Brad Jermy
@brad_jermy
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Postdoctoral researcher at University of Helsinki for https://t.co/ityW4Q1IoG SGDP Alumni Kings College London
Helsinki, Finland
Joined October 2018
RT @intervene_eu: INTERVENE biobank analysts are installing the PGS Catalog Calculator at diverse biobanks and trusted research environment….
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RT @bnwolford: Our recent @intervene_eu paper (@brad_jermy, @KristiLall, & Wolford et al) has also been summarized for a more generalized a….
helsinki.fi
New research shows that the genetic risk for many diseases is affected by age and sex: a framework developed by researchers at FIMM provides an estimate of a person’s lifetime risk of disease based...
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RT @andganna: Our flaghsip @intervene_eu paper is now published!. I think this is an important piece of work to elevate the stature of poly….
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RT @JianZengR: Our SBayesRC method is now published in Nature Genetics! SBayesRC is a full Bayesian method for polygenic score prediction t….
nature.com
Nature Genetics - SBayesRC integrates genome-wide association summary statistics with functional annotations to improve polygenic prediction of complex traits. Functional partitioning highlights a...
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RT @MaxTamlander: How do inherited factors summarized in polygenic risk scores (PRS) impact the risk of colorectal cancer?.Our work now pub….
nature.com
British Journal of Cancer - Genome-wide polygenic risk scores for colorectal cancer have implications for risk-based screening
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RT @ZhiyuHas0Memory: Is the genetic of disease susceptibility and progression shared?. We look at this question within a global biobank col….
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RT @bordinki: Really excited to share a new preprint📜, the main project I have been working on during my PhD!. Why are people not adherent….
medrxiv.org
Low drug adherence is a major obstacle to the benefits of pharmacotherapies, and it is therefore important to identify factors associated with discontinuing or being poorly adherent to a prescribed...
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RT @tuomohartonen: Check out this thread about a new preprint from our lab 👇 Really interesting analyses by @vabaliokas on fairness of a DL….
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RT @ImJiwooLee: I'm excited to share our work on quantifying the causal impact of biological risk factors on healthcare costs! Here are som….
medrxiv.org
Background A critical step in evaluating healthcare interventions is to understand their impact on healthcare costs. However, there is a limited understanding of the causal impact that biomarkers and...
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RT @andganna: Very thrilled to formally introduce FinRegistry and Risteys - But before getting into details. Do yo….
academic.oup.com
Nationwide health-related registry data provide comprehensive insights into population health and, combined with other data such as demographics, familial
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RT @bnwolford: We are excited to share a pre-print of the flagship project of @intervene_eu! .
medrxiv.org
Polygenic Scores (PGSs) offer the ability to predict genetic risk for complex disease across the life course; a key benefit over short-term prediction models. To produce risk estimates relevant for...
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RT @ATJCagan: Aoxing Liu on population analyses of mosaic X chromosome loss identify genetic drivers and widespread signatures of cellular….
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RT @chrisdwhelan: Full summary statistics for our UKB-PPP GWAS of 1,463 circulating proteins are now available at .
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RT @andganna: Now published in @NatureHumBehav 🎉. 🙏 for @tuomohartonen @brad_jermy leadership. The way to go: integrate health data, soci….
nature.com
Nature Human Behaviour - The authors use data on the entire Finnish population to develop a machine learning model for predicting COVID-19 vaccination uptake. Important predictors are proxies of...
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RT @Aoxing2: New preprint!.10% of women lose one X chromosome in a fraction of leukocytes. What’s the cause/consequence? .We leveraged gene….
medrxiv.org
Mosaic loss of the X chromosome (mLOX) is the most commonly occurring clonal somatic alteration detected in the leukocytes of women, yet little is known about its genetic determinants or phenotypic...
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RT @i_am_dr_doom: BOOM! Our genes influence which medications we are going to use in our lives! Our study on genetic predictors of lifelong….
nature.com
Nature Medicine - A new analysis of large biobanks uncovers genetic variants associated with longitudinal changes in medication for cardiometabolic diseases and presents polygenic scores of...
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RT @HHeyne: Hi all, very glad to announce our paper on “Mono- and biallelic variant effects on disease at biobank scale” is now finally pub….
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