Germline EGFR T790M mutation and lung cancer risk
Jaclyn LoPiccolo, .
Science · Published September 17, 2026
Publications
Sharing our research with the scientific community is key to our mission. Read our scientific publications, white papers and conference presentations below.
Publications
We provide access to full summary statistics from published 23andMe research.
Showing 1-15 of 352 publications
Large-scale analysis demonstrates the influence of CYP2C19 genotype on specific SSRI side effects
Chris Eijsbouts, .
The Pharmacogenomics Journal · Published August 1, 2026
Prediction of Alcohol Consumption: The Role of Genetics, Impulsivity, and Sensation Seeking from Adolescence to Adulthood
Lilia G. Geel, .
Drug and Alcohol Dependence · Published July 29, 2026
Age-Related Speech-in-Noise Hearing Loss in Parkinson’s Disease and <i>APOE</i> E4 Carriers
Matthew J. Kmiecik, .
medRxiv · Posted June 9, 2026
The genetic legacy of the 17th-century colonial capital of St. Mary’s City
Éadaoin Harney, .
Current Biology · Published May 14, 2026
Genetic predictors of GLP1 receptor agonist weight loss and side effects
Qiaojuan Jane Su, .
Nature · Published April 8, 2026
Genetic architecture of the personality meta-traits – stability and plasticity – and their overlap with psychopathology
Liam J. Veltman, .
medRxiv · Posted March 20, 2026
Health actions after direct-to-consumer genetic testing for medically actionable conditions
Amy C. Sturm, .
Genetics in Medicine Open · Published January 1, 2026
Gene‐Environment Interplay in Reading Performance
Amaia Carrión‐Castillo, .
Developmental Science · Published December 22, 2025
Viewing direct-to-consumer genetic test results for depression risk is psychologically well tolerated: Evidence from a longitudinal equivalence study
Rebecca M. K. Berns, .
Human Genetics and Genomics Advances · Published December 8, 2025
Integrating Polygenic Risk Improves Generative Forecasting of Disease Trajectories
Chris German, .
Pacific Symposium on Biocomputing (PSB) · Published December 1, 2025
Large language models identify causal genes in complex trait GWAS
Suyash Shringarpure, .
Pacific Symposium on Biocomputing (PSB) · Published December 1, 2025
Bayesian inference of population structure using identity-by-descent-based stochastic block models
Steven J. Micheletti, .
bioRxiv (Cold Spring Harbor Laboratory) · Posted November 30, 2025
Genome-wide association study of delay discounting identifies 11 loci and reveals transdiagnostic associations across mental and physical health
Hayley H. A. Thorpe, .
Molecular Psychiatry · Published November 25, 2025
Genome-wide association study and polygenic risk prediction of hypothyroidism
Søren A Rand, .
Nature Genetics · Published November 14, 2025
White Papers
Learn what 23andMe researchers have discovered with the help of 23andMe research participants.
- White Paper: Technical overview of 23andMe GWAS
- Supplementary Phenotype Table for Technical Overview of 23andMe GWAS
- Supplementary Materials for Technical Overview of 23andMe GWAS
- White Paper 23-26: Development and testing of estimating Biological Age from blood based signatures
- White Paper 23-25: A Generalized Method for the Creation and Evaluation of Polygenic Scores: Accounting for Genetic Ancestry as a Continuum
- White Paper 23-24 Health Tracks: Time to Event Modeling of Common Conditions Using Polygenic Scores and Lifestyle Factors
- White Paper 23-21: A Generalized Method for the Creation and Evaluation of Polygenic Scores
- White Paper 23-20: Standards of evidence for health and wellness recommendations
- White Paper 23-19: The science behind 23andMe's Type 2 Diabetes report
- White Paper 23-16: Ancestry Composition: A Novel, Efficient Pipeline for Ancestry Deconvolution
- White Paper 23-15: Scientific Standards for 23andMe's Health and Trait Reports
- White Paper 23-14: Ancestry Timeline
- White Paper 23-13: yHaplo™ | Identifying Y-chromosome haplogroups in arbitrarily large samples of sequenced or genotyped men
- White Paper 23-11: Estimating Carrier Frequency, Carrier Detection Rate, and Post-Test Carrier Risk for Recessive Disorders
- White Paper 23-05: Neanderthal Ancestry Inference
Publication Dataset
Access Program
23andMe's research and collaborations have been featured in more than two hundred publications, and our Publication Dataset Access Program supports sharing of these de-identified GWAS summary statistics with qualified researchers through a data transfer agreement. To initiate this process, we ask qualified researchers to provide a brief description of their research project and investigator information.
Learn more