| Genetics of rheumatoid arthritis contributes to biology and drug discovery Y Okada, D Wu, G Trynka, T Raj, C Terao, K Ikari, Y Kochi, K Ohmura, ... Nature 506 (7488), 376-381, 2014 | 2480 | 2014 |
| The polygenic and monogenic basis of blood traits and diseases D Vuckovic, EL Bao, P Akbari, CA Lareau, A Mousas, T Jiang, MH Chen, ... Cell 182 (5), 1214-1231. e11, 2020 | 448 | 2020 |
| Trans-ethnic and ancestry-specific blood-cell genetics in 746,667 individuals from 5 global populations MH Chen, LM Raffield, A Mousas, S Sakaue, JE Huffman, A Moscati, ... Cell 182 (5), 1198-1213. e14, 2020 | 427 | 2020 |
| The genetic landscape of Diamond-Blackfan anemia JC Ulirsch, JM Verboon, S Kazerounian, MH Guo, D Yuan, LS Ludwig, ... The American Journal of Human Genetics 103 (6), 930-947, 2018 | 234 | 2018 |
| Using the time and motion method to study clinical work processes and workflow: methodological inconsistencies and a call for standardized research K Zheng, MH Guo, DA Hanauer Journal of the american medical informatics Association 18 (5), 704-710, 2011 | 209 | 2011 |
| Practicality of intermittent fasting in humans and its effect on oxidative stress and genes related to aging and metabolism MP Wegman, MH Guo, DM Bennion, MN Shankar, SM Chrzanowski, ... Rejuvenation research 18 (2), 162-172, 2015 | 178 | 2015 |
| Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes AR Majithia, J Flannick, P Shahinian, M Guo, MA Bray, P Fontanillas, ... Proceedings of the National Academy of Sciences 111 (36), 13127-13132, 2014 | 177 | 2014 |
| Interrogation of human hematopoiesis at single-cell and single-variant resolution JC Ulirsch, CA Lareau, EL Bao, LS Ludwig, MH Guo, C Benner, ... Nature genetics 51 (4), 683-693, 2019 | 175 | 2019 |
| Burden testing of rare variants identified through exome sequencing via publicly available control data MH Guo, L Plummer, YM Chan, JN Hirschhorn, MF Lippincott The American Journal of Human Genetics 103 (4), 522-534, 2018 | 155 | 2018 |
| Short stature, accelerated bone maturation, and early growth cessation due to heterozygous aggrecan mutations O Nilsson, MH Guo, N Dunbar, J Popovic, D Flynn, C Jacobsen, JC Lui, ... The Journal of Clinical Endocrinology & Metabolism 99 (8), E1510-E1518, 2014 | 136 | 2014 |
| Three-dimensional genome restructuring across timescales of activity-induced neuronal gene expression JA Beagan, ED Pastuzyn, LR Fernandez, MH Guo, K Feng, KR Titus, ... Nature neuroscience 23 (6), 707-717, 2020 | 126 | 2020 |
| A shared genetic basis for self-limited delayed puberty and idiopathic hypogonadotropic hypogonadism J Zhu, REY Choa, MH Guo, L Plummer, C Buck, MR Palmert, ... The Journal of Clinical Endocrinology & Metabolism 100 (4), E646-E654, 2015 | 104 | 2015 |
| Whole exome sequencing to identify genetic causes of short stature MH Guo, Y Shen, EC Walvoord, TC Miller, JE Moon, JN Hirschhorn, ... Hormone research in paediatrics 82 (1), 44-52, 2014 | 97 | 2014 |
| Targeted application of human genetic variation can improve red blood cell production from stem cells FC Giani, C Fiorini, A Wakabayashi, LS Ludwig, RM Salem, CD Jobaliya, ... Cell stem cell 18 (1), 73-78, 2016 | 88 | 2016 |
| Estimating yields of prenatal carrier screening and implications for design of expanded carrier screening panels MH Guo, AR Gregg Genetics in Medicine 21 (9), 1940-1947, 2019 | 82 | 2019 |
| Genome-wide analysis of body proportion classifies height-associated variants by mechanism of action and implicates genes important for skeletal development Y Chan, RM Salem, YHH Hsu, G McMahon, TH Pers, S Vedantam, T Esko, ... The American Journal of Human Genetics 96 (5), 695-708, 2015 | 73 | 2015 |
| A Novel Variant in CDKN1C Is Associated With Intrauterine Growth Restriction, Short Stature, and Early-Adulthood-Onset Diabetes SL Kerns, J Guevara-Aguirre, S Andrew, J Geng, C Guevara, ... The Journal of Clinical Endocrinology & Metabolism 99 (10), E2117-E2122, 2014 | 63 | 2014 |
| TMEM106B Effect on cognition in Parkinson disease and frontotemporal dementia TF Tropea, J Mak, MH Guo, SX Xie, E Suh, J Rick, A Siderowf, ... Annals of neurology 85 (6), 801-811, 2019 | 62 | 2019 |
| Redefining the progeroid form of ehlers–danlos syndrome: Report of the fourth patient with B4GALT7 deficiency and review of the literature MH Guo, J Stoler, J Lui, O Nilsson, DW Bianchi, JN Hirschhorn, A Dauber American Journal of Medical Genetics Part A 161 (10), 2519-2527, 2013 | 61 | 2013 |
| Idiopathic short stature due to novel heterozygous mutation of the aggrecan gene JB Quintos, MH Guo, A Dauber Journal of Pediatric Endocrinology and Metabolism 28 (7-8), 927-932, 2015 | 60 | 2015 |
