Baijayanta Maiti

Proteomic identification of FHL1 as the protein mutated in human reducing body myopathy

Joachim Schessl, Yaqun Zou, Meagan J. McGrath et al. · Journal of Clinical Investigation · 2008 · 156 citations · Full text

Life Sciences, Genetics, Molecular Biology +15

Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice

Nicolas Wein, Adeline Vulin, Maria Sofia Falzarano et al. · Nature Medicine · 2014 · 118 citations · Full text

Medicine, Molecular Medicine, Pathophysiology +4

Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1

Joachim Schessl, Ana Lía Taratuto, Caroline A. Sewry et al. · Brain · 2008 · 102 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Emergent Functional Network Effects in Parkinson Disease

Caterina Gratton, Jonathan M. Koller, William D. Shannon et al. · Cerebral Cortex · 2018 · 94 citations · Full text

Life Sciences, Neurology, Neuroscience +17

A mutation in the<i>SEPN1</i>selenocysteine redefinition element (SRE) reduces selenocysteine incorporation and leads to<i>SEPN1</i>-related myopathy

Baijayanta Maiti, Sandrine Arbogast, Val��rie Allamand et al. · Human Mutation · 2008 · 79 citations

Life Sciences, Genetics, Molecular Biology +17