Year |
Citation |
Score |
2020 |
Zheng J, Haberland V, Baird D, Walker V, Haycock PC, Hurle MR, Gutteridge A, Erola P, Liu Y, Luo S, Robinson J, Richardson TG, Staley JR, Elsworth B, Burgess S, ... ... Laurin C, et al. Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases. Nature Genetics. PMID 32895551 DOI: 10.1038/S41588-020-0682-6 |
0.318 |
|
2019 |
Warrington NM, Beaumont RN, Horikoshi M, Day FR, Helgeland Ø, Laurin C, Bacelis J, Peng S, Hao K, Feenstra B, Wood AR, Mahajan A, Tyrrell J, Robertson NR, Rayner NW, et al. Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. Nature Genetics. PMID 31043758 DOI: 10.1038/S41588-019-0403-1 |
0.3 |
|
2018 |
Hemani G, Zheng J, Elsworth B, Wade KH, Haberland V, Baird D, Laurin C, Burgess S, Bowden J, Langdon R, Tan VY, Yarmolinsky J, Shihab HA, Timpson NJ, Evans DM, et al. The MR-Base platform supports systematic causal inference across the human phenome. Elife. 7. PMID 29846171 DOI: 10.7554/eLife.34408 |
0.315 |
|
2017 |
Laurin C, Cuellar-Partida G, Hemani G, Smith GD, Yang J, Evans DM. Partitioning Phenotypic Variance Due to Parent-of-Origin Effects Using Genomic Relatedness Matrices. Behavior Genetics. PMID 29098496 DOI: 10.1007/S10519-017-9880-0 |
0.387 |
|
2016 |
Zheng J, Erzurumluoglu AM, Elsworth BL, Kemp JP, Howe L, Haycock PC, Hemani G, Tansey K, Laurin C, Pourcain BS, Warrington NM, Finucane HK, Price AL, Bulik-Sullivan BK, et al. LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis. Bioinformatics (Oxford, England). PMID 27663502 DOI: 10.1093/Bioinformatics/Btw613 |
0.469 |
|
2016 |
Zheng J, Rodriguez S, Laurin C, Baird D, Trela-Larsen L, Erzurumluoglu MA, Zheng Y, White J, Giambartolomei C, Zabaneh D, Morris R, Kumari M, Casas JP, Hingorani AD, et al. HAPRAP: a haplotype-based iterative method for statistical fine mapping using GWAS summary statistics. Bioinformatics (Oxford, England). PMID 27591082 DOI: 10.1093/Bioinformatics/Btw565 |
0.386 |
|
2016 |
Laurin C, Boomsma D, Lubke G. The use of vector bootstrapping to improve variable selection precision in Lasso models. Statistical Applications in Genetics and Molecular Biology. PMID 27248122 DOI: 10.1515/Sagmb-2015-0043 |
0.64 |
|
2015 |
Laurin CA, Hottenga JJ, Willemsen G, Boomsma DI, Lubke GH. Genetic analyses benefit from using less heterogeneous phenotypes: an illustration with the hospital anxiety and depression scale (HADS). Genetic Epidemiology. 39: 317-24. PMID 25832296 DOI: 10.1002/Gepi.21897 |
0.611 |
|
2014 |
Walters RK, Laurin C, Lubke GH. Epi2Loc: an R package to investigate two-locus epistatic models. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 17: 272-8. PMID 24983251 DOI: 10.1017/Thg.2014.38 |
0.634 |
|
2014 |
Walters RK, Laurin C, Lubke GH. EpiPen: An R Package to Investigate Two-Locus Epistatic Models – RETRACTION Twin Research and Human Genetics. 17: 354-354. PMID 24970233 DOI: 10.1017/Thg.2014.37 |
0.558 |
|
2014 |
Lubke GH, Laurin C, Amin N, Hottenga JJ, Willemsen G, van Grootheest G, Abdellaoui A, Karssen LC, Oostra BA, van Duijn CM, Penninx BW, Boomsma DI. Genome-wide analyses of borderline personality features. Molecular Psychiatry. 19: 923-9. PMID 23979607 DOI: 10.1038/Mp.2013.109 |
0.648 |
|
2014 |
Walters RK, Laurin C, Lubke GH. EpiPen: An R Package to Investigate Two-Locus Epistatic Models Twin Research and Human Genetics. DOI: 10.1017/thg.2014.25 |
0.374 |
|
2013 |
Laurin C, Lubke G. Abstract: Stability Selection for Penalized Canonical Correlation Analysis. Multivariate Behavioral Research. 48: 165. PMID 26789226 DOI: 10.1080/00273171.2013.752264 |
0.551 |
|
2013 |
Lubke G, Laurin C, Walters R, Eriksson N, Hysi P, Spector T, Montgomery G, Martin N, Medland S, Boomsma D. Gradient Boosting as a SNP Filter: an Evaluation Using Simulated and Hair Morphology Data. Journal of Data Mining in Genomics & Proteomics. 4. PMID 24404405 DOI: 10.4172/2153-0602.1000143 |
0.659 |
|
2012 |
Walters R, Laurin C, Lubke GH. An integrated approach to reduce the impact of minor allele frequency and linkage disequilibrium on variable importance measures for genome-wide data. Bioinformatics (Oxford, England). 28: 2615-23. PMID 22847933 DOI: 10.1093/Bioinformatics/Bts483 |
0.636 |
|
2012 |
Lubke GH, Hottenga JJ, Walters R, Laurin C, de Geus EJ, Willemsen G, Smit JH, Middeldorp CM, Penninx BW, Vink JM, Boomsma DI. Estimating the genetic variance of major depressive disorder due to all single nucleotide polymorphisms. Biological Psychiatry. 72: 707-9. PMID 22520966 DOI: 10.1016/J.Biopsych.2012.03.011 |
0.65 |
|
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