Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 612 Records) |
Query Trace: LRRK2[original query] |
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The Avidity of Autoreactive Alpha-Synuclein Antibodies in Leucine-Rich Repeat Kinase 2 Mutation Carriers Is Not Altered Compared to Healthy Controls or Patients with Parkinson's Disease. Biomolecules 2023 9 13 (9): . Alexandra Albus, Yannick Kronimus, Monika Burg-Roderfeld, Hendrik van der Wurp, Dieter Willbold, Tamar Ziehm, Richard Dodel, Jean Alexander Ro |
Rapidly progressive multiple system atrophy in a patient carrying LRRK2 G2019S mutation. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2023 9 . Tommaso Carrer, Giulia Bonato, Michele Sandre, Aron Emmi, Marta Campagnolo, Giulia Musso, Miryam Carecchio, Piero Parchi, Angelo Antoni |
Caffeine intake interacts with Asian gene variants in Parkinson's disease: a study in 4488 subjects. The Lancet regional health. Western Pacific 2023 9 40 100877. Yi-Lin Ong, Xiao Deng, Hui-Hua Li, K Narasimhalu, Ling-Ling Chan, Kumar M Prakash, Wing-Lok Au, Pavanni Ratnagopal, Louis C S Tan, Eng-King T |
Double Trouble: Association of Malignant Melanoma with Sporadic and Genetic Forms of Parkinson's Disease and Asymptomatic Carriers of Related Genes: A Brief Report. Medicina (Kaunas, Lithuania) 2023 8 59 (8): . Christos Koros, Athina-Maria Simitsi, Anastasia Bougea, Nikolaos Papagiannakis, Roubina Antonelou, Ioanna Pachi, Efthalia Angelopoulou, Andreas Prentakis, Athena Zachou, Chrysa Chrysovitsanou, Ion Beratis, Stella Fragkiadaki, Dionysia Kontaxopoulou, Efthymia Eftymiopoulou, Evangelia Stanitsa, Constantin Potagas, Sokratis G Papageorgiou, Efstratios Karavasilis, Georgios Velonakis, Vasilios Prassopoulos, Xenia Geronicola-Trapali, Leonidas Stefan |
Proteomics of brain, CSF, and plasma identifies molecular signatures for distinguishing sporadic and genetic Alzheimer's disease. Science translational medicine 2023 7 15 (703): eabq5923. Yun Ju Sung, Chengran Yang, Joanne Norton, Matt Johnson, Anne Fagan, Randall J Bateman, Richard J Perrin, John C Morris, Martin R Farlow, Jasmeer P Chhatwal, Peter R Schofield, Helena Chui, Fengxian Wang, Brenna Novotny, Abdallah Eteleeb, Celeste Karch, Suzanne E Schindler, Herve Rhinn, Erik C B Johnson, Hamilton Se-Hwee Oh, Jarod Evert Rutledge, Eric B Dammer, Nicholas T Seyfried, Tony Wyss-Coray, Oscar Harari, Carlos Crucha |
LRRK2 exonic variants are associated with lysosomal hydrolase activities and lysosphingolipid alterations in Parkinson's disease. Gene 2023 7 882 147639. T S Usenko, K A Senkevich, K S Basharova, A I Bezrukova, G V Baydakova, A A Tyurin, M V Beletskaya, D G Kulabukhova, M N Grunina, A K Emelyanov, I V Miliukhina, A A Timofeeva, E Y Zakharova, S N Pcheli |
Increased basal forebrain volumes could prevent cognitive decline in LRRK2 Parkinson's disease. Neurobiology of disease 2023 6 183 106182. Lucia Batzu, Daniele Urso, Michel J Grothe, Dániel Veréb, K Ray Chaudhuri, Joana B Perei |
Genome-wide case-only analysis of gene-gene interactions with known Parkinson's disease risk variants reveals link between LRRK2 and SYT10. NPJ Parkinson's disease 2023 6 9 (1): 102. Milda Aleknonyt?-Resch, Joanne Trinh, Hampton Leonard, Sylvie Delcambre, Elsa Leitão, Dongbing Lai, Semra Smaji?, Avi Orr-Urtreger, Avner Thaler, Cornelis Blauwendraat, Arunabh Sharma, Mary B Makarious, Jonggeol Jeff Kim, Julie Lake, Pegah Rahmati, Sandra Freitag-Wolf, Philip Seibler, Tatiana Foroud, Andrew B Singleton, , Anne Grünewald, Frank Kaiser, Christine Klein, Michael Krawczak, Astrid Dempf |
Astrocytes Differentiated from LRRK2-I1371V Parkinson's-Disease-Induced Pluripotent Stem Cells Exhibit Similar Yield but Cell-Intrinsic Dysfunction in Glutamate Uptake and Metabolism, ATP Generation, and Nrf2-Mediated Glutathione Machinery. Cells 2023 6 12 (12): . Roon Banerjee, Aishwarya Raj, Chandrakanta Potdar, Pramod Kumar Pal, Ravi Yadav, Nitish Kamble, Vikram Holla, Indrani Dat |
Large-scale rare variant burden testing in Parkinson's disease. Brain : a journal of neurology 2023 6 . Mary B Makarious, Julie Lake, Vanessa Pitz, Allen Ye Fu, Joseph L Guidubaldi, Caroline Warly Solsberg, Sara Bandres-Ciga, Hampton L Leonard, Jonggeol Jeffrey Kim, Kimberley J Billingsley, Francis P Grenn, Pilar Alvarez Jerez, Chelsea Alvarado, Hirotaka Iwaki, Michael Ta, Dan Vitale, Dena Hernandez, Ali Torkamani, Mina Ryten, John Hardy, , Sonja W Scholz, Bryan J Traynor, Clifton L Dalgard, Debra J Ehrlich, Toshiko Tanaka, Luigi Ferrucci, Thomas G Beach, Geidy E Serrano, Raquel Real, Huw R Morris, Jinhui Ding, J Raphael Gibbs, Andrew B Singleton, Mike A Nalls, Tushar Bhangale, Cornelis Blauwendra |
Gene Panel Sequencing Analysis Revealed a Strong Contribution of Rare Coding Variants to the Risk of Parkinson's Disease in Sporadic Moroccan Patients. Journal of molecular neuroscience : MN 2023 5 . Imane Smaili, Houyam Tibar, Mounia Rahmani, Najlaa Machkour, Rachid Razine, Hajar Naciri Darai, Naima Bouslam, Ali Benomar, Wafa Regragui, Ahmed Bouhouc |
Patterns of TDP-43 Deposition in Brains with LRRK2 G2019S Mutations. Movement disorders : official journal of the Movement Disorder Society 2023 5 . Julian Agin-Liebes, Richard A Hickman, Jean Paul Vonsattel, Phyllis L Faust, Xena Flowers, Irina Utkina Sosunova, Joel Ntiri, Richard Mayeux, Matthew Surface, Karen Marder, Stanley Fahn, Serge Przedborski, Roy N Alcal |
Genetic study of early-onset Parkinson's disease in the Malaysian population. Parkinsonism & related disorders 2023 5 111 105399. Yi Wen Tay, Ai Huey Tan, Jia Lun Lim, Katja Lohmann, Khairul Azmi Ibrahim, Zariah Abdul Aziz, Yen Theng Chin, Ahmad Shahir Mawardi, Thien Thien Lim, Irene Looi, Yuen Kang Chia, Joshua Chin Ern Ooi, Wee Kooi Cheah, Alfand Marl F Dy Closas, Lei Cheng Lit, Jia Wei Hor, Tzi Shin Toh, Kalai Arasu Muthusamy, Peter Bauer, Volha Skrahin, Arndt Rolfs, Christine Klein, Azlina Ahmad-Annuar, Shen-Yang L |
Genetic risk variants in New Yorkers of Puerto Rican and Dominican Republic heritage with Parkinson's disease. NPJ Parkinson's disease 2023 12 9 (1): 160. Gabriel Miltenberger-Miltenyi, Roberto A Ortega, Aloysius Domingo, Rachita Yadav, Ayumi Nishiyama, Deborah Raymond, Viktoriya Katsnelson, Nikita Urval, Matthew Swan, Vicki Shanker, Joan Miravite, Ruth H Walker, Susan B Bressman, Laurie J Ozelius, José C Cabassa, Rachel Saunders-Pullm |
Human iPSC-derived microglia carrying the LRRK2-G2019S mutation show a Parkinson's disease related transcriptional profile and function. Scientific reports 2023 12 13 (1): 22118. Sohvi Ohtonen, Luca Giudice, Henna Jäntti, Mohammad Feroze Fazaludeen, Anastasia Shakirzyanova, Mireia Gómez-Budia, Nelli-Noora Välimäki, Jonna Niskanen, Nea Korvenlaita, Ilkka Fagerlund, Jari Koistinaho, Mahmood Amiry-Moghaddam, Ekaterina Savchenko, Laurent Roybon, Šárka Lehtonen, Paula Korhonen, Tarja Ma |
Levodopa-carbidopa intestinal gel infusion (LCIG) in Parkinson disease with genetic mutations. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2023 11 . R Balestrino, T Martone, M Toffoli, E Montanaro, M Fabbri, C A Artusi, A Romagnolo, M Zibetti, M Rizzone, S Goldwurm, L Lopiano, A H V Schapi |
Frequency of Hereditary and GBA1-Related Parkinsonism in Latin America: A Systematic Review and Meta-Analysis. Movement disorders : official journal of the Movement Disorder Society 2023 11 . Paula Saffie Awad, Daniel Teixeira-Dos-Santos, Bruno Lopes Santos-Lobato, Sarah Camargos, Mario Cornejo-Olivas, Carlos Roberto de Mello Rieder, Ignacio F Mata, Pedro Chaná-Cuevas, Christine Klein, Artur F Schumacher Sch |
The Landscape of Monogenic Parkinson's Disease in Populations of Non-European Ancestry: A Narrative Review. Genes 2023 11 14 (11): . Christos Koros, Anastasia Bougea, Athina Maria Simitsi, Nikolaos Papagiannakis, Efthalia Angelopoulou, Ioanna Pachi, Roubina Antonelou, Maria Bozi, Maria Stamelou, Leonidas Stefan |
Investigation of the genetic aetiology of Lewy body diseases with and without dementia. medRxiv : the preprint server for health sciences 2023 11 . Lesley Wu, Raquel Real, Alejandro Martinez, Ruth Chia, Michael A Lawton, Maryam Shoai, Catherine Bresner, Leon Hubbard, Cornelis Blauwendraat, Andrew B Singleton, Mina Ryten, Sonja W Scholz, Bryan J Traynor, Nigel Williams, Michele T M Hu, Yoav Ben-Shlomo, Donald G Grosset, John Hardy, Huw R Morris, |
Ethnicity- and sex-specific genome wide association study on Parkinson's disease. NPJ Parkinson's disease 2023 10 9 (1): 141. Kye Won Park, Ho-Sung Ryu, Eunsoon Shin, YoonGi Park, Sang Ryong Jeon, Seong Yoon Kim, Jae Seung Kim, Seong-Beom Koh, Sun Ju Chu |
Dopamine pathway and Parkinson's risk variants are associated with levodopa-induced dyskinesia. medRxiv : the preprint server for health sciences 2023 10 . Yuri L Sosero, Sara Bandres-Ciga, Bart Ferwerda, Maria T P Tocino, Dìaz R Belloso, Pilar Gómez-Garre, Johann Faouzi, Pille Taba, Lukas Pavelka, Tainà M Marques, Clarissa P C Gomes, Alexey Kolodkin, Patrick May, Lukasz M Milanowski, Zbigniew K Wszolek, Ryan J Uitti, Peter Heutink, Jacobus J van Hilten, David K Simon, Shirley Eberly, Ignacio Alvarez, Lynne Krohn, Eric Yu, Kathryn Freeman, Uladzislau Rudakou, Jennifer A Ruskey, Farnaz Asayesh, Manuel Menéndez-Gonzàlez, Pau Pastor, Owen A Ross, Rejko Krüger, Jean-Christophe Corvol, Sulev Koks, Pablo Mir, Rob M A De Bie, Hirotaka Iwaki, Ziv Gan- |
Genetic overlap between ALS and other neurodegenerative or neuromuscular disorders. Amyotrophic lateral sclerosis & frontotemporal degeneration 2023 10 1-11. Cathrine Goberg Olsen, Øyvind Løvold Busk, Øystein Lunde Holla, Kristian Tveten, Trygve Holmøy, Ole-Bjørn Tysnes, Helle Høy |
RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses. The Lancet. Neurology 2024 4 . Emil K Gustavsson, Jordan Follett, Joanne Trinh, Sandeep K Barodia, Raquel Real, Zhiyong Liu, Melissa Grant-Peters, Jesse D Fox, Silke Appel-Cresswell, A Jon Stoessl, Alex Rajput, Ali H Rajput, Roland Auer, Russel Tilney, Marc Sturm, Tobias B Haack, Suzanne Lesage, Christelle Tesson, Alexis Brice, Carles Vilariño-Güell, Mina Ryten, Matthew S Goldberg, Andrew B West, Michele T Hu, Huw R Morris, Manu Sharma, Ziv Gan-Or, Bedia Samanci, Pawel Lis, Maria Teresa Periñan, Rim Amouri, Samia Ben Sassi, Faycel Hentati, , Francesca Tonelli, Dario R Alessi, Matthew J Farr |
Analysis of rare Parkinson's disease variants in millions of people. NPJ Parkinson's disease 2024 1 10 (1): 11. Vanessa Pitz, Mary B Makarious, Sara Bandres-Ciga, Hirotaka Iwaki, , Andrew B Singleton, Mike Nalls, Karl Heilbron, Cornelis Blauwendra |
Genetic landscape of Parkinson's disease and related diseases in Luxembourg. Frontiers in aging neuroscience 2024 1 15 1282174. Zied Landoulsi, Sinthuja Pachchek, Dheeraj Reddy Bobbili, Lukas Pavelka, Patrick May, Rejko Krüger, |
A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinase. medRxiv : the preprint server for health sciences 2024 1 . Emil K Gustavsson, Jordan Follett, Joanne Trinh, Sandeep K Barodia, Raquel Real, Zhiyong Liu, Melissa Grant-Peters, Jesse D Fox, Silke Appel-Cresswell, A Jon Stoessl, Alex Rajput, Ali H Rajput, Roland Auer, Russel Tilney, Marc Sturm, Tobias B Haack, Suzanne Lesage, Christelle Tesson, Alexis Brice, Carles Vilariño-Güell, Mina Ryten, Matthew S Goldberg, Andrew B West, Michele T Hu, Huw R Morris, Manu Sharma, Ziv Gan-Or, Bedia Samanci, Pawel Lis, Teresa Tocino, Rim Amouri, Samia Ben Sassi, Faycel Hentati, , Francesca Tonelli, Dario R Alessi, Matthew J Farr |
The Effect of p.G2019S Mutation in the LRRK2 Gene on the Activity of Lysosomal Hydrolases and the Clinical Features of Parkinson's Disease Associated with p.N370S Mutation in the GBA1 Gene. Journal of integrative neuroscience 2024 1 23 (1): 16. Tatiana S Usenko, Alla Timofeeva, Mariia Beletskaia, Katerina Basharova, Galina Baydakova, Anastasia Bezrukova, Maria Grunina, Anton Emelyanov, Irina Miliukhina, Ekaterina Zakharova, Sofya Pcheli |
MAPT Locus in Parkinson's Disease Patients of Ashkenazi Origin: A Stratified Analysis. Genes 2024 1 15 (1): . Shachar Shani, Mali Gana-Weisz, Anat Bar-Shira, Avner Thaler, Tanya Gurevich, Anat Mirelman, Nir Giladi, Roy N Alcalay, Orly Goldstein, Avi Orr-Urtreg |
Identification of potential crucial genes and therapeutic targets for epilepsy. European journal of medical research 2024 1 29 (1): 43. Shitao Wang, Zhenrong Xie, Tian Jun, Xuelu Ma, Mengen Zhang, Feng Rao, Hui Xu, Jinghong Lu, Xiangqian Ding, Zongyou |
Gene-Level Analysis of Anthracycline-Induced Cardiomyopathy in Cancer Survivors: A Report From COG-ALTE03N1, BMTSS, and CCSS. JACC. CardioOncology 2024 1 5 (6): 807-818. Noha Sharafeldin, Liting Zhou, Purnima Singh, David K Crossman, Xuexia Wang, Lindsey Hageman, Wendy Landier, Javier G Blanco, Paul W Burridge, Yadav Sapkota, Yutaka Yasui, Gregory T Armstrong, Leslie L Robison, Melissa M Hudson, Kevin Oeffinger, Eric J Chow, Saro H Armenian, Daniel J Weisdorf, Smita Bhat |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
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