Nadine Reintjes

CNNM2 Mutations Cause Impaired Brain Development and Seizures in Patients with Hypomagnesemia

Francisco J. Arjona, Jeroen H. F. de Baaij, Karl P. Schlingmann et al. · PLoS Genetics · 2014 · 134 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies

Bodo B. Beck, Anne Baasner, Anja Buescher et al. · European Journal of Human Genetics · 2012 · 81 citations · Full text

Medicine, Internal Medicine, Molecular Medicine +6

Autosomal-Recessive Mutations in MESD Cause Osteogenesis Imperfecta

Shahida Moosa, Guilherme Lopes Yamamoto, Lutz Garbes et al. · The American Journal of Human Genetics · 2019 · 65 citations · Full text

Medicine, Genetics, Molecular Genetics +10

Normal intelligence and premature ovarian failure in an adult female with a 7.6 Mb de novo terminal deletion of chromosome 9p

Iris Bartels, I Pütz, Nadine Reintjes et al. · European Journal of Medical Genetics · 2013 · 39 citations

Life Sciences, Genetics, Molecular Genetics +17

Activating Somatic FGFR2 Mutations in Breast Cancer

Nadine Reintjes, Yun Li, Alexandra Becker et al. · PLoS ONE · 2013 · 39 citations · Full text

Medicine, Genetics, Molecular Genetics +16