Kalliopi N. Manola

National Centre of Scientific Research "Demokritos" — Greece

Medicine · Health Sciences

15h-index877citations64works0.52yr avg
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Research Topics

Acute Myeloid Leukemia Research(29), Acute Lymphoblastic Leukemia research(12), Myeloproliferative Neoplasms: Diagnosis and Treatment(9), Epigenetics and DNA Methylation(8), Chronic Lymphocytic Leukemia Research(8)

Publications64 total

FAVORABLE LONG-TERM OUTCOMES WITH IMMUNOSUPPRESSIVE THERAPY IN CHILDREN WITH SEVERE APLASTIC ANEMIA
EJC Paediatric Oncology·2025Open Access
Cohesin RAD21 Gene Promoter Methylation in Patients with Acute Myeloid Leukemia
Life·2024· 1 citedOpen Access
Epigenetic signature of ionizing radiation in therapy-related AML patients
Heliyon·2023· 4 citedOpen Access
A CASE OF KRAS-MUTATED JMML WITH HIGH METHYLATION PROFILE AND PERPLEXED CLINICAL COURSE.
EJC Paediatric Oncology·2023Open Access
BCR:ABL-NEGATIVE MYELOPROLIFERATIVE NEOPLASMS IN CHILDREN AND ADOLESCENTS: INCREASED DISEASE BURDEN IN PATIENTS WITH JAK2 MUTATION, UNMET DIAGNOSTIC NEEDS AND OPTIMAL TREATMENT OPTIONS
EJC Paediatric Oncology·2023Open Access
IMMUNOPHENOTYPE IN SAMD9/9L SYNDROME: CORRELATIONS WITH MORPHOLOGY
EJC Paediatric Oncology·2023Open Access
THERAPY-RELATED MYELODYSPLASTIC SYNDROMES (t-MDS) IN CHILDHOOD: THE EXPERIENCE OF THE HELLENIC STUDY GROUP FOR MDS/JMML/SAA, MEMBER OF THE EWOG-MDS/SAA WORKING GROUP
EJC Paediatric Oncology·2023Open Access
A 46,XX Karyotype in Men with Infertility
Journal of Human Reproductive Sciences·2022· 6 citedOpen Access
PB1914: CYTOGENETIC FINDINGS IN 18 CHILDREN WITH MYELODYSPLASTIC SYNDROMES BY KARYOTYPIC AND FISH ANALYSIS
HemaSphere·2022Open Access
P821: LATE ONSET AND/OR LONG LASTING NEUTROPENIA IN CHILDHOOD: CLINICAL AND HEMATOLOGICAL CHARACTERISTICS AND OUTCOMES
HemaSphere·2022· 1 citedOpen Access
Epigenetic Signature of Ionising Radiation In Therapy-Related AML Patients
SSRN Electronic Journal·2022Open Access
Publisher Correction: Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes
Nature Medicine·2021· 4 citedOpen Access
Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes
Nature Medicine·2021· 161 citedOpen Access
Association of unbalanced translocation der(1;7) with germline GATA2 mutations
Blood·2021· 20 citedOpen Access
Cytogenetic findings of ectopic endometriotic tissue in women with endometriosis and review of the literature
European Journal of Obstetrics & Gynecology and Reproductive Biology·2021· 2 cited
Female Reproductive Ageing and Chromosomal Abnormalities in a Large Series of Women Undergoing IVF
Cytogenetic and Genome Research·2021· 9 cited
Identification of two novel mutations in human acute myeloid leukemia cases
Leukemia & lymphoma/Leukemia and lymphoma·2020· 2 citedOpen Access
Low-level X Chromosome Mosaicism: A Common Finding in Women Undergoing IVF
In Vivo·2020· 8 citedOpen Access
Paraoxonase 1 (PON1) Q192R and L55M Polymorphisms as Potential Predisposition Factors for Chronic Lymphocytic Leukemia
Anticancer Research·2019· 4 citedOpen Access
The lysine‐specific methyltransferase <scp>KMT</scp> 2C/ <scp>MLL</scp> 3 regulates <scp>DNA</scp> repair components in cancer
EMBO Reports·2019· 127 citedOpen Access
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Frequent Co-authors

Constantina Sambani(23), Sophia Zachaki(15), Aggeliki Daraki(13), Gabriel E. Pantelias(12), Vasileios N. Georgakakos(9), Maria Karakosta(8), Maria Pagoni(8), Chryssa Stavropoulou(8), Emmanuel Kanavakis(6), Jan Starý(5), Válerie de Haas(5), Gudrun Göhring(5), Charlotte M. Niemeyer(5), C. Stavropoulou(5), Ariadni Mavrou(5), Marina Kalomoiraki(5), Barbara De Moerloose(4), Krisztián Kállay(4), Owen Smith(4), Katerina Kakosaiou(4)