Larry Walsh

  • Associate Professor of Clinical Neurology, Neurology
  • Source: Scopus
  • Calculated based on no. of publications stored in Pure and citations from Scopus
1993 …2020

Research output per year

If you made any changes in Pure these will be visible here soon.

Fingerprint

Dive into the research topics where Larry Walsh is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
  • 1 Similar Profiles

Network

Recent external collaboration on country level. Dive into details by clicking on the dots.
  • Boricua Founder Variant in FRRS1L Causes Epileptic Encephalopathy With Hyperkinetic Movements

    Abdelmoumen, I., Jimenez, S., Valencia, I., Melvin, J., Legido, A., Diaz-Diaz, M. M., Griffith, C., Massingham, L. J., Yelton, M., Rodríguez-Hernández, J., Schnur, R. E., Walsh, L. E., Cristancho, A. G., Bergqvist, C. A., McWalter, K., Mathieson, I., Belbin, G. M., Kenny, E. E., Ortiz-Gonzalez, X. R. & Schneider, M. C., 2020, (Accepted/In press) In : Journal of child neurology.

    Research output: Contribution to journalArticlepeer-review

  • Expanding the spectrum of CEP55-associated disease to viable phenotypes

    Barrie, E. S., Overwater, E., van Haelst, M. M., Motazacker, M. M., Truxal, K. V., Crist, E., Mostafavi, R., Pivnick, E. K., Choudhri, A. F., Narumanchi, T. C., Castelluccio, V., Walsh, L. E., Garganta, C. & Gastier-Foster, J. M., May 1 2020, In : American Journal of Medical Genetics, Part A. 182, 5, p. 1201-1208 8 p.

    Research output: Contribution to journalArticlepeer-review

  • Correction to: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation (Genetics in Medicine, (2018), 10.1038/s41436-018-0269-0)

    Koczkowska, M., Callens, T., Gomes, A., Sharp, A., Chen, Y., Hicks, A. D., Aylsworth, A. S., Azizi, A. A., Basel, D. G., Bellus, G., Bird, L. M., Blazo, M. A., Burke, L. W., Cannon, A., Collins, F., DeFilippo, C., Denayer, E., Digilio, M. C., Dills, S. K., Dosa, L. & 50 others, Greenwood, R. S., Griffis, C., Gupta, P., Hachen, R. K., Hernández-Chico, C., Janssens, S., Jones, K. J., Jordan, J. T., Kannu, P., Korf, B. R., Lewis, A. M., Listernick, R. H., Lonardo, F., Mahoney, M. J., Ojeda, M. M., McDonald, M. T., McDougall, C., Mendelsohn, N., Miller, D. T., Mori, M., Oostenbrink, R., Perreault, S., Pierpont, M. E., Piscopo, C., Pond, D. A., Randolph, L. M., Rauen, K. A., Rednam, S., Rutledge, S. L., Saletti, V., Schaefer, G. B., Schorry, E. K., Scott, D. A., Shugar, A., Siqveland, E., Starr, L. J., Syed, A., Trapane, P. L., Ullrich, N. J., Wakefield, E. G., Walsh, L. E., Wangler, M. F., Zackai, E., Claes, K. B. M., Wimmer, K., van Minkelen, R., De Luca, A., Martin, Y., Legius, E. & Messiaen, L. M., Mar 1 2019, In : Genetics in Medicine. 21, 3, p. 764-765 2 p.

    Research output: Contribution to journalComment/debatepeer-review

  • Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation

    Koczkowska, M., Callens, T., Gomes, A., Sharp, A., Chen, Y., Hicks, A. D., Aylsworth, A. S., Azizi, A. A., Basel, D. G., Bellus, G., Bird, L. M., Blazo, M. A., Burke, L. W., Cannon, A., Collins, F., DeFilippo, C., Denayer, E., Digilio, M. C., Dills, S. K., Dosa, L. & 50 others, Greenwood, R. S., Griffis, C., Gupta, P., Hachen, R. K., Hernández-Chico, C., Janssens, S., Jones, K. J., Jordan, J. T., Kannu, P., Korf, B. R., Lewis, A. M., Listernick, R. H., Lonardo, F., Mahoney, M. J., Ojeda, M. M., McDonald, M. T., McDougall, C., Mendelsohn, N., Miller, D. T., Mori, M., Oostenbrink, R., Perreault, S., Pierpont, M. E., Piscopo, C., Pond, D. A., Randolph, L. M., Rauen, K. A., Rednam, S., Rutledge, S. L., Saletti, V., Schaefer, G. B., Schorry, E. K., Scott, D. A., Shugar, A., Siqveland, E., Starr, L. J., Syed, A., Trapane, P. L., Ullrich, N. J., Wakefield, E. G., Walsh, L. E., Wangler, M. F., Zackai, E., Claes, K. B. M., Wimmer, K., van Minkelen, R., De Luca, A., Martin, Y., Legius, E. & Messiaen, L. M., Apr 1 2019, In : Genetics in Medicine. 21, 4, p. 867-876 10 p.

    Research output: Contribution to journalArticlepeer-review

    19 Scopus citations
  • Functional Dysregulation of CDC42 Causes Diverse Developmental Phenotypes

    The University of Washington Center for Mendelian Genomics, Feb 1 2018, In : American Journal of Human Genetics. 102, 2, p. 309-320 12 p.

    Research output: Contribution to journalArticlepeer-review

    39 Scopus citations
If you made any changes in Pure these will be visible here soon.