Genetic Counselor @StanfordCUD @UDNConnect All tweets are my own.

San Jose, CA
Joined April 2018
Devon Bonner (she/her) retweeted
TODAY is #RareDiseaseDay! 💙💚💜 All over the world, the rare disease community are sharing their colours and demanding equity for people living with a rare disease. As a global community, we have a powerful voice! 📣 How are you sharing your colours today? 👇👇👇
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Devon Bonner (she/her) retweeted
I have no idea who did this, but if you know, find them and tag them. One of the best things I’ve seen on this app this week
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Devon Bonner (she/her) retweeted
We've got 7 UDN posters coming up this afternoon at #ASHG19! Topics: precision med (417); mendelian phenotypes (1167, 1287); bioinformatics (1563); statistical genetics (2967); molecular & cyto dx (2613) & complex traits (1980)
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Devon Bonner (she/her) retweeted
Now online in @GIMJournal: Hane Lee & colleagues share findings from RNASeq on 113 undiagnosed patients referred to UDN clinical site @UCLAHealth. Questions? Come to her talk during the RNASeq session at #ASHG19 on Thursday afternoon nature.com/articles/s41436-0…
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Devon Bonner (she/her) retweeted
One month until #ASHG19! There are >20 UDN related talks and posters this year. Check out the full list below and on our website: udnconnect.org/the-undiagnos…
Devon Bonner (she/her) retweeted
Thank you #ACMGMtg19 - we learned so much and loved seeing so many new and familiar faces. See you next year!
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Devon Bonner (she/her) retweeted
Thank you #ACMGMtg19 for a fun & memorable opening reception 🥁 see you tomorrow at 9am- we’re over in 4C across from ACMG & the #ACMGFoundation Day of Caring bikes!
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Devon Bonner (she/her) retweeted
#ACMGMtg19 3.7 seconds per medical record; #ClinPhen consistent time regardless of length of record; #Phrank to rank phenotypes; 3 important phenotypes optimizes positive generank; replication across @MantonCenter @Duke_Childrens @UCLA
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Devon Bonner (she/her) retweeted
Replying to @Stanford
@stanford Johannes Birgmeier from Gil Bejerano lab presenting #ClinPhen #ACMGMtg19 #top4abstract automated extraction of #HPO terms from free text clinical notes work with @StanfordChild Jon Bernstein @stanford_CUD @MantonCenter @Duke_Childrens @UDNconnect
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Devon Bonner (she/her) retweeted
Out now - a collaborative case from @StanfordMed @stanford_CUD @UDNconnect @stanfordimmuno starting with @StanfordMedRes referral. A Patient with Sjogren’s Syndrome and Subsequent Diagnosis of Inclusion Body Myositis and Light-Chain Amyloidosis dx.doi.org/10.1007/s11606-01…
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Devon Bonner (she/her) retweeted
Information about the UDN now available in Spanish on our website! ¡La información acerca de la UDN ya está disponible en español en nuestro sitio web! undiagnosed.hms.harvard.edu/…
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Devon Bonner (she/her) retweeted
Our latest work with a national US dataset shows that cancer genetic service use is low among healthy individuals and many hold discordant risk perceptions about breast and colorectal cancer. #genomics #cancer #gcchat #PreventiveMedicine #PublicHealth authors.elsevier.com/a/1YeSe…
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Devon Bonner (she/her) retweeted
"Access to Genetic Counselor Services Act of 2018” was introduced in the House of Reps. Join us in asking your members of Congress for support of this critical bill, which would authorize CMS to recognize CGCs as healthcare providers. Learn more: bit.ly/2RcxCcP #GCchat
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Devon Bonner (she/her) retweeted
Thank you #ASHG18! We had a great time sharing the work of the UDN, catching up with collaborators, and hearing about a lot of great science being done here and around the world. See you in Houston!
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Devon Bonner (she/her) retweeted
Proud to be amongst so many fantastic female scientists at #ASHG18 #WomeninSTEM #gcchat – at San Diego, CA
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Devon Bonner (she/her) retweeted
Seven UDN posters coming up this afternoon! See what our investigators have been up to in these areas: RNASeq (1337 & 1535), bioinformatics (1412, 1580, 1682), case reports (1112 & 2894) #ASHG18
Devon Bonner (she/her) retweeted
Interested in #RNAseq for rare diseases? #Postdoc position open now with @stanford_CUD to work with RNAseq, genome and exome data and iPS cell models of rare and undiagnosed diseases
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Devon Bonner (she/her) retweeted
DM: RNASeq helped rule out many intronic & deep intronic variants by showing they don’t impact splicing #ASHG18
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Devon Bonner (she/her) retweeted
David Murdock of @bcmhouston explaining why RNASeq is relevant in clinic: 50-75% pts remain unsolved after exome, exome only 2% of the genome, hard to interpret non-coding variants, in-silico predictions don’t provide functional info #ASHG18
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