Renate Hillermann

Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23–24.1

Suzana Gispert, Rebecca C.J. Twells, Guillermo Hernández Orozco et al. · Nature Genetics · 1993 · 288 citations

Chromatin, Chromosomal Assignment, Genetic Disorder +7

Spectrum of Mutations in the HFE Gene Implicated in Haemochromatosis and Porphyria

J. Nico P. de Villiers, Renate Hillermann, L. Loubser et al. · Human Molecular Genetics · 1999 · 84 citations · Full text

The Friedreich's ataxia gene encodes a novel phosphatidylinositol–4–phosphate 5–kinase

Jaime J. Carvajal, Mark A. Pook, Maria dos Remédios Magalhães Santos et al. · Nature Genetics · 1996 · 73 citations

Protein Function, Signal Transduction, Natural Sciences +6

Prediction of Preeclampsia – A Workshop Report

Nándor Gábor Than, Roberto Romero, Renate Hillermann et al. · Placenta · 2007 · 67 citations · Full text

Hypertension, Cardiovascular Disease, Maternal Cardiovascular Outcome +11

The Glu298Asp variant of the endothelial nitric oxide synthase gene is associated with an increased risk for abruptio placentae in pre-eclampsia

Renate Hillermann, Kashefa Carelse, G. Gebhardt · Journal of Human Genetics · 2005 · 63 citations · Full text

Developmental Biology, Physiology, Glu298asp Variant +11