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Yolanda Faye Holler-Managan

Calculated based on number of publications stored in Pure and citations from Scopus
Calculated based on number of publications stored in Pure and citations from Scopus
Calculated based on number of publications stored in Pure and citations from Scopus
20082024

Research activity per year

Personal profile

Training Experience

2000Residency, Medical College of Wisconsin
2003Fellowship, University of Chicago

Education/Academic qualification

Medicine, MD, University of Illinois at Chicago

… → 1997

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  • Neurologic Evaluation

    Holler-Managan, Y. F., Jan 1 2024, Nelson Textbook of Pediatrics: Volume 1-2. Elsevier, p. 3550-3560.e1

    Research output: Chapter in Book/Report/Conference proceeding › Chapter

  • Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders

    Mannucci, I., Dang, N. D. P., Huber, H., Murry, J. B., Abramson, J., Althoff, T., Banka, S., Baynam, G., Bearden, D., Beleza-Meireles, A., Benke, P. J., Berland, S., Bierhals, T., Bilan, F., Bindoff, L. A., Braathen, G. J., Busk, Ø. L., Chenbhanich, J., Denecke, J. & Escobar, L. F. & 45 others, Estes, C., Fleischer, J., Groepper, D., Haaxma, C. A., Hempel, M., Holler-Managan, Y., Houge, G., Jackson, A., Kellogg, L., Keren, B., Kiraly-Borri, C., Kraus, C., Kubisch, C., Le Guyader, G., Ljungblad, U. W., Brenman, L. M., Martinez-Agosto, J. A., Might, M., Miller, D. T., Minks, K. Q., Moghaddam, B., Nava, C., Nelson, S. F., Parant, J. M., Prescott, T., Rajabi, F., Randrianaivo, H., Reiter, S. F., Schuurs-Hoeijmakers, J., Shieh, P. B., Slavotinek, A., Smithson, S., Stegmann, A. P. A., Tomczak, K., Tveten, K., Wang, J., Whitlock, J. H., Zweier, C., McWalter, K., Juusola, J., Quintero-Rivera, F., Fischer, U., Yeo, N. C., Kreienkamp, H. J. & Lessel, D., Dec 2021, In: Genome Medicine. 13, 1, 90.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    20 Scopus citations

  • Comprehensive systematic review summary: Treatment of tics in people with Tourette syndrome and chronic tic disorders

    Pringsheim, T., Holler-Managan, Y., Okun, M. S., Jankovic, J., Piacentini, J., Cavanna, A. E., Martino, D., Müller-Vahl, K., Woods, D. W., Robinson, M., Jarvie, E., Roessner, V. & Oskoui, M., May 7 2019, In: Neurology. 92, 19, p. 907-915 9 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    144 Scopus citations

  • GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates

    Ouyang, Q., Kavanaugh, B. C., Joesch-Cohen, L., Dubois, B., Wu, Q., Schmidt, M., Baytas, O., Pastore, S. F., Harripaul, R., Mishra, S., Hussain, A., Kim, K. H., Holler-Managan, Y. F., Ayub, M., Mir, A., Vincent, J. B., Liu, J. S. & Morrow, E. M., Oct 1 2019, In: Human Genetics. 138, 10, p. 1183-1200 18 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    8 Scopus citations

  • New Guidelines: Interpretation, Application and the Future

    Hershey, A. D., Oskoui, M., Pringsheim, T., Holler-Managan, Y., Potrebic, S., Billinghurst, L., Gloss, D., Licking, N., Sowell, M., Victorio, M. C., Gersz, E., Vrijsen, E., Zanitsch, H., Yonker, M., Mack, K., Gelfand, A. A., Szperka, C. L. & Powers, S. W., Sep 1 2019, In: Headache. 59, 8, p. 1133-1143 11 p.

    Research output: Contribution to journal › Editorial › peer-review

    2 Scopus citations
View all 12 Research outputs

  • Additional file 2 of Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders

    Mannucci, I. (Creator), Dang, N. D. P. (Creator), Huber, H. (Creator), Murry, J. B. (Creator), Abramson, J. (Creator), Althoff, T. (Creator), Banka, S. (Creator), Baynam, G. (Creator), Bearden, D. (Creator), Beleza-Meireles, A. (Creator), Benke, P. J. (Creator), Berland, S. (Creator), Bierhals, T. (Creator), Bilan, F. (Creator), Bindoff, L. A. (Creator), Braathen, G. J. (Creator), Busk, Ø. L. (Creator), Chenbhanich, J. (Creator), Denecke, J. (Creator), Escobar, L. F. (Creator), Estes, C. (Creator), Fleischer, J. (Creator), Groepper, D. (Creator), Haaxma, C. A. (Creator), Hempel, M. (Creator), Holler-Managan, Y. (Creator), Houge, G. (Creator), Jackson, A. (Creator), Kellogg, L. (Creator), Keren, B. (Creator), Kiraly-Borri, C. (Creator), Kraus, C. (Creator), Kubisch, C. (Creator), Le Guyader, G. (Creator), Ljungblad, U. W. (Creator), Brenman, L. M. (Creator), Martinez-Agosto, J. A. (Creator), Might, M. (Creator), Miller, D. T. (Creator), Minks, K. Q. (Creator), Moghaddam, B. (Creator), Nava, C. (Creator), Nelson, S. F. (Creator), Parant, J. M. (Creator), Prescott, T. (Creator), Rajabi, F. (Creator), Randrianaivo, H. (Creator), Reiter, S. F. (Creator), Schuurs-Hoeijmakers, J. (Creator), Shieh, P. B. (Creator), Slavotinek, A. (Creator), Smithson, S. (Creator), Stegmann, A. P. A. (Creator), Tomczak, K. (Creator), Tveten, K. (Creator), Wang, J. (Creator), Whitlock, J. H. (Creator), Zweier, C. (Creator), McWalter, K. (Creator), Juusola, J. (Creator), Quintero-Rivera, F. (Creator), Fischer, U. (Creator), Yeo, N. C. (Creator), Kreienkamp, H.-J. (Creator) & Lessel, D. (Creator), figshare, 2021

    DOI: 10.6084/m9.figshare.14643203, https://springernature.figshare.com/articles/dataset/Additional_file_2_of_Genotype_phenotype_correlations_and_novel_molecular_insights_into_the_DHX30-associated_neurodevelopmental_disorders/14643203

    Dataset

  • Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders

    Mannucci, I. (Creator), Dang, N. D. P. (Creator), Huber, H. (Creator), Murry, J. B. (Creator), Abramson, J. (Creator), Althoff, T. (Creator), Banka, S. (Creator), Baynam, G. (Creator), Bearden, D. (Creator), Beleza-Meireles, A. (Creator), Benke, P. J. (Creator), Berland, S. (Creator), Bierhals, T. (Creator), Bilan, F. (Creator), Bindoff, L. A. (Creator), Braathen, G. J. (Creator), Busk, Ø. L. (Creator), Chenbhanich, J. (Creator), Denecke, J. (Creator), Escobar, L. F. (Creator), Estes, C. (Creator), Fleischer, J. (Creator), Groepper, D. (Creator), Haaxma, C. A. (Creator), Hempel, M. (Creator), Holler-Managan, Y. (Creator), Houge, G. (Creator), Jackson, A. (Creator), Kellogg, L. (Creator), Keren, B. (Creator), Kiraly-Borri, C. (Creator), Kraus, C. (Creator), Kubisch, C. (Creator), Le Guyader, G. (Creator), Ljungblad, U. W. (Creator), Brenman, L. M. (Creator), Martinez-Agosto, J. A. (Creator), Might, M. (Creator), Miller, D. T. (Creator), Minks, K. Q. (Creator), Moghaddam, B. (Creator), Nava, C. (Creator), Nelson, S. F. (Creator), Parant, J. M. (Creator), Prescott, T. (Creator), Rajabi, F. (Creator), Randrianaivo, H. (Creator), Reiter, S. F. (Creator), Schuurs-Hoeijmakers, J. (Creator), Shieh, P. B. (Creator), Slavotinek, A. (Creator), Smithson, S. (Creator), Stegmann, A. P. A. (Creator), Tomczak, K. (Creator), Tveten, K. (Creator), Wang, J. (Creator), Whitlock, J. H. (Creator), Zweier, C. (Creator), McWalter, K. (Creator), Juusola, J. (Creator), Quintero-Rivera, F. (Creator), Fischer, U. (Creator), Yeo, N. C. (Creator), Kreienkamp, H.-J. (Creator) & Lessel, D. (Creator), figshare, 2021

    DOI: 10.6084/m9.figshare.c.5434178, https://springernature.figshare.com/collections/Genotype_phenotype_correlations_and_novel_molecular_insights_into_the_DHX30-associated_neurodevelopmental_disorders/5434178

    Dataset