Long-read sequencing and de novo assembly of a Chinese genome L Shi, Y Guo, C Dong, J Huddleston, H Yang, X Han, A Fu, Q Li, N Li, ... Nature communications 7 (1), 12065, 2016 | 285 | 2016 |
Early components of the complement classical activation pathway in human systemic autoimmune diseases KE Lintner, YL Wu, Y Yang, CH Spencer, G Hauptmann, LA Hebert, ... Frontiers in immunology 7, 36, 2016 | 202 | 2016 |
Glutathione reductase facilitates host defense by sustaining phagocytic oxidative burst and promoting the development of neutrophil extracellular traps J Yan, X Meng, LM Wancket, K Lintner, LD Nelin, B Chen, KP Francis, ... The Journal of Immunology 188 (5), 2316-2327, 2012 | 98 | 2012 |
Effects of Complement C4 Gene Copy Number Variations, Size Dichotomy, and C4A Deficiency on Genetic Risk and Clinical Presentation of Systemic Lupus … J Yih Chen, Y Ling Wu, M Yin Mok, YJ Jan Wu, KE Lintner, CM Wang, ... Arthritis & Rheumatology 68 (6), 1442-1453, 2016 | 69 | 2016 |
Gene copy-number variations (CNVs) of complement C4 and C4A deficiency in genetic risk and pathogenesis of juvenile dermatomyositis KE Lintner, A Patwardhan, LG Rider, R Abdul-Aziz, YL Wu, E Lundström, ... Annals of the rheumatic diseases 75 (9), 1599-1606, 2016 | 49 | 2016 |
Identification of rare variants predisposing to thyroid cancer Y Wang, S Liyanarachchi, KE Miller, TT Nieminen, D Comiskey, W Li, P Brock ... Thyroid, 2019 | 45 | 2019 |
Characterization of the genomic and immunologic diversity of malignant brain tumors through multisector analysis MO Schaettler, MM Richters, AZ Wang, ZL Skidmore, B Fisk, KE Miller, ... Cancer discovery 12 (1), 154-171, 2022 | 43 | 2022 |
Detection of brain somatic variation in epilepsy‐associated developmental lesions TA Bedrosian, KE Miller, OE Grischow, KM Schieffer, S LaHaye, H Yoon, ... Epilepsia 63 (8), 1981-1997, 2022 | 39 | 2022 |
Somatic SLC35A2 mosaicism correlates with clinical findings in epilepsy brain tissue KE Miller, DC Koboldt, KM Schieffer, TA Bedrosian, E Crist, A Sheline, ... Neurology: Genetics 6 (4), e460, 2020 | 30 | 2020 |
PTEN somatic mutations contribute to spectrum of cerebral overgrowth DC Koboldt, KE Miller, AR Miller, JM Bush, S McGrath, K Leraas, E Crist, ... Brain 144 (10), 2971-2978, 2021 | 28 | 2021 |
Patient-specific sarcoma organoids for personalized translational research: unification of the operating room with rare cancer research and clinical implications SD Forsythe, H Sivakumar, RA Erali, N Wajih, W Li, P Shen, EA Levine, ... Annals of surgical oncology 29 (12), 7354-7367, 2022 | 26 | 2022 |
Single-cell RNA sequencing reveals immunosuppressive myeloid cell diversity during malignant progression in a murine model of glioma S Rajendran, Y Hu, A Canella, C Peterson, A Gross, M Cam, M Nazzaro, ... Cell reports 42 (3), 2023 | 23 | 2023 |
Immune activity and response differences of oncolytic viral therapy in recurrent glioblastoma: gene expression analyses of a phase IB study KE Miller, KA Cassady, JC Roth, J Clements, KM Schieffer, K Leraas, ... Clinical Cancer Research 28 (3), 498-506, 2022 | 22 | 2022 |
Muscle MRI at the time of questionable disease flares in juvenile dermatomyositis (JDM) R Abdul-Aziz, CY Yu, B Adler, S Bout-Tabaku, KE Lintner, ... Pediatric Rheumatology 15, 1-6, 2017 | 21 | 2017 |
YAP1-FAM118B fusion defines a rare subset of childhood and young adulthood meningiomas KM Schieffer, V Agarwal, S LaHaye, KE Miller, DC Koboldt, T Lichtenberg, ... The American Journal of Surgical Pathology 45 (3), 329-340, 2021 | 18 | 2021 |
The financial impact of genetic diseases in a pediatric accountable care organization KE Miller, R Hoyt, S Rust, R Doerschuk, Y Huang, SM Lin Frontiers in Public Health 8, 58, 2020 | 18 | 2020 |
Cerebral organoids containing an AUTS2 missense variant model microcephaly SR Fair, W Schwind, DL Julian, A Biel, G Guo, R Rutherford, ... Brain 146 (1), 387-404, 2023 | 17 | 2023 |
Discovery of clinically relevant fusions in pediatric cancer S LaHaye, JR Fitch, KJ Voytovich, AC Herman, BJ Kelly, GE Lammi, ... BMC genomics 22, 1-16, 2021 | 17 | 2021 |
Low copy numbers of complement C4 and C4A deficiency are risk factors for myositis, its subgroups and autoantibodies D Zhou, EH King, S Rothwell, O Krystufkova, A Notarnicola, S Coss, ... Annals of the rheumatic diseases 82 (2), 235-245, 2023 | 14 | 2023 |
Gastroblastoma with a novel EWSR1‐CTBP1 fusion presenting in adolescence SC Koo, S LaHaye, BP Kovari, KM Schieffer, MA Ranalli, JH Aldrink, ... Genes, Chromosomes and Cancer 60 (9), 640-646, 2021 | 14 | 2021 |