Found: 3

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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

  • 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

  • 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