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Author Details
Full Name
Gudrun G??hring
Affiliation
Hannover Medical School
ORCID
Career Start Year
2002
Papers
234
H Index
47
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37470150
Fludarabine, cytarabine, and idarubicin with or without venetoclax in patients with relapsed/refractory acute myeloid leukemia.
Haematologica
2024
38086945
Panel-based RNA fusion sequencing improves diagnostics of pediatric acute myeloid leukemia.
Leukemia
2024
37706343
Somatic variant profiling in chronic phase pediatric chronic myeloid leukemia.
Haematologica
2024
37584291
Spontaneous remission and loss of monosomy 7: a window of opportunity for young children with SAMD9L syndrome.
Haematologica
2024
36657267
Rare and potentially fatal - Cytogenetically cryptic TNIP1::PDGFRB and PCM1::FGFR1 fusion leading to myeloid/lymphoid neoplasms with eosinophilia in children.
Cancer Genet
2023
37756525
Germ line variant GFI1-36N affects DNA repair and sensitizes AML cells to DNA damage and repair therapy.
Blood
2023
35484682
Molecular characterization and clinical outcome of B-cell precursor acute lymphoblastic leukemia with IG-MYC rearrangement.
Haematologica
2023
37104932
Generation of two human NRF2 knockout iPSC clones using CRISPR/Cas9 editing.
Stem Cell Res
2023
36775010
European standard clinical practice - Key issues for the medical care of individuals with familial leukemia.
Eur J Med Genet
2023
36463634
Generation of human induced pluripotent stem cell line encoding for a genetically encoded voltage indicator Arclight A242.
Stem Cell Res
2023
36672158
iPSC-Derived Striatal Medium Spiny Neurons from Patients with Multiple System Atrophy Show Hypoexcitability and Elevated α-Synuclein Release.
Cells
2023
36823455
Second allogeneic stem cell transplantation can rescue a significant proportion of patients with JMML relapsing after first allograft.
Bone Marrow Transplant
2023
34839233
Classification of fluorescent R-Band metaphase chromosomes using a convolutional neural network is precise and fast in generating karyograms of hematologic neoplastic cells.
Cancer Genet
2022
35406484
The Cytogenetic Landscape of Pediatric Chronic Myeloid Leukemia Diagnosed in Chronic Phase.
Cancers (Basel)
2022
35795779
Targeted biallelic integration of an inducible Caspase 9 suicide gene in iPSCs for safer therapies.
Mol Ther Methods Clin Dev
2022
35636247
Generation of an induced pluripotent stem cell line (DHMCi008-A) from an individual with TUBA1A tubulinopathy.
Stem Cell Res
2022
35362549
Evolution of severe (transfusion-dependent) anaemia in myelodysplastic syndromes with 5q deletion is characterized by a macrophage-associated failure of the eythropoietic niche.
Br J Haematol
2022
35565187
Optical Genome Mapping as a Diagnostic Tool in Pediatric Acute Myeloid Leukemia.
Cancers (Basel)
2022
35875134
Clonal Evolution at First Sight: A Combined Visualization of Diverse Diagnostic Methods Improves Understanding of Leukemic Progression.
Front Oncol
2022
36307508
Wildtype heterogeneity contributes to clonal variability in genome edited cells.
Sci Rep
2022
35930870
Generation of an induced pluripotent stem cell line (DHMCi009-A) from an individual with TUBB2A tubulinopathy.
Stem Cell Res
2022
36162332
Generation of two TMEM16A knockout iPSC clones each from a healthy human iPSC line, from a Cystic Fibrosis patient specific line with p.Phe508del mutation and from the gene corrected iPSC line.
Stem Cell Res
2022
35152180
Generation of human induced pluripotent stem cell lines encoding for genetically encoded calcium indicators RCaMP1h and GCaMP6f.
Stem Cell Res
2022
35277655
"Randomized phase II study of azacitidine ± lenalidomide in higher-risk myelodysplastic syndromes and acute myeloid leukemia with a karyotype including Del(5q)".
Leukemia
2022
34732858
A unique role of p53 haploinsufficiency or loss in the development of acute myeloid leukemia with FLT3-ITD mutation.
Leukemia
2022
34460133
Cryptic TCF3 fusions in childhood leukemia: Detection by RNA sequencing.
Genes Chromosomes Cancer
2022
32948843
IDH1/2 mutations in acute myeloid leukemia patients and risk of coronary artery disease and cardiac dysfunction-a retrospective propensity score analysis.
Leukemia
2021
33571874
Establishment of MHHi001-A-5, a GCaMP6f and RedStar dual reporter human iPSC line for in vitro and in vivo characterization and in situ tracing of iPSC derivatives.
Stem Cell Res
2021
33875720
Severe allo-immune antibody-associated peripheral and central nervous system diseases after allogeneic hematopoietic stem cell transplantation.
Sci Rep
2021
33486841
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
2021
33647814
BCR-ABL1 positive AML or CML in blast crisis? A pediatric case report with inv(3) and t(9;22) in the initial clone.
Cancer Genet
2021
33725366
Impact of PPM1D mutations in patients with myelodysplastic syndrome and deletion of chromosome 5q.
Am J Hematol
2021
33725366
Impact of PPM1D mutations in patients with myelodysplastic syndrome and deletion of chromosome 5q.
Am J Hematol
2021
33690887
Paediatric chronic myeloid leukaemia presenting in de novo or secondary blast phase - a comparison of clinical and genetic characteristics.
Br J Haematol
2021
33578365
Generation of two iPSC clones (MHHi021-A and MHHi021-B) from a patient with hypertrophic cardiomyopathy with p.Arg723Gly mutation in the MYH7 gene.
Stem Cell Res
2021
34469508
Association of unbalanced translocation der(1;7) with germline GATA2 mutations.
Blood
2021
34695767
Generation of an induced pluripotent stem cell line (DHMCi006-A) from a patient with autosomal recessive polycystic kidney disease (ARPKD) carrying a compound heterozygous missense mutation in the fibrocystin encoding PKHD1 gene.
Stem Cell Res
2021
34782764
Chromothripsis followed by circular recombination drives oncogene amplification in human cancer.
Nat Genet
2021
34688127
Generation of an induced pluripotent stem cell line (DHMCi007-A) from a patient with autosomal recessive polycystic kidney disease (ARPKD) carrying a homozygous missense mutation in the fibrocystin-encoding PKHD1 gene.
Stem Cell Res
2021
34769003
Germline POT1 Deregulation Can Predispose to Myeloid Malignancies in Childhood.
Int J Mol Sci
2021
34560000
iPSC culture expansion selects against putatively actionable mutations in the mitochondrial genome.
Stem Cell Reports
2021
34503197
The Clinical Utility of Optical Genome Mapping for the Assessment of Genomic Aberrations in Acute Lymphoblastic Leukemia.
Cancers (Basel)
2021
34244664
Hematopoietic stem cell transplantation in children and adolescents with GATA2-related myelodysplastic syndrome.
Bone Marrow Transplant
2021
34196171
A novel classification of hematologic conditions in patients with Fanconi anemia.
Haematologica
2021
33197935
SSBP2-CSF1R is a recurrent fusion in B-lineage acute lymphoblastic leukemia with diverse genetic presentation and variable outcome.
Blood
2021
33443157
Knockout of the HMG domain of the porcine SRY gene causes sex reversal in gene-edited pigs.
Proc Natl Acad Sci U S A
2021
32705308
Risk of tumor lysis syndrome in patients with acute myeloid leukemia treated with venetoclax-containing regimens without dose ramp-up.
Ann Hematol
2021
31601692
Relapses and treatment-related events contributed equally to poor prognosis in children with ABL-class fusion positive B-cell acute lymphoblastic leukemia treated according to AIEOP-BFM protocols.
Haematologica
2020
32000109
Human STAT1 gain-of-function iPSC line from a patient suffering from chronic mucocutaneous candidiasis.
Stem Cell Res
2020
31837633
Induced pluripotent stem cell line (PEIi003-A) derived from an apparently healthy male individual.
Stem Cell Res
2020
1 - 50 of 234
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Kyoto University
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The Hospital for Sick Children, University of Toronto
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Lille University Hospital, INSERM UMR-S7, CNRS UMR9020, Lille University.
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row(s) 1 - 30 of 30
Collaborators
Michael Heuser
Hannover Medical School
Co-authored papers
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Felicitas Thol
Hannover Medical School
Co-authored papers
45
Doris Steinemann
Hannover Medical School
Co-authored papers
36
Charlotte M Niemeyer
Co-authored papers
27
Michael Dworzak
St. Anna Children's Cancer Research Institute (CCRI)
Co-authored papers
10
Doris Kraemer
Co-authored papers
4
Peter Lichter
German Cancer Research Center (DKFZ)
Co-authored papers
4
Christoph Klein
Kinderklinik und Kinderpoliklinik der Ludwig-Maximilians-Universitat Munchen
Co-authored papers
3
Christian P Kratz
Co-authored papers
3
Simone Feurstein
University Hospital Heidelberg
Co-authored papers
3
Markus Metzler
University Hospital Erlangen
Co-authored papers
3
Manuela Krumbholz
University Hospital Erlangen
Co-authored papers
3
Simon J Boulton
The Francis Crick Institute
Co-authored papers
2
Wolfgang E Berdel
University Hospital Munster
Co-authored papers
2
Torsten Haferlach
Taussig Cancer Institute, Cleveland Clinic
Co-authored papers
2
Christof von Kalle
Berlin Institute of Health at Charite-Universitatsmedizin Berlin
Co-authored papers
2
Hiroko Tanaka
Tokyo Medical and Dental University
Co-authored papers
2
Hartmut Hecker
Hannover Medical School
Co-authored papers
2
Anthony V Moorman
Translational and Clinical Research Institute, Newcastle University
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2
Arndt Borkhardt
Hematology and Clinical Immunology, Heinrich Heine University Dusseldorf
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Friedrich St??lzel
University Hospital TU Dresden
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Jan O Korbel
European Bioinformatics Institute (EMBL-EBI)
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Franz Schaefer
University Children's Hospital Heidelberg
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Beat W Sch??fer
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Julian Varghese
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Udo Kontny
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Mignon L Loh
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