NHGRI at ASHG 2024 Annual Meeting
Event Details
On November 5-9, 2024, the National Human Genome Research Institute (NHGRI) will participate in the ASHG Annual Meeting - the world's largest human genetics and genomics meeting and exposition. The annual meeting provides a forum for the presentation and discussion of cutting-edge science in all areas of human genetics.
Visit with NHGRI staff at Booth #1025 in NIH Pavilion of the exhibit hall to learn more about our research, programs, career and training opportunities.
All times are in Mountain Time (MT).
Colorado Convention Center
Poster Presentations
| Presenter | Title | Board # |
|---|---|---|
| Wednesday, November 6, 2:30 – 4:30 p.m. | ||
| Anas Awan | Phenome-wide association study of MTHFR variant in UK Biobank and All of Us | 1086W |
| Amy Bentley | G6PD deficiency masks the diagnosis of abnormal glucose tolerance: insight from the Africans in America Study | 5068W |
| Kuki Davey | Functional Validation of HMCN1 as a Candidate Gene for Childhood-Onset Essential Hypertension | 2037W |
| Jennifer Johnston | Specification of frequency criteria for secondary findings genes to improve classification concordance | 3069W |
| Brynja Matthiasardottir | Optimal thresholds for variant impact prediction in human genes depend on selection | 4102W |
| Antwi Oteng | OSBPL11 is an important regulator of cholesterogenic genes in murine hepatocyte cell line | 6072W |
| Henry Taylor | Genetically-predicted protein levels in UK Biobank and NIH All of Us identify thousands of associations of proteins and clinical phenotypes | 1135W |
| Ariel Williams | SGLT2 Inhibitors Attenuate Risk of APOL1-mediated Chronic Kidney Disease | 5154W |
| Evan Ying | Validation and development of functional assays for RYR1 variants | 6092W |
| Thursday, November 7, 2:30 – 4:30 p.m. . | ||
| Seyma Eroglu | Ankylosing spine-brachydactyly syndrome: A possible novel skeletal dysplasia | 2010T |
| Kendall Flaharty | Evaluating Large Language Models on Medical, Lay Language, and Self-Reported Descriptions of Genetic Conditions | 1069T |
| Brian N Lee | Understanding ableism in abstracts for genetic and genomic autism research | 6044T |
| Dayo Shittu | Genetic Predisposition Factors for Systemic Lupus Erythematosus Within All of Us Research Program | 5123T |
| Friday, November 8, 2:30 – 4:30 p.m. | ||
| Afia Asare | Connecting with the Impact of Genomic Variation on Function (IGVF) Consortium | 1055F |
| Lily Barna | Modernizing a comprehensive measure of genetic literacy | 7069F |
| Guanjie Chen | Integrating Methylation and Transcriptomic Analyses with Whole Genome Sequencing YieldsNovel Insights into SARS-CoV-2 in African Americans | 5097F |
| Jiayu Fu | Phasing Accuracy of Long-Read Whole Genome Sequencing is Coverage and Reference Genome Dependent | 1155F |
| Slavina Goleva | Pharmacogenomic genome-wide association study of LDL response to statins using high-throughput electronic health records analysis | 4113F |
| Elizabeth Heuston | Trajectory analysis reveals islet cell depletion exacerbated in individuals of African ancestry with Type 2 diabetes | 5169F |
| Tam Tran | Efficient large scale PheWAS analysis with PheTK | 4043F |
| Nephi Walton | Defining a Clinical Data Ecosystem for Genomic Health | 1120F |
Ancillary Events
Tuesday, November 5, 2024, 12:00 – 1:15 p.m.
NIH Data Sharing Poicies
Room 601 Colorado Convention Center
ASHG 2024 Mobile App
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Last updated: October 25, 2024