Top Tweets for #thinkGenetic
“Advancing Genetic Testing in Kidney Diseases: Report from a NKF Working Group"
Recommendations will be published in an issue of AJKD and represent a significant advancement in the integration of genomic medicine into nephrology practice.
#thinkgenetic #nephtwitter
Genetic Counseling in Kidney Disease: A Perspective https://t.co/uQTFFIH8Wz @KidneyMed
New preprint from a large Geisinger health system cohort: The Phenotypic Spectrum of COL4A3 Heterozygotes https://t.co/xRbAKnm51v
ADPKD is widely recognized as the most common single-gene cause of progressive CKD. This study shows ADPKD manifesting earlier than expected on the basis of family history can identify clinically tolerant PKD1 alleles with reduced expression https://t.co/FAFPoqqCpC
Did you know? 1 in 4 adults with chronic #KidneyDisease has a family history. Renasight tests 385 genes to help determine if there is a genetic cause for someone's kidney disease or if there is an increased hereditary risk. Learn more: https://t.co/ojtDmEoxRW #KidneyMonth
Happy New Year from the entire team here at ThinkGenetic, Inc! 2022 brought us so many memories, opportunities, and discoveries, and we cannot wait to see what 2023 has in store! What are you hoping to see in 2023?
#thinkgenetic #newyears #holidays
Alonzo Mourning: How the NBA Star Rebounded from Kidney Disease #thinkgenetic #nephtwitter #APOL1 #renalgenetics https://t.co/N1NmXYZKBS
With our #Renasight test, we can help confirm a #CKD diagnosis and guide treatment decisions.
Take a look at 6 ways #GeneticTesting can make a difference for people living with #KidneyDisease. ⬇️
https://t.co/ftrWHgW5pp
What do patients want to know? | After the Diagnosis: Approach to rare d... https://t.co/ODA6Ffufzh
Dr. Anthony Bleyer, Wake Forest
#THINKGENETIC
A recent @goKDIGO publication recommends practitioners who treat CKD patients to consider genetic testing.
Read more: https://t.co/Y5p5jY719A
Genomic testing can provide targeted therapies leading to higher probabilities of success, fewer negative reactions from medications and treatments, and precise health information for better health decisions. Learn more in this statin case study. #ThinkGenetic
FindEHR helps include historically underrepresented groups in the search for patients with undiagnosed genetic disorders. However we then give results & education back to providers. What suggestions do YOU have to mitigate medical bias in that phase? #gcchat #nsgc21 #thinkgenetic
Great progress in #RareDisease research! “The ability to find so many variants that were previously missed is exciting, + holds great promise for diagnostic testing in the future.” Greg Cooper @hudsonalpha is finding answers in #RareDisease cases. See how: https://t.co/zgmdUC11w7
#Raredisease patients spend almost 8 years searching for a diagnosis, which is why our clinic uses genome sequencing & genetic testing to find genetic changes that may be causing a patient’s disease. Get in touch today! 256-327-9640 #thinkgenetic
https://t.co/HxPZ0krrvo
Great progress in #RareDisease research! “The ability to find so many variants that were previously missed is exciting, + holds great promise for diagnostic testing in the future.” Greg Cooper @hudsonalpha is finding answers in #RareDisease cases. See how: https://t.co/zgmdUC11w7
Going to be listening in on "The Future of Pediatric Rare Disease Diagnosis is NOW: Update on Genomic Sequencing in Acutely Ill Infants and Pediatric Outpatients” at #ACMGMtg21, starting of with our very own David Bick from @hudsonalpha!
Going to be listening in on "The Future of Pediatric Rare Disease Diagnosis is NOW: Update on Genomic Sequencing in Acutely Ill Infants and Pediatric Outpatients” at #ACMGMtg21, starting of with our very own David Bick from @hudsonalpha!
Through #wholegenomesequencing & #genetictesting , our clinical team can help you & your doctor establish a more accurate diagnosis for your symptoms. Learn more about the types of testing at the clinic & get in touch today! 256-327-9640 #thinkgenetic
https://t.co/IdCOsL2LtT
NEWS: @SmithGenomicMed Director David Bick discusses benefits of #wholegenomesequencing for diagnosis #raredisease #thinkgenetic #findinganswers @genomeweb
https://t.co/Kc30SfSk5m
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