Goran Čuturilo - Genetic Mutations

Author Information

Dr. Goran Cuturilo is affiliated with the Department of Clinical Genetics at the University Children's Hospital in Belgrade, Serbia. His research primarily encompasses the fields of genetics, with a focus on inherited disorders, congenital defects, and syndromes. His work contributes significantly to the understanding and treatment of genetic conditions in pediatric populations.

Research Contributions

Dr. Goran Cuturilo has made notable contributions to the field of genetics through his research on various genetic disorders and syndromes. His recent studies have explored the variable expressivity of inherited variants in CHD3 related to Snijders Blok-Campeau syndrome, and he has conducted extensive surveys on Mucopolysaccharidosis in Southern and Eastern European countries. Additionally, his work on the genetic evaluation of newborns with critical congenital heart defects and a genetics-first approach to dissecting the heterogeneity of autism have been highly impactful. His contributions are well-regarded in the scientific community, as reflected in his numerous publications and citations.

Aliases

Dr. Goran Cuturilo is also known by several aliases, including Goran Čuturilo, G Cuturilo, G. Cuturilo, and G Čuturilo. These variations appear in his publications and citations across various platforms.

Publication and Citation Metrics

Metric Value
Number of Papers 52
Citation Count 653
H-index 15

Publications:

DOI: 10.1016/j.gim.2022.02.014

Year: 2022

DOI: 10.1186/s13023-022-02285-x

Year: 2022

DOI: 10.21203/rs.3.rs-1071210/v1

Year: 2021

DOI: 10.1007/s00431-021-04097-w

Year: 2021

DOI: 10.1176/appi.ajp.2020.20010015

Year: 2021

DOI: 10.1101/2021.10.04.21264162

Year: 2021

DOI: 10.21203/rs.3.rs-17457/v1

Year: 2020

DOI: 10.1186/s13023-020-01418-4

Year: 2020

DOI: 10.21203/rs.3.rs-17457/v2

Year: 2020

DOI: 10.1101/2020.01.14.20017426

Year: 2020

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