Steven J. Pitts

Pfizer (United States) — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

38h-index9.1kcitations66works2.52yr avg
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Research Topics

Genetic Associations and Epidemiology(14), Parkinson's Disease Mechanisms and Treatments(6), Monoclonal and Polyclonal Antibodies Research(5), Epigenetics and DNA Methylation(4), Bioinformatics and Genomic Networks(4)

Publications57 total

Author Correction: Discovery of RXFP2 genetic association in resistant hypertensive men and RXFP2 antagonists for the treatment of resistant hypertension
Scientific Reports·2025Open Access
Epitope Mapping Using Yeast Display and Next Generation Sequencing
Methods in molecular biology·2025
Large-scale analysis demonstrates the influence of CYP2C19 genotype on specific SSRI side effects
2024Open Access
The impact on clinical success from the 23andMe cohort
2024· 4 citedOpen Access
Discovery of RXFP2 genetic association in resistant hypertensive men and RXFP2 antagonists for the treatment of resistant hypertension
Scientific Reports·2024· 3 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
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
Abstract 603: Discovery of CD200R1 as a novel immuno-oncology target using pleiotropic signals from 23andMe’s genetic and health survey database
Cancer Research·2022· 2 cited
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
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
Advancing drug discovery using the power of the human genome
The Journal of Pathology·2021· 25 citedOpen Access
Genetic determinants of daytime napping and effects on cardiometabolic health
Nature Communications·2021· 556 citedOpen Access
A comprehensive re-assessment of the association between vitamin D and cancer susceptibility using Mendelian randomization
Nature Communications·2021· 56 citedOpen Access
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Frequent Co-authors

Suyash Shringarpure(32), Michelle Agee(31), Pierre Fontanillas(31), Karen E. Huber(31), Aaron Kleinman(31), Nadia K. Litterman(31), Carrie A. M. Northover(31), David A. Hinds(30), Joanna L. Mountain(30), J. Fah Sathirapongsasuti(30), Janie F. Shelton(30), Katarzyna Bryc(28), Robert K. Bell(27), Matthew H. McIntyre(27), Elizabeth S. Noblin(25), Nicholas A. Furlotte(23), Babak Alipanahi(21), Catherine H. Wilson(21), Sarah L. Elson(19), Chao Tian(18)