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Steven Lubbe
Steven Lubbe
Assistant Professor of Neurology and Genetic Medicine
Verified email at northwestern.edu - Homepage
Title
Cited by
Cited by
Year
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ...
The Lancet Neurology 18 (12), 1091-1102, 2019
15292019
A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24. 21
I Tomlinson, E Webb, L Carvajal-Carmona, P Broderick, Z Kemp, S Spain, ...
Nature genetics 39 (8), 984-988, 2007
9302007
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23. 3
IPM Tomlinson, E Webb, L Carvajal-Carmona, P Broderick, K Howarth, ...
Nature genetics 40 (5), 623-630, 2008
6532008
A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk
P Broderick, L Carvajal-Carmona, AM Pittman, E Webb, K Howarth, ...
Nature genetics 39 (11), 1315-1317, 2007
6102007
Correlated gene expression supports synchronous activity in brain networks
J Richiardi, A Altmann, AC Milazzo, C Chang, MM Chakravarty, ...
Science 348 (6240), 1241-1244, 2015
6072015
Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer
L Carvajal-Carmona, K Howarth, E Jaeger, SL Spain, A Walther, ...
Nature genetics 40 (12), 1426-1435, 2008
6052008
Loss of VPS13C function in autosomal-recessive parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy
S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ...
The American Journal of Human Genetics 98 (3), 500-513, 2016
4122016
Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13. 3 influence colorectal cancer risk
E Jaeger, E Webb, K Howarth, L Carvajal-Carmona, A Rowan, ...
Nature genetics 40 (1), 26-28, 2008
3522008
Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk
MG Dunlop, SE Dobbins, SM Farrington, AM Jones, C Palles, N Whiffin, ...
Nature genetics 44 (7), 770-776, 2012
2792012
Clinical Implications of the Colorectal Cancer Risk Associated With MUTYH Mutation
SJ Lubbe, MC Di Bernardo, IP Chandler, RS Houlston
Journal of Clinical Oncology 27 (24), 3975-3980, 2009
2632009
Multiple Common Susceptibility Variants near BMP Pathway Loci GREM1, BMP4, and BMP2 Explain Part of the Missing Heritability of Colorectal Cancer
IPM Tomlinson, LG Carvajal-Carmona, SE Dobbins, A Tenesa, AM Jones, ...
PLoS genetics 7 (6), e1002105, 2011
2402011
Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers
NE Mencacci, IU Isaias, MM Reich, C Ganos, V Plagnol, JM Polke, J Bras, ...
Brain 137 (9), 2480-2492, 2014
2092014
A large-scale meta-analysis to refine colorectal cancer risk estimates associated with MUTYH variants
E Theodoratou, H Campbell, A Tenesa, R Houlston, E Webb, S Lubbe, ...
British journal of cancer 103 (12), 1875-1884, 2010
1512010
Cumulative impact of common genetic variants and other risk factors on colorectal cancer risk in 42 103 individuals
MG Dunlop, A Tenesa, SM Farrington, S Ballereau, DH Brewster, ...
Gut 62 (6), 871-881, 2013
1492013
Polygenic risk of P arkinson disease is correlated with disease age at onset
V Escott‐Price, International Parkinson's Disease Genomics Consortium, ...
Annals of neurology 77 (4), 582-591, 2015
1432015
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases
C Blauwendraat, F Faghri, L Pihlstrom, JT Geiger, A Elbaz, S Lesage, ...
Neurobiology of aging 57, 247. e9-247. e13, 2017
1392017
Evaluation of NTHL1, NEIL1, NEIL2, MPG, TDG, UNG and SMUG1genes in familial colorectal cancer predisposition
P Broderick, T Bagratuni, J Vijayakrishnan, S Lubbe, I Chandler, ...
BMC cancer 6, 1-7, 2006
1262006
Recessive mutations in VPS13D cause childhood onset movement disorders
J Gauthier, IA Meijer, D Lessel, NE Mencacci, D Krainc, M Hempel, ...
Annals of neurology 83 (6), 1089-1095, 2018
1232018
Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing
IE Jansen, H Ye, S Heetveld, MC Lechler, H Michels, RI Seinstra, ...
Genome biology 18, 1-26, 2017
1192017
Identification of candidate Parkinson disease genes by integrating genome-wide association study, expression, and epigenetic data sets
DA Kia, D Zhang, S Guelfi, C Manzoni, L Hubbard, RH Reynolds, J Botía, ...
JAMA neurology 78 (4), 464-472, 2021
1162021
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