Takip et
Emrah Yucesan
Emrah Yucesan
Istanbul University-Cerrahpasa, Institute of Neurological Sciences, Department of Neurogenetics
iuc.edu.tr üzerinde doğrulanmış e-posta adresine sahip - Ana Sayfa
Başlık
Alıntı yapanlar
Alıntı yapanlar
Yıl
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
2302019
A cross-disorder dosage sensitivity map of the human genome
E collaborative
Cell 185 (16), 3041-3055, 2022
1512022
Polygenic burden in focal and generalized epilepsies
E Collaborative
Brain 142 (11), 3473-3481, 2019
1122019
Predicting functional effects of missense variants in voltage-gated sodium and calcium channels
E Collaborative
Science Translational Medicine 12 (556), 2020
982020
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
472012
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
252017
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
192019
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
152019
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
142018
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
142018
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
132022
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
132021
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
122019
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture
ILAECC Epilepsies
Nature Genetics, 2023
112023
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
112019
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
112017
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
112016
Distinct gene-set burden patterns underlie common generalized and focal epilepsies
E Collaborative
EBioMedicine 72 (103588), 2021
102021
Sistem, işlemi şu anda gerçekleştiremiyor. Daha sonra yeniden deneyin.
Makaleler 1–20