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K. Manola · SciRah

Researcher profile · Semantic Scholar

K. Manola

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K. Manola — researcher profile on SciRah

h-index: 16
Works: 64
Citations: 781

Most-cited papers

The lysine‐specific methyltransferase KMT2C/MLL3 regulates DNA repair components in cancer
T. Rampias, Dimitris Karagiannis, M. Avgeris, A. Polyzos +10 more
2019EMBO Reports135 citations Open access
Semantic Scholar
Cytogenetics of pediatric acute myeloid leukemia
K. Manola
2009European Journal of Haematology73 citations Open access
Semantic Scholar
Cytogenetic abnormalities in acute leukaemia of ambiguous lineage: an overview
K. Manola
2013British Journal of Haematology64 citations
Semantic Scholar
Isochromosome der(17)(q10)t(15;17) in Acute Promyelocytic Leukemia Resulting in an Additional Copy of the RARA-PML Fusion Gene: Report of 4 Cases and Review of the Literature
K. Manola, Maria Karakosta, C. Sambani, G. Terzoudi +3 more
2010Acta Haematologica39 citations
Semantic Scholar
G2-checkpoint abrogation in irradiated lymphocytes: A new cytogenetic approach to assess individual radiosensitivity and predisposition to cancer.
G. Terzoudi, V. Hatzi, K. Barszczewska, K. Manola +3 more
2009International Journal of Oncology32 citations Open access
Semantic Scholar
Cytogenetic abnormalities and monosomal karyotypes in children and adolescents with acute myeloid leukemia: correlations with clinical characteristics and outcome.
K. Manola, F. Panitsas, S. Polychronopoulou, A. Daraki +7 more
2013Cancer Genetics30 citations
Semantic Scholar
ASXL1 mutations in AML are associated with specific clinical and cytogenetic characteristics
Katerina Kakosaiou, F. Panitsas, A. Daraki, M. Pagoni +9 more
2018Leukemia and Lymphoma29 citations
Semantic Scholar
Association of various risk factors with chronic lymphocytic leukemia and its cytogenetic characteristics
Maria Karakosta, E. Delicha, G. Kouraklis, K. Manola
2016Archives of Environmental & Occupational Health29 citations
Semantic Scholar
Glutathione‐S‐transferase T1 and M1 gene polymorphisms in Greek patients with multiple sclerosis: a pilot study
C. Stavropoulou, D. Korakaki, H. Rigana, G. Voutsinas +5 more
2007European Journal of Neurology27 citations
Semantic Scholar
Jumping translocations in hematological malignancies: a cytogenetic study of five cases.
K. Manola, V. N. Georgakakos, C. Stavropoulou, A. Spyridonidis +6 more
2008Cancer Genetics and Cytogenetics25 citations
Semantic Scholar
A new cytogenetic approach for the evaluation of mutagenic potential of chemicals that induce cell cycle arrest in the G2 phase.
G. Terzoudi, S. Malik, G. Pantelias, K. Margaritis +2 more
2003Mutagenesis23 citations
Semantic Scholar
The G516T CYP2B6 Germline Polymorphism Affects the Risk of Acute Myeloid Leukemia and Is Associated with Specific Chromosomal Abnormalities
A. Daraki, Sophia Zachaki, T. Koromila, P. Diamantopoulou +5 more
2014PLoS ONE21 citations Open access
Semantic Scholar
Association of Unbalanced Translocation der(1;7) with Germline GATA2 Mutations.
E. Kozyra, G. Göhring, D. Hickstein, K. Calvo +43 more
2021Blood17 citations Open access
Semantic Scholar
Leukemias associated with Turner syndrome: report of three cases and review of the literature.
K. Manola, C. Sambani, D. Karakasis, G. Kalliakosta +2 more
2008Leukemia research : a Forum for Studies on Leukemia and Normal Hemopoiesis17 citations
Semantic Scholar
A novel mechanism of NPM1 cytoplasmic localization in acute myeloid leukemia: the recurrent gene fusion NPM1–HAUS1
P. Campregher, Welbert de Oliveira Pereira, Bianca Lisboa, R. Puga +10 more
2016Haematologica16 citations Open access
Semantic Scholar
Acute Promyelocytic Leukemia: an Experience on 95 Greek Patients Treated in the All-Trans-Retinoic Acid Era
M. Pagoni, M. Garofalaki, F. Panitsas, K. Manola +14 more
2011Mediterranean Journal of Hematology and Infectious Diseases16 citations Open access
Semantic Scholar
GSTP1 and CYP2B6 Genetic Polymorphisms and the Risk of Bronchopulmonary Dysplasia in Preterm Neonates
Sophia Zachaki, A. Daraki, E. Polycarpou, C. Stavropoulou +2 more
2017American Journal of Perinatology13 citations
Semantic Scholar
5'RARA submicroscopic deletion from new variant translocation involving chromosomes 15, 17, and 18, in a case of acute promyelocytic leukemia.
C. Stavropoulou, V. N. Georgakakos, K. Manola, M. Pagoni +3 more
2008Cancer Genetics and Cytogenetics12 citations
Semantic Scholar
Leukemic recombinations involving heterochromatin in myeloproliferative disorders with t(1;9).
C. Sambani, R. la Starza, V. Pierini, P. Vandenberghe +9 more
2005Cancer Genetics and Cytogenetics12 citations
Semantic Scholar
Association of C609T-Inborn Polymorphism of NAD(P)H: Quinone Oxidoreductase 1 with the Risk of Bronchopulmonary Dysplasia in Preterm Neonates
S. Gavrili, Sophia Zachaki, A. Daraki, E. Polycarpou +4 more
2015American Journal of Perinatology10 citations
Semantic Scholar
UGT1A1*28 Polymorphism in Chronic Lymphocytic Leukemia: The First Investigation of the Polymorphism in Disease Susceptibility and Its Specific Cytogenetic Abnormalities
Maria Karakosta, V. Kalotychou, A. Kostakis, G. Pantelias +3 more
2014Acta Haematologica10 citations
Semantic Scholar
Allogeneic stem cell transplantation from donors with mosaic Turner syndrome
K. Manola, C. Sambani, D. Karakasis, I. Baltathakis +2 more
2006Bone Marrow Transplantation9 citations Open access
Semantic Scholar
Low-level X Chromosome Mosaicism: A Common Finding in Women Undergoing IVF
Sophia Zachaki, E. Kouvidi, A. Pantou, H. Tsarouha +6 more
2020In Vivo8 citations Open access
Semantic Scholar
Constitutional pericentric inversion of chromosome 9 and hematopoietic recovery after allogeneic stem cell transplantation
K. Manola, N. Harhalakis, A. Symeonidis, H. Rigana +8 more
2006Annals of Hematology8 citations
Semantic Scholar
Radioprotective effect of amifostine on cells from cancer prone patients and healthy individuals studied by the G2 and PCC assays
K. Manola, G. Terzoudi, C. Dardoufas, S. Malik +1 more
2003International Journal of Radiation Biology8 citations
Semantic Scholar
Cohesin RAD21 Gene Promoter Methylation in Patients with Chronic Lymphocytic Leukemia
Agapi Ioannidou, Sophia Zachaki, Maria Karakosta, A. Daraki +2 more
2018Cytogenetic and Genome Research7 citations
Semantic Scholar
High frequency of NAD(P)H:quinone oxidoreductase 1 (NQO1) C(609)T germline polymorphism in MDS/AML with trisomy 8.
Sophia Zachaki, C. Stavropoulou, T. Koromila, K. Manola +7 more
2013Leukemia research : a Forum for Studies on Leukemia and Normal Hemopoiesis7 citations
Semantic Scholar
Deletion of 5q as a rare abnormality in chronic lymphocytic leukemia.
Maria Karakosta, A. Tsakiridou, Ioannis Korantzis, K. Manola
2010Cancer Genetics and Cytogenetics7 citations
Semantic Scholar
Translocation (6;13)(p21;q14.1) as a rare nonrandom cytogenetic abnormality in chronic lymphocytic leukemia.
Maria Karakosta, M. Voulgarelis, Ioanna Vlachadami, K. Manola
2010Cancer Genetics and Cytogenetics7 citations
Semantic Scholar
Disruption of the ETV6 gene as a consequence of a rare translocation (12;12)(p13;q13) in treatment-induced acute myeloid leukemia after breast cancer.
K. Manola, V. N. Georgakakos, D. Margaritis, C. Stavropoulou +4 more
2008Cancer Genetics and Cytogenetics7 citations
Semantic Scholar
Low frequency of the glutathione-S-transferase T1-null genotype in patients with primary myelodysplastic syndrome and 5q deletion
Chryssa Stavropoulou, Constantina Sambani, H. Rigana, Vasileios N. Georgakakos +4 more
2008Leukemia7 citations Open access
Semantic Scholar
Female Reproductive Ageing and Chromosomal Abnormalities in a Large Series of Women Undergoing IVF
E. Kouvidi, Sophia Zachaki, Haralampia Tsarouha, A. Pantou +3 more
2022Cytogenetic and Genome Research6 citations
Semantic Scholar
Association of A313G glutathione S-transferase P1 germline polymorphism with susceptibility to de novo myelodysplastic syndrome
Sophia Zachaki, C. Stavropoulou, Marina Kalomoiraki, T. Koromila +6 more
2013Leukemia and Lymphoma6 citations
Semantic Scholar
A 46,XX Karyotype in Men with Infertility: Two New Cases and Review of the Literature
E. Kouvidi, Hara Tsimela, L. Lazaros, K. Manola +8 more
2022Journal of Human Reproductive Sciences5 citations Open access
Semantic Scholar
Polymorphisms and haplotypes of the CYP2B6 detoxification gene in the predisposition of Acute Myeloid Leukemia (AML) and induction of its cytogenetic abnormalities.
A. Daraki, Katerina Kakosaiou, Sophia Zachaki, C. Sambani +3 more
2016Cancer Genetics5 citations
Semantic Scholar
The parallel application of karyotype interphase and metaphase FISH after DSP-30/IL-2 stimulation is necessary for the investigation of chronic lymphocytic leukemia
Maria Karakosta, K. Manola
2016Hematology5 citations Open access
Semantic Scholar
Translocation t(5;18)(q35;q21) as a Rare Nonrandom Abnormality in Acute Myeloid Leukemia
A. Daraki, L. K. Bourantas, K. Manola
2013Cytogenetic and Genome Research5 citations
Semantic Scholar
Paraoxonase 1 (PON1) Q192R and L55M Polymorphisms as Potential Predisposition Factors for Chronic Lymphocytic Leukemia
Agapi Ioannidou, Sophia Zachaki, A. Daraki, Ioanna Maria Margariti +5 more
2019Anticancer Research4 citations Open access
Semantic Scholar
A novel dic(1;10) in a patient with myelodysplastic syndrome.
C. Sambani, R. la Starza, C. Stavropoulou, K. Manola +2 more
2002Cancer Genetics and Cytogenetics4 citations
Semantic Scholar
Association of GSTP1 inactivating polymorphism with acute myeloid leukemia and its specific chromosomal abnormalities
A. Daraki, Sophia Zachaki, Faidra Rosmaraki, Marina Kalomoiraki +4 more
2017Leukemia and Lymphoma3 citations
Semantic Scholar
Translocation (X;12)(p11;p13) as a sole abnormality in biphenotypic acute leukemia.
K. Manola, V. N. Georgakakos, T. Marinakis, C. Stavropoulou +4 more
2007Cancer Genetics and Cytogenetics3 citations
Semantic Scholar
Epigenetic signature of ionizing radiation in therapy-related AML patients.
G. O'Brien, Agnieszka Cecotka, K. Manola, M. Pagoni +2 more
2023Heliyon2 citations Open access
Semantic Scholar
Cytogenetic findings of ectopic endometriotic tissue in women with endometriosis and review of the literature.
Sophia Zachaki, Marina Kalomoiraki, E. Kouvidi, Emmanuel Promponas +6 more
2021European Journal of Obstetrics, Gynecology, and Reproductive Biology2 citations
Semantic Scholar
Identification of two novel mutations in human acute myeloid leukemia cases
G. O'Brien, Joanna Żyła, K. Manola, M. Pagoni +2 more
2020Leukemia and Lymphoma2 citations Open access
Semantic Scholar
A Novel Variant Translocation t(8;16;21)(q22;q24;q22) in Acute Myeloid Leukemia Expressing both Myeloid and Lymphoid Markers
Katerina Kakosaiou, A. Daraki, A. Zomas, K. Manola
20152 citations
Semantic Scholar
Plasmablastic crisis of Philadelphia chromosome-positive chronic myeloid leukemia
K. Manola, D. Pantelidou, M. Papaioannou
2010Annals of Hematology2 citations Open access
Semantic Scholar
Switch in X-inactivation in a JAK2 V617F-negative case of polycythemia vera with two acquired X-autosome translocations.
K. Manola, C. Stavropoulou, V. N. Georgakakos, K. Zoi +6 more
2007Leukemia research : a Forum for Studies on Leukemia and Normal Hemopoiesis2 citations
Semantic Scholar
Cohesin RAD21 Gene Promoter Methylation in Patients with Acute Myeloid Leukemia
K. Manola, Sophia Zachaki, Katerina Kakosaiou, Agapi Ioannidou +2 more
2024Life1 citations Open access
Semantic Scholar
Epigenetic Signature of Ionising Radiation In Therapy-Related AML Patients
G. O'Brien, Agnieszka Cecotka, K. Manola, M. Pagoni +2 more
2022Social Science Research Network0 citations Open access
Semantic Scholar
Glutathione S-transferase P1 promoter hypermethylation in acute myeloid leukemia: association with A313G germline polymorphism and chromosomal abnormalities
A. Daraki, Sophia Zachaki, C. Stavropoulou, V. Aleporou‐Marinou +2 more
2014Leukemia and Lymphoma0 citations
Semantic Scholar

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C. Sambani — researcher profile on SciRah
G. Pantelias×15
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Sophia Zachaki×15
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A. Daraki×14
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C. Stavropoulou

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Maria Karakosta×8

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Maria Karakosta — researcher profile on SciRah

V. N. Georgakakos×7

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E. Kanavakis×6

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