Showing 1 - 2 results of 2 for search 'Sitki Cem Parlar', query time: 0.02s Refine Results
  1. 1
    Are rare heterozygous SYNJ1 variants associated with Parkinson’s disease?

    Are rare heterozygous SYNJ1 variants associated with Parkinson’s disease? by Konstantin Senkevich, Sitki Cem Parlar, Cloe Chantereault, Eric Yu, Jamil Ahmad, Jennifer A. Ruskey, Farnaz Asayesh, Dan Spiegelman, Cheryl Waters, Oury Monchi, Yves Dauvilliers, Nicolas Dupré, Irina Miliukhina, Alla Timofeeva, Anton Emelyanov, Sofya Pchelina, Lior Greenbaum, Sharon Hassin-Baer, Roy N. Alcalay, Ziv Gan-Or

    Published 2024-10-01
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  2. 2
    LRRK2 rare-variant per-domain genetic burden in Parkinson’s Disease: association confined to the kinase domain

    LRRK2 rare-variant per-domain genetic burden in Parkinson’s Disease: association confined to the kinase domain by Sitki Cem Parlar, Konstantin Senkevich, Eric Yu, Jennifer A. Ruskey, Jamil Ahmad, Farnaz Asayesh, Dan Spiegelman, Cheryl Waters, Oury Monchi, Yves Dauvilliers, Nicolas Dupré, Lior Greenbaum, Sharon Hassin-Baer, Irina Miliukhina, Alla Timofeeva, Anton Emelyanov, Sofya Pchelina, Roy N. Alcalay, Edward A. Fon, Jean-François Trempe, Ziv Gan-Or

    Published 2025-04-01
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