Arash Javanmard | Genomics | Best Researcher Award

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Mr. Arash Javanmard | Genomics | Best Researcher Award

Mr. Arash Javanmard, University of Tabriz, Iran

Dr. Arash Javanmard is an Associate Professor in Animal Genomics at the University of Tabriz, Iran. With a B.Sc. and M.Sc. in Animal Science and a PhD from University Putra Malaysia, he specializes in biotechnology, molecular cloning, and bioinformatics. His notable research projects include DNA markers in livestock and molecular traceability of meat species. A recipient of multiple awards, including the Golden Medal for Innovation and Best Researcher in Agriculture, Dr. Javanmard is dedicated to advancing agricultural sciences. He is fluent in several languages and committed to enhancing livestock productivity. 🐄🔬🌱

Publication Profile

Orcid

Google Scholar

Professional Experience

Mr. Arash Javanmard has an extensive academic career in animal genomics and biotechnology. Currently serving as an Associate Professor at the University of Tabriz, he has previously held research positions at notable institutions such as the Agriculture Biotechnology Institute of Iran and the Animal Science Institute of Iran. His roles have involved significant contributions to the field of animal science, emphasizing his commitment to advancing agricultural research.

 

Educational Background

Mr. Javanmard holds a Bachelor’s degree in Animal Science from the University of Tabriz, a Master’s degree from the University of Tehran, and a PhD from University Putra Malaysia. His educational trajectory demonstrates a solid foundation in animal science and advanced studies in biotechnology and bioinformatics.

Achievements

Mr. Javanmard’s achievements include being recognized as the Best B.Sc. Student, receiving the Golden Medal for Innovation in 2009, and being named the Best Researcher in Agriculture in 2001. These accolades highlight his consistent excellence and recognition by peers and institutions.

Conclusion

Mr. Arash Javanmard’s combination of relevant experience, strong educational background, impactful research, recognized achievements, and diverse skills make him an exceptional candidate for the Best Researcher Award. His contributions significantly enhance the field of animal genomics and biotechnology, deserving recognition for his dedication and impact.

Publication Top Notes  

  • Selected microbial groups and short-chain fatty acids profile in a simulated chicken cecum supplemented with two strains of Lactobacillus – Poultry Science 89 (3), 470-476, Cited by: 131 (2010) 🐔📊
  • Polymorphism within the intron region of the bovine leptin gene in Iranian Sarabi cattle (Iranian Bos taurus) – Russian Journal of Genetics 44, 495-497, Cited by: 103 (2008) 🐄🧬
  • The allele and genotype frequencies of bovine pituitary-specific transcription factor and leptin genes in Iranian cattle and buffalo populations using PCR-RFLP – Iranian Journal of Biotechnology 3 (2), 104-108, Cited by: 96 (2005) 🧬📈
  • Study the genetic diversity of wheat landraces from northwest of Iran based on ISSR molecular markers – International Journal of Agriculture and Biology 10 (4), 466-468, Cited by: 89 (2008) 🌾🔬
  • Signatures of selection reveal candidate genes involved in economic traits and cold acclimation in five Swedish cattle breeds – Genetics Selection Evolution 52, 1-15, Cited by: 79 (2020) 🧬❄️
  • Mutations in bone morphogenetic protein 15 and growth differentiation factor 9 genes are associated with increased litter size in fat-tailed sheep breeds – Veterinary Research Communications 35, 157-167, Cited by: 79 (2011) 🐑📈
  • Application of statistical procedures for analysis of genetic diversity in domestic animal populations – Cited by: 47 (2009) 📊📉
  • The pattern of runs of homozygosity and genomic inbreeding in world-wide sheep populations – Genomics 113 (3), 1407-1415, Cited by: 39 (2021) 🐑🌍
  • Herbal hydrogel‐based encapsulated Enterococcus faecium ABRIINW. N7 improves the resistance of red hybrid tilapia against Streptococcus iniae – Journal of Applied Microbiology 131 (5), 2516-2527, Cited by: 38 (2021) 🐟💊
  • Detection of polymorphisms in the bovine leptin (LEP) Gene: Association of single nucleotide polymorphism with breeding value of milk traits in Iranian Holstein cattle – Journal of Molecular Genetics 2 (1), 10-14, Cited by: 35 (2010) 🐄🥛

 

Yuan Tian | Genomics Award | Best Researcher Award

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Mr. Yuan Tian | Genomics Award | Best Researcher Award

Mr. Yuan Tian, The third affiliated hospital of Zhengzhou University, China

Yuan Tian, a Chief Technician with a Master’s in Medical Science, specializes in genetic diagnostics and research. With extensive experience at Zhengzhou University’s Third Affiliated Hospital, he focuses on prenatal testing and whole exome sequencing analysis. Noteworthy contributions include papers on genetic disorders like spinal muscular atrophy and deafness. Yuan led projects funded by Henan Province Medical Science, earning awards for his research excellence. Passionate about preventing birth defects, he actively promotes key technologies in maternal and child health care. His dedication to advancing genetic diagnostics embodies a commitment to improving healthcare 🧬.

 

Publication Profile

Scopus

🎓 Education and Work Experience

Yuan Tian, a male Chief Technician, holds a Master’s Degree in Medical Science. He commenced his career in the Laboratory Department of the Third Affiliated Hospital of Zhengzhou University in 2015, specializing in molecular genetics. Over the years, he transitioned through various roles, focusing on prenatal testing and genetic analysis. Currently, he contributes to the Endocrinology and Immunology Laboratories at the same institution.

🏆 Awards and Recognition

Tian’s contributions have earned him accolades such as the third prize in the Science and Technology Achievement Award of Maternal and Child Health Care. His papers have been recognized for excellence in conferences and seminars, reflecting his dedication to advancing genetic diagnostics and healthcare.

 

Research focus

Yuan Tian’s research spans various categories within genetics and molecular biology, with a particular focus on understanding genetic causes of neurological and developmental disorders. His work delves into the intricate relationships between gene mutations and conditions such as spinal muscular atrophy, lissencephaly, and CHIME syndrome. Through systematic reviews, variant analyses, and exploration of allele frequencies, Tian contributes significantly to identifying pathogenic variants and understanding their implications. His dedication to unraveling the genetic basis of complex disorders reflects a commitment to improving diagnostic and therapeutic approaches in healthcare 🧬.

 

Publication Top Notes

📚 Tian, Y. et al. (2023). “Comparative analysis of allele frequencies of 15 deafness gene variants between hearing-loss and normal populations in Henan, China” published in Heliyon.

📅 Year: 2023

📚 Guo, J. et al. (2023). “Analysis of ARX gene variant in a child with X-linked lissencephaly with abnormal genitalia” in Chinese Journal of Medical Genetics.

📅 Year: 2023

📚 Tian, Y. et al. (2023). “Exploring the relationship between IGHMBP2 gene mutations and spinal muscular atrophy with respiratory distress type 1 and Charcot-Marie-Tooth disease type 2S: a systematic review” in Frontiers in Neuroscience.

🔗 Cited by: 1 📅 Year: 2023

📚 Tian, Y. et al. (2022). “Analysis of gene mutations of medium-chain acyl-coenzyme a dehydrogenase deficiency (MCADD) by next-generation sequencing in Henan, China” in Clinica Chimica Acta.

🔗 Cited by: 3 📅 Year: 2022

📚 Li, X. et al. (2021). “Newborn screening, gene variation analysis and follow-up study of very long chain acyl CoA dehydrogenase deficiency” in Chinese Journal of Applied Clinical Pediatrics.

🔗 Cited by: 1 📅 Year: 2021

📚 Zhang, L. et al. (2020). “Pathogenic variants identified by whole-exome sequencing in 43 patients with epilepsy” in Human Genomics.

🔗 Cited by: 7 📅 Year: 2020

📚 Guan, J. et al. (2020). “Case of CHIME syndrome and literature review” in Chinese Journal of Applied Clinical Pediatrics.

📅 Year: 2020

📚 Zhao, D. et al. (2020). “Variant analysis of HPD genes from two families showing elevated tyrosine upon newborn screening by tandem mass spectrometry (MS/MS)” in Journal of Pediatric Endocrinology and Metabolism.

🔗 Cited by: 5 📅 Year: 2020

📚 Tian, Y. et al. (2020). “Variant analysis of PEX11B gene from a family with peroxisome biogenesis disorder 14B by whole exome sequencing” in Molecular Genetics and Genomic Medicine.

🔗 Cited by: 12 📅 Year: 2020

📚 Tian, Y. et al. (2019). “A case of maternal 45, X/46, XX mosaicism detected by non-invasive prenatal testing” in Chinese Journal of Medical Genetics.

🔗 Cited by: 3 📅 Year: 2019