Area of research
Orthopedics and Sports Medicine · Genetics
Research interest
Research interests include Genome-wide association study, Biology, Single-nucleotide polymorphism, Genetics, Medicine, and Sarcomere.
Septin 7 Interacts With Numb To Preserve Sarcomere Structural Organization And Muscle Contractile Function
Author Response: Septin 7 Interacts With Numb To Preserve Sarcomere Structural Organization And Muscle Contractile Function
Septin 7 interacts with Numb to preserve sarcomere structural organization and muscle contractile function
Convergent genomics of longevity in rockfishes highlights the genetics of human life span variation
Septin 7 interacts with Numb to preserve sarcomere structural organization and muscle contractile function
Septin 7 Interacts With Numb To Preserve Sarcomere Structural Organization And Muscle Contractile Function
Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women
A regulatory variant at 3q21.1 confers an increased pleiotropic risk for hyperglycemia and altered bone mineral density
The Musculoskeletal Knowledge Portal: Making Omics Data Useful to the Broader Scientific Community
Searching for parent-of-origin effects on cardiometabolic traits in imprinted genomic regions
A meta-analysis of genome-wide association studies identifies multiple longevity genes
Genetics of Bone and Muscle Interactions in Humans
Meta-Analysis of Genomewide Association Studies Reveals Genetic Variants for Hip Bone Geometry
An atlas of genetic influences on osteoporosis in humans and mice
Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels
Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects
Identification of Novel Loci Associated With Hip Shape: A Meta-Analysis of Genomewide Association Studies
Disentangling the genetics of lean mass
A study of Kibbutzim in Israel reveals risk factors for cardiometabolic traits and subtle population structure
Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis
Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus
Students as anatomy near-peer teachers: a double-edged sword for an ancient skill
<scp>GWAS</scp> analysis of handgrip and lower body strength in older adults in the <scp>CHARGE</scp> consortium
A combined reference panel from the 1000 Genomes and UK10K projects improved rare variant imputation in European and Chinese samples
Novel Genetic Variants Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of <i>SLC1A3</i> and <i>EPHB2</i>
Heritability of Thoracic Spine Curvature and Genetic Correlations With Other Spine Traits: The Framingham Study
<i>FABP4</i>is a leading candidate gene associated with residual feed intake in growing Holstein calves
Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility
Rare coding variants and X-linked loci associated with age at menarche
GWAS of Longevity in CHARGE Consortium Confirms APOE and FOXO3 Candidacy