NicolineHoogerbrugge
@NicolineHoogerb
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Em. Professor Erfelijke Kanker, Radboudumc, Nijmegen, met Passie voor preventie van kanker.
The Netherlands
Joined September 2010
Jawel een steltkluten familie gezien! Prachtig hè!! Zo vlak bij de lepelaars.
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RT @GIMJournal: Staying one step ahead. Identifying patients with #PHTS before or at first primary cancer diagnosis can enable #early #dete….
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RT @insightmeeting: Submit your abstracts now! #Insight2026 Deadline 7th September #LynchSyndrome #Polyposis #EOCRC….
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RT @insightmeeting: On behalf of InSiGHT, we are delighted to welcome you to the #InSiGHT2026 meeting in Singapore, taking place from 4 – 7….
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RT @Preventable_EU: 🚨 Today is your LAST CHANCE to register for #PrevenTalk3! 🚨. 📅 Tomorrow, 6 May 2025, at 11:00 CET, with experts:.🔹Dr. R….
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RT @ejhg_journal: What factors affect access to genetic tests? .This study from Australia draws attention to the geographical and socioecon….
nature.com
European Journal of Human Genetics - Assessing the unmet needs of genomic testing in Australia: a geospatial exploration
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RT @Preventable_EU: 🎙️ Join us for #PrevenTalk3 – 6 May, 11:00 CET (Online & Free!). Theme: Advancing Care for Rare Tumour Risk Syndromes (….
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RT @kevinjmonahan: One hundred years of the St Mark’s hospital polyposis registry @LNWH_NHS @StMarksGenomics @BowelsOfStMarks
https://t.co/….
link.springer.com
Familial Cancer - The St Mark’s Hospital Polyposis Registry was founded in 1924, the first such unit in the world. This paper documents the development of the unit over the subsequent 100...
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RT @CGAIGC: 🧬 On #WorldDNADay, let’s remember: understanding DNA isn’t just science—it’s lifesaving. #HereditaryGICancer often goes undete….
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RT @LValleResearch: 🎉 Happy to share our newly published Review:. "Genetics, genomics and clinical features of adenomatous polyposis".Joo….
link.springer.com
Familial Cancer - Adenomatous polyposis syndromes are hereditary conditions characterised by the development of multiple adenomas in the gastrointestinal tract, particularly in the colon and...
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RT @HeleneLBorgne: . and excited to see @Solve_RD legacy continue & expand within @ERDERA_org with more European Reference Networks (ERNs….
cordis.europa.eu
The European Rare Diseases Research Alliance (ERDERA) aims to improve the health and well-being of the 30 million people living with a rare disease in Europe, by making Europe a world leader in Rare...
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RT @insightmeeting: Thanks to all who responded to our survey, we will be in touch if you have expressed an interest in getting more involv….
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RT @insightmeeting: We are really keen to engage with the InSiGHT membership and find out how we can improve!. Please complete this survey….
docs.google.com
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RT @caseofdees: Gisteren deelde ik dit bericht. Twee vrouwen lieten me weten niet op de hoogte te zijn en sterke verdenkingen in de familie….
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RT @PIPgen_ITN: Project 3 #PIPgeneratingART Ane's work aimed to directly impact the quality of life for PHTS patients. Her findings could l….
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RT @ahoischen: Thanks for the nice joint interview with @RMdeVoer @SteveLaurie42 and coverage @GenomeWeb!.@Solve_RD . .
genomeweb.com
Through close collaboration of more than 300 genomics and disease experts, the pan-European consortium solved more than 500 difficult cases.
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