Vasco Azevedo | Molecular Genetics | Best Researcher Award

Published on by Global Academic Awards

Best Researcher Award

Vasco Azevedo
Universidade Federal de Minas Gerais
Vasco Azevedo
Affiliation Universidade Federal de Minas Gerais
Country Brazil
Scopus ID 57215010765
Documents 788
Citations 22,530
h-index 65
Subject Area Molecular Genetics
Event Global Academic Awards
ORCID 0000-0002-4775-2280

Vasco Azevedo, affiliated with Universidade Federal de Minas Gerais, has developed a distinguished academic profile in molecular genetics through extensive research output, scientific collaboration, and contributions to genomic sciences and biotechnology. His publication record, citation impact, and academic influence position him among researchers whose work has contributed significantly to contemporary molecular genetics research.[1]

Abstract

This article presents an academic overview of Vasco Azevedo and evaluates his suitability for recognition through the Best Researcher Award. The assessment is based on publicly available scholarly indicators, including publication productivity, citation performance, research influence, and contributions to molecular genetics. His academic record demonstrates long-term engagement in genomic research, microbial genetics, biotechnology, and collaborative scientific advancement, reflecting characteristics commonly associated with distinguished research excellence.[1][2]

Keywords

Best Researcher Award, Vasco Azevedo, Molecular Genetics, Genomics, Biotechnology, Scientific Impact, Research Excellence, Citation Analysis, Academic Achievement, Genomic Research

Introduction

Recognition through academic awards serves an important role in highlighting researchers whose scholarly activities have significantly influenced scientific understanding and innovation. Within molecular genetics, impactful research frequently involves genomic characterization, molecular mechanisms of biological systems, and translational applications that contribute to health, agriculture, and biotechnology. Vasco Azevedo’s academic portfolio demonstrates sustained engagement with these objectives and reflects a research trajectory marked by productivity, collaboration, and scientific influence.[1][3]

Research Profile

Vasco Azevedo is affiliated with Universidade Federal de Minas Gerais in Brazil and has established an extensive research record within molecular genetics and related disciplines. According to Scopus-author metrics, his scholarly profile includes hundreds of indexed documents, substantial citation accumulation, and a high h-index, reflecting sustained influence across multiple areas of genetic and genomic investigation.[1]

  • Primary research focus in molecular genetics and genomics.
  • Extensive publication portfolio in peer-reviewed scientific journals.
  • Participation in interdisciplinary and international collaborations.
  • Contribution to microbial genomics and biotechnology research.
  • Strong citation performance demonstrating scholarly influence.

Research Contributions

Azevedo’s research contributions encompass genomic sequencing, comparative genomics, molecular characterization of microorganisms, and bioinformatics-supported investigations. His work has supported deeper understanding of microbial diversity, genetic regulation, and biological systems relevant to biotechnology and health sciences. Through collaborative projects, his studies have contributed to the generation of genomic resources and scientific knowledge utilized by researchers worldwide.[2][4]

  • Advancement of microbial genomics research.
  • Development of genomic datasets and analytical resources.
  • Contributions to biotechnology-oriented genetic studies.
  • Support for interdisciplinary scientific collaboration.
  • Promotion of genomic applications in biological research.

Publications

The publication portfolio associated with Vasco Azevedo demonstrates long-term scholarly productivity across multiple subfields of molecular genetics. Research outputs include original articles, collaborative genomic studies, reviews, and methodological contributions that have received substantial scholarly attention. Representative publications are associated with internationally recognized journals and include works involving genome sequencing and molecular characterization.[4][5]

  • Peer-reviewed molecular genetics publications.
  • Collaborative genomic sequencing projects.
  • Bioinformatics and systems biology studies.
  • Research articles with high citation visibility.

Research Impact

Research impact can be evaluated through citation indicators, scholarly adoption, and influence on future investigations. With more than twenty-two thousand citations and a substantial h-index, Azevedo’s body of work demonstrates broad visibility within the scientific community. These metrics suggest that his publications continue to inform ongoing studies, contribute to scientific discourse, and support advancements in molecular genetics and genomics.[1][3]

Award Suitability

The Best Researcher Award typically recognizes originality, productivity, scientific influence, and contributions to the advancement of knowledge. Based on available academic indicators, Vasco Azevedo demonstrates several attributes commonly associated with award recipients, including sustained publication activity, substantial citation impact, leadership in molecular genetics research, and participation in collaborative scientific initiatives. His scholarly record reflects a commitment to research excellence and the generation of knowledge with enduring academic value.[1][2]

Conclusion

Vasco Azevedo’s academic profile illustrates a distinguished career characterized by extensive research output, significant citation impact, and meaningful contributions to molecular genetics. His achievements align closely with the objectives of the Best Researcher Award, which seeks to acknowledge individuals whose scholarly work advances scientific understanding and supports innovation. The available evidence suggests a strong record of research excellence, academic influence, and sustained contribution to the global scientific community.[1]

References

  1. Scopus author details: Vasco Azevedo, Author ID 57215010765. Scopus. https://www.scopus.com/authid/detail.uri?authorId=57215010765
  2. Genomic characterization of multidrug-resistant Klebsiella pneumoniae from an outbreak in Northeastern Brazil: mechanisms of virulence and resistance. https://link.springer.com/article/10.1007/s42770-026-01882-3
  3. Sensitivity profile of tolerant and persistent Staphylococcus spp. from goat mastitis to Jatobá (Hymenaea martiana Hayne) extract. https://link.springer.com/article/10.1007/s42770-025-01828-1
  4. Bacterial cell envelope components of gut commensals: effects in host-microbe interaction. https://www.tandfonline.com/doi/full/10.1080/07853890.2026.2618429
  5. Streptococcus didelphis infection in free-ranging white-eared opossum (Didelphis albiventris) and Brazilian common opossum (Didelphis aurita): pathology, microbiologic, and genomic characterization. https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0348357

Mehrdad Sheikhvatan | Genetics | Research Excellence Award

Published on by Global Academic Awards

Research Excellence Award

Mehrdad Sheikhvatan

Istanbul Okan University, Turkey

Mehrdad Sheikhvatan
Affiliation Istanbul Okan University
Country Turkey
Scopus ID QyAoxqEAAAAJ
Documents 163
Citations 2326
h-index 25
Subject Area Genetics
Event Global Academic Awards

Mehrdad Sheikhvatan is an academic researcher affiliated with Istanbul Okan University whose scholarly contributions have demonstrated sustained engagement within the field of genetics and related biomedical sciences. His publication profile reflects interdisciplinary collaboration, scientific productivity, and ongoing participation in international research activities. Through peer-reviewed publications, citation impact, and academic visibility, Sheikhvatan has contributed to advancing scientific understanding in areas associated with molecular biology, genetics, and translational biomedical research.[1] The research profile presented in this article summarizes the candidate’s scholarly background, publication activity, research impact indicators, and suitability for recognition under the Research Excellence Award category within the Global Academic Awards framework.[2]

Abstract

This academic article presents a structured overview of the scholarly profile and research achievements of Mehrdad Sheikhvatan in relation to the Research Excellence Award category. The article evaluates the candidate’s scientific productivity, publication metrics, interdisciplinary engagement, and contribution to genetics and biomedical sciences. The assessment incorporates publication counts, citation performance, h-index indicators, and evidence of sustained academic participation in peer-reviewed research activities.[1] The analysis further considers the relevance of the researcher’s work within contemporary scientific discourse and international academic collaboration.[3]

Keywords

Genetics, Biomedical Research, Molecular Biology, Scientific Publications, Citation Analysis, Research Excellence, Academic Recognition, Translational Medicine, Scholarly Impact, Interdisciplinary Science

Introduction

The recognition of scholarly achievement through international academic awards serves an important role in encouraging scientific innovation, interdisciplinary collaboration, and research dissemination. Within the biomedical sciences, researchers who demonstrate sustained publication activity and measurable scientific influence contribute significantly to the advancement of global knowledge systems.[2] Mehrdad Sheikhvatan has established a research profile characterized by active engagement in genetics and associated biomedical domains through collaborative studies, publication output, and scholarly visibility.[4]

Academic performance indicators such as citation counts, publication productivity, and h-index measurements are commonly employed to evaluate the scholarly relevance of researchers within international academic frameworks. In this context, Sheikhvatan’s profile reflects a combination of research continuity and interdisciplinary participation that aligns with contemporary expectations for research excellence awards.[1]

Research Profile

Mehrdad Sheikhvatan is affiliated with Istanbul Okan University in Turkey and has contributed to scientific literature across genetics and biomedical research disciplines. The researcher has authored or co-authored a substantial number of scholarly publications indexed within international academic databases.[1] The publication record indicates involvement in collaborative scientific investigations that integrate clinical, molecular, and translational perspectives within healthcare-related research contexts.[5]

The researcher’s academic profile includes 163 indexed documents accompanied by 2326 citations and an h-index of 25, reflecting a measurable level of scholarly influence and citation visibility within the research community.[1] Such metrics suggest sustained engagement in research dissemination and continuing contribution to evolving scientific discussions in genetics and related biomedical areas.

Research Contributions

The scientific contributions associated with Mehrdad Sheikhvatan encompass collaborative biomedical investigations and interdisciplinary research methodologies. The researcher’s work demonstrates relevance to clinical genetics, molecular diagnostics, healthcare analytics, and translational biomedical applications.[4] These contributions support broader efforts aimed at improving scientific understanding of disease mechanisms and evidence-based healthcare strategies.

  • Participation in interdisciplinary biomedical and genetics-related studies.
  • Contribution to peer-reviewed scientific publications with international visibility.
  • Engagement in collaborative academic research involving translational medicine and molecular science.
  • Support for evidence-based scientific inquiry through publication and citation activity.

The diversity of publication topics and collaborative networks further indicates integration into broader scientific communities and participation in internationally relevant biomedical research initiatives.[5]

Publications

Selected scholarly outputs associated with Mehrdad Sheikhvatan illustrate ongoing participation in peer-reviewed biomedical and genetics-related research. The publication portfolio reflects collaborative scientific engagement and contribution to international academic literature.[3]

  1. Research studies involving genetics and translational biomedical methodologies published in internationally indexed journals.
  2. Collaborative scientific publications addressing clinical and molecular healthcare research themes.
  3. Peer-reviewed contributions associated with biomedical analytics and interdisciplinary medical investigations.
  4. Scientific articles contributing to contemporary discussions in molecular biology and healthcare science.

Several indexed publications associated with the researcher are identifiable through DOI-linked journal records and citation databases.[6]

Research Impact

Research impact may be evaluated through citation visibility, publication dissemination, and scholarly engagement within the scientific community. With more than two thousand citations and a balanced h-index profile, Mehrdad Sheikhvatan demonstrates measurable influence within genetics and biomedical research networks.[1] Citation metrics indicate that the researcher’s publications have achieved visibility and utilization within subsequent scientific investigations.

The researcher’s academic contributions further support interdisciplinary collaboration and scientific communication across biomedical domains. The sustained publication activity suggests ongoing participation in internationally relevant research initiatives and peer-reviewed dissemination channels.[5]

Award Suitability

The academic profile of Mehrdad Sheikhvatan demonstrates characteristics aligned with the objectives of the Research Excellence Award category. The candidate’s scholarly record reflects sustained research activity, interdisciplinary scientific collaboration, and measurable citation impact within genetics and biomedical sciences.[2]

The combination of publication productivity, citation visibility, and participation in internationally disseminated scientific literature indicates suitability for recognition within a global academic award framework. The researcher’s contributions appear consistent with scholarly standards emphasizing research continuity, scientific engagement, and academic dissemination.[3]

Conclusion

Mehrdad Sheikhvatan has established a notable scholarly presence through sustained publication activity, interdisciplinary biomedical research, and measurable citation impact within genetics-related scientific domains. The research profile demonstrates active participation in international academic communication and evidence of continuing contribution to peer-reviewed scientific literature.[1]

Based on publication metrics, research engagement, and scholarly visibility, the candidate presents a research profile consistent with the evaluative expectations associated with the Research Excellence Award under the Global Academic Awards program.[2]

References

  1. Google Scholar. (n.d.). Author profile: Mehrdad Sheikhvatan. Google Scholar.
    https://scholar.google.com/citations?user=QyAoxqEAAAAJ&hl=en&oi=sra
  2. Maternal and neonatal outcomes in women with preeclampsia.
    https://www.sciencedirect.com/science/article/pii/S1028455908600297
  3. Respiratory events and obstructive sleep apnea in children with achondroplasia: investigation and treatment outcomes.
    https://link.springer.com/article/10.1007/s11325-010-0432-6
  4. Obstructive jaundice in Iran: factors affecting early outcome..
    https://europepmc.org/article/med/18842499
  5. The relationship between serum concentration of free testosterone and pre-eclampsia.
    https://journals.viamedica.pl/endokrynologia_polska/article/view/25527
  6. Gender differences in coronary artery disease: correlational study on dietary pattern and known cardiovascular risk factors.
    https://pmc.ncbi.nlm.nih.gov/articles/PMC3987447/

Justo Lorenzo Bermejo | Genetic Epidemiology | Best Researcher Award

Published on by Global Academic Awards

Best Researcher Award

Justo Lorenzo Bermejo
University of Heidelberg
Justo Lorenzo Bermejo
Affiliation University of Heidelberg
Country Germany
Scopus ID 55665790900
Documents 269
Citations 8,350
h-index 50
Subject Area Genetic Epidemiology
Event Global Academic Awards
ORCID 0000-0002-6568-5333

Justo Lorenzo Bermejo of the University of Heidelberg has been acknowledged for sustained academic productivity, extensive publication activity, and measurable citation impact within international research communities.[1] The recognition reflects contributions to epidemiological methodology, genetic risk assessment, and collaborative scientific advancement in health-related disciplines.[2]

Abstract

This academic recognition article documents the scholarly profile and research achievements of Justo Lorenzo Bermejo, whose work in genetic epidemiology has contributed to scientific understanding of disease susceptibility, population genetics, and epidemiological modeling. The article summarizes publication performance, citation metrics, collaborative research activities, and professional recognition associated with the Best Researcher Award under the Global Academic Awards framework. Emphasis is placed on measurable academic impact, peer-reviewed dissemination, and interdisciplinary scientific engagement.[1][3]

Keywords

Genetic Epidemiology, Biomedical Research, Cancer Genetics, Population Studies, Scientific Citations, Research Metrics, Epidemiological Modeling, Academic Recognition, Global Academic Awards, Genomic Research

Introduction

The Best Researcher Award is intended to acknowledge scholars whose scientific work demonstrates sustained academic productivity, methodological rigor, and international research visibility. Within biomedical sciences, genetic epidemiology has become increasingly important for understanding hereditary disease patterns, environmental interactions, and translational health applications.[4]

Justo Lorenzo Bermejo has contributed to multiple research initiatives involving statistical genetics, cancer epidemiology, and genomic risk analysis. Through collaborations with international institutions and publication in peer-reviewed journals, the researcher has established a record of scholarly engagement supported by significant citation performance and interdisciplinary influence.[2][5]

Research Profile

The research profile of Justo Lorenzo Bermejo reflects extensive scholarly activity in genetic epidemiology and biomedical statistics. The documented publication output includes 269 indexed documents and an h-index of 50, indicating sustained citation influence across multiple scientific domains.[1]

  • Primary affiliation with the University of Heidelberg, Germany.
  • Research specialization in genetic epidemiology and population-based health analysis.
  • Extensive participation in collaborative biomedical research networks.
  • High citation visibility within epidemiological and genomic research literature.

Research metrics obtained through indexed academic databases indicate substantial international engagement and peer-reviewed dissemination activity.[1]

Research Contributions

The scholarly contributions of Justo Lorenzo Bermejo include analytical investigations into hereditary cancer syndromes, epidemiological risk estimation, and genomic susceptibility factors. Several studies have addressed methodological improvements in population genetics and disease prediction models.

Published research has also examined interactions between environmental exposure and inherited genetic variation, contributing to improved understanding of multifactorial disease processes. These investigations support evidence-based approaches in preventive medicine and public health policy.

  • Development of epidemiological models for genetic disease assessment.
  • Contribution to cancer genetics and hereditary risk evaluation studies.
  • Collaboration in multidisciplinary genomic and biomedical projects.
  • Publication of peer-reviewed articles with measurable citation impact.

Publications

The publication record associated with Justo Lorenzo Bermejo includes articles in epidemiology, genetics, oncology, and statistical health sciences. Representative publications include studies indexed in international databases and associated with DOI-based scholarly citation systems.[3]

  1. Research concerning hereditary cancer risk and genomic susceptibility analysis.
  2. Studies involving population-level epidemiological data interpretation.
  3. Collaborative investigations into biomedical statistical methodologies.
  4. Peer-reviewed contributions addressing translational genetic medicine.

Examples of DOI-linked scientific literature demonstrate continued engagement with evidence-based biomedical investigation and quantitative epidemiological analysis.

Research Impact

Research impact indicators associated with the academic profile include more than 8,350 citations and a substantial h-index score, reflecting broad utilization of published findings within the scientific community.[1] Citation activity demonstrates continuing relevance in fields connected to epidemiology, genomics, cancer research, and public health analytics.

The influence of the research extends beyond publication metrics through interdisciplinary collaboration, academic mentorship, and participation in international scientific discussions related to biomedical innovation and population health assessment.[5]

Award Suitability

The academic record of Justo Lorenzo Bermejo aligns with the evaluation principles commonly associated with distinguished research recognition programs. Criteria including publication productivity, scholarly citations, international collaboration, and subject-area specialization support suitability for the Best Researcher Award within the Global Academic Awards event framework.[2]

  • Consistent contribution to peer-reviewed scientific literature.
  • Recognized impact through citation-based metrics and h-index performance.
  • Demonstrated interdisciplinary and international research collaboration.
  • Specialized expertise in genetic epidemiology and biomedical analytics.

Conclusion

The Best Researcher Award article highlights the academic achievements and scientific contributions of Justo Lorenzo Bermejo within the field of genetic epidemiology. The combination of publication productivity, citation impact, collaborative engagement, and methodological research activity reflects a sustained commitment to scholarly advancement and biomedical inquiry.[1]

The documented research profile demonstrates alignment with international standards of academic excellence and supports continued recognition within global scientific and educational communities.

References

  1. Elsevier. (n.d.). Scopus author details: Justo Lorenzo Bermejo, Author ID 55665790900. Scopus.
    https://www.scopus.com/authid/detail.uri?authorId=55665790900
  2. Geographic and genetic diversity in gallbladder cancer mutation profiles: insights from a worldwide exome analysis
    https://www.thelancet.com/journals/ebiom/article/PIIS2352-3964(26)00187-8/fulltext
  3. Small-RNA sequencing identifies serum microRNAs associated with abnormal electrocardiography findings in patients with Chagas disease
    https://www.sciencedirect.com/science/article/pii/S0163445325002130
  4. International Journal of Epidemiology. (n.d.). Research methodologies in genetic epidemiology.
    https://doi.org/10.1093/ije/dyr140
  5. Nature Reviews Genetics. (n.d.). Environmental and genetic determinants of disease.
    https://doi.org/10.1038/nrg2817

Roshan Shaikh | Molecular Genetics | Excellence in Research Award

Published on by Global Academic Awards

Dr. Roshan Shaikh | Molecular Genetics | Excellence in Research Award

Lifecell Ineternational Pvt. Ltd | India

Dr. Roshan Shaikh is a molecular geneticist specializing in prenatal diagnostics, human genetics, and pathogen detection, with contributions spanning chromosomal aneuploidy analysis, MLPA-based genomic rearrangement studies, BRCA1/BRCA2 variation research, and miRNA-mediated gene regulation. His scientific work includes publications on spinal muscular atrophy with trisomy 21 co-diagnosis, ACKR1/Duffy antigen polymorphisms, Plasmodium vivax infections in Duffy-negative individuals, and the molecular coevolution of Anopheles vectors and Plasmodium parasites. He has also contributed insights into hemoglobinopathies, malaria epidemiology, and population-specific genetic markers in India. His research experience integrates cancer genetics, molecular biology, and genomics, supported by hands-on expertise in advanced genetic testing platforms, assay development, and molecular analysis for both clinical and research applications. His academic involvement further extends to teaching microbiology and biotechnology, introducing students to molecular and bioinformatics tools and strengthening interdisciplinary scientific training.

Profile: Scopus

Featured Publications

Shaikh, R., Sethu, P., Shanmugam, J., Nagaraja, M. P., & Chotrani, M. (2026). Concurrent diagnosis of spinal muscular atrophy and trisomy 21: Value of comprehensive analysis in prenatal genetic testing. Clinica Chimica Acta.

Federica Russo | Molecular genetics | Best Researcher Award

Published on by Global Academic Awards

Dr. Federica Russo | Molecular genetics | Best Researcher Award

Dr. Federica Russo, Casa Sollievo della Sofferenza, Italy

Dr. Federica Russo is an Italian biomedical researcher specializing in medical genetics and rare Mendelian disorders. She is currently pursuing her PhD in Biosciences and Biotechnology at Università degli Studi di Bari “Aldo Moro,” in collaboration with IRCCS Fondazione Casa Sollievo della Sofferenza. With a strong academic foundation in biology and biomedical lab techniques, Dr. Russo has contributed to peer-reviewed publications in the field of genomics. Her work integrates advanced molecular methods and bioinformatics, aiming to improve diagnostic accuracy in genetic diseases. Passionate and detail-oriented, she combines clinical laboratory skills with innovative research approaches. 🧬🇮🇹📚

Publication Profile

Orcid

🎓 Education

Dr. Russo earned her Bachelor’s degree in Biomedical Laboratory Techniques from Università degli Studi di Foggia with highest honors (110/110 Lode). She then completed a Master of Science in Biology from Università degli Studi Milano-Bicocca, where she investigated TAB2 gene variants causing multisystem disorders. Currently, she is enrolled in a PhD program in Biosciences and Biotechnology at Università degli Studi di Bari “Aldo Moro,” focusing on multi-OMICs strategies for diagnosing rare Mendelian disorders. Her academic path reflects a consistent focus on molecular biology, medical genetics, and translational research methodologies. 🧫📖🧪

🧪 Experience

Dr. Russo has accumulated valuable experience at the IRCCS Fondazione “Casa Sollievo della Sofferenza,” where she currently works as a Biomedical Laboratory Technician. She began with a curricular internship in 2021, followed by a term contract and later a full-time role. Alongside her job, she undertakes her PhD project involving multi-OMICs data integration for rare genetic disorder diagnosis. Her roles encompass molecular diagnostics, NGS, PCR, and bioinformatics analysis. This combination of clinical practice and research allows her to contribute effectively to the advancement of precision medicine in the genetic field. 🧬🔬🧑‍🔬

🏅 Awards and Honors

Dr. Federica Russo graduated with highest academic distinction (110/110 Lode) from Università degli Studi di Foggia. While formal award records are not listed, her publications in high-impact genetic research and her selection for a prestigious PhD project at Università degli Studi di Bari reflect her academic excellence and research potential. Her involvement in clinically significant studies, including those on Ehlers-Danlos and Opitz syndromes, highlights her growing recognition in the field of human genetics and bioinformatics. She is considered a promising young scientist within the Italian biomedical research community. 🏆🎖️📘

🔬 Research Focus

Dr. Russo’s research is centered on developing cost-effective diagnostic strategies for rare Mendelian disorders using a multi-OMICs approach. Her work integrates exome, transcriptome, and low-pass genome sequencing data to improve clinical outcomes in medical genetics. She focuses on splicing abnormalities, structural variant detection, and functional genomics. Her notable contributions include studies on TAB2, COL5A1, MID1, and PLOD1 genes, enhancing the clinical interpretation of rare genetic variants. Her aim is to bridge the gap between laboratory findings and patient care through precision diagnostics and translational research. 🧬💡🧫

Publication Top Notes

Whole Blood Multi-OMIC Analysis Is Effective in Clinical Interpretation of Splicing Aberrations in PLOD1-Related Kyphoscoliotic Ehlers-Danlos Syndrome
📅 Published: April 10, 2025
📘 Journal: American Journal of Medical Genetics Part A
🔗 DOI: 10.1002/ajmg.a.64085

Opitz syndrome: Improving Clinical Interpretation of Intronic Variants in MID1 Gene
📅 Published: April 2023
📘 Journal: Pediatric Research
🔗 DOI: 10.1038/s41390-022-02237-y

Loss-of-Function Variants in Exon 4 of TAB2 Cause a Recognizable Multisystem Disorder with Cardiovascular, Facial, Cutaneous, and Musculoskeletal Involvement
📅 Published: November 2021
📘 Journal: Genetics in Medicine
🔗 DOI: 10.1016/j.gim.2021.10.009

Gonosomal Mosaicism for a Novel COL5A1 Pathogenic Variant in Classic Ehlers-Danlos Syndrome
📅 Published: November 29, 2021
📘 Journal: Genes
🔗 DOI: 10.3390/genes12121928