Offene Gemeinwohldefinitionen = The public definition of common good = La définition publique du bien communENGEL, Christoph.Rechtstheorie (Berlin). 2001, Vol 32, Num 1, pp 23-52, issn 0034-1398Article

A computational model of human granulopoiesis to simulate the hematotoxic effects of multicycle polychemotherapyENGEL, Christoph; SCHOLZ, Markus; LOEFFLER, Markus et al.Blood. 2004, Vol 104, Num 8, pp 2323-2331, issn 0006-4971, 9 p.Article

Double heterozygosity for mutations in BRCA1 and BRCA2 in German breast cancer patients: implications on test strategies and clinical managementHEIDEMANN, Simone; FISCHER, Christine; JONAT, Waiter et al.Breast cancer research and treatment. 2012, Vol 134, Num 3, pp 1229-1239, issn 0167-6806, 11 p.Article

Association of the Variants CASP8 D302H and CASP10 V410I with Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation CarriersENGEL, Christoph; VERSMOLD, Beatrix; GARETH EVANS, D et al.Cancer epidemiology, biomarkers & prevention. 2010, Vol 19, Num 11, pp 2859-2868, issn 1055-9965, 10 p.Article

Common Breast Cancer-Predisposition Alleles Are Associated with Breast Cancer Risk in BRCA1 and BRCA2 Mutation CarriersANTONIOU, Antonis C; SPURDLE, Amanda B; HOFMANN, Wera et al.American journal of human genetics. 2008, Vol 82, Num 4, pp 937-948, issn 0002-9297, 12 p.Article

No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients. CommentarySCOTT, Rodney J; STEINKE, Verena; KLOOR, Matthias et al.European journal of human genetics. 2008, Vol 16, Num 5, issn 1018-4813, 531-532, 587-592 [8 p.]Article

BRCA1 R 1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer riskSPURDLE, Amanda B; WHILEY, Phillip J; KATTENTIDT-MOURAVIEVA, Anna A et al.Journal of medical genetics. 2012, Vol 49, Num 8, pp 525-532, issn 0022-2593, 8 p.Article

Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriersXIANSHU WANG; PANKRATZ, V. Shane; COOK, Margaret et al.Human molecular genetics (Print). 2010, Vol 19, Num 14, pp 2886-2897, issn 0964-6906, 12 p.Article

Acute renal failure in patients with severe sepsis and septic shock-a significant independent risk factor for mortality : results from the German Prevalence StudyOPPERT, Michael; ENGEL, Christoph; BRUNKHORST, Frank-Martin et al.Nephrology, dialysis, transplantation (Print). 2008, Vol 23, Num 3, pp 904-909, issn 0931-0509, 6 p.Article

Model-based design of chemotherapeutic regimens that account for heterogeneity in leucopoeniaSCHOLZ, Markus; ENGEL, Christoph; LOEFFLER, Markus et al.British journal of haematology. 2006, Vol 132, Num 6, pp 723-735, issn 0007-1048, 13 p.Article

Novel strategy for optimal sequential application of clinical criteria, immunohistochemistry and microsatellite analysis in the diagnosis of hereditary nonpolyposis colorectal cancerENGEL, Christoph; FORBERG, Jochen; DIETMAIER, Wolfgang et al.International journal of cancer. 2006, Vol 118, Num 1, pp 115-122, issn 0020-7136, 8 p.Article

A Breast Cancer Risk Haplotype in the Caspase-8 GeneSHEPHARD, Neil Duncan; ABO, Ryan; MEINDL, Alfons et al.Cancer research (Chicago, Ill.). 2009, Vol 69, Num 7, pp 2724-2728, issn 0008-5472, 5 p.Article

Polymorphisms in BRCA2 resulting in aberrant codon-usage and their analysis on familial breast cancer riskYANG, Rongxi; BOWANG CHEN; MEINDL, Alfons et al.Breast cancer research and treatment. 2009, Vol 118, Num 2, pp 407-413, issn 0167-6806, 7 p.Article

Practice and perception : A nationwide survey of therapy habits in sepsisBRUNKHORST, Frank M; ENGEL, Christoph; OPPERT, Michael et al.Critical care medicine. 2008, Vol 36, Num 10, pp 2719-2725, issn 0090-3493, 7 p.Article

Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: The German Hereditary Nonpolyposis Colorectal Cancer ConsortiumPLASCHKE, Jens; ENGEL, Christoph; RÜSCHOFF, Jose et al.Journal of clinical oncology. 2004, Vol 22, Num 22, pp 4486-4494, issn 0732-183X, 9 p.Article

Association of death receptor 4 variant (683A>C) with ovarian cancer risk in BRCA1 mutation carriersDICK, Michelle G; VERSMOLD, Beatrix; KAST, Karin et al.International journal of cancer (Print). 2012, Vol 130, Num 6, pp 1314-1318, issn 0020-7136, 5 p.Article

Effect of Empirical Treatment With Moxifloxacin and Meropenem vs Meropenem on Sepsis-Related Organ Dysfunction in Patients With Severe Sepsis: A Randomized TrialBRUNKHORST, Frank M; OPPERT, Michael; GRÜNDLING, Matthias et al.JAMA, the journal of the American Medical Association. 2012, Vol 307, Num 22, pp 2390-2399, issn 0098-7484, 10 p.Article

Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)MAVADDAT, Nasim; BARROWDALE, Daniel; MULLIGAN, Anna Marie et al.Cancer epidemiology, biomarkers & prevention. 2012, Vol 21, Num 1, pp 134-147, issn 1055-9965, 14 p.Article

FHL2 expression in peritumoural fibroblasts correlates with lymphatic metastasis in sporadic but not in HNPCC-associated colon cancerGULLOTTI, Lucia; CZERWITZKI, Jacqueline; FRIEDRICHS, Nicolaus et al.Laboratory investigation. 2011, Vol 91, Num 12, pp 1695-1705, issn 0023-6837, 11 p.Article

Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility geneMEINDL, Alfons; HELLEBRAND, Heide; RAMSER, Juliane et al.Nature genetics. 2010, Vol 42, Num 5, pp 410-414, issn 1061-4036, 5 p.Article

Epidemiology of sepsis in Germany : results from a national prospective multicenter studyENGEL, Christoph; BRUNKHORST, Frank M; MAYER, Konstantin et al.Intensive care medicine (Print). 2007, Vol 33, Num 4, pp 606-618, issn 0342-4642, 13 p.Article

RAD51 135G→C Modifies Breast Cancer Risk among BRCA2 Mutation Carriers : Results from a Combined Analysis of 19 StudiesANTONIOU, Antonis C; SINILNIKOVA, Olga M; COUPIER, Isabelle et al.American journal of human genetics. 2007, Vol 81, Num 6, pp 1186-1200, issn 0002-9297, 15 p.Article

Evaluating the performance of clinical criteria for predicting mismatch repair gene mutations in Lynch syndrome: A comprehensive analysis of 3,671 familiesSTEINKE, Verena; HOLZAPFEL, Stefanie; BÜTTNER, Reinhard et al.International journal of cancer (Print). 2014, Vol 135, Num 1, pp 69-77, issn 0020-7136, 9 p.Article

A Classification Model for BRCA2 DNA Binding Domain Missense Variants Based on Homology-Directed Repair ActivityGUIDUGLI, Lucia; PANKRATZ, Vernon S; SINGER, Christian et al.Cancer research (Chicago, Ill.). 2013, Vol 73, Num 1, pp 265-275, issn 0008-5472, 11 p.Article

Automatic Control of Pressure Support for Ventilator Weaning in Surgical Intensive Care PatientsSCHÄDLER, Dirk; ENGEL, Christoph; ELKE, Gunnar et al.American journal of respiratory and critical care medicine. 2012, Vol 185, Num 6, pp 637-644, issn 1073-449X, 8 p.Article