The germline variants in DNA repair genes in pediatric medulloblastoma: a challenge for current therapeutic strategies
Trubicka, Joanna, Żemojtel, Tomasz, Hecht, Jochen, Falana, Katarzyna, Piekutowska-Abramczuk, Dorota, Płoski, Rafał, Perek-Polnik, Marta, Drogosiewicz, Monika, Grajkowska, Wiesława, Ciara, Elżbieta, Moszczyńska, Elżbieta, Dembowska-Bagińska, Bożenna, Perek, Danuta, Chrzanowska, Krystyna H, Krajewska-Walasek, Małgorzata, Łastowska, Maria
Published in BMC cancer (04.04.2017)
Published in BMC cancer (04.04.2017)
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Impaired humoral and cellular immunity after SARS-CoV-2 BNT162b2 (tozinameran) prime-boost vaccination in kidney transplant recipients
Sattler, Arne, Schrezenmeier, Eva, Weber, Ulrike A, Potekhin, Alexander, Bachmann, Friederike, Straub-Hohenbleicher, Henriette, Budde, Klemens, Storz, Elena, Pross, Vanessa, Bergmann, Yasmin, Thole, Linda M.L, Tizian, Caroline, Holsken, Oliver, Diefenbach, Andreas, Schrezenmeier, Hubert, Jahrsdorfer, Bernd, Zemojtel, Tomasz, Jechow, Katharina, Conrad, Christian, Lukassen, Soren, Stauch, Diana, Lachmann, Nils, Choi, Mira, Halleck, Fabian, Kotsch, Katja
Published in The Journal of clinical investigation (15.07.2021)
Published in The Journal of clinical investigation (15.07.2021)
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Live-cell imaging of circadian clock protein dynamics in CRISPR-generated knock-in cells
Gabriel, Christian H., del Olmo, Marta, Zehtabian, Amin, Jäger, Marten, Reischl, Silke, van Dijk, Hannah, Ulbricht, Carolin, Rakhymzhan, Asylkhan, Korte, Thomas, Koller, Barbara, Grudziecki, Astrid, Maier, Bert, Herrmann, Andreas, Niesner, Raluca, Zemojtel, Tomasz, Ewers, Helge, Granada, Adrián E., Herzel, Hanspeter, Kramer, Achim
Published in Nature communications (18.06.2021)
Published in Nature communications (18.06.2021)
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Hematopoietic lineage distribution and evolutionary dynamics of clonal hematopoiesis
Arends, Christopher Maximilian, Galan-Sousa, Joel, Hoyer, Kaja, Chan, Willy, Jäger, Marten, Yoshida, Kenichi, Seemann, Ricarda, Noerenberg, Daniel, Waldhueter, Nils, Fleischer-Notter, Helga, Christen, Friederike, Schmitt, Clemens A., Dörken, Bernd, Pelzer, Uwe, Sinn, Marianne, Zemojtel, Tomasz, Ogawa, Seishi, Märdian, Sven, Schreiber, Adrian, Kunitz, Annegret, Krüger, Ulrike, Bullinger, Lars, Mylonas, Elena, Frick, Mareike, Damm, Frederik
Published in Leukemia (01.09.2018)
Published in Leukemia (01.09.2018)
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Stable expansion of high‐grade serous ovarian cancer organoids requires a low‐Wnt environment
Hoffmann, Karen, Berger, Hilmar, Kulbe, Hagen, Thillainadarasan, Sukanija, Mollenkopf, Hans‐Joachim, Zemojtel, Tomasz, Taube, Eliane, Darb‐Esfahani, Silvia, Mangler, Mandy, Sehouli, Jalid, Chekerov, Radoslav, Braicu, Elena I, Meyer, Thomas F, Kessler, Mirjana
Published in The EMBO journal (16.03.2020)
Published in The EMBO journal (16.03.2020)
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Journal Article
A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease
Smedley, Damian, Schubach, Max, Jacobsen, Julius O.B., Köhler, Sebastian, Zemojtel, Tomasz, Spielmann, Malte, Jäger, Marten, Hochheiser, Harry, Washington, Nicole L., McMurry, Julie A., Haendel, Melissa A., Mungall, Christopher J., Lewis, Suzanna E., Groza, Tudor, Valentini, Giorgio, Robinson, Peter N.
Published in American journal of human genetics (01.09.2016)
Published in American journal of human genetics (01.09.2016)
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Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genome
Zemojtel, Tomasz, Köhler, Sebastian, Mackenroth, Luisa, Jäger, Marten, Hecht, Jochen, Krawitz, Peter, Graul-Neumann, Luitgard, Doelken, Sandra, Ehmke, Nadja, Spielmann, Malte, Oien, Nancy Christine, Schweiger, Michal R, Krüger, Ulrike, Frommer, Götz, Fischer, Björn, Kornak, Uwe, Flöttmann, Ricarda, Ardeshirdavani, Amin, Moreau, Yves, Lewis, Suzanna E, Haendel, Melissa, Smedley, Damian, Horn, Denise, Mundlos, Stefan, Robinson, Peter N
Published in Science translational medicine (03.09.2014)
Published in Science translational medicine (03.09.2014)
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Multi-Parameter Analysis of Biobanked Human Bone Marrow Stromal Cells Shows Little Influence for Donor Age and Mild Comorbidities on Phenotypic and Functional Properties
Andrzejewska, Anastazja, Catar, Rusan, Schoon, Janosch, Qazi, Taimoor Hasan, Sass, Frauke Andrea, Jacobi, Dorit, Blankenstein, Antje, Reinke, Simon, Krüger, David, Streitz, Mathias, Schlickeiser, Stephan, Richter, Sarina, Souidi, Naima, Beez, Christien, Kamhieh-Milz, Julian, Krüger, Ulrike, Zemojtel, Tomasz, Jürchott, Karsten, Strunk, Dirk, Reinke, Petra, Duda, Georg, Moll, Guido, Geissler, Sven
Published in Frontiers in immunology (08.11.2019)
Published in Frontiers in immunology (08.11.2019)
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Journal Article
Walking the interactome for candidate prioritization in exome sequencing studies of Mendelian diseases
Smedley, Damian, Köhler, Sebastian, Czeschik, Johanna Christina, Amberger, Joanna, Bocchini, Carol, Hamosh, Ada, Veldboer, Julian, Zemojtel, Tomasz, Robinson, Peter N
Published in Bioinformatics (Oxford, England) (15.11.2014)
Published in Bioinformatics (Oxford, England) (15.11.2014)
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Journal Article
Genome-wide comparison of cyanobacterial transposable elements, potential genetic diversity indicators
Lin, Shen, Haas, Stefan, Zemojtel, Tomasz, Xiao, Peng, Vingron, Martin, Li, Renhui
Published in Gene (01.03.2011)
Published in Gene (01.03.2011)
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Journal Article
The phenotype‐driven computational analysis yields clinical diagnosis for patients with atypical manifestations of known intellectual disability syndromes
Jezela‐Stanek, Aleksandra, Ciara, Elżbieta, Jurkiewicz, Dorota, Kucharczyk, Marzena, Jędrzejowska, Maria, Chrzanowska, Krystyna H., Krajewska‐Walasek, Małgorzata, Żemojtel, Tomasz
Published in Molecular genetics & genomic medicine (01.09.2020)
Published in Molecular genetics & genomic medicine (01.09.2020)
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Journal Article
Longitudinal therapy monitoring of ALK-positive lung cancer by combined copy number and targeted mutation profiling of cell-free DNA
Dietz, Steffen, Christopoulos, Petros, Yuan, Zhao, Angeles, Arlou Kristina, Gu, Lisa, Volckmar, Anna-Lena, Ogrodnik, Simon J., Janke, Florian, Dalle Fratte, Chiara, Zemojtel, Tomasz, Schneider, Marc A., Kazdal, Daniel, Endris, Volker, Meister, Michael, Muley, Thomas, Cecchin, Erika, Reck, Martin, Schlesner, Matthias, Thomas, Michael, Stenzinger, Albrecht, Sültmann, Holger
Published in EBioMedicine (01.12.2020)
Published in EBioMedicine (01.12.2020)
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Journal Article
SEMA3A and IGSF10 Are Novel Contributors to Combined Pituitary Hormone Deficiency (CPHD)
Budny, Bartlomiej, Zemojtel, Tomasz, Kaluzna, Malgorzata, Gut, Pawel, Niedziela, Marek, Obara-Moszynska, Monika, Rabska-Pietrzak, Barbara, Karmelita-Katulska, Katarzyna, Stajgis, Marek, Ambroziak, Urszula, Bednarczuk, Tomasz, Wrotkowska, Elzbieta, Bukowska-Olech, Ewelina, Jamsheer, Aleksander, Ruchala, Marek, Ziemnicka, Katarzyna
Published in Frontiers in endocrinology (Lausanne) (16.06.2020)
Published in Frontiers in endocrinology (Lausanne) (16.06.2020)
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Journal Article
Recessive Inheritance of Population-Specific Intronic LINE-1 Insertion Causes a Rotor Syndrome Phenotype
Kagawa, Tatehiro, Oka, Akira, Kobayashi, Yoshinao, Hiasa, Yoichi, Kitamura, Tsuneo, Sakugawa, Hiroshi, Adachi, Yukihiko, Anzai, Kazuya, Tsuruya, Kota, Arase, Yoshitaka, Hirose, Shunji, Shiraishi, Koichi, Shiina, Takashi, Sato, Tadayuki, Wang, Ting, Tanaka, Masayuki, Hayashi, Hideki, Kawabe, Noboru, Robinson, Peter N., Zemojtel, Tomasz, Mine, Tetsuya
Published in Human mutation (01.03.2015)
Published in Human mutation (01.03.2015)
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Journal Article
Exome sequencing reveals two novel compound heterozygous XYLT1 mutations in a Polish patient with Desbuquois dysplasia type 2 and growth hormone deficiency
Jamsheer, Aleksander, Olech, Ewelina M, Kozłowski, Kazimierz, Niedziela, Marek, Sowińska-Seidler, Anna, Obara-Moszyńska, Monika, Latos-Bieleńska, Anna, Karczewski, Marek, Zemojtel, Tomasz
Published in Journal of human genetics (01.07.2016)
Published in Journal of human genetics (01.07.2016)
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Journal Article
CpG deamination creates transcription factor-binding sites with high efficiency
Zemojtel, Tomasz, Kielbasa, Szymon M, Arndt, Peter F, Behrens, Sarah, Bourque, Guillaume, Vingron, Martin
Published in Genome biology and evolution (01.01.2011)
Published in Genome biology and evolution (01.01.2011)
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Exonization of active mouse L1s: a driver of transcriptome evolution?
Zemojtel, Tomasz, Penzkofer, Tobias, Schultz, Jörg, Dandekar, Thomas, Badge, Richard, Vingron, Martin
Published in BMC genomics (26.10.2007)
Published in BMC genomics (26.10.2007)
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Journal Article
Phenotype of two Polish patients with Schaaf-Yang syndrome confirmed by identifying mutation in MAGEL2 gene
Matuszewska, Karolina E, Badura-Stronka, Magdalena, Śmigiel, Robert, Cabała, Magdalena, Biernacka, Anna, Kosinska, Joanna, Rydzanicz, Malgorzata, Winczewska-Wiktor, Anna, Sasiadek, Maria, Latos-Bieleńska, Anna, Żemojtel, Tomasz, Płoski, Rafal
Published in Clinical dysmorphology (01.04.2018)
Published in Clinical dysmorphology (01.04.2018)
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