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Elanur Yilmaz
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引用次数
引用次数
年份
Exome sequencing in routine diagnostics: a generic test for 254 patients with primary immunodeficiencies
P Arts, A Simons, MS AlZahrani, E Yilmaz, E AlIdrissi, KJ Van Aerde, ...
Genome medicine 11 (1), 1-15, 2019
692019
Recent advances in craniosynostosis
E Yilmaz, E Mihci, B Nur, ÖM Alper, Ş Taçoy
Pediatric neurology 99, 7-15, 2019
522019
Consequences of the increasing prevalence of the poisonous Lagocephalus sceleratus in southern Turkey
AB Beköz, S Beköz, E Yilmaz, S Tüzün, Ü Beköz
Emergency medicine journal 30 (11), 954-955, 2013
302013
MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss
G Bademci, C Abad, A Incesulu, A Rad, O Alper, SM Kolb, FB Cengiz, ...
Human genetics 137 (6), 479-486, 2018
242018
Copy number variation and regions of homozygosity analysis in patients with MÜLLERIAN aplasia
DD Eksi, Y Shen, M Erman, LP Chorich, ME Sullivan, M Bilekdemir, ...
Molecular cytogenetics 11 (1), 1-8, 2018
182018
A novel AXIN2 gene mutation in sagittal synostosis
E Yilmaz, E Mihci, B Guzel Nur, OM Alper
American Journal of Medical Genetics Part A 176 (9), 1976-1980, 2018
162018
Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen storage-associated mitochondriopathy
HH Wong, SH Seet, M Maier, A Gurel, RM Traspas, C Lee, S Zhang, ...
The American Journal of Human Genetics, 2021
132021
Perinatal diagnostic approach to fetal skeletal dysplasias: six years experience of a tertiary center
HS Toru, BG Nur, CY Sanhal, E Mihci, İ Mendilcioğlu, E Yilmaz, GT Yilmaz, ...
Fetal and pediatric pathology 34 (5), 287-306, 2015
122015
Nerve growth factor receptor (Ngfr) induces neurogenic plasticity by suppressing reactive astroglial Lcn2/Slc22a17 signaling in Alzheimer’s disease
T Siddiqui, MI Cosacak, S Popova, P Bhattarai, E Yilmaz, AJ Lee, Y Min, ...
NPJ Regenerative Medicine 8 (1), 33, 2023
82023
Novel Gene Variants Associated with Primary Ciliary Dyskinesia
D Demir Eksi, E Yilmaz, AE Basaran, G Erduran, B Nur, E Mihci, ...
Indian Journal of Pediatrics, 1-10, 2022
72022
Clinical and genetic findings of two cases with Apert syndrome
F Cammarata-Scalisi, E Yilmaz, M Callea, A Avendaño, E Mıhçı, OM Alper
Boletín médico del Hospital Infantil de México 76 (1), 44-48, 2019
72019
Rare genetic variation in fibronectin 1 (FN1) protects against APOEε4 in Alzheimer’s disease
P Bhattarai, TI Gunasekaran, ME Belloy, D Reyes-Dumeyer, D Jülich, ...
Acta Neuropathologica 147 (1), 1-20, 2024
32024
SNUPN deficiency causes a recessive muscular dystrophy due to RNA mis-splicing and ECM dysregulation
M Nashabat, N Nabavizadeh, HP Saraçoğlu, B Sarıbaş, Ş Avcı, E Börklü, ...
Nature Communications 15 (1), 1758, 2024
22024
Hipertansiyonda D Vitamini ile İlişkili Genetik Polimorfizmlerin Rolü
GÜL ÖZBEY, E YILMAZ, S DALAKLIOĞLU, Ö ALPER
MN Kardiyoloji 24 (1), 42-49, 2017
22017
Association Between Cystic Fibrosis Severity Markers and CFTR Genotypes in Turkish Children
AE Başaran, A Başaran, DFK Uygun, E Yılmaz, A Moballegh, L Öz, ...
infection 10, 11, 2021
12021
Coronal craniosynostosis due to TCF12 mutations in patients from Turkey
E Yilmaz, E Mihci, B Nur, OM Alper
American Journal of Medical Genetics Part A 179 (11), 2241-2245, 2019
12019
MU-BRAIN: MUltiethnic Brain Rna-seq for Alzheimer INitiative
Z Yang, B Cieza, D Reyes-Dumeyer, A Lee, Y Ma, E Yilmaz, R Lantigua, ...
bioRxiv, 2024.02. 20.581250, 2024
2024
ABCA7-dependent Neuropeptide-Y signalling is a resilience mechanism required for synaptic integrity in Alzheimer's disease
H Tayran, E Yilmaz, P Bhattarai, Y Min, X Wang, Y Ma, N Nelson, ...
bioRxiv, 2024.01. 02.573893, 2024
2024
Rare genetic variation in Fibronectin 1 (FN1) protects against APOEe4 in Alzheimer's disease
P Bhattarai, TI Gunasekaran, D Reyes-Dumeyer, D Jülich, H Tayran, ...
bioRxiv, 2024.01. 02.573895, 2024
2024
Functional investigation of the gliovascular niche‐related genes and their relevance to Alzheimer’s disease pathomechanisms in zebrafish
P Bhattarai, MI Cosacak, AJ Lee, E Yilmaz, O Is, X Wang, BN Vardarajan, ...
Alzheimer's & Dementia 19, e073812, 2023
2023
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