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Büşra Aynekin

Observed names: Aynekin, Buşra, Aynekin, Büşra, B. Aynekin, Busra Aynekin, Buşra Aynekin
Observed institutions: The Francis Crick Institute, Biruni University, UCL Queen Square Institute of Neurology, University College London, Turgut Özal University, University of Genoa, Erciyes University
ORCID: 0000-0001-9152-9783
Observed ORCID: 0000-0001-9152-9783
OpenAlex ID: A5083551361
The Investigation of a Disintegrin and Metalloproteinase with ThromboSpondin Motifs (ADAMTS) 1, 5 and 16 in Thoracic Aortic Aneurysms and Dissections
2016 · Mahmut Gunes, Mehmet Akpinar, et al. · Clinical Laboratory · 24
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
The effect of cytokine leukemia-inhibitory factor (LIF) and interleukin-11 (IL-11) gene expression on the primary infertility related to polycystic ovary syndrome, Tubal factor, and Unexplained infertility in Turkish women
2021 · Zahraa Alzaidi, Şule Menziletoğlu Yildiz, et al. · Egyptian Journal of Medical Human Genetics · 13
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COVID-19 vaccine candidates and vaccine development platforms available worldwide
2021 · Nilgun Duman, Zahraa ALzaidi, et al. · Journal of Pharmaceutical Analysis · 13
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Differentially regulated ADAMTS1, 8, and 18 in gastric adenocarcinoma
2017 · M. O. Kilic, B. Aynekin, et al. · Bratislavské lekárske listy/Bratislava medical journal · 13
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Differentially regulated ADAMTS1, 8, 9, and 18 in pancreas adenocarcinoma
2017 · Murat Özgür Kılıç, Büşra Aynekin, et al. · Gastroenterology Review · 11
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Expanding the Mutational Landscape and Clinical Phenotype of CHD2-Related Encephalopathy
2024 · Angela Clara-Hwang, Stefani Stefani, et al. · Neurology Genetics · 7
Loss of TBC1D2B causes a progressive neurological disorder with gingival overgrowth
2024 · Frederike L. Harms, Jessica Erin Rexach, et al. · European Journal of Human Genetics · 5
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Biallelic variants in ARHGAP19 cause a progressive inherited motor-predominant neuropathy
2025 · Natalia Dominik, Stephanie Efthymiou, et al. · Journal of Clinical Investigation · 3
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Phenotypic variability in progressive encephalopathy with brain atrophy and thin corpus callosum: insights from two families
2025 · Busra Aynekin, Sinan Akbaş, et al. · Neurogenetics · 3
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Novel VARS1 variants define new clinical and molecular subtypes of a rare neurodevelopmental syndrome
2026 · Busra Aynekin, Tracy Lau, et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 1
Novel PIBF1 Pathogenic Variant in Three Siblings with Joubert Syndrome Type 33
2024 · Busra Aynekin, Bahadır M. Samur, et al. · Molecular Syndromology · 1
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Biomarker potential of the GRP78 cell-free RNA in endometrial cancer
2022 · Busra Aynekin, Hilal Akalin, et al. · Egyptian Journal of Medical Human Genetics · 1
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Immunohistochemical Determination of HIF, TSP-1, ADAMTS1, and ADAMTS8 Expressions in the Brains of Alzheimer’s Disease Patients: A Preliminary Autopsy Study
2016 · Nursel Turkmen Inanir, Filiz Eren, et al. · Journal of Clinical Practice and Research · 1
Anti-CASPR2 antibody associated Morvan syndrome in adolescents: dramatic response to immunotherapy: a case series
2026 · Busra Aynekin, Stephanie Efthymiou, et al. · Brain and Development
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“Severe intellectual disability with cardiac and dermatologic involvement due to homozygous METTL23 frameshift mutation: a case report of two Turkish sisters”
2026 · Mücahid Besnek, Büşra Aynekin, et al. · Neurological Sciences
Corrigendum to “Novel VARS1 variants define new clinical and molecular subtypes of a rare neurodevelopmental syndrome” [Biochim. Biophys. Acta Mol. Basis Dis. 1872 (2026)/168184]
2026 · Busra Aynekin, Tracy Lau, et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
L-DOPA in diurnal fluctuating dystonia: two different clinical presentations, one treatment
2025 · Beyza Karataş, Ayten Güleç, et al. · Neurogenetics
Nadir Hastalıklarda Biyoteknolojik Tedaviler
2021 · Fırat Özçelik, Abdulbaki Yildirim, et al. · Turkiye Klinikleri Medical Genetics - Special Topics
Importance of ?²-APP, ADAM9, 10, 17 in Alzheimer Disease: Preliminary Autopsy Study with Immunohistochemical Expression in Human Brain
2019 · Filiz Eren, Nursel Turkmen Inanır, et al. · Bursa Uludag University - AVESIS
Investigation of autophagy, apoptosis, and er stress markers in acute appendicitis pathogenesis
2015 · Aynekin, Büşra · Malatya Turgut Özal University Institutional Repository
İmmünohistokimyasal metod ile Alzhelmer hastaları beyin dokularında HF-1, TSP-1, ADAMTS1, ADAMTS8 ekspresyonlarının incelenmesi: Prelimer otopsi çalışması
2014 · TÜRKMEN İNANIR, NURSEL, FEDAKAR, RECEP, et al. · Bursa Uludag University - AVESIS
Works count: 25
Citation count: 116
H-index: 7
I10-index: 6
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