Jasmine Lin

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 7

Top Topics

Liquid Chromatography

Autism Spectrum Disorder

Top Venues

Disease models & mechanisms

Journal of personalized medicine

European journal of human genetics : EJHG

bioRxiv : the preprint server for biology

This page only lists publications with an associated author ORCID identifier.

Publications

Shiyu Luo, Bilal Alwattar, Qifei Li, Kiran Bora, Alexandra K Blomfield, Jasmine Lin, Anne Fulton, Jing Chen, Pankaj B Agrawal
HBS1L deficiency causes retinal dystrophy in a child and in a mouse model associated with defective development of photoreceptor cells. Disease models & mechanisms 17 (8) (2024)
Shiyu Luo, Bilal Alwattar, Qifei Li, Kiran Bora, Alexandra K Blomfield, Jasmine Lin, Anne Fulton, Jing Chen, Pankaj B Agrawal
HBS1L deficiency causes retinal dystrophy in a child and in a mouse model associated with defective development of photoreceptor cells. Disease models & mechanisms 17 (8) (2024)
Shiyu Luo, Bilal Alwattar, Qifei Li, Kiran Bora, Alexandra K Blomfield, Jasmine Lin, Anne Fulton, Jing Chen, Pankaj B Agrawal
HBS1L deficiency causes retinal dystrophy in a child and a mouse model associated with defective development of photoreceptor cells. Disease models & mechanisms (2024)
Shiyu Luo, Bilal Alwattar, Qifei Li, Kiran Bora, Alexandra K Blomfield, Jasmine Lin, Anne Fulton, Jing Chen, Pankaj B Agrawal
HBS1L deficiency causes retinal dystrophy in a child and in a mouse model associated with defective development of photoreceptor cells. Disease models & mechanisms 17 (8) (2024)
Shiyu Luo, Bilal Alwattar, Qifei Li, Kiran Bora, Alexandra K Blomfield, Jasmine Lin, Anne Fulton, Jing Chen, Pankaj B Agrawal
Genetic deficiency of ribosomal rescue factor HBS1L causes retinal dystrophy associated with Pelota and EDF1 depletion. bioRxiv : the preprint server for biology (2023)
Boxun Zhao, Jill A Madden, Jasmine Lin, Gerard T Berry, Monica H Wojcik, Xuefang Zhao, Harrison Brand, Michael E Talkowski, Eunjung Alice Lee, Pankaj B Agrawal
A neurodevelopmental disorder caused by a novel de novo SVA insertion in exon 13 of the SRCAP gene. European journal of human genetics : EJHG 30 (9) (2022)
Qifei Li, Jill A Madden, Jasmine Lin, Jiahai Shi, Samantha M Rosen, Klaus Schmitz-Abe, Pankaj B Agrawal
Reanalysis of Exome Data Identifies Novel SLC25A46 Variants Associated with Leigh Syndrome. Journal of personalized medicine 11 (12) (2021)