Hasanga Manikpurage

123 posts

Hasanga Manikpurage

Hasanga Manikpurage

@HasangaDM

Genetic of cardiovascular diseases Post-Doc Fellow @Cambridge_Uni @DPHPC 🇬🇧 PhD @universitelaval @IUCPQ 🇨🇦 MSc @univ_paris_cite @lvts🇫🇷 From 🇫🇷/🇱🇰

Paris, France Katılım Mart 2011
230 Takip Edilen97 Takipçiler
Sabitlenmiş Tweet
Hasanga Manikpurage
Hasanga Manikpurage@HasangaDM·
Wow!!! Many Thanks to @JeanetteErdmann, @konradtsawicki and @Circ_Gen for highlighting all the major points of our paper through this video!
Circulation: Genomic and Precision Medicine@Circ_Gen

⚡️ Now online from Thériault + team: A Polygenic Risk Score for #CoronaryArteryDisease Improves the Prediction of Early-Onset Myocardial Infarction and Mortality in Men ahajournals.org/doi/10.1161/CI… @AHAScience #AHAjournals #CardioGen 🎬 @JeanetteErdmann @konradtsawicki

English
1
2
10
0
Hasanga Manikpurage retweetledi
Human Genetics and Genomics Advances
📣New from Zamani et al! 📄Aortic valve-specific genes dysregulated in calcific aortic valve stenosis as potential biomarkers and therapeutic targets 🫀🧬 👉bit.ly/43bMPBU
Human Genetics and Genomics Advances tweet media
English
0
1
2
90
Hasanga Manikpurage
Hasanga Manikpurage@HasangaDM·
Thank you to all colleagues involved in this project, supervised by Dr. S. Thériault. Thank you also to all scientists and participants involved in @_CARTaGENE_ , @clsa_elcv and Biobanque de l’@IUCPQ.
English
0
0
1
22
Hasanga Manikpurage
Hasanga Manikpurage@HasangaDM·
- CAD-PGS is associated with the extent of coronary artery damage observed. - In this study, not all CV-PGS are associated with the severity of CAD; lipid-PGS are.
English
1
0
0
13
Hasanga Manikpurage retweetledi
Marios Georgakis
Marios Georgakis@MariosGeorgakis·
2⃣Bridging genomics, transcriptomics, proteomics, and metabolomics In a rare combination of all 4 major omics layers, this study offers a great resource for dissecting the links between genetics, expression/slicing, molecular traits and disease risk 🔗nature.com/articles/s4158… 📊summ stats: intervalrna.org.uk/downloads/
Marios Georgakis tweet media
English
1
3
22
1.3K
Hasanga Manikpurage retweetledi
Pradeep Natarajan
Pradeep Natarajan@pnatarajanmd·
The common IL6R p.Asp358Ala missense variant is associated with 5% ↓odds for CAD (inhibiting pathway validated & more inhibitors in RCTs), & 5% ↓odds for rheumatoid arthritis (w approved inhibitors for pathway). New study shows even greater (10% ↓odds) for AAA. ahajournals.org/doi/full/10.11…
Pradeep Natarajan tweet mediaPradeep Natarajan tweet mediaPradeep Natarajan tweet media
English
0
4
19
2.5K
Hasanga Manikpurage
Hasanga Manikpurage@HasangaDM·
Finally! Happy to share my 3rd PhD paper, now published in @ATHjournal! 🚀 This study explores the impact of integrating multiple independent lipid PRSs with a CAD-PRS for CAD incidence prediction in @uk_biobank. 👉🏽Link (Open Access! 📖): #fig5" target="_blank" rel="nofollow noopener">atherosclerosis-journal.com/article/S0021-…
Hasanga Manikpurage tweet media
English
3
3
9
2.4K
Hasanga Manikpurage retweetledi
Loïc Lannelongue
Loïc Lannelongue@Loic_Lnlg·
London -> Barcelona by train ✅ (surprisingly easy! 🚄) Just arrived for the 2024 @nextflowio Summit, very excited to be delivering the keynote tonight on this mildly intimidating stage (tech tests ✔️, Segrada Familia ✔️ … we’re ready to roll)
Loïc Lannelongue tweet mediaLoïc Lannelongue tweet mediaLoïc Lannelongue tweet media
English
0
2
22
1K
Hasanga Manikpurage retweetledi
Tregouet David-Alexandre
Tregouet David-Alexandre@TregouetBPH·
The catalog of all possible SNVs altering existing upORFs or creating new ones (via both canonical  and non canonical TIS) in human transcripts is available on the mobidetails platform ( mobidetails.iurc.montp.inserm.fr/MD/) @soukarieh_omar @BPH_Research @univbordeaux_EN
bioRxiv Bioinfo@biorxiv_bioinfo

Enhancing the annotation of small ORF-altering variants using MORFEE: introducing MORFEEdb, a comprehensive catalog of SNVs ... biorxiv.org/cgi/content/sh… #biorxiv_bioinfo

English
0
6
13
767
Hasanga Manikpurage retweetledi
Ron Do
Ron Do@DoGenetics·
Our new study published in @NatureComms, led by Ghislain Rocheleau and team. Using TOPMed WGS data, estimate heritability of CAD is 34%. Ultra-rare variants with low LD score contribute ~50% of the heritability. Enrichment in several functional processes. nature.com/articles/s4146…
English
0
16
59
7K
Hasanga Manikpurage retweetledi
PGS Catalog
PGS Catalog@PGSCatalog·
>5000 Polygenic scores now available at PGSCatalog.org! As of today's release we've broken 5k PGS, indexing data from 673 unique publications. A big thank you to the authors submitting their data and our team in pursuit of #openscience, #FAIRdata, and reproducibility!
PGS Catalog tweet media
English
0
18
45
5.1K