Works by Saunders-Pullman, Rachel


Results: 71
    1

    The prodromal phase of leucine-rich repeat kinase 2-associated Parkinson disease: Clinical and imaging Studies.

    Published in:
    2017
    By:
    • Pont‐Sunyer, Claustre;
    • Tolosa, Eduardo;
    • Caspell‐Garcia, Chelsea;
    • Coffey, Christopher;
    • Alcalay, Roy N.;
    • Chan, Piu;
    • Duda, John E.;
    • Facheris, Maurizio;
    • Fernández‐Santiago, Rubén;
    • Marek, Kenneth;
    • Lomeña, Francisco;
    • Marras, Connie;
    • Mondragon, Elisabet;
    • Saunders‐Pullman, Rachel;
    • Waro, Bjorg;
    • Pont-Sunyer, Claustre;
    • Caspell-Garcia, Chelsea;
    • Fernández-Santiago, Rubén;
    • Lomeña, Francisco;
    • Saunders-Pullman, Rachel
    Publication type:
    journal 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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    Psychiatric disorders, myoclonus dystonia and SGCE: an international study.

    Published in:
    Annals of Clinical & Translational Neurology, 2016, v. 3, n. 1, p. 4, doi. 10.1002/acn3.263
    By:
    • Peall, Kathryn J.;
    • Dijk, Joke M.;
    • Saunders‐Pullman, Rachel;
    • Dreissen, Yasmine E. M.;
    • Loon, Ilke;
    • Cath, Danielle;
    • Kurian, Manju A.;
    • Owen, Michael J.;
    • Foncke, Elisabeth M. J.;
    • Morris, Huw R.;
    • Gasser, Thomas;
    • Bressman, Susan;
    • Asmus, Friedrich;
    • Tijssen, Marina A. J.
    Publication type:
    Article
    8

    GBA mutations are associated with Rapid Eye Movement Sleep Behavior Disorder.

    Published in:
    Annals of Clinical & Translational Neurology, 2015, v. 2, n. 9, p. 941, doi. 10.1002/acn3.228
    By:
    • Gan‐Or, Ziv;
    • Mirelman, Anat;
    • Postuma, Ronald B.;
    • Arnulf, Isabelle;
    • Bar‐Shira, Anat;
    • Dauvilliers, Yves;
    • Desautels, Alex;
    • Gagnon, Jean‐François;
    • Leblond, Claire S.;
    • Frauscher, Birgit;
    • Alcalay, Roy N.;
    • Saunders‐Pullman, Rachel;
    • Bressman, Susan B.;
    • Marder, Karen;
    • Monaca, Christelle;
    • Högl, Birgit;
    • Orr‐Urtreger, Avi;
    • Dion, Patrick A.;
    • Montplaisir, Jacques Y.;
    • Giladi, Nir
    Publication type:
    Article
    9

    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
    10

    Progression in the LRRK2-Asssociated Parkinson Disease Population.

    Published in:
    JAMA Neurology, 2018, v. 75, n. 3, p. 312, doi. 10.1001/jamaneurol.2017.4019
    By:
    • Saunders-Pullman, Rachel;
    • Mirelman, Anat;
    • Alcalay, Roy N.;
    • Wang, Cuiling;
    • Ortega, Roberto A.;
    • Raymond, Deborah;
    • Mejia-Santana, Helen;
    • Orbe-Reilly, Martha;
    • Johannes, Brooke A.;
    • Thaler, Avner;
    • Ozelius, Laurie;
    • Orr-Urtreger, Avi;
    • Marder, Karen S.;
    • Giladi, Nir;
    • Bressman, Susan B.
    Publication type:
    Article
    11

    Complex and Dynamic Chromosomal Rearrangements in a Family With Seemingly Non-Mendelian Inheritance of Dopa-Responsive Dystonia.

    Published in:
    JAMA Neurology, 2017, v. 74, n. 7, p. 806, doi. 10.1001/jamaneurol.2017.0666
    By:
    • Lohmann, Katja;
    • Redin, Claire;
    • Tönnies, Holger;
    • Bressman, Susan B.;
    • Subero, Jose Ignacio Martin;
    • Wiegers, Karin;
    • Hinrichs, Frauke;
    • Hellenbroich, Yorck;
    • Rakovic, Aleksandar;
    • Raymond, Deborah;
    • Ozelius, Laurie J.;
    • Schwinger, Eberhard;
    • Siebert, Reiner;
    • Talkowski, Michael E.;
    • Saunders-Pullman, Rachel;
    • Klein, Christine
    Publication type:
    Article
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    Mutations in GNAL cause primary torsion dystonia.

    Published in:
    Nature Genetics, 2013, v. 45, n. 1, p. 88, doi. 10.1038/ng.2496
    By:
    • Fuchs, Tania;
    • Saunders-Pullman, Rachel;
    • Masuho, Ikuo;
    • Luciano, Marta San;
    • Raymond, Deborah;
    • Factor, Stewart;
    • Lang, Anthony E;
    • Liang, Tsao-Wei;
    • Trosch, Richard M;
    • White, Sierra;
    • Ainehsazan, Edmond;
    • Hervé, Denis;
    • Sharma, Nutan;
    • Ehrlich, Michelle E;
    • Martemyanov, Kirill A;
    • Bressman, Susan B;
    • Ozelius, Laurie J
    Publication type:
    Article
    15
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    Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non-Ashkenazi Jewish ancestry.

    Published in:
    2017
    By:
    • Lee, Annie J.;
    • Wang, Yuanjia;
    • Alcalay, Roy N.;
    • Mejia‐Santana, Helen;
    • Saunders‐Pullman, Rachel;
    • Bressman, Susan;
    • Corvol, Jean‐Christophe;
    • Brice, Alexis;
    • Lesage, Suzanne;
    • Mangone, Graziella;
    • Tolosa, Eduardo;
    • Pont‐Sunyer, Claustre;
    • Vilas, Dolores;
    • Schüle, Birgitt;
    • Kausar, Farah;
    • Foroud, Tatiana;
    • Berg, Daniela;
    • Brockmann, Kathrin;
    • Goldwurm, Stefano;
    • Siri, Chiara
    Publication type:
    journal article
    17

    Arm swing as a potential new prodromal marker of Parkinson's disease.

    Published in:
    2016
    By:
    • Mirelman, Anat;
    • Bernad‐Elazari, Hagar;
    • Thaler, Avner;
    • Giladi‐Yacobi, Eytan;
    • Gurevich, Tanya;
    • Gana‐Weisz, Mali;
    • Saunders‐Pullman, Rachel;
    • Raymond, Deborah;
    • Doan, Nancy;
    • Bressman, Susan B.;
    • Marder, Karen S.;
    • Alcalay, Roy N.;
    • Rao, Ashwini K.;
    • Berg, Daniela;
    • Brockmann, Kathrin;
    • Aasly, Jan;
    • Waro, Bjørg Johanne;
    • Tolosa, Eduardo;
    • Vilas, Dolores;
    • Pont‐Sunyer, Claustre
    Publication type:
    journal article
    18
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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
    22

    Low-variance RNAs identify Parkinson's disease molecular signature in blood.

    Published in:
    Movement Disorders, 2015, v. 30, n. 6, p. 813, doi. 10.1002/mds.26205
    By:
    • Chikina, Maria D.;
    • Gerald, Christophe P.;
    • Li, Xianting;
    • Ge, Yongchao;
    • Pincas, Hanna;
    • Nair, Venugopalan D.;
    • Wong, Aaron K.;
    • Krishnan, Arjun;
    • Troyanskaya, Olga G.;
    • Raymond, Deborah;
    • Saunders‐Pullman, Rachel;
    • Bressman, Susan B.;
    • Yue, Zhenyu;
    • Sealfon, Stuart C.
    Publication type:
    Article
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    Parkinson disease phenotype in Ashkenazi jews with and without LRRK2 G2019S mutations.

    Published in:
    Movement Disorders, 2013, v. 28, n. 14, p. 1966, doi. 10.1002/mds.25647
    By:
    • Alcalay, Roy N.;
    • Mirelman, Anat;
    • Saunders‐Pullman, Rachel;
    • Tang, Ming‐X;
    • Mejia Santana, Helen;
    • Raymond, Deborah;
    • Roos, Ernest;
    • Orbe‐Reilly, Martha;
    • Gurevich, Tanya;
    • Bar Shira, Anat;
    • Gana Weisz, Mali;
    • Yasinovsky, Kira;
    • Zalis, Maayan;
    • Thaler, Avner;
    • Deik, Andres;
    • Barrett, Matthew James;
    • Cabassa, Jose;
    • Groves, Mark;
    • Hunt, Ann L.;
    • Lubarr, Naomi
    Publication type:
    Article
    27

    Primary dystonia: Moribund or viable.

    Published in:
    Movement Disorders, 2013, v. 28, n. 7, p. 906, doi. 10.1002/mds.25528
    By:
    • Bressman, Susan B.;
    • Saunders-Pullman, Rachel
    Publication type:
    Article
    28
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    LRRK2 G2019S mutations may be increased in Puerto Ricans.

    Published in:
    Movement Disorders, 2011, v. 26, n. 9, p. 1771, doi. 10.1002/mds.23632
    By:
    • Saunders-Pullman, Rachel;
    • Cabassa, Jose;
    • San Luciano, Marta;
    • Stanley, Kaili;
    • Raymond, Deborah;
    • Ozelius, Laurie J.;
    • Bressman, Susan B.
    Publication type:
    Article
    30

    Substantia nigra hyperechogenicity with LRRK2 G2019S mutations.

    Published in:
    Movement Disorders, 2011, v. 26, n. 5, p. 885, doi. 10.1002/mds.23644
    By:
    • Brüggemann, Norbert;
    • Hagenah, Johann;
    • Stanley, Kaili;
    • Klein, Christine;
    • Wang, Cuiling;
    • Raymond, Deborah;
    • Ozelius, Laurie;
    • Bressman, Susan;
    • Saunders-Pullman, Rachel
    Publication type:
    Article
    31

    Phenotypic spectrum of musician's dystonia: A task-specific disorder?

    Published in:
    Movement Disorders, 2011, v. 26, n. 3, p. 546, doi. 10.1002/mds.23526
    By:
    • Schmidt, Alexander;
    • Jabusch, Hans-Christian;
    • Altenmüller, Eckart;
    • Enders, Leonie;
    • Saunders-Pullman, Rachel;
    • Bressman, Susan B.;
    • Münchau, Alexander;
    • Klein, Christine;
    • Hagenah, Johann
    Publication type:
    Article
    32
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    Clinical expression of LRRK2 G2019S mutations in the elderly.

    Published in:
    Movement Disorders, 2010, v. 25, n. 15, p. 2571, doi. 10.1002/mds.23330
    By:
    • Luciano, Marta San;
    • Lipton, Richard B.;
    • Wang, Cuiling;
    • Katz, Mindy;
    • Zimmerman, Molly E.;
    • Sanders, Amy E.;
    • Ozelius, Laurie J.;
    • Bressman, Susan B.;
    • Saunders-Pullman, Rachel
    Publication type:
    Article
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    Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with ε-sarcoglycan mutations.

    Published in:
    Movement Disorders, 2008, v. 23, n. 4, p. 588, doi. 10.1002/mds.21785
    By:
    • Raymond, Deborah;
    • Saunders-Pullman, Rachel;
    • de Carvalho Aguiar, Patricia;
    • Schule, Birgitt;
    • Kock, Norman;
    • Friedman, Jennifer;
    • Harris, Juliette;
    • Ford, Blair;
    • Frucht, Steven;
    • Heiman, Gary A.;
    • Jennings, Danna;
    • Doheny, Dana;
    • Brin, Mitchell F.;
    • de Leon Brin, Deborah;
    • Multhaupt-Buell, Trisha;
    • Lang, Anthony E.;
    • Kurlan, Roger;
    • Klein, Christine;
    • Ozelius, Laurie;
    • Bressman, Susan
    Publication type:
    Article
    38

    Validity of spiral analysis in early Parkinson's disease.

    Published in:
    Movement Disorders, 2008, v. 23, n. 4, p. 531, doi. 10.1002/mds.21874
    By:
    • Saunders-Pullman, Rachel;
    • Derby, Carol;
    • Stanley, Kaili;
    • Floyd, Alicia;
    • Bressman, Susan;
    • Lipton, Richard B.;
    • Deligtisch, Amanda;
    • Severt, Lawrence;
    • Yu, Qiping;
    • Kurtis, Mónica;
    • Pullman, Seth L.
    Publication type:
    Article
    39

    Association of Dual LRRK2 G2019S and GBA Variations With Parkinson Disease Progression.

    Published in:
    JAMA Network Open, 2021, v. 4, n. 4, p. e215845, doi. 10.1001/jamanetworkopen.2021.5845
    By:
    • Ortega, Roberto A.;
    • Wang, Cuiling;
    • Raymond, Deborah;
    • Bryant, Nicole;
    • Scherzer, Clemens R.;
    • Thaler, Avner;
    • Alcalay, Roy N.;
    • West, Andrew B.;
    • Mirelman, Anat;
    • Kuras, Yuliya;
    • Marder, Karen S.;
    • Giladi, Nir;
    • Ozelius, Laurie J.;
    • Bressman, Susan B.;
    • Saunders-Pullman, Rachel
    Publication type:
    Article
    40

    Genetic risk variants in New Yorkers of Puerto Rican and Dominican Republic heritage with Parkinson's disease.

    Published in:
    NPJ Parkinson's Disease, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41531-023-00599-6
    By:
    • Miltenberger-Miltenyi, Gabriel;
    • Ortega, Roberto A.;
    • Domingo, Aloysius;
    • Yadav, Rachita;
    • Nishiyama, Ayumi;
    • Raymond, Deborah;
    • Katsnelson, Viktoriya;
    • Urval, Nikita;
    • Swan, Matthew;
    • Shanker, Vicki;
    • Miravite, Joan;
    • Walker, Ruth H.;
    • Bressman, Susan B.;
    • Ozelius, Laurie J.;
    • Cabassa, José C.;
    • Saunders-Pullman, Rachel
    Publication type:
    Article
    41
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    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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    The phenotypic spectrum of rapid-onset dystonia–parkinsonism (RDP) and mutations in the ATP1A3 gene.

    Published in:
    Brain: A Journal of Neurology, 2007, v. 130, n. 3, p. 828, doi. 10.1093/brain/awl340
    By:
    • Allison Brashear;
    • William B. Dobyns;
    • Patricia de Carvalho Aguiar;
    • Michel Borg;
    • C. J. M. Frijns;
    • Seema Gollamudi;
    • Andrew Green;
    • João Guimaraes;
    • Bret C. Haake;
    • Christine Klein;
    • Gurutz Linazasoro;
    • Alexander Münchau;
    • Deborah Raymond;
    • David Riley;
    • Rachel Saunders-Pullman;
    • Marina A. J. Tijssen;
    • David Webb;
    • Jacek Zaremba;
    • Susan B. Bressman;
    • Laurie J. Ozelius
    Publication type:
    Article
    48

    Reply to: Cognitive Effects of Deep Brain Stimulation in GBA‐Related Parkinson's Disease.

    Published in:
    Annals of Neurology, 2022, v. 92, n. 2, p. 345, doi. 10.1002/ana.26433
    By:
    • Pal, Gian;
    • Mangone, Graziella;
    • Ouyang, Bichun;
    • Ehrlich, Debra;
    • Saunders‐Pullman, Rachel;
    • Bressman, Susan;
    • Alcalay, Roy N.;
    • Marder, Karen;
    • Aasly, Jan;
    • Mouradian, M. Maral;
    • Anderson, Sharlet;
    • Bernard, Bryan;
    • Stebbins, Glenn;
    • Sani, Sepehr;
    • Afshari, Mitra;
    • Verhagen, Leo;
    • de Bie, Rob M.A.;
    • Foltynie, Tom;
    • Hall, Deborah;
    • Corvol, Jean‐Christophe
    Publication type:
    Article
    49

    Parkinson Disease and Subthalamic Nucleus Deep Brain Stimulation: Cognitive Effects in GBA Mutation Carriers.

    Published in:
    Annals of Neurology, 2022, v. 91, n. 3, p. 424, doi. 10.1002/ana.26302
    By:
    • Pal, Gian;
    • Mangone, Graziella;
    • Hill, Emily J.;
    • Ouyang, Bichun;
    • Liu, Yuanqing;
    • Lythe, Vanessa;
    • Ehrlich, Debra;
    • Saunders‐Pullman, Rachel;
    • Shanker, Vicki;
    • Bressman, Susan;
    • Alcalay, Roy N.;
    • Garcia, Priscilla;
    • Marder, Karen S.;
    • Aasly, Jan;
    • Mouradian, M. Maral;
    • Link, Samantha;
    • Rosenbaum, Marc;
    • Anderson, Sharlet;
    • Bernard, Bryan;
    • Wilson, Robert
    Publication type:
    Article
    50

    Evaluation of the role of the D2 dopamine receptor in myoclonus dystonia.

    Published in:
    Annals of Neurology, 2000, v. 47, n. 3, p. 369, doi. 10.1002/1531-8249(200003)47:3<369::AID-ANA14>3.0.CO;2-9
    By:
    • Klein, Christine;
    • Gurvich, Nadia;
    • Sena-Esteves, Miguel;
    • Bressman, Susan;
    • Brin, Mitchell F.;
    • Ebersole, Barbara J.;
    • Fink, Stephen;
    • Forsgren, Lars;
    • Friedman, Jennifer;
    • Grimes, David;
    • Holmgren, Gosta;
    • Kyllerman, Mårtin;
    • Lang, Anthony E.;
    • De Leon, Deborah;
    • Leung, Joanne;
    • Prioleau, Cassandra;
    • Raymond, Deborah;
    • Sanner, Gunnar;
    • Saunders-Pullman, Rachel;
    • Vieregge, Peter
    Publication type:
    Article