Since 2010, 23andMe has published 293 papers
23andMe customers who participate in research are helping us advance scientific knowledge in revolutionary new ways. Each discovery helps pave the way for advances in medicine.
July 2025
Genetic neurodevelopmental clustering and dyslexia
University of Edinburgh
Published in Molecular Psychiatry
January 2025
Genomics yields biological and phenotypic insights into bipolar disorder
University of Oslo
Published in Nature
January 2025
First-in-human study of 23ME-00610, an antagonistic antibody for genetically validated CD200R1 immune checkpoint, in participants with advanced solid malignancies
Oregon Health Sciences University
Published in Cancer Research Communications
December 2024
Bidirectional relationship between olfaction and Parkinson’s disease
Queen Mary University of London
Published in npj Parkinson's Disease
November 2024
The shared genetic architecture and evolution of human language and musical rhythm
Max Planck Institute for Psycholinguistics
Published in Nature Communications
November 2024
Genome-wide meta-analysis of myasthenia gravis uncovers new loci and provides insights into polygenic prediction
Charite University
Published in Nature Communications
November 2024
Risk of pregnancy-associated venous thromboembolism in sickle cell trait
Johns Hopkins Hospital
Published in Blood
October 2024
Oral and gut microbiome profiles in people with early idiopathic Parkinson’s disease
23andMe
Published in Parkinsonism & Related Disorders
October 2024
A genome-wide association analysis reveals new pathogenic pathways in gout
University of Otago
Published in Nature Genetics
October 2024
CD200R1 immune checkpoint blockade by the first-in-human anti-CD200R1 antibody 23ME-00610: Molecular mechanism and engineering of a surrogate antibody
23andMe Therapeutics
Published in mAbs
October 2024
Genome-wide association study meta-analysis of 9,619 cases with tic disorders
Karolinska Institutet
Published in Nature Communications
September 2024
Ancestry-independent risk of venous thromboembolism in individuals with sickle cell trait vs. factor V Leiden
23andMe
Published in Blood Advances
July 2024
Polygenic prediction of major depressive disorder and related traits in African ancestries UK Biobank participants
University of Edinburgh
Published in Nature Genetics
July 2024
Shortcomings of ethnicity-based carrier screening for conditions associated with Ashkenazi Jewish ancestry
23andMe
Published in Genetics in Medicine Open
June 2024
Dyslexia polygenic scores show heightened prediction of verbal working memory and arithmetic
University of Edinburgh
Published in Scientific Studies of Reading
June 2024
Genome-wide association studies of coffee intake in UK/US participants of European ancestry uncover cohort-specific genetic associations
University of Guelph
Published in Nature Neuropsychopharmacology
June 2024
Discovery of RXFP2 genetic association in resistant hypertensive men and RXFP2 antagonists for the treatment of resistant hypertension
University of California, San Francisco
Published in Hypertension Research
June 2024
Genetic analysis and natural history of Parkinson's disease due to the LRRK2 G2019S variant
Brain
Published in Brain
June 2024
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction
Nature
Published in Nature
May 2024
The genetic architecture of dog ownership: large-scale genome-wide association study in 97,552 European-ancestry individuals
Oxford Academic
Published in Oxford Academic
April 2024
An ensemble penalized regression method for multi-ancestry polygenic risk prediction
Nature
Published in Nature
April 2024
MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups
Science
Published in Science
April 2024
A phenome-wide association and Mendelian randomisation study of alcohol use variants in a diverse cohort comprising over 3 million individuals
University of California, San Diego
Published in Science Direct
January 2024
Analysis of rare Parkinson’s disease variants in millions of people
National Institutes of Health
Published in Nature
January 2024
Multi-ancestry genome-wide meta-analysis identifies novel basal cell carcinoma loci and shared genetic effects with squamous cell carcinoma
Kaiser Permanente
Published in Nature
January 2024
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference
Published in Nature Genetics
December 2023
Multi-ancestry genome-wide association meta-analysis of Parkinson's disease
National Institutes of Health
Published in PubMed
November 2023
Correlations in sleeping patterns and circadian preference between spouses
University of Bristol
Published in Communication Biology
November 2023
Executive Function and Impulsivity Predict Distinct Genetic Variance in Internalizing Problems, Externalizing Problems, Thought Disorders, and Compulsive Disorders: A Genomic Structural Equation Modeling Study
University of California, San Diego
Published in Clinical Psychological Science
October 2023
Influence of autozygosity on common disease risk across the phenotypic spectrum
Wellcome Sanger
Published in Cell
October 2023
European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation
University of Bristol
Published in Nature Communications
September 2023
A new method for multiancestry polygenic prediction improves performance across diverse populations
Johns Hopkins University
Published in Nature
September 2023
Ethical considerations when co-analyzing ancient DNA and data from private genetic databases
23andMe
Published in Science
August 2023
Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study
National Institutes of Health
Published in The Lancet
August 2023
The genetic legacy of African Americans from Catoctin Furnace
23andMe
Published in Science
July 2023
Exercise knowledge, barriers and motivators among LRRK2 G2019S mutation carriers
Radboud University Medical Center
Published in Parkinsonism & Related Disorders
June 2023
Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci
QIMR Berghofer Medical Research Institute
Published in Nature Genetics
May 2023
GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19
University of Edinburgh
Published in Nature
May 2023
CADM2 is implicated in impulsive personality and numerous other traits by genome- and phenome-wide association studies in humans and mice
University of California, San Diego
Published in Translational Psychiatry
May 2023
Shared molecular genetic factors influence subcortical brain morphometry and Parkinson’s disease risk
QIMR Berghofer Medical Research Institute
Published in NPJ Parkinson’s disease
March 2023
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
University of Oxford
Published in Nature Genetics
February 2023
Cross-trait analyses identify shared genetics between migraine, headache, and glycemic traits, and a causal relationship with fasting proinsulin
The International Headache Genetics Consortium (IHGC)
Published in Human Genetics
February 2023
The Impact of the COVID-19 Pandemic on Care Partners of People with Parkinson's Disease
Radboud University
Published in Published Movement Disorders
February 2023
Challenges of accurately estimating sex-biased admixture from X chromosomal and autosomal ancestry proportions
Georgia Institute of Technology
Published in American Journal of Human Genetics
January 2023
Exploring the genetics of rhythmic perception and musical engagement in the Vanderbilt Online Musicality Study
Published in ANNALS of the New York Academy of Sciences
December 2022
Discovery of genomic loci associated with sleep apnea risk through multi-trait GWAS analysis with snoring
Published in SLEEP
December 2022
A multi-phenotype analysis reveals 19 susceptibility loci for basal cell carcinoma and 15 for squamous cell carcinoma
QIMR Berghofer
Published in Nature
December 2022
Data related to Genetic diversity fuels gene discovery for tobacco and alcohol use
Published in Nature
December 2022
Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects
Published in Nature Communications
November 2022
A Meta-Analysis of the Genome-Wide Association Studies on Two Genetically Correlated Phenotypes Suggests Four New Risk Loci for Headaches
Published in Phenomics
October 2022
Study identifies genetic links to dyslexia
In Collaboration with University of Edinburgh
Published in Nature Genetics
October 2022
A saturated map of common genetic variants associated with human height
VA Million Veterans Program
Published in Nature
September 2022
Reliability of Ancestry-specific Prostate Cancer Genetic Risk Score in Four Racial and Ethnic Populations
Published in European Urology Open Science
September 2022
Genome-wide association study of pain sensitivity assessed by questionnaire and the cold pressor test
Grunethal
Published in Pain
August 2022
What the Polygenic Basis of Rhythm Can Tell Us About Musical Traits
Published in Scientific Reports
August 2022
A remote longitudinal observational study of individuals at genetic risk for Parkinson’s disease: Baseline results
Published in Neurology Genetics
July 2022
Are some children genetically predisposed to poor sleep. A polygenic risk study
Published in Sleep Medicine
July 2022
Genome-wide meta-analysis of insomnia in over 2.3 million individuals implicates involvement of specific biological pathways through gene-prioritization
Published in Nature Genetics
July 2022
Genetic liability to posttraumatic stress disorder and its association with postpartum depression
Published in Cambridge University Press
July 2022
Study On Side Effects of Parkinson’s Medication
Published in Annals of Clinical and Translational Neurology
June 2022
Gene-environment interplay in externalizing behavior from childhood through adulthood
Published in The Journal of Child Psychology and Psychiatry
June 2022
Further validation of the THINC-it tool and extension of the normative data set in a study of n = 10.019 typical controls
Published in International Journal of Methods in Psychiatric Research
June 2022
Elucidating the relationship between migraine risk and brain volumes: causal inference and genetic overlap analysis
Published in Brain
June 2022
We Got the Beat
Published in Nature Human Behavior
June 2022
New Study Suggests Coffee During Pregnancy May Be OK After All
Published in International Journal of Epidemiology
June 2022
Genome-wide association analysis and replication in 810,625 individuals with varicose veins
Published in Nature Communications
May 2022
Shared genetic architectures of subjective well-being in East Asian and European ancestry populations
Published in Nature Human Behavior
May 2022
Genetic analyses identify pleiotropy and causality for blood proteins and highlight Wnt/β-catenin signalling in migraine
Published in Nature Communications
May 2022
Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett’s oesophagus and provides insights into clinical heterogeneity in reflux diagnosis
Published in BMJ Journals: GUT
May 2022
Genome-Wide Association Study Identifies 15 Common Risk Variants Associated With Obsessive-Compulsive Disorder
Published in Biological Psychiatry
May 2022
Trans-ethnic genome-wide association study reveals new therapeutic targets for benign prostatic hyperplasia
Published in The Journal of Urology
March 2022
New Study on Genetics of Educational Attainment
Published in Nature
March 2022
A First Glimpse of a New Cohort to Study Depression and Bipolar Disorder
In collaboration with Lundbeck
Published in Nature
March 2022
Whole genome sequence association study in critical illness caused by COVID-19
Published in Nature
February 2022
Consumer Genetic Testing Helps People at Risk for Hard to Diagnose Condition
Published in CHEST
January 2022
23andMe Study on Loss of Smell and Taste Due to COVID-19 Published
Published in Nature Genetics
January 2022
Ancestry- and sex-specific effects underlying inguinal hernia susceptibility identified in a multiethnic genome-wide association study meta-analysis
Published in Oxford Academic
January 2022
Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis
Published in JAMA Neurology
November 2021
Multi-Trait Genetic Analysis Identifies Autoimmune Loci Associated with Cutaneous Melanoma
QIMR Berghofer
Published in Science
November 2021
A population-specific reference panel for improved genotype imputation in African Americans
23andMe
Published in Communications Biology
November 2021
Genome-wide association study of problematic opioid prescription use in 132,113 23andMe research participants of European ancestry
University of California, San Diego
Published in Nature
October 2021
Unhealthy Behaviours and Risk of Parkinson’s Disease: A Mendelian Randomisation Study
In collaboration with Queen Mary University, National Institute on Aging and University of Bristol
Published in Journal of Parkinson’s Disease
August 2021
Shared genetic aetiology between cortical brain morphology and tobacco, alcohol and cannabis use
QIMR Berghofer
Published in Oxford Academic
August 2021
Genetic insights into biological mechanisms governing human ovarian ageing
University of Cambridge
Published in Nature
August 2021
Neuroticism, smoking and the risk of Parkinson’s disease: A network Mendelian randomization study
Published in Journal of Parkinson’s Disease
July 2021
Parsing Genetically Influenced Risk Pathways: Genetic Loci Impact Problematic Alcohol Use Via Externalizing and Specific Risk
Virginia Commonwealth University
Published in MedRxiv
July 2021
pH and Proton Sensor GPR65 Determine Susceptibility to Atopic Dermatitis
Pfizer
Published in The Journal of Immunology
July 2021
Phenome-wide analysis highlights putative causal relationships between migraine and other complex traits
QIMR Berghofer
Published in The Journal of Headache and Pain
July 2021
Characterizing the genetic architecture of Parkinson's disease in Latinos
Cleveland Clinic (LARGE-PD)
Published in Annals of Neurology
June 2021
Resource profile and user guide of the Polygenic Index Repository
NBER
Published in Nature Human Behaviour
May 2021
GWAS of Depression Phenotypes in the Million Veteran Program and Meta-analysis in More than 1.2 Million Participants Yields 178 Risk Loci with Independent Replication
Yale University
Published in Nature Neuroscience
May 2021
Genome-wide association studies of LRRK2 modifiers of Parkinson’s disease
Indiana University
Published in Annals of Neurology
April 2021
Genetic analyses identify widespread sex-differential participation bias
VU Amsterdam, Broad Institute, University of Cambridge
Published in Nature Genetics
April 2021
Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity
Led by 23andMe
Published in Nature Genetics
April 2021
Genetic mechanisms of critical illness in Covid-19
University of Edinburgh
Published in Nature Genetics
April 2021
Distinct clinical phenotypes for Crohn’s disease derived from patient surveys
Published in BMC Gastroenterology
April 2021
Bonsai: An efficient method for inferring large human pedigrees from genotype data
Led by 23andMe
Published in bioRxiv
April 2021
Genetic discovery and risk characterization in type 2 diabetes across diverse populations
University of Southern California
Published in Cell
March 2021
Nuclear genome-wide associations with mitochondrial heteroplasmy
The Hospital for Sick Children
Published in Science Advances
February 2021
Predicting the effects of Tumor Necrosis Factor inhibition on Parkinson disease: A Mendelian randomization study
Karolinska Institutet
Published in Neurology
February 2021
Multiple measures of depression enhance validity of Major Depressive Disorder cases in the UK Biobank
King's College London
Published in BJPsych Open
February 2021
Elucidating the genetic architecture underlying IGF1 levels and its impact on genomic instability and cancer risk
Cambridge
Published in Wellcome Open Research
January 2021
Genome-wide meta-analysis of pneumonia suggests a role for mucin biology and provides novel drug repurposing opportunities
University of Newcastle
Published in MedRxiv
January 2021
A scalable pipeline for local ancestry inference using tens of thousands of reference haplotypes
Led by 23andMe
Published in bioRxiv
January 2021
Leveraging both individual-level genetic data and GWAS summary statistics increases polygenic prediction of psychiatric disorders and other complex diseases
Aarhus University
Published in JAMA Psychiatry
January 2021
Disease risk scores for skin cancers
23andMe
Published in Nature Cancer
December 2020
Fast and Robust Identity-by-Descent Inference with the Templated Positional Burrows–Wheeler Transform
Led by 23andMe
Published in Molecular Biology and Evolution
December 2020
Depression genetic scores are associated with major depressive disorder diagnosis and depressive episode in Mexican adolescents
QIMR Berghofer
Published in Journal of Affective Disorders
October 2020
Genome-wide association studies of antidepressant class response and treatment-resistant depression
Janssen
Published in Translational Psychiatry
October 2020
Hemochromatosis risk genotype is not associated with colorectal cancer risk or age of onset
University of Washington
Published in HGG Advances
October 2020
A large-scale genome-wide association study meta-analysis of cannabis use disorder
Aarhus University
Published in The Lancet Psychiatry
October 2020
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells
Harvard Medical School
Published in Nature
October 2020
Genome-wide Study Identifies Association between HLA-B∗55:01 and Self-Reported Penicillin Allergy
Statens Serum Institut
Published in Science Direct
September 2020
Genome-wide association study identifies 48 common genetic variants associated with left handedness
QIMR Berghofer
Published in Nature Human Behaviour
September 2020
Genetic analysis of endometriosis and depression identifies shared loci and implicates links with gastric mucosa abnormality
Queensland University of Technology
Published in Human Genetics
September 2020
Direct-to-consumer genetic testing for factor V Leiden and prothrombin 20210G>A: the Consumer Experience
23andMe
Published in Molecular Genetics and Genomics Medicine
August 2020
Evaluating lipid-lowering drug targets for Parkinson’s disease prevention using Mendelian randomization
University College London
Published in Annals of Neurology
August 2020
A two-stage approach to identifying and validating modifiable factors for the prevention of depression
Massachusetts General Hospital
Published in American Journal of Psychiatry
August 2020
Genetic correlation, pleiotropy, and causal associations between substance use and psychiatric disorder
University of Minnesota
Published in Psychological Medicine
August 2020
Genetic Consequences of the Transatlantic Slave Trade in the Americas
23andMe
Published in AJHG
July 2020
The design of a virtual Parkinson's disease cohort study
Collaboration with University of Rochester
Published in Journal of PD
June 2020
23andMe Maps the Way We Eat
Led by 23andMe
Published in Public Health Nutrition
June 2020
Genome-Wide Association Study Identifies Loci Associated with Sensitive Skin
The P&G Company
Published in MDPI
June 2020
Study suggests that partial LRRK2 inhibition may not have adverse effects
Collaboration with the Broad Institute
Published in Nature
May 2020
The method behind 23andMe health reports
Led by 23andMe
Published in
May 2020
Characterization of a 23andMe BRCA 1/2 founder variant cohort
Led by 23andMe
Published in Public Health Genomics
April 2020
Insights into Parkinson's disease etiology
Collaboration with Karolinska Institutet
Published in Nature Genetics
April 2020
SMPD1 variants do not have a major role in REM sleep behavior disorder
Collaboration with McGill University
Published in Neurobiology of Aging
April 2020
Evaluation of self-administered pain sensitivity testing
Led by 23andMe
Published in PLoS One
February 2020
Investigating the genetic relationship between endometriosis and migraine
Collaboration with Queensland University of Technology
Published in Genes
February 2020
New Genetic Associations Identified for Heart Failure
Collaboration with Johns Hopkins University
Published in Nature Communications
February 2020
New Fox Insight resource to facilitate discovery in Parkinson's disease research
Collaboration with the Michael J. Fox Foundation
Published in Scientific Data
January 2020
Genetic analysis of variants associated with rapid eye movement sleep behavior disorder
Collaboration with McGill University
Published in Annals of Neurology
December 2019
Using genetics and Electronic Health Records to examine BMI and obesity
Collaboration with Renown Health
Published in Genes, Genomes, Genetics
December 2019
The Genetic Influence on Retinal Detachment
Collaboration with University of Edinburgh
Published in Human Molecular Genetics
December 2019
New insights into the genetic associations between depression, loneliness, and coronary artery disease
Collaboration with UCSD and Vanderbilt University Medical Center
Published in Molecular Psychiatry
December 2019
New genetic insights into Parkinson's disease
Collaboration with the NIH
Published in The Lancet Neurology
November 2019
New genetic insights into GBA-associated risk for Parkinson's disease
Collaboration with the National Institute on Aging
Published in Brain
November 2019
New study uncovers genetic determinants of Y chromosome loss
Collaboration with Uppsala University and the University of Cambridge
Published in Nature
November 2019
Investigating the health outcomes associated with a genetic predisposition to loneliness
Collaboration with UCSD and Vrije Universiteit Amsterdam
Published in Human Molecular Genetics
November 2019
New study investigates risk for postpartum psychiatric disorders
Collaboration with Aarhus University
Published in Translational Psychiatry
October 2019
Investigating the genetic correlations between pain and psychiatric traits
Collaboration with the University of Dundee
Published in European Journal of Human Genetics
October 2019
New scientific resource points to traits associated with Parkinson's disease risk
Collaboration with Queen Mary University
Published in Movement Disorders
October 2019
New study reveals common genetic origins between uterine fibroids and endometriosis
Collaboration with Brigham and Women's Hospital
Published in Nature Communications
October 2019
First estimates for uniparental disomy, a rare genetic phenomenon
Led by 23andMe
Published in The American Journal of Human Genetics
September 2019
New genetic study of gastroesophageal reflux disease
Collaboration with QIMR Berghofer
Published in Nature Communications
September 2019
New genetic insights into autism-related traits
Collaboration with the University of Cambridge
Published in Communications Biology
August 2019
Sexual Behavior Not Meaningfully Predicted by Genetics, New Study Finds
Collaboration with the Broad Institute and the University of Queensland
Published in Science
August 2019
New genetic associations found in a genetic study of knee pain
Collaboration with the University of Dundee
Published in Communications Biology
August 2019
Characterization of a 23andMe BRCA1/2 founder variant cohort
Led by 23andMe
Published in medRxiv
July 2019
New insights into a potential inflammatory bowel disease therapy
Collaboration with Pfizer
Published in Mucosal Immunology
June 2019
Investigating treatment-resistant depression in the 23andMe cohort
Collaboration with Janssen
Published in Psychiatry Research
May 2019
A Study on Physicians' Knowledge of Consumer Genetic Testing
Collaboration with Duke University
Published in Journal of Personalized Medicine
April 2019
Parkinson’s disease research may offer promise for early detection
Collaboration with the NIH
Published in Movement Disorders
April 2019
The genetics of asthma and age
Collaboration with QIMR Berghofer
Published in American Journal of Human Genetics
March 2019
New Parkinson’s disease research may offer promise for early detection
Led by 23andMe
Published in npj Parkinson's Disease
March 2019
New insights into the genetics of mouth ulcers
Collaboration with University of Bristol
Published in Nature Communications
March 2019
The science behind 23andMe's Type 2 Diabetes report
Led by 23andMe
Published in
February 2019
New insights into the genetics of austism
Collaboration with Aarhus University
Published in Nature Genetics
February 2019
Genetics of insomnia more similar to psychiatric conditions than to other sleep traits
Collaboration with VU Amsterdam
Published in Nature Genetics
February 2019
New insights into the genetics of depression
Collaboration with University of Edinburgh
Published in Nature Neuroscience
February 2019
New depression loci identified
Collaboration with University of Edinburgh
Published in Nature Neuroscience
February 2019
Genetic study of impulsiveness reveals associations with drug use
Collaboration with University of California, San Diego
Published in Journal of Neuroscience
January 2019
The genetics of being a morning person
Collaboration with University of Exeter
Published in Nature Communications
January 2019
The genetics of taking risks
Collaboration with National Bureau of Economic Research
Published in Nature Genetics
January 2019
Genetic study of nicotine and alcohol use offers insight into addiction
Collaboration with University of Minnesota
Published in Nature Genetics
January 2019
New insights into genetic risk for depression
Collaboration with University of Edinburgh
Published in Biological Psychiatry
December 2018
Study points to new genetic underpinnings for polycystic ovary syndrome
Collaboration with Cambridge
Published in PLoS Genetics
November 2018
A comparison of survey platforms
Led by 23andMe
Published in Chance
November 2018
Novel research uncovers genes that contribute to risk for ADHD
Collaboration with the Broad Institute
Published in Nature Genetics
November 2018
New research shows shared genetic link between alcohol dependence and psychiatric disorders
Collaboration with Washington University St Louis
Published in Nature Neuroscience
November 2018
Study uncovers evidence of the genetic associations for appendicitis
Collaboration with University of Pittsburgh School of Medicine
Published in Human Genetics
October 2018
The genetics of alcoholism
Collaboration with UCSD and University of Edinburgh
Published in American Journal of Psychiatry
October 2018
Novel genetic research methods help to identify targets for medications
Collaboration with Merck
Published in Nature Communications
October 2018
New genetic insights into skin cancer
Collaboration with Stanford University
Published in Nature Communications
August 2018
Is the Vitamin D hype all it's made out to be? New bone fractures study provides some clues
Collaboration with Erasmus and McGill University
Published in British Medical Journal
August 2018
The power of self-report as a tool for identifying subtypes of Parkinson's disease
Collaboration with Pfizer
Published in Scientific Reports
August 2018
Scientists identify genes associated with cannabis use
Collaboration with Radboud
Published in Nature Neuroscience
August 2018
Investigating patterns in abnormal adolescent behavior
Collaboration with University of Bristol
Published in Translational Psychiatry
July 2018
Massive study on the genetics of educational attainment
Collaboration with NBER
Published in Nature Genetics
July 2018
New genetic insights into male androgenetic alopecia
Collaboration with University of Bonn
Published in Journal of Investigative Dermatology
July 2018
New genetic research on allergic rhinitis
Collaboration with COPSAC
Published in Nature Genetics
July 2018
New genetic research on spontaneous preterm birth
Collaboration with Cincinnati Children’s Hospital Medical Center
Published in PLoS Genetics
June 2018
Addressing the accuracy of direct-to-consumer genetic testing
Led by 23andMe
Published in Nature Genetics in Medicine
June 2018
New study finds genetic associations for neuroticism
Collaboration with VU Amsterdam
Published in Nature Genetics
June 2018
Study finds insights into the genetic basis of finger ratio
Collaboration with the Broad Institute
Published in Human Molecular Genetics
May 2018
New genetic research on nearsightedness
Collaboration with Consortium for Refractive Error and Myopia
Published in Nature Genetics
May 2018
Massive new study finds shared genetic basis for psychiatric disorders
Collaboration with the Broad Institute
Published in Science
May 2018
New genetic associations for rosacea found
Collaboration with GlaxoSmithKline
Published in Human Molecular Genetics
May 2018
Largest-ever family study provides new insights into migraines
Collaboration with the Broad Institute
Published in Neuron
April 2018
Findings show that common variants are associated with major depressive disorder
Collaboration with Kunming Institute of Zoology
Published in Neuropsychopharmacology
April 2018
New research identifies 44 risk variants associated with major depression
Collaboration with the Psychiatric Genomics Consortium
Published in Nature Genetics
April 2018
Research identifies new variants associated with allergies
Collaboration with QIMR and the University of Bristol
Published in Journal of Allergy and Clinical Immunology
April 2018
New genetic variants linked to hair color
Collaboration with King's College London
Published in Nature Communications
April 2018
Study finds new genetic associations for depression
Collaboration with University of Edinburgh
Published in Nature Communications
March 2018
Vitiligo-related genes and skin cancer risk
Collaboration with Indiana University
Published in Journal of Investigative Dermatology
March 2018
Researchers find genetic associations for morning sickness
Collaboration with University of California, Los Angeles
Published in Nature Communications
March 2018
Insights from direct-to-consumer genomics can be used to accelerate precision health
Collaboration with the Roundtable on Genomics and Precision Health at the National Academies of Sciences, Engineering, and Medicine
Published in National Academy of Medicine Perspectives
March 2018
New research on the genetics of empathy, and how it relates to autism
Collaboration with University of Cambridge
Published in Translational Psychiatry
February 2018
Genetics linked to adolescents' ability to read others' mental state
Collaboration with University of Cambridge
Published in Scientific Reports
January 2018
New method used in genome-wide association analysis
Collaboration with Cornell
Published in Nature Genetics
December 2017
Genetics linked to impulsivity
Collaboration with University of California, San Diego
Published in Nature Neuroscience
November 2017
New research finds genetic associations for detached earlobes
Collaboration with University of Pittsburgh
Published in American Journal of Human Genetics
November 2017
Researcher studying personality traits improve method for identifying genetic associations
Collaboration with University of San Diego and University of Oslo
Published in Human Molecular Genetics
October 2017
Genetic correlations between behavior and the alcohol use disorder identification test (AUDIT) scores
Collaboration with University of California, San Diego
Published in Addiction Biology
October 2017
New genetic associations found for restless legs syndrome
Collaboration with Helmholtz Zentrum Munich
Published in The Lancet: Neurology
October 2017
New research identifies more than a hundred immune-related genes associated with asthma and allergies
Collaboration with QIMR Berghofer Medical Research Institute
Published in Nature Genetics
October 2017
Self-reported data provides insight into use of phenome-wide association studies in drug discovery
Collaboration with GlaxoSmithKline
Published in PLoS ONE
September 2017
Study finds genetic links for vulnerability to common infectious diseases
Led by 23andMe
Published in Nature Communications
September 2017
Links between different genetic variants give hints about evolution
Collaboration with Harvard School of Public Health
Published in Nature Genetics
September 2017
New genetic associations for Parkinson’s disease identified
Collaboration with Genentech
Published in Nature Genetics
September 2017
New study finds genetic links for risk of premature births
Collaboration with Cincinnati Children's Hospital Medical Center
Published in New England Journal of Medicine
August 2017
The genetics of uterine fibroids in African Americans
Collaboration with Brigham Women's Hospital and Vanderbilt University
Published in Human Genetics
July 2017
Research confirms genetic associations for personality traits
Collaboration with University of Cambridge
Published in Heliyon
June 2017
The genetics of empathy
Collaboration with the Autism Research Center
Published in Molecular Psychiatry
May 2017
New genetic variants found to influence psoriasis risk
Collaboration with the University of Michigan
Published in Nature Communications
May 2017
New genetic variants found to influence endometriosis risk
Collaboration with the University of Queensland
Published in Nature Communications
May 2017
The role of genetics in personality and schizophrenia
Collaboration with the University of Oslo
Published in Scientific Reports
April 2017
New genetic variants found to influence puberty timing and cancer risk
Collaboration with Cambridge University
Published in Nature Genetics
March 2017
The role of genetics in male-pattern baldness
Collaboration with King's College London
Published in Nature Communications
February 2017
Genetics found to influence mosquito bite responses
Collaboration with Pfizer
Published in Human Molecular Genetics
February 2017
New genetic variant found to influence skin cancer risk
Collaboration with Stanford University
Published in Oncotarget
February 2017
The shared genetics of autoimmune disease and allergies
Collaboration with the University of Copenhagen
Published in Journal of Allergy and Clinical Immunology
January 2017
New genetic variant found to influence cognitive performance
Collaboration with Duke University
Published in Molecular Psychiatry
January 2017
Genetic evidence of assortative mating in humans
Collaboration with University of Queensland
Published in Nature Human Behavior
December 2016
Genetics found to influence personality and psychological disorders
Collaboration with the University of Oslo
Published in Nature Genetics
November 2016
Genetics found to influence menstrual cramps severity
Collaboration with Pfizer
Published in Pain
October 2016
New genetic variants found to influence fertility
Collaboration with the University of Oxford
Published in Nature Genetics
October 2016
Genetics found to influence resting heart rate
Collaboration with the University Medical Center Groningen
Published in Nature Genetics
September 2016
Genetics found to influence antidepressant efficacy
Collaboration with Janssen
Published in Translational Psychiatry
August 2016
A new methodology helps identify 4 new asthma risk genes
Collaboration with the QIMR Berghofer Medical Research Institute
Published in Journal of Allergy and Clinical Immunology
August 2016
New genetic variants found to influence risk of most common skin cancer
Collaboration with Stanford University
Published in Nature Communications
August 2016
Genetics found to influence risk of chronic pain and depression
Collaboration with Pfizer
Published in PLoS Medicine
August 2016
The genetics of being a morning person
Collaboration with University of Exeter
Published in PLoS Genetics
August 2016
New genetic variants found to influence major depression risk
Collaboration with Pfizer
Published in Nature Genetics
July 2016
New genetic variants found to influence skin cancer risk
Collaboration with Stanford University
Published in Nature Communications
June 2016
New genetic findings for rare blood cancers
Led by 23andMe
Published in Blood Journal
June 2016
The role of genetics in migraines
Collaboration with Broad Institute
Published in Nature Genetics
May 2016
Genetic variants found to influence multiple traits and conditions
Collaboration with New York Genome Center
Published in Nature Genetics
May 2016
Genetic variants linked to education level
Collaboration with Erasmus University
Published in Nature
April 2016
The role of genetics in well-being
Collaboration with Erasmus University
Published in Nature Genetics
April 2016
The identification of individuals resilient to genetic diseases
Collaboration with Mount Sinai's School of Medicine
Published in Nature Biotechnology
February 2016
New genetic variants found to influence blood clot risk
Collaboration with Karolinska Institute
Published in Human Molecular Genetics
February 2016
New genetic variants found to influence likelihood of being a morning person
Led by 23andMe
Published in Nature Communications
January 2016
Quantifying genetic risk of prion disease
Collaboration with Broad Institute
Published in Science Translational Medicine
December 2015
The genetics of esophageal cancer and GERD
Collaboration with QIMR Berghofer Medical Research Institute
Published in Human Molecular Genetics
December 2015
Genetics found to influence likelihood of developing hernias
Collaboration with Kaiser Permanente and University of California, San Francisco
Published in Nature Communications
November 2015
Genetics found to influence puberty timing in girls and boys
Collaboration with University of Cambridge
Published in Nature Communications
October 2015
Genetics found to influence eczema risk across multiple ancestries
Collaboration with University of Bristol
Published in Nature Genetics
October 2015
The impact of genetic testing on perceived risk of cancer
Collaboration with Harvard Medical School
Published in BMC Medical Genomics
September 2015
New genetic variants found to influence polycystic ovary syndrome (PCOS) risk
Collaboration with University of Cambridge
Published in Nature Communications
September 2015
New rare genetic variant found to influence bone density and risk of fractures
Collaboration with McGill University
Published in Nature
August 2015
A new model for diagnosing Parkinson's disease
Collaboration with the National Institute on Aging
Published in Lancet Neuro
August 2015
New genetic variants found to influence age at first period
Collaboration with University of Cambridge
Published in Nature Communications
August 2015
Study on what drives interest in personal genomics
Collaboration with University of Cambridge
Published in Genome Medicine
June 2015
Virtual doctor's visit and genetic testing for Parkinson's disease
Collaboration with University of Rochester
Published in Digital Health
June 2015
Consumer understanding of Personal Genomic Services test results
Collaboration with Harvard Medical School
Published in Public Health Genomics
June 2015
Genetic variants found to influence risk of depression and psychiatric disorders
Collaboration with Max Plank Institute
Published in Neuron
March 2015
Genetics found to influence risk for rosacea
Collaboration with Stanford University
Published in Journal of Investigative Dermatology
February 2015
Insight into why risk of genetic abnormalities increases with mother's age
Collaboration with Albert Einstein College of Medicine
Published in Nature Communications
January 2015
Genetics found to influence likelihood of motion sickness
Led by 23andMe
Published in Human Molecular Genetics
December 2014
An analysis of the ancestry make-up of people across the United States
Led by 23andMe
Published in AJHG
December 2014
A description of the PGen study
Collaboration with University of Cambridge
Published in Genome Medicine
October 2014
An algorithm to speed up genotype imputation
Collaboration with University of Michigan
Published in Bioinformatics
October 2014
Description of Ancestry Composition
Led by 23andMe
Published in bioRxiv
October 2014
Replication of genetic associations with behavioral traits
Collaboration with Erasmus University
Published in Psychological Science
August 2014
The design of a genotyping platform
Collaboration with the National Institute on Aging
Published in Neurobiology of Aging
July 2014
New genetic variants found to influence risk of Parkinson's disease
Collaboration with the National Institute on Aging
Published in Nature Genetics
April 2014
23andMe scientists improve method for finding relatives
Led by 23andMe
Published in Molecular Biology and Evolution
December 2013
New genetic variants found to influence risk of asthma with hay fever
Collaboration with QIMR Berghofer Medical Research Institute
Published in Journal of Allergy and Clinical Immunology
October 2013
Gradient boosting as a SNP Filter
Collaboration with University of Notre Dame
Published in Journal of Data Mining in Genomics & Proteomics
October 2013
Variants in PET1 gene influence fear and threat processing
Collaboration with Indiana University
Published in Experimental Neurology
August 2013
New genetic variants found to influence asthma risk
Collaboration with QIMR Berghofer Medical Research Institute
Published in Genes and Immunity
July 2013
Genetics found to influence likelihood of stretch marks
Led by 23andMe
Published in Journal of Investigative Dermatology
June 2013
New genetic variants found to influence allergies and asthma
Led by 23andMe
Published in Nature Genetics
June 2013
Iron levels linked to Parkinson's disease risk
Collaboration with Imperial College London
Published in PLOS Medicine
April 2013
Genetics found to influence risk of problem drinking
Collaboration with Duke University
Published in Genes, Brain and Behavior
February 2013
New genetic variants found to influence nearsightedness
Led by 23andMe
Published in PLoS Genetics
February 2013
Customer response to direct-access BRCA genetic testing
Led by 23andMe
Published in PeerJ
January 2013
New genetic variants found to influence male-pattern baldness
Collaboration with University of Bonn
Published in Journal of Investigative Dermatology
January 2013
Genetics found to influence emotion processing and psychopathology
Collaboration with University of Pennsylvania
Published in Molecular Psychiatry
November 2012
New genetics variants found to influence cilantro preference
Led by 23andMe
Published in Flavour
October 2012
Comparison of family history and genetic testing for predicting complex disease risk
Led by 23andMe
Published in PLoS Genetics
June 2012
Genetics linked to breast size and breast cancer risk
Led by 23andMe
Published in BMC Medical Genetics
May 2012
New genetic variants found to influence risk of early-onset male pattern baldness
Collaboration with McGill University
Published in PLoS Genetics
April 2012
New genetic variants found to influence risk of hypothyroidism
Led by 23andMe
Published in PLoS One
April 2012
The method behind the Relative Finder tool
Led by 23andMe
Published in PLoS One
March 2012
The creation of an online resource for Parkinson's disease research findings
Collaboration with Max Plank Institute
Published in PLoS Genetics
January 2012
Structuring a research partnership between academia and industry
Collaboration with Harvard Medical School
Published in Genetics in Medicine
August 2011
23andMe replicates over 180 genetic associations
Led by 23andMe
Published in PLoS One
June 2011
New genetic variants found to influence risk of Parkinson's disease
Led by 23andMe
Published in PLoS Genetics
March 2011
The genetics of hunter-gatherer populations
Led by 23andMe
Published in PNAS
June 2010
The discovery of new genetic associations to common traits
Led by 23andMe
Published in PLoS Genetics
See here for full bibliography
