Author

Seval Türkmen

Observed names: S Turkmen, S Türkmen, S. Turkmen, S. Türkmen, SEVAL TURKMEN, Seval Turkmen, Seval Türkmen, Seval Türkmen (263554), Türkmen, Seval

Observed institutions: Max Planck Society, Humboldt-Universität zu Berlin, Istanbul University-Cerrahpaşa, Berlin Institute of Health at Charité - Universitätsmedizin Berlin, Max Planck Institute for Molecular Genetics, Laboratoire National de Santé, Stiftung Charité, Afyon Kocatepe University, Istanbul University, Freie Universität Berlin, Charité - Universitätsmedizin Berlin

ORCID: 0000-0002-4016-4777

Observed ORCID: 0000-0002-4016-4777

OpenAlex ID: A5013478491

Genotype-Phenotype Associations in Sotos Syndrome: An Analysis of 266 Individuals with NSD1 Aberrations

2005 · Katrina Tatton-Brown, Jenny Douglas, et al. · The American Journal of Human Genetics · 338

PDF

Mesenchymal stromal cells of myelodysplastic syndrome and acute myeloid leukemia patients have distinct genetic abnormalities compared with leukemic blasts

2011 · Olga Blau, Claudia Dorothea Baldus, et al. · Blood · 173

CA8 Mutations Cause a Novel Syndrome Characterized by Ataxia and Mild Mental Retardation with Predisposition to Quadrupedal Gait

2009 · Seval Türkmen, Gao Guo, et al. · PLoS Genetics · 153

PDF

Loss-of-function mutations in ATP6V0A2 impair vesicular trafficking, tropoelastin secretion and cell survival

2009 · V. Hucthagowder, E. Morava, et al. · Human Molecular Genetics · 140

Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes

2003 · Seval Türkmen, Gabriele Gillessen-Kaesbach, et al. · European Journal of Human Genetics · 129

Circulating proteasome levels are an independent prognostic factor for survival in multiple myeloma

2006 · Christian Jakob, Karl Egerer, et al. · Blood · 128

Hi-C Identifies Complex Genomic Rearrangements and TAD-Shuffling in Developmental Diseases

2020 · Uirá Souto Melo, Robert Schöpflin, et al. · The American Journal of Human Genetics · 125

PDF

Homeobox genes d11–d13 and a13 control mouse autopod cortical bone and joint formation

2010 · Pablo Villavicencio-Lorini, Pia Kuss, et al. · Journal of Clinical Investigation · 83

PDF

Acute myeloid leukemia in the elderly is characterized by a distinct genetic and epigenetic landscape

2017 · P Silva, M Neumann, et al. · Leukemia · 72

TGGE screening of the entireFBN1coding sequence in 126 individuals with marfan syndrome and related fibrillinopathies

2002 · Stefanie Katzke, Patrick Booms, et al. · Human Mutation · 71

PDF

Brachydactyly type C caused by a homozygous missense mutation in the prodomain of CDMP1

2003 · Georg C. Schwabe, Seval Türkmen, et al. · American Journal of Medical Genetics Part A · 67

Cerebellar hypoplasia, with quadrupedal locomotion, caused by mutations in the very low-density lipoprotein receptor gene

2008 · S Türkmen, K Hoffmann, et al. · European Journal of Human Genetics · 65

BRCA1 and BRCA2 mutations in Turkish breast/ovarian families and young breast cancer patients

2000 · H Yazici, O Bitisik, et al. · British Journal of Cancer · 62

PDF

Multilayered Omics-Based Analysis of a Head and Neck Cancer Model of Cisplatin Resistance Reveals Intratumoral Heterogeneity and Treatment-Induced Clonal Selection

2017 · Franziska Niehr, Theresa Eder, et al. · Clinical Cancer Research · 57

Copy number genome alterations are associated with treatment response and outcome in relapsed childhood ETV6/RUNX1-positive acute lymphoblastic leukemia

2013 · A. Bokemeyer, C. Eckert, et al. · Haematologica · 51

PDF

Integration of Hi-C with short and long-read genome sequencing reveals the structure of germline rearranged genomes

2022 · Robert Schöpflin, Uirá Souto Melo, et al. · Nature Communications · 50

PDF

Cerebellar hypoplasia and quadrupedal locomotion in humans as a recessive trait mapping to chromosome 17p

2005 · S Türkmen, O Demirhan, et al. · Journal of Medical Genetics · 47

PDF

Impact of additional chromosomal aberrations and BCR-ABL kinase domain mutations on the response to nilotinib in Philadelphia chromosome-positive chronic myeloid leukemia

2009 · T. D. Kim, S. Turkmen, et al. · Haematologica · 45

PDF

Synergistic action of the novel HSP90 inhibitor NVP‐AUY922 with histone deacetylase inhibitors, melphalan, or doxorubicin in multiple myeloma

2009 · Martin Kaiser, Britta Lamottke, et al. · European Journal Of Haematology · 44

Aneuploidy in children with relapsed B‐cell precursor acute lymphoblastic leukaemia: clinical importance of detecting a hypodiploid origin of relapse

2019 · Stefanie Groeneveld‐Krentz, Michael P. Schroeder, et al. · British Journal of Haematology · 38

Clinical and molecular characterization of two adults with autosomal recessive Robinow syndrome

2005 · Fatih Tufan, Kivanc Cefle, et al. · American Journal of Medical Genetics Part A · 36

AML: high serum ferritin at initial diagnosis has a negative impact on long-term survival

2018 · Jana Ihlow, Sophia Gross, et al. · Leukemia & lymphoma/Leukemia and lymphoma · 27

A BACH2‐BCL2L1 fusion gene resulting from a t(6;20)(q15;q11.2) chromosomal translocation in the lymphoma cell line BLUE‐1

2011 · Seval Türkmen, Mathias Riehn, et al. · Genes Chromosomes and Cancer · 26

Genome sequencing in families with congenital limb malformations

2021 · Jonas Elsner, Martin A. Mensah, et al. · Human Genetics · 25

PDF

Cytogenetic studies in acute leukemia patients relapsing after allogeneic stem cell transplantation

2010 · Martin Schmidt-Hieber, Igor W. Blau, et al. · Cancer Genetics and Cytogenetics · 24

Works count: 66

Citation count: 2,284

H-index: 24

I10-index: 35