#Genomic #MedicalScientist, technophile, progress enthusiast. All views my own.
Joined April 2016
- Tweets 872
- Following 517
- Followers 614
- Likes 1,456
65 Photos and videos
8 Oct 2024
This 👇👇👇!!! I think data sharing is an absolute must, and can be done in a way that ensures privacy and patient autonomy while providing huge benefits to individuals, research and society. Even a small start is a start, let’s break down the silos. Please do!
8 Oct 2024
👉 Out now @NatureRevGenet: we CAN and we SHOULD do more to enable #genomic data sharing! 🧬🌏
👉Best practice examples and 12 actions we can all take together
👉 rdcu.be/dWfsu
@GA4GH @AusGenomics @GenomicsEngland @NHSgms @AllofUsResearch @uk_biobank @ukfuturehealth
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Seb Lunke retweeted
3 Jul 2024
New publications from @AusGenomics & @MCRI_for_kids in @AJHGNews led by A/Prof Amy Nisselle & @bronwynterrill aim to improve #genomicmedicine #education for healthcare professionals through rigorous evaluation, ultimately to provide better health outcomes for Australians. 1/4
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Seb Lunke retweeted
3 Jul 2024
Looking forward to the partnership between @MCRI_for_kids @TeamVCGS and @nanopore becoming prosperous for numerous patients. Innovative times ahead!! @GenomeSeb #RareDisease #genetics
Congrats to #MCRI's A/Prof Sebastian Lunke who has received a Victorian Medical Research Acceleration Fund grant to develop a faster technique to screen for rare #genetic disorders. | #MCRIresearch #Grants #RareDisease #Genetics
➡️mcri.edu.au/news/awards/asso…
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Seb Lunke retweeted
Congrats to #MCRI's A/Prof Sebastian Lunke who has received a Victorian Medical Research Acceleration Fund grant to develop a faster technique to screen for rare #genetic disorders. | #MCRIresearch #Grants #RareDisease #Genetics
➡️mcri.edu.au/news/awards/asso…
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Seb Lunke retweeted
29 Jun 2024
The most exciting part for me will be seeing how this work will improve the lives of those suffering from hard to diagnose neurological and neuromuscular genetic disorders.
28 Jun 2024
Excited to receive VMRAF 💰 by @VicGovAu @VicGov_DJSIR to pilot @nanopore to detect repeat expansion disorders! This will enable us to substantially improve #genetic #diagnosis for many #neurological conditions. djsir.vic.gov.au/medical-res… @MCRI_for_kids @TeamVCGS
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Seb Lunke retweeted
28 Jun 2024
#InternationalNeonatalScreeningDay: A call for global implementation of neonatal screening programmes.
Read at bit.ly/3XvNIDQ
@screen4rare #PressRelease
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Seb Lunke retweeted
28 Jun 2024
28 Jun 2024
Excited to receive VMRAF 💰 by @VicGovAu @VicGov_DJSIR to pilot @nanopore to detect repeat expansion disorders! This will enable us to substantially improve #genetic #diagnosis for many #neurological conditions. djsir.vic.gov.au/medical-res… @MCRI_for_kids @TeamVCGS
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28 Jun 2024
Excited to receive VMRAF 💰 by @VicGovAu @VicGov_DJSIR to pilot @nanopore to detect repeat expansion disorders! This will enable us to substantially improve #genetic #diagnosis for many #neurological conditions. djsir.vic.gov.au/medical-res… @MCRI_for_kids @TeamVCGS
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Seb Lunke retweeted
Translating the outcomes of this project will be transformative for mainstreaming #genomics in Australian healthcare. Exciting times!
25 Jun 2024
The diagnosis of rare genetic disorders is one of the places where AI will have the earliest and largest clinical impact. Delighted to be leading a new consortium to help make this happen, along with an awesome team of Australian and global partners: mcri.edu.au/news/funding-awa…
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Seb Lunke retweeted
25 Jun 2024
Exploring the benefits, harms and costs of genomic newborn screening for rare diseases.
Comment from @ZornitzaS and colleagues @AusGenomics @GreatOrmondSt @GenomicsEngland
nature.com/articles/s41591-0…
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Seb Lunke retweeted
25 Jun 2024
Stoked that we get to extend our already hyper-productive work together in a whole bunch of fun new directions, and help so many more patients! (Here’s a Thor-themed fist bump to celebrate 🥳)
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Seb Lunke retweeted
25 Jun 2024
Sooooo excited to be doing this with you @dgmacarthur and building on the 💪 collaborations we have established in automation for #raredisease diagnosis 🤗🤗🤗 @TeamVCGS @MCRI_for_kids #translation 🤖🧬
25 Jun 2024
The diagnosis of rare genetic disorders is one of the places where AI will have the earliest and largest clinical impact. Delighted to be leading a new consortium to help make this happen, along with an awesome team of Australian and global partners: mcri.edu.au/news/funding-awa…
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25 Jun 2024
Exited to be part of this new initiative! The promises of AI are many fold, this project will help us harness them the right way to help more people with rare genetic diseases.
25 Jun 2024
The diagnosis of rare genetic disorders is one of the places where AI will have the earliest and largest clinical impact. Delighted to be leading a new consortium to help make this happen, along with an awesome team of Australian and global partners: mcri.edu.au/news/funding-awa…
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Seb Lunke retweeted
25 Jun 2024
The diagnosis of rare genetic disorders is one of the places where AI will have the earliest and largest clinical impact. Delighted to be leading a new consortium to help make this happen, along with an awesome team of Australian and global partners: mcri.edu.au/news/funding-awa…
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Seb Lunke retweeted
22 Jun 2024
📣 our latest BabyScreen paper now out @ejhg_journal
Process changes needed to deliver #genomic NBS: what, when and who?
Key informant interviews 🇦🇺
👉rdcu.be/dLzRV
👏@drstephbest @erin_tutty @AlisonArchiba19 @drlildownie @ClaraGaff @DanyaVears @GenomeSeb
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Seb Lunke retweeted
19 Jun 2024
Out now @NatureMedicine 🔥🔥
#genomic NBS: the challenges are daunting
But we have a responsibility to lead research in public health systems 🇬🇧🇦🇺
@RDExeter @Rich_Genomics @smbanka @LouiseFish1 @swynn_unique @NeonatalEthics @jbuchanan_ox @dgmacarthur
nature.com/articles/s41591-0…
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Seb Lunke retweeted
7 Jun 2024
In a new paper published in @NatureMedicine, we show that @EmotiveTrial early detection & bundled treatment of #postpartum_hemorrhage is cost-effective
Paper nature.com/articles/s41591-0…
- with @arricoomarasamy @IoannisGallos @terobertsbham @e_vwilliams ...
@unibirmingham @UniMelb
🧵
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Seb Lunke retweeted
3 Jun 2024
On now in A3, the new gene 🧬 discovery of the year: RNU4-2 is a frequent cause of DD/ID. A fantastic, whirlwind collaboration to have been part of 🤩 @quenchentin @nickywhiffin @dgmacarthur @AnneOtation and many more 👏👏👏
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Seb Lunke retweeted
3 Jun 2024
Starting now in A6/7 #eshg2024 Nonsense mediated mRNA decay: variant interpretation challenges with @GeczSquadGoals and @GenomeSeb
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