Calculated based on number of publications stored in Pure and citations from Scopus
20012016

Research activity per year

Search results

  • 2016

    Neural correlates of abnormal sensory discrimination in laryngeal dystonia

    Termsarasab, P., Ramdhani, R. A., Battistella, G., Rubien-Thomas, E., Choy, M., Farwell, I. M., Velickovic, M., Blitzer, A., Frucht, S. J., Reilly, R. B., Hutchinson, M., Ozelius, L. J. & Simonyan, K., 2016, In: NeuroImage: Clinical. 10, p. 18-26 9 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    42 Scopus citations
  • 2014
    1428 Scopus citations
  • What's special about task in dystonia? A voxel-based morphometry and diffusion weighted imaging study

    Ramdhani, R. A., Kumar, V., Velickovic, M., Frucht, S. J., Tagliati, M. & Simonyan, K., Aug 2014, In: Movement Disorders. 29, 9, p. 1141-1150 10 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    56 Scopus citations
  • 2008

    Cervical dystonia: Etiology and pathophysiology

    Singer, C. & Velickovic, M., May 2008, In: Neurologic Clinics. 26, SUPPL.1, p. 9-22 14 p.

    Research output: Contribution to journalArticlepeer-review

    18 Scopus citations
  • Long-term treatment with botulinum toxin type A in cervical dystonia has low immunogenicity by mouse protection assay

    Brin, M. F., Comella, C. L., Jankovic, J., Lai, F., Naumann, M., Ahmed, F., Brashear, A., Chehrenama, M., Erjanti, H., Evatt, M., Gordon, M. F., Grimes, D., Hauser, R., Hefter, H., Hermanowicz, N., Ilmavirta, M., Jennings, D., Jolma, T., Kaiňovský, P. & Knecht, S. & 16 others, Martinez-Castrillo, J. C., Massey, J. M., Molho, E., Miyasaki, J., Rajput, A., Reiners, K., Ružčka, E., Schramm, A., Seeberger, L., Sherman, S., Subramanian, T., Suchowersky, O., Swope, D., Tsui, J., Velickovic, M. & Walker, F., 30 Jul 2008, In: Movement Disorders. 23, 10, p. 1353-1360 8 p.

    Research output: Contribution to journalArticlepeer-review

    179 Scopus citations
  • 2007

    R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation

    Nichols, W. C., Marek, D. K., Pauciulo, M. W., Pankratz, N., Halter, C. A., Rudolph, A., Shults, C. W., Wojcieszek, J., Foroud, T., Shults, C., Marshall, F., Oakes, D., Rudolph, A., Shinaman, A., Marder, K., Conneally, P. M., Halter, C., Lyons, K., Siemers, E. & Factor, S. & 197 others, Higgins, D., Evans, S., Shill, H., Stacy, M., Danielson, J., Marlor, L., Williamson, K., Jankovic, J., Hunter, C., Simon, D., Ryan, P., Scollins, L., Saunders-Pullman, R., Boyar, K., Costan-Toth, C., Ohmann, E., Sudarsky, L., Joubert, C., Friedman, J., Chou, K., Fernandez, H., Lannon, M., Galvez-Jimenez, N., Podichetty, A., Lewitt, P., DeAngelis, M., O'Brien, C., Seeberger, L., Dingmann, C., Judd, D., Marder, K., Fraser, J., Harris, J., Bertoni, J., Peterson, C., Chouinard, S., Panisset, M., Hall, J., Poiffaut, H., Calabrese, V., Roberge, P., Wojcieszek, J., Belden, J., Halter, C., Jennings, D., Marek, K., Mendick, S., Reich, S., Dunlop, B., Jog, M., Horn, C., Rao, J., Cook, M., Uitti, R., Turk, M., Ajax, T., Mannetter, J., Panisset, M., Hall, J., Sethi, K., Carpenter, J., Ligon, K., Narayan, S., Woodward, L., Blindauer, K., Petit, J., Elmer, L., Aiken, E., Davis, K., Schell, C., Wilson, S., Velickovic, M., Koller, W., Phipps, S., Feigin, A., Gordon, M., Hamann, J., Licari, E., Marotta-Kollarus, M., Shannon, B., Winnick, R., Simuni, T., Kaczmarek, A., Williams, K., Wolff, M., Fernandez, M., Hubble, J., Kostyk, S., Campbell, A., Reider, C., Camicioli, R., Carter, J., Andrews, P., Morehouse, S., Stone, C., Mendis, T., Grimes, D., Gray, P., Haas, K., Sutton, J., Hutchinson, B., Young, J., Rajput, A., Rajput, A., Klassen, L., Shirley, T., Manyam, B., Simpson, P., Whetteckey, J., Wulbrecht, B., Truong, D., Pathak, M., Luong, N., Tra, T., Tran, A., Vo, J., Lang, A., Kleiner-Fisman, G., Nieves, A., So, J., Podskalny, G., Giffin, L., Atchison, P., Allen, C., Martin, W., Wieler, M., Suchowersky, O., Klimek, M., Hermanowicz, N., Niswonger, S., Shults, C., Fontaine, D., Aminoff, M., Christine, C., Diminno, M., Hevezi, J., Dalvi, A., Kang, U., Richman, J., Uy, S., Young, J., Dalvi, A., Sahay, A., Schwieterman, D., Leehey, M., Culver, S., Derian, T., Demarcaida, T., Belber, S., Rodnitzky, R., Dobson, J., Pahwa, R., Lyons, K., Gales, T., Thomas, S., Shulman, L., Weiner, W., Dustin, K., Singer, C., Koller, W., Lyons, K., Weiner, W., Zelaya, L., Tuite, P., Hagen, V., Rolandelli, S., Schacherer, R., Gordon, P., Werner, J., Serrano, C., Roque, S., Kurlan, R., Berry, D., Gardiner, I., Hauser, R., Sanchez-Ramos, J., Zesiewicz, T., Delgado, H., Price, K., Rodriguez, P., Pfeiffer, R., Davis, L., Pfeiffer, B., Dewey, R., Hayward, B., Meacham, M., Walker, F., Hunt, V., Racette, B., Good, L., Rundle, M., Watts, A., Wang, A., Ross, T., Bennett, S., Kamp, D. & Julian-Baros, E., 15 Jan 2007, In: Movement Disorders. 22, 2, p. 254-256 3 p.

    Research output: Contribution to journalArticlepeer-review

    7 Scopus citations
  • 2006

    Mutations in LRRK2 other than G2019S are rare in a north-American based sample of familial Parkinson's didease

    Pankratz, N., Pauciulo, M. W., Elsaesser, V. E., Marek, D. K., Halter, C. A., Rudolph, A., Shults, C. W., Foroud, T., Nichols, W. C., Shults, C., Marshall, F., Oakes, D., Shinaman, A., Marder, K., Conneally, P. M., Lyons, K., Siemers, E., Factor, S., Higgins, D. & Evans, S. & 79 others, Shill, H., Stacy, M., Danielson, J., Marlor, L., Williamson, K., Jankovic, J., Hunter, C., Simon, D., Ryan, P., Scollins, L., Saunders-Pullman, R., Boyar, K., Costan-Toth, C., Ohmann, E., Sudarsky, L., Joubert, C., Friedman, J., Chou, K., Fernandez, H., Lannon, M., Galvez-Jimenez, N., Podichetty, A., Lewitt, P., DeAngelis, M., O'Brien, C., Seeberger, L., Dingmann, C., Judd, D., Fraser, J., Harris, J., Bertoni, J., Peterson, C., Chouinard, S., Panisset, M., Hall, J., Poiffaut, H., Calabrese, V., Roberge, P., Wojcieszek, J., Belden, J., Halter, C., Jennings, D., Marek, K., Mendick, S., Reich, S., Dunlop, B., Jog, M., Horn, C., Rao, J., Cook, M., Uitti, R., Turk, M., Ajax, T., Mannetter, J., Sethi, K., Carpenter, J., Ligon, K., Narayan, S., Woodward, L., Blindauer, K., Petit, J., Elmer, L., Aiken, E., Davis, K., Schell, C., Wilson, S., Velickovic, M., Koller, W., Phipps, S., Feigin, A., Gordon, M., Hamann, J., Licari, E., Marotta-Kollarus, M., Shannon, B., Winnick, R., Simuni, T., Kaczmarek, A. & Williams, K., Dec 2006, In: Movement Disorders. 21, 12, p. 2257-2260 4 p.

    Research output: Contribution to journalArticlepeer-review

    28 Scopus citations
  • 2004

    Corticospinal excitability accompanying ballistic wrist movements in primary dystonia

    MacKinnon, C. D., Velickovic, M., Drafta, C., Hesquijarosa, A. & Brin, M. F., Mar 2004, In: Movement Disorders. 19, 3, p. 273-284 12 p.

    Research output: Contribution to journalReview articlepeer-review

    19 Scopus citations
  • Parkinson's disease without expected neuropathologic abnormality

    Velickovic, M., Lesser, G., Purohit, D., Neufeld, R. R., Tarshish, C. Y. & Libow, L. S., 2004, In: Journal of the American Medical Directors Association. 5, 6, p. 407-409 3 p.

    Research output: Contribution to journalArticlepeer-review

    3 Scopus citations
  • 2003

    Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families

    Pankratz, N., Nichols, W. C., Uniacke, S. K., Halter, C., Murrell, J., Rudolph, A., Shults, C. W., Conneally, P. M., Foroud, T., Truong, D., Pathak, M., Tran, A., Rodnitzky, R., Dobson, J., Koller, W., Weiner, W., Lyons, K., Kurlan, R., Berry, D. & Bertoni, J. & 71 others, Peterson, C., Martin, W., Wieler, M., Tuite, P., Schacherer, R., Marder, K., Harris, J., Jankovic, J., Hunter, C., Lang, A., Kleimer-Fisman, G., Nieves, A., So, J., Factor, S., Evans, S., Manyam, B., Wulbrecht, B., Walker, F., Hunt, V., Gordon, M. F., Hamman, J., Kang, U. J., Young, J., Blindauer, K., Petit, J., Rao, J., Cook, M., Stacy, M., Williamson, K., Pullman, R. S., Boyar, K., Leehey, M., Derian, T., Gordon, P., Werner, J., Racette, B., Good, L., Simon, D., Scollins, L., Schwieterman, D., Dewey, R., Meacham, M., Sutton, J., Hutchinson, B., Jog, M., Horn, C., Sethi, K., Carpenter, J., Atchison, P., Rolli, S., Sudarsky, L., Corwin, C., Velickovic, M., Phipps, S., Simuni, T., Kaczmarek, A., Hermanowicz, N., Niswonger, S., Feigin, A., Shannon, B., Calabrese, V., Roberge, P., Homes, H., Shulman, L., Dustin, K., Ajax, T., Mannetter, J., Podskalny, G. D., Giffin, L., Uitti, R. & Turk, M. F., 15 Oct 2003, In: Human Molecular Genetics. 12, 20, p. 2599-2608 10 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    130 Scopus citations
  • 2002

    Autonomic cardiovascular reflexes in Wilson's disease

    Bhattacharya, K., Velickovic, M., Schilsky, M. & Kaufmann, H., 2002, In: Clinical Autonomic Research. 12, 3, p. 190-192 3 p.

    Research output: Contribution to journalArticlepeer-review

    20 Scopus citations
  • Clinical findings of a myoclonus-dystonia family with two distinct mutations

    Doheny, D., Danisi, F., Smith, C., Morrison, C., Velickovic, M., De Leon, D., Bressman, S. B., Leung, J., Ozelius, L., Klein, C., Breakefield, X. O., Brin, M. F. & Silverman, J. M., 22 Oct 2002, In: Neurology. 59, 8, p. 1244-1246 3 p.

    Research output: Contribution to journalArticlepeer-review

    51 Scopus citations
  • Open Access
    154 Scopus citations
  • Linkage stratification and mutation analysis at the parkin locus identifies mutation positive Parkinson's disease families [1]

    Nichols, W. C., Pankratz, N., Uniacke, S. K., Pauciulo, M. W., Halter, C., Rudolph, A., Conneally, P. M., Foroud, T., Carter, J., Camicioli, R., Wojcieszek, J., Fernandez, M., Hubble, J., Rajput, A., Panisset, M., Mendis, T., Grimes, D. A., Serrano Ramos, C., Reich, S. & Hauser, R. & 53 others, Sanchez-Ramos, J., Zesiewicz, T., Pfeiffer, R., Friedman, J., Fernandez, H., Shults, C., Seeberger, L., O'Brien, C., Pahwa, R., Elmer, L., Jennings, D., Marek, K., Truong, D., Pathak, M., Rodnitzyk, R., Kurlan, R., Tuite, P., Aminoff, M., Marder, K., Lewitt, P., Koller, W., Martin, W., Jankovic, J., Bertoni, J., Factor, S., Walker, F., Jung Kang, U., Stacy, M., Simon, D., Blindauer, K., Manyam, B., Nieves, A., Velickovic, M., Gordon, M. F., Leehey, M., Gordon, P., Rao, J., Dalvi, A., Racette, B., Sethi, K., Sudarsky, L., Saunders Pullman, R., Simuni, T., Dewey, R., Hermanowicz, N., Feigin, A., Calabresse, V., Sutton, J., Ajax, T., Podakalny, G. D., Suchowersky, O., Uitti, R. & Shulman, L., 2002, In: Journal of Medical Genetics. 39, 7, p. 489-492 4 p.

    Research output: Contribution to journalLetterpeer-review

    51 Scopus citations
  • Movement disorders: Keys to identifying and treating tremor

    Velickovic, M. & Gracies, J. M., 2002, In: Geriatrics. 57, 7, p. 32-36 5 p.

    Research output: Contribution to journalReview articlepeer-review

    8 Scopus citations
  • ε-sarcoglycan mutations found in combination with other dystonia gene mutations

    Klein, C., Liu, L., Doheny, D., Kock, N., Müller, B., De Carvalho Aguiar, P., Leung, J., De Leon, D., Bressman, S. B., Silverman, J., Smith, C., Danisi, F., Morrison, C., Walker, R. H., Velickovic, M., Schwinger, E., Kramer, P. L., Breakefield, X. O., Brin, M. F. & Ozelius, L. J., 1 Nov 2002, In: Annals of Neurology. 52, 5, p. 675-679 5 p.

    Research output: Contribution to journalArticlepeer-review

    85 Scopus citations
  • 2001

    Cervical Dystonia: Pathophysiology and Treatment Options

    Velickovic, M., Benabou, R. & Brin, M. F., 2001, In: Drugs. 61, 13, p. 1921-1943 23 p.

    Research output: Contribution to journalArticlepeer-review

    67 Scopus citations
  • Myoclonus

    Abbasi, S., Velickovic, M. & Brin, M. F., 2001, In: Neurologist. 7, 3, p. 171-179 9 p.

    Research output: Contribution to journalReview articlepeer-review

    1 Scopus citations