檢索結果 - Cornelis Blauwendraat

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  1. 1
    The genetic architecture of Parkinson's disease

    The genetic architecture of Parkinson's disease 由 Cornelis Blauwendraat, Mike A. Nalls, Andrew Singleton

    出版 2019
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  2. 2
    The role of monogenic genes in idiopathic Parkinson’s disease

    The role of monogenic genes in idiopathic Parkinson’s disease 由 Xylena Reed, Sara Bandrés‐Ciga, Cornelis Blauwendraat, Mark Cookson

    出版 2018
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  3. 3
    <scp>DNAJC</scp> proteins and pathways to parkinsonism

    <scp>DNAJC</scp> proteins and pathways to parkinsonism 由 Dorien A. Roosen, Cornelis Blauwendraat, Mark Cookson, Patrick A. Lewis

    出版 2019
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  4. 4
    Exploration of Neurodegenerative Diseases Using Long‐Read Sequencing and Optical Genome Mapping Technologies

    Exploration of Neurodegenerative Diseases Using Long‐Read Sequencing and Optical Genome Mapping Technologies 由 Guillaume Cogan, Kensuke Daida, Cornelis Blauwendraat, Kimberley J. Billingsley, Alexis Brice

    出版 2025
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  5. 5
    Transcriptomic changes in oligodendrocytes and precursor cells associate with clinical outcomes of Parkinson’s disease

    Transcriptomic changes in oligodendrocytes and precursor cells associate with clinical outcomes of Parkinson’s disease 由 Mohammad Dehestani, Velina Kozareva, Cornelis Blauwendraat, Ernest Fraenkel, Thomas Gasser, V. Bansal

    出版 2024
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  6. 6
    Increased brain expression of GPNMB is associated with genome wide significant risk for Parkinson’s disease on chromosome 7p15.3

    Increased brain expression of GPNMB is associated with genome wide significant risk for Parkinson’s disease on chromosome 7p15.3 由 Megha Murthy, Cornelis Blauwendraat, Sebastian Guelfi, John Hardy, Patrick A. Lewis, Daniah Trabzuni

    出版 2017
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  7. 7
    Molecular Fingerprinting of Mycobacterium abscessus Strains in a Cohort of Pediatric Cystic Fibrosis Patients

    Molecular Fingerprinting of Mycobacterium abscessus Strains in a Cohort of Pediatric Cystic Fibrosis Patients 由 Kathryn Harris, D. Kenna, Cornelis Blauwendraat, John C. Hartley, Jane F. Turton, Paul Aurora, Garth Dixon

    出版 2012
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  8. 8
    Lower Lymphocyte Count is Associated With Increased Risk of Parkinson's Disease

    Lower Lymphocyte Count is Associated With Increased Risk of Parkinson's Disease 由 Melanie P. Jensen, Benjamin Meir Jacobs, Ruth Dobson, Sara Bandrés‐Ciga, Cornelis Blauwendraat, Anette Schrag, Alastair Noyce

    出版 2021
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  9. 9
    Association of a common genetic variant with Parkinson’s disease is mediated by microglia

    Association of a common genetic variant with Parkinson’s disease is mediated by microglia 由 Rebekah G. Langston, Alexandra Beilina, Xylena Reed, Alice Kaganovich, Andrew Singleton, Cornelis Blauwendraat, J. Raphael Gibbs, Mark Cookson

    出版 2022
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  10. 10
    Gender Differences in the Prevalence of Parkinson's Disease

    Gender Differences in the Prevalence of Parkinson's Disease 由 Alexandra Zirra, Shilpa C. Rao, Jonathan P. Bestwick, Rajasumi Rajalingam, Connie Marras, Cornelis Blauwendraat, Ignácio F. Mata, Alastair Noyce

    出版 2022
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  11. 11
    Virus exposure and neurodegenerative disease risk across national biobanks

    Virus exposure and neurodegenerative disease risk across national biobanks 由 Kristin Levine, Hampton L. Leonard, Cornelis Blauwendraat, Hirotaka Iwaki, Nicholas L. Johnson, Sara Bandrés‐Ciga, Luigi Ferrucci, Faraz Faghri, Andrew Singleton, Mike A. Nalls

    出版 2023
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  12. 12
    Association of CSF α‐synuclein seed amplification assay positivity with disease progression and cognitive decline: A longitudinal Alzheimer's Disease Neuroimaging Initiative study

    Association of CSF α‐synuclein seed amplification assay positivity with disease progression and cognitive decline: A longitudinal Alzheimer's Disease Neuroimaging Initiative study... 由 Duygu Tosun, Zachary Hausle, Pamela Thropp, Luis Concha‐Marambio, Jennifer Lamoureux, Russ Lebovitz, Leslie M. Shaw, Andrew B. Singleton, Michael W. Weiner, Cornelis Blauwendraat

    出版 2024
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  13. 13
    Functionalization of the TMEM175 p.M393T variant as a risk factor for Parkinson disease

    Functionalization of the TMEM175 p.M393T variant as a risk factor for Parkinson disease 由 Sarah Jinn, Cornelis Blauwendraat, Dawn Toolan, Cheryl A. Gretzula, Robert E. Drolet, Sean M. Smith, Mike A. Nalls, Jacob Marcus, Andrew Singleton, David J. Stone

    出版 2019
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  14. 14
    Effect Modification between Genes and Environment and Parkinson's Disease Risk

    Effect Modification between Genes and Environment and Parkinson's Disease Risk 由 María Teresa Periñán, Kajsa Brolin, Sara Bandrés‐Ciga, Cornelis Blauwendraat, Christine Klein, Ziv Gan‐Or, Andrew Singleton, Pilar Gómez‐Garre, Maria Swanberg, Pablo Mir, Alastair Noyce

    出版 2022
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  15. 15
    Comprehensive assessment of PINK1 variants in Parkinson's disease

    Comprehensive assessment of PINK1 variants in Parkinson's disease 由 Lynne Krohn, Francis P. Grenn, Mary B. Makarious, Jonggeol Jeffrey Kim, Sara Bandrés‐Ciga, Dorien A. Roosen, Ziv Gan‐Or, Mike A. Nalls, Andrew Singleton, Cornelis Blauwendraat

    出版 2020
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  16. 16
    Assessing methylation detection for primary human tissue using Nanopore sequencing

    Assessing methylation detection for primary human tissue using Nanopore sequencing 由 Rylee M. Genner, Stuart Akeson, Melissa Meredith, Pilar Álvarez Jerez, Laksh Malik, Breeana Baker, Abigail Miano‐Burkhardt, Benedict Paten, Kimberley J. Billingsley, Cornelis Blauwendraat, Miten Jain

    出版 2024
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  17. 17
    C9orf72 is differentially expressed in the central nervous system and myeloid cells and consistently reduced in C9orf72, MAPT and GRN mutation carriers

    C9orf72 is differentially expressed in the central nervous system and myeloid cells and consistently reduced in C9orf72, MAPT and GRN mutation carriers 由 Patrizia Rizzu, Cornelis Blauwendraat, Sasja Heetveld, Emily M. Lynes, Melissa Castillo-Lizardo, Ashutosh Dhingra, Elwira Pyż, Markus A. Hobert, Matthis Synofzik, Javier Simón‐Sánchez, Margherita Francescatto, Peter Heutink

    出版 2016
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  18. 18
    Penetrance of Parkinson's Disease in <i>LRRK2</i> p.G2019S Carriers Is Modified by a Polygenic Risk Score

    Penetrance of Parkinson's Disease in <i>LRRK2</i> p.G2019S Carriers Is Modified by a Polygenic Risk Score 由 Hirotaka Iwaki, Cornelis Blauwendraat, Mary B. Makarious, Sara Bandrés‐Ciga, Hampton L. Leonard, J. Raphael Gibbs, Dena Hernández, Sonja W. Scholz, Faraz Faghri, Mike A. Nalls, Andrew Singleton

    出版 2020
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  19. 19
    The wide genetic landscape of clinical frontotemporal dementia: systematic combined sequencing of 121 consecutive subjects

    The wide genetic landscape of clinical frontotemporal dementia: systematic combined sequencing of 121 consecutive subjects 由 Cornelis Blauwendraat, Carlo Wilke, Javier Simón‐Sánchez, Iris E. Jansen, Anika Reifschneider, Anja Capell, Christian Haass, Melissa Castillo-Lizardo, Saskia Biskup, Walter Maetzler, Patrizia Rizzu, Peter Heutink, Matthis Synofzik

    出版 2017
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  20. 20
    Assessing the relationship between monoallelic <i>PRKN</i> mutations and Parkinson’s risk

    Assessing the relationship between monoallelic <i>PRKN</i> mutations and Parkinson’s risk 由 Steven Lubbe, Bernabé I. Bustos, Jing Hu, Dimitri Krainc, Theresita Joseph, Jason Hehir, Manuela Tan, Weijia Zhang, Valentina Escott‐Price, Nigel Williams, Cornelis Blauwendraat, Andrew Singleton, Huw R. Morris

    出版 2021
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