Heather Mefford, MD, PhD
@hcmefford.bsky.social
Physician scientist @ St. Jude
(neuro)genetics | genomics
epilepsy | rare disease | precision medicine
(neuro)genetics | genomics
epilepsy | rare disease | precision medicine
Oops - WED poster correction
🧬🧠🧬
WEDNESDAY 10/15
4027W Genome seq in unsolved epilepsy
@sohamsg90.bsky.social
**8062W** a new repeat expansion locus as a potential cause for epilepsy @cwlaflamme.bsky.social (presented by Dianne Laboy)
🧬🧠🧬
WEDNESDAY 10/15
4027W Genome seq in unsolved epilepsy
@sohamsg90.bsky.social
**8062W** a new repeat expansion locus as a potential cause for epilepsy @cwlaflamme.bsky.social (presented by Dianne Laboy)
October 15, 2025 at 2:54 PM
Oops - WED poster correction
🧬🧠🧬
WEDNESDAY 10/15
4027W Genome seq in unsolved epilepsy
@sohamsg90.bsky.social
**8062W** a new repeat expansion locus as a potential cause for epilepsy @cwlaflamme.bsky.social (presented by Dianne Laboy)
🧬🧠🧬
WEDNESDAY 10/15
4027W Genome seq in unsolved epilepsy
@sohamsg90.bsky.social
**8062W** a new repeat expansion locus as a potential cause for epilepsy @cwlaflamme.bsky.social (presented by Dianne Laboy)
Looking forward to seeing you!
October 13, 2025 at 7:12 PM
Looking forward to seeing you!
More 🧬🧠🧬 from @stjuderesearch.bsky.social
THURSDAY 10/16
7025T NatHx of CHD2 and methylation sig for diagnosis @edithalmanzafuerte.bsky.social
4040T Multiomics analysis of Ring14 syndrome @esbonkowski.bsky.social
6011T Antisense oligonucleotide (ASO) therapy for GNAI1 epilepsy
THURSDAY 10/16
7025T NatHx of CHD2 and methylation sig for diagnosis @edithalmanzafuerte.bsky.social
4040T Multiomics analysis of Ring14 syndrome @esbonkowski.bsky.social
6011T Antisense oligonucleotide (ASO) therapy for GNAI1 epilepsy
October 13, 2025 at 3:35 PM
More 🧬🧠🧬 from @stjuderesearch.bsky.social
THURSDAY 10/16
7025T NatHx of CHD2 and methylation sig for diagnosis @edithalmanzafuerte.bsky.social
4040T Multiomics analysis of Ring14 syndrome @esbonkowski.bsky.social
6011T Antisense oligonucleotide (ASO) therapy for GNAI1 epilepsy
THURSDAY 10/16
7025T NatHx of CHD2 and methylation sig for diagnosis @edithalmanzafuerte.bsky.social
4040T Multiomics analysis of Ring14 syndrome @esbonkowski.bsky.social
6011T Antisense oligonucleotide (ASO) therapy for GNAI1 epilepsy
Come visit our rare disease / epilepsy / genetics posters 🧬🧠🧬 from @stjuderesearch.bsky.social
WEDNESDAY 10/15
4027W Genome seq in unsolved epilepsy @sohamsg90.bsky.social
8026W a new repeat expansion locus as a potential cause for epilepsy
WEDNESDAY 10/15
4027W Genome seq in unsolved epilepsy @sohamsg90.bsky.social
8026W a new repeat expansion locus as a potential cause for epilepsy
October 13, 2025 at 3:35 PM
Come visit our rare disease / epilepsy / genetics posters 🧬🧠🧬 from @stjuderesearch.bsky.social
WEDNESDAY 10/15
4027W Genome seq in unsolved epilepsy @sohamsg90.bsky.social
8026W a new repeat expansion locus as a potential cause for epilepsy
WEDNESDAY 10/15
4027W Genome seq in unsolved epilepsy @sohamsg90.bsky.social
8026W a new repeat expansion locus as a potential cause for epilepsy
Congrats to both @mrvollger.bsky.social and to UofU!
June 5, 2025 at 9:58 PM
Congrats to both @mrvollger.bsky.social and to UofU!
Agree - amazing talk! Thanks for visiting and sharing your beautiful work @melikel.bsky.social!
April 29, 2025 at 6:14 PM
Agree - amazing talk! Thanks for visiting and sharing your beautiful work @melikel.bsky.social!
So great to have you! Thanks again for coming. What a great #womeninstem epilepsy session! 🧬🧠🤩
April 5, 2025 at 7:13 PM
So great to have you! Thanks again for coming. What a great #womeninstem epilepsy session! 🧬🧠🤩