Thomas Lennert

Human laminin β2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities

Martin Zenker, Thomas Aigner, Olaf Wendler et al. · Human Molecular Genetics · 2004 · 499 citations

Medicine, Genetics, Molecular Genetics +17

Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21–cen

Klaus Zerres, Gabi Mücher, L Bachner et al. · Nature Genetics · 1994 · 258 citations

Medicine, Genetics, Molecular Genetics +14

The nephronophthisis complex

R. Waldherr, Thomas Lennert, H.P. Weber et al. · Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin · 1982 · 153 citations

Aminoglycoside Pretreatment Partially Restores the Function of Truncated V₂Vasopressin Receptors Found in Patients with Nephrogenic Diabetes Insipidus

Angela Schulz, Katrin Sangkuhl, Thomas Lennert et al. · The Journal of Clinical Endocrinology & Metabolism · 2002 · 64 citations · Full text

Medicine, Molecular Biology, Molecular Genetics +14

Bilateral Wilms Tumor in a Boy with Severe Hypospadias and Cryptorchidism Due to a Heterozygous Mutation in the WT1 Gene

Birgit Köhler, Valerié Schumacher, U. Schulte-Overberg et al. · Pediatric Research · 1999 · 29 citations

Life Sciences, Genetics, Molecular Genetics +15