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    Fosphenytoin: An intravenous option for the management of acute trigeminal neuralgia crisis

    Cheshire, W. P., 2001, In: Journal of pain and symptom management. 21, 6, p. 506-510 5 p.

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

    52 Scopus citations

  • Four distinct trajectories of tau deposition identified in Alzheimer’s disease

    The Alzheimer's Disease Neuroimaging Initiative, May 2021, In: Nature Medicine. 27, 5, p. 871-881 11 p.

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

    3 Scopus citations

  • Frequency and accuracy of prehospital diagnosis of acute stroke

    Kothari, R., Barsan, W., Brott, T., Broderick, J. & Ashbrock, S. N., Jun 1995, In: Stroke. 26, 6, p. 937-941 5 p.

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

    169 Scopus citations

  • Frequency and patterns of abnormality detected by iodine-123 amine emission CT after cerebral infarction

    Brott, T. G., Gelfand, M. J., Williams, C. C., Spilker, J. A. & Hertzberg, V. S., Jan 1 1986, In: Radiology. 158, 3, p. 729-734 6 p.

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

    27 Scopus citations

  • Frequency of APOE, MTHFR and ACE polymorphisms in the Zambian population

    Atadzhanov, M., Mwaba, M. H., Mukomena, P. N., Lakhi, S., Mwaba, P., Rayaprolu, S., Meschia, J. F. & Ross, O. A., Mar 28 2014, In: BMC Research Notes. 7, 1, 194.

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

    11 Scopus citations

  • Frequency of bitemporal independent interictal epileptiform discharges in temporal lobe epilepsy

    Ergene, E., Shih, J. J., Blum, D. E. & So, N. K., 2000, In: Epilepsia. 41, 2, p. 213-218 6 p.

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

    48 Scopus citations

  • Frequency of mutations in PRKN, PINK1, and DJ1 in Patients With Early-Onset Parkinson Disease from neighboring countries in Central Europe

    Milanowski, Ł. M., Lindemann, J. A., Hoffman-Zacharska, D., Soto-Beasley, A. I., Barcikowska, M., Boczarska-Jedynak, M., Deutschlander, A., Kłodowska, G., Dulski, J., Fedoryshyn, L., Friedman, A., Jamrozik, Z., Janik, P., Karpinsky, K., Koziorowski, D., Krygowska-Wajs, A., Jasińska-Myga, B., Opala, G., Potulska-Chromik, A., Pulyk, A., & 10 othersRektorova, I., Sanotsky, Y., Siuda, J., Sławek, J., Śmiłowska, K., Szczechowski, L., Rudzińska-Bar, M., Walton, R. L., Ross, O. A. & Wszolek, Z. K., May 2021, In: Parkinsonism and Related Disorders. 86, p. 48-51 4 p.

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

  • Frequency of spinocerebellar ataxia mutations in patients with multiple system atrophy

    Wernick, A. I., Walton, R. L., Soto-Beasley, A. I., Koga, S., Heckman, M. G., Valentino, R. R., Milanowski, L. M., Hoffman-Zacharska, D., Koziorowski, D., Hassan, A., Uitti, R. J., Cheshire, W. P., Singer, W., Wszolek, Z. K., Dickson, D. W., Low, P. A. & Ross, O. A., Feb 2021, In: Clinical Autonomic Research. 31, 1, p. 117-125 9 p.

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

  • Frontal degenerative dementia and neuroimaging.

    Graff-Radford, N. R., Russell, J. W. & Rezai, K., 1995, In: Advances in neurology. 66, p. 37-47; discussion 47-4750

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

    10 Scopus citations

  • Frontal lobe 1H MR spectroscopy in asymptomatic and symptomatic MAPT mutation carriers

    Chen, Q., Boeve, B. F., Tosakulwong, N., Lesnick, T., Brushaber, D., Dheel, C., Fields, J., Forsberg, L., Gavrilova, R., Gearhart, D., Haley, D., Gunter, J. L., Graff-Radford, J., Jones, D., Knopman, D., Graff-Radford, N., Kraft, R., Lapid, M., Rademakers, R., Syrjanen, J., & 4 othersWszolek, Z. K., Rosen, H., Boxer, A. L. & Kantarci, K., 2019, In: Neurology. 93, 8, p. E758-E765

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

    8 Scopus citations

  • Frontotemporal dementia and its subtypes: A genome-wide association study

    Ferrari, R., Hernandez, D. G., Nalls, M. A., Rohrer, J. D., Ramasamy, A., Kwok, J. B. J., Dobson-Stone, C., Brooks William S., B. S., Schofield, P. R., Halliday, G. M., Hodges, J. R., Piguet, O., Bartley, L., Thompson, E., Haan, E., Hernández, I., Ruiz, A., Boada, M., Borroni, B., Padovani, A., & 138 othersCruchaga, C., Cairns, N. J., Benussi, L., Binetti, G., Ghidoni, R., Forloni, G., Galimberti, D., Fenoglio, C., Serpente, M., Scarpini, E., Clarimón, J., Lleó, A., Blesa, R., Waldö, M. L., Nilsson, K., Nilsson, C., Mackenzie, I. R. A., Hsiung, G. Y. R., Mann, D. M. A., Grafman, J., Morris, C. M., Attems, J., Griffiths, T. D., McKeith, I. G., Thomas, A. J., Pietrini, P., Huey, E. D., Wassermann, E. M., Baborie, A., Jaros, E., Tierney, M. C., Pastor, P., Razquin, C., Ortega-Cubero, S., Alonso, E., Perneczky, R., Diehl-Schmid, J., Alexopoulos, P., Kurz, A., Rainero, I., Rubino, E., Pinessi, L., Rogaeva, E., St George-Hyslop, P., Rossi, G., Tagliavini, F., Giaccone, G., Rowe, J. B., Schlachetzki, J. C. M., Uphill, J., Collinge, J., Mead, S., Danek, A., Van Deerlin, V. M., Grossman, M., Trojanowski, J. Q., Van der Zee, J., Deschamps, W., Van Langenhove, T., Cruts, M., Van Broeckhoven, C., Cappa, S. F., Le Ber, I., Hannequin, D., Golfier, V., Vercelletto, M., Brice, A., Nacmias, B., Sorbi, S., Bagnoli, S., Piaceri, I., Nielsen, J. E., Hjermind, L. E., Riemenschneider, M., Mayhaus, M., Ibach, B., Gasparoni, G., Pichler, S., Gu, W., Rossor, M. N., Fox, N. C., Warren, J. D., Spillantini, M. G., Morris, H. R., Rizzu, P., Heutink, P., Snowden, J. S., Rollinson, S., Richardson, A., Gerhard, A., Bruni, A. C., Maletta, R., Frangipane, F., Cupidi, C., Bernardi, L., Anfossi, M., Gallo, M., Conidi, M. E., Smirne, N., Rademakers, R., Baker, M., Dickson, D. W., Graff-Radford, N. R., Petersen, R. C., Knopman, D., Josephs, K. A., Boeve, B. F., Parisi, J. E., Seeley, W. W., Miller, B. L., Karydas, A. M., Rosen, H., van Swieten, J. C., Dopper, E. G. P., Seelaar, H., Pijnenburg, Y. A. L., Scheltens, P., Logroscino, G., Capozzo, R., Novelli, V., Puca, A. A., Franceschi, M., Postiglione, A., Milan, G., Sorrentino, P., Kristiansen, M., Chiang, H. H., Graff, C., Pasquier, F., Rollin, A., Deramecourt, V., Lebert, F., Kapogiannis, D., Ferrucci, L., Pickering-Brown, S., Singleton, A. B., Hardy, J. & Momeni, P., Jul 2014, In: The Lancet Neurology. 13, 7, p. 686-699 14 p.

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

    157 Scopus citations

  • Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17): PPND family. A longitudinal videotape demonstration

    Wszolek, Z. K., Kardon, R. H., Wolters, E. C. & Pfeiffer, R. F., Jul 2001, In: Movement Disorders. 16, 4, p. 756-760 5 p.

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

    10 Scopus citations

  • Frontotemporal dementia and parkinsonism linked to chromosome 17 - the first Polish family

    Narozdańska, E., Jasinska-Myga, B., Sitek, E. J., Robowski, P., Brockhuis, B., Lass, P., Dubaniewicz, M., Wieczorek, D., Baker, M., Rademakers, R., Wszolek, Z. K. & Sławek, J., Mar 2011, In: European Journal of Neurology. 18, 3, p. 535-537 3 p.

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

    11 Scopus citations

  • Frontotemporal dementia and parkinsonism linked to chromosome 17 with the N279K tau mutation

    Slowinski, J., Dominik, J., Uitti, R. J., Ahmed, Z., Dickson, D. D. & Wszolek, Z. K., Feb 2007, In: Neuropathology. 27, 1, p. 73-80 8 p.

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

    17 Scopus citations

  • Frontotemporal dementia-associated N279K tau mutant disrupts subcellular vesicle trafficking and induces cellular stress in iPSC-derived neural stem cells

    Wren, M. C., Zhao, J., Liu, C. C., Murray, M. E., Atagi, Y., Davis, M. D., Fu, Y., Okano, H. J., Ogaki, K., Strongosky, A. J., Tacik, P., Rademakers, R., Ross, O. A., Dickson, D. W., Wszolek, Z. K., Kanekiyo, T. & Bu, G., Sep 15 2015, In: Molecular neurodegeneration. 10, 1, 42.

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

    Open Access
    36 Scopus citations

  • Frontotemporal lobar degeneration with ubiquitin-positive, but TDP-43-negative inclusions

    Josephs, K. A., Lin, W. L., Ahmed, Z., Stroh, D. A., Graff-Radford, N. R. & Dickson, D. W., Aug 2008, In: Acta neuropathologica. 116, 2, p. 159-167 9 p.

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

    42 Scopus citations

  • FTDP-17 with Pick body-like inclusions associated with a novel tau mutation, p.E372G

    Tacik, P., DeTure, M. A., Carlomagno, Y., Lin, W. L., Murray, M. E., Baker, M. C., Josephs, K. A., Boeve, B. F., Wszolek, Z. K., Graff-Radford, N. R., Parisi, J. E., Petrucelli, L., Rademakers, R., Isaacson, R. S., Heilman, K. M., Petersen, R. C., Dickson, D. W. & Kouri, N., Sep 2017, In: Brain Pathology. 27, 5, p. 612-626 15 p.

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

    9 Scopus citations

  • Functional analysis of the SIM1 variant p.G715V in 2 patients with obesity

    Blackburn, P. R., Sullivan, A. E., Gerassimou, A. G., Kleinendorst, L., Bersten, D. C., Cooiman, M., Harris, K. G., Wierenga, K. J., Klee, E. W., van Gerpen, J. A., Ross, O. A., van Haelst, M. M., Whitelaw, M. L., Atwal, P. S. & Caulfield, T. R., Jan 1 2020, In: Journal of Clinical Endocrinology and Metabolism. 105, 1, p. 355-361 7 p.

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

    Open Access
    5 Scopus citations

  • Functional and genetic analysis of haplotypic sequence variation at the nicastrin genomic locus

    the Genetic and Environmental Risk for Alzheimer’s Disease (GERAD1) Consortium, the Translational Genomics Research Institute (TGen) Consortium & the European Alzheimer Disease Initiative (EADI), Aug 1 2012, In: Neurobiology of aging. 33, 8, p. 1848.e1-1848.e13

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

    4 Scopus citations

  • Functional brain architecture is associated with the rate of tau accumulation in Alzheimer’s disease

    Alzheimer’s Disease Neuroimaging Initiative (ADNI), Dec 1 2020, In: Nature communications. 11, 1, 347.

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

    Open Access
    34 Scopus citations

  • Functional characterization of brain tumor-initiating cells and establishment of GBM preclinical models that incorporate heterogeneity, therapy, and sex differences

    Garcia, C. A., Bhargav, A. G., Brooks, M., Suarez-Meade, P., Mondal, S. K., Zarco, N., ReFaey, K., Jentoft, M., Middlebrooks, E. H., Snuderl, M., Carrano, A., Guerrero-Cazares, H., Schiapparelli, P., Sarabia-Estrada, R. & Quiñones-Hinojosa, A., Dec 2021, In: Molecular cancer therapeutics. 20, 12, p. 2585-2597 13 p.

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

    Open Access

  • Functional validation of a novel AAAS variant in an atypical presentation of Allgrove syndrome

    Macke, E. L., Morales-Rosado, J. A., Macklin-Mantia, S. K., Schmitz, C. T., Oskarsson, B., Klee, E. W. & Wierenga, K. J., Jul 2022, In: Molecular Genetics and Genomic Medicine. 10, 7, e1966.

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

    Open Access

  • FUS gene mutations in familial and sporadic amyotrophic lateral sclerosis

    Rademakers, R., Stewart, H., Dejesus-Hernandez, M., Krieger, C., Graff-Radford, N., Fabros, M., Briemberg, H., Cashman, N., Eisen, A. & Mackenzie, I. R. A., Aug 2010, In: Muscle and Nerve. 42, 2, p. 170-176 7 p.

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

    79 Scopus citations

  • FUS pathology defines the majority of tau-and TDP-43-negative frontotemporal lobar degeneration

    Urwin, H., Josephs, K. A., Rohrer, J. D., MacKenzie, I. R., Neumann, M., Authier, A., Seelaar, H., Van Swieten, J. C., Brown, J. M., Johannsen, P., Nielsen, J. E., Holm, I. E., Dickson, D. W., Rademakers, R., Graff-Radford, N. R., Parisi, J. E., Petersen, R. C., Hatanpaa, K. J., White, C. L., Weiner, M. F., & 27 othersGeser, F., Van Deerlin, V. M., Trojanowski, J. Q., Miller, B. L., Seeley, W. W., Van Der Zee, J., Kumar-Singh, S., Engelborghs, S., De Deyn, P. P., Van Broeckhoven, C., Bigio, E. H., Deng, H. X., Halliday, G. M., Kril, J. J., Munoz, D. G., Mann, D. M., Pickering-Brown, S. M., Doodeman, V., Adamson, G., Ghazi-Noori, S., Fisher, E. M. C., Holton, J. L., Revesz, T., Rossor, M. N., Collinge, J., Mead, S. & Isaacs, A. M., Jul 2010, In: Acta neuropathologica. 120, 1, p. 33-41 9 p.

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

    175 Scopus citations

  • Future Neurohospitalist: Teleneurohospitalist

    Freeman, W. D., Barrett, K. M., Vatz, K. A. & Demaerschalk, B. M., Oct 2012, In: The Neurohospitalist. 2, 4, p. 132-143 12 p.

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

    14 Scopus citations

  • GBA variation and susceptibility to multiple system atrophy

    Wernick, A. I., Walton, R. L., Koga, S., Soto-Beasley, A. I., Heckman, M. G., Gan-Or, Z., Ren, Y., Rademakers, R., Uitti, R. J., Wszolek, Z. K., Cheshire, W. P., Dickson, D. W. & Ross, O. A., Aug 2020, In: Parkinsonism and Related Disorders. 77, p. 64-69 6 p.

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

  • GCH1 expression in human cerebellum from healthy individuals is not gender dependant

    Wider, C., Lincoln, S., Dachsel, J. C., Kapatos, G., Heckman, M. G., Diehl, N. N., Papapetropoulos, S., Mash, D., Rajput, A., Rajput, A. H., Dickson, D. W., Wszolek, Z. K. & Farrer, M. J., Sep 18 2009, In: Neuroscience Letters. 462, 1, p. 73-75 3 p.

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

    1 Scopus citations

  • GCH1 in early-onset Parkinson's disease

    Cobb, S. A., Wider, C., Ross, O. A., Mata, I. F., Adler, C. H., Rajput, A., Rajput, A. H., Wu, R. M., Hauser, R., Josephs, K. A., Carr, J., Gwinn, K., Heckman, M. G., Aasly, J. O., Lynch, T., Uitti, R. J., Wszolek, Z. K., Kapatos, G. & Farrer, M. J., Oct 30 2009, In: Movement Disorders. 24, 14, p. 2070-2075 6 p.

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

    15 Scopus citations

  • Gender and the Parkinson's disease phenotype

    Baba, Y., Putzke, J. D., Whaley, N. R., Wszolek, Z. K. & Uitti, R. J., Oct 1 2005, In: Journal of Neurology. 252, 10, p. 1201-1205 5 p.

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

    89 Scopus citations

  • Gene-based GWAS and biological pathway analysis of the resilience of executive functioning

    Mukherjee, S., Kim, S., Ramanan, V. K., Gibbons, L. E., Nho, K., Glymour, M. M., Ertekin-Taner, N., Montine, T. J., Saykin, A. J. & Crane, P. K., Mar 2014, In: Brain Imaging and Behavior. 8, 1, p. 110-118 9 p.

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

    23 Scopus citations

  • Gene expression, methylation and neuropathology correlations at progressive supranuclear palsy risk loci

    Allen, M., Burgess, J. D., Ballard, T., Serie, D., Wang, X., Younkin, C. S., Sun, Z., Kouri, N., Baheti, S., Wang, C., Carrasquillo, M. M., Nguyen, T., Lincoln, S., Malphrus, K., Murray, M., Golde, T. E., Price, N. D., Younkin, S. G., Schellenberg, G. D., Asmann, Y., & 4 othersOrdog, T., Crook, J., Dickson, D. & Ertekin-Taner, N., Aug 1 2016, In: Acta neuropathologica. 132, 2, p. 197-211 15 p.

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

    24 Scopus citations

  • Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes

    International FTD-Genomics Consortium, Apr 15 2021, In: Biological psychiatry. 89, 8, p. 825-835 11 p.

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

    Open Access
    1 Scopus citations

  • Gene expression levels as endophenotypes in genome-wide association studies of Alzheimer disease

    Zou, F., Carrasquillo, M. M., Pankratz, V. S., Belbin, O., Morgan, K., Allen, M., Wilcox, S. L., Ma, L., Walker, L. P., Kouri, N., Burgess, J. D., Younkin, L. H., Younkin, S. G., Younkin, C. S., Bisceglio, G. D., Crook, J. E., Dickson, D. W., Petersen, R. C., Graff-Radford, N., Younkin, S. G., & 1 othersErtekin-Taner, N., Feb 2010, In: Neurology. 74, 6, p. 480-486 7 p.

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

    26 Scopus citations

  • Genetically-controlled Vesicle-Associated Membrane Protein 1 expression may contribute to Alzheimer's pathophysiology and susceptibility

    Sevlever, D., Zou, F., Ma, L., Carrasquillo, S., Crump, M. G., Culley, O. J., Hunter, T. A., Bisceglio, G. D., Younkin, L., Allen, M., Carrasquillo, M. M., Sando, S. B., Aasly, J. O., Dickson, D. W., Graff-Radford, N. R., Petersen, R. C., Morgan, K. & Belbin, O., Apr 9 2015, In: Molecular neurodegeneration. 10, 1, 18.

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

    8 Scopus citations

  • Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease

    ARUK Consortium, GERAD/PERADES, CHARGE, ADGC, EADI, International Genomics of Alzheimer's Project (IGAP), ARUK Consortium & GERAD/PERADES, CHARGE, ADGC, EADI, Jan 1 2018, In: Alzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoring. 10, p. 595-598 4 p.

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

    Open Access

  • Genetically Elevated LDL Associates with Lower Risk of Intracerebral Hemorrhage

    Falcone, G. J., Kirsch, E., Acosta, J. N., Noche, R. B., Leasure, A., Marini, S., Chung, J., Selim, M., Meschia, J. F., Brown, D. L., Worrall, B. B., Tirschwell, D. L., Jagiella, J. M., Schmidt, H., Jimenez-Conde, J., Fernandez-Cadenas, I., Lindgren, A., Slowik, A., Gill, D., Holmes, M., & 18 othersPhuah, C. L., Petersen, N. H., Matouk, MD, C. N., Gunel, M., Sansing, L., Bennett, D., Chen, Z., Sun, L. L., Clarke, R., Walters, R. G., Gill, T. M., Biffi, A., Kathiresan, S., Langefeld, C. D., Woo, D., Rosand, J., Sheth, K. N. & Anderson, C. D., Jul 1 2020, In: Annals of neurology. 88, 1, p. 56-66 11 p.

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

  • Genetically predicted body mass index and Alzheimer's disease-related phenotypes in three large samples: Mendelian randomization analyses

    Adult Changes in Thought Study Investigators, Religious Orders Study/Memory and Aging Project Investigators & Alzheimer’s Disease Genetics Consortium, Dec 1 2015, In: Alzheimer's and Dementia. 11, 12, p. 1439-1451 13 p.

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

    28 Scopus citations

  • Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies

    Bras, J., Guerreiro, R., Darwent, L., Parkkinen, L., Ansorge, O., Escott-Price, V., Hernandez, D. G., Nalls, M. A., Clark, L. N., Honig, L. S., Marder, K., Van Der Flier, W. M., Lemstra, A., Scheltens, P., Rogaeva, E., St George-Hyslop, P., Londos, E., Zetterberg, H., Ortega-Cubero, S., Pastor, P., & 22 othersFerman, T. J., Graff-Radford, N. R., Ross, O. A., Barber, I., Braae, A., Brown, K., Morgan, K., Maetzler, W., Berg, D., Troakes, C., Al-Sarraj, S., Lashley, T., Compta, Y., Revesz, T., Lees, A., Cairns, N., Halliday, G. M., Mann, D., Pickering-Brown, S., Dickson, D. W., Singleton, A. & Hardy, J., Dec 1 2014, In: Human molecular genetics. 23, 23, p. 6139-6146 8 p.

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

    Open Access
    128 Scopus citations

  • Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration

    Chen-Plotkin, A. S., Martinez-Lage, M., Sleiman, P. M. A., Hu, W., Greene, R., Wood, E. M. C., Bing, S., Grossman, M., Schellenberg, G. D., Hatanpaa, K. J., Weiner, M. F., White, C. L., Brooks, W. S., Halliday, G. M., Kril, J. J., Gearing, M., Beach, T. G., Graff-Radford, N. R., Dickson, D. W., Rademakers, R., & 35 othersBoeve, B. F., Pickering-Brown, S. M., Snowden, J., Van Swieten, J. C., Heutink, P., Seelaar, H., Murrell, J. R., Ghetti, B., Spina, S., Grafman, J., Kaye, J. A., Woltjer, R. L., Mesulam, M., Bigio, E., Lladó, A., Miller, B. L., Alzualde, A., Moreno, F., Rohrer, J. D., Mackenzie, I. R. A., Feldman, H. H., Hamilton, R. L., Cruts, M., Engelborghs, S., De Deyn, P. P., Van Broeckhoven, C., Bird, T. D., Cairns, N. J., Goate, A., Frosch, M. P., Riederer, P. F., Bogdanovic, N., Lee, V. M. Y., Trojanowski, J. Q. & Van Deerlin, V. M., Apr 2011, In: Archives of neurology. 68, 4, p. 488-497 10 p.

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

    82 Scopus citations

  • Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting

    Stroke Genetics Network (SiGN), International Stroke Genetics Consortium (ISGC), METASTROKE, Alzheimer’s Disease Genetics Consortium (ADGC) & Neurology Working Group of the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium, Jan 29 2019, In: Neurology. 92, 5, p. E486-E503

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

    Open Access
    10 Scopus citations

  • Genetic architecture of resilience of executive functioning

    Mukherjee, S., Kim, S., Gibbons, L. E., Nho, K., Risacher, S. L., Glymour, M. M., Habeck, C., Lee, G. J., Mormino, E., Ertekin-Taner, N., Montine, T. J., DeCarli, C., Saykin, A. J. & Crane, P. K., Dec 2012, In: Brain Imaging and Behavior. 6, 4, p. 621-633 13 p.

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

    19 Scopus citations

  • Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases

    The IFGC and IPDGC members, Feb 1 2017, In: Journal of Neurology, Neurosurgery and Psychiatry. 88, 2, p. 152-164 13 p.

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

    56 Scopus citations

  • Genetic architecture of white matter hyperintensities differs in hypertensive and nonhypertensive ischemic stroke

    Adib-Samii, P., Devan, W., Traylor, M., Lanfranconi, S., Zhang, C. R., Cloonan, L., Falcone, G. J., Radmanesh, F., Fitzpatrick, K., Kanakis, A., Rothwell, P. M., Sudlow, C., Boncoraglio, G. B., Meschia, J. F., Levi, C., Dichgans, M., Bevan, S., Rosand, J., Rost, N. S. & Markus, H. S., Feb 6 2015, In: Stroke. 46, 2, p. 348-353 6 p.

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

    20 Scopus citations

  • Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

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

    Open Access
    236 Scopus citations

  • Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies

    Helsinki Stroke, Study Dutch Parelsnoer Institute-Cerebrovascular Accident (CVA) Study Group, National Institute of Neurological Disorders and Stroke (NINDS) Stroke Genetics Network, UK DNA Lacunar Stroke Study Investigators & International Stroke Genetics Consortium, May 2021, In: The Lancet Neurology. 20, 5, p. 351-361 11 p.

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

    Open Access

  • Genetic disorders with tau pathology: A review of the literature and report of two patients with tauopathy and positive family histories

    Tacik, P., Sanchez-Contreras, M., Rademakers, R., Dickson, D. W. & Wszolek, Z. K., Feb 1 2016, In: Neurodegenerative Diseases. 16, 1-2, p. 12-21 10 p.

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

    Open Access
    21 Scopus citations

  • Genetic effects on sleep/wake variation of seizures

    Winawer, M. R., Shih, J., Beck, E. S., Hunter, J. E. & Epstein, M. P., Apr 1 2016, In: Epilepsia. 57, 4, p. 557-565 9 p.

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

    10 Scopus citations

  • 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.

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  • 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