Lot Snijders Blok
@Lot_SB
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researcher & clinical geneticist 🧬 | cyclist 🚴🏼♀️
Nijmegen, Nederland
Joined July 2015
RT @ahoischen: It’s a privilege to announce Solve-RD’s latest manuscript based on years of work: “Genomic reanalysis of a pan-European rare….
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RT @ahoischen: Image a set of 100 rare disease cases with the most difficult-to-detect mutations a human genetics lab can be faced with. …m….
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Wow! 😀.
My lab has been working for the past 15 years to develop a method to isolate specific genomic loci to identify its chromatin composition & protein interactome. Finally,… our superb physician/scientist Dr. Bercin Cenik @bkcenik did it and here it is Not
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Very happy to be one of the ZonMw Clinical Fellows grant awardees this year!. Thanks to all colleagues for the help and support, especially @LisenkaVissers @ahoischen and @WendyStams . Looking forward to finally have more time for research again! 🧬👩🔬.
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RT @doctorveera: Analysis of sequencing data of 320k individuals (75k cases and 245k controls) shows heterozygous carriers of cystic fibros….
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RT @SolidEvidence: I knew there were a lot of fake accounts on this platform, but they are usually obvious. I had no idea how intricate an….
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RT @michaelkosicki: Updated VISTA Enhancer Browser, 7 years in the making, out in @NAR_Open! >4,500 transgenic in vivo enhancer experiments….
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RT @rafeequemavoor: Free scientific illustrations for biologists! 😍. @NIH has released a library of 500+ free scientific illustrations to….
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RT @szuchner: Somatic repeat expansion field is getting more interesting!! @DavidPellerin_2 @NAF_Ataxia @ataxia_global @CureFA_org #….
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RT @tycheleturner: Excited to share that denovo-db is now available on @ZENODO_ORG (! The new version of denovo-db….
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RT @eshg_young: 📢📢📢Opportunity for young geneticists! @eshgsociety opens application for the.ESHG Mentorship Programm! Apply until 30th Nov….
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RT @DeSpeld: 13:00 Experts: toneelspel Yeşilgöz valt onder hoog btw-tarief. #AlgemeneBeschouwingen #APB #APB2024
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RT @doctorveera: A Sunday read for you. A new blog post on a discovery of a noncoding mutation that causes a Mendelian cardiac arrhythmia t….
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RT @StefanBarakat: 👋We are hiring a PhD student for rare disease diagnostics project .#genetics #RareDisease #WGS #ONT #AI #job #PhDpositio….
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