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Publications

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

Aragam KG. et al, (2022), Nat Genet

Determining the Relationship Between Blood Pressure, Kidney Function, and Chronic Kidney Disease: Insights From Genetic Epidemiology.

Staplin N. et al, (2022), Hypertension

Are polygenic risk scores for systolic blood pressure and LDL-cholesterol associated with treatment effectiveness, and clinical outcomes among those on treatment?

Tapela NM. et al, (2021), Eur J Prev Cardiol

Assessment of the causal relevance of ECG parameters for risk of atrial fibrillation: A mendelian randomisation study.

Gajendragadkar PR. et al, (2021), PLoS Med, 18

Genome-wide scans of myopia in Pennsylvania Amish families reveal significant linkage to 12q15, 8q21.3 and 5p15.33.

Musolf AM. et al, (2019), Human genetics, 138, 339 - 354

Exome genotyping and linkage analysis identifies two novel linked regions and replicates two others for myopia in Ashkenazi Jewish families.

Simpson CL. et al, (2019), BMC medical genetics, 20

Effects of smoking status, history and intensity on heart rate variability in the general population: The CHRIS study.

Murgia F. et al, (2019), PLoS One, 14

Myopia in Chinese families shows linkage to 10q26.13.

Musolf AM. et al, (2018), Molecular vision, 24, 29 - 42

Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity.

Joshi PK. et al, (2017), Nat Commun, 8

Caucasian Families Exhibit Significant Linkage of Myopia to Chromosome 11p.

Musolf AM. et al, (2017), Investigative ophthalmology & visual science, 58, 3547 - 3554

Genetic Variants Associated with Circulating Parathyroid Hormone.

Robinson-Cohen C. et al, (2017), Journal of the American Society of Nephrology : JASN, 28, 1553 - 1565

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.

Pattaro C. et al, (2016), Nat Commun, 7

Height-reducing variants and selection for short stature in Sardinia.

Zoledziewska M. et al, (2015), Nature genetics, 47, 1352 - 1356

Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium.

Li Q. et al, (2015), Hum Genet, 134, 131 - 146

Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium

Li Q. et al, (2015), Human Genetics, 134, 131 - 146

Ancestry of the Timorese: age-related macular degeneration associated genotype and allele sharing among human populations from throughout the world.

Morrison MA. et al, (2015), Frontiers in genetics, 6

Modulation of genetic associations with serum urate levels by body-mass-index in humans.

Huffman JE. et al, (2015), PLoS One, 10

Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium

Li Q. et al, (2014), Human Genetics

Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci.

Simpson CL. et al, (2014), PLoS One, 9

Common variants in Mendelian kidney disease genes and their association with renal function.

Parsa A. et al, (2013), J Am Soc Nephrol, 24, 2105 - 2117

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