University for Business and Technology, Albania
Author Profile
Early Academic Pursuits:
Gazmend Temaj embarked on his academic journey with a Bachelor's degree in General Biology and Molecular biologyfrom the University of Pristina in 1998. This foundational education provided him with a solid understanding of the fundamental principles of biology, setting the stage for his subsequent achievements in the field of genetics and biomedicine. He furthered his education with a Master of Sciences degree from the University of Zagreb/Sarajevo in 2004, where he delved deeper into subjects such as genetic populations, molecular biology, and biochemistry. This postgraduate study equipped him with specialized knowledge and skills necessary for his future endeavors in the realm of genetics.
Professional Endeavors:
Throughout his career, Gazmend Temaj has held various positions in prestigious institutions around the world, showcasing his expertise in molecular biology, cytogenetics, and clinical genetics. From his role as a Prof. Assistant at the Medical Faculty in Kosovo to his guest doctor positions at institutions like Goethe Uniklinik in Frankfurt and University Rezonanca in Prishtina, Temaj has consistently demonstrated his proficiency in a wide array of molecular techniques, including ELISA, PCR, gel electrophoresis, and cell culture. His contributions extend beyond his academic appointments, as evidenced by his participation in international conferences and collaborations with renowned institutes such as the Human Genetic Institute in Jena, Germany, and the DEBRA Institute at Salzburg University Clinic in Austria.
Contributions and Research Focus:
His research interests primarily revolve around rare genetic diseases, with a particular focus on Epidermolysis Bullosa (EB). His dissertation on the molecular environment and expression strategy of the therapeutic target RpL35/uL29 in EB underscores his dedication to unraveling the complexities of this debilitating condition. His presentations at international summer academies and conferences highlight his commitment to raising awareness and sharing insights into the management, therapy, and genetic implications of rare diseases, including ribosomopathies and carcinogenic diseases. Temaj's involvement in professional organizations such as ANUBIH, the Albanian Association of Human Molecular Genetics, and membership in consortia like PharmVar and CPIC further attest to his active engagement in advancing the field of genetics and personalized medicine.
Accolades and Recognition:
His contributions to the field have been recognized through invitations to review for esteemed journals and his participation in conferences as an invited lecturer. His commitment to excellence is evident in his pursuit of continuous education, as demonstrated by his completion of courses like the Clinical Laboratory Genetics program in Zagreb, Croatia, and his attendance at webinars on oncology NGS testing.
Impact and Influence:
Through his research, teaching, and professional engagements, Gazmend Temaj has made significant contributions to the field of genetics and biomedicine. His expertise, combined with his passion for advancing knowledge and improving patient care, continues to inspire colleagues and students alike.
Legacy and Future Contributions:
As Gazmend Temaj continues his journey in academia and research, his legacy will be defined by his dedication to unraveling the mysteries of rare genetic diseases and his efforts to translate scientific discoveries into tangible benefits for patients. His future contributions are poised to further enrich our understanding of human genetics and pave the way for innovative therapies and personalized medicine approaches.
A total of 112 citations for his publications, demonstrating the impact and recognition of his research within the academic community.
- Citations 112
- h-index 7
- i10-index 5
Notable Publications
Ribosome-directed therapies in cancer
The impact of consanguinity on human health and disease with an emphasis on rare diseases
Comparative analysis of dermatoglyphic traits in Albanian and Turkish population living in Kosovo
Joubert syndrome: Molecular basis and treatment
Comparative analysis of qualitative dermatoglyphic traits of Albanian and Turkish populations living in the area of Dukagjin Valley in Kosovo
Mucopolysaccharidosis III: Molecular basis and treatment
Three patterns of inheritance of quantitative dermatoglyphic traits: Kosovo albanian twin study
Suspicions regarding the genetic inheritance of acute lymphoblastic leukemia in patients with down syndrome
Correlation between level of vitamin D in serum and value of lung function in children diagnosed with bronchial asthma
Case Report: Identification of likely recurrent CEP290 mutation in a child with Joubert syndrome and cerebello-retinal-renal features.