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The impact of Polymorphisms of rs689 and rs757110 in Familial Type 2 Diabetes: A Case-Control Study in the Iranian Population by Amin Haghighi, Amaneh Javid, Ali Khodadadian, Mohammad Yahya Vahidi Mehrjardi

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A nationwide cross-sectional study in Saudi Arabia for the assessment of understanding and practices of clinicians towards personalized genetic testing by Mohy Uddin, Ahmad Deeb, Husam Ardah, Marwan Nashbat, Mohammad Yahya Ayoub, Majid Alfadhel

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Investigation of rs328 polymorphism of lipoprotein lipase and rs1260326 polymorphism of glucokinase regulatory genes in individuals with type 2 diabetes in Yazd, Iran by Mohammad Javad Rezazadeh Khabaz, Sanaz Dastghaib, Mohammad Yahya Vahidi Mehrjardi, Mohammad Hasan Sheikhha

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From Clinical Presentation to Genetic Confirmation: A Case of L2HGDH-Related Leukodystrophy in an 11-Year-Old by Negareh Poursalehi, Mojtaba Movahedinia, Mohammad Hossein Mohammadi, Mohamammad Ebrahim Ghanei, Mohammad Yahya Vahidi Mehrjerdi, Seyed Mehdi Kalantar

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Topically Applied Luteolin /Quercetin-Capped Silver Nanoparticle Ointment as Antileishmanial Composite: Acceleration Wound Healing in BALB/c Mice by Azadeh Ebrahimzadeh, Mehdi Karamian, Farshid Abedi, Mohammad Yahya Hanafi-Bojd, Mohammd Amin Ghatee, Mina Hemmati, Effat Alemzadeh

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Central line-associated bloodstream infections (CLABSI) in critical care: understanding incidence, and risk factors in Palestine by Sameer Alomari, Mohammad Yahya, Nadeem Alabadlah, Khader Thiab, Walid Basha, Haneen Dhaidel, Razan Rabi, Dina Abugaber, Ahmad Enaya

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Predictive analytics technique based on hybrid sampling to manage unbalanced data in smart cities by Ayushi Chahal, Preeti Gulia, Nasib Singh Gill, Mohammad Yahya, Mohd Anul Haq, Mohammed Aleisa, Abdullah Alenizi, Arfat Ahmad Khan, Piyush Kumar Shukla

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Circulating long non-coding RNAs NKILA, NEAT1, MALAT1, and MIAT expression and their association in type 2 diabetes mellitus by Irfan Ahmad, Mohammed Alfaifi, Mirza Masroor Ali Beg, Ali Gaithan Alkhathami, Prakash C Joshi, Osama M Alshehri, Abdulrahman Manaa Alamri, Amit Kumar Verma, Mohammad Yahya Alshahrani

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Uncovering the genetic architecture of inherited retinal disease in a consanguineous Iranian cohort by Lieselot Vincke, Kristof Van Schil, Hamid Ahmadieh, Afrooz Moghaddasi, Hamideh Sabbaghi, Narsis Daftarian, Tahmineh Motevasseli, Leila Javanparast Sheykhani, Mohammadreza Dehghani, Mohammad Yahya Vahidi Mehrjardi, Julie De Zaeytijd, Marieke De Bruyne, Quinten Mahieu, Ebrahim Al-Hajj, Marta Del Pozo-Valero, Toon Rosseel, Mattias Van Heetvelde, Reza Maroofian, Fatemeh Suri, Miriam Bauwens, Elfride De Baere

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