Genetics of early onset Parkinson’s disease in Finland: exome sequencing and genome-wide association study

Por Siitonen, A, Nalls, MA, Hernández, D, Gibbs, JR, Ding, J, Ylikotila, P, Edsall, C, Singleton, A, Majamaa, K
Publicado no Neurobiol Aging (2017)

The endocytic membrane trafficking pathway plays a major role in the risk of Parkinson disease

Por Bandres-Ciga, S, Saez-Atienzar, S, Bonet-Ponce, L, Billingsley, K, Vitale, D, Blauwendraat, C, Gibbs, JR, Pihlstrom, L, Gan-Or, Z, Cookson, MR, Nalls, MA, Singleton, AB
Publicado no Mov Disord (2019)

Genome Wide assessment of Parkinson’s disease in a Southern Spanish population

Por Bandrés-Ciga, S, Price, TR, Barrero, FJ, Escamilla-Sevilla, F, Pelegrina, J, Arepalli, S, Hernández, D, Gutiérrez, B, Cervilla, J, Rivera, M, Rivera, AM, Ding, J, Vives, F, Nalls, MA, Singleton, AB, Durán, R
Publicado no Neurobiol Aging (2016)

Multilocus genetic risk score associates with ischemic stroke in case-control and prospective cohort studies

Por Malik, R, Bevan, S, Nalls, MA, Holliday, EG, Devan, WJ, Cheng, YC, Ibrahim-Verbaas, CA, Verhaaren, BF, Bis, JC, Joon, AY, de Stefano, AL, Fornage, M, Psaty, BM, Ikram, MA, Launer, LJ, van Duijn, CM, Sharma, P, Mitchell, BD, Rosand, J, Meschia, JF, Levi, C, Rothwell, PM, Sudlow, C, Markus, HS, Seshadri, S, Dichgans, M
Publicado em 2014

Common genetic variation near the connexin-43 gene is associated with resting heart rate in African Americans: A genome-wide association study of 13,372 participants

Por Deo, R., Nalls, M.A., Avery, C.L., Smith, J.G., Evans, D.S., Keller, M.F., Butler, A.M., Buxbaum, S.G., Li, G., Quibrera, P. Miguel, Smith, E.N., Tanaka, T., Akylbekova, E.L., Alonso, A., Arking, D.E., Benjamin, E.J., Berenson, G.S., Bis, J.C., Chen, L.Y., Chen, W., Cummings, S.R., Ellinor, P.T., Evans, M.K., Ferrucci, L., Fox, E.R., Heckbert, S.R., Heiss, G., Hsueh, W.C., Kerr, K.F., Limacher, M.C., Liu, Y., Lubitz, S.A., Magnani, J.W., Mehra, R., Marcus, G.M., Murray, S.S., Newman, A.B., Njajou, O., North, K.E., Paltoo, D.N., Psaty, B.M., Redline, S.S., Reiner, A.P., Robinson, J.G., Rotter, J.I., Samdarshi, T.E., Schnabel, R.B., Schork, N.J., Singleton, A.B., Siscovick, D., Soliman, E.Z., Sotoodehnia, N., Srinivasan, S.R., Taylor, H.A., Trevisan, M., Zhang, Z., Zonderman, A.B., Newton-Cheh, C., Whitsel, E.A.
Publicado em 2012

MUC5B Promoter Variant and Rheumatoid Arthritis with Interstitial Lung Disease

Por Juge, P.-A., Lee, J.S., Ebstein, E., Furukawa, H., Dobrinskikh, E., Gazal, S., Kannengiesser, C., Ottaviani, S., Oka, S., Tohma, S., Tsuchiya, N., Rojas-Serrano, J., González-Pérez, M.I., Mejía, M., Buendía-Roldán, I., Falfán-Valencia, R., Ambrocio-Ortiz, E., Manali, E., Papiris, S.A., Karageorgas, T., Boumpas, D., Antoniou, K., van Moorsel, C.H.M., van der Vis, J., de Man, Y.A., Grutters, J.C., Wang, Y., Borie, R., Wemeau-Stervinou, L., Wallaert, B., Flipo, R.-M., Nunes, H., Valeyre, D., Saidenberg-Kermanac’h, N., Boissier, M.-C., Marchand-Adam, S., Frazier, A., Richette, P., Allanore, Y., Sibilia, J., Dromer, C., Richez, C., Schaeverbeke, T., Lioté, H., Thabut, G., Nathan, N., Amselem, S., Soubrier, M., Cottin, V., Clément, A., Deane, K., Walts, A.D., Fingerlin, T., Fischer, A., Ryu, J.H., Matteson, E.L., Niewold, T.B., Assayag, D., Gross, A., Wolters, P., Schwarz, M.I., Holers, M., Solomon, J.J., Doyle, T., Rosas, I.O., Blauwendraat, C., Nalls, M.A., Debray, M.-P., Boileau, C., Crestani, B., Schwartz, D.A., Dieudé, P.
Publicado no N Engl J Med (2018)

Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson's

Por Liu, Ganqiang, Boot, Brendon, Locascio, Joseph J., Jansen, Iris E., Winder‐Rhodes, Sophie, Eberly, Shirley, Elbaz, Alexis, Brice, Alexis, Ravina, Bernard, van Hilten, Jacobus J., Cormier‐Dequaire, Florence, Corvol, Jean‐Christophe, Barker, Roger A., Heutink, Peter, Marinus, Johan, Williams‐Gray, Caroline H., Scherzer, Clemens R., Scherzer, C., Hyman, B.T., Ivinson, A.J., Trisini‐Lipsanopoulos, A., Franco, D., Burke, K., Sudarsky, L.R., Hayes, M.T., Umeh, C.C., Growdon, J.H., Schwarzschild, M.A., Hung, A.Y., Flaherty, A.W., Wills, A.‐M., Mejia, N.I., Gomperts, S.N., Khurana, V., Selkoe, D.J., Yi, T., Page, K., Liao, Z., Barker, R., Foltynie, T., Williams‐Gray, C.H., Mason, S., Winder‐Rhodes, S., Barker, R., Williams‐Gray, C.H., Breen, D., Cummins, G., Evans, J., Winder‐Rhodes, S., Corvol, J.‐C., Brice, A., Elbaz, A., Mallet, A., Vidailhet, M., Bonnet, A.‐M., Bonnet, C., Grabli, D., Hartmann, A., Klebe, S., Lacomblez, L., Mangone, G., Bourdain, F., Brandel, J.‐P., Derkinderen, P., Durif, F., Mesnage, V., Pico, F., Rascol, O., Forlani, S., Lesage, S., Tahiri, K., van Hilten, J.J., Marinus, J., Liao, Z., Page, K., Franco, D., Duong, K., Yi, T., Trisini‐Lipsanopoulos, A., Dong, X., Sudarsky, L.R., Hutten, S.J., Amr, S.S., Shoulson, I., Tanner, C.M., Lang, A.E., Nalls, M.A.
Publicado no Ann Neurol (2016)