Works by Clark, Lorraine

Results: 69
    1

    LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson disease.

    Published in:
    Neurogenetics, 2010, v. 11, n. 4, p. 401, doi. 10.1007/s10048-010-0241-x
    By:
    • Vilariño-Güell, Carles;
    • Wider, Christian;
    • Ross, Owen;
    • Jasinska-Myga, Barbara;
    • Kachergus, Jennifer;
    • Cobb, Stephanie;
    • Soto-Ortolaza, Alexandra;
    • Behrouz, Bahareh;
    • Heckman, Michael;
    • Diehl, Nancy;
    • Testa, Claudia;
    • Wszolek, Zbigniew;
    • Uitti, Ryan;
    • Jankovic, Joseph;
    • Louis, Elan;
    • Clark, Lorraine;
    • Rajput, Alex;
    • Farrer, Matthew
    Publication type:
    Article
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    Olfactory identification in LRRK2 G2019S mutation carriers: a relevant marker?

    Published in:
    Annals of Clinical & Translational Neurology, 2014, v. 1, n. 9, p. 670, doi. 10.1002/acn3.95
    By:
    • Saunders‐Pullman, Rachel;
    • Mirelman, Anat;
    • Wang, Cuiling;
    • Alcalay, Roy N.;
    • San Luciano, Marta;
    • Ortega, Robert;
    • Raymond, Deborah;
    • Mejia‐Santana, Helen;
    • Ozelius, Laurie;
    • Clark, Lorraine;
    • Orr‐Utreger, Avi;
    • Marder, Karen;
    • Giladi, Nir;
    • Bressman, Susan B.
    Publication type:
    Article
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    Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis.

    Published in:
    JAMA Neurology, 2022, v. 79, n. 2, p. 185, doi. 10.1001/jamaneurol.2021.4781
    By:
    • Liao, Calwing;
    • Castonguay, Charles-Etienne;
    • Heilbron, Karl;
    • Vuokila, Veikko;
    • Medeiros, Miranda;
    • Houle, Gabrielle;
    • Akçimen, Fulya;
    • Ross, Jay P.;
    • Catoire, Helene;
    • Diez-Fairen, Monica;
    • Kang, Jooeun;
    • Mueller, Stefanie H.;
    • Girard, Simon L.;
    • Hopfner, Franziska;
    • Lorenz, Delia;
    • Clark, Lorraine N.;
    • Soto-Beasley, Alexandra I.;
    • Klebe, Stephan;
    • Hallett, Mark;
    • Wszolek, Zbigniew K.
    Publication type:
    Article
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    Clinical Correlations With Lewy Body Pathology in LRRK2-Related Parkinson Disease.

    Published in:
    JAMA Neurology, 2015, v. 72, n. 1, p. 100, doi. 10.1001/jamaneurol.2014.2704
    By:
    • Kalia, Lorraine V.;
    • Lang, Anthony E.;
    • Hazrati, Lili-Naz;
    • Fujioka, Shinsuke;
    • Wszolek, Zbigniew K.;
    • Dickson, Dennis W.;
    • Ross, Owen A.;
    • Van Deerlin, Vivianna M.;
    • Trojanowski, John Q.;
    • Hurtig, Howard I.;
    • Alcalay, Roy N.;
    • Marder, Karen S.;
    • Clark, Lorraine N.;
    • Gaig, Carles;
    • Tolosa, Eduardo;
    • Ruiz-Martínez, Javier;
    • Marti-Masso, Jose F.;
    • Ferrer, Isidre;
    • López de Munain, Adolfo;
    • Goldman, Samuel M.
    Publication type:
    Article
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    Clinical and Pathological Characteristics of LRRK2 G2019S Patients with PD.

    Published in:
    Journal of Molecular Neuroscience, 2012, v. 47, n. 1, p. 139, doi. 10.1007/s12031-011-9696-y
    By:
    • Poulopoulos, Markos;
    • Cortes, Etty;
    • Vonsattel, Jean-Paul;
    • Fahn, Stanley;
    • Waters, Cheryl;
    • Cote, Lucien;
    • Moskowitz, Carol;
    • Honig, Lawrence;
    • Clark, Lorraine;
    • Marder, Karen;
    • Alcalay, Roy
    Publication type:
    Article
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    Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene.

    Published in:
    Movement Disorders, 2015, v. 30, n. 7, p. 981, doi. 10.1002/mds.26213
    By:
    • Mirelman, Anat;
    • Alcalay, Roy N.;
    • Saunders‐Pullman, Rachel;
    • Yasinovsky, Kira;
    • Thaler, Avner;
    • Gurevich, Tanya;
    • Mejia‐Santana, Helen;
    • Raymond, Deborah;
    • Gana‐Weisz, Mali;
    • Bar‐Shira, Anat;
    • Ozelius, Laurie;
    • Clark, Lorraine;
    • Orr‐Urtreger, Avi;
    • Bressman, Susan;
    • Marder, Karen;
    • Giladi, Nir
    Publication type:
    Article
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    Genetic variants of α-synuclein are not associated with essential tremor.

    Published in:
    Movement Disorders, 2011, v. 26, n. 14, p. 2552, doi. 10.1002/mds.23909
    By:
    • Ross, Owen A.;
    • Conneely, Karen N.;
    • Wang, Tao;
    • Vilarino-Guell, Carles;
    • Soto-Ortolaza, Alexandra I.;
    • Rajput, Alex;
    • Wszolek, Zbigniew K.;
    • Uitti, Ryan J.;
    • Louis, Elan D.;
    • Clark, Lorraine N.;
    • Farrer, Matthew J.;
    • Testa, Claudia M.
    Publication type:
    Article
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    Clinical exome sequencing for inherited retinal degenerations at a tertiary care center.

    Published in:
    Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-13026-2
    By:
    • Ganapathi, Mythily;
    • Thomas-Wilson, Amanda;
    • Buchovecky, Christie;
    • Dharmadhikari, Avinash;
    • Barua, Subit;
    • Lee, Winston;
    • Ruan, Merry Z. C.;
    • Soucy, Megan;
    • Ragi, Sara;
    • Tanaka, Joy;
    • Clark, Lorraine N.;
    • Naini, Ali B.;
    • Liao, Jun;
    • Mansukhani, Mahesh;
    • Tsang, Stephen;
    • Jobanputra, Vaidehi
    Publication type:
    Article
    20

    Gene-Wise Association of Variants in Four Lysosomal Storage Disorder Genes in Neuropathologically Confirmed Lewy Body Disease.

    Published in:
    PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0125204
    By:
    • Clark, Lorraine N.;
    • Chan, Robin;
    • Cheng, Rong;
    • Liu, Xinmin;
    • Park, Naeun;
    • Parmalee, Nancy;
    • Kisselev, Sergey;
    • Cortes, Etty;
    • Torres, Paola A.;
    • Pastores, Gregory M.;
    • Vonsattel, Jean P.;
    • Alcalay, Roy;
    • Marder, Karen;
    • Honig, Lawrence L.;
    • Fahn, Stanley;
    • Mayeux, Richard;
    • Shelanski, Michael;
    • Di Paolo, Gilbert;
    • Lee, Joseph H.
    Publication type:
    Article
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    Current Opinions and Consensus for Studying Tremor in Animal Models.

    Published in:
    Cerebellum, 2019, v. 18, n. 6, p. 1036, doi. 10.1007/s12311-019-01037-1
    By:
    • Kuo, Sheng-Han;
    • Louis, Elan D.;
    • Faust, Phyllis L.;
    • Handforth, Adrian;
    • Chang, Su-youne;
    • Avlar, Billur;
    • Lang, Eric J.;
    • Pan, Ming-Kai;
    • Miterko, Lauren N.;
    • Brown, Amanda M.;
    • Sillitoe, Roy V.;
    • Anderson, Collin J.;
    • Pulst, Stefan M.;
    • Gallagher, Martin J.;
    • Lyman, Kyle A.;
    • Chetkovich, Dane M.;
    • Clark, Lorraine N.;
    • Tio, Murni;
    • Tan, Eng-King;
    • Elble, Rodger J.
    Publication type:
    Article
    23

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

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 23, p. 6139, doi. 10.1093/hmg/ddu334
    By:
    • Bras, Jose;
    • Guerreiro, Rita;
    • Darwent, Lee;
    • Parkkinen, Laura;
    • Ansorge, Olaf;
    • Escott-Price, Valentina;
    • Hernandez, Dena G.;
    • Nalls, Michael A.;
    • Clark, Lorraine N.;
    • Honig, Lawrence S.;
    • Marder, Karen;
    • Van Der Flier, Wiesje M.;
    • Lemstra, Afina;
    • Scheltens, Philip;
    • Rogaeva, Ekaterina;
    • St George-Hyslop, Peter;
    • Londos, Elisabet;
    • Zetterberg, Henrik;
    • Ortega-Cubero, Sara;
    • Pastor, Pau
    Publication type:
    Article
    24

    Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 17, p. 4693, doi. 10.1093/hmg/ddu158
    By:
    • Vacic, Vladimir;
    • Ozelius, Laurie J.;
    • Clark, Lorraine N.;
    • Bar-Shira, Anat;
    • Gana-Weisz, Mali;
    • Gurevich, Tanya;
    • Gusev, Alexander;
    • Kedmi, Merav;
    • Kenny, Eimear E.;
    • Liu, Xinmin;
    • Mejia-Santana, Helen;
    • Mirelman, Anat;
    • Raymond, Deborah;
    • Saunders-Pullman, Rachel;
    • Desnick, Robert J.;
    • Atzmon, Gil;
    • Burns, Edward R.;
    • Ostrer, Harry;
    • Hakonarson, Hakon;
    • Bergman, Aviv
    Publication type:
    Article
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    Genome-wide association study in essential tremor identifies three new loci.

    Published in:
    Brain: A Journal of Neurology, 2016, v. 139, n. 12, p. 3163, doi. 10.1093/brain/aww242
    By:
    • Müller, Stefanie H.;
    • Girard, Simon L.;
    • Hopfner, Franziska;
    • Merner, Nancy D.;
    • Bourassa, Cynthia V.;
    • Lorenz, Delia;
    • Clark, Lorraine N.;
    • Tittmann, Lukas;
    • Soto-Ortolaza, Alexandra I.;
    • Klebe, Stephan;
    • Hallett, Mark;
    • Schneider, Susanne A.;
    • Hodgkinson, Colin A.;
    • Lieb, Wolfgang;
    • Wszolek, Zbigniew K.;
    • Pendziwiat, Manuela;
    • Lorenzo-Betancor, Oswaldo;
    • Poewe, Werner;
    • Ortega-Cubero, Sara;
    • Seppi, Klaus
    Publication type:
    Article
    27

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

    Published in:
    2021
    By:
    • Lai, Dongbing;
    • Alipanahi, Babak;
    • Fontanillas, Pierre;
    • Schwantes‐An, Tae‐Hwi;
    • Aasly, Jan;
    • Alcalay, Roy N.;
    • Beecham, Gary W.;
    • Berg, Daniela;
    • Bressman, Susan;
    • Brice, Alexis;
    • Brockman, Kathrin;
    • Clark, Lorraine;
    • Cookson, Mark;
    • Das, Sayantan;
    • Van Deerlin, Vivianna;
    • Follett, Jordan;
    • Farrer, Matthew J.;
    • Trinh, Joanne;
    • Gasser, Thomas;
    • Goldwurm, Stefano
    Publication type:
    journal article
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    Meta-analysis of Parkinson's Disease: Identification of a novel locus, RIT2.

    Published in:
    Annals of Neurology, 2012, v. 71, n. 3, p. 370, doi. 10.1002/ana.22687
    By:
    • Pankratz, Nathan;
    • Beecham, Gary W.;
    • DeStefano, Anita L.;
    • Dawson, Ted M.;
    • Doheny, Kimberly F.;
    • Factor, Stewart A.;
    • Hamza, Taye H.;
    • Hung, Albert Y.;
    • Hyman, Bradley T.;
    • Ivinson, Adrian J.;
    • Krainc, Dmitri;
    • Latourelle, Jeanne C.;
    • Clark, Lorraine N.;
    • Marder, Karen;
    • Martin, Eden R.;
    • Mayeux, Richard;
    • Ross, Owen A.;
    • Scherzer, Clemens R.;
    • Simon, David K.;
    • Tanner, Caroline
    Publication type:
    Article
    31

    SORCS1 alters amyloid precursor protein processing and variants may increase Alzheimer's disease risk.

    Published in:
    Annals of Neurology, 2011, v. 69, n. 1, p. 47, doi. 10.1002/ana.22308
    By:
    • Reitz, Christiane;
    • Tokuhiro, Shinya;
    • Clark, Lorraine N.;
    • Conrad, Christopher;
    • Vonsattel, Jean-Paul;
    • Hazrati, Lili-Naz;
    • Palotás, András;
    • Lantigua, Raphael;
    • Medrano, Martin;
    • Z. Jiménez -Velázquez, Ivonne;
    • Vardarajan, Badri;
    • Simkin, Irene;
    • Haines, Jonathan L.;
    • Pericak -Vance, Margaret A.;
    • Farrer, Lindsay A.;
    • Lee, Joseph H.;
    • Rogaeva, Ekaterina;
    • George- Hyslop, Peter St.;
    • Mayeux, Richard
    Publication type:
    Article
    32

    From genotype to phenotype: a clinical pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation.

    Published in:
    1999
    By:
    • Nasreddine, Ziad S.;
    • Loginov, Maxim;
    • Clark, Lorraine N.;
    • Lamarche, Jacques;
    • Miller, Bruce L.;
    • Lamontagne, Albert;
    • Zhukareva, Victoria;
    • Lee, Virginia M.-Y.;
    • Wilhelmsen, Kirk C.;
    • Geschwind, Daniel H.;
    • Nasreddine, Z S;
    • Loginov, M;
    • Clark, L N;
    • Lamarche, J;
    • Miller, B L;
    • Lamontagne, A;
    • Zhukareva, V;
    • Lee, V M;
    • Wilhelmsen, K C;
    • Geschwind, D H
    Publication type:
    journal article
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    PCDH10 promoter hypermethylation is frequent in most histologic subtypes of mature lymphoid malignancies and occurs early in lymphomagenesis.

    Published in:
    Genes, Chromosomes & Cancer, 2013, v. 52, n. 11, p. 1030, doi. 10.1002/gcc.22098
    By:
    • Narayan, Gopeshwar;
    • Xie, Dongxu;
    • Freddy, Allen J.;
    • Ishdorj, Ganchimeg;
    • Do, Catherine;
    • Satwani, Prakash;
    • Liyanage, Hema;
    • Clark, Lorraine;
    • Kisselev, Sergey;
    • Nandula, Subhadra V.;
    • Scotto, Luigi;
    • Alobeid, Bachir;
    • Savage, David;
    • Tycko, Benjamin;
    • O'Connor, Owen A.;
    • Bhagat, Govind;
    • Murty, Vundavalli V.
    Publication type:
    Article
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    Application of the Movement Disorder Society prodromal criteria in healthy G2019S-LRRK2 carriers.

    Published in:
    2018
    By:
    • Mirelman, Anat;
    • Saunders‐Pullman, Rachel;
    • Alcalay, Roy N.;
    • Shustak, Shiran;
    • Thaler, Avner;
    • Gurevich, Tanya;
    • Raymond, Deborah;
    • Mejia‐Santana, Helen;
    • Orbe Reilly, Martha;
    • Ozelius, Laurie;
    • Clark, Lorraine;
    • Gana‐Weisz, Mali;
    • Bar‐Shira, Anat;
    • Orr‐Utreger, Avi;
    • Bressman, Susan B.;
    • Marder, Karen;
    • Giladi, Nir;
    • the AJ LRRK2 Consortium;
    • Saunders-Pullman, Rachel;
    • Mejia-Santana, Helen
    Publication type:
    journal article
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