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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

πŸŽ“ 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.

πŸ† 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

πŸ“š 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.

πŸ“… Year: 2023

πŸ“š 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.

πŸ“… Year: 2023

πŸ“š 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.

πŸ”— Cited by: 1 πŸ“… Year: 2023

πŸ“š 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.

πŸ”— Cited by: 3 πŸ“… Year: 2022

πŸ“š 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.

πŸ”— Cited by: 1 πŸ“… Year: 2021

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

πŸ”— Cited by: 7 πŸ“… Year: 2020

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

πŸ“… Year: 2020

πŸ“š 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.

πŸ”— Cited by: 5 πŸ“… Year: 2020

πŸ“š 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.

πŸ”— Cited by: 12 πŸ“… Year: 2020

πŸ“š 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.

πŸ”— Cited by: 3 πŸ“… Year: 2019


Yuan Tian | Genomics Award | Best Researcher Award

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