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| Linkage disequilibrium in the human genome DE Reich, M Cargill, S Bolk, J Ireland, PC Sabeti, DJ Richter, T Lavery, ... Nature 411 (6834), 199-204, 2001 | 2231 | 2001 |
| Discovery of T cell receptor β motifs specific to HLA–B27–positive ankylosing spondylitis by deep repertoire sequence analysis M Faham, V Carlton, M Moorhead, J Zheng, M Klinger, F Pepin, T Asbury, ... Arthritis & rheumatology 69 (4), 774-784, 2017 | 100 | 2017 |
| Analysis of molecular inversion probe performance for allele copy number determination Y Wang, M Moorhead, G Karlin-Neumann, NJ Wang, J Ireland, S Lin, ... Genome biology 8, 1-14, 2007 | 86 | 2007 |
| Method and kits for multiplex hybridization assays X Miao, J Ireland, P Hardenbol, TM Daly, DJ Fu, RD Hockett US Patent 7,368,242, 2008 | 50 | 2008 |
| Single nucleotide polymorphisms in genes ES Lander, M Cargill, JS Ireland, S Bolk, GQ Daley, JJ McCarthy US Patent 6,727,063, 2004 | 44 | 2004 |
| Functional single nucleotide polymorphism-based association studies VEH Carlton, JS Ireland, F Useche, M Faham Human genomics 2 (6), 391, 2006 | 43 | 2006 |
| Generic SBE-FRET protocol S Bolk, JN Hirschhorn, JS Ireland, ES Lander US Patent 6,642,001, 2003 | 43 | 2003 |
| High-throughput method for analyzing methylation of CpGs in targeted genomic regions S Nautiyal, VEH Carlton, Y Lu, JS Ireland, D Flaucher, M Moorhead, ... Proceedings of the National Academy of Sciences 107 (28), 12587-12592, 2010 | 41 | 2010 |
| Optimal genotype determination in highly multiplexed SNP data M Moorhead, P Hardenbol, F Siddiqui, M Falkowski, C Bruckner, J Ireland, ... European journal of human genetics 14 (2), 207-215, 2006 | 36 | 2006 |
| Rapid identification of somatic mutations in colorectal and breast cancer tissues using mismatch repair detection (MRD) S Bentivegna, J Zheng, E Namsaraev, VEH Carlton, A Pavlicek, ... Human mutation 29 (3), 441-450, 2008 | 29 | 2008 |
| High-throughput, high-accuracy array-based resequencing J Zheng, M Moorhead, L Weng, F Siddiqui, VEH Carlton, JS Ireland, L Lee, ... Proceedings of the National Academy of Sciences 106 (16), 6712-6717, 2009 | 27 | 2009 |
| Human single nucleotide polymorphisms M Cargill, J Ireland, E Lander US Patent App. 09/765,081, 2002 | 21 | 2002 |
| Large-scale characterization of public database SNPs causing non-synonymous changes in three ethnic groups J Ireland, VEH Carlton, M Falkowski, M Moorhead, K Tran, F Useche, ... Human genetics 119, 75-83, 2006 | 15 | 2006 |
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| Stroke Biomarkers PV Peplow, B Martinez, SA Dambinova Springer New York, 2020 | 6 | 2020 |
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| Performance of molecular inversion probes (MIP) in allele copy number determination Y Wang, M Moorhead, G Karlin-Neumann, NJ Wang, J Ireland, S Lin, ... | 3 | 2008 |
| Coding sequence polymorphisms in vascular pathology genes ES Lander, GQ Daley, M Cargill, JS Ireland, SG Rozen US Patent 6,692,909, 2004 | 3 | 2004 |
