Prof. Liu Qicai – Human Genetics- Best Researcher Award

Prof. Liu Qicai – Human Genetics- Best Researcher Award

Fujian Medical University – China

Author Profile

Orcid

🎓 Academic and Professional Background

Liu Qicai is a distinguished researcher in human genetics and an influential academic leader. He was selected for the Outstanding Youth Research Talent Cultivation Program in Colleges and Universities in Fujian Province, China, recognizing his significant contributions to scientific research.

🏆 Awards and Recognitions

Liu Qicai has been honored with the Fujian Provincial Science and Technology Award (First Prize) in 2009, 2014, 2016, and 2022 for his groundbreaking work. His dedication to scientific advancement was further acknowledged when he received the prestigious May 4th Youth Medal in Fuzhou, China.

🔬 Professional Memberships and Editorial Roles

He actively contributes to the scientific community as a member of the Standing Committee of Reproductive Health under the Chinese Rehabilitation Medical Association and a member of the Fujian Medical Genetics Society. Additionally, he serves as a member of the Standing Committee of Cancer Sequencing and Large Data Collaboration Group of the China Anti-Cancer Association. His expertise is further recognized as an editorial board member for the journal Endocrine, Metabolic & Immune Disorders – Drug Targets.

🤝 Collaborations and Research Focus

Liu Qicai collaborates with Tsinghua University, fostering advancements in human genetics and related medical research. His primary research interests lie in genetic mechanisms of diseases, contributing to breakthroughs in reproductive health, cancer genetics, and medical rehabilitation.

Notable Publications📝

📝Myeloperoxidase-mediated immature dendritic cell promotes vascular remodeling and functional placenta formation
  • Authors: F. Gao, J. Jiang, Y. Lin, Q. Chen, Q. Liu
    Journal: Placenta
    Year: 2025

📝EZH2 G553C significantly increases the risk of brain metastasis from lung cancer due to salt bridge instability
  • Authors: H. Wang, L. Wang, S. Zhang, Q. Liu, F. Gao
    Journal: Cancer Cell International
    Year: 2024

📝Neu5Gc regulates decidual macrophages leading to abnormal embryo implantation
  • Authors: W. Yue, Z. Huiling, L. Yuxin, F. Gao, Q. Liu
    Journal: Genes and Immunity
    Year: 2024

📝A pH-Sensitive I-Motif Aptamer Probe for Dual Targeting and Imaging of Pancreatic Cancer Cells via Nucleolin Interactions
  • Authors: Q. Li, Q. Chen, J. Tang, Q. Liu, F. Gao
    Journal: Journal of Bio-X Research
    Year: 2024

📝High-Speed and Accurate Diagnosis of Gastrointestinal Disease: Learning on Endoscopy Images Using Lightweight Transformer with Local Feature Attention
  • Authors: S. Wu, R. Zhang, J. Yan, L. Wang, H. Wang
    Journal: Bioengineering
    Year: 2023

 

Dr. Christina Tise | Human Genetics | Best Researcher Award

Dr. Christina Tise | Human Genetics | Best Researcher Award

Doctorate at Stanford University, United States

Professional Profile

Scopus

🎓 Education Background

Dr. Christina G. Tise has an exceptional academic background that reflects her dedication to advancing knowledge in genetics and medicine. She earned her Bachelor of Science in Biochemistry in May 2009 from Virginia Tech, graduating Summa Cum Laude and as a Commonwealth Scholar. Her medical journey continued at the University of Maryland School of Medicine, where she completed her Doctor of Medicine (MD) in May 2018 and concurrently pursued a PhD in Epidemiology and Human Genetics, specializing in Human Genetics and Genomic Medicine (June 2012 – December 2015).

Her advanced training includes an Internship in Pediatrics (2018–2019) at the Lucile Packard Children’s Hospital, Stanford, CA, followed by a Residency in Medical Genetics (2019–2021) and a Fellowship in Clinical Biochemical Genetics (2021–2022) at the Stanford University Medical Center.

👩‍🔬 Employment and Research Experience

In addition to her academic achievements, Dr. Tise gained valuable experience during her Postdoctoral Research in Translational Genetics at the Regeneron Genetics Center LLC (January – April 2016). She worked on cutting-edge genetic research that paved the way for advancements in personalized medicine.

🏆 Honors and Awards

Dr. Christina G. Tise’s career has been marked by a series of prestigious accolades, showcasing her dedication to excellence in both research and education. As an undergraduate, she consistently demonstrated academic brilliance, earning a spot on the Virginia Tech Dean’s List (2006–2009) and graduating Summa Cum Laude. Her groundbreaking research during her doctoral studies at the University of Maryland School of Medicine was recognized with the PhD Thesis of the Year Award (2016).

In 2018, Dr. Tise was honored with the J. Edmund and Kathryn S. Bradley Award for Excellence in Pediatrics, acknowledging her outstanding contributions to pediatric medicine. Her innovative work continued to gain recognition, earning her the Henry Christian Award from the American Federation for Medical Research (2020) and the Pfizer/ACMGF Next Generation Biochemical Genetics Fellowship Award (2021), highlighting her leadership in the field of medical genetics.

Dr. Tise’s commitment to mentorship and education has also been celebrated. In 2023, she received the Golden Helix Faculty Teaching Award from the Stanford Medical Genetics Residency Program, underscoring her impact as an educator. Additionally, her expertise in genetics research is reflected in her Top-Rated Abstracts, presented at highly esteemed conferences such as the American College of Medical Genetics and the American Society of Human Genetics. These honors collectively highlight Dr. Tise’s significant contributions to advancing medical science and fostering the next generation of healthcare leaders.

Publications Top Notedđź“‘

Considerations for reporting variants in novel candidate genes identified during clinical genomic testing

Authors: Chong, J.X.; Berger, S.I.; Baxter, S.; … Bamshad, M.J.; Rehm, H.L.

Journal: Genetics in Medicine

Year: 2024

Fetal phenotype and diagnosis of autosomal dominant Robinow syndrome due to novel DVL1 variant

Authors: Smith, C.M.; Guinon, K.; Bachir, S.; Tise, C.G.

Journal: Prenatal Diagnosis

Year: 2024

Newborn Screening for X-Linked Adrenoleukodystrophy (X-ALD): Biochemical, Molecular, and Clinical Characteristics of Other Genetic Conditions

Authors: Mares Beltran, C.F.; Tise, C.G.; Barrick, R.; … Enns, G.M.; Abdenur, J.E.

Journal: Genes

Year: 2024

Molecular testing in newborn screening: VUS burden among true positives and secondary reproductive limitations via expanded carrier screening panels

Authors: Cook, S.; Dunn, E.; Kornish, J.; … Cusmano-Ozog, K.P.; Tise, C.G.

Journal: Genetics in Medicine

Year: 2024

Monozygotic twins discordant for a congenital cranial dysinnervation disorder with features of Moebius syndrome

Authors: Gates, R.W.; Webb, B.D.; Stevenson, D.A.; … Ruzhnikov, M.R.Z.; Tise, C.G.

Journal: American Journal of Medical Genetics, Part A

Year: 2023