Discover Community Create You

t/gene-fmr1

FMR1 gene

Discuss publications and research concerning the FMR1 gene.

0 followers0 posts138 articles

All posts discussion question review note

Create the first post

Ask a question, share an idea or link scientific evidence.

Topic rules

Follow Noodle’s community and scientific integrity rules.

Moderators

Managed by the Noodle moderation team.

Related literature

Psychiatric and Cognitive Features in Italian Women With the FMR1 Premutation: A Comprehensive Assessment Using SCID-5 and Standardized Cognitive Measures.
FMR1
Why Speech Motor Blocks Emerge in a Communicative Context: An Active Inference Model of Stuttering
FMR1
Autonomic Nervous System Function and Sensory Sensitivity in 12-Month-Old Infants with the FMR1 Premutation.
FMR1
Beyond Repeats: Intragenic Variants in FMR1 and Their Contribution to Fragile X Syndrome Pathogenesis.
FMR1
Virtual Speech Therapist: A Clinician-in-the-Loop AI Speech Therapy Agent for Personalized and Supervised Therapy
FMR1
The Breastfeeding Experiences of Mother-Infant Dyads and the Effects of an FMR1 Mutation.
FMR1
Virtual Speech Therapist: A Clinician-in-the-Loop AI Speech Therapy Agent for Personalized and Supervised Therapy
FMR1
Using Generative AI for the Objective Assessment of Language in Healthcare
FMR1
Identification of a De Novo Heterozygous Frameshift Variant in FMR1 in a Female With Fragile X Syndrome.
FMR1
FMR1 KH0-KH1 domains coordinate m6A binding and phase separation in Fragile X syndrome.
FMR1

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details