Reduced neutrophil count in people of African descent is due to a regulatory variant in the Duffy antigen receptor for chemokines gene

by Reich D., Nalls M.A., Kao W.H.L., Akylbekova E.L., Tandon A., Patterson N., Mullikin J., Hsueh W.-C., Cheng C.-Y., Coresh J., Boerwinkle E., Li M., Waliszewska A., Neubauer J., Li R., Leak T.S., Ekunwe L., Files J.C., Hardy C.L., Zmuda J.M., Taylor H.A., Ziv E., Harris T.B., Wilson J.G.
Published 2018

Genetic variation at 16q24.2 is associated with small vessel stroke

by Traylor, M, Malik, R, Nalls, M.A
Published 2020

Genetic comorbidities in Parkinson's disease

by Nalls, M.A., Saad, M., Noyce, A.J., Keller, M.F., Schrag, A., Bestwick, J.P., Traynor, B.J., Gibbs, J.R., Hernandez, D.G., Cookson, M.R., Morris, H.R., Williams, N., Gasser, T., Heutink, P., Wood, N., Hardy, J., Martinez, M., Singleton, A.B., IPDGC, WTCCC2, NABEC, UKBEC
Published 2014

Admixture mapping of 15,280 African Americans identifies obesity susceptibility loci on chromosomes 5 and X

by Cheng C.-Y., Kao W.H.L., Patterson N., Tandon A., Haiman C.A., Harris T.B., Xing C., John E.M., Ambrosone C.B., Brancati F.L., Coresh J., Press M.F., Parekh R.S., Klag M.J., Meoni L.A., Hsueh W.-C., Fejerman L., Pawlikowska L., Freedman M.L., Jandorf L.H., Bandera E.V., Ciupak G.L., Nalls M.A., Akylbekova E.L., Orwoll E.S., Leak T.S., Miljkovic I., Li R., Ursin G., Bernstein L., Ardlie K., Taylor H.A., Boerwinckle E., Zmuda J.M., Henderson B.E., Wilson J.G., Reich D.
Published 2018

Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease

by Beilina, A., Rudenko, I.N., Kaganovich, A., Civiero, L., Chau, H., Kalia, S.K., Kalia, L.V., Lobbestael, E., Chi, R., Ndukwe, K., Ding, J., Nalls, M.A., Olszewski, M., Hauser, D.N., Kumaran, R., Lozano, A.M., Baekelandt, V., Greene, L.E., Taymans, J.M., Greggio, E., Cookson, M.R., Int Parkinson's Dis Genomics Conso, North Amer Brain Expression Consor
Published 2014

Genome-Wide Association Study of Retinopathy in Individuals without Diabetes

by Jensen, R.A., Sim, X., Li, X., Cotch, M.F., Ikram, M.K., Holliday, E.G., Eiriksdottir, G., Harris, T.B., Jonasson, F., Klein, B.E.K., Launer, L.J., Smith, A.V., Boerwinkle, E., Cheung, N., Hewitt, A.W., Liew, G., Mitchell, P., Wang, J.J., Attia, J., Scott, R., Glazer, N.L., Lumley, T., McKnight, B., Psaty, B.M., Taylor, K., Hofman, A., de Jong, P.T.V.M., Rivadeneira, F., Uitterlinden, A.G., Tay, W.-T., Teo, Y.Y., Seielstad, M., Liu, J., Cheng, C.-Y., Saw, S.-M., Aung, T., Ganesh, S.K., O'Donnell, C.J., Nalls, M.A., Wiggins, K.L., Kuo, J.Z., van Duijn, C.M., Gudnason, V., Klein, R., Siscovick, D.S., Rotter, J.I., Tai, E.S., Vingerling, J., Wong, T.Y.
Published 2014

Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing

by Jansen, I.E., Ye, H., Heetveld, S., Lechler, M.C., Michels, H., Seinstra, R.I., Lubbe, S.J., Drouet, V., Lesage, S., Majounie, E., Gibbs, J.R., Nalls, M.A., Ryten, M., Botia, J.A., Vandrovcova, J., Simon-Sanchez, J., Castillo-Lizardo, M., Rizzu, P., Blauwendraat, C., Chouhan, A.K., Li, Y.R., Yogi, P., Amin, N., Duijn, C.M. van, Morris, H.R., Brice, A., Singleton, A.B., David, D.C., Nollen, E.A., Jain, S., Shulman, J.M., Heutink, P., IPGDC
Published 2017

Loss of VPS1 3C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

by Lesage, S., Drouet, V., Majounie, E., Deramecourt, V., Jacoupy, M., Nicolas, A., Cormier-Dequaire, F., Hassoun, S.M., Pujol, C., Ciura, S., Erpapazoglou, Z., Usenko, T., Maurage, C.A., Sahbatou, M., Liebau, S., Ding, J.H., Bilgic, B., Emre, M., Erginel-Unaltuna, N., Guven, G., Tison, F., Tranchant, C., Vidailhet, M., Corvol, J.C., Krack, P., Leutenegger, A.L., Nalls, M.A., Hernandez, D.G., Heutink, P., Gibbs, J.R., Hardy, J., Wood, N.W., Gasser, T., Durr, A., Deleuze, J.F., Tazir, M., Destee, A., Lohmann, E., Kabashi, E., Singleton, A., Corti, O., Brice, A., French Parkinson's Dis Genetics St, IPDGC
Published 2016

NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases

by Nalls, M.A., Bras, J., Hernandez, D.G., Keller, M.F., Majounie, E., Renton, A.E., Saad, M., Jansen, I., Guerreiro, R., Lubbe, S., Plagnol, V., Gibbs, J.R., Schulte, C., Pankratz, N., Sutherland, M., Bertram, L., Lill, C.M., DeStefano, A.L., Faroud, T., Eriksson, N., Tung, J.Y., Edsall, C., Nichols, N., Brooks, J., Arepalli, S., Pliner, H., Letson, C., Heutink, P., Martinez, M., Gasser, T., Traynor, B.J., Wood, N., Hardy, J., Singleton, A.B., Int Parkinson's Dis Genomics Conso, Parkinson's Dis Meta-Anal Consorti
Published 2015

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease

by Sidransky, E., Nalls, M.A., Aasly, J.O., Aharon-Peretz, J., Annesi, G., Barbosa, E.R., Bar-Shira, A., Berg, D., Bras, J., Brice, A., Chen, C.-M., Clark, L.N., Condroyer, C., De Marco, E.V., Dürr, A., Eblan, M.J., Fahn, S., Farrer, M.J., Fung, H.-C., Gan-Or, Z., Gasser, T., Gershoni-Baruch, R., Giladi, N., Griffith, A., Gurevich, T., Januario, C., Kropp, P., Lang, A.E., Lee-Chen, G.-J., Lesage, S., Marder, K., Mata, I.F., Mirelman, A., Mitsui, J., Mizuta, I., Nicoletti, G., Oliveira, C., Ottman, R., Orr-Urtreger, A., Pereira, L.V., Quattrone, A., Rogaeva, E., Rolfs, A., Rosenbaum, H., Rozenberg, R., Samii, A., Samaddar, T., Schulte, C., Sharma, M., Singleton, A., Spitz, M., Tan, E.-K., Tayebi, N., Toda, T., Troiano, A.R., Tsuji, S., Wittstock, M., Wolfsberg, T.G., Wu, Y.-R., Zabetian, C.P., Zhao, Y., Ziegler, S.G.
Published 2014

Genetic risk of Parkinson disease and progression: An analysis of 13 longitudinal cohorts

by Iwaki, H., Blauwendraat, C., Leonard, H.L., Liu, G.Q., Maple-Grodem, J., Corvol, J.C., Pihlstrom, L., Nimwegen, M. van, Hutten, S.J., Nguyen, K.D.H., Rick, J., Eberly, S., Faghri, F., Auinger, P., Scott, K.M., Wijeyekoon, R., Deerlin, V.M. van, Hernandez, D.G., Day-Williams, A.G., Brice, A., Alves, G., Noyce, A.J., Tysnes, O.B., Evans, J.R., Breen, D.P., Estrada, K., Wegel, C.E., Danjou, F., Simon, D.K., Ravina, B., Toft, M., Heutink, P., Bloem, B.R., Weintraub, D., Barker, R.A., Williams-Gray, C.H., Warrenburg, B.P. van de, Hilten, J.J. van, Scherzer, C.R., Singleton, A.B., Nalls, M.A.
Published 2019

Genome-Wide Association Analysis Identifies Variants Associated with Nonalcoholic Fatty Liver Disease That Have Distinct Effects on Metabolic Traits

by Speliotes, E.K., Yerges-Armstrong, L.M., Wu, J., Hernaez, R., Kim, L.J., Palmer, C.D., Gudnason, V., Eiriksdottir, G., Garcia, M.E., Launer, L.J., Nalls, M.A., Clark, J.M., Mitchell, B.D., Shuldiner, A.R., Butler, J.L., Tomas, M., Hoffmann, U., Hwang, S.J., Massaro, J.M., O'Donnell, C.J., Sahani, D.V., Salomaa, V., Schadt, E.E., Schwartz, S.M., Siscovick, D.S., Voight, B.F., Carr, J.J., Feitosa, M.F., Harris, T.B., Fox, C.S., Smith, A.V., Kao, W.H.L., Hirschhorn, J.N., Borecki, I.B., NASH CRN, GIANT Consortium, MAGIC Investigators, GOLD Consortium
Published 2011

Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and alpha-synuclein mechanisms

by Blauwendraat, C., Heilbron, K., Vallerga, C.L., Bandres-Ciga, S., Coelln, R. von, Pihlstrom, L., Simon-Sanchez, J., Schulte, C., Sharma, M., Krohn, L., Siitonen, A., Iwaki, H., Leonard, H., Noyce, A.J., Tan, M., Gibbs, J.R., Hernandez, D.G., Scholz, S.W., Jankovic, J., Shulman, L.M., Lesage, S., Corvol, J.C., Brice, A., Hilten, J.J. van, Marinus, J., Eerola-Rautio, J., Tienari, P., Majamaa, K., Toft, M., Grosset, D.G., Gasser, T., Heutink, P., Shulman, J.M., Wood, N., Hardy, J., Morris, H.R., Hinds, D.A., Gratten, J., Visscher, P.M., Gan-Or, Z., Nalls, M.A., Singleton, A.B., 23andMe Res Team, IPDGC
Published 2019

Systematic identification of trans eQTLs as putative drivers of known disease associations

by Westra, H.J., Peters, M.J., Esko, T., Yaghootkar, H., Schurmann, C., Kettunen, J., Christiansen, M.W., Fairfax, B.P., Schramm, K., Powell, J.E., Zhernakova, A., Zhernakova, D.V., Veldink, J.H., Berg, L.H. van den, Karjalainen, J., Withoff, S., Uitterlinden, A.G., Hofman, A., Rivadeneira, F., Hoen, P.A.C. 't, Reinmaa, E., Fischer, K., Nelis, M., Milani, L., Melzer, D., Ferrucci, L., Singleton, A.B., Hernandez, D.G., Nalls, M.A., Homuth, G., Nauck, M., Radke, D., Volker, U., Perola, M., Salomaa, V., Brody, J., Suchy-Dicey, A., Gharib, S.A., Enquobahrie, D.A., Lumley, T., Montgomery, G.W., Makino, S., Prokisch, H., Herder, C., Roden, M., Grallert, H., Meitinger, T., Strauch, K., Li, Y., Jansen, R.C., Visscher, P.M., Knight, J.C., Psaty, B.M., Ripatti, S., Teumer, A., Frayling, T.M., Metspalu, A., Meurs, J.B.J. van, Franke, L.
Published 2013

Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts

by Iwaki, H., Blauwendraat, C., Leonard, H.L., Kim, J.J., Liu, G.Q., Maple-Grodem, J., Corvol, J.C., Pihlstrom, L., Nimwegen, M. van, Hutten, S.J., Nguyen, K.D.H., Rick, J., Eberly, S., Faghri, F., Auinger, P., Scott, K.M., Wijeyekoon, R., Deerlin, V.M. van, Hernandez, D.G., Gibbs, J.R., Chitrala, K.N., Day-Williams, A.G., Brice, A., Alves, G., Noyce, A.J., Tysnes, O.B., Evans, J.R., Breen, D.P., Estrada, K., Wegel, C.E., Danjou, F., Simon, D.K., Andreassen, O., Ravina, B., Toft, M., Heutink, P., Bloem, B.R., Weintraub, D., Barker, R.A., Williams-Gray, C.H., Warrenburg, B.P. van de, Hilten, J.J. van, Scherzer, C.R., Singleton, A.B., Nalls, M.A., Int Parkinson's Dis Genomics Cons
Published 2019

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

by Nalls, M.A., Pankratz, N., Lill, C.M., , C.B. do, Hernandez, D.G., Saad, M., DeStefano, A.L., Kara, E., Bras, J., Sharma, M., Schulte, C., Keller, M.F., Arepalli, S., Letson, C., Edsall, C., Stefansson, H., Liu, X., Pliner, H., Lee, J.H., Cheng, R., Ikram, M.A., Ioannidis, J.P.A., Hadjigeorgiou, G.M., Bis, J.C., Martinez, M., Perlmutter, J.S., Goate, A., Marder, K., Fiske, B., Sutherland, M., Xiromerisiou, G., Myers, R.H., Clark, L.N., Stefansson, K., Hardy, J.A., Heutink, P., Chen, H., Wood, N.W., Houlden, H., Payami, H., Brice, A., Scott, W.K., Gasser, T., Bertram, L., Eriksson, N., Foroud, T., Singleton, A.B., IPDG, GParkinson's Study Grp PSG Parkins, 23AndMe, GenePD, NGRC, HIHG, Ashkenazi Jewish Dataset Investiga, CHARGE, NABEC, UKBEC, Greek Parkinson's Dis Consortium, Alzheimer Genetic Analysis Gr
Published 2014

Is the adiposity-associated FTO gene variant related to all-cause mortality independent of adiposity? Meta-analysis of data from 169,551 Caucasian adults

by Zimmermann, E., Angquist, L.H., Mirza, S.S., Zhao, J.H., Chasman, D.I., Fischer, K., Qi, Q., Smith, A.V., Thinggaard, M., Jarczok, M.N., Nalls, M.A., Trompet, S., Timpson, N.J., Schmidt, B., Jackson, A.U., Lyytikainen, L.P., Verweij, N., Mueller-Nurasyid, M., Vikstrom, M., Marques-Vidal, P., Wong, A., Meidtner, K., Middelberg, R.P., Strawbridge, R.J., Christiansen, L., Kyvik, K.O., Hamsten, A., Jaaskelainen, T., Tjonneland, A., Eriksson, J.G., Whitfield, J.B., Boeing, H., Hardy, R., Vollenweider, P., Leander, K., Peters, A., Harst, P. van der, Kumari, M., Lehtimaki, T., Meirhaeghe, A., Tuomilehto, J., Jockel, K.H., Ben-Shlomo, Y., Sattar, N., Baumeister, S.E., Smith, G.D., Casas, J.P., Houston, D.K., Marz, W., Christensen, K., Gudnason, V., Hu, F.B., Metspalu, A., Ridker, P.M., Wareham, N.J., Loos, R.J.F., Tiemeier, H., Sonestedt, E., Sorensen, T.I.A., The FTO-Mortality Collaborating
Published 2015

Genome-Wide Interactions with Dairy Intake for Body Mass Index in Adults of European Descent

by Smith, C.E., Follis, J.L., Dashti, H.S., Tanaka, T., Graff, M., Fretts, A.M., Kilpelainen, T.O., Wojczynski, M.K., Richardson, K., Nalls, M.A., Schulz, C.A., Liu, Y.M., Frazier-Wood, A.C., Eekelen, E. van, Wang, C., Vries, P.S. de, Mikkila, V., Rohde, R., Psaty, B.M., Hansen, T., Feitosa, M.F., Lai, C.Q., Houston, D.K., Ferruci, L., Ericson, U., Wang, Z., Mutsert, R. de, Oddy, W.H., Jonge, E.A.L. de, Seppala, I., Justice, A.E., Lemaitre, R.N., Sorensen, T.I.A., Province, M.A., Parnell, L.D., Garcia, M.E., Bandinelli, S., Orho-Melander, M., Rich, S.S., Rosendaal, F.R., Pennell, C.E., Kiefte-de Jong, J.C., Kahonen, M., Young, K.L., Pedersen, O., Aslibekyan, S., Rotter, J.I., Mook-Kanamori, D.O., Zillikens, M.C., Raitakari, O.T., North, K.E., Overvad, K., Arnett, D.K., Hofman, A., Lehtimaki, T., Tjonneland, A., Uitterlinden, A.G., Rivadeneira, F., Franco, O.H., German, J.B., Siscovick, D.S., Cupples, L.A., Ordovas, J.M.
Published 2018

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies

by Traylor, M., Farrall, M., Holliday, E.G., Sudlow, C., Hopewell, J.C., Cheng, Y.C., Fomage, M., Ikram, M.A., Malik, R., Bevan, S., Thorsteinsdottir, U., Nalls, M.A., Longstreth, W.T., Wiggins, K.L., Yadav, S., Parati, E.A., DeStefano, A.L., Worrall, B.B., Kittner, S., Khan, M.S., Reiner, A.P., Helgadottir, A., Achterberg, S., Fernandez-Cadenas, I., Abboud, S., Schmidt, R., Walters, M., Chen, W.M., Ringelstein, E.B., O'Donnell, M., Ho, W.K., Pera, J., Lemmens, R., Norrving, B., Higgins, P., Benn, M., Sale, M., Kuhlenbaumer, G., Doney, A.S.F., Vicente, A.M., Delavaran, H., Algra, A., Davies, G., Oliveira, S.A., Palmer, C.N.A., Deary, I., Schmidt, H., Pandolfo, M., Montaner, J., Carty, C., Bakker, P.I.W. de, Kostulas, K., Ferro, J.M., Zuydam, N.R. van, Valdimarsson, E., Nordestgaard, B.G., Lindgren, A., Thijs, V., Slowik, A., Saleheen, D., Pare, G., Berger, K., Thorleifsson, G., Hofman, A., Mosley, T.H., Mitchell, B.D., Furie, K., Clarke, R., Levi, C., Seshadri, S., Gschwendtner, A., Boncoraglio, G.B., Sharma, P., Bis, J.C., Gretarsdottir, S., Psaty, B.M., Rothwell, P.M., Rosand, J., Meschia, J.F., Stefansson, K., Dichgans, M., Markus, H.S., Australian Stroke Genetics Collabo, WTCCC 2, Int Stroke Genetics Consortium
Published 2012

Sequential screening nominates the Parkinson's disease associated kinase LRRK2 as a regulator of Clathrin-mediated endocytosis

by Heaton, G.R., Landeck, N., Mamais, A., Nalls, M.A., Nixon-Abell, J., Kumaran, R., Beilina, A., Pellegrini, L., Li, Y., Harvey, K., Cookson, M.R., IPDGC
Published 2020