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Lamiya Aliyeva

Observed names: ALİYEVA, LAMİYA, Aliyeva, Lamiya, Alıyeva, Lamiya, L Aliyeva, LAMIYA ALIYEVA, Lamiya ALİYEVA, Lamiya Aliyeva Cavit
ORCID: 0000-0001-9436-9279
Observed ORCID: 0000-0001-9436-9279
OpenAlex ID: A5018937345
Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium
2022 · Munis Dundar, Umut Fahrioglu, et al. · Functional & Integrative Genomics · 20
BRCA Variations Risk Assessment in Breast Cancers Using Different Artificial Intelligence Models
2021 · Niyazi Senturk, Gulten Tuncel, et al. · Genes · 11
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Genotype and Phenotype Correlation of Patients with Osteogenesis Imperfecta
2024 · Lamiya Aliyeva, Yasemin Denkboy Ongen, et al. · Journal of Molecular Diagnostics · 10
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Frequency of germline pathogenic variants in breast cancer predisposition genes among young Turkish breast cancer patients
2023 · Aysun Dauti Isiklar, Lamiya Aliyeva, et al. · Breast Cancer Research and Treatment · 3
Frequency and Distribution of MEFV Gene Mutation in Familial Mediterranean Fever Patients: A Single Center Experience
2020 · Şebnem ÖZEMRİ SAĞ, Adem ALEMDAR, et al. · SDÜ Tıp Fakültesi Dergisi · 1
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The Development of a Fuzzy Logic System Using MATLAB for Early Detection of Hereditary Cancer in BRCA1/2 Negative Cases
2025 · N Senturk, GP Volkan, et al. · Balkan Journal of Medical Genetics
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ITGB4-Related pyloric atresia without epidermolysis in two siblings
2024 · Lamiya Aliyeva, Serdar Beken, et al. · European Journal of Medical Genetics
Kalıtsal meme kanserinde multigen panel test analizlerinin retrospektif olarak değerlendirilmesi
2022 · Lamiya Aliyeva Cavit, Selin Ekiz, et al. · EURASIAN JOURNAL OF CLINICAL SCIENCES
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Bilgisayar-Tabanlı Bulanık Mantık Yöntemi Kullanılarak Brca-Negatif Kalıtsal eme Kanseri Klinik Ve Varyant Risk Değerlendirmesi
2021 · TEMEL, ŞEHİME GÜLSÜN, ÖZEMRİ SAĞ, ŞEBNEM, et al. · Bursa Uludag University - AVESIS
Germline landscape of BRCAs by 7-site collaborations as a BRCA consortium in Turkey
2021 · Doğan, Berkcan, Alemdar, Adem, et al. · Bursa Uludag University - AVESIS
Kedi Miyavlama Sendromu
2020 · BODUR, MUHİTTİN, OKAN, MEHMET SAİT, et al. · Bursa Uludag University - AVESIS
Diagnostic Efficiency of Clinical Exome Solution Panel in patients with Hearing loss/Hereditary Deafness by using Next Generation Sequencing
2020 · Şehime Gülsün Temel, Adem Alemdar, et al. · Bursa Uludag University - AVESIS
Osteogenezis imperfekta tanılı hastaların genotip ve fenotip korelasyonu
2020 · LAMIYA ALIYEVA · Bursa Uludag University - AVESIS
Next generation sequencing-based gene panel tests for the diagnosis of hereditary cancers
2019 · PİRİM, DİLEK, UZ YILDIRIM, ELİF, et al. · Bursa Uludag University - AVESIS
Molecular diagnosis of connective tissue disorders using targeted gene panel screening
2019 · PİRİM, DİLEK, UZ YILDIRIM, ELİF, et al. · Bursa Uludag University - AVESIS
Genetic evaluation of the CFTR gene and comprehensive analysis of the sequence
2019 · PİRİM, DİLEK, UZ YILDIRIM, ELİF, et al. · Bursa Uludag University - AVESIS
Identification of BRCA1/2 Variants via Next Generation Sequencing for Therapeutic Approach
2019 · Uz Yıldırım, Elif, Pirim, DİLEK, et al. · Bursa Uludag University - AVESIS
A rare case report of SMARD1 (SPINAL MUSCULAR ATROPHY WITH RESPIRATORY DISTRESS 1 syndrome.
2019 · TEMEL, ŞEHİME GÜLSÜN, ÖZEMRİ SAĞ, ŞEBNEM, et al. · Bursa Uludag University - AVESIS
Osteogenezis imperfekta ön tanılı hastaların hedefe yönelik gen paneli kullanilarak yeni nesil tekniği ile dizilenmesi
2019 · PİRİM, DİLEK, UZ YILDIRIM, ELİF, et al. · Bursa Uludag University - AVESIS
A case with a de novoheterozygote ACTG1 variant:Genotype-phenotype correlation
2019 · ÖZEMRİ SAĞ, ŞEBNEM, TEMEL, ŞEHİME GÜLSÜN, et al. · Bursa Uludag University - AVESIS
Identification and analysis of novel variants associated with breast and ovarian cancer in BRCA1 and BRCA2 Genes
2018 · PİRİM, DİLEK, UZ YILDIRIM, ELİF, et al. · Bursa Uludag University - AVESIS
Screening of common and novel variants in the MEFV Gene in patients with familial mediterranean fever (FMF) symptoms by using next generation sequencing
2018 · UZ YILDIRIM, ELİF, PİRİM, DİLEK, et al. · Bursa Uludag University - AVESIS
Lysinuric protein intolerance and HOIP deficiency in a boy: SLCA7A and RNF31 gene disruptions
2018 · Lamiya Aliyeva, Sahin Erdol, et al. · Journal of Biotechnology
Works count: 23
Citation count: 45
H-index: 3
I10-index: 3
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