Works matching AU Hernandez, Dena

Results: 122
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    Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson's Disease.

    Published in:
    Journal of Parkinson's Disease, 2022, v. 12, n. 1, p. 267, doi. 10.3233/JPD-212851
    By:
    • Domenighetti, Cloé;
    • Sugier, Pierre-Emmanuel;
    • Sreelatha, Ashwin Ashok Kumar;
    • Schulte, Claudia;
    • Grover, Sandeep;
    • Mohamed, Océane;
    • Portugal, Berta;
    • May, Patrick;
    • Bobbili, Dheeraj R.;
    • Radivojkov-Blagojevic, Milena;
    • Lichtner, Peter;
    • Singleton, Andrew B.;
    • Hernandez, Dena G.;
    • Edsall, Connor;
    • Mellick, George D.;
    • Zimprich, Alexander;
    • Pirker, Walter;
    • Rogaeva, Ekaterina;
    • Lang, Anthony E.;
    • Koks, Sulev
    Publication type:
    Article
    3

    Structural genomic variation in ischemic stroke.

    Published in:
    Neurogenetics, 2008, v. 9, n. 2, p. 101, doi. 10.1007/s10048-008-0119-3
    By:
    • Matarin, Mar;
    • Simon-Sanchez, Javier;
    • Fung, Hon-Chung;
    • Scholz, Sonja;
    • Gibbs, J.;
    • Hernandez, Dena;
    • Crews, Cynthia;
    • Britton, Angela;
    • Wavrant De Vrieze, Fabienne;
    • Brott, Thomas;
    • Brown, Robert;
    • Worrall, Bradford;
    • Silliman, Scott;
    • Case, L.;
    • Hardy, John;
    • Rich, Stephen;
    • Meschia, James;
    • Singleton, Andrew
    Publication type:
    Article
    4

    Kohlschütter-Tönz Syndrome: Mutations in ROGDI and Evidence of Genetic Heterogeneity.

    Published in:
    Human Mutation, 2013, v. 34, n. 2, p. 296, doi. 10.1002/humu.22241
    By:
    • Tucci, Arianna;
    • Kara, Eleanna;
    • Schossig, Anna;
    • Wolf, Nicole I.;
    • Plagnol, Vincent;
    • Fawcett, Katherine;
    • Paisán‐Ruiz, Coro;
    • Moore, Matthew;
    • Hernandez, Dena;
    • Musumeci, Sebastiano;
    • Tennison, Michael;
    • Hennekam, Raoul;
    • Palmeri, Silvia;
    • Malandrini, Alessandro;
    • Raskin, Salmo;
    • Donnai, Dian;
    • Hennig, Corina;
    • Tzschach, Andreas;
    • Hordijk, Roel;
    • Bast, Thomas
    Publication type:
    Article
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    Use of support vector machines for disease risk prediction in genome-wide association studies: Concerns and opportunities.

    Published in:
    Human Mutation, 2012, v. 33, n. 12, p. 1708, doi. 10.1002/humu.22161
    By:
    • Mittag, Florian;
    • Büchel, Finja;
    • Saad, Mohamad;
    • Jahn, Andreas;
    • Schulte, Claudia;
    • Bochdanovits, Zoltan;
    • Simón-Sánchez, Javier;
    • Nalls, Mike A.;
    • Keller, Margaux;
    • Hernandez, Dena G.;
    • Gibbs, J. Raphael;
    • Lesage, Suzanne;
    • Brice, Alexis;
    • Heutink, Peter;
    • Martinez, Maria;
    • Wood, Nicholas W;
    • Hardy, John;
    • Singleton, Andrew B.;
    • Zell, Andreas;
    • Gasser, Thomas
    Publication type:
    Article
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    MIDN locus structural variants and Parkinson's Disease risk.

    Published in:
    Annals of Clinical & Translational Neurology, 2020, v. 7, n. 4, p. 602, doi. 10.1002/acn3.51012
    By:
    • Billingsley, Kimberley J.;
    • Bandres‐Ciga, Sara;
    • Ding, Jinhui;
    • Hernandez, Dena;
    • Gibbs, J. Raphael;
    • Blauwendraat, Cornelis
    Publication type:
    Article
    8

    Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease.

    Published in:
    JAMA Neurology, 2018, v. 75, n. 11, p. 1416, doi. 10.1001/jamaneurol.2018.1885
    By:
    • Blauwendraat, Cornelis;
    • Reed, Xylena;
    • Kia, Demis A.;
    • Gan-Or, Ziv;
    • Lesage, Suzanne;
    • Pihlstrøm, Lasse;
    • Guerreiro, Rita;
    • Gibbs, J. Raphael;
    • Sabir, Marya;
    • Ahmed, Sarah;
    • Ding, Jinhui;
    • Alcalay, Roy N.;
    • Hassin-Baer, Sharon;
    • Pittman, Alan M.;
    • Brooks, Janet;
    • Edsall, Connor;
    • Hernandez, Dena G.;
    • Chung, Sun Ju;
    • Goldwurm, Stefano;
    • Toft, Mathias
    Publication type:
    Article
    9

    Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases.

    Published in:
    JAMA Neurology, 2017, v. 74, n. 7, p. 780, doi. 10.1001/jamaneurol.2017.0469
    By:
    • Witoelar, Aree;
    • Jansen, Iris E.;
    • Yunpeng Wang;
    • Desikan, Rahul S.;
    • Gibbs, J. Raphael;
    • Blauwendraat, Cornelis;
    • Thompson, Wesley K.;
    • Hernandez, Dena G.;
    • Djurovic, Srdjan;
    • Schork, Andrew J.;
    • Bettella, Francesco;
    • Ellinghaus, David;
    • Franke, Andre;
    • Lie, Benedicte A.;
    • McEvoy, Linda K.;
    • Karlsen, Tom H.;
    • Lesage, Suzanne;
    • Morris, Huw R.;
    • Brice, Alexis;
    • Wood, Nicholas W.
    Publication type:
    Article
    10

    A Genome-Wide Association Study of Myasthenia Gravis.

    Published in:
    JAMA Neurology, 2015, v. 72, n. 4, p. 396, doi. 10.1001/jamaneurol.2014.4103
    By:
    • Renton, Alan E.;
    • Pliner, Hannah A.;
    • Provenzano, Carlo;
    • Evoli, Amelia;
    • Ricciardi, Roberta;
    • Nalls, Michael A.;
    • Marangi, Giuseppe;
    • Abramzon, Yevgeniya;
    • Arepalli, Sampath;
    • Sean Chong;
    • Hernandez, Dena G.;
    • Johnson, Janel O.;
    • Bartoccioni, Emanuela;
    • Scuderi, Flavia;
    • Maestri, Michelangelo;
    • Gibbs, J. Raphael;
    • Errichiello, Edoardo;
    • Chiò, Adriano;
    • Restagno, Gabriella;
    • Sabatelli, Mario
    Publication type:
    Article
    11

    A 6.4 Mb Duplication of the a-Synuclein Locus Causing Frontotemporal Dementia and Parkinsonism Phenotype-Genotype Correlations.

    Published in:
    JAMA Neurology, 2014, v. 71, n. 9, p. 1162, doi. 10.1001/jamaneurol.2014.994
    By:
    • Kara, Eleanna;
    • Kiely, Aoife P.;
    • Proukakis, Christos;
    • Giffin, Nicola;
    • Love, Seth;
    • Hehir, Jason;
    • Rantell, Khadija;
    • Pandraud, Amelie;
    • Hernandez, Dena G.;
    • Nacheva, Elizabeth;
    • Pittman, Alan M.;
    • Nalls, Mike A.;
    • Singleton, Andrew B.;
    • Revesz, Tamas;
    • Bhatia, Kailash P.;
    • Quinn, Niall;
    • Hardy, John;
    • Holton, Janice L.;
    • Houlden, Henry
    Publication type:
    Article
    12

    Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk.

    Published in:
    JAMA Neurology, 2013, v. 70, n. 10, p. 1268, doi. 10.1001/jamaneurol.2013.448
    By:
    • Moskvina, Valentina;
    • Harold, Denise;
    • Russo, GianCarlo;
    • Vedernikov, Alexey;
    • Sharma, Manu;
    • Saad, Mohamad;
    • Holmans, Peter;
    • Bras, Jose M.;
    • Bettella, Francesco;
    • Keller, Margaux F.;
    • Nicolaou, Nayia;
    • Simón-Sánchez, Javier;
    • Gibbs, J. Raphael;
    • Schulte, Claudia;
    • Durr, Alexandra;
    • Guerreiro, Rita;
    • Hernandez, Dena;
    • Brice, Alexis;
    • Stefánsson, Hreinn;
    • Majamaa, Kari
    Publication type:
    Article
    13

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

    Published in:
    Nature Genetics, 2014, v. 46, n. 9, p. 989, doi. 10.1038/ng.3043
    By:
    • Nalls, Mike A;
    • Pankratz, Nathan;
    • Lill, Christina M;
    • Do, Chuong B;
    • Hernandez, Dena G;
    • Saad, Mohamad;
    • DeStefano, Anita L;
    • Kara, Eleanna;
    • Bras, Jose;
    • Sharma, Manu;
    • Schulte, Claudia;
    • Keller, Margaux F;
    • Arepalli, Sampath;
    • Letson, Christopher;
    • Edsall, Connor;
    • Stefansson, Hreinn;
    • Liu, Xinmin;
    • Pliner, Hannah;
    • Lee, Joseph H;
    • Cheng, Rong
    Publication type:
    Article
    14

    Genome-wide association study reveals genetic risk underlying Parkinson's disease.

    Published in:
    Nature Genetics, 2009, v. 41, n. 12, p. 1308, doi. 10.1038/ng.487
    By:
    • Simón-Sánchez, Javier;
    • Schulte, Claudia;
    • Bras, Jose M.;
    • Sharma, Manu;
    • Gibbs, J. Raphael;
    • Berg, Daniela;
    • Paisan-Ruiz, Coro;
    • Lichtner, Peter;
    • Scholz, Sonja W.;
    • Hernandez, Dena G.;
    • Krüger, Rejko;
    • Federoff, Monica;
    • Klein, Christine;
    • Goate, Alison;
    • Perlmutter, Joel;
    • Bonin, Michael;
    • Nalls, Michael A.;
    • Illig, Thomas;
    • Gieger, Christian;
    • Houlden, Henry
    Publication type:
    Article
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    A common variation in deiodinase 1 gene DIO1 is associated with the relative levels of free thyroxine and triiodothyronine.

    Published in:
    2008
    By:
    • Panicker, Vijay;
    • Cluett, Christie;
    • Shields, Beverley;
    • Murray, Anna;
    • Parnell, Kirstie S;
    • Perry, John R B;
    • Weedon, Michael N;
    • Singleton, Andrew;
    • Hernandez, Dena;
    • Evans, Jonathan;
    • Durant, Claire;
    • Ferrucci, Luigi;
    • Melzer, David;
    • Saravanan, Ponnusamy;
    • Visser, Theo J;
    • Ceresini, Graziano;
    • Hattersley, Andrew T;
    • Vaidya, Bijay;
    • Dayan, Colin M;
    • Frayling, Timothy M
    Publication type:
    journal article
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    Phenomenology of 'Lubag' or X-linked dystonia-parkinsonism.

    Published in:
    Movement Disorders, 2002, v. 17, n. 6, p. 1271, doi. 10.1002/mds.10271
    By:
    • Evidente, Virgilio Gerald H.;
    • Advincula, Joel;
    • Esteban, Raymund;
    • Pasco, Paul;
    • Alfon, Jhoe Anthony;
    • Natividad, Filipinas F.;
    • Cuanang, Joven;
    • Luis, Amado San;
    • Gwinn-Hardy, Katrina;
    • Hardy, John;
    • Hernandez, Dena;
    • Singleton, Andrew
    Publication type:
    Article
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    Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2).

    Published in:
    NPJ Parkinson's Disease, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41531-023-00533-w
    By:
    • Towns, Clodagh;
    • Richer, Madeleine;
    • Jasaityte, Simona;
    • Stafford, Eleanor J.;
    • Joubert, Julie;
    • Antar, Tarek;
    • Martinez-Carrasco, Alejandro;
    • Makarious, Mary B.;
    • Casey, Bradford;
    • Vitale, Dan;
    • Levine, Kristin;
    • Leonard, Hampton;
    • Pantazis, Caroline B.;
    • Screven, Laurel A.;
    • Hernandez, Dena G.;
    • Wegel, Claire E.;
    • Solle, Justin;
    • Nalls, Mike A.;
    • Blauwendraat, Cornelis;
    • Singleton, Andrew B.
    Publication type:
    Article
    28

    Fine-Mapping, Gene Expression and Splicing Analysis of the Disease Associated <i>LRRK2</i> Locus.

    Published in:
    PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0070724
    By:
    • Trabzuni, Daniah;
    • Ryten, Mina;
    • Emmett, Warren;
    • Ramasamy, Adaikalavan;
    • Lackner, Karl J.;
    • Zeller, Tanja;
    • Walker, Robert;
    • Smith, Colin;
    • Lewis, Patrick A.;
    • Mamais, Adamantios;
    • de Silva, Rohan;
    • Vandrovcova, Jana;
    • Hernandez, Dena;
    • Nalls, Michael A.;
    • Sharma, Manu;
    • Garnier, Sophie;
    • Lesage, Suzanne;
    • Simon-Sanchez, Javier;
    • Gasser, Thomas;
    • Heutink, Peter
    Publication type:
    Article
    29

    Imputation of Variants from the 1000 Genomes Project Modestly Improves Known Associations and Can Identify Low-frequency Variant - Phenotype Associations Undetected by HapMap Based Imputation

    Published in:
    PLoS ONE, 2013, v. 8, n. 5, p. 1, doi. 10.1371/journal.pone.0064343
    By:
    • Wood, Andrew R.;
    • Perry, John R. B.;
    • Tanaka, Toshiko;
    • Hernandez, Dena G.;
    • Zheng, Hou-Feng;
    • Melzer, David;
    • Gibbs, J. Raphael;
    • Nalls, Michael A.;
    • Weedon, Michael N.;
    • Spector, Tim D.;
    • Richards, J. Brent;
    • Bandinelli, Stefania;
    • Ferrucci, Luigi;
    • Singleton, Andrew B.;
    • Frayling, Timothy M.
    Publication type:
    Article
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    Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes.

    Published in:
    Human Molecular Genetics, 2015, v. 24, n. 5, p. 1504, doi. 10.1093/hmg/ddu560
    By:
    • Wood, Andrew R.;
    • Tuke, Marcus A.;
    • Nalls, Mike;
    • Hernandez, Dena;
    • Gibbs, J. Raphael;
    • Lin, Haoxiang;
    • Xu, Christopher S.;
    • Li, Qibin;
    • Shen, Juan;
    • Jun, Goo;
    • Almeida, Marcio;
    • Tanaka, Toshiko;
    • Perry, John R. B.;
    • Gaulton, Kyle;
    • Rivas, Manny;
    • Pearson, Richard;
    • Curran, Joanne E.;
    • Johnson, Matthew P.;
    • Göring, Harald H. H.;
    • Duggirala, Ravindranath
    Publication type:
    Article
    33

    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
    34

    Genetic comorbidities in Parkinson's disease.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 3, p. 831
    By:
    • Nalls, Mike A.;
    • Saad, Mohamad;
    • Noyce, Alastair J.;
    • Keller, Margaux F.;
    • Schrag, Anette;
    • Bestwick, Jonathan P.;
    • Traynor, Bryan J.;
    • Gibbs, J. Raphael;
    • Hernandez, Dena G.;
    • Cookson, Mark R.;
    • Morris, Huw R.;
    • Williams, Nigel;
    • Gasser, Thomas;
    • Heutink, Peter;
    • Wood, Nick;
    • Hardy, John;
    • Martinez, Maria;
    • Singleton, Andrew B.
    Publication type:
    Article
    35

    A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 2, p. 562
    By:
    • Holmans, Peter;
    • Moskvina, Valentina;
    • Jones, Lesley;
    • Sharma, Manu;
    • Vedernikov, Alexey;
    • Buchel, Finja;
    • Saad, Mohamad;
    • Bras, Jose M.;
    • Bettella, Francesco;
    • Nicolaou, Nayia;
    • Simón-Sánchez, Javier;
    • Mittag, Florian;
    • Gibbs, J. Raphael;
    • Schulte, Claudia;
    • Durr, Alexandra;
    • Guerreiro, Rita;
    • Hernandez, Dena;
    • Brice, Alexis;
    • Stefánsson, Hreinn;
    • Majamaa, Kari
    Publication type:
    Article
    36

    Using genome-wide complex trait analysis to quantify ‘missing heritability’ in Parkinson's disease.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 14, p. 2973
    By:
    • Keller, Margaux F.;
    • Saad, Mohamad;
    • Bras, Jose;
    • Bettella, Francesco;
    • Nicolaou, Nayia;
    • Simón-Sánchez, Javier;
    • Mittag, Florian;
    • chel, Finja Bü;
    • Sharma, Manu;
    • Gibbs, J. Raphael;
    • Schulte, Claudia;
    • Moskvina, Valentina;
    • Durr, Alexandra;
    • Holmans, Peter;
    • Kilarski, Laura L.;
    • Guerreiro, Rita;
    • Hernandez, Dena G.;
    • Brice, Alexis;
    • Ylikotila, Pauli;
    • Stefánsson, Hreinn
    Publication type:
    Article
    37

    Using genome-wide complex trait analysis to quantify ‘missing heritability’ in Parkinson's disease.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 8, p. 1696
    By:
    • Keller, Margaux F.;
    • Saad, Mohamad;
    • Bras, Jose;
    • Bettella, Francesco;
    • Nicolaou, Nayia;
    • Simón-Sánchez, Javier;
    • Mittag, Florian;
    • Büchel, Finja;
    • Sharma, Manu;
    • Gibbs, J. Raphael;
    • Schulte, Claudia;
    • Moskvina, Valentina;
    • Durr, Alexandra;
    • Holmans, Peter;
    • Kilarski, Laura L.;
    • Guerreiro, Rita;
    • Hernandez, Dena G.;
    • Brice, Alexis;
    • Ylikotila, Pauli;
    • Stefánsson, Hreinn
    Publication type:
    Article
    38

    A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 5, p. 1039
    By:
    • Holmans, Peter;
    • Moskvina, Valentina;
    • Jones, Lesley;
    • Sharma, Manu;
    • Vedernikov, Alexey;
    • Buchel, Finja;
    • Sadd, Mohamad;
    • Bras, Jose M.;
    • Bettella, Francesco;
    • Nicolaou, Nayia;
    • Simón-Sánchez, Javier;
    • Mittag, Florian;
    • Gibbs, J. Raphael;
    • Schulte, Claudia;
    • Durr, Alexandra;
    • Guerreiro, Rita;
    • Hernandez, Dena;
    • Brice, Alexis;
    • Stefánsson, Hreinn;
    • Majamaa, Kari
    Publication type:
    Article
    39

    Multimodal assessment of mitochondrial function in Parkinson's disease.

    Published in:
    Brain: A Journal of Neurology, 2024, v. 147, n. 1, p. 267, doi. 10.1093/brain/awad364
    By:
    • Payne, Thomas;
    • Burgess, Toby;
    • Bradley, Stephen;
    • Roscoe, Sarah;
    • Sassani, Matilde;
    • Dunning, Mark J;
    • Hernandez, Dena;
    • Scholz, Sonja;
    • McNeill, Alisdair;
    • Taylor, Rosie;
    • Su, Li;
    • Wilkinson, Iain;
    • Jenkins, Thomas;
    • Mortiboys, Heather;
    • Bandmann, Oliver
    Publication type:
    Article
    40

    Large-scale rare variant burden testing in Parkinson's disease.

    Published in:
    Brain: A Journal of Neurology, 2023, v. 146, n. 11, p. 4622, doi. 10.1093/brain/awad214
    By:
    • Makarious, Mary B;
    • Lake, Julie;
    • Pitz, Vanessa;
    • Fu, Allen Ye;
    • Guidubaldi, Joseph L;
    • Solsberg, Caroline Warly;
    • Bandres-Ciga, Sara;
    • Leonard, Hampton L;
    • Kim, Jonggeol Jeffrey;
    • Billingsley, Kimberley J;
    • Grenn, Francis P;
    • Jerez, Pilar Alvarez;
    • Alvarado, Chelsea X;
    • Iwaki, Hirotaka;
    • Ta, Michael;
    • Vitale, Dan;
    • Hernandez, Dena;
    • Torkamani, Ali;
    • Ryten, Mina;
    • Hardy, John
    Publication type:
    Article
    41
    42

    Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia.

    Published in:
    Brain: A Journal of Neurology, 2020, v. 143, n. 1, p. 234, doi. 10.1093/brain/awz350
    By:
    • Blauwendraat, Cornelis;
    • Reed, Xylena;
    • Krohn, Lynne;
    • Heilbron, Karl;
    • Bandres-Ciga, Sara;
    • Tan, Manuela;
    • Gibbs, J Raphael;
    • Hernandez, Dena G;
    • Kumaran, Ravindran;
    • Langston, Rebekah;
    • Bonet‐Ponce, Luis;
    • Alcalay, Roy N;
    • Hassin-Baer, Sharon;
    • Greenbaum, Lior;
    • Iwaki, Hirotaka;
    • Leonard, Hampton L;
    • Grenn, Francis P;
    • Ruskey, Jennifer A;
    • Sabir, Marya;
    • Ahmed, Sarah
    Publication type:
    Article
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    Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease.

    Published in:
    Brain: A Journal of Neurology, 2012, v. 135, n. 9, p. 2875, doi. 10.1093/brain/aws161
    By:
    • Johnson, Janel O.;
    • Gibbs, J. Raphael;
    • Megarbane, Andre;
    • Urtizberea, J. Andoni;
    • Hernandez, Dena G.;
    • Foley, A. Reghan;
    • Arepalli, Sampath;
    • Pandraud, Amelie;
    • Simón-Sánchez, Javier;
    • Clayton, Peter;
    • Reilly, Mary M.;
    • Muntoni, Francesco;
    • Abramzon, Yevgeniya;
    • Houlden, Henry;
    • Singleton, Andrew B.
    Publication type:
    Article
    45

    Genome‐Wide Analysis of Structural Variants in Parkinson Disease.

    Published in:
    Annals of Neurology, 2023, v. 93, n. 5, p. 1012, doi. 10.1002/ana.26608
    By:
    • Billingsley, Kimberley J.;
    • Ding, Jinhui;
    • Jerez, Pilar Alvarez;
    • Illarionova, Anastasia;
    • Levine, Kristin;
    • Grenn, Francis P.;
    • Makarious, Mary B.;
    • Moore, Anni;
    • Vitale, Daniel;
    • Reed, Xylena;
    • Hernandez, Dena;
    • Torkamani, Ali;
    • Ryten, Mina;
    • Hardy, John;
    • Chia, Ruth;
    • Scholz, Sonja W.;
    • Traynor, Bryan J.;
    • Dalgard, Clifton L.;
    • Ehrlich, Debra J.;
    • Tanaka, Toshiko
    Publication type:
    Article
    46

    Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease.

    Published in:
    Annals of Neurology, 2021, v. 90, n. 1, p. 35, doi. 10.1002/ana.26090
    By:
    • Blauwendraat, Cornelis;
    • Iwaki, Hirotaka;
    • Makarious, Mary B.;
    • Bandres‐Ciga, Sara;
    • Leonard, Hampton L.;
    • Grenn, Francis P.;
    • Lake, Julie;
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