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Manuela MX Tan
Manuela MX Tan
Oslo University hospital
Verified email at medisin.uio.no - Homepage
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A García, AE Welch, ML Mandelli, ML Henry, S Lukic, MJT Prioris, ...
Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson’s disease
EE Brown, C Blauwendraat, J Trinh, M Rizig, MA Nalls, E Leveille, ...
Neurobiology of Aging 97, 148. e17-148. e24, 2021
222021
Andme Research T
C Blauwendraat, K Heilbron, CL Vallerga, S Bandres-Ciga, R Von Coelln, ...
Eerola-Rautio J, Tienari P, Majamaa K, Toft M, Grosset DG, Gasser T, Heutink …, 2019
252019
Assessing the relationship between monoallelic PRKN mutations and Parkinson’s risk
SJ Lubbe, BI Bustos, J Hu, D Krainc, T Joseph, J Hehir, M Tan, W Zhang, ...
Human molecular genetics 30 (1), 78-86, 2021
412021
Association between the LRP1B and APOE loci and the development of Parkinson’s disease dementia
R Real, A Martinez-Carrasco, RH Reynolds, MA Lawton, MMX Tan, ...
Brain 146 (5), 1873-1887, 2023
302023
Association of Body Mass Index and Parkinson Disease: A Bidirectional Mendelian Randomization Study
C Domenighetti, PE Sugier, A Ashok Kumar Sreelatha, C Schulte, ...
Neurology 103 (3), e209620, 2024
2024
Association of genetic variation at the GJA5/ACP6 locus with motor progression in Parkinson’s
A Martinez-Carrasco, R Real, M Lawton, RH Reynolds, MMX Tan, L Wu, ...
medRxiv, 2022.10. 28.22281645, 2022
12022
Author Correction: The IPDGC/GP2 Hackathon-an open science event for training in data science, genomics, and collaboration using Parkinson’s disease data
HL Leonard, R Murtadha, A Martinez-Carrasco, A Jama, ...
npj Parkinson's Disease 9 (1), 77, 2023
2023
Building a Global Parkinson's Genetics Program (GP2): Clinical Cohorts Integration Working Group
J Joubert, M Tan, T Antar, A Martinez-Carrasco, H Iwaki, H Morris
MOVEMENT DISORDERS 36, S313-S313, 2021
2021
Cognitive impairment in early onset and familial Parkinson's disease
M Tan, J Bras, J Hong, C Brugaletta, T Samakomva, K Hoffmann, S Lubbe, ...
MOVEMENT DISORDERS 32, 2017
2017
Combining biomarkers for prognostic modelling of Parkinson’s disease
N Vijiaratnam, M Lawton, AJ Heslegrave, T Guo, M Tan, E Jabbari, R Real, ...
Journal of Neurology, Neurosurgery & Psychiatry 93 (7), 707-715, 2022
142022
Common variation at the LRRK2 locus is associated with survival in the primary tauopathy progressive supranuclear palsy
E Jabbari, MMX Tan, RH Reynolds, KY Mok, R Ferrari, DP Murphy, ...
bioRxiv, 2020.02. 04.932335, 2020
62020
Dairy intake and Parkinson's disease: a Mendelian randomization study
C Domenighetti, PE Sugier, A Ashok Kumar Sreelatha, C Schulte, ...
Movement Disorders 37 (4), 857-864, 2022
212022
Defining candidate Parkinson’s disease genes through the analysis of genome-wide homozygosity
SJ Lubbe, YC Wong, B Bustos, S Kim, J Vandrovcova, BP Norman, M Tan, ...
medRxiv, 2020.11. 23.20235671, 2020
12020
Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
C Towns, M Richer, S Jasaityte, EJ Stafford, J Joubert, T Antar, ...
npj Parkinson's Disease 9 (1), 131, 2023
82023
Developing New Insights Into Clinical and Genetic Features of PD-The Global Parkinson's Genetics Program (GP2) Clinical Cohorts Working Group
M Richer, C Towns, A Martinez-Carrasco, J Solle, A Singleton, ...
MOVEMENT DISORDERS 37, S575-S575, 2022
2022
Diagnosis across the spectrum of progressive supranuclear palsy and corticobasal syndrome
E Jabbari, N Holland, V Chelban, PS Jones, R Lamb, C Rawlinson, T Guo, ...
JAMA neurology 77 (3), 377-387, 2020
1302020
Dissecting the limited genetic overlap of Parkinson's and Alzheimer's disease
M Stolp Andersen, M Tan, IR Holtman, J Hardy, ...
Annals of clinical and translational neurology 9 (8), 1289-1295, 2022
82022
Early Onset Parkinson’s Disease in a family of Moroccan origin caused by a p.A217D mutation in PINK1: a case report
BP Norman, SJ Lubbe, M Tan, N Warren, HR Morris
BMC neurology 17, 1-5, 2017
32017
Epigenome-wide association study, meta-analysis and risk profiling of whole blood in Parkinson's disease
IH Lie, MMX Tan, MS Andersen, M Toft, L Pihlstrom
medRxiv, 2024.05. 28.24308034, 2024
2024
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