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Lara Mariah Lange

Calculated based on number of publications stored in Pure and citations from PlumX
20212024

Research activity per year

  • 3 Journal articles
  • 1 Comments/Debates
  • 1 Scientific review articles
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Journal articles

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  • 2024

    Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson’s disease study

    Westenberger, A., Skrahina, V., Usnich, T., Beetz, C., Vollstedt, E. J., Laabs, B. H., Paul, J. J., Curado, F., Skobalj, S., Gaber, H., Olmedillas, M., Bogdanovic, X., Ameziane, N., Schell, N., Aasly, J. O., Afshari, M., Agarwal, P., Aldred, J., Alonso-Frech, F. & Anderson, R. & 139 others, Araújo, R., Arkadir, D., Avenali, M., Balal, M., Benizri, S., Bette, S., Bhatia, P., Bonello, M., Braga-Neto, P., Brauneis, S., Cardoso, F. E. C., Cavallieri, F., Classen, J., Cohen, L., Coletta, D., Crosiers, D., Cullufi, P., Dashtipour, K., Demirkiran, M., de Carvalho Aguiar, P., De Rosa, A., Djaldetti, R., Dogu, O., dos Santos Ghilardi, M. G., Eggers, C., Elibol, B., Ellenbogen, A., Ertan, S., Fabiani, G., Falkenburger, B. H., Farrow, S., Fay-Karmon, T., Ferencz, G. J., Fonoff, E. T., Fragoso, Y. D., Genç, G., Gorospe, A., Grandas, F., Gruber, D., Gudesblatt, M., Gurevich, T., Hagenah, J., Hanagasi, H. A., Hassin-Baer, S., Hauser, R. A., Hernández-Vara, J., Herting, B., Hinson, V. K., Hogg, E., Hu, M. T., Hummelgen, E., Hussey, K., Infante, J., Isaacson, S. H., Jauma, S., Koleva-Alazeh, N., Kuhlenbäumer, G., Kühn, A., Litvan, I., López-Manzanares, L., Luxmore, M., Manandhar, S., Marcaud, V., Markopoulou, K., Marras, C., McKenzie, M., Matarazzo, M., Merello, M., Mollenhauer, B., Morgan, J. C., Mullin, S., Musacchio, T., Myers, B., Negrotti, A., Nieves, A., Nitsan, Z., Oskooilar, N., Öztop-Çakmak, Ö., Pal, G., Pavese, N., Percesepe, A., Piccoli, T., de Souza, C. P., Prell, T., Pulera, M., Raw, J., Reetz, K., Reiner, J., Rosenberg, D., Ruiz-Lopez, M., Martinez, J. R., Sammler, E., Santos-Lobato, B. L., Saunders-Pullman, R., Schlesinger, I., Schofield, C. M., Schumacher-Schuh, A. F., Scott, B., Sesar, Á., Shafer, S. J., Sheridan, R., Silverdale, M., Sophia, R., Spitz, M., Stathis, P., Stocchi, F., Tagliati, M., Tai, Y. F., Terwecoren, A., Thonke, S., Tönges, L., Toschi, G., Tumas, V., Urban, P. P., Vacca, L., Vandenberghe, W., Valente, E. M., Valzania, F., Vela-Desojo, L., Weill, C., Weise, D., Wojcieszek, J., Wolz, M., Yahalom, G., Yalcin-Cakmakli, G., Zittel, S., Zlotnik, Y., Kandaswamy, K. K., Balck, A., Hanssen, H., Borsche, M., Lange, L. M., Csoti, I., Lohmann, K., Kasten, M., Brüggemann, N., Rolfs, A., Klein, C. & Bauer, P., 01.08.2024, In: Brain. 147, 8, p. 2652-2667 16 p.

    Research output: Journal Articles › Journal articles › Research › peer-review

  • 2023

    Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2)

    Global Parkinson’s Genetic Program (GP2), 13.09.2023, In: NPJ Parkinson's disease. 9, 1, p. 133

    Research output: Journal Articles › Journal articles › Research › peer-review

  • MDSGene: Extending the List of Isolated Dystonia Genes by VPS16, EIF2AK2, and AOPEP

    Thomsen, M., Lange, L. M., Klein, C. & Lohmann, K., 03.2023, In: Movement disorders : official journal of the Movement Disorder Society. 38, 3, p. 507-508 2 p.

    Research output: Journal Articles › Journal articles › Research › peer-review