Concetta Scimone | Molecular genetics | Women Researcher Award

Published on by Global Scholar Awards

šŸŒŸDr. Concetta Scimone, Molecular genetics, Women Researcher AwardšŸ†

Doctorate at University of Messina, Italy

Concetta Scimone is an accomplished professional in the field of applied biology and genetics, hailing from Italy. With a diverse educational background in biotechnology, she has established herself as an Associate Professor at the University of Messina. Her expertise encompasses various domains such as molecular biology, bioinformatics, and cellular biotechnology. Throughout her career, she has been actively involved in research, teaching, and editorial roles, contributing significantly to the advancement of scientific knowledge.

Author Metrics:

Scopus Profile

ORCID Profile

Concetta Scimone’s contributions to the scientific community are reflected in her author metrics. With an SCOPUS H-index of 22, she has co-authored numerous scientific papers published in esteemed international journals. Additionally, she has presented oral communications and posters at both national and international conferences, showcasing her expertise and research findings to a broader audience.

  • Citations: 1,067 citations from 498 documents
  • Documents: 53 documents authored by Concetta Scimone
  • h-index: 26

Education:

Scimone’s academic journey is marked by a series of achievements. She holds a Ph.D. in Biology and Cellular Biotechnology from the University of Messina, along with a Master’s degree and a Bachelor’s degree in Biotechnology. Her educational background has provided her with a strong foundation in molecular and cell biology, enabling her to pursue a successful career in academia and research.

Research Focus:

Concetta Scimone’s research interests span various areas within biology and genetics. She has focused on elucidating molecular mechanisms and genetic bases of genetic rare diseases, including cerebral cavernous malformations, brain arteriovenous malformations, retinitis pigmentosa, and trimethylaminuria. Her research endeavors aim to advance understanding in these fields, potentially leading to improved diagnostics and therapeutic interventions.

Professional Journey:

Scimone’s professional journey is characterized by a rich tapestry of roles and responsibilities. From her early days as a teaching assistant at the University of Messina to her current position as an Associate Professor, she has demonstrated a strong commitment to education and research. Alongside her academic roles, she has also engaged in editorial assignments, serving as a board member and guest editor for esteemed scientific journals.

Honors & Awards:

Throughout her career, Concetta Scimone has been recognized for her contributions to the field of biology and genetics. While specific honors and awards may not be listed, her achievements, including her SCOPUS H-index and authorship of numerous publications, attest to her standing as a respected professional in her field.

Publications Noted & Contributions:

Scimone’s contributions to scientific literature are notable, with a significant number of co-authored papers published in impactful international journals. Her research findings, presented through oral communications and posters, have contributed to the advancement of knowledge in various domains of biology and genetics.

Title: Bridging Retinal and Cerebral Neurodegeneration: A Focus on Crosslinks between Alzheimerā€“Perusiniā€™s Disease and Retinal Dystrophies

Journal: Biomedicines

Publication Date: December 2023

DOI: 10.3390/biomedicines11123258

Contributors: Luigi Donato, Domenico MordĆ , Concetta Scimone, Simona Alibrandi, Rosalia d’Angelo, Antonina Sidoti

Title: How Many Alzheimerā€“Perusiniā€™s Atypical Forms Do We Still Have to Discover?

Journal: Biomedicines

Publication Date: July 2023

DOI: 10.3390/biomedicines11072035

Contributors: Luigi Donato, Domenico MordĆ , Concetta Scimone, Simona Alibrandi, Rosalia d’Angelo, Antonina Sidoti

Title: Impaired Nuclear and Mitochondrial Cross-Talk Might Alter mtDNA Epigenetic Regulation in Maternally Inherited Diabetes- and Deafness-Affected Patients

Journal: Biology and Life Sciences Forum

Publication Date: March 2023

DOI: 10.3390/blsf2023021026

Contributors: Luigi Donato, Concetta Scimone, Simona Alibrandi, Maria Vadala, Massimo Castellucci, Domenico MordĆ , Carmela Rinaldi, Rosalia d’Angelo, Antonina Sidoti

Title: Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes

Journal: Molecules

Publication Date: November 2021

DOI: 10.3390/molecules26227045

Contributors: Simona Alibrandi, Fabiana Nicita, Luigi Donato, Concetta Scimone, Carmela Rinaldi, Rosalia d’Angelo, Antonina Sidoti

Research Timeline:

Concetta Scimone’s research timeline highlights her progression and involvement in various research projects and initiatives. From her early years as a voluntary researcher to her current role as a principal investigator and associate professor, she has continuously engaged in research activities aimed at addressing key questions in biology and genetics.

Collaborations and Projects:

Scimone has been actively involved in collaborations and projects spanning national and international boundaries. Her work with institutions such as the University of Messina and the Istituto Euromediterraneo di Scienza e Tecnologia underscores her collaborative spirit and commitment to advancing scientific knowledge through interdisciplinary efforts. These collaborations have resulted in impactful research outcomes and contributions to the scientific community.

Dongye He | Medical Genetics | Best Researcher Award

Published on by Global Scholar Awards

šŸŒŸDr. Dongye He, Medical Genetics, Best Researcher AwardšŸ†

  • Ā Doctorate at Affiliated Hospital of Jining Medical University, China

Dongye He is a research associate at the Medical Research Center at the Affiliated Hospital of Jining Medical University in Shandong Province, China. He specializes in investigating the molecular etiology and disease mechanisms underlying rare genetic diseases in the endocrine system. Dongye holds a degree from Dalian University of Technology and has made significant contributions to understanding various endocrine disorders through his research.

Author Metrics

Dongye He has published 17 documents and garnered 165 citations from 149 documents, indicating the impact of his research in the field. His h-index, which measures both the productivity and citation impact of the publications, is 8. These metrics demonstrate Dongye’s contribution to the scholarly literature on endocrine disorders.

Scopus Profile

ORCID Profile

Education

Dongye He pursued his education at Dalian University of Technology, where he gained expertise in his field of study. He completed his education from September 2012 to June 2018, preparing him for a career in medical research focusing on rare genetic diseases in the endocrine system.

Research Focus

Dongye He’s research focuses on investigating the molecular mechanisms underlying rare genetic diseases in the endocrine system. He is particularly interested in disorders such as growth hormone deficiency and idiopathic hypogonadotropic hypogonadism. His work aims to enhance understanding of these conditions and develop effective diagnostic and therapeutic strategies.

Professional Journey

Dongye He began his professional journey as a research associate at the Medical Research Center at the Affiliated Hospital of Jining Medical University in September 2018. Since then, he has been actively involved in conducting research, publishing papers, and contributing to advancements in the field of endocrinology.

Honors & Awards

Dongye He’s contributions to the field of endocrinology have likely been recognized through various forms of academic recognition, such as conference presentations, scholarships, or institutional awards.

Publications Noted & Contributions

Dongye He has contributed to numerous publications focusing on topics ranging from molecular diagnosis and therapeutic evaluations of endocrine disorders to the pharmacological properties of natural compounds. His research has shed light on the genetic basis of rare genetic diseases and explored potential treatment options for these conditions.

“Identification and functional analysis of first heterozygous frameshift mutation in the GHRH gene in a Chinese boy with isolated growth hormone deficiency” was published in the journal Gene in May 2024. The DOI for this article is 10.1016/j.gene.2024.148283. The contributors to this article are Shuoshuo Wei, Mei Zhang, Yanying Li, Wanling Yang, Chuanpeng Zhang, Fupeng Liu, Shuxiong Chen, Bo Ban, and Dongye He.

“Functional investigation of a novel ANKRD11 frameshift variant identified in a Chinese family with KBG syndrome” was published in the journal Heliyon in March 2024. The DOI for this article is 10.1016/j.heliyon.2024.e28082. The contributors to this article are Shuoshuo Wei, Yanying Li, Wanling Yang, Shuxiong Chen, Fupeng Liu, Mei Zhang, Bo Ban, and Dongye He.

“Letrozole combined with rhGH treatment increases the adult height of short pubertal boys” was published in the Journal of Pediatric Endocrinology & Metabolism (JPEM) on November 30, 2023. The DOI for this article is 10.1515/jpem-2023-0459. The PMID for this article is 38018388. The contributors to this article are He M, Zhang Y, Zhao Q, He D, Li Y, Zhang M, and Ban B.

“Clinical Manifestations, Genetic Variants and Therapeutic Evaluation in Sporadic Chinese Patients with Idiopathic Hypogonadotropic Hypogonadism” was published in the International Journal of General Medicine in September 2023. The DOI for this article is 10.2147/IJGM.S430904. The contributors to this article are Dongye He, Hailing Sun, Mei Zhang, Yanying Li, Fupeng Liu, Yanhong Zhang, Mingming He, and Bo Ban.

“Serum triglyceride glucose index is a valuable predictor for visceral obesity in patients with type 2 diabetes: a cross-sectional study” was published in the journal Cardiovascular Diabetology on April 29, 2023. The DOI for this article is 10.1186/s12933-023-01834-3. The PMID for this article is 37120516. The contributors to this article are Yang Q, Xu H, Zhang H, Li Y, Chen S, He D, Yang G, Ban B, Zhang M, and Liu F.

Research Timeline

Dongye He’s research journey has spanned several years, beginning with his education at Dalian University of Technology from September 2012 to June 2018. He then transitioned into his role as a research associate at the Medical Research Center at the Affiliated Hospital of Jining Medical University in September 2018, where he continues to contribute to advancements in the field.

Collaborations and Projects

Dongye He likely collaborates with colleagues and researchers within his institution and possibly from other institutions as well. His projects involve multidisciplinary approaches to understanding the molecular mechanisms of endocrine disorders and developing innovative solutions for diagnosis and treatment. Collaborations and projects play a crucial role in advancing scientific knowledge and addressing complex research questions in the field of endocrinology.