Marjo Kestilä

Positionally Cloned Gene for a Novel Glomerular Protein—Nephrin—Is Mutated in Congenital Nephrotic Syndrome

Marjo Kestilä, Ulla Lenkkeri, Minna Männikkö et al. · Molecular Cell · 1998 · 1.9K citations · Full text

Medicine, Genetics, Molecular Genetics +12

Nephrin is specifically located at the slit diaphragm of glomerular podocytes

Vesa Ruotsalainen, Päivi Ljungberg, Jorma Wartiovaara et al. · Proceedings of the National Academy of Sciences · 1999 · 762 citations

Medicine, Molecular Biology, Nephrology +16

Loss-of-function mutations in TYROBP (DAP12) result in a presenile dementia with bone cysts

Juha Paloneva, Marjo Kestilä, Jun Wu et al. · Nature Genetics · 2000 · 472 citations

Medicine, Genetics, Neurology +15

Structure of the Gene for Congenital Nephrotic Syndrome of the Finnish Type (NPHS1) and Characterization of Mutations

Ulla Lenkkeri, Minna Männikkö, Paula McCready et al. · The American Journal of Human Genetics · 1999 · 402 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Congenital nephrotic syndrome (NPHS1): Features resulting from different mutations in Finnish patients

Jaakko Patrakka, Marjo Kestilä, Jorma Wartiovaara et al. · Kidney International · 2000 · 305 citations · Full text

Medicine, Genetics, Molecular Genetics +15