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About the database ScholarIQanswers from OpenAlex & ORCID
How has Orhan Görükmez's publication output changed over time?
ScholarIQpublication output · 2010–2025
Output declined50% over the shown period — from 2 works in 2010 to 1 in 2025.
2
1
1
1
1
1
2
1
1
201020122015201620172019202020212025
What are the most-cited papers on Orhan Görükmez?
ScholarIQmost cited works
Lack of association of ACE gene I/D polymorphism with obstructive sleep apnea syndrome in Turkish patients
Tahsin Yakut, Mutlu Karkucak, Ahmet Ursavaş, T Gulten, Başak Burgazlıoğlu, Orhan Görükmez, Mehmet Karadağ
Genetics and Molecular Research. 201026 CitationsOPEN ACCESS
The role of genetic mutations in intrahepatic cholestasis of pregnancy
Gültekin Adanaş Aydın, Gülten Özgen, Orhan Görükmez
S180931821. 202022 CitationsOPEN ACCESS
Evaluation of the JAK2-V617F gene mutation in Turkish patients with essential thrombocythemia and polycythemia vera
Mutlu Karkucak, Tahsin Yakut, Vildan Özkocaman, Fahir Özkalemkaş, Rıdvan Ali, Murat Bayram, Orhan Görükmez, Gökhan Ocakoğlu
S197962172. 201220 Citations
Lack of association of genetic polymorphisms of angiotensin-converting enzyme gene I/D and glutathione-S-transferase enzyme T1 and M1 with retinopathy of prematures
Meral Yıldız, Mutlu Karkucak, Tahsin Yakut, Orhan Görükmez, Ahmet Özmen
Genetics and Molecular Research. 201018 CitationsOPEN ACCESS
Patients with cerebrotendinous xanthomatosis diagnosed with diverse multisystem involvement
Pelin Teke Kısa, Gonca Kılıç Yıldırım, Burcu Öztürk Hişmi, Sevil Dorum, Özge Yılmaz Küsbeci, Ali Topak, Figen Baydan, Nazlı Durmaz Çelik, Orhan Görükmez, Zümrüt Arslan Gülten, Arzu Ekici, Serhat Özkan, Aylın Yaman, Nur Arslan
S31409034. 202117 Citations
Related on ScholarIQ
Bursa Yuksek Ihtisas Egitim Ve Arastirma Hastanesi
Institution
Lack of association of ACE gene I/D polymorphism with obstructive sleep apnea syndrome in Turkish patients
Paper
The role of genetic mutations in intrahepatic cholestasis of pregnancy
Paper
Evaluation of the JAK2-V617F gene mutation in Turkish patients with essential thrombocythemia and polycythemia vera
Paper
Lack of association of genetic polymorphisms of angiotensin-converting enzyme gene I/D and glutathione-S-transferase enzyme T1 and M1 with retinopathy of prematures
Paper
Patients with cerebrotendinous xanthomatosis diagnosed with diverse multisystem involvement
Paper