Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPaseAlfredo Ramı́rez, Christian Kubisch, A. S. Najim Al-Din et al.|Nature Genetics|2006Cited by 1.2k
Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosinEtgar Levy‐Nissenbaum, Elon Pras, Regina C. Betz et al.|Nature Genetics|2003Cited by 176
Functional Subclone Profiling for Prediction of Treatment-Induced Intratumor Population Shifts and Discovery of Rational Drug Combinations in Human GlioblastomaRoman Reinartz, Björn Scheffler, Shanshan Wang et al.|Clinical Cancer Research|2016Cited by 72
KEAP1/NFE2L2 Pathway Signature Outperforms KEAP1/NFE2L2 Mutation Status and Reveals Alternative Pathway-Activating Mutations in NSCLCChristoph Arolt, Axel M. Hillmer|Journal of Thoracic Oncology|2023Cited by 24
Esophageal adenocarcinoma relapse after chemoradiation is dominated by a basal-like subtypeSascha Hoppe, Axel M. Hillmer|bioRxiv (Cold Spring Harbor Laboratory)|2025Cited by 0