| Blood metabolite markers of preclinical Alzheimer's disease in two longitudinally followed cohorts of older individuals R Casanova, S Varma, B Simpson, M Kim, Y An, S Saldana, C Riveros, ... Alzheimer's & Dementia 12 (7), 815-822, 2016 | 161 | 2016 |
| Genetics, epigenetic mechanism NM Al Aboud, C Tupper, I Jialal | 111 | 2018 |
| Impaired cognition and brain atrophy decades after hypertensive pregnancy disorders MM Mielke, NM Milic, TL Weissgerber, WM White, K Kantarci, TH Mosley, ... Circulation: Cardiovascular Quality and Outcomes 9 (2_suppl_1), S70-S76, 2016 | 98 | 2016 |
| Blood metabolite markers of cognitive performance and brain function in aging BN Simpson, M Kim, YF Chuang, L Beason-Held, M Kitner-Triolo, M Kraut, ... Journal of Cerebral Blood Flow & Metabolism 36 (7), 1212-1223, 2016 | 62 | 2016 |
| Associations between inflammation and cognitive function in African Americans and European Americans BG Windham, BN Simpson, S Lirette, J Bridges, L Bielak, PA Peyser, ... Journal of the American Geriatrics Society 62 (12), 2303-2310, 2014 | 61 | 2014 |
| De novo pathogenic variants in N-cadherin cause a syndromic neurodevelopmental disorder with corpus callosum, axon, cardiac, ocular, and genital defects A Accogli, S Calabretta, J St-Onge, N Boudrahem-Addour, ... The American Journal of Human Genetics 105 (4), 854-868, 2019 | 36 | 2019 |
| Evaluation and classification of severity for 176 genes on an expanded carrier screening panel A Arjunan, H Bellerose, R Torres, R Ben‐Shachar, JD Hoffman, B Angle, ... Prenatal Diagnosis 40 (10), 1246-1257, 2020 | 26 | 2020 |
| Genetics, histone code Z Shahid, B Simpson, KH Miao, G Singh | 23 | 2019 |
| Genetics, human major histocompatibility complex (MHC) G Tumer, B Simpson, TK Roberts | 20 | 2019 |
| Statpearls H Saleem, B Simpson StatPearls Publishing,, 2022 | 17 | 2022 |
| Genetics, autosomal dominant RG Lewis, B Simpson | 15 | 2020 |
| Biotinidase deficiency H Saleem, B Simpson | 13 | 2020 |
| Genetics, DNA packaging B Simpson, C Tupper, NM Al Aboud | 12 | 2018 |
| The natural history of adults with Rubinstein-Taybi syndrome: a families-reported experience S Douzgou, J Dell’Oro, CR Fonseca, A Rei, J Mullins, I Jusiewicz, ... European Journal of Human Genetics 30 (7), 841-847, 2022 | 11 | 2022 |
| Genetics, Histone Code; StatPearls Z Shahid, B Simpson, KH Miao, G Singh StatPearls Publishing LLC.: Treasure Island, FL, USA, 2022 | 11 | 2022 |
| A new leukocyte hyperadhesion syndrome of delayed cord separation, skin infection, and nephrosis BN Simpson, N Hogg, LM Svensson, A McDowall, W Daley, K Yarbrough, ... Pediatrics 133 (1), e257-e262, 2014 | 9 | 2014 |
| CHARGE syndrome in the era of molecular diagnosis: similar outcomes in those without coloboma or choanal atresia BN Simpson, D Khattar, H Saal, CE Prada, D Choo, L Marcheschi, ... European Journal of Medical Genetics 64 (1), 104103, 2021 | 7 | 2021 |
| Genetics, mitosis I Rehman, A Gulani, M Farooq, B Simpson | 6 | 2018 |
| Insights into the genotype–phenotype relationship of ocular manifestations in Kabuki syndrome SS Shah, A Fulton, M Jabroun, D Brightman, BN Simpson, OA Bodamer American Journal of Medical Genetics Part A 191 (5), 1325-1338, 2023 | 3 | 2023 |
| Motor Function and Physiology in Youth With Neurofibromatosis Type 1 AC Doherty, DA Huddleston, PS Horn, N Ratner, BN Simpson, EK Schorry, ... Pediatric Neurology 143, 34-43, 2023 | 2 | 2023 |
