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C

Christian P. Kratz

hannover medical school

60H指数
364论文数
2.1W被引数
收录论文 122
发表时间
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Tumor patterns and cancer risk in carriers of TP53 exonic germline variants that alter mRNA splicingTP53外显子胚系变异携带者的肿瘤模式和癌症风险
errEuropean Journal of Human Genetics
IF4.6
err2026-03-03
err0
errOAAI
errDeborah Schönegger; Emilie Montellier; Sandrine Blanchet; Claire Freycon; Paola Monti; Catherine Goudie; Gaëlle Bougeard; Christian P. Kratz; Pierre Hainaut; Anna Reymer
err分享
err收藏
Neoantigenic properties of TP53 variants influence cancer risk in individuals with Li-Fraumeni syndromeTP53变体的neoantigenic properties影响具有Li-Fraumeni综合征个体的癌症风险
erreBioMedicine
IF10.8
err2025-12-09
err0
errOAAI
errEmilie Montellier; Olivier Manches; Jonathan Gaucher; Claire Freycon; David Hoyos; Sandrine Blanchet; Murielle Verboom; Christina M. Dutzmann; Sophie Coutant; Jacqueline Bou; Bertrand Fin; Robert Olaso; Jean-François Deleuze; Thierry Frébourg; Benjamin D. Greenbaum; Arnold J. Levine; Christian P. Kratz; Gaëlle Bougeard; Pierre Hainaut
err分享
err收藏
Psychosocial burdens and unmet supportive care needs of partners and relatives of individuals with Li-Fraumeni syndrome: A mixed-methods study心理社会负担及支持性照护需求未获满足的Li-Fraumeni综合征患者伴侣与亲属：一项混合方法研究
errJournal of Genetic Counseling
IF0
err2025-12-01
err0
errOAAI
errKiermeier, Senta; Schott, Sarah; Nees, Juliane; Dutzmann, Christina M.; Silchmuller, Farina; Kratz, Christian P.; Keymling, Myriam; Maatouk, Imad
err分享
err收藏
Unique Hematological Presentation of Patients with Biallelic Inactivation of FANCD1/BRCA2Biallelic FANCD1/BRCA2失活患者的独特血液学表现
errBlood Advances
IF7.1
err2025-11-01
err0
errOAAI
errMarena R Niewisch; Michelle Dierolf; Anna B Herba; Felicitas Thol; Christian Reimann; Isabell Popp; Susanne Holzhauer; Yvonne L Behrens; Marius Rohde; Jörg Leyh; Ingrid Kühnle; Dagmar Dilloo; Martina Stiefel; Stephan Schwarz-Furlan; Irith Baumann; Reinhard Kalb; Christian P Kratz
err分享
err收藏
FANCE MISSENSE VARIANT WITH MILD PHENOTYPE BUT RETAINS HIGH MMC SENSITIVITY
errEJC Paediatric Oncology
IF0
err2025-11-01
err0
errOAAI
errDroste, A.; Beyrle, K.; Popp, I.; Kratz, C. P.; Feurstein, S.; Sobeck, A.; Kalb, R.
err分享
err收藏
BRCA1-, BRCA2-, and PALB2-related Fanconi anemia: Scope to expand disease phenotypic features and predict breast cancer risk in heterozygotesBRCA1-、BRCA2-和PALB2相关的范可尼贫血：扩展疾病表型特征并预测杂合子乳腺癌风险的潜力
errThe American Journal of Human Genetics
IF0
err2025-10-30
err0
PREAI
errSharon E. Johnatty; Emma Tudini; Michael T. Parsons; Kyriaki Michailidou; Maria Zanti; Daffodil M. Canson; Aimee L. Davidson; Tamar Berger; Rasim Ozgur Rosti; Christian P. Kratz; Reinhard Kalb; Lisa J. McReynolds; Neelam Giri; Marcy E. Richardson; Tina Pesaran; Jordi Surrallés; Roser Pujol; Babu Rao Vundinti; Merin George; Kara N. Maxwell; Kate Nathanson; Susan Domchek; Moisés Ó. Fiesco-Roa; Sara Frias; Benilde García-de-Teresa; Marjolijn Jongmans; Seema Lalani; Merel Maiburg; Katrina Prescott; Rachel Robinson; Sulekha Rajagopalan; Lot Snijders Blok; Suzanna E.L. Temple; Kathy Tucker; Arleen D. Auerbach; Maria I. Cancio; Jennifer A. Kennedy; Margaret L. MacMillan; Rebecca Tryon; John E. Wagner; Michael Walsh; Nicholas J. Boddicker; Chunling Hu; Jeffrey N. Weitzel; Alexander J.M. Dingemans; Johanna Hadler; Nitsan Rotenberg; Lobna Ramadane-Morchadi; Miguel de la Hoya; Paul James; Thomas Van Overeem Hansen; Maaike P.G. Vreeswijk; Logan C. Walker; Shyam K. Sharan; Douglas F. Easton; Fergus Couch; Agata Smogorzewska; Adam Nelson; Joanne Ngeow; Marc Tischkowitz; Encarnacion Gomez-Garcia; Amanda B. Spurdle
err分享
err收藏
A quantitative, Bayesian-informed approach to gene-specific variant classification: Updated Expert Panel recommendations improve classification of TP53 germline variants for Li-Fraumeni syndrome一种基于贝叶斯定量分析的基因特异性变异分类方法：更新的专家小组建议改进了TP53生殖细胞变异在Li-Fraumeni综合征中的分类
errGenome Medicine
IF11.2
err2025-10-24
err0
errOAAI
errCristina Fortuno; Megan N. Frone; Jessica Mester; Miguel de la Hoya; Phuong L. Mai; Tina Pesaran; Maria Isabel Achatz; Rebecca Bassett; Carolina Bustamante; Stephanie Crowley; Kelvin Cesar de Andrade; D. Gareth Evans; Bingjian Feng; Laura Fuqua; Maria Isabel Harrell; Jessica N. Hatton; Robert Huether; Chimene Kesserwan; Kristy Lee; Suzanne P. MacFarland; Jamie L. Maciaszek; Kara Maxwell; Kelly McGoldrick; Maureen Murphy; Bita Nehoray; Judith Penkert; Emilia Modolo Pinto; Sharon E. Plon; Alison Schwartz-Levine; Ashley S. Thompson; Wenyi Wang; Gerard P. Zambetti; Kristin Zelley; Paul A. James; Sharon A. Savage; Christian P. Kratz; Amanda B. Spurdle
err分享
err收藏
Optimizing whole-body MRI for early cancer detection in Li-Fraumeni syndrome: a prospective bicentric study优化全身MRI以用于Li-Fraumeni综合征的早期癌症检测：一项前瞻性双中心研究
errEuropean Radiology
IF4.7
err2025-10-21
err0
errOAAI
errMyriam Margareta Keymling; Felix Tobias Kurz; Tristan Anselm Kuder; Sebastian Bickelhaupt; Thomas Hielscher; Robert Hog; Theresa Mokry; Tawfik Moher Alsady; Sarah Schott; Christian Kratz; Diane Miriam Renz; Heinz-Peter Schlemmer
err分享
err收藏
Opening of a phase Ib/II study to investigate the safety and efficacy of Afatinib in patients with Fanconi anemia and unresectable locally advanced or metastatic head and neck squamous cell carcinoma开展一项Ib/II期研究，以评估Afatinib在Fanconi贫血合并不可切除的局部晚期或转移性头颈部鳞状细胞癌患者中的安全性与有效性。
errBMC Cancer
IF3.4
err2025-08-29
err0
errOAAI
errGeorgia Anguera; Oscar Gallego; Mireia Llobet; Núria Berga; Maria-Estela Moreno-Martinez; Xavier Leon; Christian Kratz; Ramon Garcia-Escudero; Jordi Minguillón; Jordi Surrallés
err分享
err收藏
A cancer predisposition screening tool for young adults with cancer癌症易感倾向筛查工具，适用于患有癌症的年轻成人
errJNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE
IF7.2
err2025-08-01
err0
PREAI
errRipperger, Tim; Kratz, Christian P.
err分享
err收藏
Model of care for individuals with rare cancer predisposition syndromes in Germany德国针对具有罕见癌症易患倾向综合征个体的护理模式
errlancet regional health europe
IF0
err2025-06-26
err0
PREAI
errValentina Härter; Birte Sänger; Josephine C. Gieseke; Tanja Gerasimov; Beatrice Hoffmann; Carolin Huisinga; Anja Karow; Lucas J. Müntnich; Natalie E. Palmaers; Stefanie Paquet; Judith Penkert; Diane M. Renz; Tim Ripperger; Farina J. Silchmüller; Christina M. Dutzmann; Christian P. Kratz
err分享
err收藏
Genetic predisposition in sarcomas: clinical implications and management软组织肉瘤中的遗传易感性：临床意义与管理
errECLINICALMEDICINE
IF10
err2025-05-01
err0
PREAI
errConnolly, Elizabeth A.; Boye, Kjetil; Bonvalot, Sylvie; Kratz, Christian P.; Leithner, Andreas; Malkin, David; Messiou, Christina; Miah, Aisha B.; Pantziarka, Pan; Timmermann, Beate; van der Graaf, Winette T. A.; Thomas, David M.; Stacchiotti, Silvia
err分享
err收藏
RE: Childhood, adolescent, and young adulthood cancer risk in BRCA1 or BRCA2 pathogenic variant carriers主题：BRCA1或BRCA2致病性变异携带者儿童期、青春期及青年期癌症风险
errJNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE
IF7.2
err2025-02-05
err1
PREAI
errKratz, Christian P.; Plon, Sharon E.; Lupo, Philip J.
err分享
err收藏
MSH2, MSH6, MLH1, and PMS2 immunohistochemistry as highly sensitive screening method for DNA mismatch repair deficiency syndromes in pediatric high-grade gliomaMSH2、MSH6、MLH1和PMS2免疫组化作为儿科高级别胶质瘤中DNA错配修复缺陷综合征的高敏感性筛查方法
errACTA NEUROPATHOLOGICA
IF9.3
err2025-02-02
err0
errOAAI
errFriker, LL; Perwein, T; Waha, A; Dörner, E; Klein, R; Blattner-Johnson, M; Layer, JP; Sturm, D; Nussbaumer, G; Kwiecien, R; Spier, I; Aretz, S; Kerl, K; Hennewig, U; Rohde, M; Karow, A; Bluemcke, I; Schmitz, AK; Reinhard, H; Driever, PH; Wendt, S; Weiser, A; Stücklin, ASG; Gerber, NU; von Bueren, AO; Khurana, C; Jorch, N; Wiese, M; Kratz, CP; Eyrich, M; Karremann, M; Herrlinger, U; Hölzel, M; Jones, DTW; Hoffmann, M; Pietsch, T; Gielen, GH; Kramm, CM
err分享
err收藏
Cancer risk in carriers of TP53 germline variants grouped into different functional categories
errJNCI CANCER SPECTRUM
IF4.1
err2025-01-28
err0
errOAAI
errMuentnich, Lucas John; Dutzmann, Christina M.; Grosshennig, Anika; Haerter, Valentina; Keymling, Myriam; Mastronuzzi, Angela; Montellier, Emilie; Nees, Juliane; Palmaers, Natalie E.; Penkert, Judith; Pfister, Stefan M.; Ripperger, Tim; Schott, Sarah; Silchmueller, Farina; Hainaut, Pierre; Kratz, Christian P.
err分享
err收藏
Re-envisioning genetic predisposition to childhood and adolescent cancers重新设想儿童和青少年癌症的遗传易感性
errNATURE REVIEWS CANCER
IF66.8
err2024-12-03
err0
PREAI
errKratz, Christian P.
err分享
err收藏
ERN GENTURIS guidelines on constitutional mismatch repair deficiency diagnosis, genetic counselling, surveillance, quality of life, and clinical management
errEUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
err2024-10-17
err3
errOAAI
errColas, Chrystelle; Guerrini-Rousseau, Lea; Suerink, Manon; Gallon, Richard; Kratz, Christian P.; Ayuso, Eloise; Brugieres, Laurence; Wimmer, Katharina
err分享
err收藏
TP53 variant clusters stratify the Li-Fraumeni spectrum and reveal an osteosarcoma-prone subgroup
errCANCER RESEARCH
IF16.6
err2024-09-05
err0
PREAI
errFischer, Nicholas W.; Laverty, Brianne; Alon, Noa; Montellier, Emilie; Hainaut, Pierre; Maxwell, Kara N.; Kratz, Christian P.; Malkin, David
err分享
err收藏
Liver disease and transplantation in telomere biology disorders: An international multicenter cohort
errHEPATOLOGY COMMUNICATIONS
IF4.6
err2024-07-01
err0
errOAAI
errWang, YunZu Michele; Kaj-Carbaidwala, Batul; Lane, Adam; Agarwal, Suneet; Beier, Fabian; Bertuch, Alison; Borovsky, Kristin A.; Brennan, Steven K.; Calado, Rodrigo T.; Catto, Luiz Fernando B.; Dufour, Carlo; Ebens, Christen L.; Fioredda, Francesca; Giri, Neelam; Gloude, Nicholas; Goldman, Frederick; Hertel, Paula M.; Himes, Ryan; Keel, Sioban B.; Koura, Divya T.; Kratz, Christian P.; Kulkarni, Sakil; Liou, Iris; Nakano, Taizo A.; Nastasio, Silvia; Niewisch, Marena R.; Penrice, Daniel D.; Sasa, Ghadir S.; Savage, Sharon A.; Simonetto, Douglas A.; Ziegler, David S.; Miethke, Alexander G.; Myers, Kasiani C.
err分享
err收藏
AGE ABOVE 12 MONTHS, ABSENCE OF SYNCHRONOUS, MULTIFOCAL DISEASE AND PATHOGENIC GERMLINE VARIANTS AT C-TERMINI ARE POSITIVE PROGNOSTIC FACTORS IN CHILDREN WITH RTPS1 (RHABDOID-TUMOR-PREDISPOSITION-SYNDROME)
errNEURO-ONCOLOGY
IF13.4
err2024-06-18
err0
errOAAI
errFruehwald, Michael C.; Boros, Matej; Dahlum, Sonja; Bens, Susanne; Johann, Pascal D.; Kachanov, Denis; Hauser, Peter; Kratz, Christian P.; Hernaiz-Driever, Pablo; Eyrich, Matthias; Sumerauer, David; Milde, Till; Reinhard, Harald; van de Wetering, Marianne; Gil-da-Costa, Maria Joao; Elisabetta, Schiavello; Kerl, Kornelius; Furtwaengler, Rhoikos; Kordes, Uwe; Gerss, Joachim; Hasselblatt, Martin; Nysom, Karsten; Nemes, Karolina
err分享
err收藏

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