Stebėti
Christina M. Lill
Christina M. Lill
Professor, University of Münster, Germany; Lecturer, Imperial College London, UK
Patvirtintas el. paštas uni-luebeck.de
Pavadinimas
Cituota
Cituota
Metai
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
MA Nalls, N Pankratz, CM Lill, CB Do, DG Hernandez, M Saad, ...
Nature genetics 46 (9), 989-993, 2014
21042014
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
International IBD Genetics Consortium (IIBDGC), C Agliardi, L Alfredsson, ...
Nature genetics 45 (11), 1353-1360, 2013
14032013
The genetics of Alzheimer disease: back to the future
L Bertram, CM Lill, RE Tanzi
Neuron 68 (2), 270-281, 2010
11402010
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility
International Multiple Sclerosis Genetics Consortium*†, ANZgene, ...
Science 365 (6460), eaav7188, 2019
8632019
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
G Davies, M Lam, SE Harris, JW Trampush, M Luciano, WD Hill, ...
Nature communications 9 (1), 2098, 2018
7172018
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
R Karlsson Linnér, P Biroli, E Kong, SFW Meddens, R Wedow, ...
Nature genetics 51 (2), 245-257, 2019
7162019
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database
CM Lill, JT Roehr, MB McQueen, FK Kavvoura, S Bagade, BMM Schjeide, ...
PLoS genetics 8 (3), e1002548, 2012
6312012
Genetics of Parkinson's disease
CM Lill
Molecular and cellular probes 30 (6), 386-396, 2016
4972016
Class II HLA interactions modulate genetic risk for multiple sclerosis
Nature genetics 47 (10), 1107-1113, 2015
4432015
Fine-mapping the genetic association of the major histocompatibility complex in multiple sclerosis: HLA and non-HLA effects
NA Patsopoulos, LF Barcellos, RQ Hintzen, C Schaefer, CM Van Duijn, ...
PLoS genetics 9 (11), e1003926, 2013
3992013
Genotype‐Phenotype Relations for the Parkinson's Disease Genes Parkin, PINK1, DJ1: MDSGene Systematic Review
M Kasten, C Hartmann, J Hampf, S Schaake, A Westenberger, ...
Movement Disorders 33 (5), 730-741, 2018
3212018
The Multiple Sclerosis Genomic Map: Role of peripheral immune cells and resident microglia in susceptibility
International Multiple Sclerosis Genetics Consortium, NA Patsopoulos, ...
BioRxiv, 143933, 2017
3112017
Genotype‐phenotype relations for the Parkinson's disease genes SNCA, LRRK2, VPS35: MDSGene systematic review
J Trinh, FMJ Zeldenrust, J Huang, M Kasten, S Schaake, S Petkovic, ...
Movement Disorders 33 (12), 1857-1870, 2018
1922018
The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease
CM Lill, A Rengmark, L Pihlstrøm, I Fogh, A Shatunov, PM Sleiman, ...
Alzheimer's & Dementia 11 (12), 1407-1416, 2015
1802015
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity
PK Joshi, N Pirastu, KA Kentistou, K Fischer, E Hofer, KE Schraut, ...
Nature communications 8 (1), 910, 2017
1732017
Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study
I Pichler, F Del Greco M, M Gögele, CM Lill, L Bertram, CB Do, N Eriksson, ...
PLoS medicine 10 (6), e1001462, 2013
1712013
Network-based multiple sclerosis pathway analysis with GWAS data from 15,000 cases and 30,000 controls
SE Baranzini, P Khankhanian, NA Patsopoulos, M Li, J Stankovich, ...
The American Journal of Human Genetics 92 (6), 854-865, 2013
1652013
Large-scale replication and heterogeneity in Parkinson disease genetic loci
M Sharma, JPA Ioannidis, JO Aasly, G Annesi, A Brice, ...
Neurology 79 (7), 659-667, 2012
1622012
Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation
TFM Andlauer, D Buck, G Antony, A Bayas, L Bechmann, A Berthele, ...
Science advances 2 (6), e1501678, 2016
1562016
Low-frequency and rare-coding variation contributes to multiple sclerosis risk
M Mitrovič, NA Patsopoulos, AH Beecham, T Dankowski, A Goris, ...
Cell 175 (6), 1679-1687. e7, 2018
1472018
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Straipsniai 1–20