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Emmanouil Kanavakis
Observed names:
E Kanavakis,
E. Kanavakis
Observed institutions:
National and Kapodistrian University of Athens,
Children's Hospital Agia Sophia,
Panagiotis & Aglaia Kyriakou Children's Hospital
OpenAlex ID:
A5112066569
The lysine‐specific methyltransferase KMT2C/MLL3 regulates DNA repair components in cancer
2019
·
Theodoros Rampias
, Dimitris Karagiannis
, et al.
·
EMBO Reports
·
135
Melanocortin Receptor-1 Gene Polymorphisms and the Risk of Cutaneous Melanoma in a Low-Risk Southern European Population
2006
·
Alexander J. Stratigos
, Gerasimos Dimisianos
, et al.
·
Journal of Investigative Dermatology
·
99
Diagnostic Exome Sequencing to Elucidate the Genetic Basis of Likely Recessive Disorders in Consanguineous Families
2014
·
Periklis Makrythanasis
, Mari Nelis
, et al.
·
Human Mutation
·
87
PDF
De novo interstitial duplication of the 15q11.2‐q14 PWS/AS region of maternal origin: Clinical description, array CGH analysis, and review of the literature
2010
·
Sophia Kitsiou‐Tzeli
, Maria Tzetis
, et al.
·
American Journal of Medical Genetics Part A
·
75
Clinical manifestations in 17 Greek patients with Goldenhar syndrome.
2006
·
V Touliatou
, H Fryssira
, et al.
·
PubMed
·
60
Diabetic neuropathy in children and adolescents with type 1 diabetes mellitus: Diagnosis, pathogenesis, and associated genetic markers
2019
·
Dimitra Kallinikou
, Alexandra Soldatou
, et al.
·
Diabetes/Metabolism Research and Reviews
·
56
Association of repeat polymorphisms in the estrogen receptors alpha, beta (ESR1, ESR2) and androgen receptor (AR) genes with the occurrence of breast cancer
2007
·
A. Tsezou
, M. Tzetis
, et al.
·
The Breast
·
42
Detection of 22q11.2 deletion among 139 patients with Di George/Velocardiofacial syndrome features.
2004
·
S Kitsiou-Tzeli
, A Kolialexi
, et al.
·
PubMed
·
41
Association ofMMP-1-1607 1G/2G (rs1799750) polymorphism with primary knee osteoarthritis in the Greek population
2014
·
Panagiotis Lepetsos
, Andreas Pampanos
, et al.
·
Journal of Orthopaedic Research®
·
26
PDF
The interaction of α° thalassaemia with Hb Icaria: three unusual cases of haemoglobinopathy H
1996
·
E. Kanavakis
, J. Traeger‐Synodinos
, et al.
·
British Journal of Haematology
·
21
Severe hypertriglyceridaemia in diabetic ketoacidosis: clinical and genetic study
2004
·
C. Karagianni
, S. Stabouli
, et al.
·
Diabetic Medicine
·
20
GILBERT SYNDROME ASSOCIATED WITH β-THALASSEMIA
2001
·
M. Tzetis
, E. Kanavakis
, et al.
·
Pediatric Hematology and Oncology
·
19
Impact of cytogenetic and molecular cytogenetic studies on hematologic malignancies.
2005
·
A Kolialexi
, G Th Tsangaris
, et al.
·
PubMed
·
17
Synthesized allosteric effectors of the hemoglobin molecule: a possible mechanism for improved erythrocyte oxygen release capability in hemoglobinopathy H disease.
1998
·
I Papassotiriou
, J Kister
, et al.
·
PubMed
·
10
Association of NADPH oxidase p22phox gene C242T, A640G and −930A/G polymorphisms with primary knee osteoarthritis in the Greek population
2013
·
Panagiotis Lepetsos
, Andreas Pampanos
, et al.
·
Molecular Biology Reports
·
9
Unilateral microtia in an infant with trisomy 18 mosaicism.
2009
·
E Giannatou
, H Leze
, et al.
·
PubMed
·
8
Steroid hormones polymorphisms and cholelithiasis in Greek population
2006
·
S. Kitsiou‐Tzeli
, E. Giannatou
, et al.
·
Liver International
·
8
A variant of uncertain significance of the HMGA2 gene in a child with Silver-Russell syndrome-like phenotype: a case report
2024
·
Evangelos Bourousis
, Maria Xatzipsalti
, et al.
·
HORMONES
·
3
Retrocollis as the cardinal feature in a de novo ITRP1 variant
2022
·
Athena Zachou
, Danai Palaiologou
, et al.
·
Brain and Development
·
3
Homozygosity of the Z‐2 polymorphic variant in the aldose reductase gene promoter confers increased risk for neuropathy in children and adolescents with Type 1 diabetes
2021
·
Dimitra Kallinikou
, Charalampos Tsentidis
, et al.
·
Pediatric Diabetes
·
3
Application of high-resolution array comparative genomic hybridization in children with unknown syndromic microcephaly
2017
·
Eirini Tsoutsou
, Maria Tzetis
, et al.
·
Pediatric Research
·
2
Jérôme Lejeune (1926-1994): father of modern genetics.
2012
·
Marianna Karamanou
, Emmanouil Kanavakis
, et al.
·
PubMed
·
2
PDF
The Effect of 5-Azacitidine Treatment on the Biologic Characteristics of Bone Marrow Mesenchymal Stem Cells in Patients with Myelodysplastic Syndromes
2017
·
Ioannis Liapis
, Aristea Batsali
, et al.
·
Blood
·
1
Feasibility of Neonatal Wilson Disease Screening by Mutation Analysis
2005
·
G Loudianos
, A Zappu
, et al.
·
Journal of Pediatric Gastroenterology and Nutrition
·
1
PDF
#925 Genotyping and phenotyping early and very early autosomal dominant polycystic kidney disease onset
2025
·
Maria Varveri
, Myrto Kostopoulou
, et al.
·
Nephrology Dialysis Transplantation
PDF
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Works count:
36
Citation count:
748
H-index:
13
I10-index:
14
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