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Bilgin Yüksel

cukurova university

28H指数
249论文数
3.6K被引数
收录论文 34
发表时间
Targeting Hypercalciuria in SLC34A1-Related Disorders: Impact of Oral Phosphate Therapy and Novel Genetic Insights in Pediatric Case Series
err2026-01-16
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errOAAI
errIhsan Turan; Muge Atar; Mehmet Eltan; Ahmet Anik; Eda Celebi Bitkin; Semine Ozdemir Dilek; Mevra Cay; Sevcan Tuğ Bozdogan; Hakan Döneray; Damla Kotan; Serap Turan; Bilgin Yüksel; Ali Kemal Topaloglu
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Diagnostic pitfalls in aldosterone defects: a 9-year follow-up of early-onset pseudohypoaldosteronism type 2醛固酮缺陷中的诊断陷阱:对早期发病假性醛固酮减少症2型的9年随访研究
err2025-12-01
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PREAI
errCay, Mevra; Turan, Ihsan; Atmis, Bahriye; Kotan, Leman Damla; Celebi, Sukriye Tugce; Cimen, Ayse Merve; Mengen, Eda; Bayazit, Aysun Karabay; Yuksel, Bilgin
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A Novel Mutation in the Androgen Receptor Gene of Female Patients with 46,XY Karyotype46,XY核型女性患者雄激素受体基因中的新发突变
err2025-05-10
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errUslu, Inayet Nur; Gokce, Nuriye; Aksoy, Gulsevinc; Inandiklioglu, Nihal; Yuksel, Bilgin; Dundar, Munis; Demirhan, Osman
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Provider Perspectives on Contraceptive Care: A Systematic Review
err2024-12-01
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errOAAI
errManzer, Jamie L.; Ouellette, Lexi; Tingey, Lauren; Carrillo-Perez, Amanda; Hogan, Clare; Atkins, Nia; Carmichael, Katherine; Ramirez, Grace Guerrero; Magee, Maggie M.; Miller, Macy A.; Nwankwo, Chidinma; Reid, Simone; Strelevitz, Tara; Taylor, Vanessa; Waddell, William; Wong, Mindy; Yuksel, Burak; Blum, Jennifer
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Client Perspectives on Contraceptive Care: A Systematic Review
err2024-12-01
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errOAAI
errManzer, Jamie L.; Carrillo-Perez, Amanda; Tingey, Lauren; Ouellette, Lexi; Hogan, Clare; Atkins, Nia; Carmichael, Katherine; Ramirez, Grace Guerrero; Magee, Maggie M.; Miller, Macy A.; Nwankwo, Chidinma; Reid, Simone; Strelevitz, Tara; Taylor, Vanessa; Waddell, William; Wong, Mindy; Yuksel, Burak; Blum, Jennifer
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17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort
err2024-07-17
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errOAAI
errSiklar, Zeynep; Camtosun, Emine; Bolu, Semih; Yildiz, Melek; Akinci, Aysehan; Bas, Firdevs; Dundar, Ismail; Bestas, Asli; Unal, Edip; Kocaay, Pinar; Guran, Tulay; Buyukyilmaz, Gonul; Ugurlu, Aylin Kilinc; Tosun, Busra Gurpinar; Turan, Ihsan; Kurnaz, Erdal; Yuksel, Bilgin; Turkkahraman, Doga; Cayir, Atilla; Celmeli, Gamze; Gonc, E. Nazli; Eklioglu, Beray Selver; Cetinkaya, Semra; Yilmaz, Seniha Kiremitci; Atabek, Mehmet Emre; Buyukinan, Muammer; Arslan, Emrullah; Mengen, Eda; Cakir, Esra Deniz Papatya; Karaoglan, Murat; Hatipoglu, Nihal; Orbak, Zerrin; Ucar, Ahmet; Akyurek, Nesibe; Akbas, Emine Demet; Isik, Emregul; Kaygusuz, Sare Betul; Sutcu, Zumrut Kocabey; Seymen, Gulcan; Berberoglu, Merih
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Plasma pentraxin-3 levels and its role in childhood obesity-Is it anti-inflammatory? A matched group study
err2024-05-01
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PREAI
errUysal, Merve; Mete, Burak; Kara, Ertan; Demirhindi, Hakan; Haytoglu, Zeliha; Yuksel, Bilgin; Turan, Ihsan; Daglioglu, Gulcin; Dogus, Yusuf
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POU6F2 mutation in humans with pubertal failure alters GnRH transcript expression
err2023-08-01
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errCho, Hyun-Ju; Gurbuz, Fatih; Stamou, Maria; Kotan, Leman Damla; Farmer, Stephen Matthew; Can, Sule; Tompkins, Miranda Faith; Mammadova, Jamala; Altincik, S. Ayca; Gokce, Cumali; Catli, Gonul; Bugrul, Fuat; Bartlett, Keenan; Turan, Ihsan; Balasubramanian, Ravikumar; Yuksel, Bilgin; Seminara, Stephanie B.; Wray, Susan; Topaloglu, A. Kemal
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PLXNB1 mutations in the etiology of idiopathic hypogonadotropic hypogonadism特发性低促性腺激素性性腺功能减退症的病因中的PLXNB1突变
err2022-02-16
err4
PREAI
errWelch, Bradley A.; Cho, Hyun-Ju; Ucakturk, Seyit Ahmet; Farmer, Stephen Matthew; Cetinkaya, Semra; Abaci, Ayhan; Akkus, Gamze; Simsek, Enver; Kotan, Leman Damla; Turan, Ihsan; Gurbuz, Fatih; Yuksel, Bilgin; Wray, Susan; Topaloglu, A. Kemal
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Inactivating NHLH2 variants cause idiopathic hypogonadotropic hypogonadism and obesity in humans
err2022-01-23
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errTopaloglu, A. Kemal; Simsek, Enver; Kocher, Matthew A.; Mammadova, Jamala; Bober, Ece; Kotan, Leman Damla; Turan, Ihsan; Celiloglu, Can; Gurbuz, Fatih; Yuksel, Bilgin; Good, Deborah J.
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Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism
err2021-06-01
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errKotan, Leman Damla; Ternier, Gaetan; Cakir, Aydilek Dagdeviren; Emeksiz, Hamdi Cihan; Turan, Ihsan; Delpouve, Gaspard; Kardelen, Asli Derya; Ozcabi, Bahar; Isik, Emregul; Mengen, Eda; Cakir, Esra Deniz P.; Yuksel, Aysegul; Agladioglu, Sebahat Yilmaz; Dilek, Semine Ozdemir; Evliyaoglu, Olcay; Darendeliler, Feyza; Gurbuz, Fatih; Akkus, Gamze; Yuksel, Bilgin; Giacobini, Paolo; Kemal Topaloglu, A.
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Clinical Characteristics and Long-term Follow-of Patients with Diabetes Due To PTF1A Enhancer Mutations
err2020-09-07
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errDemirbilek, Huseyin; Cayir, Atilla; Flanagan, Sarah E.; Yildirim, Ruken; Kor, Yilmaz; Gurbuz, Fatih; Haliloglu, Belma; Yildiz, Melek; Baran, Riza Taner; Akbas, Emine Demet; Demiral, Meliha; Unal, Edip; Arslan, Gulcin; Vuralli, Dogus; Buyukyilmaz, Gonul; Al-Khawaga, Sara; Saeed, Amira; Al Maadheed, Maryam; Khalifa, Amel; Onal, Hasan; Yuksel, Bilgin; Ozbek, Mehmet Nuri; Bereket, Abdullah; Hattersley, Andrew T.; Hussain, Khalid; De Franco, Elisa
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Molecular genetic studies in a case series of isolated hypoaldosteronism due to biosynthesis defects or aldosterone resistance
err2018-04-18
err15
PREAI
errTuran, Ihsan; Kotan, Leman Damla; Tastan, Mehmet; Gurbuz, Fatih; Topaloglu, Ali Kemal; Yuksel, Bilgin
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CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism
err2017-01-23
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errTuran, Ihsan; Hutchins, B. Ian; Hacihamdioglu, Bulent; Kotan, L. Damla; Gurbuz, Fatih; Ulubay, Ayca; Mengen, Eda; Yuksel, Bilgin; Wray, Susan; Topaloglu, A. Kemal
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CCDC141 Mutation Identified in Anosmic Hypogonadotropic Hypogonadism (Kallmann Syndrome) Alters GnRH Neuronal Migration
err2016-03-25
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errHutchins, B. Ian; Kotan, L. Damla; Taylor-Burds, Carol; Ozkan, Yusuf; Cheng, Paul J.; Gurbuz, Fatih; Tiong, Jean D. R.; Mengen, Eda; Yuksel, Bilgin; Topaloglu, A. Kemal; Wray, Susan
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Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort
err2016-01-01
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errGuran, Tulay; Buonocore, Federica; Saka, Nurcin; Ozbek, Mehmet Nuri; Aycan, Zehra; Bereket, Abdullah; Bas, Firdevs; Darcan, Sukran; Bideci, Aysun; Guven, Ayla; Demir, Korcan; Akinci, Aysehan; Buyukinan, Muammer; Aydin, Banu Kucukemre; Turan, Serap; Agladioglu, Sebahat Yilmaz; Atay, Zeynep; Abali, Zehra Yavas; Tarim, Omer; Catli, Gonul; Yuksel, Bilgin; Akcay, Teoman; Yildiz, Metin; Ozen, Samim; Doger, Esra; Demirbilek, Huseyin; Ucar, Ahmet; Isik, Emregul; Ozhan, Bayram; Bolu, Semih; Ozgen, Ilker Tolga; Suntharalingham, Jenifer P.; Achermann, John C.
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Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study
err2014-12-11
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PREAI
errBas, Firdevs; Uyguner, Z. Oya; Darendeliler, Feyza; Aycan, Zehra; Cetinkaya, Ergun; Berberoglu, Merih; Siklar, Zeynep; Ocal, Gonul; Darcan, Sukran; Goksen, Damla; Topaloglu, Ali Kemal; Yuksel, Bilgin; Ozbek, Mehmet Nuri; Ercan, Oya; Evliyaoglu, Olcay; Cetinkaya, Semra; Sen, Yasar; Atabek, Emre; Toksoy, Guven; Aydin, Banu Kucukemre; Bundak, Ruveyde
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Normosmic idiopathic hypogonadotropic hypogonadism due to a novel homozygous nonsense c.C969A (p.Y323X) mutation in the KISS1R gene in three unrelated families
err2014-11-07
err20
PREAI
errDemirbilek, Huseyin; Ozbek, M. Nuri; Demir, Korcan; Kotan, L. Damla; Cesur, Yasar; Dogan, Murat; Temiz, Fatih; Mengen, Eda; Gurbuz, Fatih; Yuksel, Bilgin; Topaloglu, A. Kemal
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Loss-of-Function Mutations in PNPLA6 Encoding Neuropathy Target Esterase Underlie Pubertal Failure and Neurological Deficits in Gordon Holmes Syndrome
err2014-10-01
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errTopaloglu, A. Kemal; Lomniczi, Alejandro; Kretzschmar, Doris; Dissen, Gregory A.; Kotan, L. Damla; McArdle, Craig A.; Koc, A. Filiz; Hamel, Ben C.; Guclu, Metin; Papatya, Esra D.; Eren, Erdal; Mengen, Eda; Gurbuz, Fatih; Cook, Mandy; Castellano, Juan M.; Kekil, M. Burcu; Mungan, Neslihan O.; Yuksel, Bilgin; Ojeda, Sergio R.
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