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List of works by Benjamin H Mullin

A cohort study of the effects of serum osteoprotegerin and osteoprotegerin gene polymorphisms on cardiovascular mortality in elderly women

article

A non-synonymous coding change in the CYP19A1 gene Arg264Cys (rs700519) does not affect circulating estradiol, bone structure or fracture.

scientific article

Advanced Genetic Approaches in Discovery and Characterization of Genes Involved With Osteoporosis in Mouse and Human

article

Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study.

scientific article published on May 2008

Bone structural effects of variation in the TNFRSF1B gene encoding the tumor necrosis factor receptor 2

article

Characterisation of genetic regulatory effects for osteoporosis risk variants in human osteoclasts

scientific article published on 26 March 2020

Collaborative meta-analysis: associations of 150 candidate genes with osteoporosis and osteoporotic fracture

scientific article

Conditional testing of multiple variants associated with bone mineral density in the FLNB gene region suggests that they represent a single association signal

scientific article

Erratum: Whole-genome sequence-based analysis of thyroid function

scientific article published on 20 May 2015

Expression Quantitative Trait Locus Study of Bone Mineral Density GWAS Variants in Human Osteoclasts

scientific article published on 23 February 2018

Functional Assessment of Calcium-Sensing Receptor Variants Confirms Familial Hypocalciuric Hypercalcemia

scientific article published on 18 February 2022

Genetic regulatory mechanisms in human osteoclasts suggest a role for the STMP1 and DCSTAMP genes in Paget's disease of bone

scientific article published in Scientific Reports

Genome-wide association study meta-analysis for quantitative ultrasound parameters of bone identifies five novel loci for broadband ultrasound attenuation

scientific article published on 4 May 2017

Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density

scientific article

Homozygous deletion of the UGT2B17 gene is not associated with osteoporosis risk in elderly Caucasian women.

scientific article published on 29 September 2010

Identification of novel loci associated with hip shape: a meta-analysis of genome-wide association studies

Impact of Neuritin 1 (NRN1) polymorphisms on fluid intelligence in schizophrenia

scientific article

Influence of ARHGEF3 and RHOA knockdown on ACTA2 and other genes in osteoblasts and osteoclasts

scientific article

Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria

scientific article published on 19 December 2018

Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects

scientific article published in January 2018

Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

No associations between OPG gene polymorphisms or serum levels and measures of osteoporosis in elderly Australian women

article

Polymorphism in HSD17B6 is associated with key features of polycystic ovary syndrome.

scientific article

Polymorphism in postinsulin receptor signaling pathway is not associated with polycystic ovary syndrome.

scientific article

Polymorphism of the follistatin gene in polycystic ovary syndrome

scientific article

Polymorphisms in ALOX12, but not ALOX15, Are Significantly Associated With BMD in Postmenopausal Women

scientific article published on 23 May 2007

Significant Association between Common Polymorphisms in the Aromatase Gene CYP19A1 and Bone Mineral Density in Postmenopausal Women

article

Use of the collaborative cross gene mine mouse phenotype library to identify novel genes regulating bone mass and bone architecture

article

Whole-genome sequence-based analysis of thyroid function.

scientific article

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