Matthew J Thomas

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Matthew J Thomas

Matthew J Thomas

@matthewjthomas

Cardiovascular genetic counselor

University of Virginia Katılım Ağustos 2014
157 Takip Edilen347 Takipçiler
Matthew J Thomas retweetledi
Randy K. Ramcharitar
Randy K. Ramcharitar@Doc_RKR·
Thank you @adityasharmamd It's an honor to lead a dedicated team including @PeterNDean & @matthewjthomas at @UVAhealth We are committed to providing high level care for those with heritable aneurysms Grateful for recognition & support from @MarfanFdn @ChrisKramerMD @OPreventzaMD
Aditya Sharma@adityasharmamd

Proud to announce the Heritable Aneurysm and Arteriopathy Program at @UVAHealth is the only one in Virginia recognized by @MarfanFdn! Kudos to Dr. Randy Ramcharitar @Doc_RKR for leading the initiative. Thanks to @ChrisKramerMD and @OPreventzaMD for their support.

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Sana Syed
Sana Syed@SyedLabGI_AI·
Incredibly honored to receive this award - thank you @gumbo_amando @PRodriguezMD Dr Mathieu & Lozano allowing me to be a part of your lives + @thriv_i @UVAPediatrics for your support
UVA Research@UVAResearchNews

Congratulations to all the 2022 Research Achievement Award winners, recognized last night for their excellence in research, collaboration, mentorship, and public impact focused research #research @UVA @UVAEngineers @uvahealthnews @UVAEdu @UVaAstro research.virginia.edu/initiatives/re…

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Matthew J Thomas
Matthew J Thomas@matthewjthomas·
Papers by @gravesjl55 & @ATDeyrupMDPhD heavily cited in a new video by one of the best medical YouTube channels around. My advice: watch this and invite the duo to give Grand Rounds like @UVAPediatrics & @UVA_Pathology did
Healthcare Triage@HCTriage

In medical education, health disparities are often (incorrectly) attributed to biological differences between races, and this leads healthcare professionals to make false assumptions about patients, which then affects how they are diagnosed and treated. youtu.be/PMGKHM3YlUk

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Matthew J Thomas retweetledi
Small Special Collections Library (UVA)
Small Special Collections Library (UVA)@RareUVA·
So proud of our @UVALibrary colleague @EzeAmosp on the launch of “The Story of Us: Reclaiming the Narrative of #Charlottesville Through Storytelling and Portraits of Community Resilience,” an installation on display August 11- September 29 on the Downtown mall.
Small Special Collections Library (UVA) tweet media
C-VILLE Weekly@cville_weekly

“My hope is that this project will get more people to tell their stories.” In honor of the fifth anniversary of the deadly Unite the Right rally, photojournalist Eze Amos’ powerful new memorial will be unveiled on the downtown mall tomorrow. c-ville.com/the-story-of-us

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Jordy Yager
Jordy Yager@jordyyager·
[tw/cw] As an homage to my dear friend @EzeAmosp I'm sharing some thoughts from this day 5 years ago. It’s a truism among documentarians—we rarely center ourselves in the stories we relay & until recently neither of us had really talked about 8/12/2017. youtube.com/watch?v=Rk7QiH…
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Dena DNA
Dena DNA@DenaTalksDNA·
“Don’t be Scooby do and split up”, if you find discrepancies in Clinvar when looking at a variant, let the labs know! #NSGC21 @matthewjthomas
GIF
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Genetic Counselors
Genetic Counselors@GeneticCouns·
Congratulations to Gretchen MacCarrick, MS, CGC for winning this year's Heart of Genetic Counseling Award! #NSGC20 ❤️🧬
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Amy R. Kontorovich, MD, PhD
Amy R. Kontorovich, MD, PhD@GeneticHeartDoc·
Our genotype-first study of FBN1- and RASopathy-related disorders is out! What happens when you approach a possible diagnosis of #Marfan or #Noonan syndrome from the genotype-first perspective? (1/n)
Genetics in Medicine@GIMJournal

The seminal features of both #Marfan syndrome and the RASopathies may be less prevalent in affected individuals than previously thought: a proposal for genotype-first identification go.nature.com/2SqXggB #Marfansyndrome #CHD #Genetics

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Annals of Int Med
Annals of Int Med@AnnalsofIM·
New guidelines focus on the diagnosis and management of hereditary hemorrhagic telangiectasia ow.ly/4D1x50Bm26a.
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Emily Brown
Emily Brown@EE_Brown42·
This is an important finding! We have started adding ABCG5/8 testing for most FH patients for this reason along with trying to find hidden sitosterolemia cases.
Sek Kathiresan MD@skathire

Attn: sequencing panels testing for genetic causes high LDL & heart attack "Although familial sitosterolemia is traditionally considered as a recessive disorder, het carriers of ABCG5 LoF variant: *25mg/dl higher LDL *two-fold increase in risk of CAD ahajournals.org/doi/abs/10.116…

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Keşfet

@adityasharmamd @PeterNDean @UVAhealth @MarfanFdn @ChrisKramerMD @OPreventzaMD @PRodriguezMD @thriv_i