Robert H Listernick

  • Source: Scopus
1983 …2021

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Personal profile

Research Interests

I am a general academic pediatrician in the Department of Pediatrics.

I study the natural history and treatment of optic pathway tumors in children who have neurofibromatosis-1. My clinic is a site of the Department of Defense Neurofibromatosis Clinical Trials Consortium which conducts clinical trials on individuals with NF-1, NF-2 and schwannomatosis. I am very involved in the education program of the Department of Pediatrics

My main clinical focuses are: 1) The care and management of children with Neurofibromatosis-1 2) Consultative pediatrics for difficult diagnostic problems 3) The management of hospitalized children

Certifications and Licenses

Pediatrics

Training Experience

1982Residency, Northwestern University, McGaw Medical Center (Children’s Memorial Hospital)

Education/Academic qualification

MD, University of Pennsylvania

… → 1979

Research interests

  • Neurofibromatosis

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  • Neurofibromatosis Type 1-Associated Optic Pathway Glioma in Children: A Follow-Up of 10 Years or More

    Kinori, M., Armarnik, S., Listernick, R., Charrow, J. & Zeid, J. L., Jan 2021, In: American journal of ophthalmology. 221, p. 91-96 6 p.

    Research output: Contribution to journalArticlepeer-review

    1 Scopus citations
  • Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation

    International Consensus Group on Neurofibromatosis Diagnostic Criteria (I-NF-DC), Aug 2021, In: Genetics in Medicine. 23, 8, p. 1506-1513 8 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    6 Scopus citations
  • Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype–phenotype study in neurofibromatosis type 1

    Koczkowska, M., Callens, T., Chen, Y., Gomes, A., Hicks, A. D., Sharp, A., Johns, E., Uhas, K. A., Armstrong, L., Bosanko, K. A., Babovic-Vuksanovic, D., Baker, L., Basel, D. G., Bengala, M., Bennett, J. T., Chambers, C., Clarkson, L. K., Clementi, M., Cortés, F. M., Cunningham, M. & 88 others, D'Agostino, M. D., Delatycki, M. B., Digilio, M. C., Dosa, L., Esposito, S., Fox, S., Freckmann, M. L., Fauth, C., Giugliano, T., Giustini, S., Goetsch, A., Goldberg, Y., Greenwood, R. S., Griffis, C., Gripp, K. W., Gupta, P., Haan, E., Hachen, R. K., Haygarth, T. L., Hernández-Chico, C., Hodge, K., Hopkin, R. J., Hudgins, L., Janssens, S., Keller, K., Kelly-Mancuso, G., Kochhar, A., Korf, B. R., Lewis, A. M., Liebelt, J., Lichty, A., Listernick, R. H., Lyons, M. J., Maystadt, I., Martinez Ojeda, M., McDougall, C., McGregor, L. K., Melis, D., Mendelsohn, N., Nowaczyk, M. J. M., Ortenberg, J., Panzer, K., Pappas, J. G., Pierpont, M. E., Piluso, G., Pinna, V., Pivnick, E. K., Pond, D. A., Powell, C. M., Rogers, C., Ruhrman Shahar, N., Rutledge, S. L., Saletti, V., Sandaradura, S. A., Santoro, C., Schatz, U. A., Schreiber, A., Scott, D. A., Sellars, E. A., Sheffer, R., Siqveland, E., Slopis, J. M., Smith, R., Spalice, A., Stockton, D. W., Streff, H., Theos, A., Tomlinson, G. E., Tran, G., Trapane, P. L., Trevisson, E., Ullrich, N. J., Van den Ende, J., Schrier Vergano, S. A., Wallace, S. E., Wangler, M. F., Weaver, D. D., Yohay, K. H., Zackai, E., Zonana, J., Zurcher, V., Claes, K. B. M., Eoli, M., Martin, Y., Wimmer, K., De Luca, A., Legius, E. & Messiaen, L. M., Jan 1 2020, In: Human mutation. 41, 1, p. 299-315 17 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    27 Scopus citations
  • Visual field outcomes in children treated for neurofibromatosis type 1–associated optic pathway gliomas: a multicenter retrospective study

    Heidary, G., Fisher, M. J., Liu, G. T., Ferner, R. E., Gutmann, D. H., Listernick, R. H., Kapur, K., Loguidice, M., Ardern-Holmes, S. L., Avery, R. A., Hammond, C., Hoffman, R. O., Hummel, T. R., Kuo, A., Reginald, A. & Ullrich, N. J., Dec 2020, In: Journal of AAPOS. 24, 6, p. 349.e1-349.e5

    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