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    Genetic evaluation of dementia with Lewy bodies implicates distinct disease subgroups

    Kaivola, K., Shah, Z., Chia, R., Black, S. E., Gan-Or, Z., Keith, J., Masellis, M., Rogaeva, E., Brice, A., Lesage, S., Xiromerisiou, G., Calvo, A., Canosa, A., Chio, A., Logroscino, G., Mora, G., Krüger, R., May, P., Alcolea, D., Clarimon, J., & 67 othersFortea, J., Gonzalez-Aramburu, I., Infante, J., Lage, C., Lleó, A., Pastor, P., Sanchez-Juan, P., Brett, F., Aarsland, D., Al-Sarraj, S., Attems, J., Gentleman, S., Hardy, J. A., Hodges, A. K., Love, S., Mckeith, I. G., Morris, C. M., Morris, H. R., Palmer, L., Pickering-Brown, S., Ryten, M., Thomas, A. J., Troakes, C., Albert, M. S., Barrett, M. J., Beach, T. G., Bekris, L. M., Bennett, D. A., Boeve, B. F., Dalgard, C. L., Dawson, T. M., Dickson, D. W., Faber, K., Ferman, T., Ferrucci, L., Flanagan, M. E., Foroud, T. M., Ghetti, B., Gibbs, J. R., Goate, A., Goldstein, D. S., Graff-Radford, N. R., Kaufmann, H., Kukull, W. A., Leverenz, J. B., Mao, Q., Masliah, E., Monuki, E., Newell, K. L., Palma, J. A., Pletnikova, O., Renton, A. E., Resnick, S. M., Rosenthal, L. S., Ross, O. A., Scherzer, C. R., Serrano, G. E., Shakkottai, V. G., Sidransky, E., Tanaka, T., Topol, E., Torkamani, A., Troncoso, J. C., Woltjer, R., Wszolek, Z. K., Scholz, S. W. & Scholz, S. W., May 1 2022, In: Brain. 145, 5, p. 1757-1762 6 p.

    Research output: Contribution to journal › Article › peer-review

  • Genetic factors influencing age at onset in LRRK2-linked Parkinson disease

    Golub, Y., Berg, D., Calne, D. B., Pfeiffer, R. F., Uitti, R. J., Stoessl, A. J., Wszolek, Z. K., Farrer, M. J., Mueller, J. C., Gasser, T. & Fuchs, J., Aug 2009, In: Parkinsonism and Related Disorders. 15, 7, p. 539-541 3 p.

    Research output: Contribution to journal › Article › peer-review

    27 Scopus citations

  • Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease)

    Oliveira, J. R. M., Spiteri, E., Sobrido, M. J., Hopfer, S., Klepper, J., Voit, T., Gilbert, J., Wszolek, Z. K., Calne, D. B., Stoessl, A. J., Hutton, M., Manyam, B. V., Boller, F., Baquero, M. & Geschwind, D. H., Dec 14 2004, In: Neurology. 63, 11, p. 2165-2167 3 p.

    Research output: Contribution to journal › Article › peer-review

    91 Scopus citations

  • Genetic linkage studies in autosomal dominantly inherited L-DOPA responsive parkinsonism. Evaluation of candidate genes.

    Gasser, T., Wszolek, Z., Supala, A., Trofatter, J., Ozelius, L., Uitti, R. J., Pfeiffer, R. F., Gusella, J., Calne, D. & Breakefield, X. O., 1996, In: Advances in neurology. 69, p. 87-95 9 p.

    Research output: Contribution to journal › Article › peer-review

    1 Scopus citations

  • Genetic linkage studies in autosomal dominant parkinsonism: Evaluation of seven candidate genes

    Gasser, T., Wszolek, Z. K., Trofatter, J., Ozelius, L., Uitti, R. J., Lee, C. S., Gusella, J., Pfeiffer, R. F., Calne, D. B. & Breakefield, X. O., Sep 1994, In: Annals of neurology. 36, 3, p. 387-396 10 p.

    Research output: Contribution to journal › Article › peer-review

    85 Scopus citations

  • Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

    Alzheimer Disease Genetics Consortium (ADGC), The European Alzheimer’s Disease Initiative (EADI), Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium (CHARGE), & Genetic and Environmental Risk in AD/Defining Genetic, Polygenic and Environmental Risk for Alzheimer’s Disease Consortium (GERAD/PERADES), Mar 1 2019, In: Nature Genetics. 51, 3, p. 414-430 17 p.

    Research output: Contribution to journal › Article › peer-review

    474 Scopus citations

  • Genetic modifiers in carriers of repeat expansions in the C9ORF72 gene

    van Blitterswijk, M., Mullen, B., Wojtas, A., Heckman, M. G., Diehl, N. N., Baker, M. C., DeJesus-Hernandez, M., Brown, P. H., Murray, M. E., Hsiung, G. Y. R., Stewart, H., Karydas, A. M., Finger, E., Kertesz, A., Bigio, E. H., Weintraub, S., Mesulam, M., Hatanpaa, K. J., White, C. L., Neumann, M., & 19 othersStrong, M. J., Beach, T. G., Wszolek, Z. K., Lippa, C., Caselli, R., Petrucelli, L., Josephs, K. A., Parisi, J. E., Knopman, D. S., Petersen, R. C., Mackenzie, I. R., Seeley, W. W., Grinberg, L. T., Miller, B. L., Boylan, K. B., Graff-Radford, N. R., Boeve, B. F., Dickson, D. W. & Rademakers, R., 2014, In: Molecular neurodegeneration. 9, p. 38 1 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    43 Scopus citations

  • Genetic overlap between diagnostic subtypes of ischemic stroke

    Holliday, E. G., Traylor, M., Malik, R., Bevan, S., Falcone, G., Hopewell, J. C., Cheng, Y. C., Cotlarciuc, I., Bis, J. C., Boerwinkle, E., Boncoraglio, G. B., Clarke, R., Cole, J. W., Fornage, M., Furie, K. L., Ikram, M. A., Jannes, J., Kittner, S. J., Lincz, L. F., Maguire, J. M., & 20 othersMeschia, J. F., Mosley, T. H., Nalls, M. A., Oldmeadow, C., Parati, E. A., Psaty, B. M., Rothwell, P. M., Seshadri, S., Scott, R. J., Sharma, P., Sudlow, C., Wiggins, K. L., Worrall, B. B., Rosand, J., Mitchell, B. D., Dichgans, M., Markus, H. S., Levi, C., Attia, J. & Wray, N. R., Mar 1 2015, In: Stroke. 46, 3, p. 615-619 5 p.

    Research output: Contribution to journal › Article › peer-review

    28 Scopus citations

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

    Traylor, M., Farrall, M., Holliday, E. G., Sudlow, C., Hopewell, J. C., Cheng, Y. C., Fornage, 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. J., Khan, M. S., & 62 othersReiner, 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., Kuhlenbäumer, 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., de Bakker, P. I. W., Kostulas, K., Ferro, J. M., van Zuydam, N. R., Valdimarsson, E., Nordestgaard, B. G., Lindgren, A., Thijs, V., Slowik, A., Saleheen, D., Paré, 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., Nov 2012, In: The Lancet Neurology. 11, 11, p. 951-962 12 p.

    Research output: Contribution to journal › Article › peer-review

    326 Scopus citations

  • Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's disease

    Schott, J. M., Crutch, S. J., Carrasquillo, M. M., Uphill, J., Shakespeare, T. J., Ryan, N. S., Yong, K. X., Lehmann, M., Ertekin-Taner, N., Graff-Radford, N. R., Boeve, B. F., Murray, M. E., Khan, Q. U. A., Petersen, R. C., Dickson, D. W., Knopman, D. S., Rabinovici, G. D., Miller, B. L., González, A. S., Gil-Néciga, E., & 24 othersSnowden, J. S., Harris, J., Pickering-Brown, S. M., Louwersheimer, E., van der Flier, W. M., Scheltens, P., Pijnenburg, Y. A., Galasko, D., Sarazin, M., Dubois, B., Magnin, E., Galimberti, D., Scarpini, E., Cappa, S. F., Hodges, J. R., Halliday, G. M., Bartley, L., Carrillo, M. C., Bras, J. T., Hardy, J., Rossor, M. N., Collinge, J., Fox, N. C. & Mead, S., Aug 1 2016, In: Alzheimer's and Dementia. 12, 8, p. 862-871 10 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    44 Scopus citations

  • Genetics and genomics for the prevention and treatment of cardiovascular disease: Update a scientific statement from the american heart association

    Ganesh, S. K., Arnett, D. K., Assimes, T. L., Basson, C. T., Chakravarti, A., Ellinor, P. T., Engler, M. B., Goldmuntz, E., Herrington, D. M., Hershberger, R. E., Hong, Y., Johnson, J. A., Kittner, S. J., McDermott, D. A., Meschia, J. F., Mestroni, L., O'Donnell, C. J., Psaty, B. M., Vasan, R. S., Ruel, M., & 3 othersShen, W. K., Terzic, A. & Waldman, S. A., Dec 24 2013, In: Circulation. 128, 25, p. 2813-2851 39 p.

    Research output: Contribution to journal › Article › peer-review

    58 Scopus citations

  • Genetic Screening and Functional Characterization of PDGFRB Mutations Associated with Basal Ganglia Calcification of Unknown Etiology

    Sanchez-Contreras, M., Baker, M. C., Finch, N. A., Nicholson, A., Wojtas, A., Wszolek, Z. K., Ross, O. A., Dickson, D. W. & Rademakers, R., Aug 2014, In: Human mutation. 35, 8, p. 964-971 8 p.

    Research output: Contribution to journal › Article › peer-review

    32 Scopus citations

  • Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases

    on behalf of the ARTFL/LEFFTDS consortium, Jan 1 2020, In: Alzheimer's and Dementia. 16, 1, p. 118-130 13 p.

    Research output: Contribution to journal › Article › peer-review

    11 Scopus citations

  • Genetics of cerebrovascular disorders

    Meschia, J. F., Brott, T. G. & Brown, R. D., Jan 2005, In: Mayo Clinic proceedings. 80, 1, p. 122-132 11 p.

    Research output: Contribution to journal › Article › peer-review

    36 Scopus citations

  • Genetics of Gene Expression in the Aging Human Brain Reveal TDP-43 Proteinopathy Pathophysiology

    Yang, H. S., White, C. C., Klein, H. U., Yu, L., Gaiteri, C., Ma, Y., Felsky, D., Mostafavi, S., Petyuk, V. A., Sperling, R. A., Ertekin-Taner, N., Schneider, J. A., Bennett, D. A. & De Jager, P. L., Aug 5 2020, In: Neuron. 107, 3, p. 496-508.e6

    Research output: Contribution to journal › Article › peer-review

    Open Access
    6 Scopus citations

  • Genetics of ischemic stroke: Inheritance of a sporadic disorder

    Ross, O. A. & Meschia, J. F., Jan 1 2009, In: Current neurology and neuroscience reports. 9, 1, p. 19-27 9 p.

    Research output: Contribution to journal › Article › peer-review

    5 Scopus citations

  • Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke

    Cole, J. W., Xu, H., Ryan, K., Jaworek, T., Dueker, N., McArdle, P., Gaynor, B., Cheng, Y. C., O'Connell, J., Bevan, S., Malik, R., Ahmed, N. U., Amouyel, P., Anjum, S., Bis, J. C., Crosslin, D., Danesh, J., Engelter, S. T., Fornage, M., Frossard, P., & 58 othersGieger, C., Giese, A. K., Grond-Ginsbach, C., Ho, W. K., Holliday, E., Hopewell, J., Hussain, M., Iqbal, W., Jabeen, S., Jannes, J., Kamal, A., Kamatani, Y., Kanse, S., Kloss, M., Lathrop, M., Leys, D., Lindgren, A., LongstrethJr, W. T., Mahmood, K., Meisinger, C., Metso, T. M., Mosley, T., Müller-Nurasyid, M., Norrving, B., Parati, E., Peters, A., Pezzini, A., Quereshi, I., Rasheed, A., Rauf, A., Salam, T., Shen, J., Slowik, A., Stanne, T., Strauch, K., Tatlisumak, T., Thijs, V. N., Tiedt, S., Traylor, M., Waldenberger, M., Walters, M., Zhao, W., Boncoraglio, G., Debette, S., Jern, C., Levi, C., Markus, H., Meschia, J., Rolfs, A., Rothwell, P., Saleheen, D., Seshadri, S., Sharma, P., Sudlow, C., Worrall, B., Stine, O. C., Kittner, S. J. & Mitchell, B. D., Nov 2018, In: PloS one. 13, 11, e0206554.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    4 Scopus citations

  • Genetic studies of body mass index yield new insights for obesity biology

    LifeLines Cohort Study & ADIPOGen Consortium; AGEN-BMI Working Group; CARDIOGRAMplusC4D Consortium; CKDGen Consortium; GLGC; ICBP; MAGIC Investigators; MuTHER Consortium; MIGen Consortium; PAGE Consortium; ReproGen Consortium; GENIE Consortium; International Endogene Consortium, Feb 12 2015, In: Nature. 518, 7538, p. 197-206 10 p.

    Research output: Contribution to journal › Article › peer-review

    2006 Scopus citations

  • Genetic variants associated with myocardial infarction in the PSMA6 gene and Chr9p21 are also associated with ischaemic stroke

    Heckman, M. G., Soto-Ortolaza, A. I., Diehl, N. N., Rayaprolu, S., Brott, T. G., Wszolek, Z. K., Meschia, J. F. & Ross, O. A., Feb 2013, In: European Journal of Neurology. 20, 2, p. 300-308 9 p.

    Research output: Contribution to journal › Article › peer-review

    19 Scopus citations

  • Genetic variants associated with susceptibility to psychosis in late-onset Alzheimer's disease families

    NIA-LOAD/NCRAD Family Study Group, Nov 2015, In: Neurobiology of aging. 36, 11, p. 3116.e9-3116.e16

    Research output: Contribution to journal › Article › peer-review

    Open Access
    8 Scopus citations

  • Genetic Variants in a Haplotype Block Spanning IDE are Significantly Associated with Plasma Aβ42 Levels and Risk for Alzheimer Disease

    Ertekin-Taner, N., Allen, M., Fadale, D., Scanlin, L., Younkin, L., Petersen, R. C., Graff-Radford, N. & Younkin, S. G., 2004, In: Human mutation. 23, 4, p. 334-342 9 p.

    Research output: Contribution to journal › Article › peer-review

    87 Scopus citations

  • Genetic variants in CETP increase risk of intracerebral hemorrhage

    on behalf of the Global Lipids Genetics Consortium and International Stroke Genetics Consortium, Nov 1 2016, In: Annals of neurology. 80, 5, p. 730-740 11 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    18 Scopus citations

  • Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

    Ehret, G. B., Munroe, P. B., Rice, K. M., Bochud, M., Johnson, A. D., Chasman, D. I., Smith, A. V., Tobin, M. D., Verwoert, G. C., Hwang, S. J., Pihur, V., Vollenweider, P., O'Reilly, P. F., Amin, N., Bragg-Gresham, J. L., Teumer, A., Glazer, N. L., Launer, L., Zhao, J. H., Aulchenko, Y., & 326 othersHeath, S., Sober, S., Parsa, A., Luan, J., Arora, P., Dehghan, A., Zhang, F., Lucas, G., Hicks, A. A., Jackson, A. U., Peden, J. F., Tanaka, T., Wild, S. H., Rudan, I., Igl, W., Milaneschi, Y., Parker, A. N., Fava, C., Chambers, J. C., Fox, E. R., Kumari, M., Go, M. J., van der Harst, P., Kao, W. H. L., Sjögren, M., Vinay, D. G., Alexander, M., Tabara, Y., Shaw-Hawkins, S., Whincup, P. H., Liu, Y., Shi, G., Kuusisto, J., Tayo, B., Seielstad, M., Sim, X., Hoang Nguyen, K. D., Lehtimäki, T., Matullo, G., Wu, Y., Gaunt, T. R., Charlotte Onland-Moret, N., Cooper, M. N., Platou, C. G. P., Org, E., Hardy, R., Dahgam, S., Palmen, J., Vitart, V., Braund, P. S., Kuznetsova, T., Uiterwaal, C. S. P. M., Adeyemo, A., Palmas, W., Campbell, H., Ludwig, B., Tomaszewski, M., Tzoulaki, I., Palmer, N. D., Aspelund, T., Garcia, M., Chang, Y. P. C., O'Connell, J. R., Steinle, N. I., Grobbee, D. E., Arking, D. E., Kardia, S. L., Morrison, A. C., Hernandez, D., Najjar, S., McArdle, W. L., Hadley, D., Brown, M. J., Connell, J. M., Hingorani, A. D., Day, I. N. M., Lawlor, D. A., Beilby, J. P., Lawrence, R. W., Clarke, R., Hopewell, J. C., Ongen, H., Dreisbach, A. W., Li, Y., Hunter Young, J., Bis, J. C., Kähönen, M., Viikari, J., Adair, L. S., Lee, N. R., Chen, M. H., Olden, M., Pattaro, C., Bolton, J. A. H., Köttgen, A., Bergmann, S., Mooser, V., Chaturvedi, N., Frayling, T. M., Islam, M., Jafar, T. H., Erdmann, J., Kulkarni, S. R., Bornstein, S. R., Grässler, J., Groop, L., Voight, B. F., Kettunen, J., Howard, P., Taylor, A., Guarrera, S., Ricceri, F., Emilsson, V., Plump, A., Barroso, I., Khaw, K. T., Weder, A. B., Hunt, S. C., Sun, Y. V., Bergman, R. N., Collins, F. S., Bonnycastle, L. L., Scott, L. J., Stringham, H. M., Peltonen, L., Perola, M., Vartiainen, E., Brand, S. M., Staessen, J. A., Wang, T. J., Burton, P. R., Artigas, M. S., Dong, Y., Snieder, H., Wang, X., Zhu, H., Lohman, K. K., Rudock, M. E., Heckbert, S. R., Smith, N. L., Wiggins, K. L., Doumatey, A., Shriner, D., Veldre, G., Viigimaa, M., Kinra, S., Prabhakaran, D., Tripathy, V., Langefeld, C. D., Rosengren, A., Thelle, D. S., Corsi, A. M., Singleton, A., Forrester, T., Hilton, G., McKenzie, C. A., Salako, T., Iwai, N., Kita, Y., Ogihara, T., Ohkubo, T., Okamura, T., Ueshima, H., Umemura, S., Eyheramendy, S., Meitinger, T., Wichmann, H. E., Cho, Y. S., Kim, H. L., Lee, J. Y., Scott, J., Sehmi, J. S., Zhang, W., Hedblad, B., Nilsson, P., Smith, G. D., Wong, A., Narisu, N., Stančáková, A., Raffel, L. J., Yao, J., Kathiresan, S., O'Donnell, C. J., Schwartz, S. M., Arfan Ikram, M., Longstreth, W. T., Mosley, T. H., Seshadri, S., Shrine, N. R. G., Wain, L. V., Morken, M. A., Swift, A. J., Laitinen, J., Prokopenko, I., Zitting, P., Cooper, J. A., Humphries, S. E., Danesh, J., Rasheed, A., Goel, A., Hamsten, A., Watkins, H., Bakker, S. J. L., van Gilst, W. H., Janipalli, C. S., Radha Mani, K., Yajnik, C. S., Hofman, A., Mattace-Raso, F. U. S., Oostra, B. A., Demirkan, A., Isaacs, A., Rivadeneira, F., Lakatta, E. G., Orru, M., Scuteri, A., Ala-Korpela, M., Kangas, A. J., Lyytikäinen, L. P., Soininen, P., Tukiainen, T., Würtz, P., Twee-HeeOng, R., Dörr, M., Kroemer, H. K., Völker, U., Völzke, H., Galan, P., Hercberg, S., Lathrop, M., Zelenika, D., Deloukas, P., Mangino, M., Spector, T. D., Zhai, G., Meschia, J. F., Nalls, M. A., Sharma, P., Terzic, J., Kranthi Kumar, M. V., Denniff, M., Zukowska-Szczechowska, E., Wagenknecht, L. E., Fowkes, F. G. R., Charchar, F. J., Schwarz, P. E. H., Hayward, C., Guo, X., Rotimi, C., Bots, M. L., Brand, E., Samani, N. J., Polasek, O., Talmud, P. J., Nyberg, F., Kuh, D., Laan, M., Hveem, K., Palmer, L. J., van der Schouw, Y. T., Casas, J. P., Mohlke, K. L., Vineis, P., Raitakari, O., Ganesh, S. K., Wong, T. Y., Shyong Tai, E., Cooper, R. S., Laakso, M., Rao, D. C., Harris, T. B., Morris, R. W., Dominiczak, A. F., Kivimaki, M., Marmot, M. G., Miki, T., Saleheen, D., Chandak, G. R., Coresh, J., Navis, G., Salomaa, V., Han, B. G., Zhu, X., Kooner, J. S., Melander, O., Ridker, P. M., Bandinelli, S., Gyllensten, U. B., Wright, A. F., Wilson, J. F., Ferrucci, L., Farrall, M., Tuomilehto, J., Pramstaller, P. P., Elosua, R., Soranzo, N., Sijbrands, E. J. G., Altshuler, D., Loos, R. J. F., Shuldiner, A. R., Gieger, C., Meneton, P., Uitterlinden, A. G., Wareham, N. J., Gudnason, V., Rotter, J. I., Rettig, R., Uda, M., Strachan, D. P., Witteman, J. C. M., Hartikainen, A. L., Beckmann, J. S., Boerwinkle, E., Vasan, R. S., Boehnke, M., Larson, M. G., Järvelin, M. R., Psaty, B. M., Abecasis, G. R., Chakravarti, A., Elliott, P., van Duijn, C. M., Newton-Cheh, C., Levy, D., Caulfield, M. J. & Johnson, T., Oct 6 2011, In: Nature. 478, 7367, p. 103-109 7 p.

    Research output: Contribution to journal › Article › peer-review

    1430 Scopus citations

  • Genetic variants of α-synuclein are not associated with essential tremor

    Ross, O. A., Conneely, K. N., Wang, T., Vilarino-Guell, C., Soto-Ortolaza, A. I., Rajput, A., Wszolek, Z. K., Uitti, R. J., Louis, E. D., Clark, L. N., Farrer, M. J. & Testa, C. M., Dec 2011, In: Movement Disorders. 26, 14, p. 2552-2556 5 p.

    Research output: Contribution to journal › Article › peer-review

    9 Scopus citations

  • Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

    International FTD-Genomics Consortium (IFGC), Dec 1 2019, In: Scientific reports. 9, 1, 10854.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    4 Scopus citations

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

    on behalf of the International Stroke Genetics Consortium & METASTROKE, UK Young Lacunar DNA Study, NINDS Stroke Genetics Network, Neurology Working Group of the CHARGE Consortium, Mar 1 2017, In: Annals of neurology. 81, 3, p. 383-394 12 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    39 Scopus citations

  • Genetic variation at CR1 increases risk of cerebral amyloid angiopathy

    Biffi, A., Shulman, J. M., Jagiella, J. M., Cortellini, L., Ayres, A. M., Schwab, K., Brown, D. L., Silliman, S. L., Selim, M., Worrall, B. B., Meschia, J. F., Slowik, A., De Jager, P. L., Greenberg, S. M., Schneider, J. A., Bennett, D. A. & Rosand, J., Jan 31 2012, In: Neurology. 78, 5, p. 334-341 8 p.

    Research output: Contribution to journal › Article › peer-review

    68 Scopus citations

  • Genetic variation in PCDH11X is associated with susceptibility to late onset alzheimer's disease

    Carrasquillo, M. M., Zou, F., Pankratz, V. S., Wilcox, S. L., Ma, L., Walker, L. P., Younkin, C. S., Younkin, L. H., Bisceglio, G. D., Ertekin-Taner, N., Crook, J. E., Dickson, D. W., Petersen, R. C., Graff-Radford, N. R. & Younkin, S. G., Jul 8 2010, In: Hirosaki Medical Journal. 61, SUPPL., p. S125-S134

    Research output: Contribution to journal › Article › peer-review

  • Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease

    Carrasquillo, M. M., Zou, F., Pankratz, V. S., Wilcox, S. L., Ma, L., Walker, L. P., Younkin, S. G., Younkin, C. S., Younkin, L. H., Bisceglio, G. D., Ertekin-Taner, N., Crook, J. E., Dickson, D. W., Petersen, R. C., Graff-Radford, N. R. & Younkin, S. G., Feb 2009, In: Nature Genetics. 41, 2, p. 192-198 7 p.

    Research output: Contribution to journal › Article › peer-review

    222 Scopus citations

  • Genetic variation of Omi/HtrA2 and Parkinson's disease

    Ross, O. A., Soto, A. I., Vilariño-Güell, C., Heckman, M. G., Diehl, N. N., Hulihan, M. M., Aasly, J. O., Sando, S., Gibson, J. M., Lynch, T., Krygowska-Wajs, A., Opala, G., Barcikowska, M., Czyzewski, K., Uitti, R. J., Wszolek, Z. K. & Farrer, M. J., Nov 2008, In: Parkinsonism and Related Disorders. 14, 7, p. 539-543 5 p.

    Research output: Contribution to journal › Article › peer-review

    56 Scopus citations

  • Genetic variation of the retromer subunits VPS26A/B-VPS29 in Parkinson's disease

    Shannon, B., Soto-Ortolaza, A., Rayaprolu, S., Cannon, H. D., Labbé, C., Benitez, B. A., Choi, J., Lynch, T., Boczarska-Jedynak, M., Opala, G., Krygowska-Wajs, A., Barcikowska, M., Van Gerpen, J. A., Uitti, R. J., Springer, W., Cruchaga, C., Wszolek, Z. K. & Ross, O. A., Aug 2014, In: Neurobiology of aging. 35, 8, p. 1958.e1-1958.e2

    Research output: Contribution to journal › Article › peer-review

    17 Scopus citations

  • Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations

    Parkinson study group, 2002, In: American journal of human genetics. 71, 1, p. 124-135 12 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    149 Scopus citations

  • Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

    The American Genome Center, Mar 2021, In: Nature Genetics. 53, 3, p. 294-303 10 p.

    Research output: Contribution to journal › Article › peer-review

    2 Scopus citations

  • Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD

    Pottier, C., Ren, Y., Perkerson, R. B., Baker, M., Jenkins, G. D., van Blitterswijk, M., DeJesus-Hernandez, M., van Rooij, J. G. J., Murray, M. E., Christopher, E., McDonnell, S. K., Fogarty, Z., Batzler, A., Tian, S., Vicente, C. T., Matchett, B., Karydas, A. M., Hsiung, G. Y. R., Seelaar, H., Mol, M. O., & 85 othersFinger, E. C., Graff, C., Öijerstedt, L., Neumann, M., Heutink, P., Synofzik, M., Wilke, C., Prudlo, J., Rizzu, P., Simon-Sanchez, J., Edbauer, D., Roeber, S., Diehl-Schmid, J., Evers, B. M., King, A., Mesulam, M. M., Weintraub, S., Geula, C., Bieniek, K. F., Petrucelli, L., Ahern, G. L., Reiman, E. M., Woodruff, B. K., Caselli, R. J., Huey, E. D., Farlow, M. R., Grafman, J., Mead, S., Grinberg, L. T., Spina, S., Grossman, M., Irwin, D. J., Lee, E. B., Suh, E. R., Snowden, J., Mann, D., Ertekin-Taner, N., Uitti, R. J., Wszolek, Z. K., Josephs, K. A., Parisi, J. E., Knopman, D. S., Petersen, R. C., Hodges, J. R., Piguet, O., Geier, E. G., Yokoyama, J. S., Rissman, R. A., Rogaeva, E., Keith, J., Zinman, L., Tartaglia, M. C., Cairns, N. J., Cruchaga, C., Ghetti, B., Kofler, J., Lopez, O. L., Beach, T. G., Arzberger, T., Herms, J., Honig, L. S., Vonsattel, J. P., Halliday, G. M., Kwok, J. B., White, C. L., Gearing, M., Glass, J., Rollinson, S., Pickering-Brown, S., Rohrer, J. D., Trojanowski, J. Q., Van Deerlin, V., Bigio, E. H., Troakes, C., Al-Sarraj, S., Asmann, Y., Miller, B. L., Graff-Radford, N. R., Boeve, B. F., Seeley, W. W., Mackenzie, I. R. A., van Swieten, J. C., Dickson, D. W., Biernacka, J. M. & Rademakers, R., Jun 1 2019, In: Acta neuropathologica. 137, 6, p. 879-899 21 p.

    Research output: Contribution to journal › Article › peer-review

    28 Scopus citations

  • Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

    ITALSGEN Consortium, Genomic Translation for ALS Care (GTAC) Consortium, ALS Sequencing Consortium, NYGC ALS Consortium, Answer ALS Foundation, Clinical Research in ALS and Related Disorders for Therapeutic Development (CReATe) Consortium, SLAGEN Consortium, French ALS Consortium & Project MinE ALS Sequencing Consortium, Mar 21 2018, In: Neuron. 97, 6, p. 1268-1283.e6

    Research output: Contribution to journal › Article › peer-review

    Open Access
    184 Scopus citations

  • Genome-wide analysis identifies a novel LINC-PINT splice variant associated with vascular amyloid pathology in Alzheimer’s disease

    Reddy, J. S., Allen, M., Ho, C. C. G., Oatman, S. R., Iş, Ö., Quicksall, Z. S., Wang, X., Jin, J., Patel, T. A., Carnwath, T. P., Nguyen, T. T., Malphrus, K. G., Lincoln, S. J., Carrasquillo, M. M., Crook, J. E., Kanekiyo, T., Murray, M. E., Bu, G., Dickson, D. W. & Ertekin-Taner, N., Dec 2021, In: Acta Neuropathologica Communications. 9, 1, 93.

    Research output: Contribution to journal › Article › peer-review

    Open Access

  • Genome-wide analysis of blood pressure variability and ischemic stroke

    Yadav, S., Cotlarciuc, I., Munroe, P. B., Khan, M. S., Nalls, M. A., Bevan, S., Cheng, Y. C., Chen, W. M., Malik, R., Mccarthy, N. S., Holliday, E. G., Speed, D., Hasan, N., Pucek, M., Rinne, P. E., Sever, P., Stanton, A., Shields, D. C., Maguire, J. M., Mcevoy, M., & 14 othersScott, R. J., Ferrucci, L., Macleod, M. J., Attia, J., Markus, H. S., Sale, M. M., Worrall, B. B., Mitchell, B. D., Dichgans, M., Sudlow, C., Meschia, J. F., Rothwell, P. M., Caulfield, M. & Sharma, P., Oct 2013, In: Stroke. 44, 10, p. 2703-2709 7 p.

    Research output: Contribution to journal › Article › peer-review

    15 Scopus citations

  • Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases

    International Parkinson's Disease Genomics Consortium (IPDGC), Oct 13 2016, In: Neurobiology of aging. 38, p. 214.e7-214.e10

    Research output: Contribution to journal › Article › peer-review

    Open Access
    42 Scopus citations

  • Genome-wide analysis of genetic loci associated with Alzheimer disease

    Seshadri, S., Fitzpatrick, A. L., Ikram, M. A., DeStefano, A. L., Gudnason, V., Boada, M., Bis, J. C., Smith, A. V., Carassquillo, M. M., Lambert, J. C., Harold, D., Schrijvers, E. M. C., Ramirez-Lorca, R., Debette, S., Longstreth, W. T., Janssens, A. C. J. W., Pankratz, V. S., Dartigues, J. F., Hollingworth, P., Aspelund, T., & 43 othersHernandez, I., Beiser, A., Kuller, L. H., Koudstaal, P. J., Dickson, D. W., Tzourio, C., Abraham, R., Antunez, C., Du, Y., Rotter, J. I., Aulchenko, Y. S., Harris, T. B., Petersen, R. C., Berr, C., Owen, M. J., Lopez-Arrieta, J., Varadarajan, B. N., Becker, J. T., Rivadeneira, F., Nalls, M. A., Graff-Radford, N. R., Campion, D., Auerbach, S., Rice, K., Hofman, A., Jonsson, P. V., Schmidt, H., Lathrop, M., Mosley, T. H., Au, R., Psaty, B. M., Uitterlinden, A. G., Farrer, L. A., Lumley, T., Ruiz, A., Williams, J., Amouyel, P., Younkin, S. G., Wolf, P. A., Launer, L. J., Lopez, O. L., Van Duijn, C. M. & Breteler, M. M. B., May 12 2010, In: JAMA. 303, 18, p. 1832-1840 9 p.

    Research output: Contribution to journal › Article › peer-review

    874 Scopus citations

  • Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

    Köttgen, A., Albrecht, E., Teumer, A., Vitart, V., Krumsiek, J., Hundertmark, C., Pistis, G., Ruggiero, D., O'Seaghdha, C. M., Haller, T., Yang, Q., Tanaka, T., Johnson, A. D., Kutalik, Z., Smith, A. V., Shi, J., Struchalin, M., Middelberg, R. P. S., Brown, M. J., Gaffo, A. L., & 205 othersPirastu, N., Li, G., Hayward, C., Zemunik, T., Huffman, J., Yengo, L., Zhao, J. H., Demirkan, A., Feitosa, M. F., Liu, X., Malerba, G., Lopez, L. M., Van Der Harst, P., Li, X., Kleber, M. E., Hicks, A. A., Nolte, I. M., Johansson, A., Murgia, F., Wild, S. H., Bakker, S. J. L., Peden, J. F., Dehghan, A., Steri, M., Tenesa, A., Lagou, V., Salo, P., Mangino, M., Rose, L. M., Lehtimäki, T., Woodward, O. M., Okada, Y., Tin, A., Müller, C., Oldmeadow, C., Putku, M., Czamara, D., Kraft, P., Frogheri, L., Thun, G. A., Grotevendt, A., Gislason, G. K., Harris, T. B., Launer, L. J., McArdle, P., Shuldiner, A. R., Boerwinkle, E., Coresh, J., Schmidt, H., Schallert, M., Martin, N. G., Montgomery, G. W., Kubo, M., Nakamura, Y., Tanaka, T., Munroe, P. B., Samani, N. J., Jacobs, D. R., Liu, K., D'Adamo, P., Ulivi, S., Rotter, J. I., Psaty, B. M., Vollenweider, P., Waeber, G., Campbell, S., Devuyst, O., Navarro, P., Kolcic, I., Hastie, N., Balkau, B., Froguel, P., Esko, T., Salumets, A., Khaw, K. T., Langenberg, C., Wareham, N. J., Isaacs, A., Kraja, A., Zhang, Q., Wild, P. S., Scott, R. J., Holliday, E. G., Org, E., Viigimaa, M., Bandinelli, S., Metter, J. E., Lupo, A., Trabetti, E., Sorice, R., Döring, A., Lattka, E., Strauch, K., Theis, F., Waldenberger, M., Wichmann, H. E., Davies, G., Gow, A. J., Bruinenberg, M., Stolk, R. P., Kooner, J. S., Zhang, W., Winkelmann, B. R., Boehm, B. O., Lucae, S., Penninx, B. W., Smit, J. H., Curhan, G., Mudgal, P., Plenge, R. M., Portas, L., Persico, I., Kirin, M., Wilson, J. F., Leach, I. M., Van Gilst, W. H., Goel, A., Ongen, H., Hofman, A., Rivadeneira, F., Uitterlinden, A. G., Imboden, M., Von Eckardstein, A., Cucca, F., Nagaraja, R., Piras, M. G., Nauck, M., Schurmann, C., Budde, K., Ernst, F., Farrington, S. M., Theodoratou, E., Prokopenko, I., Stumvoll, M., Jula, A., Perola, M., Salomaa, V., Shin, S. Y., Spector, T. D., Sala, C., Ridker, P. M., Kähönen, M., Viikari, J., Hengstenberg, C., Nelson, C. P., Meschia, J. F., Nalls, M. A., Sharma, P., Singleton, A. B., Kamatani, N., Zeller, T., Burnier, M., Attia, J., Laan, M., Klopp, N., Hillege, H. L., Kloiber, S., Choi, H., Pirastu, M., Tore, S., Probst-Hensch, N. M., Völzke, H., Gudnason, V., Parsa, A., Schmidt, R., Whitfield, J. B., Fornage, M., Gasparini, P., Siscovick, D. S., Polašek, O., Campbell, H., Rudan, I., Bouatia-Naji, N., Metspalu, A., Loos, R. J. F., Van Duijn, C. M., Borecki, I. B., Ferrucci, L., Gambaro, G., Deary, I. J., Wolffenbuttel, B. H. R., Chambers, J. C., März, W., Pramstaller, P. P., Snieder, H., Gyllensten, U., Wright, A. F., Navis, G., Watkins, H., Witteman, J. C. M., Sanna, S., Schipf, S., Dunlop, M. G., Tönjes, A., Ripatti, S., Soranzo, N., Toniolo, D., Chasman, D. I., Raitakari, O., Kao, W. H. L., Ciullo, M., Fox, C. S., Caulfield, M., Bochud, M. & Gieger, C., Feb 1 2013, In: Nature Genetics. 45, 2, p. 145-154 10 p.

    Research output: Contribution to journal › Article › peer-review

    442 Scopus citations

  • Genome-wide association analysis of hippocampal volume identifies enrichment of neurogenesis-related pathways

    Alzheimer’s Disease Neuroimaging Initiative (ADNI), Dec 1 2019, In: Scientific reports. 9, 1, 14498.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    4 Scopus citations

  • Genome-wide association analysis of ischemic stroke in young adults

    Cheng, Y. C., O'Connell, J. R., Cole, J. W., Colin Stine, O., Dueker, N., McArdle, P. F., Sparks, M. J., Shen, J., Laurie, C. C., Nelson, S., Doheny, K. F., Ling, H., Pugh, E. W., Brott, T. G., Brown, R. D., Meschia, J. F., Nalls, M., Rich, S. S., Worrall, B., Anderson, C. D., & 8 othersBiffi, A., Cortellini, L., Furie, K. L., Rost, N. S., Rosand, J., Manolio, T. A., Kittner, S. J. & Mitchell, B. D., Nov 2011, In: G3: Genes, Genomes, Genetics. 1, 6, p. 505-514 10 p.

    Research output: Contribution to journal › Article › peer-review

    24 Scopus citations

  • Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2

    Cheng, Y. C., Stanne, T. M., Giese, A. K., Ho, W. K., Traylor, M., Amouyel, P., Holliday, E. G., Malik, R., Xu, H., Kittner, S. J., Cole, J. W., O'Connell, J. R., Danesh, J., Rasheed, A., Zhao, W., Engelter, S., Grond-Ginsbach, C., Kamatani, Y., Lathrop, M., Leys, D., & 43 othersThijs, V., Metso, T. M., Tatlisumak, T., Pezzini, A., Parati, E. A., Norrving, B., Bevan, S., Rothwell, P. M., Sudlow, C., Slowik, A., Lindgren, A., Walters, M. R., Jannes, J., Shen, J., Crosslin, D., Doheny, K., Laurie, C. C., Kanse, S. M., Bis, J. C., Fornage, M., Mosley, T. H., Hopewell, J. C., Strauch, K., Müller-Nurasyid, M., Gieger, C., Waldenberger, M., Peters, A., Meisinger, C., Ikram, M. A., Longstreth, W. T., Meschia, J. F., Seshadri, S., Sharma, P., Worrall, B., Jern, C., Levi, C., Dichgans, M., Boncoraglio, G. B., Markus, H. S., Debette, S., Rolfs, A., Saleheen, D. & Mitchell, B. D., Feb 1 2016, In: Stroke. 47, 2, p. 307-316 10 p.

    Research output: Contribution to journal › Article › peer-review

    32 Scopus citations

  • Genome-wide association interaction analysis for Alzheimer's disease

    GERAD1 Consortium, Nov 1 2014, In: Neurobiology of aging. 35, 11, p. 2436-2443 8 p.

    Research output: Contribution to journal › Article › peer-review

    44 Scopus citations

  • Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease

    The 23andMe Research Team, Jul 2021, In: Annals of neurology. 90, 1, p. 76-88 13 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access

  • Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

    Bellenguez, C., Bevan, S., Gschwendtner, A., Spencer, C. C. A., Burgess, A. I., Pirinen, M., Jackson, C. A., Traylor, M., Strange, A., Su, Z., Band, G., Syme, P. D., Malik, R., Pera, J., Bo, N., Lemmens, R., Freeman, C., Schanz, R., James, T., Poole, D., & 68 othersMurphy, L., Segal, H., Cortellini, L., Cheng, Y. C., Woo, D., Nalls, M. A., Müller-Myhsok, B., Meisinger, C., Seedorf, U., Ross-Adams, H., Boonen, S., Wloch-Kopec, D., Valant, V., Slark, J., Furie, K., Delavaran, H., Langford, C., Deloukas, P., Edkins, S., Hunt, S., Gray, E., Dronov, S., Peltonen, L., Gretarsdottir, S., Thorleifsson, G., Thorsteinsdottir, U., Stefansson, K., Boncoraglio, G. B., Parati, E. A., Attia, J., Holliday, E., Levi, C., Franzosi, M. G., Goel, A., Helgadottir, A., Blackwell, J. M., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Duncanson, A., Jankowski, J., Mathew, C. G., Palmer, C. N. A., Plomin, R., Rautanen, A., Sawcer, S. J., Trembath, R. C., Viswanathan, A. C., Wood, N. W., Worrall, B. B., Kittner, S. J., Mitchell, B. D., Kissela, B., Meschia, J. F., Thijs, V., Lindgren, A., MacLeod, M. J., Slowik, A., Walters, M., Rosand, J., Sharma, P., Farrall, M., Sudlow, C. L. M., Rothwell, P. M., Dichgans, M., Donnelly, P. & Markus, H. S., Mar 2012, In: Nature Genetics. 44, 3, p. 328-333 6 p.

    Research output: Contribution to journal › Article › peer-review

    296 Scopus citations

  • Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma

    Alcohol Genome-wide Association (AlcGen) Consortium; Diabetes Genetics Replication and Meta-analyses (DIAGRAM+) Study; Genetic Investigation of Anthropometric Traits (GIANT) Consortium; Global Lipids Genetics Consortium; Genetics of Liver Disease (GOLD) Consortium; International Consortium for Blood Pressure (ICBP-GWAS); Meta-analyses of Glucose and Insulin-Related Traits Consortium (MAGIC) & Collaborators, Nov 1 2011, In: Nature Genetics. 43, 11, p. 1131-1138 8 p.

    Research output: Contribution to journal › Article › peer-review

    350 Scopus citations

  • Genome-Wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1

    Winkelmann, J., Czamara, D., Schormair, B., Knauf, F., Schulte, E. C., Trenkwalder, C., Dauvilliers, Y., Polo, O., Högl, B., Berger, K., Fuhs, A., Gross, N., Stiasny-Kolster, K., Oertel, W., Bachmann, C. G., Paulus, W., Xiong, L., Montplaisir, J., Rouleau, G. A., Fietze, I., & 37 othersVávrová, J., Kemlink, D., Sonka, K., Nevsimalova, S., Lin, S. C., Wszolek, Z., Vilariño-Güell, C., Farrer, M. J., Gschliesser, V., Frauscher, B., Falkenstetter, T., Poewe, W., Allen, R. P., Earley, C. J., Ondo, W. G., Le, W. D., Spieler, D., Kaffe, M., Zimprich, A., Kettunen, J., Perola, M., Silander, K., Cournu-Rebeix, I., Francavilla, M., Fontenille, C., Fontaine, B., Vodicka, P., Prokisch, H., Lichtner, P., Peppard, P., Faraco, J., Mignot, E., Gieger, C., Illig, T., Wichmann, H. E., Müller-Myhsok, B. & Meitinger, T., Jul 2011, In: PLoS genetics. 7, 7, e1002171.

    Research output: Contribution to journal › Article › peer-review

    134 Scopus citations

  • Genome-wide association study in essential tremor identifies three new loci

    Müller, S. H., Girard, S. L., Hopfner, F., Merner, N. D., Bourassa, C. V., Lorenz, D., Clark, L. N., Tittmann, L., Soto-Ortolaza, A. I., Klebe, S., Hallett, M., Schneider, S. A., Hodgkinson, C. A., Lieb, W., Wszolek, Z. K., Pendziwiat, M., Lorenzo-Betancor, O., Poewe, W., Ortega-Cubero, S., Seppi, K., & 29 othersRajput, A., Hussl, A., Rajput, A. H., Berg, D., Dion, P. A., Wurster, I., Shulman, J. M., Srulijes, K., Haubenberger, D., Pastor, P., Vilariño-Güell, C., Postuma, R. B., Bernard, G., Ladwig, K. H., Dupré, N., Jankovic, J., Strauch, K., Panisset, M., Winkelmann, J., Testa, C. M., Reischl, E., Zeuner, K. E., Ross, O. A., Arzberger, T., Chouinard, S., Deuschl, G., Louis, E. D., Kuhlenbäumer, G. & Rouleau, G. A., Dec 2016, In: Brain. 139, 12, p. 3163-3169 7 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    53 Scopus citations

  • Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations with Stroke

    Keene, K. L., Hyacinth, H. I., Bis, J. C., Kittner, S. J., Mitchell, B. D., Cheng, Y. C., Pare, G., Chong, M., O'Donnell, M., Meschia, J. F., Chen, W. M., Sale, M. M., Rich, S. S., Nalls, M. A., Zonderman, A. B., Evans, M. K., Wilson, J. G., Correa, A., Markus, H. S., Traylor, M., & 27 othersLewis, C. M., Carty, C. L., Reiner, A., Haessler, J., Langefeld, C. D., Gottesman, R., Mosley, T. H., Woo, D., Yaffe, K., Liu, Y. M., Longstreth, W. T., Psaty, B. M., Kooperberg, C., Lange, L. A., Sacco, R., Rundek, T., Lee, J. M., Cruchaga, C., Furie, K. L., Arnett, D. K., Benavente, O. R., Grewal, R. P., Peddareddygari, L. R., Dichgans, M., Malik, R., Worrall, B. B. & Fornage, M., Aug 1 2020, In: Stroke. 51, 8, p. 2454-2463 10 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access