Prech Uapinyoying

ORCID: 0000-0003-1950-4164

Also affiliated with Children's National, National Institute of Neurological Disorders and Stroke

Biochemistry, Genetics and Molecular BiologyMedicine

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 12 papers. Top paper: “A long-read RNA-seq approach to identify novel transcripts of very large genes”.

A long-read RNA-seq approach to identify novel transcripts of very large genes

Genome Research(2020)10.1101/gr.259903.119

N/A

0.617DataRank · unranked

60 citations

Jeremy Goecks, Susan M. Knoblach, Karuna Panchapakesan, Carsten G. Bönnemann, Terence A. Partridge +3 more

Exploring the therapeutic potential of fibroadipogenic progenitors in muscle disease

Journal of Neuromuscular Diseases(2025)10.1177/22143602241298545

N/A

0.241DataRank · unranked

4 citations

Medha Kurukunda, Karim Ismat, Prech Uapinyoying, Jyoti K. Jaiswal, Marshall W. Hogarth

A new long-read RNA-seq analysis approach identifies and quantifies novel transcripts of very large genes

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.01.08.898627

N/A

0.165DataRank · unranked

2 citations

Jeremy Goecks, Susan M. Knoblach, Karuna Panchapakesan, Carsten G. Bönnemann, Terence A. Partridge +3 more

Gene delivery corrects N-acetylglutamate synthase deficiency and enables insights in the physiological impact of L-arginine activation of N-acetylglutamate synthase

Scientific Reports(2021)10.1038/s41598-021-82994-8

N/A

0DataRank · unranked

15 citations

Emilee Senkevitch, Nantaporn Haskins, Prech Uapinyoying, Markey McNutt, Hiroki Morizono +3 more

Single-cell transcriptomic analysis of the identity and function of fibro/adipogenic progenitors in healthy and dystrophic muscle

iScience(2023)10.1016/j.isci.2023.107479

N/A

0DataRank · unranked

23 citations

Marshall W. Hogarth, Surajit Battacharya, Davi A. G. Mázala, Karuna Panchapakesan, Carsten G. Bönnemann +2 more

Collecting, freezing and shipping frozen post mortem skeletal muscle for single nuclear and spatial RNAseq v1

(2023)10.17504/protocols.io.dm6gp3zz1vzp/v1

N/A

0DataRank · unranked

0 citations

Prech Uapinyoying

Allele-specific CRISPR-Cas9 editing inactivates a single nucleotide variant associated with collagen VI muscular dystrophy

Molecular Therapy — Nucleic Acids(2024)10.1016/j.omtn.2024.102269

N/A

0DataRank · unranked

9 citations

Katherine Sizov, Astrid Brull, Eric Esposito, Grace S. Chen, Prech Uapinyoying +4 more

Transcriptome analysis of collagen VI‐related muscular dystrophy muscle biopsies

Annals of Clinical and Translational Neurology(2021)10.1002/acn3.51450

N/A

0DataRank · unranked

25 citations

Payam Mohassel, Kory R. Johnson, Lin Yang, Mariarita Santi, Prech Uapinyoying +7 more

Differential inclusion of NEB exons 143 and 144 provides insight into NEB -related myopathy variant interpretation and disease manifestation

medRxiv(2024)10.1101/2024.03.25.24304535

N/A

0DataRank · unranked

0 citations

Rotem Orbach, Safoora Syeda, A. Reghan Foley, Svetlana Gorokhova, Katherine G. Meilleur +6 more

Failure to resolve inflammation contributes to juvenile onset cardiac damage in a mouse model of Duchenne Muscular Dystrophy

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.08.15.607998

N/A

0DataRank · unranked

0 citations

Amy Lischin, Prech Uapinyoying, Ravi Hindupur, Young Jae Moon, Surajit Bhattacharya +7 more

Differential inclusion of NEB exons 143 and 144 provides insight into NEB-related myopathy variant interpretation and disease manifestation

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100354

N/A

0DataRank · unranked

0 citations

Rotem Orbach, Safoora Syeda, A. Reghan Foley, Svetlana Gorokhova, Katherine G. Meilleur +6 more

Allele-specific CRISPR/Cas9 editing inactivates a single nucleotide variant associated with collagen VI muscular dystrophy

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.03.22.586265

N/A

0DataRank · unranked

1 citations

Katherine Sizov, Astrid Brull, Eric Esposito, Grace S. Chen, Prech Uapinyoying +4 more