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Christian P. Kratz

hannover medical school

60H-index
364Paper Count
2.1WCitation Count
Published Papers 122
Publication Date
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Tumor patterns and cancer risk in carriers of TP53 exonic germline variants that alter mRNA splicing
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
errShare
errSave
Neoantigenic properties of TP53 variants influence cancer risk in individuals with Li-Fraumeni syndrome
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
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errSave
Psychosocial burdens and unmet supportive care needs of partners and relatives of individuals with Li-Fraumeni syndrome: A mixed-methods study
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
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errSave
Unique Hematological Presentation of Patients with Biallelic Inactivation of FANCD1/BRCA2
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
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errSave
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.
errShare
errSave
BRCA1-, BRCA2-, and PALB2-related Fanconi anemia: Scope to expand disease phenotypic features and predict breast cancer risk in heterozygotes
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
errShare
errSave
A quantitative, Bayesian-informed approach to gene-specific variant classification: Updated Expert Panel recommendations improve classification of TP53 germline variants for Li-Fraumeni syndrome
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
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errSave
Optimizing whole-body MRI for early cancer detection in Li-Fraumeni syndrome: a prospective bicentric study
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
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errSave
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
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
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errSave
A cancer predisposition screening tool for young adults with cancer
errJNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE
IF7.2
err2025-08-01
err0
PREAI
errRipperger, Tim; Kratz, Christian P.
errShare
errSave
Model of care for individuals with rare cancer predisposition syndromes in Germany
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
errShare
errSave
Genetic predisposition in sarcomas: clinical implications and management
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
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errSave
RE: Childhood, adolescent, and young adulthood cancer risk in BRCA1 or BRCA2 pathogenic variant carriers
errJNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE
IF7.2
err2025-02-05
err1
PREAI
errKratz, Christian P.; Plon, Sharon E.; Lupo, Philip J.
errShare
errSave
MSH2, MSH6, MLH1, and PMS2 immunohistochemistry as highly sensitive screening method for DNA mismatch repair deficiency syndromes in pediatric high-grade glioma
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
errShare
errSave
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.
errShare
errSave
Re-envisioning genetic predisposition to childhood and adolescent cancers
errNATURE REVIEWS CANCER
IF66.8
err2024-12-03
err0
PREAI
errKratz, Christian P.
errShare
errSave
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
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errSave
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
errShare
errSave
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.
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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
errShare
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Research Directions

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Co-authors
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