| The allelic landscape of human blood cell trait variation and links to common complex disease WJ Astle, H Elding, T Jiang, D Allen, D Ruklisa, AL Mann, D Mead, ... Cell 167 (5), 1415-1429. e19, 2016 | 1229 | 2016 |
| Genetic drivers of epigenetic and transcriptional variation in human immune cells L Chen, B Ge, FP Casale, L Vasquez, T Kwan, D Garrido-Martín, S Watt, ... Cell 167 (5), 1398-1414. e24, 2016 | 680 | 2016 |
| Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture HF Zheng, V Forgetta, YH Hsu, K Estrada, A Rosello‐Diez, PJ Leo, ... Nature 526 (7571), 112-117, 2015 | 554 | 2015 |
| The relationship between DNA methylation, genetic and expression inter-individual variation in untransformed human fibroblasts JR Wagner, S Busche, B Ge, T Kwan, T Pastinen, M Blanchette Genome biology 15, 1-17, 2014 | 502 | 2014 |
| ARSACS, a spastic ataxia common in northeastern Quebec, is caused by mutations in a new gene encoding an 11.5-kb ORF JC Engert, P Bérubé, J Mercier, C Doré, P Lepage, B Ge, JP Bouchard, ... Nature genetics 24 (2), 120-125, 2000 | 486 | 2000 |
| Global analysis of DNA methylation variation in adipose tissue from twins reveals links to disease-associated variants in distal regulatory elements E Grundberg, E Meduri, JK Sandling, ÅK Hedman, S Keildson, A Buil, ... The American Journal of Human Genetics 93 (5), 876-890, 2013 | 391 | 2013 |
| Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease DJ Verlaan, S Berlivet, GM Hunninghake, AM Madore, M Larivière, ... The American Journal of Human Genetics 85 (3), 377-393, 2009 | 337 | 2009 |
| A survey of genetic and epigenetic variation affecting human gene expression T Pastinen, R Sladek, S Gurd, B Ge, P Lepage, K Lavergne, A Villeneuve, ... Physiological genomics, 2004 | 325 | 2004 |
| Differential Allelic Expression in the Human Genome: A Robust Approach To Identify Genetic and Epigenetic Cis-Acting Mechanisms Regulating Gene Expression D Serre, S Gurd, B Ge, R Sladek, D Sinnett, E Harmsen, M Bibikova, ... PLoS genetics 4 (2), e1000006, 2008 | 301 | 2008 |
| Novel promoter polymorphism in insulin-like growth factor-binding protein-3: correlation with serum levels and interaction with known regulators C Deal, J Ma, F Wilkin, J Paquette, F Rozen, B Ge, T Hudson, M Stampfer, ... The Journal of Clinical Endocrinology & Metabolism 86 (3), 1274-1280, 2001 | 270 | 2001 |
| Global patterns of cis variation in human cells revealed by high-density allelic expression analysis B Ge, DK Pokholok, T Kwan, E Grundberg, L Morcos, DJ Verlaan, J Le, ... Nature genetics 41 (11), 1216-1222, 2009 | 267 | 2009 |
| Influence of human genome polymorphism on gene expression T Pastinen, B Ge, TJ Hudson Human molecular genetics 15 (suppl_1), R9-R16, 2006 | 184 | 2006 |
| Analysis of expressed SNPs identifies variable extents of expression from the human inactive X chromosome AM Cotton, B Ge, N Light, V Adoue, T Pastinen, CJ Brown Genome biology 14, 1-17, 2013 | 178 | 2013 |
| Survey of allelic expression using EST mining B Ge, S Gurd, T Gaudin, C Dore, P Lepage, E Harmsen, TJ Hudson, ... Genome research 15 (11), 1584-1591, 2005 | 166 | 2005 |
| Increased DNA methylation variability in type 1 diabetes across three immune effector cell types DS Paul, AE Teschendorff, MAN Dang, R Lowe, MI Hawa, S Ecker, ... Nature communications 7 (1), 13555, 2016 | 160 | 2016 |
| Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment JP Kemp, C Medina-Gomez, K Estrada, B St Pourcain, DHM Heppe, ... PLoS genetics 10 (6), e1004423, 2014 | 160 | 2014 |
| Hyperhomocysteinemia due to methionine synthase deficiency, cblG: structure of the MTR gene, genotype diversity, and recognition of a common mutation, P1173L D Watkins, M Ru, HY Hwang, CD Kim, A Murray, NS Philip, W Kim, ... The American Journal of Human Genetics 71 (1), 143-153, 2002 | 155 | 2002 |
| Long-range epigenetic regulation is conferred by genetic variation located at thousands of independent loci M Lemire, SHE Zaidi, M Ban, B Ge, D Aïssi, M Germain, I Kassam, ... Nature communications 6 (1), 6326, 2015 | 148 | 2015 |
| Radiation hybrid map of the mouse genome WJ Van Etten, RG Steen, H Nguyen, AB Castle, DK Slonim, B Ge, ... Nature genetics 22 (4), 384-387, 1999 | 145 | 1999 |
| Toward further mapping of the association between the IL2RA locus and type 1 diabetes HQ Qu, A Montpetit, B Ge, TJ Hudson, C Polychronakos Diabetes 56 (4), 1174-1176, 2007 | 140 | 2007 |
