Sehime Gulsun Temel (Sehime G Temel, Şehime Gülsün Temel)

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 20

Top Venues

Journal of medical virology

Life science alliance

Biomedicines

European journal of human genetics : EJHG

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

Publications

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, 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)
Aslıhan Kiraz, Ozlem Sezer, Adem Alemdar, Sezin Canbek, Nilgun Duman, Atıl Bisgin, Tulin Cora, Hatice Ilgın Ruhi, Mahmut Cerkez Ergoren, Bilgen Bilge Geçkinli, Sebnem Ozemri Sag, Hilmi Erdem Gözden, Ozlem Oz, Zuhal Mert Altıntaş, Sinem Yalcıntepe, Adem Keskin, Ayşegül Yabacı Tak, Şeyma Aktaş Paskal, Uğur Fahri Yürekli, Mercan Demirtas, Emine Unal Evren, Abdullah Hanta, Müşerref Başdemirci, Huseyin Kaya Suer, Burhan Balta, Nadir Kocak, Halil Gürhan Karabulut, Havva Cobanogulları, Esra Arslan Ateş, Sevcan Tuğ Bozdoğan, Damla Eker, Sadiye Ekinci, Süleyman Nergiz, Timur Tuncalı, Serap Yagbasan, Ceren Alavanda, Nuket Yurur Kutlay, Hakan Evren, Murat Erdoğan, Sule Altıner, Tamer Sanlidag, Gizem Akıncı Gonen, Arzu Vicdan, Nazan Eras, Hatice Koçak Eker, Ozgür Balasar, Gulten Tuncel, Munis Dundar, Hakan Gurkan, Sehime Gulsun Temel
Contribution of genotypes in Prothrombin and Factor V Leiden to COVID-19 and disease severity in patients at high risk for hereditary thrombophilia. Journal of medical virology (2023)
Aslıhan Kiraz, Ozlem Sezer, Adem Alemdar, Sezin Canbek, Nilgun Duman, Atıl Bisgin, Tulin Cora, Hatice Ilgın Ruhi, Mahmut Cerkez Ergoren, Bilgen Bilge Geçkinli, Sebnem Ozemri Sag, Hilmi Erdem Gözden, Ozlem Oz, Zuhal Mert Altıntaş, Sinem Yalcıntepe, Adem Keskin, Ayşegül Yabacı Tak, Şeyma Aktaş Paskal, Uğur Fahri Yürekli, Mercan Demirtas, Emine Unal Evren, Abdullah Hanta, Müşerref Başdemirci, Kaya Suer, Burhan Balta, Nadir Kocak, Halil Gürhan Karabulut, Havva Cobanogulları, Esra Arslan Ateş, Sevcan Tuğ Bozdoğan, Damla Eker, Sadiye Ekinci, Süleyman Nergiz, Timur Tuncalı, Serap Yagbasan, Ceren Alavanda, Nuket Yurur Kutlay, Hakan Evren, Murat Erdoğan, Sule Altıner, Tamer Sanlidag, Gizem Akıncı Gonen, Arzu Vicdan, Nazan Eras, Hatice Koçak Eker, Ozgür Balasar, Gulten Tuncel, Munis Dundar, Hakan Gurkan, Sehime Gulsun Temel
Contribution of genotypes in Prothrombin and Factor V Leiden to COVID-19 and disease severity in patients at high risk for hereditary thrombophilia. Journal of medical virology 95 (2) (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)
Aslıhan Kiraz, Ozlem Sezer, Adem Alemdar, Sezin Canbek, Nilgun Duman, Atıl Bisgin, Tulin Cora, Hatice Ilgın Ruhi, Mahmut Cerkez Ergoren, Bilgen Bilge Geçkinli, Sebnem Ozemri Sag, Hilmi Erdem Gözden, Ozlem Oz, Zuhal Mert Altıntaş, Sinem Yalcıntepe, Adem Keskin, Ayşegül Yabacı Tak, Şeyma Aktaş Paskal, Uğur Fahri Yürekli, Mercan Demirtas, Emine Unal Evren, Abdullah Hanta, Müşerref Başdemirci, Kaya Suer, Burhan Balta, Nadir Kocak, Halil Gürhan Karabulut, Havva Cobanogulları, Esra Arslan Ateş, Sevcan Tuğ Bozdoğan, Damla Eker, Sadiye Ekinci, Süleyman Nergiz, Timur Tuncalı, Serap Yagbasan, Ceren Alavanda, Nuket Yurur Kutlay, Hakan Evren, Murat Erdoğan, Sule Altıner, Tamer Sanlidag, Gizem Akıncı Gonen, Arzu Vicdan, Nazan Eras, Hatice Koçak Eker, Ozgür Balasar, Gulten Tuncel, Munis Dundar, Hakan Gurkan, Sehime Gulsun Temel
Contribution of genotypes in Prothrombin and Factor V Leiden to COVID-19 and disease severity in patients at high risk for hereditary thrombophilia. Journal of medical virology 95 (2) (2023)
Nihat Buğra Ağaoğlu, Busra Unal, Ozlem Akgun Dogan, Martin Orlinov Kanev, Payam Zolfagharian, Sebnem Ozemri Sag, Sehime Gulsun Temel, Levent Doganay
Consistency of variant interpretations among bioinformaticians and clinical geneticists in hereditary cancer panels. European journal of human genetics : EJHG 30 (3) (2022)
Nilgun Duman, Gulten Tuncel, Atil Bisgin, Sevcan Tug Bozdogan, Sebnem Ozemri Sag, Seref Gul, Aslihan Kiraz, Burhan Balta, Murat Erdogan, Bulent Uyanik, Sezin Canbek, Pinar Ata, Bilgen Bilge Geckinli, Esra Arslan Ates, Ceren Alavanda, Sevda Yesim Ozdemir, Ozlem Sezer, Gulay Oner Ozgon, Hakan Gurkan, Kubra Guler, Ibrahim Boga, Niyazi Kaya, Adem Alemdar, Murat Sayan, Munis Dundar, Mahmut Cerkez Ergoren, Sehime Gulsun Temel
Analysis of ACE2 and TMPRSS2 coding variants as a risk factor for SARS-CoV-2 from 946 whole-exome sequencing data in the Turkish population. Journal of medical virology 94 (11) (2022)
Eda Hasal, Emel Bulbul Baskan, Şeref Gül, Aslı Görek Dilektaşlı, Sebnem Ozemri Sag, Saduman Balaban Adim, Sehime Gulsun Temel
Birt-Hogg-Dubé Syndrome: Diagnostic Journey of Three Cases from Skin to Gene. Annals of dermatology 34 (1) (2022)
Ahmet Umit Sabancı, Perihan Erkan Alkan, Cem Mujde, Hivda Ulbeği Polat, Cemre Ornek Erguzeloglu, Serdar Ceylaner, Cüneyt Özakın, Sehime Gulsun Temel
Nanobubble Ozone Stored in Hyaluronic Acid Decorated Liposomes: Antibacterial, Anti-SARS-CoV-2 Effect and Biocompatibility Tests. International journal of nanomedicine 17 (2022)
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)
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)
Sehime Gulsun Temel, B Karakaş, Ü Şeker, B Turkgenç, Ö Zorlu, H Sarıcaoğlu, Ç Oğur, Ö Kütük, D P Kelsell, M C Yakıcıer
A novel homozygous nonsense mutation in CAST associated with PLACK syndrome. Cell and tissue research 378 (2) (2019)
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)
Burcu Turkgenc, Burcin Sanlidag, Amber Eker, Aslı Giray, Ozgur Kutuk, Cengiz Yakicier, Aslıhan Tolun, Sehime Gulsun Temel
STUB1 polyadenylation signal variant AACAAA does not affect polyadenylation but decreases STUB1 translation causing SCAR16. Human mutation 39 (10) (2018)
Mahmut Cerkez Ergoren, Burcu Turkgenc, Kerem Terali, Orhan Rodoplu, Aline Verstraeten, Lut Van Laer, Gamze Mocan, Bart Loeys, Omer Tetik, Sehime Gulsun Temel
Identification and characterization of a novel FBN1 gene variant in an extended family with variable clinical phenotype of Marfan syndrome. Connective tissue research 60 (2) (2018)

Sehime Gulsun Temel.css-eqlu8i{font-size:small;padding-left:4px;} (Sehime G Temel, Şehime Gülsün Temel)

Publication Activity (10 Years)

Top Topics

Top Venues

Sehime Gulsun Temel (Sehime G Temel, Şehime Gülsün Temel)