Tom H. Lindner

Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

Yukio Horikawa, Naohisa Oda, Nancy J. Cox et al. · Nature Genetics · 2000 · 1.5K citations

Metabolic Syndrome, Genetic Determinant, Genetics +9

A genome–wide search for human non–insulin–dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2

Craig L. Hanis, Eric Boerwinkle, Ranajit Chakraborty et al. · Nature Genetics · 1996 · 592 citations

Genome-wide Association Study, Transcriptional Regulation, Genetic Determinant +13

Mutations in the Cilia Gene ARL13B Lead to the Classical Form of Joubert Syndrome

Vincent Cantagrel, Jennifer L. Silhavy, Stephanie Bielas et al. · The American Journal of Human Genetics · 2008 · 395 citations · Full text

Developmental Biology, Mendelian Disorder, Joubert Syndrome +10

A novel syndrome of diabetes mellitus, renal dysfunction and genital malformation associated with a partial deletion of the pseudo-POU domain of hepatocyte nuclear factor-1beta

Tom H. Lindner · Human Molecular Genetics · 1999 · 362 citations · Full text

Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger–Huët anomaly)

Katrin Hoffmann, Christine Karin Dreger, Ada L. Olins et al. · Nature Genetics · 2002 · 346 citations

Lamin B Receptor, Granulocyte, Cell Signaling +7