André Heimbach

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase

Alfredo Ramı́rez, André Heimbach, Jan Gründemann et al. · Nature Genetics · 2006 · 1.2K citations

Alzheimer's Disease, P-type Atpase, Hereditary Parkinsonism +10

Prevalence of deleterious germline variants in risk genes including BRCA1/2 in consecutive ovarian cancer patients (AGO-TR-1)

Philipp Harter, Jan Hauke, Florian Heitz et al. · PLoS ONE · 2017 · 129 citations · Full text

Pathogenic effects of novel mutations in the P‐type ATPase <i>ATP13A2</i> ( <i>PARK9</i> ) causing Kufor‐Rakeb syndrome, a form of early‐onset parkinsonism

Jin‐Sung Park, Prachi Mehta, Antony A. Cooper et al. · Human Mutation · 2011 · 114 citations

Genetics, Molecular Biology, Early‐onset Parkinsonism +17

The severity of human peri‐implantitis lesions correlates with the level of submucosal microbial dysbiosis

Annika Kröger, Claudia Hülsmann, Stefan Fickl et al. · Journal Of Clinical Periodontology · 2018 · 93 citations · Full text

CHD1L: a new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT)

Antje Brockschmidt, Byung Ha Chung, Stefanie Weber et al. · Nephrology Dialysis Transplantation · 2011 · 46 citations · Full text