Tim Ripperger

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 20

Top Venues

Journal of the National Cancer Institute

European journal of public health

Blood

Pediatric blood & cancer

This page only lists publications with an associated author ORCID identifier.

Publications

J Matt McCrary, Els Van Valckenborgh, Hélène A Poirel, Robin de Putter, Jeroen G J van Rooij, Denis Horgan, Marie-Luise Dierks, Olga Antonova, Joan Brunet, Adela Chirita-Emandi, Chrystelle Colas, Miriam Dalmas, Hans Ehrencrona, Claire Grima, Ramūnas Janavičius, Barbara Klink, Katalin Koczok, Mateja Krajc, Baiba Lace, Liis Leitsalu, Martin Mistrik, Milena Paneque, Dragan Primorac, Katharina M Roetzer, Joelle Ronez, Lucie Slámová, Elena Spanou, Kostas Stamatopoulos, Tomasz Stoklosa, Sonja Strang-Karlsson, Katalin Szakszon, Krzysztof Szczałuba, Jacqueline Turner, Marieke F van Dooren, Wendy A G van Zelst-Stams, Loredana-Maria Vassallo, Karin A W Wadt, Tamara Žigman, Tim Ripperger, Maurizio Genuardi, Marc Van den Bulcke, Anke Katharina Bergmann
Genetic counselling legislation and practice in cancer in EU Member States. European journal of public health 34 (4) (2024)
J Matt McCrary, Els Van Valckenborgh, Hélène A Poirel, Robin de Putter, Jeroen G J van Rooij, Denis Horgan, Marie-Luise Dierks, Olga Antonova, Joan Brunet, Adela Chirita-Emandi, Chrystelle Colas, Miriam Dalmas, Hans Ehrencrona, Claire Grima, Ramūnas Janavičius, Barbara Klink, Katalin Koczok, Mateja Krajc, Baiba Lace, Liis Leitsalu, Martin Mistrik, Milena Paneque, Dragan Primorac, Katharina M Roetzer, Joelle Ronez, Lucie Slámová, Elena Spanou, Kostas Stamatopoulos, Tomasz Stoklosa, Sonja Strang-Karlsson, Katalin Szakszon, Krzysztof Szczałuba, Jacqueline Turner, Marieke F van Dooren, Wendy A G van Zelst-Stams, Loredana-Maria Vassallo, Karin A W Wadt, Tamara Žigman, Tim Ripperger, Maurizio Genuardi, Marc Van den Bulcke, Anke Katharina Bergmann
Genetic counselling legislation and practice in cancer in EU Member States. European journal of public health 34 (4) (2024)
J Matt McCrary, Els Van Valckenborgh, Hélène A Poirel, Robin de Putter, Jeroen G J van Rooij, Denis Horgan, Marie-Luise Dierks, Olga Antonova, Joan Brunet, Adela Chirita-Emandi, Chrystelle Colas, Miriam Dalmas, Hans Ehrencrona, Claire Grima, Ramūnas Janavičius, Barbara Klink, Katalin Koczok, Mateja Krajc, Baiba Lace, Liis Leitsalu, Martin Mistrik, Milena Paneque, Dragan Primorac, Katharina M Roetzer, Joelle Ronez, Lucie Slámová, Elena Spanou, Kostas Stamatopoulos, Tomasz Stoklosa, Sonja Strang-Karlsson, Katalin Szakszon, Krzysztof Szczałuba, Jacqueline Turner, Marieke F van Dooren, Wendy A G van Zelst-Stams, Loredana-Maria Vassallo, Karin A W Wadt, Tamara Žigman, Tim Ripperger, Maurizio Genuardi, Marc Van den Bulcke, Anke Katharina Bergmann
Genetic counselling legislation and practice in cancer in EU Member States. European journal of public health (2024)
Christian Peter Kratz, Dmitrii Smirnov, Robert Autry, Natalie Jäger, Sebastian M Waszak, Anika Großhennig, Riccardo Berutti, Mareike Wendorff, Pierre Hainaut, Stefan M Pfister, Holger Prokisch, Tim Ripperger, David Malkin
Reply to Evans and Woodward. Journal of the National Cancer Institute 115 (2) (2023)
Jelena Lazic, Oskar A Haas, Ugur Özbek, Tim Ripperger, Anna Byrjalsen, Geertruij Te Kronnie, null null
Perception and management of cancer predisposition in pediatric cancer centers: A European-wide questionnaire-based survey. Pediatric blood & cancer 70 (5) (2023)
Christian Peter Kratz, Dmitrii Smirnov, Robert Autry, Natalie Jäger, Sebastian M Waszak, Anika Großhennig, Riccardo Berutti, Mareike Wendorff, Pierre Hainaut, Stefan M Pfister, Holger Prokisch, Tim Ripperger, David Malkin
Reply to Evans and Woodward. Journal of the National Cancer Institute 115 (2) (2023)
Claire C Homan, Michael W Drazer, Kai Yu, David Michael Lawrence, Jinghua Feng, Luis Alberto Arriola-Martinez, Matthew J Pozsgai, Kelsey E McNeely, Thuong Thi Ha, Parvathy Venugopal, Peer Arts, Sarah King-Smith, Jesse Jc Cheah, Mark Armstrong, Paul Wang, Csaba Bödör, Alan B Cantor, Mario Cazzola, Erin S Degelman, Courtney D D DiNardo, Nicolas Duployez, Rémi Favier, Stefan Fröhling, Ana Rio-Machin, Jeffery M Klco, Alwin Krämer, Mineo Kurokawa, Joanne Lee, Luca Malcovati, Neil V Morgan, Natsoulis Georges, Carolyn Owen, Keyur Pravinchandra Patel, Claude Preudhomme, Hana Raslova, Hugh Young Rienhoff, Tim Ripperger, Rachael R Schulte, Kiran Tawana, Elvira Velloso, Yan Benedict, Erika Mijin Kwon Kim, Raman Sood, Amy P Hsu, Steven M Holland, Kerry Phillips, Nicola Poplawski, Milena Babic, Andrew H Wei, Cecily Jane Forsyth, Helen Mar Fan, Ian Lewis, Julian P Cooney, Rachel Susman, Lucy C Fox, Piers Blombery, Deepak Singhal, Devendra K Hiwase, Belinda Phipson, Andreas W Schreiber, Christopher N Hahn, Hamish S Scott, Paul P Liu, Lucy A Godley, Anna L Brown
Somatic mutational landscape of hereditary hematopoietic malignancies caused by germ line RUNX1, GATA2, and DDX41 variants. Blood advances (2023)
Tim Ripperger
Seeding the future: the natural history of RUNX1 deficiency. Blood 142 (25) (2023)
Tim Ripperger
Seeding the future: the natural history of RUNX1 deficiency. Blood 142 (25) (2023)
Tim Ripperger
Seeding the future: the natural history of RUNX1 deficiency. Blood 142 (25) (2023)
Jelena Lazic, Oskar A Haas, Ugur Özbek, Tim Ripperger, Anna Byrjalsen, Geertruij Te Kronnie, null null
Perception and management of cancer predisposition in pediatric cancer centers: A European-wide questionnaire-based survey. Pediatric blood & cancer 70 (5) (2023)
Christian Peter Kratz, Dmitrii Smirnov, Robert Autry, Natalie Jäger, Sebastian M Waszak, Anika Großhennig, Riccardo Berutti, Mareike Wendorff, Pierre Hainaut, Stefan M Pfister, Holger Prokisch, Tim Ripperger, David Malkin
Reply to Evans and Woodward. Journal of the National Cancer Institute 115 (2) (2023)
Jelena Lazic, Oskar A Haas, Ugur Özbek, Tim Ripperger, Anna Byrjalsen, Geertruij Te Kronnie, null null
Perception and management of cancer predisposition in pediatric cancer centers: A European-wide questionnaire-based survey. Pediatric blood & cancer (2023)
Alisa Förster, Melanie Decker, Brigitte Schlegelberger, Tim Ripperger
Beyond Pathogenic RUNX1 Germline Variants: The Spectrum of Somatic Alterations in RUNX1-Familial Platelet Disorder with Predisposition to Hematologic Malignancies. Cancers 14 (14) (2022)
Melanie Decker, Anupriya Agarwal, Andreas Benneche, Jane Churpek, Nicolas Duployez, Adam Duvall, Martijn P T Ernst, Alisa Förster, Hildegunn Høberg Vetti, Inga Hofmann, Michelle Nash, Marc H G P Raaijmakers, Tor H A Tvedt, Adrianna Vlachos, Brigitte Schlegelberger, Thomas Illig, Tim Ripperger
Validation and clinical application of transactivation assays for RUNX1 variant classification. Blood advances 6 (11) (2022)
Christian Peter Kratz, Dmitrii Smirnov, Robert Autry, Natalie Jäger, Sebastian M Waszak, Anika Großhennig, Riccardo Berutti, Mareike Wendorff, Pierre Hainaut, Stefan M Pfister, Holger Prokisch, Tim Ripperger, David Malkin
Heterozygous BRCA1 and BRCA2 and Mismatch Repair Gene Pathogenic Variants in Children and Adolescents With Cancer. Journal of the National Cancer Institute 114 (11) (2022)
Melanie Decker, Tim Lammens, Alina Ferster, Miriam Erlacher, Ayami Yoshimi, Charlotte M Niemeyer, Martijn P T Ernst, Marc H G P Raaijmakers, Nicolas Duployez, Andreas Flaum, Doris Steinemann, Brigitte Schlegelberger, Thomas Illig, Tim Ripperger
Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies. Leukemia 35 (11) (2021)
Greta Winter, Renate Kirschner-Schwabe, Stefanie Groeneveld-Krentz, Gabriele Escherich, Anja Möricke, Arend von Stackelberg, Martin Stanulla, Simon Bailey, Lisa Richter, Doris Steinemann, Tim Ripperger, Adela Escudero, Roula Farah, Olli Lohi, Karin Wadt, Marjolijn Jongmans, Nienke van Engelen, Cornelia Eckert, Christian Peter Kratz
Clinical and genetic characteristics of children with acute lymphoblastic leukemia and Li-Fraumeni syndrome. Leukemia 35 (5) (2021)
Mariola Monika Golas, Bernd Auber, Tim Ripperger, Brigitte Pabst, Gunnar Schmidt, Michel Morlot, Uta Diebold, Doris Steinemann, Brigitte Schlegelberger, Susanne Morlot
Looking for the hidden mutation: Bannayan-Riley-Ruvalcaba syndrome caused by constitutional and mosaic 10q23 microdeletions involving PTEN and BMPR1A. American journal of medical genetics. Part A 179 (7) (2019)
Astrid Behnert, Bernd Auber, Doris Steinemann, Michael C Frühwald, Carolin Huisinga, Kais Hussein, Christian Peter Kratz, Tim Ripperger
KBG syndrome patient due to 16q24.3 microdeletion presenting with a paratesticular rhabdoid tumor: Coincidence or cancer predisposition? American journal of medical genetics. Part A 176 (6) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Tim Ripperger