Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals E Collaborative American Journal of Human Genetics 105 (2), 267-282, 2019 | 230 | 2019 |
A cross-disorder dosage sensitivity map of the human genome E collaborative Cell 185 (16), 3041-3055, 2022 | 151 | 2022 |
Polygenic burden in focal and generalized epilepsies E Collaborative Brain 142 (11), 3473-3481, 2019 | 112 | 2019 |
Predicting functional effects of missense variants in voltage-gated sodium and calcium channels E Collaborative Science Translational Medicine 12 (556), 2020 | 98 | 2020 |
Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy. ST Møller RS, Weber YG, Klitten LL, Trucks H, Muhle H, Kunz WS, Mefford HC ... Epilepsia 54 (12), 2232, 2013 | 74* | 2013 |
Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects E Collaborative Brain 143 (7), 2106-2118, 2020 | 52* | 2020 |
Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies. Epilepsia 53 (2), 308-18, 2012 | 47 | 2012 |
Fresh tissue parathyroid allotransplantation with short‐term immunosuppression: one year follow‐up E Yucesan, B Goncu, H Basoglu, N Ozten Kandas, YE Ersoy, F Akbas, ... Clinical Transplantation, 2017 | 25 | 2017 |
Microencapsulated parathyroid allotransplantation in the omental tissue E Yucesan, H Basoglu, B Goncu, F Akbas, YE Ersoy, E Aysan Artificial Organs 43 (10), 1022-1027, 2019 | 19 | 2019 |
Biallelic loss of EEF1D function links heat shock response pathway to autosomal recessive intellectual disability SA Ugur Iseri, E Yucesan, FN Tuncer, M Calik, Y Kesim, G Altiokka Uzun, ... Journal of Human Genetics 64 (5), 421-426, 2019 | 15 | 2019 |
A new transport solution for parathyroid allotransplantation: effects on cell viability and calcium-sensing receptors B Goncu, E Yucesan, B Ozdemir, H Basoglu, NO Kandas, F Akbas, ... Biopreservation and biobanking 16 (4), 278-284, 2018 | 14 | 2018 |
Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span D Yücel-Yılmaz, E Yücesan, D Yalnızoğlu, KK Oğuz, MŞ Sağıroğlu, ... Brain and Development 40 (6), 458-464, 2018 | 14 | 2018 |
Biallelic loss of TRAPPC9 function links vesicle trafficking pathway to autosomal recessive intellectual disability AD Aslanger, B Goncu, OF Duzenli, E Yucesan, E Sengenc, G Yesil Journal of Human Genetics 67 (5), 279-284, 2022 | 13 | 2022 |
Investigating differential miRNA expression profiling using serum and urine specimensfor detecting potential biomarkers for early prostate cancer diagnosis S Hasanoğlu, BS Göncü, E Yücesan, S Atasoy, Y Kayali, NÖ Kandaş Turkish journal of medical sciences 51 (4), 1764-1774, 2021 | 13 | 2021 |
Importance of HLA typing, PRA and DSA tests for successful parathyroid allotransplantation E Yucesan, B Goncu, B Ozdemir, O Idiz, YE Ersoy, E Aysan Immunobiology 224 (4), 485-489, 2019 | 12 | 2019 |
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture ILAECC Epilepsies Nature Genetics, 2023 | 11 | 2023 |
Discharging a patient treated with parathyroid allotransplantation after having been hospitalized for 3.5 years with permanent hypoparathyroidism: a case report E Aysan, E Yucesan, UO Idiz, B Goncu Transplantation Proceedings 51 (9), 3186-3188, 2019 | 11 | 2019 |
SYNE1 related cerebellar ataxia presents with variable phenotypes in a consanguineous family from Turkey E Yucesan, SA Ugur Iseri, B Bilgic, Z Gormez, B Bakir Gungor, A Sarac, ... Neurological Sciences 38, 2203-2207, 2017 | 11 | 2017 |
Screening LGI1 in a cohort of 26 lateral temporal lobe epilepsy patients with auditory aura from Turkey detects a novel de novo mutation YF Kesim, GA Uzun, E Yucesan, FN Tuncer, O Ozdemir, N Bebek, ... Epilepsy Research 120, 73-78, 2016 | 11 | 2016 |
Distinct gene-set burden patterns underlie common generalized and focal epilepsies E Collaborative EBioMedicine 72 (103588), 2021 | 10 | 2021 |