Sophia Ceulemans
@SophiaCeulemans
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Sign. Gnaw. High. Phlegm. Just a few of the words in which 'G' is completely useless. https://t.co/j7UjY5gl9I
merriam-webster.com
How every letter can be (annoyingly) silent
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The coffin of the "new MS gene" is now nailed shut. @ccots looks in 32K MS cases and 36K controls - no association:
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Adherence to NCCN guidelines for referral to #genetics professionals #gynonc, new article April 2015 http://t.co/3sGNn3Zft5
#GC #cancer
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"Doctor, Have You Had Your DNA Tested?" NYTeditorial on #DNA sequencing http://t.co/xpGvSXxoGJ
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"Certainty generally is illusion, repose is not the destiny of man"OliverWHolmes, @NEJM article on #uncertainty
http://t.co/695BnDhpKd
#GC
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Best blizzard pic so far, a wind-induced double helix. (via @reddit) http://t.co/aJCWiWHvO8
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recent article on trends of Public Awareness of Direct-to-Consumer #Genetic Tests, http://t.co/j9zu0j1t9f
#DTCgenetic #GC #geneticcounseling
pubmed.ncbi.nlm.nih.gov
Although the availability of direct-to-consumer (DTC) genetic testing has increased in recent years, the general public's awareness of this testing is not well understood. This study examined levels...
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First set of guidelines for #22q11.2 deletion syndrome, Genet in Med Jan 2015, http://t.co/vb2aMRXjOE
#22q #GC #genetic #cardiogenetics
pubmed.ncbi.nlm.nih.gov
22q11.2 Deletion syndrome (22q11.2DS) is the most common microdeletion syndrome in humans, estimated to affect up to 1 in 2,000 live births. Major features of this multisystem condition include...
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parent's perspective of whole exome sequencing http://t.co/imwFlcaEAz
#genetic #pediatric #WES #GC #developmentaldelay #lifeisajourney
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#MRI +mammo for #BRCA mut carriers ≥50 y/o sig increased screening sensitivity, new JCO article http://t.co/IFh61ksvzd
#cancergenetics #GC
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not sure if a #genetic test is warranted based on family hx? Check CDC's tiered list with the evidence #GC #genomic
http://t.co/QG8rtweOh3
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2014 Top Ten #Genetics Stories on DNAExchange blog, by @laurahercher
http://t.co/NzSIWUCLnt
#topten #GC #genes #science
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new study, if #WES #WGS done @ symp onset in kids w neurodev disorders, #genomic dx made 77 months earlier http://t.co/hxwvpreQms
#GC
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#ASCO endorses EuropeanSocietyMedOnc guidelines on #colorectalcancer #cancergenetics #GC, pub in JCO, free full text http://t.co/aPdP1bkz8e
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#RAD51C mut 1% in #HBOC families, 9% risk of #ovariancancer by age 80, Narod et al http://t.co/tERm8gdbvf
#cancergenetics #GC
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7-13% #BRCA mut in AJ pts are nonfounder, may be skewed for high risk families #cancergenetics #GC #myriad
http://t.co/XE4sYW0lqB
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