| Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5 MJ McMillin, AE Beck, JX Chong, KM Shively, KJ Buckingham, ... The American Journal of Human Genetics 94 (5), 734-744, 2014 | 214 | 2014 |
| Preclinical safety evaluation of intravitreal injection of full-length humanized vascular endothelial growth factor antibody in rabbit eyes UU Inan, B Avci, T Kusbeci, B Kaderli, R Avci, SG Temel Investigative ophthalmology & visual science 48 (4), 1773-1781, 2007 | 173 | 2007 |
| European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death F Fellmann, CG Van El, P Charron, K Michaud, HC Howard, SN Boers, ... European Journal of Human Genetics 27 (12), 1763-1773, 2019 | 106 | 2019 |
| Arterial tortuosity syndrome: 40 new families and literature review. Genetics in Medicine, 2018 | 101 | 2018 |
| Bi-allelic mutations in M1AP are a frequent cause of meiotic arrest and severely impaired spermatogenesis leading to male infertility MJ Wyrwoll, ŞG Temel, L Nagirnaja, MS Oud, AM Lopes, ... The American Journal of Human Genetics 107 (2), 342-351, 2020 | 79 | 2020 |
| Effects of citicoline used alone and in combination with mild hypothermia on apoptosis induced by focal cerebral ischemia in rats S Sahin, T Alkan, SG Temel, K Tureyen, S Tolunay, E Korfali Journal of Clinical Neuroscience 17 (2), 227-231, 2010 | 61 | 2010 |
| A new material for prevention of epidural fibrosis after laminectomy: oxidized regenerated cellulose (interceed), an absorbable barrier SG Temel, C Ozturk, A Temiz, S Ersozlu, U Aydinli Clinical Spine Surgery 19 (4), 270-275, 2006 | 57 | 2006 |
| Aven blocks DNA damage-induced apoptosis by stabilising Bcl-xL O Kutuk, SG Temel, S Tolunay, H Basaga European journal of cancer 46 (13), 2494-2505, 2010 | 54 | 2010 |
| Expression of estrogen receptor-α and cFos in norepinephrine and epinephrine neurons of young and middle-aged rats during the steroid-induced luteinizing hormone surge S Temel, W Lin, S Lakhlani, L Jennes Endocrinology 143 (10), 3974-3983, 2002 | 53 | 2002 |
| Extended Pedigree with Multiple Cases of XX Sex Reversal in the Absence of SRY and of a Mutation at the SOX9 Locus SG Temel, T Gulten, T Yakut, H Saglam, N Kilic, E Bausch, WJ Jin, ... Sexual Development 1 (1), 24-34, 2006 | 49 | 2006 |
| Cyclooxygenase-2 expression in astrocytes and microglia in human oligodendroglioma and astrocytoma SG Temel, Z Kahveci Journal of molecular histology 40, 369-377, 2009 | 36 | 2009 |
| Strong association between VDR FokI (rs2228570) gene variant and serum vitamin D levels in Turkish Cypriots G Tuncel, SG Temel, MC Ergoren Molecular biology reports 46 (3), 3349-3355, 2019 | 33 | 2019 |
| Impact of SARS-CoV-2 infection and COVID-19 on patients with inborn errors of immunity SG Tangye, L Abel, S Al-Muhsen, A Aiuti, S Al-Muhsen, F Al-Mulla, ... Journal of Allergy and Clinical Immunology 151 (4), 818-831, 2023 | 30 | 2023 |
| Evaluation of bioaccessibility and functional properties of kombucha beverages fortified with different medicinal plant extracts CE Tamer, ŞG TEMEL, S Suna, AÖ KARABACAK, T ÖZCAN, LY ERSAN, ... Turkish Journal of Agriculture and Forestry 45 (1), 13-32, 2021 | 30 | 2021 |
| Biphasic ROS production, p53 and BIK dictate the mode of cell death in response to DNA damage in colon cancer cells. BH Kutuk O, Aytan N, Karakas B, Kurt AG, Acikbas U, Temel SG Plos One 12 (8), 2017 | 26 | 2017 |
| Localization of serotonin 5-HT7-receptor immunoreactivity in the rat brain MJ Duncan, S Temel, L Jennes Soc Neurosci Abstr 380, 18, 2001 | 20 | 2001 |
| University of Washington Center for Mendelian Genomics Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5 MJ McMillin, AE Beck, JX Chong, KM Shively, KJ Buckingham, ... Am. J. Hum. Genet 94, 734-744, 2014 | 18 | 2014 |
| The association between the chromosome 9p21 CDKN2B-AS1 gene variants and the lipid metabolism: A pre-diagnostic biomarker for coronary artery disease. ŞG Temel, MÇ Ergören Anatolian Journal of Cardiology/Anadolu Kardiyoloji Dergisi 21 (1), 2019 | 17 | 2019 |
| A Novel TBX19 Gene Mutation in a Case of Congenital Isolated Adrenocorticotropic Hormone Deficiency Presenting with Recurrent Respiratory Tract Infections N Akcan, N Serakıncı, B Turkgenc, R Bundak, N Bahceciler, SG Temel Frontiers in endocrinology 8, 64, 2017 | 17 | 2017 |
| A simple and rapid microwave-assisted hematoxylin and eosin staining method using 1, 1, 1 trichloroethane as a dewaxing and a clearing agent SG Temel, S Noyan, I Cavusoglu, Z Kahveci Biotechnic & Histochemistry 80 (3-4), 123-132, 2005 | 17 | 2005 |
Mahmut Cerkez ErgorenNear East University Hospital, Head of the Laboratory of Medical Genetic DiagnosticsVerified email at neu.edu.tr
