Ian N.M. Day

United Kingdom Atomic Energy Authority — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

62h-index24.6kcitations250works0.02yr avg
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Research Topics

Genetic Associations and Epidemiology(57), Lipoproteins and Cardiovascular Health(31), Genomics and Rare Diseases(22), Growth Hormone and Insulin-like Growth Factors(15), Epigenetics and DNA Methylation(14)

Publications240 total

A shinethrough detector and interlock for neutral beam injection operations on MAST-U
Fusion Engineering and Design·2025Open Access
DUNE PERFORMANCE IN 2050 AND 2100 SUBJECTED TO EXTREME AND NUISANCE EROSION EVENTS
Coastal Engineering Proceedings·2025Open Access
Quantifying the influence of profile variability on dune impacts during Hurricane Sandy
Shore & Beach·2023· 1 cited
Microarrays and Microplates
Garland Science eBooks·2023· 1 cited
Developing guidance for the application of Natural and Nature Based Features (NNBF) on developed shores: A case study from New Jersey, USA
Regional Studies in Marine Science·2023· 6 cited
The molecular basis of genetic variation: mutation detection methodologies and limitations
Garland Science eBooks·2020· 1 cited
Genetics of Common Diseases
Garland Science eBooks·2020· 6 cited
Candidate-Gene Studies of the Atherogenic Lipoprotein Phenotype: A Sib-Pair Linkage Analysis of DZ Women Twins
UNC Libraries·2020Open Access
Common variants near MC4R are associated with fat mass, weight and risk of obesity
UNC Libraries·2020Open Access
Lipids, obesity and gallbladder disease in women: insights from genetic studies using the cardiovascular gene-centric 50K SNP array
UNC Libraries·2020Open Access
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
UNC Libraries·2019Open Access
Aortic aneurysms: A brief overview and dental implications
International journal of anatomical variations·2018· 1 cited
A rare observation of mandibular buccal ramus variant of stafne bone defect
International journal of anatomical variations·2018
Possible positive effect of the APOE ε2 allele on cognition in early to mid-adult life
Neurobiology of Learning and Memory·2017· 18 citedOpen Access
Cardiometabolic phenotypes and mitochondrial DNA copy number in two cohorts of UK women
Mitochondrion·2017· 23 citedOpen Access
Genetic evidence of assortative mating in humans
Nature Human Behaviour·2017· 356 cited
HAPRAP: a haplotype-based iterative method for statistical fine mapping using GWAS summary statistics
Bioinformatics·2016· 7 citedOpen Access
Frequency of <i>KLK3</i> gene deletions in the general population
Annals of Clinical Biochemistry International Journal of Laboratory Medicine·2016Open Access
Mendelian Randomisation study of the influence of eGFR on coronary heart disease
Scientific Reports·2016· 17 citedOpen Access
Correction: Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport
Nature Communications·2016· 259 citedOpen Access
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Frequent Co-authors

Tom R. Gaunt(25), George Davey Smith(23), Debbie A. Lawlor(17), Steve E. Humphries(16), Nicholas J. Timpson(15), Meena Kumari(10), Shah Ebrahim(9), Inês Barroso(8), Marta Futema(7), Petr Danecek(7), Richard Durbin(7), Yoav Ben‐Shlomo(6), Lucy Crooks(6), Audrey E. Hendricks(6), Peter Clapham(6), Guy Coates(6), Sarah Edkins(6), Peter Ellis(6), Paul Flicek(6), Chris Boustred(6)