| Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts SR Rashkin, RE Graff, L Kachuri, KK Thai, SE Alexeeff, MA Blatchins, ... Nature Communications 11 (1), 1-14, 2020 | 181 | 2020 |
| Pan-cancer analysis demonstrates that integrating polygenic risk scores with modifiable risk factors improves risk prediction L Kachuri, RE Graff, K Smith-Byrne, TJ Meyers, SR Rashkin, E Ziv, ... Nature communications 11 (1), 6084, 2020 | 125 | 2020 |
| The landscape of host genetic factors involved in immune response to common viral infections L Kachuri, SS Francis, ML Morrison, GA Wendt, Y Bossé, TB Cavazos, ... Genome Medicine 12 (1), 1-18, 2020 | 95* | 2020 |
| Cross-cancer evaluation of polygenic risk scores for 16 cancer types in two large cohorts RE Graff, TB Cavazos, KK Thai, L Kachuri, SR Rashkin, JD Hoffman, ... Nature Communications 12 (1), 1-9, 2021 | 58 | 2021 |
| Genomewide Meta‐Analysis Validates a Role for S1PR1 in Microtubule Targeting Agent‐Induced Sensory Peripheral Neuropathy KC Chua, C Xiong, C Ho, T Mushiroda, C Jiang, F Mulkey, D Lai, ... Clinical Pharmacology & Therapeutics 108 (3), 625-634, 2020 | 31 | 2020 |
| Immune-mediated genetic pathways resulting in pulmonary function impairment increase lung cancer susceptibility L Kachuri, M Johansson, SR Rashkin, RE Graff, Y Bossé, V Manem, ... Nature Communications 11 (1), 1-14, 2020 | 30 | 2020 |
| Optimal sequencing strategies for identifying disease-associated singletons S Rashkin, G Jun, S Chen, ... PLoS genetics 13 (6), e1006811, 2017 | 24* | 2017 |
| A Pharmacogenetic Prediction Model of Progression‐Free Survival in Breast Cancer using Genome‐Wide Genotyping Data from CALGB 40502 (Alliance) SR Rashkin, KC Chua, C Ho, F Mulkey, C Jiang, T Mushiroda, M Kubo, ... Clinical Pharmacology & Therapeutics 105 (3), 738-745, 2019 | 17 | 2019 |
| A large-scale association study detects novel rare variants, risk genes, functional elements, and polygenic architecture of prostate cancer susceptibility NC Emami, TB Cavazos, SR Rashkin, RE Graff, CG Tai, JA Mefford, ... Cancer Research, 2020 | 16* | 2020 |
| A polygenic score for acute vaso-occlusive pain in pediatric sickle cell disease E Rampersaud, G Kang, LE Palmer, SR Rashkin, S Wang, W Bi, ... Blood Advances 5 (14), 2839-2851, 2021 | 14 | 2021 |
| Genetic analysis of lung cancer and the germline impact on somatic mutation burden AAG Gabriel, JR Atkins, RCC Penha, K Smith-Byrne, V Gaborieau, ... Journal Of The National Cancer Institute 114 (8), 1159-1166, 2022 | 13* | 2022 |
| Discovery of novel predisposing coding and noncoding variants in familial Hodgkin lymphoma JE Flerlage, JR Myers, JL Maciaszek, N Oak, SR Rashkin, Y Hui, ... Blood 141 (11), 1293-1307, 2023 | 10 | 2023 |
| T‐helper cells and liver fibrosis in hepatitis C virus‐monoinfected patients S Rashkin, S Rouster, ZD Goodman, KE Sherman Journal of viral hepatitis 17 (3), 222-226, 2010 | 10 | 2010 |
| Fetal hemoglobin modulates neurocognitive performance in sickle cell anemia✰,✰✰ AM Heitzer, J Longoria, E Rampersaud, SR Rashkin, JH Estepp, ... Current Research in Translational Medicine 70 (3), 103335, 2022 | 6 | 2022 |
| Genetic Variation and Sickle Cell Disease Severity: A Systematic Review and Meta-Analysis JK Kirkham, JH Estepp, MJ Weiss, SR Rashkin JAMA Network Open 6 (10), e2337484-e2337484, 2023 | 5 | 2023 |
| Imputed genomic data reveals a moderate effect of low frequency variants to the heritability of complex human traits KA Hartman, SR Rashkin, JS Witte, RD Hernandez bioRxiv, 2019.12. 18.879916, 2019 | 4 | 2019 |
| A genome‐wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study SR Rashkin, M Cleves, GM Shaw, WN Nembhard, E Nestoridi, ... American Journal of Medical Genetics Part A 188 (8), 2303-2314, 2022 | 3 | 2022 |
| Generalization of a genetic risk score for time to first albuminuria in children with sickle cell anaemia: SCCRIP cohort study results SR Rashkin, E Rampersaud, G Kang, KI Ataga, JS Hankins, W Wang, ... British Journal of Haematology 194 (2), 469-473, 2021 | 2 | 2021 |
| The genetic dissection of fetal haemoglobin persistence in sickle cell disease in Nigeria OO Ojewunmi, TA Adeyemo, AI Oyetunji, B Inyang, A Akinrindoye, ... Human Molecular Genetics, ddae014, 2024 | 1 | 2024 |
| A Versatile and Efficient Novel Approach for Mendelian Randomization Analysis with Application to Assess the Causal Effect of Fetal Hemoglobin on Anemia in Sickle Cell Anemia JSS Liyanage, JH Estepp, K Srivastava, SR Rashkin, VA Sheehan, ... Mathematics 10 (20), 3743, 2022 | 1 | 2022 |
