Genetics lab @chudelyon and @jcourchet group at Institut NeuroMyoGène
Lyon, France
Joined March 2009
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Croyez le ou non : j’ai répondu à sondage téléphonique dur mes attentes à propos de cette bibliothèque pour le centre-ville de Clermont-Ferrand… en 2007 !!!
PHOTOS - Découvrez le chantier de la future bibliothèque de l'Hôtel-Dieu, avant son ouverture au printemps 2027
➡️ l.ici.fr/wKSY
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Le timing est risqué 😔mais je profite du buzz : si la journée d’aujourd’hui a réveillé en vous le généticien 🧬qui dormait et que vous envisagez cette option pour plus tard, DM pour toute question 😜#ecos #edn #oncogenetique #genetique
Before @JorisVermeesch closes the fantastic #ECA2025 in 🇧🇪Leuven, @CharlotteTardy1 presented our work in @CHUdeLyon around chromosomal breakpoint characterization in the prenatal🤰 setting with @nanopore . Ongoing but already 5/5 success including a clear pathogenic variant👏
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Took advantage of T2T assembly to resolve one. @EichlerLab questioned whether this will to use T2T in the clinic was consensus to decide whether this was to be annotated or not. So ?
0%Yes go for T2T annotation
100%No I’ll stick with GRCh38
0%I am a GRCh37 fan 🤭
0%What is this about ? 🫣
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🚨It is sometimes a difficult exercise but the assembly of the pieces of the #ESHG2026 program is completed. 🤩👏 to an amazing team 🎉👍Stay tuned and see you in Gothenburg ! 🇸🇪
ALT An AI-edited IKEA style drawing showing that taking a great team of experts worldwide and DNA ends uo to an amazing ESHG conference
Today, the Scientific Programme Committee wrapped a fantastic and exciting programme for #eshg2026 conference! More information will available on our conference website soon. We look forward to welcoming you in Gothenburg!
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To give the better for patients, team work is crucial . I am part of an amazing one. Some gathered in Milan #ESHG2025 for 4 exciting days of science and networking, thanks 🙏 to others that stayed @CHUdeLyon @gaetan_lesca @LouisJanuel
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Fully packed room for #eshg2025 chromosomal structural variants workshop session. Cytogeneticists are in the place !
Day#1 at #eshg2025 Amazing long read génome session. Already astonished by the speakers of this “prologue”.
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Just arrived in 🇮🇹 Milan for #eshg2025 . Train 20 minutes ahead of time… Never seen such miracle on the other side of the Alps 🇫🇷. Ready for 🧬!!!
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Nico Chatron retweeted
The #eshg2025 virtual platform & the ESHG 2025 app are now online! Read through our tips of using the platform, check out the conference programme and prepare your visit to Milan today: 2025.eshg.org/myconference/h… and 2025.eshg.org/myconference/c…
Nico Chatron retweeted
2 PLACES POUR LE GRAND PRIX DE MONACO À GAGNER 🤩🇲🇨
🌟 Pour participer :
- RT ce post
- Abonnez-vous à @canalplusf1
BONUS : Doublez vos chances sur tous nos réseaux 🤞
Tirage au sort le 21/05 🍀
Règlement en bio.
Nico Chatron retweeted
Proud to be the first geneticist to have reached the 1000th genome on the AURAGEN laboratory of the french national genomic plan (PFMG 2025) 😊. Mainly for patients with rare epilepies. Please to share with you my price 😄 @TeamHcl @AURAGEN2 @EpiCARE_ERN @IlaeWeb #pfmg2025
Nico Chatron retweeted
One more week until the abstract submission deadline for #eshg2025 #hybridconference! Do not forget to submit your abstract until Thursday, January 30, 2025, 23.59 h CET. All information can be found on our website:
2025.eshg.org/abstracts/
#genetics #genomes
Nico Chatron retweeted
A new editorial describes the science behind a study linking a severe neurodevelopmental disorder with deletions in a gene (𝘊𝘏𝘈𝘚𝘌𝘙𝘙) that encodes a long noncoding RNA. Read the full editorial: nej.md/4hkctuu
ALT A diagram of CHASERR haploinsufficiency in a neurodevelopmental disorder.
Nico Chatron retweeted
Thank you to Prof. Ling-Ling Chen and the illustrators and editors at @NEJM for nicely summarizing our study and its implications. 🙏
A new editorial describes the science behind a study linking a severe neurodevelopmental disorder with deletions in a gene (𝘊𝘏𝘈𝘚𝘌𝘙𝘙) that encodes a long noncoding RNA. Read the full editorial: nej.md/4hkctuu
ALT A diagram of CHASERR haploinsufficiency in a neurodevelopmental disorder.
🚨New 🧬disease mechanism described. 🤞Hope this will help to end other odysseys. Excited for @curechd2 ! Amazing being part of this with @VGaneshMDPhD @AnneOtation @CarvillLab @IgorUlitsky @BezieauStephane @dgmacarthur @chaserrdad and many others 👇🍾@HCL_research @AURAGEN2
Excited to report our study in @NEJM on the discovery of deletions in a long noncoding RNA gene 🧬 (𝘊𝘏𝘈𝘚𝘌𝘙𝘙) as the cause of a newly defined human neurodevelopmental disorder 🧠. 🧵1/10 nejm.org/doi/full/10.1056/NE…
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Genomes, non-coding variants, diagnoses++ and huge collab : awesome times for genomics ! Glad to be part of this 👇Bravo @ChristelDepienn
Thrilled to share a new preprint on the role of RNU4-2 and RNU5B-1 variants in neurodevelopmental disorders, now online in MedRxiv. 1/12 🧵medrxiv.org/content/10.1101/…
💡 Et si on était obligés de lier un numéro de portable perso à notre fiche RPPS dans un espace réservé aux pros ? Pas bien compliqué tout de même…
Toi aussi essayes d’appeler le CHU pour des résultats bio très perturbés (3 dossiers, 3 services) :
- impossible de joindre les médecins en question (« on n’a pas les no directs » dit le standard)
- no sur les ordo : tombe sur les secrétariats, fermés dès 16:30
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