Eimear Kenny

@eimearekenny.bsky.social

Genomics, Computer Science, Medicine. Professor @ Mount Sinai in NYC. Director of Institute for Genomic Health. 🇮🇪 VMO

📢 Just posted: Our preprint introducing SPC — Spectral Components — is now live on medRxiv! Led by Dr. Ruhollah Shemirani and years in the making, this method offers a robust, scalable way to adjust for recent population structure in genomic analyses. 🔗 www.medrxiv.org/content/10.1... 1/9

SPC: a SPectral Component approach to address recent population structure in genomic analysis

Population structure is a well-known confounder in statistical genetics, particularly in genome-wide association studies (GWAS), where it can lead to inflated test statistics and spurious associations...

medrxiv.org

Truveta has built a database of 120M de-identified EHRs for digital phenotyping—and now they're teaming up with Regeneron and Illumina to sequence 10M patients across 30 US health systems. 🧬 Major move for precision medicine! www.geekwire.com/2025/seattle...

Seattle’s newest unicorn: Truveta lands $320M to fuel creation of massive new genome project

The Truveta team at its Bellevue, Wash., headquarters last year. (Truveta Photo) Seattle-area health data company Truveta announced $320 million in

geekwire.com

🚨 Calling human geneticists! 🚨 Featured Symposium & Interactive Workshop submissions for #ASHG2025 are OPEN! 🧬✨ Got cutting-edge research or ideas to share? Now’s the time to showcase them on a global stage. Spread the word & submit! 🌍📝 🔗 www.ashg.org/meetings/202... 1/ #HumanGenomics #ASHG25

Featured Symposia

Questions: programs@ashg.org Looking to make your mark on the ASHG Annual Meeting? Propose a Featured Symposium on a topic that excites you. Our Program Committee is here to provide guidance and suppo...

ashg.org

Thrilled to be a part of the Leena Peltonen School of Human Genomics this year -- an opportunity for PhD students to learn and interact 1:1 with many experts (and genuinely nice people) in the field! Apply by March 7th at: lpshg.org Program runs July 27-31 at the Wellcome Genome Campus, UK.

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🚨 New Paper Alert! 🚨 Led by Dr. Amy Kontorovich and Dr. Noura Abul-husn, our latest study in Genetics in Medicine explores “red flag” clinical features for hereditary transthyretin amyloidosis (ATTRv) associated with the TTR p.(Val142Ile) variant. 🫀🧬 1/

Evolving knowledge of “red flag” clinical features associated with TTR p.(Val142Ile) in a diverse electronic health record-linked biobank

Previous studies have established “red flags” that raise clinical suspicion for the hereditary form of transthyretin amyloidosis (ATTRv). However, the…

sciencedirect.com