Human Genetics Nijmegen, Radboudumc Profile
Human Genetics Nijmegen, Radboudumc

@GeneticNijmegen

Followers
547
Following
94
Media
7
Statuses
128

Radboudumc Nijmegen Genetica. Research, erfelijkheidsonderzoek, genoomdiagnostiek en onderwijs.

Joined February 2020
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@GeneticNijmegen
Human Genetics Nijmegen, Radboudumc
3 years
May is PHTS Awareness Month! See https://t.co/5kDZYmz18D for more information! @Radboudumc #PHTS #PTEN #awareness #research #cancer #genetics
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@ahoischen
Alexander Hoischen
4 years
Great opportunity to join us @GeneticNijmegen! Anyone up for this opportunity - @eshg_young @juhumgen maybe?
@hannie_kremer
Hannie Kremer
4 years
Are you a postdoc who wants to perform exciting research on understanding the genetics of hearing loss as a basis for treatment development, then apply. You will work in a multidisciplinairy team and an internationally oriented department.
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@GeneticNijmegen
Human Genetics Nijmegen, Radboudumc
4 years
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@PIPgen_ITN
PIPgen
4 years
Discover our PhD Positions! Project 13: To identify PI3K vascular-related therapies which enhance immunoregulation flux | PI: @MarionaGraupera To apply VISIT: https://t.co/7YUl0aHtH3 #WeAreHiring @MSCActions @CarrerasIJC @raicex_es @COSCEorg @criscancer @CRISCANCERUK @twitamit_es
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@GeneticNijmegen
Human Genetics Nijmegen, Radboudumc
4 years
For more information and registration go to https://t.co/3CzupKpGl4
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@ProfSimonFisher
Simon Fisher
4 years
“Capturing the brain for neuroimaging genomics” 28-29 June, 2-7pm CEST, has keynotes on environmental effects on brain health, transcriptomics of neural oscillations, & genome screens with EEG & fMRI. Register now & submit your work for a breakout session: https://t.co/AWiH0mobhS
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@GeneticNijmegen
Human Genetics Nijmegen, Radboudumc
4 years
May is PHTS Awareness Month! See https://t.co/JiCI9CRnHG for more information! #PHTS #PTEN #awareness #research #cancer #genetics
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@GeneticNijmegen
Human Genetics Nijmegen, Radboudumc
4 years
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@SusanneRoosing
Susanne Roosing
4 years
A new publication of my PhD student Zeinab Fadaie appeared online in @JMG_BMJ. Thanks to a wonderful collaboration with (amongst others) @PhDWithLaura and @j_ellingford 'BBS1 branchpoint variant is associated with non-syndromic retinitis pigmentosa'. https://t.co/psPahlMx1y
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@radboudumc
Radboudumc
4 years
Met behulp van ‘omics’-technieken meer te weten komen over foutjes op het DNA die zeldzame ziekten kunnen veroorzaken. @LisenkaVissers gaat nieuwe methoden ontwikkelen om deze mutaties in kaart te brengen. #UCD21 #UCD @Vsopzeldzaam @geneticnijmegen
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@radboudumc
Radboudumc
4 years
Vandaag is het Undiagnosed Child Day. @WendyStams, net benoemd hoogleraar Zorg voor Zeldzaam, heeft als doel kinderen met een zeldzame ziekte sneller van een diagnose te voorzien én hun zorg te verbeteren. #UCD21 #UCD @vsopzeldzaam @geneticnijmegen https://t.co/a0PpVBqNB1
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@ahoischen
Alexander Hoischen
4 years
Great opportunity! If you are an ambitious postdoc and want to work in Nijmegen @radboudumc you could get great support to apply for MSCA-PF grant by our institution: https://t.co/NDTuRTDkaQ
radboudumc.nl
Are you a postdoc or almost graduated PhD candidate looking to give your academic career a boost? Then an postdoctoral fellowship abroad might be of i
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@GeneticNijmegen
Human Genetics Nijmegen, Radboudumc
4 years
Two new professors appointed at the Radboudumc Human Genetics department, @LisenkaVissers and @WendyStams - congratulations to an honour very well-deserved! We look forward to valuable contributions in the fields of Translational Genomics and Care for Rare (Zorg voor Zeldzaam).
@radboudumc
Radboudumc
4 years
Radboudumc benoemt 13 vrouwelijke academici tot hoogleraar. https://t.co/9zkh9FdQEM
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@cathrynlewis
Dr Cathryn Lewis
5 years
This year's IoPPN Youth Awards are launched! Please RT to your local networks, and schools - and follow @IoPPNYouthAward
@IoPPNYouthAward
IoPPN Youth Awards
5 years
👀👀 Students aged 15-18 at schools in a 5 mile radius to @KingsIoPPN can APPLY NOW! Win £50 book token, gain first-hand experience of life in a university and research, make connections with scientists, tailor the topics to your interests, build your CV & UCAS application 💪💪
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@camillabellone
camilla
5 years
FENSFriday webinar on May 21 Registration is now open
@FENSorg
FENS
5 years
Registration is now open for the #FENSFriday webinar “Brain development and neuropsychiatric disorders”! 📆 Friday 21 May, 2-3:00 pm CEST ✍️ Info & Registration: https://t.co/lg1tx4xr1O 💡 Free event Organised by the #FENS Committee for Higher Education and Training
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@GeneticNijmegen
Human Genetics Nijmegen, Radboudumc
4 years
33rd Course on Clinical Genomics and next generation sequencing, jointly organized by ESHG and CEUB, with several experts from our department. While virtual this year, it will certainly be a treat, as it is every year!
@ksamocha
Kaitlin Samocha
5 years
Coming up soon is the (virtual) course on Clinical Genomics and NGS! Join us to learn about the basics of medical genetics, bioinformatics, emerging therapies, and the application of new technologies. There is still time to register: https://t.co/UgNvqCiPqc #bertinoro2021
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@Radboud_Uni
Radboud University
5 years
👑💐Trots: zeven Radboud-medewerkers ontvangen vandaag een koninklijke onderscheiding! Felicitaties aan René ten Bos, Jan Buitelaar, Béatrice van der Heijden, Nicoline Hoogerbrugge, Angélique Janssens, Hans de Kroon en Jolanda de Vries #lintjesregen2021
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@ProfSimonFisher
Simon Fisher
4 years
New paper! Comprehensive overview of speech & language deficits due to loss-of-function variants of SETBP1, a gene that we previously implicated in childhood apraxia of speech. https://t.co/AjKE1SMqJo Read it for free here: https://t.co/pZPYshsWOi
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@RMdeVoer
Richarda de Voer
4 years
Our manuscript that deficiency of MBD4 causes colorectal polyposis and AML is now available on bioRxiv. A great collaboration with @clpalles @saragalavotti8 @JEGrolleman @CFlensburg @ianjmajewski and many others! #cancergenomics @radboudumc @RIMLSInstitute @GeneticNijmegen
@biorxivpreprint
bioRxiv
4 years
Germline loss-of-function variants in the base-excision repair gene MBD4 cause a Mendelian recessive syndrome of adenomatous colorectal polyposis and acute myeloid leukaemia https://t.co/fnjkE8v1HI #bioRxiv
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