ASHG 2026 · Biopharma

Regeneron at ASHG 2026

Tarrytown, New York

Regeneron at ASHG 2026 in Montréal: 10 presentations (9 posters, 1 platform talk); Booth 507.

10
presentations on the program
1
sessions invited to or moderated
2
Reviewers’ Choice abstracts
507
exhibit booth

Explore everyone at ASHG 2026 →

OrganizationASHG 2026 Attendance
Regeneron
Tarrytown, New York
1 Employee · 1 Senior Manager, RGC · 1 Statistical Geneticist · 1 SVP and Chief Genomics and Data Sciences Officer
Public company~15,400 people
Regeneron invents, develops, and commercializes medicines for serious diseases. Its work spans biologics, genetic medicines, and cell therapies.
Won FDA approval for Pasatru, the first treatment for a rare bone-growth disorder called FOP, adding a new rare-disease product.
Won FDA approval for Pasatru, the first treatment for a rare bone-growth disorder called FOP, adding a new rare-disease product.
2026-08 · source
Launched a research collaboration with Parabilis Medicines to develop antibody-peptide conjugate therapies, expanding its drug-discovery pipeline.
2026-05 · source
Agreed to provide its newly approved genetic-hearing-loss gene therapy Otarmeni for free in the US, expanding patient access.
2026-04 · source
Source: company newsroom
Q2 2026 revenue $4.3B, up 17% YoY
2026 guidance includes R&D spend of $6.5-6.635 billion and SG&A of $2.83-2.96 billion. · 2026-07-30
“Second quarter 2026 revenues increased 17% to $4.3 billion versus second quarter 2025; GAAP R&D $6.500–$6.635 billion”
Source: results release
Currently hiring: 662 open roles
Source: careers page
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 validation
Genetic, Genomic, and Epigenomic Resources and Databases
Complex 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 Targets
Complex Traits and Polygenic Disorders
Collaborators: National Heart Foundation Hospital & Research Institute, Bangladesh Medical University +4 more
DiabetesLarge-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.
Statistical Genetics and Genetic Epidemiology
Exome/genome sequencingRare variantsNeurodegenerationTriplet and other repeats
Poster
Thu Oct 22
4:15 pm
Identification of proteins reflecting baseline effects and ongoing aging from cross-sectional proteomic data
Omics Technologies
Proteomics
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 Genetics and Genetic Epidemiology
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
Mendelian Phenotypes
Collaborators: Boston Children's Hospital
Clinical geneticsDiagnosticsGastrointestinal systemImmune system
Poster
Fri Oct 23
2:30 pm
Identifying genetic variants with large effects on risk of depression using severe phenotypes
Complex Traits and Polygenic Disorders
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 Intelligence and Machine Learning
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 Traits and Polygenic Disorders
Collaborators: University of Oxford, Universidad Nacional Autónoma de México +7 more
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
From Autoimmune Risk Variants to Cell States and Target Genes: Integrative Genetic Dissection of Immune-Mediated Disease
Collaborators: University of Pittsburgh, Skåne University Hospital +2 more
Autoimmune disorderIdentification of disease genesGenome-wide association studyRare variants
Session
Sat Oct 24
11:15 am
Globalizing Human Genetics: From Discovery Through Implementation
1 invited symposium speaker

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