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Doris Steinemann

ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 14

Top Venues

Leukemia

Genes, chromosomes & cancer

Molecular genetics & genomic medicine

Gene therapy

Medizinische Hochschule Hannover

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

Affiliation History

Medizinische Hochschule Hannover Mar 15o 2001

Germany

Prof. Dr. rer. nat. :: Human Genetics

Publications

Željko Antić, Alena van Bömmel, Konstantin Riege, Jana Lentes, Charlotte Schröder, Julia Alten, Cornelia Eckert, Lara Fuhrmann, Doris Steinemann, Lennart Lenk, Denis Martin Schewe, Martin Zimmermann, Martin Schrappe, Brigitte Schlegelberger, Gunnar Cario, Steve Hoffmann, Anke Katharina Bergmann
Recurrent DNMT3B rearrangements are associated with unfavorable outcome in dicentric (9;20)-positive pediatric BCP-ALL. Leukemia (2023)
Christopher Hakkaart, John F Pearson, Louise Marquart, Joe G Dennis, George A R Wiggins, Daniel R Barnes, Bridget A Robinson, Peter D Mace, Kristiina Aittomäki, Irene L Andrulis, Banu K Arun, Jacopo Azzollini, Judith Balmaña, Rosa B Barkardottir, Sami Belhadj, Lieke Berger, Marinus J Blok, Susanne E Boonen, Julika Borde, Angela R Bradbury, Joan Brunet, Saundra S Buys, Maria A Caligo, Ian G Campbell, Wendy K Chung, Kathleen B M Claes, null null, null null, Marie-Agnès Collonge-Rame, Jackie Cook, Casey Cosgrove, Fergus J Couch, Mary B Daly, Sita Dandiker, Rosemarie Davidson, Miguel de la Hoya, Robin de Putter, Capucine Delnatte, Mallika Dhawan, Orland Diez, Yuan Chun Ding, Susan M Domchek, Alan Donaldson, Jacqueline Eason, Douglas F Easton, Hans Ehrencrona, Christoph Engel, D Gareth Evans, Ulrike Faust, Lidia Feliubadaló, Florentia Fostira, Eitan Friedman, Megan Frone, Debra Frost, Judy Garber, Simon A Gayther, Andrea Gehrig, Paul Gesta, Andrew K Godwin, David E Goldgar, Mark H Greene, Eric Hahnen, Christopher R Hake, Ute Hamann, Thomas V O Hansen, Jan Hauke, Julia Hentschel, Natalie Herold, Ellen Honisch, Peter J Hulick, Evgeny N Imyanitov, null null, null null, null null, Claudine Isaacs, Louise Izatt, Angel Izquierdo, Anna Jakubowska, Paul A James, Ramunas Janavicius, Esther M John, Joseph Vijai, Beth Y Karlan, Zoe Kemp, Judy Kirk, Irene Konstantopoulou, Marco Koudijs, Ava Kwong, Yael Laitman, Fiona Lalloo, Christine Lasset, Charlotte Lautrup, Conxi Lazaro Garcia, Clémentine Legrand, Goska Leslie, Fabienne Lesueur, Phuong L Mai, Siranoush Manoukian, Véronique Mari, John W M Martens, Lesley McGuffog, Noura Mebirouk, Alfons Meindl, Austin Miller, Marco Montagna, Lidia Moserle, Emmanuelle Mouret-Fourme, Hannah Musgrave, Sophie Nambot, Katherine L Nathanson, Susan L Neuhausen, Heli Nevanlinna, Joanne Ngeow Yuen Yie, Tu Nguyen-Dumont, Liene Nikitina-Zake, Kenneth Offit, Edith Olah, Olufunmilayo I Olopade, Ana Osorio, Claus-Eric Ott, Sue-Kyung Park, Michael T Parsons, Inge Sokilde Pedersen, Ana Peixoto, Pedro Perez-Segura, Paolo Peterlongo, Timea Pocza, Paolo Radice, Juliane Ramser, Johanna Rantala, Gustavo C Rodriguez, Karina Rønlund, Efraim H Rosenberg, Maria Rossing, Rita K Schmutzler, Payal D Shah, Saba Sharif, Priyanka Sharma, Lucy E Side, Jacques Simard, Christian F Singer, Katie Snape, Doris Steinemann, Dominique Stoppa-Lyonnet, Christian Sutter, Yen Yen Tan, Manuel R Teixeira, Soo-Hwang Teo, Mads Thomassen, Darcy L Thull, Marc Tischkowitz, Amanda Ewart Toland, Alison H Trainer, Vishakha Tripathi, Nadine Tung, Klaartje van Engelen, Elizabeth J vanRensburg, Ana Vega, Alessandra Viel, Lisa Walker, Jeffrey N Weitzel, Marijke R Wevers, Georgia Chenevix-Trench, Amanda B Spurdle, Antonis C Antoniou, Logan C Walker
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers. Communications biology 5 (1) (2022)
Reto Eggenschwiler, Thomas Gschwendtberger, Christian Felski, Christopher Jahn, Florian Langer, Jared Sterneckert, Andreas Hermann, Jonathan Lukas Lühmann, Doris Steinemann, Alexandra Haase, Ulrich Martin, Susanne Petri, Tobias Cantz
A selectable all-in-one CRISPR prime editing piggyBac transposon allows for highly efficient gene editing in human cell lines. Scientific reports 11 (1) (2021)
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)
Mustafa Salim, Frederik Heldt, Kathrin Thomay, Jana Lentes, Yvonne Lisa Behrens, Beate Kaune, Anja Möricke, Gunnar Cario, Maximilian Schieck, Winfried Hofmann, Claudia Davenport, Doris Steinemann, Martin Schrappe, Brigitte Schlegelberger, Gudrun Göhring
Cryptic TCF3 fusions in childhood leukemia: Detection by RNA sequencing. Genes, chromosomes & cancer 61 (1) (2021)
Daria Warnstorf, Randa Bawadi, Andrea Schienke, Renate Strasser, Gunnar Schmidt, Thomas Illig, Marcel Tauscher, Felicitas Thol, Michael Heuser, Doris Steinemann, Claudia Davenport, Brigitte Schlegelberger, Yvonne Lisa Behrens, Gudrun Göhring
Unbalanced translocation der(5;17) resulting in a TP53 loss as recurrent aberration in myelodysplastic syndrome and acute myeloid leukemia with complex karyotype. Genes, chromosomes & cancer 60 (6) (2021)
Mareike Jung, Maximilian Schieck, Winfried Hofmann, Marcel Tauscher, Jana Lentes, Anke Bergmann, Marie Stelter, Anja Möricke, Julia Alten, Brigitte Schlegelberger, Martin Schrappe, Martin Zimmermann, Martin Stanulla, Gunnar Cario, Doris Steinemann
Frequency and prognostic impact of PAX5 p.P80R in pediatric acute lymphoblastic leukemia patients treated on an AIEOP-BFM acute lymphoblastic leukemia protocol. Genes, chromosomes & cancer 59 (11) (2020)
Dirk Hoffmann, Johannes Kuehle, Daniela Lenz, Friederike Philipp, Daniela Zychlinski, Nico Lachmann, Thomas Moritz, Doris Steinemann, Michael Morgan, Julia Skokowa, Christoph Klein, Axel Schambach
Lentiviral gene therapy and vitamin B3 treatment enable granulocytic differentiation of G6PC3-deficient induced pluripotent stem cells. Gene therapy 27 (6) (2020)
Ana Rio-Machin, Tom Vulliamy, Nele Hug, Amanda Walne, Kiran Tawana, Shirleny Cardoso, Alicia Ellison, Nikolas Pontikos, Jun Wang, Hemanth Tummala, Ahad Fahad H Al Seraihi, Jenna Alnajar, Findlay Bewicke-Copley, Hannah Armes, Michael Barnett, Adrian Bloor, Csaba Bödör, David Bowen, Pierre Fenaux, Andrew Green, Andrew Hallahan, Henrik Hjorth-Hansen, Upal Hossain, Sally Killick, Sarah Lawson, Mark Layton, Alison M Male, Judith Marsh, Priyanka Mehta, Rogier Mous, Josep F Nomdedéu, Carolyn Owen, Jiří Pavlů, Elspeth M Payne, Rachel E Protheroe, Claude Preudhomme, Nuria Pujol-Moix, Aline Renneville, Nigel Russell, Anand Saggar, Gabriela Sciuccati, David Taussig, Cynthia L Toze, Anne Uyttebroeck, Peter Vandenberghe, Brigitte Schlegelberger, Tim Ripperger, Doris Steinemann, John Wu, Joanne Mason, Paula Page, Susanna Akiki, Kim Reay, Jamie D Cavenagh, Vincent Plagnol, Javier F Caceres, Jude Fitzgibbon, Inderjeet Dokal
The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants. Nature communications 11 (1) (2020)
Stephanie Schubert, Jana L van Luttikhuizen, Bernd Auber, Gunnar Schmidt, Winfried Hofmann, Judith Penkert, Colin F Davenport, Ursula Hille-Betz, Lena Wendeburg, Janin Bublitz, Marcel Tauscher, Karl Hackmann, Evelin Schröck, Caroline Scholz, Hannah Wallaschek, Brigitte Schlegelberger, Thomas Illig, Doris Steinemann
The identification of pathogenic variants in BRCA1/2 negative, high risk, hereditary breast and/or ovarian cancer patients: High frequency of FANCM pathogenic variants. International journal of cancer 144 (11) (2019)
Jonas Samuel Jutzi, Titiksha Basu, Maximilian Pellmann, Sandra Kaiser, Doris Steinemann, Mathijs Arnoud Sanders, Adil S A Hinai, Annelieke Zeilemaker, Sarolta Bojtine Kovacs, Christoph Koellerer, Jenny Ostendorp, Konrad Aumann, Wei Wang, Emmanuel Raffoux, Bruno Cassinat, Lars Bullinger, Brigitte Schlegelberger, Peter J M Valk, Heike Luise Pahl
Altered NFE2 activity predisposes to leukemic transformation and myelosarcoma with AML-specific aberrations. Blood 133 (16) (2019)
Jana Lisa van Luttikhuizen, Janin Bublitz, Stephanie Schubert, Gunnar Schmidt, Winfried Hofmann, Susanne Morlot, Reena Buurman, Bernd Auber, Brigitte Schlegelberger, Doris Steinemann
From a variant of unknown significance to pathogenic: Reclassification of a large novel duplication in BRCA2 by high-throughput sequencing. Molecular genetics & genomic medicine 8 (9) (2019)
Lisa Pahl, Rita Beier, Nils von Neuhoff, Bernd Auber, Michaela Höfs, Eva-Christina Prott, Brigitte Schlegelberger, Dirk Reinhardt, Doris Steinemann
Two cancer-predisposing variants in one family: Incidental finding of a fumarate hydrogenase (FH) germline variant in a family with Li-Fraumeni syndrome. Pediatric blood & cancer 65 (10) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Doris Steinemann