Mahmut Çerkez Ergoren (M C Ergoren, Mahmut Çerkez Ergören, Mahmut Cerkez Ergoren, Mahmut C Ergoren)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 32

Top Venues

Global medical genetics

Biomedicines

Journal of clinical medicine

Genes

University of Leicester (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

University of Leicester

United Kingdom

PHD :: Genetics

Publications

Aya Badeea Ismail, Özlem Balcıoğlu, Barçın Özcem, Mahmut Çerkez Ergoren
APOE Gene Variation's Impact on Cardiovascular Health: A Case-Control Study. Biomedicines 12 (3) (2024)
Aya Badeea Ismail, Mehmet Sait Dundar, Cemre Ornek Erguzeloglu, Mahmut Çerkez Ergoren, Adem Alemdar, Sebnem Ozemri Sag, Sehime Gulsun Temel
Alzheimer Disease Associated Loci: APOE Single Nucleotide Polymorphisms in Marmara Region. Biomedicines 12 (5) (2024)
Angelina Haesoo Kim, Irmak Sakin, Stephen Viviano, Gulten Tuncel, Stephanie Marie Aguilera, Gizem Goles, Lauren Jeffries, Weizhen Ji, Saquib A Lakhani, Canan Ceylan Kose, Fatma Silan, Sukru Sadik Oner, Oktay Ismail Kaplan, null null, Mahmut Çerkez Ergoren, Ketu Mishra-Gorur, Murat Gunel, Sebnem Ozemri Sag, Sehime Gulsun Temel, Engin Deniz
CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow. Life science alliance 7 (10) (2024)
Aya Badeea Ismail, Özlem Balcıoğlu, Barçın Özcem, Mahmut Çerkez Ergoren
APOE Gene Variation's Impact on Cardiovascular Health: A Case-Control Study. Biomedicines 12 (3) (2024)
Aya Badeea Ismail, Mehmet Sait Dundar, Cemre Ornek Erguzeloglu, Mahmut Çerkez Ergoren, Adem Alemdar, Sebnem Ozemri Sag, Sehime Gulsun Temel
Alzheimer Disease Associated Loci: APOE Single Nucleotide Polymorphisms in Marmara Region. Biomedicines 12 (5) (2024)
Angelina Haesoo Kim, Irmak Sakin, Stephen Viviano, Gulten Tuncel, Stephanie Marie Aguilera, Gizem Goles, Lauren Jeffries, Weizhen Ji, Saquib A Lakhani, Canan Ceylan Kose, Fatma Silan, Sukru Sadik Oner, Oktay Ismail Kaplan, null null, Mahmut Çerkez Ergoren, Ketu Mishra-Gorur, Murat Gunel, Sebnem Ozemri Sag, Sehime Gulsun Temel, Engin Deniz
CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow. Life science alliance 7 (10) (2024)
Angelina Haesoo Kim, Irmak Sakin, Stephen Viviano, Gulten Tuncel, Stephanie Marie Aguilera, Gizem Goles, Lauren Jeffries, Weizhen Ji, Saquib A Lakhani, Canan Ceylan Kose, Fatma Silan, Sukru Sadik Oner, Oktay Ismail Kaplan, null null, Mahmut Çerkez Ergoren, Ketu Mishra-Gorur, Murat Gunel, Sebnem Ozemri Sag, Sehime Gulsun Temel, Engin Deniz
CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow. Life science alliance 7 (10) (2024)
Qendresa Hoti, Gokce Akan, Gulten Tuncel, Emine Unal Evren, Hakan Evren, Kaya Suer, Tamer Sanlidag, Mahmut Çerkez Ergoren
Altered expression levels of TAS1R2 and TAS1R3 genes among SARS-CoV-2 variants of concerns. Molecular biology reports (2023)
Aziz Suat Gunsel, Mahmut Çerkez Ergoren, Hatice Kemal, Haniyeh Rahbar Kafshboran, Levent Cerit, Ayla Turgay, Hamza Duygu
Determination of Carrier Frequency of Actionable Pathogenic Variants in Autosomal Recessive Genetic Diseases in the Turkish Cypriot Population. Genes 14 (10) (2023)
Gulten Tuncel, Burcin Sanlıdag, Eray Dirik, Tugba Baris, Mahmut Çerkez Ergoren, Sehime Gulsun Temel
Lessons from Real Life Experience: Importance of In-House Sequencing and Smart Ratio-Based Real-Time PCR Outperform Multiplex Ligation-Dependent Probe Amplification in Prenatal Diagnosis for Spinal Muscular Atrophy: Bench to Bedside Diagnosis. Global medical genetics 10 (3) (2023)
Mahmut Çerkez Ergoren, Gokce Akan, Emrah Guler, Gulten Tuncel, Damla Akovalı, Emine Unal Evren, Hakan Evren, Huseyin Kaya Suer, Tamer Sanlidag
Sex and ABO Blood Differences in SARS-CoV-2 Infection Susceptibility. Global medical genetics 10 (1) (2023)
Mahmut Çerkez Ergoren, Gokce Akan, Emrah Guler, Gulten Tuncel, Damla Akovalı, Emine Unal Evren, Hakan Evren, Huseyin Kaya Suer, Tamer Sanlidag
Sex and ABO Blood Differences in SARS-CoV-2 Infection Susceptibility. Global medical genetics 10 (1) (2023)
Ibrahim Boga, Sebnem Ozemri Sag, Nilgun Duman, Sevda Yesim Ozdemir, Mahmut Çerkez Ergoren, Kubilay Dalcı, Cem Mujde, Cem Kaan Parsak, Cagla Rencuzogullari, Ozge Sonmezler, Orçun Yalav, Adem Alemdar, Lamiya Aliyeva, Özlem Bozkurt, Sibel Cetintas, Erdem Cubukcu, Adem Deligonul, Berkcan Dogan, Cemre Ornek Erguzeloglu, Türkkan Evrensel, Mustafa Şehsuvar Gökgöz, Kazım Şenol, Sahsine Tolunay, Esra Akyurek, Neslihan Basgoz, Nuriye Coskun, Bilge Dundar, Figen Öztürk, Duygu Taskin, Mercan Demirtas, Murat Cag, Omer Diker, Polat Olgun, Munis Dündar, Serdar Ceylaner, Sehime Gulsun Temel
A Multicenter Study of Genotype Variation/Demographic Patterns in 2475 Individuals Including 1444 Cases With Breast Cancer in Turkey. European journal of breast health 19 (3) (2023)
Gulten Tuncel, Mahmut Çerkez Ergoren, Buket Baddal, Pinar Tulay, Cenk Serhan Ozverel, Emrah Guler, Huseyin Kaya Suer, Murat Sayan, Tamer Sanlidag
Detection of SARS-CoV-2 N501Y mutation among SARS-CoV-2 variants of concern circulating in Northern Cyprus. Future virology (2022)
Lizzy Teleboshe Paul, Mahmut Çerkez Ergoren
Comparison of Bioinformatics Approaches for Fetal Microdeletions and Monogenic Variations Estimation in Non-invasive Prenatal Testing. Global medical genetics 9 (2) (2022)
Gabriele Bonetti, Kristjana Dhuli, Maria Rachele Ceccarini, Jurgen Kaftalli, Michele Samaja, Vincenza Precone, Stefano Cecchin, Paolo Enrico Maltese, Giulia Guerri, Giuseppe Marceddu, Tommaso Beccari, Barbara Aquilanti, Valeria Velluti, Giuseppina Matera, Marco Alfonso Merrone, Amerigo Iaconelli, Francesca Colombo, Francesco Greco, Marco Raffaelli, Mahmut Çerkez Ergoren, Matteo Bertelli
Next-Generation Sequencing of a Large Gene Panel for Outcome Prediction of Bariatric Surgery in Patients with Severe Obesity. Journal of clinical medicine 11 (24) (2022)
Gabriele Bonetti, Kristjana Dhuli, Maria Rachele Ceccarini, Jurgen Kaftalli, Michele Samaja, Vincenza Precone, Stefano Cecchin, Paolo Enrico Maltese, Giulia Guerri, Giuseppe Marceddu, Tommaso Beccari, Barbara Aquilanti, Valeria Velluti, Giuseppina Matera, Marco Alfonso Merrone, Amerigo Iaconelli, Francesca Colombo, Francesco Greco, Marco Raffaelli, Mahmut Çerkez Ergoren, Matteo Bertelli
Next-Generation Sequencing of a Large Gene Panel for Outcome Prediction of Bariatric Surgery in Patients with Severe Obesity. Journal of clinical medicine 11 (24) (2022)
Aya Badeea Ismail, Marwan 'Mohammad Saeed' Naji, İnci Nebih, Gulten Tuncel, Burcu Ozbakir, Sehime Gulsun Temel, Pınar Tulay, Gamze Mocan, Mahmut Çerkez Ergoren
The expression profile of WNT/β-catanin signalling genes in human oocytes obtained from polycystic ovarian syndrome (PCOS) patients. Zygote (Cambridge, England) 30 (4) (2022)
Gabriele Bonetti, Kristjana Dhuli, Maria Rachele Ceccarini, Jurgen Kaftalli, Michele Samaja, Vincenza Precone, Stefano Cecchin, Paolo Enrico Maltese, Giulia Guerri, Giuseppe Marceddu, Tommaso Beccari, Barbara Aquilanti, Valeria Velluti, Giuseppina Matera, Marco Alfonso Merrone, Amerigo Iaconelli, Francesca Colombo, Francesco Greco, Marco Raffaelli, Mahmut Çerkez Ergoren, Matteo Bertelli
Next-Generation Sequencing of a Large Gene Panel for Outcome Prediction of Bariatric Surgery in Patients with Severe Obesity. Journal of clinical medicine 11 (24) (2022)
Mahmut Çerkez Ergoren, Kubra Komurcu, Gulten Tuncel, Gokce Akan, Cenk Serhan Ozverel, Ceyhun Dalkan, Melis Kalayci, Tamer Sanlıdag
Impact of SARS-CoV-2 Delta and Omicron variants on viral burden and cycle threshold in BNT162b2-vaccinated 12-18 years group. Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] 53 (4) (2022)
Mahmut Çerkez Ergoren, Gokce Akan, Ender Volkan, Emine Kandemis, Emine U Evren, Hakan Evren, Eliz Volkan, Gulten Tuncel, Kaya Suer, Tamer Sanlidag
The "vaccine" hubbub: Viral load comparisons of SARS-CoV-2 Delta and Omicron variants against different vaccine-booster vaccine combinations. Journal of medical virology (2022)
Mahmut Çerkez Ergoren, Gulten Tuncel, Cenk Serhan Ozverel, Tamer Sanlidag
Designing In-House SARS-CoV-2 RT-qPCR Assay for Variant of Concerns. Global medical genetics 9 (3) (2022)
Gabriele Bonetti, Kristjana Dhuli, Maria Rachele Ceccarini, Jurgen Kaftalli, Michele Samaja, Vincenza Precone, Stefano Cecchin, Paolo Enrico Maltese, Giulia Guerri, Giuseppe Marceddu, Tommaso Beccari, Barbara Aquilanti, Valeria Velluti, Giuseppina Matera, Marco Alfonso Merrone, Amerigo Iaconelli, Francesca Colombo, Francesco Greco, Marco Raffaelli, Mahmut Çerkez Ergoren, Matteo Bertelli
Next-Generation Sequencing of a Large Gene Panel for Outcome Prediction of Bariatric Surgery in Patients with Severe Obesity. Journal of clinical medicine 11 (24) (2022)
A Curukoglu, Mahmut Çerkez Ergoren, F E Ozgencil, S Sayiner, M E Ince, T Sanlidag
First direct human-to-cat transmission of the SARS-CoV-2 B.1.1.7 variant. Australian veterinary journal 99 (11) (2021)
Mahmut Çerkez Ergoren, Sehime Gulsun Temel, Gamze Mocan, Munis Dündar
The Story of a Ship Journey, Malaria, and the HBB Gene IVS-II-745 Mutation: Circassian Immigration to Cyprus. Global medical genetics 8 (2) (2021)
Niyazi Senturk, Gulten Tuncel, Berkcan Dogan, Lamiya Aliyeva, Mehmet Sait Dundar, Sebnem Ozemri Sag, Gamze Mocan, Sehime Gulsun Temel, Munis Dündar, Mahmut Çerkez Ergoren
BRCA Variations Risk Assessment in Breast Cancers Using Different Artificial Intelligence Models. Genes 12 (11) (2021)
Gulten Tuncel, Bahar Kaymakamzade, Yeliz Engindereli, Sehime G Temel, Mahmut Çerkez Ergoren
A Homozygous Synonymous Variant Likely Cause of Severe Ciliopathy Phenotype. Genes 12 (6) (2021)
Sehime Gulsun Temel, Mahmut Çerkez Ergoren, Elena Manara, Stefano Paolacci, Gulten Tuncel, Şeref Gül, Matteo Bertelli
Unique combination and in silico modeling of biallelic POLR3A variants as a cause of Wiedemann-Rautenstrauch syndrome. European journal of human genetics : EJHG 28 (12) (2020)
Umut Fahrioğlu, Mahmut Çerkez Ergoren, Gamze Mocan
CCR5-Δ32 gene variant frequency in the Turkish Cypriot population. Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] 51 (4) (2020)
Niyazi Senturk, Mahmut Çerkez Ergoren
Developing an Online Portal for Determining the Genomic Signature of Archaic DNA that are Associated to Modern Human Genetic Diseases: A Meta-Analysis Study. The Eurasian journal of medicine 52 (2) (2020)
Gulten Tuncel, Sehime Gulsun Temel, Mahmut Çerkez Ergoren
Strong association between VDR FokI (rs2228570) gene variant and serum vitamin D levels in Turkish Cypriots. Molecular biology reports 46 (3) (2019)
Gulten Tuncel, Mahmut Çerkez Ergoren
Functional coding and non-coding variants in human BRCA1 gene and their use in genetic screening. Medical oncology (Northwood, London, England) 36 (8) (2019)

Mahmut Çerkez Ergoren.css-eqlu8i{font-size:small;padding-left:4px;} (M C Ergoren, Mahmut Çerkez Ergören, Mahmut Cerkez Ergoren, Mahmut C Ergoren)

Publication Activity (10 Years)

Top Topics

Top Venues

Mahmut Çerkez Ergoren (M C Ergoren, Mahmut Çerkez Ergören, Mahmut Cerkez Ergoren, Mahmut C Ergoren)