Author details

Full Name

John P Kemp

Affiliation

ORCID

Career Start Year

2009

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37096546	Lowering of Circulating Sclerostin May Increase Risk of Atherosclerosis and Its Risk Factors: Evidence From a Genome-Wide Association Meta-Analysis Followed by Mendelian Randomization.	Arthritis Rheumatol	2023
37619450	The identification of distinct protective and susceptibility mechanisms for hip osteoarthritis: findings from a genome-wide association study meta-analysis of minimum joint space width and Mendelian randomisation cluster analyses.	EBioMedicine	2023
37402774	Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis.	Commun Biol	2023
36662418	A Genome-Wide Association Study Meta-Analysis of Alpha Angle Suggests Cam-Type Morphology May Be a Specific Feature of Hip Osteoarthritis in Older Adults.	Arthritis Rheumatol	2023
34995520	Limb development genes underlie variation in human fingerprint patterns.	Cell	2022
36320039	Mendelian randomization analysis of factors related to ovulation and reproductive function and endometrial cancer risk.	BMC Med	2022
34784738	Investigating a Potential Causal Relationship Between Maternal Blood Pressure During Pregnancy and Future Offspring Cardiometabolic Health.	Hypertension	2022
35057801	Regenerating zebrafish scales express a subset of evolutionary conserved genes involved in human skeletal disease.	BMC Biology	2022
34698806	Dnmt3a-mutated clonal hematopoiesis promotes osteoporosis.	J Exp Med	2021
33798441	Osteoclasts recycle via osteomorphs during RANKL-stimulated bone resorption.	Cell	2021
33636130	Osteoclasts recycle via osteomorphs during RANKL-stimulated bone resorption.	Cell	2021
33953184	Osteocyte transcriptome mapping identifies a molecular landscape controlling skeletal homeostasis and susceptibility to skeletal disease.	Nat Commun	2021
33517400	Genome-wide association study of circulating interleukin 6 levels identifies novel loci.	Hum Mol Genet	2021
33658983	Opportunities and Challenges in Functional Genomics Research in Osteoporosis: Report From a Workshop Held by the Causes Working Group of the Osteoporosis and Bone Research Academy of the Royal Osteoporosis Society on October 5th 2020.	Front Endocrinol (Lausanne)	2021
32989287	Genome-wide association study identifies 48 common genetic variants associated with handedness.	Nat Hum Behav	2021
31525280	A Rare Mutation in SMAD9 Associated With High Bone Mass Identifies the SMAD-Dependent BMP Signaling Pathway as a Potential Anabolic Target for Osteoporosis.	J Bone Miner Res	2020
32163637	The Effect of Plasma Lipids and Lipid-Lowering Interventions on Bone Mineral Density: A Mendelian Randomization Study.	J Bone Miner Res	2020
32493999	RSPO3 impacts body fat distribution and regulates adipose cell biology in vitro.	Nat Commun	2020
32614825	Development of a polygenic risk score to improve screening for fracture risk: A genetic risk prediction study.	PLoS Med	2020
32777102	The Musculoskeletal Knowledge Portal: Making Omics Data Useful to the Broader Scientific Community.	J Bone Miner Res	2020
30882941	A Metabolic Screen in Adolescents Reveals an Association Between Circulating Citrate and Cortical Bone Mineral Density.	J Bone Miner Res	2019
31824424	Use of Mendelian Randomization to Examine Causal Inference in Osteoporosis.	Front Endocrinol (Lausanne)	2019
30888730	Meta-Analysis of Genomewide Association Studies Reveals Genetic Variants for Hip Bone Geometry.	J Bone Miner Res	2019
29659830	Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero.	Hum Mol Genet	2018
29883787	Genome-wide association study of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes.	Bone	2018
30388399	Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.	Am J Hum Genet	2018
29304378	Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects.	Am J Hum Genet	2018
27663502	LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis.	Bioinformatics	2017
28552196	Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.	Am J Hum Genet	2017
28628106	Variants in the fetal genome near FLT1 are associated with risk of preeclampsia.	Nat Genet	2017
28934396	Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus.	Hum Mol Genet	2017
28743860	Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus.	Nat Commun	2017
28869591	Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis.	Nat Genet	2017
27663945	A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Pediatric Cohorts.	J Am Acad Child Adolesc Psychiatry	2016
27299648	Erratum to: Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence.	Hum Genet	2016
27020472	Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error.	Nat Commun	2016
27045867	Common Genetic Variants Influence Whorls inÂ Fingerprint Patterns.	J Invest Dermatol	2016
27215616	Using Mendelian randomization to investigate a possible causal relationship between adiposity and increased bone mineral density at different skeletal sites in children.	Int J Epidemiol	2016
27257477	The case for genome-wide association studies of bone acquisition in paediatric and adolescent populations.	Bonekey Rep	2016
26362575	Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium.	Behav Genet	2016
26087016	A genome-wide approach to children's aggressive behavior: The EAGLE consortium.	Am J Med Genet B Neuropsychiatr Genet	2016
26367794	Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.	Nature	2015
25281659	A novel common variant in DCST2 is associated with length in early life and height in adulthood.	Hum Mol Genet	2015
25367360	Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium.	Hum Genet	2015
25488826	Associations of vitamin D pathway genes with circulating 25-hydroxyvitamin-D, 1,25-dihydroxyvitamin-D, and prostate cancer: a nested case-control study.	Cancer Causes Control	2015
25820613	Genome-wide association study of blood lead shows multiple associations near ALAD.	Hum Mol Genet	2015
25515860	Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence.	Hum Genet	2015
25953783	A genome-wide association study of body mass index across early life and childhood.	Int J Epidemiol	2015
25941325	Genetic variants in adult bone mineral density and fracture risk genes are associated with the rate of bone mineral density acquisition in adolescence.	Hum Mol Genet	2015
26482879	Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis.	Nat Genet	2015