Regeneron at ASHG 2026
Oct 20–24, 2026 Montréal, Canada ~7.5k attendees Website
Regeneron brings 10 presentations to ASHG 2026 in Montréal, and exhibits at Booth 507. Its program at this meeting centres on population genetics, computational analysis, and therapeutic discovery. Its presentations cover imaging-based genetic discovery in 95,000 UK Biobank participants and protective variants linked to type 2 diabetes in 132,045 South Asians.
| Organization | ASHG 2026 Attendance |
|---|---|
Regeneron Tarrytown, New York | 1 Employee · 1 Senior Manager, RGC · 1 Statistical Geneticist · 1 SVP and Chief Genomics and Data Sciences Officer |
Regeneron invents, develops, and commercializes medicines for serious diseases. Its work spans biologics, genetic medicines, and cell therapies.
| Booth Exhibiting at Booth 507 Wed, Oct 219:45am–4:30pmThu, Oct 229:45am–1:30pmFri, Oct 239:45am–4:30pm Poster Wed Oct 21 2:30 pm ★ Reviewers’ Choice Systematic extraction of 4,434 imaging-derived phenotypes in 95,000 UK Biobank participants drives genetic discovery and validationComplex traitsLarge-scale biobanksRare variantsIdentification of disease genes Poster Wed Oct 21 2:30 pm ★ Reviewers’ Choice Exome-Wide Association Study of Type 2 Diabetes in 132,045 South Asians reveals Population-Enriched Protective Variants and Novel Therapeutic TargetsDiabetesLarge-scale biobanksRare variantsGenomics Poster Thu Oct 22 4:15 pm Loss-of-function variants in the DNA Mismatch Repair genes POLD1, PMS1 and FAN1 modify age at onset of motor symptoms in Huntington’s Disease. Exome/genome sequencingRare variantsNeurodegenerationTriplet and other repeats Poster Thu Oct 22 4:15 pm Poster Fri Oct 23 2:30 pm SBAT-REMETA: Combining rare-variant burden scores from summary statistics boosts gene discovery in multi-cohort studies Statistical geneticsRare variantsLarge-scale biobanksGenome-wide association study Poster Fri Oct 23 2:30 pm Whole-Exome Sequencing for Severe Inflammatory Bowel Disease: Genetic Architecture and Emerging Candidate Genes Clinical geneticsDiagnosticsGastrointestinal systemImmune system Poster Fri Oct 23 2:30 pm Identifying genetic variants with large effects on risk of depression using severe phenotypes DepressionPolygenic risk scorePsychiatric geneticsGenetic epidemiology Poster Fri Oct 23 2:30 pm Predicting diseases of high mortality and morbidity from 4,434 imaging and 99 non-imaging biomarkers in 95,000 UK Biobank participants Artificial intelligenceMathematical modelingMachine learningLarge-scale biobanks Poster Fri Oct 23 2:30 pm Ancestry-specific associations with adult height in 2.1 million diverse exomes Complex traitsExome/genome sequencingRare variantsSkeletal system Talk Sat Oct 24 8:15 am A distinct subset of autoimmune diseases defined by profound co-prevalence and genetic risk association with the IL12 pathway Autoimmune disorderIdentification of disease genesGenome-wide association studyRare variants Session Sat Oct 24 11:15 am 1 invited symposium speaker |
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