Number of items: 5.
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Billingsley, Kimberley, Barbosa, Ines, Bandrés-Ciga, Sara, Quinn, John ORCID: 0000-0003-3551-7803, Bubb, Vivien, Deshpande, Charu, Botia, Juan, Reynolds, Regina, Zhang, David, Simpson, Michael ORCID: 0000-0002-8539-8753 et al (show 8 more authors) , Blauwendraat, Cornelis, Gan-Or, Ziv, Gibbs, Raphael ORCID: 0000-0002-6985-0658, Nalls, Mike, Singleton, Andrew, Ryten, Mina, Koks, Sulev ORCID: 0000-0001-6087-6643 and International Parkinson’s Disease Genomics Consortium (IPDGC),
(2018)
Genetic variation within genes associated with mitochondrial function is significantly associated with later age at onset of Parkinson disease and contributes to disease risk.
BioRxiv.
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Billingsley, Kimberley J, Ding, Jinhui, Jerez, Pilar Alvarez, Illarionova, Anastasia, Levine, Kristin, Grenn, Francis P, Makarious, Mary B, Moore, Anni, Vitale, Daniel, Reed, Xylena et al (show 31 more authors) , Hernandez, Dena, Torkamani, Ali, Ryten, Mina, Hardy, John, UK Brain Expression Consortium UKBEC, Ruth, Chia, Ruth W, Scholz, Sonja J, Traynor, Bryan L, Dalgard, Clifton J, Ehrlich, Debra, Tanaka, Toshiko, Ferrucci, Luigi G, Beach, Thomas E, Serrano, Geidy P, Quinn, John J, Bubb, Vivien ORCID: 0000-0003-2763-7004, Collins, Ryan L, Zhao, Xuefang, Walker, Mark, Pierce-Hoffman, Emma, Brand, Harrison E, Talkowski, Michael, Casey, Bradford, Cookson, Mark R, Markham, Androo A, Nalls, Mike, Mahmoud, Medhat, Sedlazeck, Fritz J, Blauwendraat, Cornelis, Gibbs, J Raphael B and Singleton, Andrew
(2023)
Genome-Wide Analysis of Structural Variants in Parkinson Disease.
ANNALS OF NEUROLOGY, 93 (5).
pp. 1012-1022.
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Bandres-Ciga, Sara ORCID: 0000-0003-0056-1361, Faghri, Faraz ORCID: 0000-0001-5744-8728, Majounie, Elisa, Koretsky, Mathew J ORCID: 0000-0003-4341-3991, Kim, Jeffrey ORCID: 0000-0003-0738-0512, Levine, Kristin S, Leonard, Hampton ORCID: 0000-0003-2390-8110, Makarious, Mary B ORCID: 0000-0002-7978-1051, Iwaki, Hirotaka ORCID: 0000-0002-8982-7885, Crea, Peter Wild ORCID: 0000-0001-8944-5716 et al (show 24 more authors) , Hernandez, Dena G ORCID: 0000-0002-0188-9927, Arepalli, Sampath, Billingsley, Kimberley ORCID: 0000-0002-8003-4029, Lohmann, Katja ORCID: 0000-0002-5121-1460, Klein, Christine ORCID: 0000-0003-2102-3431, Lubbe, Steven J ORCID: 0000-0002-7103-6671, Jabbari, Edwin ORCID: 0000-0001-6844-882X, Saffie-Awad, Paula ORCID: 0000-0002-8056-365X, Narendra, Derek ORCID: 0000-0002-8696-9108, Reyes-Palomares, Armando ORCID: 0000-0002-0289-6889, Quinn, John P ORCID: 0000-0003-3551-7803, Schulte, Claudia ORCID: 0000-0003-4006-1265, Morris, Huw R ORCID: 0000-0002-5473-3774, Traynor, Bryan J ORCID: 0000-0003-0527-2446, Scholz, Sonja W ORCID: 0000-0002-6623-0429, Houlden, Henry ORCID: 0000-0002-2866-7777, Hardy, John ORCID: 0000-0002-3122-0423, Dumanis, Sonya ORCID: 0000-0002-3345-9497, Riley, Ekemini ORCID: 0000-0001-7040-5191, Blauwendraat, Cornelis ORCID: 0000-0001-9358-8111, Singleton, Andrew ORCID: 0000-0001-5606-700X, Nalls, Mike, Jeff, Janina and Vitale, Dan ORCID: 0000-0002-0637-3671
(2023)
NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations.
medRxiv.
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Kraja, Aldi T, Chasman, Daniel I, North, Kari E, Reiner, Alexander P, Yanek, Lisa R, Kilpeläinen, Tuomas O, Smith, Jennifer A, Dehghan, Abbas, Dupuis, Josée, Johnson, Andrew D et al (show 58 more authors) , Feitosa, Mary F, Tekola-Ayele, Fasil, Chu, Audrey Y, Nolte, Ilja M, Dastani, Zari, Morris, Andrew, Pendergrass, Sarah A, Sun, Yan V, Ritchie, Marylyn D, Vaez, Ahmad, Lin, Honghuang, Ligthart, Symen, Marullo, Letizia, Rohde, Rebecca, Shao, Yaming, Ziegler, Mark A, Im, Hae Kyung, Schnabel, Renate B, Jørgensen, Torben, Jørgensen, Marit E, Hansen, Torben, Pedersen, Oluf, Stolk, Ronald P, Snieder, Harold, Hofman, Albert, Uitterlinden, Andre G, Franco, Oscar H, Ikram, M Arfan, Richards, J Brent, Rotimi, Charles, Wilson, James G, Lange, Leslie, Ganesh, Santhi K, Nalls, Mike, Rasmussen-Torvik, Laura J, Pankow, James S, Coresh, Josef, Tang, Weihong, Linda Kao, WH, Boerwinkle, Eric, Morrison, Alanna C, Ridker, Paul M, Becker, Diane M, Rotter, Jerome I, Kardia, Sharon LR, Loos, Ruth JF, Larson, Martin G, Hsu, Yi-Hsiang, Province, Michael A, Tracy, Russell, Voight, Benjamin F, Vaidya, Dhananjay, O'Donnell, Christopher J, Benjamin, Emelia J, Alizadeh, Behrooz Z, Prokopenko, Inga, Meigs, James B and Borecki, Ingrid B
(2014)
Pleiotropic genes for metabolic syndrome and inflammation.
Molecular Genetics and Metabolism, 112 (4).
pp. 317-338.
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Liu, Hui ORCID: 0000-0001-5308-0874, Dehestani, Mohammad, Blauwendraat, Cornelis ORCID: 0000-0001-9358-8111, Makarious, Mary B, Leonard, Hampton, Kim, Jonggeol J, Schulte, Claudia, Noyce, Alastair ORCID: 0000-0003-3027-5497, Jacobs, Benjamin M, Foote, Isabelle ORCID: 0000-0002-0253-4116 et al (show 6 more authors) , Sharma, Manu ORCID: 0000-0002-1260-5416, International Parkinson's Disease Genomics Consortium; Comprehen, , Nalls, Mike, Singleton, Andrew, Gasser, Thomas and Bandres-Ciga, Sara ORCID: 0000-0003-0056-1361
(2022)
Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk Factors.
Annals of neurology, 92 (2).
pp. 270-278.
This list was generated on Sun Feb 11 08:34:02 2024 GMT.