Kate E Stanley retweetledi
Kate E Stanley
19 posts

Kate E Stanley
@KateEStanley1
marie curie PhD fellow @CHG_CME @karolinskainst formerly @Columbia @ColumbiaMed @Ox_wrh human genetics | reproductive genomics
Brussels, Belgium Katılım Ekim 2019
178 Takip Edilen87 Takipçiler
Kate E Stanley retweetledi

We have a new 'Dr. House' in the house! PhD researcher Benjamin Huremagic participated in the #undiagnosedhackathon2024. Together with a bioinformatician from @UAntwerpen solving a case in only 2 hours: nieuwsblad.be/cnt/dmf2024060…
@KU_Leuven @Nieuwsblad_be @JorisVermeesch
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Kate E Stanley retweetledi

Delighted to share our work published in @NatureComms exploring cell type signatures in cell free DNA sequencing data. A big thanks to many great collaborators @CHG_CME, @KU_Leuven, and @VHIO.
nature.com/articles/s4146…
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Kate E Stanley retweetledi

A study in @NatureMedicine shows that a liquid-biopsy approach that measures DNA-methylation levels in the blood may improve the detection of pregnancies at risk of developing preeclampsia at early stages. go.nature.com/45HyMn0

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#EMBLTranscript cell free DNA profiling in pregnancy infers placental contributions in health and disease


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Kate E Stanley retweetledi
Kate E Stanley retweetledi

Prenatal tests promise to detect rare genetic diseases in babies by scanning DNA.
Labs market them as "reliable." They tell women to have "total confidence" in results.
It turns out, the grave predictions made by those tests are usually wrong. (1/5)
nytimes.com/2022/01/01/ups…
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Kate E Stanley retweetledi

Eric Lander of Broad Institute named White House science adviser to president elect Joe Biden.
A short thread w/ a few observations about Eric Lander who i have previously called "the single most influential and powerful scientist in America."
1/n
washingtonpost.com/science/2021/0…
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Kate E Stanley retweetledi
Kate E Stanley retweetledi

Very excited to share our analysis of exome sequencing data from 200K participants in the @uk_biobank. @AstraZeneca @kerencarss @DrAndrewHarper @ruth_march #SlavePetrovski
biorxiv.org/content/10.110…
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Kate E Stanley retweetledi

Using rare-variant collapsing we showed that even patients with presumed ischemic heart failure often have rare deleterious variants in cardiomyopathy genes such as TTN. Thanks to everyone involved. @GoldsteinDB @OlympeChazara @carolin56741829 @dirk_paul @kerencarss et al.
JAMA Cardiology@JAMACardio
Exome sequencing of a broad group of 5,942 patients with heart failure of mostly ischemic etiology shows a significant enrichment of rare protein-truncating variants in the TTN gene and in general an increased burden of Mendelian cardiomyopathy variants. ja.ma/3oWs1s1
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Kate E Stanley retweetledi

Causal Genetic Variants in Stillbirth | NEJM nejm.org/doi/full/10.10… Important paper for #PediPath. Congratulations to our colleague, Halit Pinar! @SocPediPath
Català
Kate E Stanley retweetledi
Kate E Stanley retweetledi

In addition, @NEJM published an accompanying Editorial on our findings!
nejm.org/doi/full/10.10…
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Check out our paper on causal genetic variants in stillbirth, at @NEJM! We found evidence to suggest that depletion of loss-of-function variants in certain genes in post-natal populations may be due to a critical role for these genes in fetal development.
nejm.org/doi/full/10.10…
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