Showing results (11-20 of 20) with videos related to
Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Genetics in Medicine Open|February 10, 2025
Biallelic SLC13A1 loss-of-function variants result in impaired sulfate transport and skeletal phenotypes, including short stature, scoliosis, and skeletal dysplasiaChristina G Tise, Katie Ashton, Lachlan de Hayr, et al.American Journal of Human Genetics|November 4, 2023
RAB1A haploinsufficiency phenocopies the 2p14-p15 microdeletion and is associated with impaired neuronal differentiationJonathan J Rios, Yang Li, Nandina Paria, et al.Genes|February 25, 2022
Y-Chromosomal Insights into Breeding History and Sire Line Genealogies of Arabian HorsesViktoria Remer, Elif Bozlak, Sabine Felkel, et al.The Journal of Clinical Investigation|November 14, 2023
Impaired glycine neurotransmission causes adolescent idiopathic scoliosisXiaolu Wang, Ming Yue, Jason Pui Yin Cheung, et al.Biorxiv : the Preprint Server for Biology|June 9, 2023
Association of genetic variation inHao Yu, Anas M Khanshour, Aki Ushiki, et al.Elife|January 26, 2024
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosisHao Yu, Anas M Khanshour, Aki Ushiki, et al.Human Molecular Genetics|November 6, 2018
Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility lociAnas M Khanshour, Ikuyo Kou, Yanhui Fan, et al.Elife|July 15, 2025
EPHA4 signaling dysregulation links abnormal locomotion and the development of idiopathic scoliosisLianlei Wang, Xinyu Yang, Sen Zhao, et al.Frontiers in Endocrinology|July 7, 2023
Evidence of causality of low body mass index on risk of adolescent idiopathic scoliosis: a Mendelian randomization studyNao Otomo, Anas M Khanshour, Masaru Koido, et al.Journal of Medical Genetics|May 9, 2020
Diagnostic yield and clinical impact of exome sequencing in early-onset scoliosis (EOS)Sen Zhao, Yuanqiang Zhang, Weisheng Chen, et al.Pageof 2