Maria Asif

Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome

Daniela A. Braun, Svjetlana Lovric, David Schapiro et al. · Journal of Clinical Investigation · 2018 · 138 citations · Full text

Glomerular Disease, Genetics, Renal Pathology +22

Altered paracellular cation permeability due to a rare CLDN10B variant causes anhidrosis and kidney damage

Joakim Klar, Jörg Piontek, Susanne Milatz et al. · PLoS Genetics · 2017 · 64 citations · Full text

Protein Secretion, Pathology, Cellular Physiology +21

Genetic heterogeneity in Pakistani microcephaly families revisited

Ilyas Ahmad, Shahid Mahmood Baig, Adnan Abdulkareem et al. · Clinical Genetics · 2016 · 33 citations

An update of pathogenic variants in <i>ASPM</i>, <i>WDR62, CDK5RAP2</i>,<i> STIL, CENPJ,</i> and<i> CEP135</i> underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan

Sajida Rasool, Jamshaid Mahmood Baig, Abubakar Moawia et al. · Molecular Genetics & Genomic Medicine · 2020 · 33 citations · Full text

Unilateral L4-dorsal root ganglion stimulation evokes pain relief in chronic neuropathic postsurgical knee pain and changes of inflammatory markers: part II whole transcriptome profiling

Thomas M. Kinfe, Maria Asif, Krishnan Chakravarthy et al. · Journal of Translational Medicine · 2019 · 30 citations · Full text