| A 46, XX ovotesticular disorder of sex development likely caused by a steroidogenic factor-1 (NR5A1) variant JM Swartz, R Ciarlo, MH Guo, A Abrha, B Weaver, DA Diamond, YM Chan, ... Hormone Research in Paediatrics 87 (3), 191-195, 2017 | 52 | 2017 |
| A CLK3-HMGA2 alternative splicing axis impacts human hematopoietic stem cell molecular identity throughout development M Cesana, MH Guo, D Cacchiarelli, L Wahlster, J Barragan, S Doulatov, ... Cell Stem Cell 22 (4), 575-588. e7, 2018 | 49 | 2018 |
| A closer look at attrition in MD–PhD programs PN Mittwede, EK Noch, MH Guo Academic Medicine 89 (7), 958-959, 2014 | 3 | 2014 |
| 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 | 65 | 2014 |
| 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 | 103 | 2015 |
| Accelerated skeletal maturation in disorders of retinoic acid metabolism: a case report and focused review of the literature O Nilsson, N Isoherranen, MH Guo, JC Lui, YH Jee, I Guttmann-Bauman, ... Hormone and Metabolic Research 48 (11), 737-744, 2016 | 19 | 2016 |
| Alzheimer’s Disease Genetic Risk Variants Predict Cognitive Decline in Parkinson’s Disease (P2. 8-026) L Baratta, T Tropea, K Maddy, M Guo, J Rick, J Trojanowski, D Weintraub, ... Neurology 92 (15_supplement), P2. 8-026, 2019 | | 2019 |
| Application of Genomics to the Study of Human Growth Disorders MH Guo, A Dauber Pediatric Biomedical Informatics: Computer Applications in Pediatric …, 2016 | | 2016 |
| Basal ganglia calcifications-etiological relationship to strokes from mild head trauma? MH Guo, LA Beslow European journal of paediatric neurology: EJPN: official journal of the …, 2021 | | 2021 |
| 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 | 157 | 2018 |
| Case of serotonin syndrome initially presenting as diffuse body pain MH Guo, RL Monir, A Wright, NP Holland The American journal of case reports 19, 1227, 2018 | 8 | 2018 |
| Clinical management in Alzheimer’s disease in the era of disease-modifying therapies MH Guo, SN Vaishnavi Current Treatment Options in Neurology 25 (5), 121-133, 2023 | 1 | 2023 |
| Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms MH Guo, SK Nandakumar, JC Ulirsch, SM Zekavat, JD Buenrostro, ... Proceedings of the National Academy of Sciences 114 (3), E327-E336, 2017 | 44 | 2017 |
| Determinants of power in gene-based burden testing for monogenic disorders MH Guo, A Dauber, MF Lippincott, YM Chan, RM Salem, JN Hirschhorn The American Journal of Human Genetics 99 (3), 527-539, 2016 | 41 | 2016 |
| Disparities in genetic testing for neurologic disorders A Baldwin, J Copeland, M Azage, L Dratch, K Johnson, RA Paul, ... Neurology 102 (6), e209161, 2024 | 2 | 2024 |
| Dissecting the Regulation of Human Hematopoiesis at Single-Cell and Single-Variant Resolution EL Bao, JC Ulirsch, CA Lareau, LS Ludwig, MH Guo, C Benner, ... Blood 132, 531, 2018 | | 2018 |
| Dissection of multiple sclerosis genetics identifies B and CD4+ T cells as driver cell subsets MH Guo, P Sama, BA LaBarre, H Lokhande, J Balibalos, C Chu, X Du, ... Genome Biology 23 (1), 127, 2022 | 12 | 2022 |
| Epigenetic profiling of growth plate chondrocytes sheds insight into regulatory genetic variation influencing height M Guo, Z Liu, J Willen, CP Shaw, D Richard, E Jagoda, AC Doxey, ... elife 6, e29329, 2017 | 35 | 2017 |
| 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 | 84 | 2019 |
| Expanding Genetic and Functional Diagnoses of IGF1R Haploinsufficiencies P Ocaranza, MC Golekoh, SF Andrew, MH Guo, P Kaplowitz, H Saal, ... Hormone research in paediatrics 87 (6), 412-422, 2017 | 23 | 2017 |
