H Kääriäinen

The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.

Alan H. Beggs, Mary B. Moyer, S. Scherpf et al. · PubMed · 1989 · 961 citations

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

Mendelian Disorder, Genetic Disorder, Medicine +11

Cancer in Patients With Ataxia-Telangiectasia and in Their Relatives in the Nordic Countries

Jørgen H. Olsen, Johanne M D Hahnemann, A.L. Børresen-Dale et al. · JNCI Journal of the National Cancer Institute · 2001 · 239 citations

A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10

Stanislas Lyonnet, Alessandra Bolino, Anna Pelet et al. · Nature Genetics · 1993 · 192 citations

Chromatin, Developmental Biology, Cytogenetics +11

Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q

Eeva‐Marja Sankila, Leenamaija Pakarinen, H Kääriäinen et al. · Human Molecular Genetics · 1995 · 185 citations