusuke Ohno et al. · Human Molecular Genetics · 2013 · 56 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Essential role of carbonic anhydrase XII in secretory gland fluid and HCO₃⁻ secretion revealed by disease causing human mutation

Jeong Hee Hong, Emad Muhammad, Changyu Zheng et al. · The Journal of Physiology · 2015 · 45 citations · Full text

Dentistry, Biochemistry, Physiology +17

Autosomal recessive hyponatremia due to isolated salt wasting in sweat associated with a mutation in the active site of Carbonic Anhydrase 12

Emad Muhammad, Neta Leventhal, Galit Parvari et al. · Human Genetics · 2010 · 39 citations

Life Sciences, Genetics, Physiology +12