| Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ... Nature 590 (7845), 290-299, 2021 | 1628 | 2021 |
| Sickle Hemoglobin (Hb S) Allele and Sickle Cell Disease: A HuGE Review A Ashley-Koch, Q Yang, RS Olney American journal of epidemiology 151 (9), 839-845, 2000 | 777 | 2000 |
| The genetic architecture of the human cerebral cortex KL Grasby, N Jahanshad, JN Painter, L Colodro-Conde, J Bralten, ... Science 367 (6484), eaay6690, 2020 | 686 | 2020 |
| A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10) E Reid, M Kloos, A Ashley-Koch, L Hughes, S Bevan, IK Svenson, ... The American Journal of Human Genetics 71 (5), 1189-1194, 2002 | 644 | 2002 |
| International meta-analysis of PTSD genome-wide association studies identifies sex-and ancestry-specific genetic risk loci CM Nievergelt, AX Maihofer, T Klengel, EG Atkinson, CY Chen, KW Choi, ... Nature communications 10 (1), 4558, 2019 | 540 | 2019 |
| Largest GWAS of PTSD (N= 20 070) yields genetic overlap with schizophrenia and sex differences in heritability LE Duncan, A Ratanatharathorn, AE Aiello, LM Almli, AB Amstadter, ... Molecular psychiatry 23 (3), 666-673, 2018 | 488 | 2018 |
| Epidemiologic and genetic aspects of spina bifida and other neural tube defects KS Au, A Ashley‐Koch, H Northrup Developmental disabilities research reviews 16 (1), 6-15, 2010 | 449 | 2010 |
| Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism DQ Ma, PL Whitehead, MM Menold, ER Martin, AE Ashley-Koch, H Mei, ... The American Journal of Human Genetics 77 (3), 377-388, 2005 | 438 | 2005 |
| Relationship between methylome and transcriptome in patients with nonalcoholic fatty liver disease SK Murphy, H Yang, CA Moylan, H Pang, A Dellinger, MF Abdelmalek, ... Gastroenterology 145 (5), 1076-1087, 2013 | 404 | 2013 |
| Self-regulation of emotion, functional impairment, and comorbidity among childrenwith AD/HD AD Anastopoulos, TF Smith, ME Garrett, E Morrissey-Kane, NK Schatz, ... Journal of attention disorders 15 (7), 583-592, 2011 | 366 | 2011 |
| Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus Y Lu, V Vitart, KP Burdon, CC Khor, Y Bykhovskaya, A Mirshahi, ... Nature genetics 45 (2), 155-163, 2013 | 360 | 2013 |
| The psychencode project S Akbarian, C Liu, JA Knowles, FM Vaccarino, PJ Farnham, GE Crawford, ... Nature neuroscience 18 (12), 1707-1712, 2015 | 357 | 2015 |
| Factors associated with survival in a contemporary adult sickle cell disease cohort H Elmariah, ME Garrett, LM De Castro, JC Jonassaint, KI Ataga, ... American journal of hematology 89 (5), 530-535, 2014 | 355 | 2014 |
| Hepatic gene expression profiles differentiate presymptomatic patients with mild versus severe nonalcoholic fatty liver disease CA Moylan, H Pang, A Dellinger, A Suzuki, ME Garrett, CD Guy, ... Hepatology 59 (2), 471-482, 2014 | 319 | 2014 |
| Identification of MeCP2 mutations in a series of females with autistic disorder RM Carney, CM Wolpert, SA Ravan, M Shahbazian, A Ashley-Koch, ... Pediatric neurology 28 (3), 205-211, 2003 | 315 | 2003 |
| Genomic screen and follow‐up analysis for autistic disorder Y Shao, CM Wolpert, KL Raiford, MM Menold, SL Donnelly, SA Ravan, ... American journal of medical genetics 114 (1), 99-105, 2002 | 309 | 2002 |
| Pulmonary hypertension associated with sickle cell disease: clinical and laboratory endpoints and disease outcomes LM De Castro, JC Jonassaint, FL Graham, A Ashley‐Koch, MJ Telen American journal of hematology 83 (1), 19-25, 2008 | 295 | 2008 |
| Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31 S Züchner, G Wang, KN Tran-Viet, MA Nance, PC Gaskell, JM Vance, ... The American Journal of Human Genetics 79 (2), 365-369, 2006 | 289 | 2006 |
| Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma JNC Bailey, SJ Loomis, JH Kang, RR Allingham, P Gharahkhani, CC Khor, ... Nature genetics 48 (2), 189-194, 2016 | 278 | 2016 |
| HLA-DR15 Haplotype and Multiple Sclerosis: A HuGE Review H Schmidt, D Williamson, A Ashley-Koch American journal of epidemiology 165 (10), 1097-1109, 2007 | 275 | 2007 |
