| Year |
Citation |
Score |
| 2024 |
Gaynor SM, Joseph T, Bai X, Zou Y, Boutkov B, Maxwell EK, Delaneau O, Hofmeister RJ, Krasheninina O, Balasubramanian S, Marcketta A, Backman J, Reid JG, Overton JD, Lotta LA, ... Marchini J, et al. Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank. Nature Genetics. PMID 39322778 DOI: 10.1038/s41588-024-01930-4 |
0.694 |
|
| 2024 |
Shi S, Rubinacci S, Hu S, Moutsianas L, Stuckey A, Need AC, Palamara PF, Caulfield M, Marchini J, Myers S. A Genomics England haplotype reference panel and imputation of UK Biobank. Nature Genetics. PMID 39134668 DOI: 10.1038/s41588-024-01868-7 |
0.379 |
|
| 2024 |
Sun KY, Bai X, Chen S, Bao S, Zhang C, Kapoor M, Backman J, Joseph T, Maxwell E, Mitra G, Gorovits A, Mansfield A, Boutkov B, Gokhale S, Habegger L, ... ... Marchini J, et al. A deep catalogue of protein-coding variation in 983,578 individuals. Nature. PMID 38768635 DOI: 10.1038/s41586-024-07556-0 |
0.352 |
|
| 2023 |
Ziyatdinov A, Torres J, Alegre-Díaz J, Backman J, Mbatchou J, Turner M, Gaynor SM, Joseph T, Zou Y, Liu D, Wade R, Staples J, Panea R, Popov A, Bai X, ... ... Marchini J, et al. Genotyping, sequencing and analysis of 140,000 adults from Mexico City. Nature. PMID 37821707 DOI: 10.1038/s41586-023-06595-3 |
0.404 |
|
| 2023 |
Sun KY, Bai X, Chen S, Bao S, Kapoor M, Backman J, Joseph T, Maxwell E, Mitra G, Gorovits A, Mansfield A, Boutkov B, Gokhale S, Habegger L, Marcketta A, ... ... Marchini J, et al. A deep catalog of protein-coding variation in 985,830 individuals. Biorxiv : the Preprint Server For Biology. PMID 37214792 DOI: 10.1101/2023.05.09.539329 |
0.306 |
|
| 2022 |
Kessler MD, Damask A, O'Keeffe S, Banerjee N, Li D, Watanabe K, Marketta A, Van Meter M, Semrau S, Horowitz J, Tang J, Kosmicki JA, Rajagopal VM, Zou Y, Houvras Y, ... ... Marchini J, et al. Common and rare variant associations with clonal haematopoiesis phenotypes. Nature. PMID 36450978 DOI: 10.1038/s41586-022-05448-9 |
0.329 |
|
| 2021 |
Backman JD, Li AH, Marcketta A, Sun D, Mbatchou J, Kessler MD, Benner C, Liu D, Locke AE, Balasubramanian S, Yadav A, Banerjee N, Gillies C, Damask A, Liu S, ... ... Marchini J, et al. Exome sequencing and analysis of 454,787 UK Biobank participants. Nature. PMID 34662886 DOI: 10.1038/s41586-021-04103-z |
0.322 |
|
| 2021 |
Sesia M, Bates S, Candès E, Marchini J, Sabatti C. False discovery rate control in genome-wide association studies with population structure. Proceedings of the National Academy of Sciences of the United States of America. 118. PMID 34580220 DOI: 10.1073/pnas.2105841118 |
0.405 |
|
| 2021 |
Kosmicki JA, Horowitz JE, Banerjee N, Lanche R, Marcketta A, Maxwell E, Bai X, Sun D, Backman JD, Sharma D, Kury FSP, Kang HM, O'Dushlaine C, Yadav A, Mansfield AJ, ... ... Marchini J, et al. Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals. American Journal of Human Genetics. PMID 34115965 DOI: 10.1016/j.ajhg.2021.05.017 |
0.34 |
|
| 2021 |
Mbatchou J, Barnard L, Backman J, Marcketta A, Kosmicki JA, Ziyatdinov A, Benner C, O'Dushlaine C, Barber M, Boutkov B, Habegger L, Ferreira M, Baras A, Reid J, Abecasis G, ... ... Marchini J, et al. Computationally efficient whole-genome regression for quantitative and binary traits. Nature Genetics. PMID 34017140 DOI: 10.1038/s41588-021-00870-7 |
0.313 |
|
| 2020 |
Rubinacci S, Delaneau O, Marchini J. Genotype imputation using the Positional Burrows Wheeler Transform. Plos Genetics. 16: e1009049. PMID 33196638 DOI: 10.1371/journal.pgen.1009049 |
0.664 |
|
| 2020 |
Van Hout CV, Tachmazidou I, Backman JD, Hoffman JD, Liu D, Pandey AK, Gonzaga-Jauregui C, Khalid S, Ye B, Banerjee N, Li AH, O'Dushlaine C, Marcketta A, Staples J, Schurmann C, ... ... Marchini J, et al. Exome sequencing and characterization of 49,960 individuals in the UK Biobank. Nature. PMID 33087929 DOI: 10.1038/s41586-020-2853-0 |
0.378 |
|
| 2020 |
Kerin M, Marchini J. Inferring Gene-by-Environment Interactions with a Bayesian Whole-Genome Regression Model. American Journal of Human Genetics. PMID 32888427 DOI: 10.1016/J.Ajhg.2020.08.009 |
0.412 |
|
| 2020 |
Cai N, Bigdeli TB, Kretzschmar WW, Li Y, Liang J, Hu J, Peterson RE, Bacanu S, Webb BT, Riley B, Li Q, Marchini J, Mott R, Kendler KS, Flint J. Retraction Note: 11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project. Scientific Data. 7: 123. PMID 32300216 DOI: 10.1038/S41597-020-0430-X |
0.369 |
|
| 2019 |
Delaneau O, Zagury JF, Robinson MR, Marchini JL, Dermitzakis ET. Accurate, scalable and integrative haplotype estimation. Nature Communications. 10: 5436. PMID 31780650 DOI: 10.1038/S41467-019-13225-Y |
0.765 |
|
| 2019 |
Wiberg A, Ng M, Al Omran Y, Alfaro-Almagro F, McCarthy P, Marchini J, Bennett DL, Smith S, Douaud G, Furniss D. Handedness, language areas and neuropsychiatric diseases: insights from brain imaging and genetics. Brain : a Journal of Neurology. PMID 31504236 DOI: 10.1093/Brain/Awz257 |
0.413 |
|
| 2019 |
Jung M, Wells D, Rusch J, Ahmad S, Marchini J, Myers SR, Conrad DF. Unified single-cell analysis of testis gene regulation and pathology in 5 mouse strains. Elife. 8. PMID 31237565 DOI: 10.7554/Elife.43966 |
0.349 |
|
| 2018 |
Bycroft C, Freeman C, Petkova D, Band G, Elliott LT, Sharp K, Motyer A, Vukcevic D, Delaneau O, O'Connell J, Cortes A, Welsh S, Young A, Effingham M, McVean G, ... ... Marchini J, et al. The UK Biobank resource with deep phenotyping and genomic data. Nature. 562: 203-209. PMID 30305743 DOI: 10.1038/S41586-018-0579-Z |
0.721 |
|
| 2018 |
Elliott LT, Sharp K, Alfaro-Almagro F, Shi S, Miller KL, Douaud G, Marchini J, Smith SM. Genome-wide association studies of brain imaging phenotypes in UK Biobank. Nature. 562: 210-216. PMID 30305740 DOI: 10.1038/S41586-018-0571-7 |
0.349 |
|
| 2018 |
Mahajan A, Taliun D, Thurner M, Robertson NR, Torres JM, Rayner NW, Payne AJ, Steinthorsdottir V, Scott RA, Grarup N, Cook JP, Schmidt EM, Wuttke M, Sarnowski C, Mägi R, ... ... Marchini J, et al. Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps. Nature Genetics. PMID 30297969 DOI: 10.1038/S41588-018-0241-6 |
0.403 |
|
| 2018 |
Wang DR, Agosto-Pérez FJ, Chebotarov D, Shi Y, Marchini J, Fitzgerald M, McNally KL, Alexandrov N, McCouch SR. An imputation platform to enhance integration of rice genetic resources. Nature Communications. 9: 3519. PMID 30158584 DOI: 10.1038/S41467-018-05538-1 |
0.477 |
|
| 2018 |
Wray NR, Ripke S, Mattheisen M, Trzaskowski M, Byrne EM, Abdellaoui A, Adams MJ, Agerbo E, Air TM, Andlauer TMF, Bacanu SA, Bækvad-Hansen M, Beekman AFT, Bigdeli TB, Binder EB, ... ... Marchini J, et al. Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Nature Genetics. PMID 29700475 DOI: 10.1038/S41588-018-0090-3 |
0.323 |
|
| 2018 |
Mahajan A, Wessel J, Willems SM, Zhao W, Robertson NR, Chu AY, Gan W, Kitajima H, Taliun D, Rayner NW, Guo X, Lu Y, Li M, Jensen RA, Hu Y, ... ... Marchini J, et al. Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. Nature Genetics. 50: 559-571. PMID 29632382 DOI: 10.1038/S41588-018-0084-1 |
0.394 |
|
| 2017 |
Justice AE, Winkler TW, Feitosa MF, Graff M, Fisher VA, Young K, Barata L, Deng X, Czajkowski J, Hadley D, Ngwa JS, Ahluwalia TS, Chu AY, Heard-Costa NL, Lim E, ... ... Marchini J, et al. Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Nature Communications. 8: 14977. PMID 28443625 DOI: 10.1038/Ncomms14977 |
0.389 |
|
| 2017 |
Cai N, Bigdeli TB, Kretzschmar WW, Li Y, Liang J, Hu J, Peterson RE, Bacanu S, Webb BT, Riley B, Li Q, Marchini J, Mott R, Kendler KS, Flint J. 11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project. Scientific Data. 4: 170011. PMID 28195579 DOI: 10.1038/Sdata.2017.11 |
0.517 |
|
| 2016 |
Astle WJ, Elding H, Jiang T, Allen D, Ruklisa D, Mann AL, Mead D, Bouman H, Riveros-Mckay F, Kostadima MA, Lambourne JJ, Sivapalaratnam S, Downes K, Kundu K, Bomba L, ... ... Marchini J, et al. The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Cell. 167: 1415-1429.e19. PMID 27863252 DOI: 10.1016/J.Cell.2016.10.042 |
0.68 |
|
| 2016 |
Amos CI, Dennis J, Wang Z, Byun J, Schumacher FR, Gayther SA, Casey G, Hunter DJ, Sellers TA, Gruber SB, Dunning AM, Michailidou K, Fachal L, Doheny K, Spurdle AB, ... ... Marchini J, et al. The OncoArray Consortium: a Network for Understanding the Genetic Architecture of Common Cancers. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. PMID 27697780 DOI: 10.1158/1055-9965.Epi-16-0106 |
0.434 |
|
| 2016 |
Hore V, Viñuela A, Buil A, Knight J, McCarthy MI, Small K, Marchini J. Tensor decomposition for multiple-tissue gene expression experiments. Nature Genetics. PMID 27479908 DOI: 10.1038/Ng.3624 |
0.39 |
|
| 2016 |
O'Connell J, Sharp K, Shrine N, Wain L, Hall I, Tobin M, Zagury JF, Delaneau O, Marchini J. Haplotype estimation for biobank-scale data sets. Nature Genetics. PMID 27270105 DOI: 10.1038/Ng.3583 |
0.731 |
|
| 2016 |
Sharp K, Kretzschmar W, Delaneau O, Marchini J. Phasing for medical sequencing using rare variants and large haplotype reference panels. Bioinformatics (Oxford, England). 32: 1974-80. PMID 27153703 DOI: 10.1093/Bioinformatics/Btw065 |
0.709 |
|
| 2016 |
Dahl A, Iotchkova V, Baud A, Johansson Å, Gyllensten U, Soranzo N, Mott R, Kranis A, Marchini J. A multiple-phenotype imputation method for genetic studies. Nature Genetics. 48: 466-72. PMID 26901065 DOI: 10.1038/Ng.3513 |
0.477 |
|
| 2016 |
Cai N, Bigdeli T, Kretzschmar W, Li Y, Liang J, Song L, Hu J, Li Q, Jin W, Hu Z, Wang G, Wang L, Qian P, Liu Y, Jiang T, ... ... Marchini J, et al. CONVERGE dataset: 12,000 whole-genome sequences representative of the Han Chinese population Gigascience. 5. DOI: 10.1186/S13742-016-0123-8 |
0.397 |
|
| 2015 |
Auton A, Brooks LD, Durbin RM, Garrison EP, Kang HM, Korbel JO, Marchini JL, McCarthy S, McVean GA, Abecasis GR. A global reference for human genetic variation. Nature. 526: 68-74. PMID 26432245 DOI: 10.1038/Nature15393 |
0.453 |
|
| 2015 |
Wain LV, Shrine N, Miller S, Jackson VE, Ntalla I, Artigas MS, Billington CK, Kheirallah AK, Allen R, Cook JP, Probert K, Obeidat M, Bossé Y, Hao K, Postma DS, ... ... Marchini J, et al. Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank. The Lancet. Respiratory Medicine. PMID 26423011 DOI: 10.1016/S2213-2600(15)00283-0 |
0.626 |
|
| 2015 |
Huang J, Howie B, McCarthy S, Memari Y, Walter K, Min JL, Danecek P, Malerba G, Trabetti E, Zheng HF, Gambaro G, Richards JB, Durbin R, Timpson NJ, ... Marchini J, et al. Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel. Nature Communications. 6: 8111. PMID 26368830 DOI: 10.1038/Ncomms9111 |
0.531 |
|
| 2015 |
Martin HC, Christ R, Hussin JG, O'Connell J, Gordon S, Mbarek H, Hottenga JJ, McAloney K, Willemsen G, Gasparini P, Pirastu N, Montgomery GW, Navarro P, Soranzo N, Toniolo D, ... ... Marchini J, et al. Multicohort analysis of the maternal age effect on recombination. Nature Communications. 6: 7846. PMID 26242864 DOI: 10.1038/Ncomms8846 |
0.337 |
|
| 2015 |
Cai N, Bigdeli TB, Kretzschmar W, Lei Y, Liang J, Song L, Hu J, Li Q, Jin W, Hu Z, Wang G, Wang L, Qian P, Liu Y, Jiang T, ... ... Marchini J, et al. Sparse whole-genome sequencing identifies two loci for major depressive disorder Nature. 523: 588-591. DOI: 10.1038/Nature14659 |
0.361 |
|
| 2014 |
Delaneau O, Marchini J. Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel. Nature Communications. 5: 3934. PMID 25653097 DOI: 10.1038/Ncomms4934 |
0.739 |
|
| 2014 |
O'Connell J, Gurdasani D, Delaneau O, Pirastu N, Ulivi S, Cocca M, Traglia M, Huang J, Huffman JE, Rudan I, McQuillan R, Fraser RM, Campbell H, Polasek O, Asiki G, ... ... Marchini J, et al. A general approach for haplotype phasing across the full spectrum of relatedness. Plos Genetics. 10: e1004234. PMID 24743097 DOI: 10.1371/Journal.Pgen.1004234 |
0.748 |
|
| 2013 |
Stephens SH, Hartz SM, Hoft NR, Saccone NL, Corley RC, Hewitt JK, Hopfer CJ, Breslau N, Coon H, Chen X, Ducci F, Dueker N, Franceschini N, Frank J, Han Y, ... ... Marchini J, et al. Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking. Genetic Epidemiology. 37: 846-59. PMID 24186853 DOI: 10.1002/Gepi.21760 |
0.32 |
|
| 2013 |
Delaneau O, Howie B, Cox AJ, Zagury JF, Marchini J. Haplotype estimation using sequencing reads. American Journal of Human Genetics. 93: 687-96. PMID 24094745 DOI: 10.1016/J.Ajhg.2013.09.002 |
0.746 |
|
| 2013 |
Montgomery SB, Goode DL, Kvikstad E, Albers CA, Zhang ZD, Mu XJ, Ananda G, Howie B, Karczewski KJ, Smith KS, Anaya V, Richardson R, Davis J, MacArthur DG, ... ... Marchini J, et al. The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes. Genome Research. 23: 749-61. PMID 23478400 DOI: 10.1101/Gr.148718.112 |
0.49 |
|
| 2013 |
Delaneau O, Zagury JF, Marchini J. Improved whole-chromosome phasing for disease and population genetic studies. Nature Methods. 10: 5-6. PMID 23269371 DOI: 10.1038/Nmeth.2307 |
0.717 |
|
| 2013 |
Churchhouse C, Marchini J. Multiway admixture deconvolution using phased or unphased ancestral panels. Genetic Epidemiology. 37: 1-12. PMID 23136122 DOI: 10.1002/Gepi.21692 |
0.456 |
|
| 2013 |
Menelaou A, Marchini J. Genotype calling and phasing using next-generation sequencing reads and a haplotype scaffold. Bioinformatics (Oxford, England). 29: 84-91. PMID 23093610 DOI: 10.1093/Bioinformatics/Bts632 |
0.503 |
|
| 2013 |
Wang J, Bansal AT, Martin M, Germer S, Benayed R, Essioux L, Lee JS, Begovich A, Hemmings A, Kenwright A, Taylor KE, Upmanyu R, Cutler P, Harari O, Marchini J, et al. Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis. The Pharmacogenomics Journal. 13: 235-41. PMID 22491018 DOI: 10.1038/Tpj.2012.8 |
0.364 |
|
| 2012 |
Hancock DB, Artigas MS, Gharib SA, Henry A, Manichaikul A, Ramasamy A, Loth DW, Imboden M, Koch B, McArdle WL, Smith AV, Smolonska J, Sood A, Tang W, Wilk JB, ... ... Marchini J, et al. Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function. Plos Genetics. 8: e1003098. PMID 23284291 DOI: 10.1371/Journal.Pgen.1003098 |
0.402 |
|
| 2012 |
Hartz SM, Short SE, Saccone NL, Culverhouse R, Chen L, Schwantes-An TH, Coon H, Han Y, Stephens SH, Sun J, Chen X, Ducci F, Dueker N, Franceschini N, Frank J, ... ... Marchini J, et al. Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Archives of General Psychiatry. 69: 854-60. PMID 22868939 DOI: 10.1001/Archgenpsychiatry.2012.124 |
0.328 |
|
| 2012 |
O'Connell J, Marchini J. Joint genotype calling with array and sequence data. Genetic Epidemiology. 36: 527-37. PMID 22821426 DOI: 10.1002/Gepi.21657 |
0.519 |
|
| 2012 |
Howie B, Fuchsberger C, Stephens M, Marchini J, Abecasis GR. Fast and accurate genotype imputation in genome-wide association studies through pre-phasing. Nature Genetics. 44: 955-9. PMID 22820512 DOI: 10.1038/Ng.2354 |
0.541 |
|
| 2011 |
Howie B, Marchini J, Stephens M. Genotype imputation with thousands of genomes. G3 (Bethesda, Md.). 1: 457-70. PMID 22384356 DOI: 10.1534/G3.111.001198 |
0.529 |
|
| 2011 |
Delaneau O, Marchini J, Zagury JF. A linear complexity phasing method for thousands of genomes. Nature Methods. 9: 179-81. PMID 22138821 DOI: 10.1038/Nmeth.1785 |
0.764 |
|
| 2011 |
Soler Artigas M, Wain LV, Repapi E, Obeidat M, Sayers I, Burton PR, Johnson T, Zhao JH, Albrecht E, Dominiczak AF, Kerr SM, Smith BH, Cadby G, Hui J, Palmer LJ, ... ... Marchini J, et al. Effect of five genetic variants associated with lung function on the risk of chronic obstructive lung disease, and their joint effects on lung function. American Journal of Respiratory and Critical Care Medicine. 184: 786-95. PMID 21965014 DOI: 10.1164/Rccm.201102-0192Oc |
0.384 |
|
| 2011 |
Soler Artigas M, Loth DW, Wain LV, Gharib SA, Obeidat M, Tang W, Zhai G, Zhao JH, Smith AV, Huffman JE, Albrecht E, Jackson CM, Evans DM, Cadby G, Fornage M, ... ... Marchini J, et al. Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. Nature Genetics. 43: 1082-90. PMID 21946350 DOI: 10.1038/Ng.941 |
0.334 |
|
| 2011 |
Cardin N, Holmes C, Donnelly P, Marchini J. Bayesian hierarchical mixture modeling to assign copy number from a targeted CNV array. Genetic Epidemiology. 35: 536-48. PMID 21769931 DOI: 10.1002/Gepi.20604 |
0.422 |
|
| 2011 |
Tomlinson IP, Carvajal-Carmona LG, Dobbins SE, Tenesa A, Jones AM, Howarth K, Palles C, Broderick P, Jaeger EE, Farrington S, Lewis A, Prendergast JG, Pittman AM, Theodoratou E, Olver B, ... ... Marchini J, et al. Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer. Plos Genetics. 7: e1002105. PMID 21655089 DOI: 10.1371/Journal.Pgen.1002105 |
0.419 |
|
| 2011 |
Su Z, Marchini J, Donnelly P. HAPGEN2: simulation of multiple disease SNPs. Bioinformatics (Oxford, England). 27: 2304-5. PMID 21653516 DOI: 10.1093/Bioinformatics/Btr341 |
0.413 |
|
| 2011 |
Southam L, Panoutsopoulou K, Rayner NW, Chapman K, Durrant C, Ferreira T, Arden N, Carr A, Deloukas P, Doherty M, Loughlin J, McCaskie A, Ollier WE, Ralston S, Spector TD, ... ... Marchini J, et al. The effect of genome-wide association scan quality control on imputation outcome for common variants. European Journal of Human Genetics : Ejhg. 19: 610-4. PMID 21267008 DOI: 10.1038/Ejhg.2010.242 |
0.447 |
|
| 2011 |
Ferreira T, Marchini J. Modeling interactions with known risk loci-a Bayesian model averaging approach. Annals of Human Genetics. 75: 1-9. PMID 21118191 DOI: 10.1111/J.1469-1809.2010.00618.X |
0.457 |
|
| 2010 |
Marchini J, Howie B. Genotype imputation for genome-wide association studies. Nature Reviews. Genetics. 11: 499-511. PMID 20517342 DOI: 10.1038/Nrg2796 |
0.467 |
|
| 2010 |
Liu JZ, Tozzi F, Waterworth DM, Pillai SG, Muglia P, Middleton L, Berrettini W, Knouff CW, Yuan X, Waeber G, Vollenweider P, Preisig M, Wareham NJ, Zhao JH, Loos RJ, ... ... Marchini J, et al. Meta-analysis and imputation refines the association of 15q25 with smoking quantity. Nature Genetics. 42: 436-40. PMID 20418889 DOI: 10.1038/Ng.572 |
0.417 |
|
| 2010 |
Craddock N, Hurles ME, Cardin N, Pearson RD, Plagnol V, Robson S, Vukcevic D, Barnes C, Conrad DF, Giannoulatou E, Holmes C, Marchini JL, Stirrups K, Tobin MD, et al. Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls. Nature. 464: 713-20. PMID 20360734 DOI: 10.1038/Nature08979 |
0.374 |
|
| 2009 |
Howie BN, Donnelly P, Marchini J. A flexible and accurate genotype imputation method for the next generation of genome-wide association studies. Plos Genetics. 5: e1000529. PMID 19543373 DOI: 10.1371/Journal.Pgen.1000529 |
0.513 |
|
| 2009 |
Spencer CCA, Su Z, Donnelly P, Marchini J. Designing genome-wide association studies: Sample size, power, imputation, and the choice of genotyping chip Plos Genetics. 5. PMID 19492015 DOI: 10.1371/Journal.Pgen.1000477 |
0.467 |
|
| 2009 |
Jallow M, Teo YY, Small KS, Rockett KA, Deloukas P, Clark TG, Kivinen K, Bojang KA, Conway DJ, Pinder M, Sirugo G, Sisay-Joof F, Usen S, Auburn S, Bumpstead SJ, ... ... Marchini J, et al. Genome-wide and fine-resolution association analysis of malaria in West Africa. Nature Genetics. 41: 657-65. PMID 19465909 DOI: 10.1038/Ng.388 |
0.465 |
|
| 2009 |
Su Z, Cardin N, Donnelly P, Marchini J. A Bayesian Method for Detecting and Characterizing Allelic Heterogeneity and Boosting Signals in Genome-Wide Association Studies Statistical Science. 24: 430-450. DOI: 10.1214/09-Sts311 |
0.484 |
|
| 2009 |
Zheng G, Marchini J, Geller NL. Introduction to the Special Issue: Genome-Wide Association Studies Statistical Science. 24: 387-387. DOI: 10.1214/09-Sts310 |
0.381 |
|
| 2008 |
Marchini J, Howie B. Comparing algorithms for genotype imputation. American Journal of Human Genetics. 83: 535-9; author reply . PMID 18940314 DOI: 10.1016/J.Ajhg.2008.09.007 |
0.432 |
|
| 2008 |
Barnes C, Plagnol V, Fitzgerald T, Redon R, Marchini J, Clayton D, Hurles ME. A robust statistical method for case-control association testing with copy number variation. Nature Genetics. 40: 1245-52. PMID 18776912 DOI: 10.1038/Ng.206 |
0.428 |
|
| 2008 |
Barrett JC, Hansoul S, Nicolae DL, Cho JH, Duerr RH, Rioux JD, Brant SR, Silverberg MS, Taylor KD, Barmada MM, Bitton A, Dassopoulos T, Datta LW, Green T, Griffiths AM, ... ... Marchini J, et al. Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. Nature Genetics. 40: 955-62. PMID 18587394 DOI: 10.1038/Ng.175 |
0.44 |
|
| 2007 |
Sabeti PC, Varilly P, Fry B, Lohmueller J, Hostetter E, Cotsapas C, Xie X, Byrne EH, McCarroll SA, Gaudet R, Schaffner SF, Lander ES, Frazer KA, Ballinger DG, ... ... Marchini J, et al. Genome-wide detection and characterization of positive selection in human populations. Nature. 449: 913-8. PMID 17943131 DOI: 10.1038/Nature06250 |
0.434 |
|
| 2007 |
Frazer KA, Ballinger DG, Cox DR, Hinds DA, Stuve LL, Gibbs RA, Belmont JW, Boudreau A, Hardenbol P, Leal SM, Pasternak S, Wheeler DA, Willis TD, Yu F, ... ... Marchini J, et al. A second generation human haplotype map of over 3.1 million SNPs. Nature. 449: 851-61. PMID 17943122 DOI: 10.1038/Nature06258 |
0.472 |
|
| 2007 |
Marchini J, Howie B, Myers S, McVean G, Donnelly P. A new multipoint method for genome-wide association studies by imputation of genotypes. Nature Genetics. 39: 906-13. PMID 17572673 DOI: 10.1038/Ng2088 |
0.515 |
|
| 2007 |
Eyheramendy S, Marchini J, McVean G, Myers S, Donnelly P. A model-based approach to capture genetic variation for future association studies. Genome Research. 17: 88-95. PMID 17095708 DOI: 10.1101/Gr.5675406 |
0.507 |
|
| 2006 |
Evans DM, Marchini J, Morris AP, Cardon LR. Two-stage two-locus models in genome-wide association. Plos Genetics. 2: e157. PMID 17002500 DOI: 10.1371/Journal.Pgen.0020157 |
0.436 |
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| 2006 |
de Bakker PI, McVean G, Sabeti PC, Miretti MM, Green T, Marchini J, Ke X, Monsuur AJ, Whittaker P, Delgado M, Morrison J, Richardson A, Walsh EC, Gao X, Galver L, et al. A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC. Nature Genetics. 38: 1166-72. PMID 16998491 DOI: 10.1038/Ng1885 |
0.393 |
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| 2006 |
Marchini J, Cutler D, Patterson N, Stephens M, Eskin E, Halperin E, Lin S, Qin ZS, Munro HM, Abecasis GR, Donnelly P. A comparison of phasing algorithms for trios and unrelated individuals. American Journal of Human Genetics. 78: 437-50. PMID 16465620 DOI: 10.1086/500808 |
0.482 |
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| 2005 |
Marchini J, Donnelly P, Cardon LR. Genome-wide strategies for detecting multiple loci that influence complex diseases. Nature Genetics. 37: 413-7. PMID 15793588 DOI: 10.1038/Ng1537 |
0.468 |
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| 2004 |
Marchini J, Cardon LR, Phillips MS, Donnelly P. The effects of human population structure on large genetic association studies Nature Genetics. 36: 512-517. PMID 15052271 DOI: 10.1038/Ng1337 |
0.424 |
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| 2004 |
Marchini J, Cardon LR, Phillips MS, Donnelly P. Reply to "Genomic Control to the extreme" Nature Genetics. 36: 1131-1131. DOI: 10.1038/Ng1104-1131 |
0.338 |
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| 2003 |
Belmont JW, Hardenbol P, Willis TD, Yu F, Yang H, Ch'Ang LY, Huang W, Liu B, Shen Y, Tam PKH, Tsui LC, Waye MMY, Wong JTF, Zeng C, Zhang Q, ... ... Marchini J, et al. The international HapMap project Nature. 426: 789-796. DOI: 10.1038/Nature02168 |
0.434 |
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