The relation between distant metastasis and genetic change type in stage IV lung adenocarcinoma patients at diagnosis

Authors: Ermin, Sinem, Batum, Özgür, Saka Güvenç, Merve, Diniz, Gülden, Ayrancı, Aysu, Erdoğan, Kadri Murat, Yücel, Nur, Yıldırım, Eylem, Özdemir, Taha Reşid, Hacar, Alev Gülşah, Güldaval, Filiz, Koç, Altuğ, Aydoğdu, Zekiye, Balcı, Günseli, Özyılmaz, Berk, Akşit Yaşar, Hacer, Özer Kaya, Özge, Gayaf, Mine, Kırbıyık, Özgür, Aksel, Nimet, Kutbay, Yaşar Bekir, Ursavaş, Tuba Nihal, Karadeniz, Gülistan, Polat, Gülru, Kömürcüoğlu, Berna, Çırak, Ali Kadri, Yılmaz, Ufuk

Source: Clinical respiratory journal. 15(2):196-202

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100115396856.0x000001&indx=1&recIds=ETOCvdc_100115396856.0x000001

SURF1 related Leigh syndrome: Clinical and molecular findings of 16 patients from Turkey

Authors: Kose, Melis, Canda, Ebru, Kagnici, Mehtap, Aykut, Ayça, Adebali, Ogün, Durmaz, Asude, Bircan, Aylin, Diniz, Gulden, Eraslan, Cenk, Kose, Engin, Ünalp, Aycan, Yılmaz, Ünsal, Ozyilmaz, Berk, Özdemir, Taha Reşid, Atik, Tahir, Uçar, Sema Kalkan, McFarland, Robert, Taylor, Robert W., Brown, Garry K., Çoker, Mahmut, Özkınay, Ferda

Source: In Molecular Genetics and Metabolism Reports December 2020 25

A Case of Late-onset Hyperinsulinemic Hypoglycemia: HNF4A Mutation

Authors: Arslan, Gülçin, Acar, Sezer, Özdemir, Taha Reşid, Nalbantoğlu, Özlem, Kirbiyik, Özgür, Köprülü, Özge, Özkaya, Beyhan, Özkan, Behzat

Source: Journal of pediatric research. 7(2):168-171

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN624039772&indx=1&recIds=ETOCRN624039772

Targeted Next-Generation Sequencing of MLH1, MSH2, and MSH6 Genes in Patients with Endometrial Carcinoma under 50 Years of Age

Authors: Özdemir, Taha Reşid, Alan, Murat, Sanci, Muzaffer, Koç, Altuğ

Source: Balkan medical journal. 36(1):37-42

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN621826991&indx=1&recIds=ETOCRN621826991

A case of spastic paraplegia-15 with a novel pathogenic variant in ZFYVE26 gene

Authors: Özdemir, Taha Reşid, Gençpınar, Pınar, Arıcan, Pınar, Öztekin, Özgür, Dündar, Nihal Olgaç, Özyılmaz, Berk

Source: International journal of neuroscience. 129(12):1198-1202

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100089987225.0x000001&indx=1&recIds=ETOCvdc_100089987225.0x000001

The Histopathological Findings of High-grade Serous Ovarian Carcinomas in Patients with BRCA Germline Mutations, Single Center Experience.

Alternate Title: BRCA Germline Mutasyonu Olan Hastalarda Yüksek Dereceli Seröz Over Karsinomlarının Histopatolojik Özellikleri; Tek Merkez Deneyimi. (Turkish)

Authors: Aköz, Gamze, Kaya, Özge Özer, Özdemir, Taha Reşid, Çakır, İlker, Talu, Canan Kelten

Source: Anatolian Journal of General Medical Research; 2024, Vol. 34 Issue 1, p50-56, 7p

A Novel De Novo Missense Mutation in HNFA Resulting in Sulfonylurea-Responsive Maturity-onset Diabetes of the Young

Authors: Acar, Sezer, Abaci, Ayhan, Demir, Korcan, Özdemir, Taha Reşid, Özyilmaz, Berk, Böber, Ece

Source: Journal of pediatric research. 5(3):156-160

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN617491720&indx=1&recIds=ETOCRN617491720

Prognostic and predictive role of liquid biopsy in lung cancer patients.

Authors: Goksel, Tuncay, Özgür, Su, Vardarlı, Aslı Tetik, Koç, Altuğ, Karakuş, Haydar Soydaner, Özdemir, Taha Reşid, Erdoğan, Kadri Murat, Aldağ, Ceyda, Veral, Ali, Komurcuoglu, Berna, Gursoy, Pınar, Arayici, Mehmet Emin, Leblebici, Asim, Yiğitbaşı, Türkan, Ellidokuz, Hülya, Basbinar, Yasemin

Source: Frontiers in Oncology; 2024, p1-10, 10p

The Frequency and Management of TP53 Mutation Carriers in Turkish Patients with BRCA-Negative Breast Cancer Under 50 Years of Age.

Authors: ÖZDEMİR, Taha Reşid¹ dr.tahaoz@gmail.com, ÖZER KAYA, Özge¹, EMİROĞLU, Mustafa², ERDOĞAN, Kadri Murat¹, DEĞİRMENCİ, Mustafa³, SAKA GÜVENÇ, Merve¹, DEMİR, Gönül⁴, KOÇ, Altuğ¹, ÖZYILMAZ, Berk¹, KIRBIYIK, Özgür¹

Source: Turkish Journal of Oncology / Türk Onkoloji Dergisi. 2020, Vol. 35 Issue 2, p178-188. 11p.

Subject Terms: *BREAST tumor risk factors, *TUMOR suppressor genes, *BREAST tumors, *GENETIC counseling, *HEALTH care teams, *GENETIC mutation, *POLYMERASE chain reaction, *RISK assessment, *BRCA genes, *LI-Fraumeni syndrome, *SEQUENCE analysis

Geographic Terms: TURKEY

The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey

Authors: Ozantürk, Ayşegül, Marshall, Jan D, Collin, Gayle B, Düzenli, Selma, Marshall, Robert P, Candan, Şükrü, Tos, Tülay, Esen, İhsan, Taşkesen, Mustafa, Çayır, Atilla, Öztürk, Şükrü, Üstün, İhsan, Ataman, Esra, Karaca, Emin, Özdemir, Taha Reşid, Erol, İlknur, Eroğlu, Fehime Kara, Torun, Deniz, Parıltay, Erhan, Yılmaz-Güleç, Elif, Karaca, Ender, Atabek, M Emre, Elçioğlu, Nursel, Satman, İlhan, Möller, Claes, Muller, Jean, Naggert, Jürgen K, Özgül, Rıza Köksal

Source: Journal of human genetics. 60(1):1-9

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100194164420.0x000001&indx=1&recIds=ETOCvdc_100194164420.0x000001

Evaluation of chromosomal abnormalities and Y-chromosome microdeletions in 1696 Turkish cases with primary male infertility: A single-center study.

Authors: Özdemir, Taha Reşid¹ dr.tahaoz@gmail.com, Özyılmaz, Berk¹, Çakmak, Özgür², Kaya, Özge Özer¹, Köse, Can³, Kırbıyık, Özgür¹, Keskin, Mehmet Zeynel², Koç, Altuğ¹, Zeyrek, Tuğba¹, Kutbay, Yaşar Bekir¹, Erdoğan, Kadri Murat¹, Güvenç, Merve Saka¹

Source: Turkish Journal of Urology. Mar2020, Vol. 46 Issue 2, p95-100. 6p.

Subject Terms: *HUMAN reproductive technology, *INFERTILITY, *KARYOTYPES, *MEN'S health, *GENETIC mutation, *POLYMERASE chain reaction, *SEX chromosome abnormalities

Geographic Terms: TURKEY

The Role of Interleukin-1 Beta C-511T as a Modifier Polymorphism in Cryopyrin-associated Periodic Syndromes.

Authors: Özyılmaz, Berk¹ drberk@gmail.com, Özdemir, Taha Reşid¹

Source: Journal of Pediatric Research. 2019, Vol. 6 Issue 3, p247-251. 5p.

Subject Terms: *ALLELES, *GENES, *GENETIC polymorphisms, *INTERLEUKINS, *GENETIC mutation, *PROTEOLYTIC enzymes, *PHENOTYPES, *SIGNAL peptides, *CRYOPYRIN-associated periodic syndromes, *GENOTYPES

IFNG and IFNGR1 gene polymorphisms in children with nonresponse to the hepatitis B vaccine

Authors: Çiftdoğan, Dilek Yılmaz, Onay, Hüseyin, Tosun, Selam, Özdemir, Taha Reşid, Özkınay, Ferda, Vardar, Fadıl

Source: Future virology. 9(2):123-130

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100115557994.0x000001&indx=1&recIds=ETOCvdc_100115557994.0x000001

Whole-genome gene expression analysis in urine samples of patients with prostate cancer and benign prostate hyperplasia

Authors: Özdemir, Taha Reşid, Şimşir, Adnan, Onay, Hüseyin, Cüreklibatır, İbrahim, Özkınay, Ferda, Akın, Haluk

Source: In Urologic Oncology: Seminars and Original Investigations October 2017 35(10):607-607

The Case Report of Hemoglobin Hamadan: HBB:c.169G>C (B 56 (D7) Gly-Arg) in Istanbul.

Authors: HÜRMEYDAN, Özlem, ÇAKIR MADENCİ, Özlem, ERDOĞMUŞ, Fatma, ÖZYILMAZ, Berk, ÖZDEMİR, Taha Reşid, YÜCEL, Nihal

Source: Türkiye Klinikleri Journal of Case Reports; 2023, Vol. 31 Issue 1, p58-62, 5p

Subject Terms: CAPILLARY electrophoresis, HEMOGLOBINS, HEMOGLOBINOPATHY, THALASSEMIA, CANCER chemotherapy, HIGH performance liquid chromatography, ELECTROPHORESIS, GLYCOSYLATED hemoglobin, GLOBIN genes

Geographic Terms: ISTANBUL (Turkey)

Topiramate-Responsive Tremor in a Novel Pathogenic Variant of SPG15 Patient

Authors: Ersen, Atilla, Gençpınar, Pınar, Arıcan, Pınar, Bozkaya Yılmaz, Sema, Aliyeva, Nargiz, Özdemir, Taha Reşid, Öztekin, Özgür, Olgaç Dündar, Nihal

Source: Clinical neuropharmacology. 43(4):121-122

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100178663304.0x000001&indx=1&recIds=ETOCvdc_100178663304.0x000001

Gilbert Syndrome and Genetic Findings in Children: A Tertiary-Center Experience from Turkey.

Authors: Appak, Yeliz Çağan, Aksoy, Betül, Özyılmaz, Berk, Özdemir, Taha Reşid, Baran, Maşallah

Source: Turkish Archives of Pediatrics; May2022, Vol. 57 Issue 3, p295-299, 5p

Subject Terms: SEQUENCE analysis, DIFFERENTIAL diagnosis, GENETIC polymorphisms, TERTIARY care, GILBERT disease, GENETIC markers, TRANSFERASES

Geographic Terms: TURKEY

The utility of next-generation sequencing technologies in diagnosis of Mendelian mitochondrial diseases and reflections on clinical spectrum.

Authors: Kose, Melis, Isik, Esra, Aykut, Ayça, Durmaz, Asude, Kose, Engin, Ersoy, Melike, Diniz, Gulden, Adebali, Ogun, Ünalp, Aycan, Yilmaz, Ünsal, Karaoğlu, Pakize, Edizer, Selvinaz, Tekin, Hande Gazeteci, Özdemir, Taha Reşid, Atik, Tahir, Onay, Hüseyin, Özkınay, Ferda

Source: Journal of Pediatric Endocrinology & Metabolism; Apr2021, Vol. 34 Issue 4, p417-430, 14p

Neuronal ceroid lipofuscinosis: genetic and phenotypic spectrum of 14 patients from Turkey.

Authors: Kose, Melis, Kose, Engin, Ünalp, Aycan, Yılmaz, Ünsal, Edizer, Selvinaz, Tekin, Hande Gazeteci, Karaoğlu, Pakize, Özdemir, Taha Reşid, Er, Esra, Onay, Hüseyin, Yildirim, Eser Sozmen

Source: Neurological Sciences; 2021, Vol. 42 Issue 3, p1103-1111, 9p, 2 Charts

Subject Terms: NEURONAL ceroid-lipofuscinosis, GENETIC counseling, CONGENITAL disorders, GENES, INBORN errors of metabolism

Geographic Terms: TURKEY

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