Carrie A. M. Northover

Biochemistry, Genetics and Molecular Biology · Life Sciences

41h-index9.7kcitations61works4.72yr avg
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Research Topics

Genetic Associations and Epidemiology(14), Parkinson's Disease Mechanisms and Treatments(8), Migraine and Headache Studies(8), Epigenetics and DNA Methylation(4), Bioinformatics and Genomic Networks(4)

Publications50 total

Diagnosing migraine from genome-wide genotype data: a machine learning analysis
Brain·2025· 1 citedOpen Access
HMG-CoA reductase is a potential therapeutic target for migraine: a mendelian randomization study
Scientific Reports·2024· 5 citedOpen Access
A causal effects of gut microbiota in the development of migraine
The Journal of Headache and Pain·2023· 42 citedOpen Access
Migraine, chronic kidney disease and kidney function: observational and genetic analyses
Human Genetics·2023· 10 citedOpen Access
Extensive embryonic patterning without cellular differentiation primes the plant epidermis for efficient post-embryonic stomatal activities
Developmental Cell·2023· 21 citedOpen Access
Causal relationships between migraine and microstructural white matter: a Mendelian randomization study
The Journal of Headache and Pain·2023· 29 citedOpen Access
Author Correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis
Nature Communications·2022· 1 citedOpen Access
Slow and not so furious: <i>de novo</i> stomatal pattern formation during plant embryogenesis
2022Open Access
Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways
Nature Genetics·2022· 219 citedOpen Access
The genetic architecture of pneumonia susceptibility implicates mucin biology and a relationship with psychiatric illness
Nature Communications·2022· 20 citedOpen Access
Genome-wide association analysis and replication in 810,625 individuals with varicose veins
Nature Communications·2022· 27 citedOpen Access
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals
Nature Genetics·2022· 650 citedOpen Access
Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders
Nature Genetics·2021· 261 citedOpen Access
Genome-wide association study of problematic opioid prescription use in 132,113 23andMe research participants of European ancestry
Molecular Psychiatry·2021· 63 citedOpen Access
Genetic overlap analysis of endometriosis and asthma identifies shared loci implicating sex hormones and thyroid signalling pathways
Human Reproduction·2021· 42 citedOpen Access
Incorporating functional priors improves polygenic prediction accuracy in UK Biobank and 23andMe data sets
Nature Communications·2021· 146 citedOpen Access
Resource profile and user guide of the Polygenic Index Repository
Nature Human Behaviour·2021· 172 citedOpen Access
pH and Proton Sensor GPR65 Determine Susceptibility to Atopic Dermatitis
The Journal of Immunology·2021· 25 citedOpen Access
Genetic analyses identify widespread sex-differential participation bias
Nature Genetics·2021· 255 citedOpen Access
Author Correction: Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways
Nature Communications·2021· 6 citedOpen Access
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Frequent Co-authors

Pierre Fontanillas(43), Michelle Agee(42), Karen E. Huber(42), Aaron Kleinman(42), Nadia K. Litterman(42), Suyash Shringarpure(42), Joanna L. Mountain(41), J. Fah Sathirapongsasuti(41), Janie F. Shelton(41), Katarzyna Bryc(37), Matthew H. McIntyre(37), David A. Hinds(35), Robert K. Bell(35), Steven J. Pitts(34), Elizabeth S. Noblin(33), Babak Alipanahi(32), Catherine H. Wilson(31), Nicholas A. Furlotte(29), Chao Tian(25), Sarah L. Elson(25)