Feride İffet Şahi̇n - Genetic Mutations

Author Information

Feride İffet Şahin is a distinguished researcher affiliated with the Department of Medical Genetics at Başkent University, Faculty of Medicine in Ankara, Turkey. Şahin's expertise in genetics is reflected in her extensive research contributions that span various topics in the field, including gene polymorphisms, diagnostic criteria in familial Mediterranean fever, and placental gene expression patterns.

Research Contributions

Feride İffet Şahin's research has primarily focused on genetic disorders and their clinical implications. Her notable works include studies on the KANSL1 gene deletion, MEFV gene variants in the Turkish population, and the genetic underpinnings of familial Mediterranean fever. Additionally, Şahin has explored the impact of matrix metalloproteinase gene polymorphisms on allograft rejection in pediatric renal transplant recipients and examined the role of heredity in strabismus. Her research has significantly contributed to the understanding of genetic factors in various medical conditions.

Aliases

Over the course of her academic career, Feride İffet Şahin has published under several variations of her name, including Feride İ. Şahin, F. İffet Şahin, and Feride İffet Sahin. This diversity of aliases reflects the transliteration of her name across different publications and databases.

Publication and Citation Metrics

Metric	Value
Total Papers	179
Total Citations	1454
H-index	21

Publications:

MLPA Method does not Always Confirm the Results of aCGH: A Study of KANSL1 Gene Deletion Patients

DOI: 10.12996/gmj.2022.37

Year: 2022

Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium.

DOI: 10.1007/s10142-021-00819-3

Year: 2022

Comparison of diagnostic criteria for children with familial Mediterranean fever

DOI: 10.1007/s00431-021-04370-y

Year: 2022

Model Organisms and Systems in Life Sciences

DOI: 10.7197/cmj.991430

Year: 2022

The Comparison of Diagnostic Criteria in Children with Familial Mediterranean Fever

DOI: 10.21203/RS.3.RS-705764/V1

Year: 2021

Placental Maspin Gene Expression Pattern May Be Used to Distinguish Between Preeclampsia and Intrauterine Growth Restriction

DOI: 10.21613/gorm.2019.969

Year: 2021

99 G2019-045 Placental Maspin Gene Expression Pattern May_Layout 1

DOI:

Year: 2021

Impact of Matrix Metalloproteinases 2 and 9 and Tissue Inhibitor of Metalloproteinase 2 Gene Polymorphisms on Allograft Rejection in Pediatric Renal Transplant Recipients.

DOI: 10.6002/ect.2020.0036

Year: 2020

Investigation of ARHGEF12 Single Nucleotide Polymorphism in Hypercholesterolemia and Primary Open Angle Glaucoma

DOI: 10.12996/gmj.2020.142

Year: 2020

The Role of Heredity and the Prevalence of Strabismus in Families with Accommodative, Partial Accommodative, and Infantile Esotropia

DOI: 10.4274/tjo.galenos.2019.49204

Year: 2020

How Does Hemoglobin Electrophoresis Work?

What are Synonymous Codons?

Can Genetics Explain Individual Differences in Cognitive Abilities?

What is a Substitution Mutation?

What is Polyploidy?

What Are the Implications of Genetic Research on ASD?

How do PAHs cause genetic mutations?

What is the Impact of Inherited Mutations?

What are the Applications of Induced Mutations in Agriculture?

How Are Synonymous Mutations Detected?

Partnered Content Networks

Relevant Topics