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ScreenPlus @ScreenPlusNY

We are the largest newborn pilot screening program in the United States. Our goal is to identify babies with rare disorders earlier #2025NBS #rarediseases

Joined December 2020
  • Tweets 532
  • Following 174
  • Followers 183
95 Photos and videos
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ScreenPlus@ScreenPlusNY
18 Dec 2023
Excited to announce that ScreenPlus has another published paper out! Our marker paper gives you a great detailed overview of what we do! Congrats and thank you to everyone involved! doi.org/10.1016/j.ymgmr.2023…
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ScreenPlus retweeted
NNPDF@nnpdf
21 Oct 2025
Is someone you love living with the effects of Niemann-Pick disease? NNPDF is dedicated to supporting families every step of the way with programs, resources, and advocacy. Learn more about our work or make a donation at nnpdf.org/
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Excited and proud to announce that we have officially enrolled over 35,000 babies into our study! Incredible work and huge thanks to all of our recruiters and to all involved in this project! #RareDisease #newbornscreening
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Today we wrap up this month's awareness on GM1 gangliosidosis 💡Thank you for tuning in on this important #RareDisease ! #newbornscreening
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Check out one of the advocacy groups, Cure GM1 Foundation, to connect with the community: 👉 curegm1.org/

GM1 Gangliosidosis Research & Support | Cure GM1 Foundation

Cure GM1 Foundation funds GM1 gangliosidosis research, clinical trials & patient advocacy to find treatments for this rare disease. Join us.

curegm1.org
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For more information about #GM1 gangliosidosis, symptoms, or causes, make sure to visit: rarediseases.info.nih.gov/di…
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For rare diseases like #GM1 gangliosidosis, #research focusing on early detection and treatment can improve outcomes. 🧬 Check out the link below ⬇️ for more info on current clinical trials: clinicaltrials.gov/search?co…
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There are also less severe forms of #GM1 gangliosidosis that progress more slowly. For more information about #GM1, check out this link: medlineplus.gov/genetics/con…

GM1 gangliosidosis: MedlinePlus Genetics

GM1 gangliosidosis is an inherited disorder that destroys neurons in the brain and spinal cord. Explore symptoms, inheritance, genetics of this condition.

medlineplus.gov
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#RareDisease
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#newbornscreening #RareDisease
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This month we’re spreading #awareness about #GM1 gangliosidosis, one of the rare conditions on our ScreenPlus panel. Throughout the month, we’ll share some information and helpful resources, so follow along! #newbornscreening #RareDisease
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Team selfie! Hello from the ScreenPlus Team: @MontefioreNYC @MontefiorePeds @EinsteinMed @nyulangone @NYULangoneBK @MountSinaiNYC @NorthwellHealth @MaimoHealth #newbornscreening #RareDisease
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Happy 4th of July from the ScreenPlus Team!! 🇺🇸📷🎆 @MontefiorePeds @EinsteinMed
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📢30,000 babies enrolled! Congratulations team! 🎉 @EinsteinMed @MontefiorePeds @nyulangone @MountSinaiNYC @NorthwellHealth @MaimoHealth #PublicHealth #RareDiseases
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ScreenPlus retweeted
Michael Cabana, MD@cabanam
28 Apr 2025
Dr Melissa Wasserstein presents her work on @ScreenPlusNY at the Children’s Hospital at Montefiore (#CHAM) at @PASMeeting. @MontefioreNYC @SuzettePediMD @i_jsmiles @DrFerdowsi @SocPedResearch @RareDiseases @RFK_Center @JoeBalagtas
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#RareDiseaseDay 2025🧬 @EinsteinMed
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📢 Reminder to register for the #RareDiseaseDay Symposium below! 👇 @EinsteinMed @MontefiorePeds
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#RareDiseaseDay
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#RareDiseaseDay
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