Carrie Ris‐Stalpers

Inactivating Mutations in the Gene for Thyroid Oxidase 2 (<i>THOX2</i>) and Congenital Hypothyroidism

J.C. Moreno, Hennie Bikker, Marlies Kempers et al. · New England Journal of Medicine · 2002 · 474 citations · Full text

Two Frequent Missense Mutations in Pendred Syndrome

Peter Van Hauwe, Lorraine A. Everett, Paul Coucke et al. · Human Molecular Genetics · 1998 · 189 citations · Full text

Up to date with human thyroglobulin

S.A. van de Graaf, Carrie Ris‐Stalpers, Erwin Pauws et al. · Journal of Endocrinology · 2001 · 148 citations · Full text

Allelic Variant, Genetic Disorder, Medicine +15

Type II and type III deiodinase activity in human placenta as a function of gestational age.

Jolanda M. Koopdonk-Kool, J J de Vijlder, Geertruda J. M. Veenboer et al. · The Journal of Clinical Endocrinology & Metabolism · 1996 · 143 citations · Full text

Genetics, Gynecology, Type Ii +21

A Premature Stopcodon in Thyroglobulin Messenger RNA Results in Familial Goiter and Moderate Hypothyroidism

Simone A. R. van de Graaf, Carrie Ris‐Stalpers, Geertruda J. M. Veenboer et al. · The Journal of Clinical Endocrinology & Metabolism · 1999 · 85 citations

Genetics, Molecular Biology, Thyroid Gland +18