Ebrahim Sakhinia - Genetic Mutations

Author Information

Ebrahim Sakhinia is a prominent researcher affiliated with the Connective Tissue Research Center, Department of Medical Genetics, Faculty of Medicine, and Tabriz Genetic Analysis Centre (TGAC) at Tabriz University of Medical Sciences, located in Tabriz, Iran. His work primarily involves genetic research, with a significant focus on various genetic disorders and cancer studies. Ebrahim Sakhinia's contributions to the field are reflected in his extensive research on genetic mutations, methylation status, and gene expression related to diseases such as Behcet's disease and various forms of cancer.

Research Contributions

Ebrahim Sakhinia has made substantial contributions to the field of medical genetics, particularly in understanding the genetic basis of reproductive health issues and cancer. His research in 2021 includes significant studies on the genetic aspects of spermatozoa in men with fertility issues and mutations in the TP53 gene in colorectal cancer patients. Notably, his work often explores gene expression and methylation patterns, which are crucial for understanding disease mechanisms and potential therapeutic targets. Sakhinia’s systematic reviews and evaluations of genetic markers highlight his dedication to advancing genetic analysis techniques and improving clinical outcomes through personalized medicine.

Aliases

Throughout his academic career, Ebrahim Sakhinia has been referenced under several aliases, including E Sakhinia and E. Sakhinia. These variations are common in scientific literature and databases, reflecting different naming conventions or transliterations of his name.

Publication and Citation Metrics

Metric Value
Total Citation Count 1451
H-index 22
Total Number of Papers 127

Publications:

Partnered Content Networks

Relevant Topics