Papers matching “chromosomal abnormalities” 172
Not finding it? Sign in to also search OpenAlex live.
-
Complex karyotype but not other cytogenetic abnormalities is associated with worse posttransplant survival of patients with nucleophosmin 1‐mutated acute myeloid leukemia: A study from the European Society for Blood and Marrow Transplantation Acute Leukemia Working Party
Nour M. Moukalled, Myriam Labopin, Jurjen Versluis, Gèrard Socié, Didier Blaise, Urpu Salmenniemi, +12 more
7citations -
Impact of cytogenetic abnormalities on treatment outcomes in patients with amyloid light-chain amyloidosis: subanalyses from the ANDROMEDA study2023 Amyloid article Biochemistry, Genetics and Molecular Biology Amyloidosis: Diagnosis, Treatment, Outcomes Open access
Shaji Kunnathu Kumar, Angela A. Dispenzieri, Divaya Bhutani, Morie Abraham Gertz, Ashutosh D. Wechalekar, Giovanni O. Palladini, +9 more
23citations -
In uveal melanoma Gα-protein GNA11 mutations convey a shorter disease-specific survival and are more strongly associated with loss of BAP1 and chromosomal alterations than Gα-protein GNAQ mutations
Francesca Piaggio, Michela Croce, Francesco Reggiani, Paola Monti, Cinzia Bernardi, Marianna Ambrosio, +16 more
29citations -
OAB-034: Evaluating the impact of cytogenetic abnormalities on treatment outcomes in patients with AL amyloidosis: subanalyses from the ANDROMEDA study2021 Clinical Lymphoma Myeloma & Leukemia conference-abstract Biochemistry, Genetics and Molecular Biology Amyloidosis: Diagnosis, Treatment, Outcomes
Shaji Kunnathu Kumar, Angela A. Dispenzieri, Divaya Bhutani, Morie Abraham Gertz, Ashutosh D. Wechalekar, Giovanni O. Palladini, +10 more
2citations -
The cumulative effect of cytogenetic abnormalities on the outcomes of myeloma patients with del(17p) undergoing AHSCT in EBMT centres between 2016 and 20222026 British Journal of Haematology article Medicine Multiple Myeloma Research and Treatments Open access
Claire Comerford, Patrick John Hayden, Diderik-Jan Eikema, Linda Köster, Sandra Sauer, Annoek E. C. Broers, +20 more
0citations -
Dynamic X-chromosomal reactivation enhances female brain resilience2023 bioRxiv (Cold Spring Harbor Laboratory) preprint Biochemistry, Genetics and Molecular Biology Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities Open access
Stephan Käseberg, Ramkumar Menon, Elisa Gabassi, Hristo Todorov, Sarah Frank, Heiko Brennenstuhl, +13 more
4citations -
New developments and future trajectories in supernumerary sex chromosome abnormalities: a summary of the 2022 3rd International Workshop on Klinefelter Syndrome, Trisomy X, and XYY2023 Endocrine Connections article Biochemistry, Genetics and Molecular Biology Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities Open access
Claus Højbjerg Gravholt, Alberto Ferlin, Joerg Gromoll, Anders Juul, Armin Raznahan, Sophie van Rijn, +4 more
12citations -
A novel genetic strategy to interrogate an unknown phenotypic modifier: Sdhc KO-Robertsonian mice develop frequent thyroid abnormalities with papillary thyroid carcinoma-like features0citations
-
Prognostic value of CPSS cytogenetic risk classification in patients with CMML after allogeneic hematopoietic cell transplantation: a retrospective multicenter study of the Chronic Malignancies Working Party of the EBMT2022 Bone Marrow Transplantation article Medicine Hematopoietic Stem Cell Transplantation Open access
Christian Koenecke, Dirk‐Jan Eikema, Sheree Hazelaar, Thomas A. Schroeder, Victoria T. Potter, Nicolaus Martin Kröger, +19 more
5citations -
540. Allele specific expression as an indication of ploidy in pig IPECJ2 and chicken SL-29 cell lines2022 World Congress on Genetics Applied to Livestock Production (WCGALP) conference-paper Agricultural and Biological Sciences Chromosomal and Genetic Variations Open access
Jani de Vos, Richard P. M. A. Crooijmans, Martijn F. L. Derks, Susan L. Kloet, Martien A. M. Groenen, Ole Madsen
1citations -
P-495 Effectiveness and feasibility of integrating genome-wide non-invasive prenatal testing (GW-NIPT) into standard care for recurrent pregnancy loss: A systematic review and SWOT analysis
Matea Skojo, Lisanne van Prooyen Schuurman, Karin E. M. Diderich, Marieke Joosten, Annemarie G. M. G. J. Mulders, Eileen E. L. O. Lashley, +3 more
0citations -
Acquisition of chromosome 1q duplication in parental and genome‐edited human‐induced pluripotent stem cell‐derived neural stem cells results in their higher proliferation rate in vitro and in vivo2020 Cell Proliferation article Biochemistry, Genetics and Molecular Biology Pluripotent Stem Cells Research Open access
Narges Zare Mehrjardi, Marek Molčányi, Firuze Fulya Hatay, Marco Timmer, Ebrahim Shahbazi, Justus P. Ackermann, +10 more
10citations -
Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 study2022 The American Journal of Human Genetics article Medicine Prenatal Screening and Diagnostics Open access
Lisanne van Prooyen Schuurman, Erik A. Sistermans, Diane Van Opstal, Lidewij Henneman, Mireille N. Bekker, Caroline J. Bax, +28 more
98citations