• 3671 Citations
  • 24 h-Index
1985 …2018
If you made any changes in Pure, your changes will be visible here soon.

Fingerprint Dive into the research topics where Jay W Schneider is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 26 Similar Profiles
Isoxazoles Medicine & Life Sciences
Cardiac Myocytes Medicine & Life Sciences
Genes Medicine & Life Sciences
Protein Isoforms Medicine & Life Sciences
Gene Expression Medicine & Life Sciences
Stem Cells Medicine & Life Sciences
Messenger RNA Medicine & Life Sciences
Molecular Cloning Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 1985 2018

  • 3671 Citations
  • 24 h-Index
  • 42 Article
  • 1 Chapter
36 Citations (Scopus)

Correction of diverse muscular dystrophy mutations in human engineered heart muscle by single-site genome editing

Long, C., Li, H., Tiburcy, M., Rodriguez-Caycedo, C., Kyrychenko, V., Zhou, H., Zhang, Y., Min, Y. L., Shelton, J. M., Mammen, P. P. A., Liaw, N. Y., Zimmermann, W. H., Bassel-Duby, R., Schneider, J. W. & Olson, E. N., Jan 1 2018, In : Science advances. 4, 1, eaap9004.

Research output: Contribution to journalArticle

Duchenne Muscular Dystrophy
Muscular Dystrophies
Myocardium
Mutation
Dystrophin
2 Citations (Scopus)

Down syndrome critical region 1 gene, rcan1, helps maintain a more fused mitochondrial network

Parra, V., Altamirano, F., Hernández-Fuentes, C. P., Tong, D., Kyrychenko, V., Rotter, D., Pedrozo, Z., Hill, J. A., Eisner, V., Lavandero, S., Schneider, J. W. & Rothermel, B. A., Mar 1 2018, In : Circulation Research. 122, 6, p. e20-e33

Research output: Contribution to journalArticle

Calcineurin
Genes
Induced Pluripotent Stem Cells
Mitochondria
Ischemia
22 Citations (Scopus)

Functional correction of dystrophin actin binding domain mutations by genome editing

Kyrychenko, V., Kyrychenko, S., Tiburcy, M., Shelton, J. M., Long, C., Schneider, J. W., Zimmermann, W. H., Bassel-Duby, R. S. & Olson, E. N., Sep 21 2017, In : JCI insight. 2, 18

Research output: Contribution to journalArticle

Open Access
Dystrophin
Duchenne Muscular Dystrophy
Actins
Exons
Mutation
1 Citation (Scopus)

Priapism in a Fabry disease mouse model is associated with upregulated penile nNOS and eNOS expression

Meng, X. L., Arning, E., Wight-Carter, M., Day, T. S., Jabbarzadeh-Tabrizi, S., Chen, S., Ziegler, R. J., Bottiglieri, T., Schneider, J. W., Cheng, S. H., Schiffmann, R. & Shen, J. S., Nov 6 2017, (Accepted/In press) In : Journal of Inherited Metabolic Disease. p. 1-8 8 p.

Research output: Contribution to journalArticle

Priapism
Fabry Disease
Nitric Oxide Synthase Type I
Penis
Galactosidases
11 Citations (Scopus)

Retinoblastoma protein controls growth, survival and neuronal migration in human cerebral organoids

Matsui, T., Nieto-Estévez, V., Kyrychenko, S., Schneider, J. W. & Hsieh, J., Apr 1 2017, In : Journal of Cell Science. 130, 7, p. 1025-1034 10 p.

Research output: Contribution to journalArticle

Organoids
Retinoblastoma Protein
Survival
Growth
Neural Stem Cells