George A. Tanteles - Concepedia

Author

George A. Tanteles

Cyprus Institute of Neurology and Genetics ORCID

Also Known As

Danielle M. Andrade, Emanuela Scarano, G A Tanteles, G Tanteles, G. A. Tanteles, G. Tanteles, G.A. Tanteles, GA Tanteles, GEORGE A. TANTELES, George A. Tanteles

118

Publications

Citations

H-Index

Concepts

All Affiliations

Cyprus Institute of Neurology and Genetics Archbishop Makarios III Hospital University of Nicosia University of Leicester Limassol General Hospital

About

George A. Tanteles is an author at Cyprus Institute of Neurology and Genetics specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	19	884
2	Public Health	5	5	281
3	Engineering	2	2	56
4	Social Sciences	1	1	20
5	Molecular Biology	1	1	15

George A. Tanteles

Publications

1.3K

Citations

H-Index

Page 1

	Year	Citations
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals Yen‐Chen Anne Feng, Daniel P. Howrigan, Liam Abbott, The American Journal of Human Genetics Allelic VariantUltra-rare Genetic VariationWhole-exome Sequencing StudyGeneticsGenetic Disorder	2019	298
A genome wide association study (GWAS) providing evidence of an association between common genetic variants and late radiotherapy toxicity Gillian C. Barnett, Deborah J. Thompson, Laura Fachal, Radiotherapy and Oncology Genome-wide Association StudyLate Radiotherapy ToxicityGenotype-phenotype AssociationMedicineGenetic Epidemiology	2014	153
A replicated association between polymorphisms near TNFα and risk for adverse reactions to radiotherapy Chris J. Talbot, George A. Tanteles, Gillian C. Barnett, British Journal of Cancer	2012	70
Standardized Total Average Toxicity Score: A Scale- and Grade-Independent Measure of Late Radiotherapy Toxicity to Facilitate Pooling of Data From Different Studies Gillian C. Barnett, Catharine West, Charlotte E. Coles, International Journal of Radiation OncologyBiologyPhysics Adaptive RadiotherapyFacilitate PoolingGrade-independent MeasureRadiation MedicineOncology	2011	67
Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals Joshua E. Motelow, Gundula Povysil, Ryan S. Dhindsa, The American Journal of Human Genetics Mendelian DisorderFemale InfertilityWhole-exome Sequencing StudyGenetic DisorderGenetics	2021	58
263.4 kb deletion within the TCF4 gene consistent with Pitt–Hopkins syndrome, inherited from a mosaic parent with normal phenotype Ludmila Kousoulidou, George A. Tanteles, Maria Moutafi, European Journal of Medical Genetics Tcf4 GeneKb DeletionMendelian DisorderGenetic DisorderMedicine	2013	54
Accurate Breakpoint Mapping in Apparently Balanced Translocation Families with Discordant Phenotypes Using Whole Genome Mate-Pair Sequencing Constantia Aristidou, Costas Koufaris, Athina Theodosiou, PLoS ONE EngineeringNovo TranslocationsGeneticsLinkage AnalysisPathology	2017	41
European lipodystrophy registry: background and structure Julia von Schnurbein, Claire Adams, Giovanni Ceccarini, Orphanet Journal of Rare Diseases	2020	33
GnRH Deficient Patients With Congenital Hypogonadotropic Hypogonadism: Novel Genetic Findings in ANOS1, RNF216, WDR11, FGFR1, CHD7, and POLR3A Genes in a Case Series and Review of the Literature Vassos Neocleous, Pavlos Fanis, Meropi Toumba, Frontiers in Endocrinology	2020	32
A novel HCFC1 variant in male siblings with intellectual disability and microcephaly in the absence of cobalamin disorder Costas Koufaris, Angelos Alexandrou, George A. Tanteles, Biomedical Reports GeneticsGenetic EpidemiologyPathologyDisease Gene IdentificationGenomics	2015	31

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