Tina Pesaran @tinapesaran

Joined July 2009

Tweets

46
Followers

60
Following

225
Likes

202

Genetic Counselors @GeneticCouns

4 years ago

We’re deeply concerned about the leaked #SCOTUS draft opinion that would overturn Roe and Casey and stand by our position statement on reproductive freedom, supporting the right of all individuals to make reproductive choices, including having access to safe abortion. #GeneChat

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Pesaran Lab @pesaranlab

4 years ago

We are delighted to be part of this exciting team! NYU Langone Health awarded $8 million NIH grant to develop implantable device to study epileptic seizures news-medical.net/news/20220217/…

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Tina Pesaran @tinapesaran

5 years ago

The future looks bright for pancreatic cancer! #precedestudy

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Tina Pesaran @tinapesaran

5 years ago

“PRECEDE is a unique, unparalleled opportunity to re-imagine how we detect, treat, and prevent pancreatic cancer in our lifetime." It's an honor to be part of this initiative! #PancreaticCancer #earlydetection #precedestudy #precedeconsortium #ambrygenetics #realm #invicro

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Tina Pesaran @tinapesaran

5 years ago

@helenkimgc @dgmacarthur @katiehelbig @Invitae @gnomad_project @AmbryGenetics Are you referring to the genomic coordinates? @AmbryGenetics we use and report gnomAD.

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Tina Pesaran @tinapesaran

5 years ago

@ColYou There is more risk of blood clots for women taking birth control. 🤷🏻‍♀️

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ClinGen @ClinGenResource

5 years ago

Attending #ACMGMtg21 this week? Don't miss these ClinGen-related presentations and posters clinicalgenome.org/about/events/c…

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Center for the Multiplex Assessment of Phenotype @CEGS_CMAP

5 years ago

Introducing the Atlas of Variant Effects Alliance. A roadmap to precision medicine at nucleotide resolution. Breakout rooms are now open! #varianteffect21 @FPRoth @rubin_af @BenLehner @clare__turnbull

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Center for the Multiplex Assessment of Phenotype @CEGS_CMAP

5 years ago

Martin Kampmann on deep mutational scanning to capture disease-relevant protein conformations in neurodegenerative diseases #varianteffect21 @MartinUCSF

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Genetic Counselors @GeneticCouns

5 years ago

We're excited to announce the #AccesstoGCs Act, which would authorize @CMSGov to recognize CGCs as healthcare providers, has been reintroduced to US House of Reps as #HR2144! Help us improve #AccesstoGCs so patients can make informed decisions about their healthcare #GCChat

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Heather Hampel @HHampel1

5 years ago

If your personal or family history includes the following, see a genetic counselor to consider testing bc you may need earlier & more frequent screening: 🧩 #colorectalcancer dx<50 🧩 3 cases total of CRC, endometrial, stomach or ovarian cancer #colorectalcancerAwarenessMonth

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Genetic Counselors @GeneticCouns

5 years ago

Members, the newest NSGC Podcast Series episode is here! Listen in to hear from @Naomi_CGC and Ryan Kuehl as they speak with molecular pathologist Brian Shirts & GC @GenesintheD about family testing for cancer VUS reclassification: bit.ly/35pzuZS #GCchat

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Bita Nehoray @BeetsWhoTweets

5 years ago

Variant interpretation is challenging! #TP53 c.1000C>G;p.G334R has discordant calls (#VUS & #VLP) in #ClinVar. Paper below suggests that this variant leads to low penetrance #LFS Highlights the importance of LFS research! #LiFraumeniSyndromeAwarenessMonth

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Sohnee Ahmed @SohneeAhmed

6 years ago

So...just found out that the ACMG has sent letters to all states with GC licensure asking sponsors to change bill lang, saying we can't order tests without a dr. Not without a geneticist. Just any doctor. #GCChat

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Mark Ruffalo @MarkRuffalo

6 years ago

Imagine if this was our side. There would be rivers of our blood in the streets and not a single one of us would be armed. This has been allowed. #CoupAttempt

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Tina Pesaran @tinapesaran

6 years ago

@JimGaffigan Happy new year!

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Tina Pesaran @tinapesaran

6 years ago

@ColYou Now you are definitely going to get covid

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Tina Pesaran @tinapesaran

6 years ago

@ColYou Add cognac and eggnog to your coffee and you will feel amazing 🤩

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Heidi Rehm @HeidiRehm

6 years ago

At launch, GenCC DB contains 3728 gene-disease assertions on 2282 genes from 8 submitters @AmbryGenetics @ClinGenResource @PanelAppTeam @illumina @Invitae @MyrWomensHealth @PanelAppAus @theTGMI More submissions from these groups as well as @OmimOrg and LMM are coming soon (3/4)