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George A. Tanteles

Observed names: G A Tanteles, G Tanteles, G. A. Tanteles, G. Tanteles, G.A. Tanteles, GA Tanteles, GEORGE A. TANTELES, George A Tanteles, George Tanteles, Tanteles, George, Tanteles, George A.
Observed institutions: Nottingham University Hospitals NHS Trust, University of Leicester, Philipps University of Marburg, University of Nicosia, Leicester Royal Infirmary, Nicosia General Hospital, University Hospitals of Leicester NHS Trust, Nottingham City Hospital, Centre for Life, Christian-Albrechts-Universität zu Kiel, City Hospital, Goldfinch Bio (United States), Queen's Medical Centre, Hertie Institute for Clinical Brain Research, Archbishop Makarios III Hospital, Derby Hospitals NHS Foundation Trust, The Cyprus Institute of Neurology & Genetics - Postgraduate Education, Cyprus Institute of Neurology and Genetics, University of Tübingen
ORCID: 0000-0002-8117-9852
Observed ORCID: 0000-0002-8117-9852
OpenAlex ID: A5017884591
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals
2019 · Yen-Chen Anne Feng, Daniel P. Howrigan, et al. · The American Journal of Human Genetics · 283
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GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture
2023 · Remi Stevelink, Ciarán Campbell, et al. · Nature Genetics · 224
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A genome wide association study (GWAS) providing evidence of an association between common genetic variants and late radiotherapy toxicity
2014 · Gillian C. Barnett, Deborah Thompson, et al. · Radiotherapy and Oncology · 151
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes
2024 · Epi25 Collaborative, Siwei Chen, et al. · Nature Neuroscience · 88
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Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects
2020 · Lisa-Marie Niestroj, Eduardo Perez-Palma, et al. · Brain · 80
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A replicated association between polymorphisms near TNFα and risk for adverse reactions to radiotherapy
2012 · C J Talbot, G A Tanteles, et al. · British Journal of Cancer · 73
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Standardized Total Average Toxicity Score: A Scale- and Grade-Independent Measure of Late Radiotherapy Toxicity to Facilitate Pooling of Data From Different Studies
2011 · Gillian C. Barnett, Catharine M.L. West, et al. · International Journal of Radiation Oncology*Biology*Physics · 69
7q11.23 Microduplication: a recognizable phenotype
2012 · A Dixit, S McKee, et al. · Clinical Genetics · 66
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals
2023 · Ludovica Montanucci, David Lewis-Smith, et al. · Nature Communications · 56
Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals
2021 · Joshua E. Motelow, Gundula Povysil, et al. · The American Journal of Human Genetics · 53
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263.4 kb deletion within the TCF4 gene consistent with Pitt–Hopkins syndrome, inherited from a mosaic parent with normal phenotype
2013 · Ludmila Kousoulidou, George Tanteles, et al. · European Journal of Medical Genetics · 53
Accurate Breakpoint Mapping in Apparently Balanced Translocation Families with Discordant Phenotypes Using Whole Genome Mate-Pair Sequencing
2017 · Constantia Aristidou, Costas Koufaris, et al. · PLoS ONE · 41
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Natural history of KBG syndrome in a large European cohort
2022 · Lorenzo Loberti, Lucia Pia Bruno, et al. · Human Molecular Genetics · 37
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European lipodystrophy registry: background and structure
2020 · Julia von Schnurbein, Claire Adams, et al. · Orphanet Journal of Rare Diseases · 35
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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
2020 · Vassos Neocleous, Pavlos Fanis, et al. · Frontiers in Endocrinology · 34
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Biallelic loss-of-function variants in PLD1 cause congenital right-sided cardiac valve defects and neonatal cardiomyopathy
2021 · Najim Lahrouchi, Alex V. Postma, et al. · Journal of Clinical Investigation · 31
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A novel HCFC1 variant in male siblings with intellectual disability and microcephaly in the absence of cobalamin disorder
2015 · COSTAS KOUFARIS, ANGELOS ALEXANDROU, et al. · Biomedical Reports · 29
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Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With KCNC2 Pathogenic Variants
2022 · Niklas Schwarz, Simone Seiffert, et al. · Neurology · 26
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Surveillance and monitoring in vascular Ehlers-Danlos syndrome in European Reference Network For Rare Vascular Diseases (VASCERN)
2022 · Ingrid M.B.H. van de Laar, Annette F. Baas, et al. · European Journal of Medical Genetics · 21
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Variation in Telangiectasia Predisposing Genes Is Associated With Overall Radiation Toxicity
2012 · George A. Tanteles, Robert J.S. Murray, et al. · International Journal of Radiation Oncology*Biology*Physics · 21
Mowat-Wilson syndrome: growth charts
2020 · Ivan Ivanovski, Olivera Djuric, et al. · Orphanet Journal of Rare Diseases · 20
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Epidemiology of ATTRV30M neuropathy in Cyprus and the modifier effect of complement C1q on the age of disease onset
2018 · Savanna Andreou, Elena Panayiotou, et al. · Amyloid · 20
Pathogenic and Low-Frequency Variants in Children With Central Precocious Puberty
2021 · Vassos Neocleous, Pavlos Fanis, et al. · Frontiers in Endocrinology · 19
Epidemiology of Huntington disease in Cyprus: A 20‐year retrospective study
2017 · C.A. Demetriou, A. Heraclides, et al. · Clinical Genetics · 19
Open-Label Fosmetpantotenate, a Phosphopantothenate Replacement Therapy in a Single Patient with Atypical PKAN
2017 · Yiolanda-Panayiota Christou, George A. Tanteles, et al. · Case Reports in Neurological Medicine · 19
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Works count: 131
Citation count: 2,105
H-index: 20
I10-index: 49
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