Jasmine Lin

Also affiliated with Boston Children's Hospital, Harvard University, Sanofi (United States), Boston Children's Museum

MedicineChemistry

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 16 papers. Top paper: “Dynamin-2 reduction rescues the skeletal myopathy of a SPEG-deficient mouse model”.

Dynamin-2 reduction rescues the skeletal myopathy of a SPEG-deficient mouse model

JCI Insight(2022)10.1172/jci.insight.157336

N/A

0.460DataRank · unranked

12 citations

Jasmine Lin, Jeffrey J. Widrick, Shiyu Luo, Gu Li, Tracy Zhang +5 more

Striated Preferentially Expressed Protein Kinase (SPEG)-Deficient Skeletal Muscles Display Fewer Satellite Cells with Reduced Proliferation and Delayed Differentiation

American Journal Of Pathology(2020)10.1016/j.ajpath.2020.08.012

N/A

0DataRank · unranked

6 citations

Jasmine Lin, Samantha M. Rosen, Tian Zhang, Shideh Kazerounian, Shiyu Luo +2 more

A neurodevelopmental disorder caused by a novel de novo SVA insertion in exon 13 of the SRCAP gene

European Journal of Human Genetics(2022)10.1038/s41431-022-01137-3

N/A

0DataRank · unranked

18 citations

Jill A. Madden, Jasmine Lin, Gerard T. Berry, Monica H. Wojcik, Xuefang Zhao +5 more

Unique Capabilities of Genome Sequencing for Rare Disease Diagnosis

medRxiv(2023)10.1101/2023.08.08.23293829

N/A

0DataRank · unranked

8 citations

Gabrielle Lemire, Maha S. Zaki, Mariel Wissman, Wathone Win, S. White +70 more

WNT2B Deficiency Causes Increased Susceptibility to Colitis in Mice and Impairs Intestinal Epithelial Development in Humans

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.04.21.537894

N/A

0DataRank · unranked

2 citations

Sathuwarman Raveenthiraraj, Comfort Adegboye, Wanshu Qi, Radhika S. Khetani, Akaljot Singh +11 more

Genetic deficiency of ribosomal rescue factor HBS1L causes retinal dystrophy associated with Pelota and EDF1 depletion

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.10.18.562924

N/A

0DataRank · unranked

1 citations

Bilal K. AlWattar, Qifei Li, Kiran Bora, Alexandra K. Blomfield, Jasmine Lin +4 more

Integrated multi-omics approach reveals the role of SPEG in skeletal muscle biology including its relationship with myospryn complex

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.04.24.538136

N/A

0DataRank · unranked

0 citations

Jasmine Lin, Shiyu Luo, Klaus Schmitz‐Abe, Rohan Agrawal, Melissa Meng +6 more

Genome Sequencing for Diagnosing Rare Diseases

New England Journal of Medicine(2024)10.1056/nejmoa2314761

N/A

0DataRank · unranked

189 citations

Gabrielle Lemire, Eva Berger, Maha S. Zaki, Mariel Wissmann, Wathone Win +84 more

WNT2B Deficiency Causes Enhanced Susceptibility to Colitis Due to Increased Inflammatory Cytokine Production

Cellular and Molecular Gastroenterology and Hepatology(2024)10.1016/j.jcmgh.2024.04.006

N/A

0DataRank · unranked

12 citations

Sathuwarman Raveenthiraraj, Luiz Fernando Silva Oliveira, Comfort Adegboye, Venkata Siva Dasuri, Wanshu Qi +14 more

The solute carrier family 26 member 9 modifies rapidly progressing cystic fibrosis associated with homozygous F508del CFTR mutation

Clinica Chimica Acta(2024)10.1016/j.cca.2024.119765

N/A

0DataRank · unranked

3 citations

S.D. Rollins, Klaus Schmitz‐Abe, Amy Tam, Qifei Li, Jiahai Shi +4 more

HBS1L deficiency causes retinal dystrophy in a child and in a mouse model associated with defective development of photoreceptor cells

Disease Models & Mechanisms(2024)10.1242/dmm.050557

N/A

0DataRank · unranked

3 citations

Bilal K. AlWattar, Qifei Li, Kiran Bora, Alexandra K. Blomfield, Jasmine Lin +4 more

Integrated multi‐omics approach reveals the role of striated muscle preferentially expressed protein kinase in skeletal muscle including its relationship with myospryn complex

Journal of Cachexia Sarcopenia and Muscle(2024)10.1002/jcsm.13470

N/A

0DataRank · unranked

4 citations

Jasmine Lin, Shiyu Luo, Klaus Schmitz‐Abe, Rohan Agrawal, Melissa Meng +6 more

The Solute Carrier Family 26 Member 9 Is a Modifier of the Rapidly Progressing Cystic Fibrosis Associated with F508del CFTR Mutations

medRxiv(2024)10.1101/2024.01.04.23300546

N/A

0DataRank · unranked

0 citations

S.D. Rollins, Klaus Schmitz‐Abe, Amy Tam, Qifei Li, Jiahai Shi +4 more

Long-Read Sequencing is Required for Precision Diagnosis of Incontinentia Pigmenti

Research Square(2025)10.21203/rs.3.rs-5811417/v1

N/A

0DataRank · unranked

0 citations

Robin D. Clark, Abdallah F. Elias, Casie A. Genetti, Jill A. Madden, Dana Simpson +21 more

SPEG binds with desmin and its deficiency causes defects in triad and focal adhesion proteins

Human Molecular Genetics(2020)10.1093/hmg/ddaa276

N/A

0DataRank · unranked

13 citations

Qifei Li, Jasmine Lin, Quinn Murphy, Isabelle Marty, Tracy Zhang +3 more

Long-read sequencing is required for precision diagnosis of incontinentia pigmenti

Human Genetics and Genomics Advances(2025)10.1016/j.xhgg.2025.100468

N/A

0DataRank · unranked

0 citations

Robin D. Clark, Abdallah F. Elias, Casie A. Genetti, Jill A. Madden, Dana Simpson +21 more