Publications by authors named "Seval Turkmen"

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Integration of Hi-C with short and long-read genome sequencing reveals the structure of germline rearranged genomes.
Robert Schöpflin, Uirá Souto Melo, Hossein Moeinzadeh, David Heller, Verena Laupert

Nat Commun· October 2022

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Acute myeloid leukemia: negative prognostic impact of early blast persistence can be in part overcome by a later remission prior to post-induction therapy.
Jana Ihlow, Sophia Gross, Leonie Busack, Anne Flörcken, Julia Jesse

Haematologica· August 2022

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Understanding the new BRD4-related syndrome: Clinical and genomic delineation with an international cohort study.
Guillaume Jouret, Solveig Heide, Arthur Sorlin, Laurence Faivre, Sandra Chantot-Bastaraud

Clin Genet· August 2022

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A conserved long-distance telomeric silencing mechanism suppresses mTOR signaling in aging human fibroblasts.
Kathrin Jäger, Juliane Mensch, Maria Elisabeth Grimmig, Bruno Neuner, Kerstin Gorzelniak

Sci Adv· August 2022

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Method Optimization of Skin Biopsy-Derived Fibroblast Culture for Reprogramming Into Induced Pluripotent Stem Cells.
Kathleen Mommaerts, Camille Bellora, Pauline Lambert, Seval Türkmen, Jens C Schwamborn

Biopreserv Biobank· February 2022

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Genome sequencing in families with congenital limb malformations.
Jonas Elsner, Martin A Mensah, Manuel Holtgrewe, Jakob Hertzberg, Stefania Bigoni

Hum Genet· August 2021

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Clinical outcome of older adults with acute myeloid Leukemia: An analysis of a large tertiary referral Center over two decades.
Jana Ihlow, Sophia Gross, Nina Rosa Neuendorff, Leonie Busack, Alma Herneth

J Geriatr Oncol· May 2021

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Hi-C Identifies Complex Genomic Rearrangements and TAD-Shuffling in Developmental Diseases.
Uirá Souto Melo, Robert Schöpflin, Rocio Acuna-Hidalgo, Martin Atta Mensah, Björn Fischer-Zirnsak

Am J Hum Genet· June 2020

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Aneuploidy in children with relapsed B-cell precursor acute lymphoblastic leukaemia: clinical importance of detecting a hypodiploid origin of relapse.
Stefanie Groeneveld-Krentz, Michael P Schroeder, Michael Reiter, Malwine J Pogodzinski, Helia J Pimentel-Gutiérrez

Br J Haematol· April 2019

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AML: high serum ferritin at initial diagnosis has a negative impact on long-term survival.
Jana Ihlow, Sophia Gross, Annabel Sick, Tanja Schneider, Anne Flörcken

Leuk Lymphoma· January 2019

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Multilayered Omics-Based Analysis of a Head and Neck Cancer Model of Cisplatin Resistance Reveals Intratumoral Heterogeneity and Treatment-Induced Clonal Selection.
Franziska Niehr, Theresa Eder, Tanja Pilz, Robert Konschak, Denise Treue

Clin Cancer Res· January 2018

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A Novel de novo Mutation in a Patient with Autosomal Dominant Omodysplasia.
Seval Türkmen, Malte Spielmann, Nilay Güneş, Alexej Knaus, Ricarda Flöttmann

Mol Syndromol· November 2017

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A Rare Case of Acute Myeloid Leukemia with a t(2;3) Chromosomal Translocation Characterized by Thrombophilia and Chemoresistance.
Cecilia Bozzetti, Seval Türkmen, Ulrich Richter, Lars Fransecky, Gürkan Bal

J Clin Exp Hematop· March 2017

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Flow cytometric maturity score as a novel prognostic parameter in patients with acute myeloid leukemia.
Tanja Schneider, Anne Flörcken, Anju Singh, Seval Türkmen, Thomas Burmeister

Ann Hematol· August 2015

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BCR-ABL1(+) acute myeloid leukemia: clonal selection of a BCR-ABL1(-) subclone as a cause of refractory disease with nilotinib treatment.
Nina Rosa Neuendorff, Michaela Schwarz, Philipp Hemmati, Seval Türkmen, Christiane Bommer

Acta Haematol· April 2015

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High prevalence of immunoglobulin light chain gene aberrations as revealed by FISH in multiple myeloma and MGUS.
Seval Türkmen, Anastasia Binder, Antje Gerlach, Sylke Niehage, Maria Theodora Melissari

Genes Chromosomes Cancer· August 2014

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Copy number genome alterations are associated with treatment response and outcome in relapsed childhood ETV6/RUNX1-positive acute lymphoblastic leukemia.
Almut Bokemeyer, Cornelia Eckert, Franziska Meyr, Gabriele Koerner, Arend von Stackelberg

Haematologica· April 2014

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Involvement of the MLL gene in adult T-lymphoblastic leukemia.
Seval Türkmen, Bernd Timmermann, Gesine Bartels, Daniela Gröger, Claus Meyer

Genes Chromosomes Cancer· December 2012

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Mesenchymal stromal cells of myelodysplastic syndrome and acute myeloid leukemia patients have distinct genetic abnormalities compared with leukemic blasts.
Olga Blau, Claudia Dorothea Baldus, Wolf-Karsten Hofmann, Gundula Thiel, Florian Nolte

Blood· November 2011

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A BACH2-BCL2L1 fusion gene resulting from a t(6;20)(q15;q11.2) chromosomal translocation in the lymphoma cell line BLUE-1.
Seval Türkmen, Mathias Riehn, Eva Klopocki, Mara Molkentin, Richard Reinhardt

Genes Chromosomes Cancer· June 2011

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Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation.
Pablo Villavicencio-Lorini, Pia Kuss, Julia Friedrich, Julia Haupt, Muhammed Farooq

J Clin Invest· June 2010

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Impact of additional chromosomal aberrations and BCR-ABL kinase domain mutations on the response to nilotinib in Philadelphia chromosome-positive chronic myeloid leukemia.
Theo D Kim, Seval Türkmen, Michaela Schwarz, Gökben Koca, Hendrik Nogai

Haematologica· April 2010

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Synergistic action of the novel HSP90 inhibitor NVP-AUY922 with histone deacetylase inhibitors, melphalan, or doxorubicin in multiple myeloma.
Martin Kaiser, Britta Lamottke, Maren Mieth, Michael R Jensen, Cornelia Quadt

Eur J Haematol· April 2010

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Cytogenetic studies in acute leukemia patients relapsing after allogeneic stem cell transplantation.
Martin Schmidt-Hieber, Igor W Blau, Gregor Richter, Seval Türkmen, Christiane Bommer

Cancer Genet Cytogenet· April 2010

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CA8 mutations cause a novel syndrome characterized by ataxia and mild mental retardation with predisposition to quadrupedal gait.
Seval Türkmen, Gao Guo, Masoud Garshasbi, Katrin Hoffmann, Amjad J Alshalah

PLoS Genet· May 2009

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