about
Polymorphism of the follistatin gene in polycystic ovary syndromeWhole-genome sequence-based analysis of thyroid function.Influence of ARHGEF3 and RHOA knockdown on ACTA2 and other genes in osteoblasts and osteoclasts.A non-synonymous coding change in the CYP19A1 gene Arg264Cys (rs700519) does not affect circulating estradiol, bone structure or fracture.Polymorphism in HSD17B6 is associated with key features of polycystic ovary syndrome.Conditional testing of multiple variants associated with bone mineral density in the FLNB gene region suggests that they represent a single association signal.Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density.Homozygous deletion of the UGT2B17 gene is not associated with osteoporosis risk in elderly Caucasian women.Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study.Genome-wide association study meta-analysis for quantitative ultrasound parameters of bone identifies five novel loci for broadband ultrasound attenuation.Impact of Neuritin 1 (NRN1) polymorphisms on fluid intelligence in schizophrenia.Erratum: Whole-genome sequence-based analysis of thyroid functionPolymorphism in postinsulin receptor signaling pathway is not associated with polycystic ovary syndrome.Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects.Expression Quantitative Trait Locus Study of Bone Mineral Density GWAS Variants in Human Osteoclasts.Identification of novel loci associated with hip shape: a meta-analysis of genome-wide association studiesSignificant Association between Common Polymorphisms in the Aromatase Gene CYP19A1 and Bone Mineral Density in Postmenopausal WomenA cohort study of the effects of serum osteoprotegerin and osteoprotegerin gene polymorphisms on cardiovascular mortality in elderly womenBone structural effects of variation in the TNFRSF1B gene encoding the tumor necrosis factor receptor 2No associations between OPG gene polymorphisms or serum levels and measures of osteoporosis in elderly Australian womenUse of the collaborative cross gene mine mouse phenotype library to identify novel genes regulating bone mass and bone architecturePolymorphisms in ALOX12, but not ALOX15, Are Significantly Associated With BMD in Postmenopausal WomenLarge-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteriaAdvanced Genetic Approaches in Discovery and Characterization of Genes Involved With Osteoporosis in Mouse and Human
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description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Benjamin H Mullin
@ast
Benjamin H Mullin
@en
Benjamin H Mullin
@es
Benjamin H Mullin
@nl
type
label
Benjamin H Mullin
@ast
Benjamin H Mullin
@en
Benjamin H Mullin
@es
Benjamin H Mullin
@nl
prefLabel
Benjamin H Mullin
@ast
Benjamin H Mullin
@en
Benjamin H Mullin
@es
Benjamin H Mullin
@nl
P106
P1153
15027205800
P21
P31
P496
0000-0003-0743-770X