Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish familiesMelanie M. Mahtani, Leif Groop, Timo Kanninen et al.|Nature Genetics|1996Cited by 327
Characterization of the MODY3 phenotype. Early-onset diabetes caused by an insulin secretion defect.Markku Lehto, Leif Groop, Melanie M. Mahtani et al.|Journal of Clinical Investigation|1997Cited by 199
Heritability of albumin excretion rate in families of patients with Type II diabetesCarol Forsblom, Leif Groop, Timo Kanninen et al.|Diabetologia|1999Cited by 87
Genome-Wide Association Study of Peripheral Artery DiseaseNatalie R. van Zuydam, Paul McKeague, Alexander Stiby et al.|Circulation Genomic and Precision Medicine|2021Cited by 86
A paired-sibling analysis of the XbaI polymorphism in the muscle glycogen synthase geneMarju Orho‐Melander, Leif Groop, P. Almgren et al.|Diabetologia|1999Cited by 43