Works by Hernandez, Dena

Results: 120
    1

    Towards a gene expression biomarker set for human biological age.

    Published in:
    Aging Cell, 2013, v. 12, n. 2, p. 324, doi. 10.1111/acel.12044
    By:
    • Holly, Alice C.;
    • Melzer, David;
    • Pilling, Luke C.;
    • Henley, William;
    • Hernandez, Dena G.;
    • Singleton, Andrew B.;
    • Bandinelli, Stefania;
    • Guralnik, Jack M.;
    • Ferrucci, Luigi;
    • Harries, Lorna W.
    Publication type:
    Article
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    Epigenetic signature of human immune aging in the GESTALT study.

    Published in:
    eLife, 2023, p. 1, doi. 10.7554/eLife.86136
    By:
    • Roy, Roshni;
    • Pei-Lun Kuo;
    • Candia, Julián;
    • Sarantopoulou, Dimitra;
    • Ubaida-Mohien, Ceereena;
    • Hernandez, Dena;
    • Kaileh, Mary;
    • Arepalli, Sampath;
    • Singh, Amit;
    • Bektas, Arsun;
    • Kim, Jaekwan;
    • Moore, Ann Z.;
    • Toshiko Tanaka;
    • McKelvey, Julia;
    • Zukley, Linda;
    • Cuong Nguyen;
    • Wallace, Tonya;
    • Dunn, Christopher;
    • Wood, William;
    • Yulan Piao
    Publication type:
    Article
    5

    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
    6

    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
    7

    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
    8

    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
    9

    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
    10

    QTL mapping of human retina DNA methylation identifies 87 gene-epigenome interactions in age-related macular degeneration.

    Published in:
    Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-46063-8
    By:
    • Advani, Jayshree;
    • Mehta, Puja A.;
    • Hamel, Andrew R.;
    • Mehrotra, Sudeep;
    • Kiel, Christina;
    • Strunz, Tobias;
    • Corso-Díaz, Ximena;
    • Kwicklis, Madeline;
    • van Asten, Freekje;
    • Ratnapriya, Rinki;
    • Chew, Emily Y.;
    • Hernandez, Dena G.;
    • Montezuma, Sandra R.;
    • Ferrington, Deborah A.;
    • Weber, Bernhard H. F.;
    • Segrè, Ayellet V.;
    • Swaroop, Anand
    Publication type:
    Article
    11
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    Initial Assessment of the Pathogenic Mechanisms of the Recently Identified Alzheimer Risk Loci.

    Published in:
    Annals of Human Genetics, 2013, v. 77, n. 2, p. 85, doi. 10.1111/ahg.12000
    By:
    • Holton, Patrick;
    • Ryten, Mina;
    • Nalls, Michael;
    • Trabzuni, Daniah;
    • Weale, Michael E.;
    • Hernandez, Dena;
    • Crehan, Helen;
    • Gibbs, J. Raphael;
    • Mayeux, Richard;
    • Haines, Jonathan L.;
    • Farrer, Lindsay A.;
    • Pericak‐Vance, Margaret A.;
    • Schellenberg, Gerard D.;
    • Ramirez‐Restrepo, Manuel;
    • Engel, Anzhelika;
    • Myers, Amanda J.;
    • Corneveaux, Jason J.;
    • Huentelman, Matthew J.;
    • Dillman, Allissa;
    • Cookson, Mark R.
    Publication type:
    Article
    13

    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
    14

    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;
    • Krohn, Lynne;
    • Tan, Manuela;
    • Kim, Jonggeol J.;
    • Gibbs, Jesse R.;
    • Hernandez, Dena G.;
    • Ruskey, Jennifer A.;
    • Pihlstrøm, Lasse;
    • Toft, Mathias;
    • Hilten, Jacobus J.;
    • Marinus, Johan;
    • Schulte, Claudia;
    • Brockmann, Kathrin;
    • Sharma, Manu
    Publication type:
    Article
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    Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis.

    Published in:
    Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-68848-9
    By:
    • Gao, Yixin;
    • Wang, Ting;
    • Yu, Xinghao;
    • International FTD-Genomics Consortium (IFGC);
    • Ferrari, Raffaele;
    • Hernandez, Dena G.;
    • Nalls, Michael A.;
    • Rohrer, Jonathan D.;
    • Ramasamy, Adaikalavan;
    • Kwok, John B. J.;
    • Dobson-Stone, Carol;
    • Brooks, William S.;
    • Schofield, Peter R.;
    • Halliday, Glenda M.;
    • Hodges, John R.;
    • Piguet, Olivier;
    • Bartley, Lauren;
    • Thompson, Elizabeth;
    • Haan, Eric;
    • Hernández, Isabel
    Publication type:
    Article
    19
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    Analysis of repeated leukocyte DNA methylation assessments reveals persistent epigenetic alterations after an incident myocardial infarction.

    Published in:
    Clinical Epigenetics, 2018, v. 10, n. 1, p. N.PAG, doi. 10.1186/s13148-018-0588-7
    By:
    • Ward-Caviness, Cavin K.;
    • Agha, Golareh;
    • Chen, Brian H.;
    • Pfeiffer, Liliane;
    • Wilson, Rory;
    • Wolf, Petra;
    • Gieger, Christian;
    • Schwartz, Joel;
    • Vokonas, Pantel S.;
    • Hou, Lifang;
    • Just, Allan C.;
    • Bandinelli, Stefania;
    • Hernandez, Dena G.;
    • Singleton, Andrew B.;
    • Prokisch, Holger;
    • Meitinger, Thomas;
    • Kastenmüller, Gabi;
    • Ferrucci, Luigi;
    • Baccarelli, Andrea A.;
    • Waldenberger, Melanie
    Publication type:
    Article
    21

    Characterization of PLA2G6 as a locus for dystonia-parkinsonism.

    Published in:
    Annals of Neurology, 2009, v. 65, n. 1, p. 19, doi. 10.1002/ana.21415
    By:
    • Paisan-Ruiz, Coro;
    • Bhatia, Kailash P.;
    • Li, Abi;
    • Hernandez, Dena;
    • Davis, Mary;
    • Wood, Nick W.;
    • Hardy, John;
    • Houlden, Henry;
    • Singleton, Andrew;
    • Schneider, Susanne A.
    Publication type:
    Article
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    Clinical and positron emission tomography of Parkinson's disease caused by LRRK2.

    Published in:
    Annals of Neurology, 2005, v. 57, n. 3, p. 453
    By:
    • Dena G. Hernandez;
    • Coro Paisán‐Ruíz;
    • Aideen McInerney‐Leo;
    • Shushant Jain;
    • Andreas Meyer‐Lindenberg;
    • E. Whitney Evans;
    • Karen F. Berman;
    • Janel Johnson;
    • Georg Auburger;
    • Alejandro A. Schäffer;
    • Grisel J. Lopez;
    • Robert L. Nussbaum;
    • Andrew B. Singleton
    Publication type:
    Article
    25

    Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation.

    Published in:
    Annals of Neurology, 2003, v. 54, n. 2, p. 271
    By:
    • Stephen Hague;
    • Ekaterina Rogaeva;
    • Dena Hernandez;
    • Cindy Gulick;
    • Amanda Singleton;
    • Melissa Hanson;
    • Janel Johnson;
    • Roberto Weiser;
    • Marisol Gallardo;
    • Bernard Ravina;
    • Katrina Gwinn-Hardy;
    • Anthony Crawley;
    • Peter H. St. George-Hyslop;
    • Anthony E. Lang;
    • Peter Heutink;
    • Vincenzo Bonifati;
    • John Hardy;
    • Andrew Singleton
    Publication type:
    Article
    26

    Case-Control study of the extended tau gene haplotype in Parkinson's disease.

    Published in:
    2001
    By:
    • Maraganore, Demetrius M.;
    • Hernandez, Dena G.;
    • Singleton, Andrew B.;
    • Farrer, Matthew J.;
    • McDonnell, Shannon K.;
    • Hutton, Michael L.;
    • Hardy, John A.;
    • Rocca, Walter A.;
    • Maraganore, D M;
    • Hernandez, D G;
    • Singleton, A B;
    • Farrer, M J;
    • McDonnell, S K;
    • Hutton, M L;
    • Hardy, J A;
    • Rocca, W A
    Publication type:
    journal article
    27

    Lewy bodies and parkinsonism in families with parkin mutations.

    Published in:
    2001
    By:
    • Farrer, Matt;
    • Chan, Piu;
    • Chen, Rong;
    • Tan, Louis;
    • Lincoln, Sarah;
    • Hernandez, Dena;
    • Forno, Lysia;
    • Gwinn-Hardy, Katrina;
    • Petrucelli, Leonard;
    • Hussey, Jennifer;
    • Singleton, Andrew;
    • Tanner, Caroline;
    • Hardy, John;
    • Langston, J. William;
    • Farrer, M;
    • Chan, P;
    • Chen, R;
    • Tan, L;
    • Lincoln, S;
    • Hernandez, D
    Publication type:
    journal article
    28

    NeuroBooster Array: A Genome‐Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations.

    Published in:
    Movement Disorders, 2024, v. 39, n. 11, p. 2039, doi. 10.1002/mds.29902
    By:
    • Bandres‐Ciga, Sara;
    • Faghri, Faraz;
    • Majounie, Elisa;
    • Koretsky, Mathew J.;
    • Kim, Jeffrey;
    • Levine, Kristin S.;
    • Leonard, Hampton;
    • Makarious, Mary B.;
    • Iwaki, Hirotaka;
    • Crea, Peter Wild;
    • Hernandez, Dena G.;
    • Arepalli, Sampath;
    • Billingsley, Kimberley;
    • Lohmann, Katja;
    • Klein, Christine;
    • Lubbe, Steven J.;
    • Jabbari, Edwin;
    • Saffie‐Awad, Paula;
    • Narendra, Derek;
    • Reyes‐Palomares, Armando
    Publication type:
    Article
    29
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    A Double‐Blind, Randomized, Placebo‐Controlled Trial of Ursodeoxycholic Acid (UDCA) in Parkinson's Disease.

    Published in:
    Movement Disorders, 2023, v. 38, n. 8, p. 1493, doi. 10.1002/mds.29450
    By:
    • Payne, Thomas;
    • Appleby, Matthew;
    • Buckley, Ellen;
    • van Gelder, Linda M.A.;
    • Mullish, Benjamin H.;
    • Sassani, Matilde;
    • Dunning, Mark J.;
    • Hernandez, Dena;
    • Scholz, Sonja W.;
    • McNeill, Alisdair;
    • Libri, Vincenzo;
    • Moll, Sarah;
    • Marchesi, Julian R.;
    • Taylor, Rosie;
    • Su, Li;
    • Mazzà, Claudia;
    • Jenkins, Thomas M.;
    • Foltynie, Thomas;
    • Bandmann, Oliver
    Publication type:
    Article
    31

    Polygenic Parkinson's Disease Genetic Risk Score as Risk Modifier of Parkinsonism in Gaucher Disease.

    Published in:
    Movement Disorders, 2023, v. 38, n. 5, p. 899, doi. 10.1002/mds.29342
    By:
    • Blauwendraat, Cornelis;
    • Tayebi, Nahid;
    • Woo, Elizabeth Geena;
    • Lopez, Grisel;
    • Fierro, Luca;
    • Toffoli, Marco;
    • Limbachiya, Naomi;
    • Hughes, Derralynn;
    • Pitz, Vanessa;
    • Patel, Dhairya;
    • Vitale, Dan;
    • Koretsky, Mathew J.;
    • Hernandez, Dena;
    • Real, Raquel;
    • Alcalay, Roy N.;
    • Nalls, Mike A.;
    • Morris, Huw R.;
    • Schapira, Anthony H.V.;
    • Balwani, Manisha;
    • Sidransky, Ellen
    Publication type:
    Article
    32

    Profiling the NOTCH2NLC GGC Repeat Expansion in Parkinson's Disease in the European Population.

    Published in:
    Movement Disorders, 2022, v. 37, n. 10, p. 2161, doi. 10.1002/mds.29155
    By:
    • Billingsley, Kimberley J.;
    • Alvarez Jerez, Pilar;
    • Grenn, Francis P.;
    • Bandres‐Ciga, Sara;
    • Malik, Laksh;
    • Hernandez, Dena;
    • Torkamani, Ali;
    • Ryten, Mina;
    • Hardy, John;
    • Scholz, Sonja W.;
    • Traynor, Bryan J.;
    • Dalgard, Clifton L.;
    • Ehrlich, Debra J.;
    • Tanaka, Toshiko;
    • Ferrucci, Luigi;
    • Beach, Thomas G.;
    • Serrano, Geidy E.;
    • Ding, Jinhui;
    • Gibbs, J. Raphael;
    • Blauwendraat, Cornelis
    Publication type:
    Article
    33

    The Interaction between HLA-DRB1 and Smoking in Parkinson's Disease Revisited.

    Published in:
    2022
    By:
    • Domenighetti, Cloé;
    • Douillard, Venceslas;
    • Sugier, Pierre‐Emmanuel;
    • Sreelatha, Ashwin Ashok Kumar;
    • Schulte, Claudia;
    • Grover, Sandeep;
    • May, Patrick;
    • Bobbili, Dheeraj R.;
    • Radivojkov‐Blagojevic, Milena;
    • Lichtner, Peter;
    • Singleton, Andrew B.;
    • Hernandez, Dena G.;
    • Edsall, Connor;
    • Gourraud, Pierre‐Antoine;
    • Mellick, George D.;
    • Zimprich, Alexander;
    • Pirker, Walter;
    • Rogaeva, Ekaterina;
    • Lang, Anthony E.;
    • Koks, Sulev
    Publication type:
    journal article
    34

    Dairy Intake and Parkinson's Disease: A Mendelian Randomization Study.

    Published in:
    Movement Disorders, 2022, v. 37, n. 4, p. 857, doi. 10.1002/mds.28902
    By:
    • Domenighetti, Cloé;
    • Sugier, Pierre‐Emmanuel;
    • Ashok Kumar Sreelatha, Ashwin;
    • 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
    35

    Accelerating Medicines Partnership: Parkinson's Disease. Genetic Resource.

    Published in:
    Movement Disorders, 2021, v. 36, n. 8, p. 1795, doi. 10.1002/mds.28549
    By:
    • Iwaki, Hirotaka;
    • Leonard, Hampton L.;
    • Makarious, Mary B.;
    • Bookman, Matt;
    • Landin, Barry;
    • Vismer, David;
    • Casey, Bradford;
    • Gibbs, J. Raphael;
    • Hernandez, Dena G.;
    • Blauwendraat, Cornelis;
    • Vitale, Daniel;
    • Song, Yeajin;
    • Kumar, Dinesh;
    • Dalgard, Clifton L.;
    • Sadeghi, Mahdiar;
    • Dong, Xianjun;
    • Misquitta, Leonie;
    • Scholz, Sonja W.;
    • Scherzer, Clemens R.;
    • Nalls, Mike A.
    Publication type:
    Article
    36

    The Parkinson's Disease DNA Variant Browser.

    Published in:
    Movement Disorders, 2021, v. 36, n. 5, p. 1250, doi. 10.1002/mds.28488
    By:
    • Kim, Jonggeol J.;
    • Makarious, Mary B.;
    • Bandres‐Ciga, Sara;
    • Gibbs, Jesse Raphael;
    • Ding, Jinhui;
    • Hernandez, Dena G.;
    • Brooks, Janet;
    • Grenn, Francis P.;
    • Iwaki, Hirotaka;
    • Singleton, Andrew B.;
    • Nalls, Mike A.;
    • Blauwendraat, Cornelis
    Publication type:
    Article
    37

    Penetrance of Parkinson's Disease in LRRK2 p.G2019S Carriers Is Modified by a Polygenic Risk Score.

    Published in:
    2020
    By:
    • Iwaki, Hirotaka;
    • Blauwendraat, Cornelis;
    • Makarious, Mary B.;
    • Bandrés‐Ciga, Sara;
    • Leonard, Hampton L.;
    • Gibbs, J. Raphael;
    • Hernandez, Dena G.;
    • Scholz, Sonja W.;
    • Faghri, Faraz;
    • Nalls, Mike A.;
    • Singleton, Andrew B.;
    • Noyce, Alastair J;
    • Kaiyrzhanov, Rauan;
    • Middlehurst, Ben;
    • Kia, Demis A;
    • Tan, Manuela;
    • Houlden, Henry;
    • Morris, Huw R;
    • Plun‐Favreau, Helene;
    • Holmans, Peter
    Publication type:
    journal article
    38

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

    Published in:
    2019
    By:
    • Iwaki, Hirotaka;
    • Blauwendraat, Cornelis;
    • Leonard, Hampton L.;
    • Kim, Jonggeol J.;
    • Liu, Ganqiang;
    • Maple‐Grødem, Jodi;
    • Corvol, Jean‐Christophe;
    • Pihlstrøm, Lasse;
    • Nimwegen, Marlies;
    • Hutten, Samantha J.;
    • Nguyen, Khanh‐Dung H.;
    • Rick, Jacqueline;
    • Eberly, Shirley;
    • Faghri, Faraz;
    • Auinger, Peggy;
    • Scott, Kirsten M.;
    • Wijeyekoon, Ruwani;
    • Van Deerlin, Vivianna M.;
    • Hernandez, Dena G.;
    • Gibbs, J. Raphael
    Publication type:
    journal article
    39

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

    Published in:
    2019
    By:
    • Blauwendraat, Cornelis;
    • Heilbron, Karl;
    • Vallerga, Costanza L.;
    • Bandres‐Ciga, Sara;
    • von Coelln, Rainer;
    • Pihlstrøm, Lasse;
    • Simón‐Sánchez, Javier;
    • Schulte, Claudia;
    • Sharma, Manu;
    • Krohn, Lynne;
    • Siitonen, Ari;
    • Iwaki, Hirotaka;
    • Leonard, Hampton;
    • Noyce, Alastair J.;
    • Tan, Manuela;
    • Gibbs, J. Raphael;
    • Hernandez, Dena G.;
    • Scholz, Sonja W.;
    • Jankovic, Joseph;
    • Shulman, Lisa M.
    Publication type:
    journal 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
    50

    Peripheral Blood Transcriptomic Signatures of Fasting Glucose and Insulin Concentrations.

    Published in:
    2016
    By:
    • Chen, Brian H;
    • Hivert, Marie-France;
    • Peters, Marjolein J;
    • Pilling, Luke C;
    • Hogan, John D;
    • Pham, Lisa M;
    • Harries, Lorna W;
    • Fox, Caroline S;
    • Bandinelli, Stefania;
    • Dehghan, Abbas;
    • Hernandez, Dena G;
    • Hofman, Albert;
    • Hong, Jaeyoung;
    • Joehanes, Roby;
    • Johnson, Andrew D;
    • Munson, Peter J;
    • Rybin, Denis V;
    • Singleton, Andrew B;
    • Uitterlinden, André G;
    • Ying, Saixia
    Publication type:
    journal article