Author

Christopher Grace

Centre for Human GeneticsORCID 0000-0002-8082-7504Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:GWAS / association mapping· 2 Approach:Bayesian inference· 1 Research Focus:differential expression· 1 Research Focus:fine-mapping· 1 Assay:GWAS summary statistics· 1 Assay:imaging· 1

Frequent Co-Authors

Anuj GoeliD· 3 shared Hugh C WatkinsiD· 2 shared Abdulaziz HassaniD· 1 shared Adam S. ButterworthiD· 1 shared Adnan KastratiiD· 1 shared Afolashade Akinrindoye· 1 shared Ajoke Idayat Oyetunji· 1 shared Alanna C. MorrisoniD· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Anuj GoelORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJul 30, 2026

Genotype-Phenotype Correlations Identify Phenotypic Differences in Sarcomere Mutation-Positive Hypertrophic Cardiomyopathy in the NHLBI HCM Registry

Jonathan Chan, Christopher Grace, Kate L. Thomson…·Anuj Goel

The paper identifies phenotypic differences in sarcomere mutation-positive hypertrophic cardiomyopathy using CMR data from the NHLBI HCM Registry, resolving prior discrepancies through meta-analysis.

DOI 10.64898/2026.07.28.26359171

humanimaging

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Genetic & Genomic MedicineHuman Molecular GeneticsPeer-reviewedJan 18, 2024

The genetic dissection of fetal haemoglobin persistence in sickle cell disease in Nigeria

Oyesola Oyewole Ojewunmi, Titilope Adenike Adeyemo, Ajoke Idayat Oyetunji…·Stephan Menzel

This paper conducts a genome-wide association study in Nigerian sickle cell disease patients to identify genetic variants associated with fetal hemoglobin levels, finding significant associations at BCL11A and HBS1L-MYB and novel signals in the Nigerian cohort.

17 citations

humanstatistical model

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Genetic & Genomic MedicinemedRxivPreprintMay 24, 2021

✦ In-depth digest

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants.

Krishna G. Aragam, Tao Jiang, Anuj Goel…·Adam S. Butterworth

A coronary artery disease GWAS of 181,522 cases among 1,165,690 participants yields 241 associations (54 new); an eight-predictor consensus nominates 185 candidate causal genes, 94 with ≥3 predictors.

67 citations

humanGWAS summary statistics

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