| Cancer health disparities in racial/ethnic minorities in the United States VA Zavala, PM Bracci, JM Carethers, L Carvajal-Carmona, NB Coggins, ... British journal of cancer 124 (2), 315-332, 2021 | 671 | 2021 |
| A new highly penetrant form of obesity due to deletions on chromosome 16p11. 2 RG Walters, S Jacquemont, A Valsesia, AJ de Smith, D Martinet, ... Nature 463 (7281), 671-675, 2010 | 602 | 2010 |
| FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity M Fanciulli, PJ Norsworthy, E Petretto, R Dong, L Harper, L Kamesh, ... Nature genetics 39 (6), 721-723, 2007 | 575 | 2007 |
| A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism AJ de Smith, C Purmann, RG Walters, RJ Ellis, SE Holder, MM Van Haelst, ... Human molecular genetics 18 (17), 3257-3265, 2009 | 312 | 2009 |
| Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases AJ de Smith, A Tsalenko, N Sampas, A Scheffer, NA Yamada, P Tsang, ... Human molecular genetics 16 (23), 2783-2794, 2007 | 259 | 2007 |
| PDGFRα demarcates the cardiogenic clonogenic Sca1+ stem/progenitor cell in adult murine myocardium M Noseda, M Harada, S McSweeney, T Leja, E Belian, DJ Stuckey, ... Nature communications 6 (1), 6930, 2015 | 165 | 2015 |
| Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly Y Li, H Zheng, R Luo, H Wu, H Zhu, R Li, H Cao, B Wu, S Huang, H Shao, ... Nature biotechnology 29 (8), 723-730, 2011 | 147 | 2011 |
| Human genes involved in copy number variation: mechanisms of origin, functional effects and implications for disease AJ De Smith, RG Walters, P Froguel, AI Blakemore Cytogenetic and genome research 123 (1-4), 17-26, 2009 | 111 | 2009 |
| A global DNA methylation and gene expression analysis of early human B-cell development reveals a demethylation signature and transcription factor network ST Lee, Y Xiao, MO Muench, J Xiao, ME Fomin, JK Wiencke, S Zheng, ... Nucleic acids research 40 (22), 11339-11351, 2012 | 110 | 2012 |
| Cortical Lewy bodies and Aβ burden are associated with prevalence and timing of dementia in Lewy body diseases C Ruffmann, FCF Calboli, I Bravi, D Gveric, LK Curry, A de Smith, ... Neuropathology and applied neurobiology 42 (5), 436-450, 2016 | 91 | 2016 |
| GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24. 21 JL Wiemels, KM Walsh, AJ de Smith, C Metayer, S Gonseth, HM Hansen, ... Nature communications 9 (1), 286, 2018 | 84 | 2018 |
| In utero cytomegalovirus infection and development of childhood acute lymphoblastic leukemia SS Francis, AD Wallace, GA Wendt, L Li, F Liu, LW Riley, S Kogan, ... Blood, The Journal of the American Society of Hematology 129 (12), 1680-1684, 2017 | 82 | 2017 |
| Imprinted expression of UBE3A in non-neuronal cells from a Prader–Willi syndrome patient with an atypical deletion K Martins-Taylor, JS Hsiao, PF Chen, H Glatt-Deeley, AJ De Smith, ... Human molecular genetics 23 (9), 2364-2373, 2014 | 76 | 2014 |
| Small Deletion Variants Have Stable Breakpoints Commonly Associated with Alu Elements AJ de Smith, RG Walters, LJM Coin, I Steinfeld, Z Yakhini, R Sladek, ... PloS one 3 (8), e3104, 2008 | 74 | 2008 |
| Genetic variation associated with longer telomere length increases risk of chronic lymphocytic leukemia J Ojha, V Codd, CP Nelson, NJ Samani, IV Smirnov, NR Madsen, ... Cancer Epidemiology, Biomarkers & Prevention 25 (7), 1043-1049, 2016 | 73 | 2016 |
| Common genetic variants associated with telomere length confer risk for neuroblastoma and other childhood cancers KM Walsh, TP Whitehead, AJ de Smith, IV Smirnov, M Park, AA Endicott, ... Carcinogenesis 37 (6), 576-582, 2016 | 66 | 2016 |
| Associations between genome-wide Native American ancestry, known risk alleles and B-cell ALL risk in Hispanic children KM Walsh, AP Chokkalingam, LI Hsu, C Metayer, AJ De Smith, DI Jacobs, ... Leukemia 27 (12), 2416-2419, 2013 | 62 | 2013 |
| Inherited genetic susceptibility to acute lymphoblastic leukemia in Down syndrome AL Brown, AJ De Smith, VU Gant, W Yang, ME Scheurer, KM Walsh, ... Blood, The Journal of the American Society of Hematology 134 (15), 1227-1237, 2019 | 55 | 2019 |
| Epigenetic remodeling in B-cell acute lymphoblastic leukemia occurs in two tracks and employs embryonic stem cell-like signatures ST Lee, MO Muench, ME Fomin, J Xiao, M Zhou, A De Smith, ... Nucleic acids research 43 (5), 2590-2602, 2015 | 54 | 2015 |
| cnvHap: an integrative population and haplotype–based multiplatform model of SNPs and CNVs LJM Coin, JE Asher, RG Walters, JS El-Sayed Moustafa, AJ De Smith, ... Nature methods 7 (7), 541-546, 2010 | 53 | 2010 |
