Hasil Pencarian - Mike A. Nalls

Perbaiki Hasil
  1. 1
    Proteomics and Epidemiological Models of Human Aging

    Proteomics and Epidemiological Models of Human Aging oleh Ceereena Ubaida-Mohien, Ruin Moaddel, Ann Zenobia Moore, Pei-Lun Kuo, Faraz Faghri, Faraz Faghri, Faraz Faghri, Ravi Tharakan, Toshiko Tanaka, Mike A. Nalls, Mike A. Nalls, Mike A. Nalls, Luigi Ferrucci

    Diterbitkan 2021-05-01
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  2. 2
    Association of red cell distribution width with all-cause and cardiovascular-specific mortality in African American and white adults: a prospective cohort study

    Association of red cell distribution width with all-cause and cardiovascular-specific mortality in African American and white adults: a prospective cohort study oleh Salman M. Tajuddin, Mike A. Nalls, Alan B. Zonderman, Michele K. Evans

    Diterbitkan 2017-10-01
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  3. 3
    Lack of genetic evidence for NLRP3 inflammasome involvement in Parkinson’s disease pathogenesis

    Lack of genetic evidence for NLRP3 inflammasome involvement in Parkinson’s disease pathogenesis oleh Konstantin Senkevich, Lang Liu, Chelsea X. Alvarado, Hampton L. Leonard, Mike A. Nalls, Global Parkinson’s Genetics Program (GP2), Ziv Gan-Or

    Diterbitkan 2024-08-01
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  4. 4
    A population scale analysis of rare SNCA variation in the UK Biobank

    A population scale analysis of rare SNCA variation in the UK Biobank oleh Cornelis Blauwendraat, Mary B. Makarious, Hampton L. Leonard, Sara Bandres-Ciga, Hirotaka Iwaki, Mike A. Nalls, Alastair J. Noyce, Andrew B. Singleton

    Diterbitkan 2021-01-01
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  5. 5
    Sequential screening nominates the Parkinson's disease associated kinase LRRK2 as a regulator of Clathrin-mediated endocytosis

    Sequential screening nominates the Parkinson's disease associated kinase LRRK2 as a regulator of Clathrin-mediated endocytosis oleh George R. Heaton, Natalie Landeck, Adamantios Mamais, Mike A. Nalls, Jonathon Nixon-Abell, Ravindran Kumaran, Alexandra Beilina, Laura Pellegrini, Yan Li, Kirsten Harvey, Mark R. Cookson

    Diterbitkan 2020-07-01
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  6. 6
    A fully automated FAIMS-DIA mass spectrometry-based proteomic pipeline

    A fully automated FAIMS-DIA mass spectrometry-based proteomic pipeline oleh Luke Reilly, Erika Lara, Daniel Ramos, Ziyi Li, Caroline B. Pantazis, Julia Stadler, Marianita Santiana, Jessica Roberts, Faraz Faghri, Ying Hao, Mike A. Nalls, Priyanka Narayan, Yansheng Liu, Andrew B. Singleton, Mark R. Cookson, Michael E. Ward, Yue A. Qi

    Diterbitkan 2023-10-01
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  7. 7
    Application of Aligned-UMAP to longitudinal biomedical studies

    Application of Aligned-UMAP to longitudinal biomedical studies oleh Anant Dadu, Vipul K. Satone, Rachneet Kaur, Mathew J. Koretsky, Hirotaka Iwaki, Yue A. Qi, Daniel M. Ramos, Brian Avants, Jacob Hesterman, Roger Gunn, Mark R. Cookson, Michael E. Ward, Andrew B. Singleton, Roy H. Campbell, Mike A. Nalls, Faraz Faghri

    Diterbitkan 2023-06-01
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  8. 8
    Rare coding variation in paraoxonase-1 is associated with ischemic stroke in the NHLBI Exome Sequencing Project[S]

    Rare coding variation in paraoxonase-1 is associated with ischemic stroke in the NHLBI Exome Sequencing Project[S] oleh Daniel Seung Kim, David R. Crosslin, Paul L. Auer, Stephanie M. Suzuki, Judit Marsillach, Amber A. Burt, Adam S. Gordon, James F. Meschia, Mike A. Nalls, Bradford B. Worrall, W.T. Longstreth, Jr., Rebecca F. Gottesman, Clement E. Furlong, Ulrike Peters, Stephen S. Rich, Deborah A. Nickerson, Gail P. Jarvik

    Diterbitkan 2014-06-01
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  9. 9
    Identification and prediction of Parkinson’s disease subtypes and progression using machine learning in two cohorts

    Identification and prediction of Parkinson’s disease subtypes and progression using machine learning in two cohorts oleh Anant Dadu, Vipul Satone, Rachneet Kaur, Sayed Hadi Hashemi, Hampton Leonard, Hirotaka Iwaki, Mary B. Makarious, Kimberley J. Billingsley, Sara Bandres‐Ciga, Lana J. Sargent, Alastair J. Noyce, Ali Daneshmand, Cornelis Blauwendraat, Ken Marek, Sonja W. Scholz, Andrew B. Singleton, Mike A. Nalls, Roy H. Campbell, Faraz Faghri

    Diterbitkan 2022-12-01
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  10. 10
    Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain

    Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain oleh Dena G. Hernandez, Mike A. Nalls, Matthew Moore, Sean Chong, Allissa Dillman, Daniah Trabzuni, J. Raphael Gibbs, Mina Ryten, Sampath Arepalli, Michael E. Weale, Alan B. Zonderman, Juan Troncoso, Richard O'Brien, Robert Walker, Colin Smith, Stefania Bandinelli, Bryan J. Traynor, John Hardy, Andrew B. Singleton, Mark R. Cookson

    Diterbitkan 2012-07-01
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  11. 11
    Profiling complex repeat expansions in RFC1 in Parkinson’s disease

    Profiling complex repeat expansions in RFC1 in Parkinson’s disease oleh Pilar Alvarez Jerez, Kensuke Daida, Abigail Miano-Burkhardt, Hirotaka Iwaki, Laksh Malik, Guillaume Cogan, Mary B. Makarious, Roisin Sullivan, Jana Vandrovcova, Jinhui Ding, J. Raphael Gibbs, Androo Markham, Mike A. Nalls, Rupesh K. Kesharwani, Fritz J. Sedlazeck, Bradford Casey, John Hardy, Henry Houlden, Cornelis Blauwendraat, Andrew B. Singleton, Kimberley J. Billingsley

    Diterbitkan 2024-05-01
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  12. 12
    Estimating the causal influence of body mass index on risk of Parkinson disease: A Mendelian randomisation study.

    Estimating the causal influence of body mass index on risk of Parkinson disease: A Mendelian randomisation study. oleh Alastair J Noyce, Demis A Kia, Gibran Hemani, Aude Nicolas, T Ryan Price, Eduardo De Pablo-Fernandez, Philip C Haycock, Patrick A Lewis, Thomas Foltynie, George Davey Smith, International Parkinson Disease Genomics Consortium, Anette Schrag, Andrew J Lees, John Hardy, Andrew Singleton, Mike A Nalls, Neil Pearce, Debbie A Lawlor, Nicholas W Wood

    Diterbitkan 2017-06-01
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  13. 13
    Characterizing a complex CT-rich haplotype in intron 4 of SNCA using large-scale targeted amplicon long-read sequencing

    Characterizing a complex CT-rich haplotype in intron 4 of SNCA using large-scale targeted amplicon long-read sequencing oleh Pilar Alvarez Jerez, Kensuke Daida, Francis P. Grenn, Laksh Malik, Abigail Miano-Burkhardt, Mary B. Makarious, Jinhui Ding, J. Raphael Gibbs, Anni Moore, Xylena Reed, Mike A. Nalls, Syed Shah, Medhat Mahmoud, Fritz J. Sedlazeck, Egor Dolzhenko, Morgan Park, Hirotaka Iwaki, Bradford Casey, Mina Ryten, Cornelis Blauwendraat, Andrew B. Singleton, Kimberley J. Billingsley

    Diterbitkan 2024-07-01
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  14. 14
    Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information

    Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information oleh Sebastian Guelfi, Karishma D’Sa, Juan A. Botía, Jana Vandrovcova, Regina H. Reynolds, David Zhang, Daniah Trabzuni, Leonardo Collado-Torres, Andrew Thomason, Pedro Quijada Leyton, Sarah A. Gagliano Taliun, Mike A. Nalls, International Parkinson’s Disease Genomics Consortium (IPDGC), UK Brain Expression Consortium (UKBEC), Kerrin S. Small, Colin Smith, Adaikalavan Ramasamy, John Hardy, Michael E. Weale, Mina Ryten

    Diterbitkan 2020-02-01
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  15. 15
    Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)

    Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2) oleh Clodagh Towns, Madeleine Richer, Simona Jasaityte, Eleanor J. Stafford, Julie Joubert, Tarek Antar, Alejandro Martinez-Carrasco, Mary B. Makarious, Bradford Casey, Dan Vitale, Kristin Levine, Hampton Leonard, Caroline B. Pantazis, Laurel A. Screven, Dena G. Hernandez, Claire E. Wegel, Justin Solle, Mike A. Nalls, Cornelis Blauwendraat, Andrew B. Singleton, Manuela M. X. Tan, Hirotaka Iwaki, Huw R. Morris, the Global Parkinson’s Genetics Program (GP2)

    Diterbitkan 2023-09-01
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  16. 16
    Multi-modality machine learning predicting Parkinson’s disease

    Multi-modality machine learning predicting Parkinson’s disease oleh Mary B. Makarious, Hampton L. Leonard, Dan Vitale, Hirotaka Iwaki, Lana Sargent, Anant Dadu, Ivo Violich, Elizabeth Hutchins, David Saffo, Sara Bandres-Ciga, Jonggeol Jeff Kim, Yeajin Song, Melina Maleknia, Matt Bookman, Willy Nojopranoto, Roy H. Campbell, Sayed Hadi Hashemi, Juan A. Botia, John F. Carter, David W. Craig, Kendall Van Keuren-Jensen, Huw R. Morris, John A. Hardy, Cornelis Blauwendraat, Andrew B. Singleton, Faraz Faghri, Mike A. Nalls

    Diterbitkan 2022-04-01
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  17. 17
    GWAS of QRS duration identifies new loci specific to Hispanic/Latino populations.

    GWAS of QRS duration identifies new loci specific to Hispanic/Latino populations. oleh Brenton R Swenson, Tin Louie, Henry J Lin, Raúl Méndez-Giráldez, Jennifer E Below, Cathy C Laurie, Kathleen F Kerr, Heather Highland, Timothy A Thornton, Kelli K Ryckman, Charles Kooperberg, Elsayed Z Soliman, Amanda A Seyerle, Xiuqing Guo, Kent D Taylor, Jie Yao, Susan R Heckbert, Dawood Darbar, Lauren E Petty, Barbara McKnight, Susan Cheng, Natalie A Bello, Eric A Whitsel, Craig L Hanis, Mike A Nalls, Daniel S Evans, Jerome I Rotter, Tamar Sofer, Christy L Avery, Nona Sotoodehnia

    Diterbitkan 2019-01-01
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  18. 18
    A novel MMP12 locus is associated with large artery atherosclerotic stroke using a genome-wide age-at-onset informed approach.

    A novel MMP12 locus is associated with large artery atherosclerotic stroke using a genome-wide age-at-onset informed approach. oleh Matthew Traylor, Kari-Matti Mäkelä, Laura L Kilarski, Elizabeth G Holliday, William J Devan, Mike A Nalls, Kerri L Wiggins, Wei Zhao, Yu-Ching Cheng, Sefanja Achterberg, Rainer Malik, Cathie Sudlow, Steve Bevan, Emma Raitoharju, METASTROKE, International Stroke Genetics Consortium, Wellcome Trust Case Consortium 2 (WTCCC2), Niku Oksala, Vincent Thijs, Robin Lemmens, Arne Lindgren, Agnieszka Slowik, Jane M Maguire, Matthew Walters, Ale Algra, Pankaj Sharma, John R Attia, Giorgio B Boncoraglio, Peter M Rothwell, Paul I W de Bakker, Joshua C Bis, Danish Saleheen, Steven J Kittner, Braxton D Mitchell, Jonathan Rosand, James F Meschia, Christopher Levi, Martin Dichgans, Terho Lehtimäki, Cathryn M Lewis, Hugh S Markus

    Diterbitkan 2014-07-01
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  19. 19
    Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson’s disease in Chinese population

    Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson’s disease in Chinese population oleh Hongxu Pan, Zhenhua Liu, Jinghong Ma, Yuanyuan Li, Yuwen Zhao, Xiaoxia Zhou, Yaqin Xiang, Yige Wang, Xun Zhou, Runcheng He, Yali Xie, Qiao Zhou, Kai Yuan, Qian Xu, Qiying Sun, Junling Wang, Xinxiang Yan, Hainan Zhang, Chunyu Wang, Lifang Lei, Weiguo Liu, Xuejing Wang, Xuebing Ding, Tao Wang, Zheng Xue, Zhentao Zhang, Ling Chen, Qing Wang, Yonghong Liu, Jiayu Tang, Xuewei Zhang, Shifang Peng, Chaodong Wang, Jianqing Ding, Chunfeng Liu, Lijuan Wang, Haibo Chen, Lu Shen, Hong Jiang, Xinyin Wu, Hongzhuan Tan, Dan Luo, Shuiyuan Xiao, Xiang Chen, Jieqiong Tan, Zhengmao Hu, Chao Chen, Kun Xia, Zhuohua Zhang, Jia Nee Foo, Cornelis Blauwendraat, Mike A. Nalls, Andrew B. Singleton, Jun Liu, Piu Chan, Houfeng Zheng, Jinchen Li, Jifeng Guo, Jian Yang, Beisha Tang, the Parkinson’s Disease & Movement Disorders Multicenter Database and Collaborative Network in China (PD-MDCNC)

    Diterbitkan 2023-02-01
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  20. 20
    Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects

    Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects oleh Lynne Krohn, Karl Heilbron, Cornelis Blauwendraat, Regina H. Reynolds, Eric Yu, Konstantin Senkevich, Uladzislau Rudakou, Mehrdad A. Estiar, Emil K. Gustavsson, Kajsa Brolin, Jennifer A. Ruskey, Kathryn Freeman, Farnaz Asayesh, Ruth Chia, Isabelle Arnulf, Michele T. M. Hu, Jacques Y. Montplaisir, Jean-François Gagnon, Alex Desautels, Yves Dauvilliers, Gian Luigi Gigli, Mariarosaria Valente, Francesco Janes, Andrea Bernardini, Birgit Högl, Ambra Stefani, Abubaker Ibrahim, Karel Šonka, David Kemlink, Wolfgang Oertel, Annette Janzen, Giuseppe Plazzi, Francesco Biscarini, Elena Antelmi, Michela Figorilli, Monica Puligheddu, Brit Mollenhauer, Claudia Trenkwalder, Friederike Sixel-Döring, Valérie Cochen De Cock, Christelle Charley Monaca, Anna Heidbreder, Luigi Ferini-Strambi, Femke Dijkstra, Mineke Viaene, Beatriz Abril, Bradley F. Boeve, 23andMe Research Team, Sonja W. Scholz, Mina Ryten, Sara Bandres-Ciga, Alastair Noyce, Paul Cannon, Lasse Pihlstrøm, Mike A. Nalls, Andrew B. Singleton, Guy A. Rouleau, Ronald B. Postuma, Ziv Gan-Or

    Diterbitkan 2022-12-01
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