Author Information
Seher Başaran is affiliated with the Istanbul University, Istanbul Medical Faculty, Department of Medical Genetics, Turkey. Her research focuses on the genetic underpinnings of various medical conditions, including disorders of sex development, Parkinson's disease, chromosomal abnormalities, and more. She has made significant contributions to the field through her extensive research and numerous publications.Research Contributions
Seher Başaran has made significant contributions to the field of medical genetics. Her research encompasses a broad range of topics including mutations in AR or SRD5A2 genes, distal arthrogryposis phenotypes, holoprosencephaly, gonadal pathology, hereditary Parkinson's disease, 22q11.2 microdeletion syndrome, Fanconi anemia, and prenatal diagnostic techniques. Her work has been instrumental in advancing the understanding of these genetic conditions, offering insights into their clinical and molecular characteristics, and improving diagnostic and therapeutic approaches.Aliases
Seher Başaran is also known by several aliases including Seher Başaran, S. Başaran, S. Basaran, S Basaran, and Seher Basaran. These variations of her name appear in different publications and databases.Publication and Citation Metrics
| Metric |
Value |
| Citation Count |
1401 |
| H-index |
21 |
| Paper Count |
106 |
