Calculated based on number of publications stored in Pure and citations from Scopus
20112024

Research activity per year

Personal profile

Expertise related to UN Sustainable Development Goals

In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):

  • SDG 3 - Good Health and Well-being

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Collaborations and top research areas from the last five years

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  • A Novel Variant in SQSTM1 Gene Causing Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy in a Peruvian Family

    Chacaltana-Vinas, C., Ramirez-Pajares, P., Manrique-Palomino, A., Clause, A. R., Chawla, A., Thorpe, E., Taft, R., Rivera-Valdivia, A., Sarapura-Castro, E., Bazalar-Montoya, J. & Cornejo-Olivas, M., 2024, (Accepted/In press) In: Movement Disorders Clinical Practice.

    Research output: Contribution to journalLetterpeer-review

  • Frequency of Hereditary and GBA1-Related Parkinsonism in Latin America: A Systematic Review and Meta-Analysis

    Saffie Awad, P., Teixeira-dos-Santos, D., Santos-Lobato, B. L., Camargos, S., Cornejo-Olivas, M., de Mello Rieder, C. R., Mata, I. F., Chaná-Cuevas, P., Klein, C. & Schumacher Schuh, A. F., Jan 2024, In: Movement Disorders. 39, 1, p. 6-16 11 p.

    Research output: Contribution to journalReview articlepeer-review

    Open Access
    1 Scopus citations
  • Genetic Testing for Parkinson's Disease and Movement Disorders in Less Privileged Areas: Barriers and Opportunities

    Tan, A. H., Cornejo-Olivas, M., Okubadejo, N., Pal, P. K., Saranza, G., Saffie-Awad, P., Ahmad-Annuar, A., Schumacher-Schuh, A. F., Okeng'o, K., Mata, I. F., Gatto, E. M. & Lim, S. Y., Jan 2024, In: Movement Disorders Clinical Practice. 11, 1, p. 14-20 7 p.

    Research output: Contribution to journalArticlepeer-review

    1 Scopus citations
  • Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease

    Kim, J. J., Vitale, D., Otani, D. V., Lian, M. M., Heilbron, K., Aslibekyan, S., Auton, A., Babalola, E., Bell, R. K., Bielenberg, J., Bryc, K., Bullis, E., Cannon, P., Coker, D., Partida, G. C., Dhamija, D., Das, S., Elson, S. L., Eriksson, N., Filshtein, T., & 279 othersFitch, A., Fletez-Brant, K., Fontanillas, P., Freyman, W., Granka, J. M., Hernandez, A., Hicks, B., Hinds, D. A., Jewett, E. M., Jiang, Y., Kukar, K., Kwong, A., Lin, K. H., Llamas, B. A., Lowe, M., McCreight, J. C., McIntyre, M. H., Micheletti, S. J., Moreno, M. E., Nandakumar, P., Nguyen, D. T., Noblin, E. S., O’Connell, J., Petrakovitz, A. A., Poznik, G. D., Reynoso, A., Schloetter, M., Schumacher, M., Shastri, A. J., Shelton, J. F., Shi, J., Shringarpure, S., Su, Q. J., Tat, S. A., Tchakouté, C. T., Tran, V., Tung, J. Y., Wang, X., Wang, W., Weldon, C. H., Wilton, P., Wong, C. D., Iwaki, H., Lake, J., Solsberg, C. W., Leonard, H., Makarious, M. B., Tan, E. K., Singleton, A. B., Bandres-Ciga, S., Noyce, A. J., Gatto, E. M., Kauffman, M., Khachatryan, S., Tavadyan, Z., Shepherd, C. E., Hunter, J., Kumar, K., Ellis, M., Rentería, M. E., Koks, S., Zimprich, A., Schumacher-Schuh, A. F., Rieder, C., Awad, P. S., Tumas, V., Camargos, S., Fon, E. A., Monchi, O., Fon, T., Galleguillos, B. P., Miranda, M., Bustamante, M. L., Olguin, P., Chana, P., Tang, B., Shang, H., Guo, J., Chan, P., Luo, W., Arboleda, G., Orozc, J., del Rio, M. J., Hernandez, A., Salama, M., Kamel, W. A., Zewde, Y. Z., Brice, A., Corvol, J. C., Westenberger, A., Illarionova, A., Mollenhauer, B., Klein, C., Vollstedt, E. J., Hopfner, F., Höglinger, G., Madoev, H., Trinh, J., Junker, J., Lohmann, K., Lange, L. M., Sharma, M., Groppa, S., Gasser, T., Fang, Z. H., Akpalu, A., Xiromerisiou, G., Hadjigorgiou, G., Dagklis, I., Tarnanas, I., Stefanis, L., Stamelou, M., Dadiotis, E., Medina, A., Chan, G. H. F., Ip, N., Cheung, N. Y. F., Chan, P., Zhou, X., Kishore, A., Divya, K. P., Pal, P., Kukkle, P. L., Rajan, R., Borgohain, R., Salari, M., Quattrone, A., Valente, E. M., Parnetti, L., Avenali, M., Schirinzi, T., Funayama, M., Hattori, N., Shiraishi, T., Karimova, A., Kaishibayeva, G., Shambetova, C., Krüger, R., Tan, A. H., Ahmad-Annuar, A., Norlinah, M. I., Murad, N. A. A., Azmin, S., Lim, S. Y., Mohamed, W., Tay, Y. W., Martinez-Ramirez, D., Rodriguez-Violante, M., Reyes-Pérez, P., Tserensodnom, B., Ojha, R., Anderson, T. J., Pitcher, T. L., Sanyaolu, A., Okubadejo, N., Ojo, O., Aasly, J. O., Pihlstrøm, L., Tan, M., Ur-Rehman, S., Veliz-Otani, D., Cornejo-Olivas, M., Doquenia, M. L., Rosales, R., Vinuela, A., Iakovenko, E., Mubarak, B. A., Umair, M., Amod, F., Carr, J., Bardien, S., Jeon, B., Kim, Y. J., Cubo, E., Alvarez, I., Hoenicka, J., Beyer, K., Periñan, M. T., Pastor, P., El-Sadig, S., Brolin, K., Zweier, C., Tinkhauser, G., Krack, P., Lin, C. H., Wu, H. C., Kung, P. J., Wu, R. M., Wu, Y., Amouri, R., Sassi, S. B., Başak, A. N., Genc, G., Çakmak, Ö. Ö., Ertan, S., Martínez-Carrasco, A., Schrag, A., Schapira, A., Carroll, C., Bale, C., Grosset, D., Stafford, E. J., Houlden, H., Morris, H. R., Hardy, J., Mok, K. Y., Rizig, M., Wood, N., Williams, N., Okunoye, O., Lewis, P. A., Kaiyrzhanov, R., Weil, R., Love, S., Stott, S., Jasaityte, S., Dey, S., Obese, V., Espay, A., O’Grady, A., Sobering, A. K., Siddiqi, B., Casey, B., Fiske, B., Jonas, C., Cruchaga, C., Pantazis, C. B., Comart, C., Wegel, C., Hall, D., Hernandez, D., Shiamim, E., Riley, E., Faghri, F., Serrano, G. E., Chen, H., Mata, I. F., Sarmiento, I. J. K., Williamson, J., Jankovic, J., Shulman, J., Solle, J. C., Murphy, K., Nuytemans, K., Kieburtz, K., Markopoulou, K., Marek, K., Levine, K. S., Chahine, L. M., Ibanez, L., Screven, L., Ruffrage, L., Shulman, L., Marsili, L., Kuhl, M., Dean, M., Koretsky, M., Puckelwartz, M. J., Inca-Martinez, M., Louie, N., Mencacci, N. E., Albin, R., Alcalay, R., Walker, R., Chowdhury, S., Dumanis, S., Lubbe, S., Xie, T., Foroud, T., Beach, T., Sherer, T., Song, Y., Nguyen, D., Nguyen, T., Atadzhanov, M., Blauwendraat, C., Nalls, M. A., Foo, J. N. & Mata, I., Jan 2024, In: Nature Genetics. 56, 1, p. 27-36 10 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    6 Scopus citations
  • Spinocerebellar ataxia type 2 has multiple ancestral origins

    Rede Neurogenetica, Mar 2024, In: Parkinsonism and Related Disorders. 120, 105985.

    Research output: Contribution to journalArticlepeer-review

    Open Access