Top Tweets for #GenomeFirst
The advancements in #genomesequencing in clinical care are growing, but integrating it into routine medical practice remains a challenge. Two clinical studies, #GenomeFirst and #GeMed, aim to improve predictive #genomics in healthcare.
Via @Nature:
https://t.co/dWUf7bld6m
Do #Fanconi Anemia heterozygotes have an increased #cancer risk? It looks like the long awaited answer is likely to be no. #genomefirst #DiscovEHR #populationgenetics https://t.co/06nqQH4Umq
Join the upcoming #CancerPredisposition #ASPHOWebinar on Wednesday, January 24, 3 pm CT. Speakers Kris Ann Schultz @ppbDICER1 and #DouglasStewart will describe the #genomefirst approach to understanding #cancer risk. Register here: https://t.co/pkoTjuG3qN #PHODocs #PedsHemeOnc
Around 1% of the population carry a pathogenic DNA variant that confers 3-fold increased risk of sudden cardiac death #genomefirst #AHA19
@MGHHeartHealth @AHA_Research @AHAScience @amitvkhera
Genome-first! Enhancing knowledge of rare genetic variants associated with #cardiomyopathy and #kidneydisease and improving diagnostic accuracy. #CardioGen #genomefirst #CKD https://t.co/qVElbduf8I
Is #HealthCare ready for routine #DNA screening? Interesting ready from @sciencemagazine about @geisingerhealth #MyCode #GenomeFIRST initiative: https://t.co/2cN9DMMJ06
Thrilled to return to my alma mater and intellectual home to present the work of @GeisingerRsrch #GenomeFIRST @UWMadison @uwalumni https://t.co/eyKRqwoQor
Friday, 9/22: Join us to hear Marc Williams from @GeisingerRsrch talk about a new paradigm in #genomics research.
https://t.co/hMgHvw4fFX
A focus for our #MyCodeRoR @GeisingerRsrch #GenomeFIRST @GeisingerHealth does universal tumor screening for colorectal and endo cancer https://t.co/1p7naPPHWM
Expanding Lynch Syndrome screening. VIEW 1-hour Webinar presentation via @theNCI. https://t.co/uzEdHZXpOe
Preliminary data in our population suggests penetrance not that much lower than estimates. Manuscript in prep #GenomeFIRST @GeisingerRsrch https://t.co/E3a3aG4E21
The pros & cons of population wide screening for BRCA mutations: Many unresolved issues. https://t.co/91DJ0t3tx1
In our population closer to 3.5%. For CDC Tier 1 conditions just over 1%. #GenomeFIRST @GeisingerRsrch https://t.co/pmAc57rps9
We screen newborns, don’t we? What’s the case for population genetic screening in healthy adults? https://t.co/erf5SWO47w #tier1
Current status of our return of results progrmam. #GenomeFirst #GenomicMedicineInstitute https://t.co/IWYnJbmyYF
This is especially true when doing non-indication testing. Emphasizing specificity for MyCode RoR. #GenomeFirst @GeisingerRsrch https://t.co/1LDVzrkpbv
Addressing monogenic risk 1st. Fairly low incidence, 2%, MI event due to LDLR mutation #NLASessions @skathire
LJ: poster at tv 17 on Early follow-up in genetically identified FH individuals #NLASessions #GeisingerResearch #GenomeFIRST #GeisingerCPIO
302 patients got results from #GeisingerMyCode, including 223 CDC Tier 1 conditions. See latest monthly table: https://t.co/6pGzRxLe7c
This emphasizes the importance of finding 1 individual with a genetic condition and reaching out to the family @GeisingerRsrch #GenomeFIRST https://t.co/PQ6Ul3qvgA
I still can't get over the incredible power of relationships in #DiscovEHR - e.g. this LDLR dup carrier pedigree... https://t.co/L7jpykuHXw
#ACMGMtg17 Hot Topic - Developing Care Models for Patients with Secondary Genomic Findings #secondaryfindings
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