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Nature Genetics|October 28, 2008
TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathyAlena Cízková, Viktor Stránecký, Johannes A Mayr, et al.Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|May 23, 2024
Development and benchmarking of a Deep Learning-based MRI-guided gross tumor segmentation algorithm for Radiomics analyses in extremity soft tissue sarcomasJan C Peeken, Lucas Etzel, Tim Tomov, et al.Nature Communications|June 1, 2019
Publisher Correction: Clonal replacement and heterogeneity in breast tumors treated with neoadjuvant HER2-targeted therapyJennifer L Caswell-Jin, Katherine McNamara, Johannes G Reiter, et al.Nature Communications|February 10, 2019
Clonal replacement and heterogeneity in breast tumors treated with neoadjuvant HER2-targeted therapyJennifer L Caswell-Jin, Katherine McNamara, Johannes G Reiter, et al.Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|September 10, 2021
MRI-based delta-radiomics predicts pathologic complete response in high-grade soft-tissue sarcoma patients treated with neoadjuvant therapyJan C Peeken, Rebecca Asadpour, Katja Specht, et al.American Journal of Clinical Oncology|July 23, 2013
ACR Appropriateness Criteria® management of locoregionally advanced squamous cell carcinoma of the vulva, Elizabeth Kidd, David Moore, et al.American Journal of Human Genetics|July 16, 2013
ELAC2 mutations cause a mitochondrial RNA processing defect associated with hypertrophic cardiomyopathyTobias B Haack, Robert Kopajtich, Peter Freisinger, et al.International Journal of Radiation Oncology, Biology, Physics|December 18, 2023
Overview and Recommendations for Prospective Multi-institutional Spatially Fractionated Radiation Therapy Clinical TrialsHeng Li, Nina A Mayr, Robert J Griffin, et al.Cell|February 26, 2021
Increased stem cell proliferation in atherosclerosis accelerates clonal hematopoiesisAlexander Heyde, David Rohde, Cameron S McAlpine, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 7, 2020
Heterozygous truncating variants in SUFU cause congenital ocular motor apraxiaSimone Schröder, Yun Li, Gökhan Yigit, et al.Pageof 69