Mingyan Fang

Mutation in the<i>SYNJ1</i>Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism

Marialuisa Quadri, Mingyan Fang, Marina Picillo et al. · Human Mutation · 2013 · 309 citations

Neurodegenerative Diseases, Early-onset Parkinsonism, Mendelian Disorder +15

<i>D</i><scp><i>NAJC</i></scp><i>6</i><scp>M</scp>utations <scp>A</scp>ssociated <scp>W</scp>ith <scp>E</scp>arly‐<scp>O</scp>nset <scp>P</scp>arkinson's <scp>D</scp>isease

Simone Olgiati, Marialuisa Quadri, Mingyan Fang et al. · Annals of Neurology · 2015 · 198 citations · Full text

Combined immunodeficiency and Epstein-Barr virus–induced B cell malignancy in humans with inherited CD70 deficiency

Hassan Abolhassani, Emily S.J. Edwards, Aydan İkincioğulları et al. · The Journal of Experimental Medicine · 2016 · 149 citations · Full text

T cell receptor β repertoires as novel diagnostic markers for systemic lupus erythematosus and rheumatoid arthritis

Xiao Liu, Wei Zhang, Ming Zhao et al. · Annals of the Rheumatic Diseases · 2019 · 148 citations

Novel mutations in TNFRSF7/CD27: Clinical, immunologic, and genetic characterization of human CD27 deficiency

Omar K. Alkhairy, Ruy Perez‐Becker, Gertjan J. Driessen et al. · Journal of Allergy and Clinical Immunology · 2015 · 129 citations

Human Cd27 Deficiency, Autoimmune Disease, Genetic Disorder +9