| Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases MM Clark, Z Stark, L Farnaes, TY Tan, SM White, D Dimmock, ... NPJ genomic medicine 3 (1), 16, 2018 | 504 | 2018 |
| Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization L Farnaes, A Hildreth, NM Sweeney, MM Clark, S Chowdhury, S Nahas, ... NPJ genomic medicine 3 (1), 10, 2018 | 365 | 2018 |
| A randomized, controlled trial of the analytic and diagnostic performance of singleton and trio, rapid genome and exome sequencing in ill infants SF Kingsmore, JA Cakici, MM Clark, M Gaughran, M Feddock, S Batalov, ... The American Journal of Human Genetics 105 (4), 719-733, 2019 | 274 | 2019 |
| Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation MM Clark, A Hildreth, S Batalov, Y Ding, S Chowdhury, K Watkins, ... Science translational medicine 11 (489), eaat6177, 2019 | 244 | 2019 |
| Project Baby Bear: Rapid precision care incorporating rWGS in 5 California children’s hospitals demonstrates improved clinical outcomes and reduced costs of care D Dimmock, S Caylor, B Waldman, W Benson, C Ashburner, ... The American Journal of Human Genetics 108 (7), 1231-1238, 2021 | 152 | 2021 |
| A cell-penetrating peptide from a novel pVII–pIX phage-displayed random peptide library C Gao, S Mao, HJ Ditzel, L Farnaes, P Wirsching, RA Lerner, KD Janda Bioorganic & medicinal chemistry 10 (12), 4057-4065, 2002 | 144 | 2002 |
| An RCT of rapid genomic sequencing among seriously ill infants results in high clinical utility, changes in management, and low perceived harm DP Dimmock, MM Clark, M Gaughran, JA Cakici, SA Caylor, C Clarke, ... The American Journal of Human Genetics 107 (5), 942-952, 2020 | 118 | 2020 |
| Rapid whole genome sequencing has clinical utility in children in the PICU EF Sanford, MM Clark, L Farnaes, MR Williams, JC Perry, EG Ingulli, ... Pediatric Critical Care Medicine 20 (11), 1007-1020, 2019 | 116 | 2019 |
| Effect of whole-genome sequencing on the clinical management of acutely ill infants with suspected genetic disease: a randomized clinical trial ID Krantz, L Medne, JM Weatherly, KT Wild, S Biswas, B Devkota, ... JAMA pediatrics 175 (12), 1218-1226, 2021 | 95 | 2021 |
| Cloning and expression of a novel human antibody–antigen pair associated with Felty's syndrome HJ Ditzel, Y Masaki, H Nielsen, L Farnaes, DR Burton Proceedings of the National Academy of Sciences 97 (16), 9234-9239, 2000 | 77 | 2000 |
| Napyradiomycin derivatives, produced by a marine-derived actinomycete, illustrate cytotoxicity by induction of apoptosis L Farnaes, NG Coufal, CA Kauffman, AL Rheingold, AG DiPasquale, ... Journal of natural products 77 (1), 15-21, 2014 | 58 | 2014 |
| Community-acquired pneumonia in children: cell-free plasma sequencing for diagnosis and management L Farnaes, J Wilke, KR Loker, JS Bradley, CR Cannavino, DK Hong, ... Diagnostic microbiology and infectious disease 94 (2), 188-191, 2019 | 57 | 2019 |
| Emergence of an early SARS-CoV-2 epidemic in the United States M Zeller, K Gangavarapu, C Anderson, AR Smither, JA Vanchiere, ... Cell 184 (19), 4939-4952. e15, 2021 | 40 | 2021 |
| Dissecting the cellular functions of annexin XI using recombinant human annexin XI-specific autoantibodies cloned by phage display L Farnaes, HJ Ditzel Journal of Biological Chemistry 278 (35), 33120-33126, 2003 | 38 | 2003 |
| Bactericidal Kinetics of Marine-Derived Napyradiomycins against Contemporary Methicillin-Resistant Staphylococcus aureus NM Haste, L Farnaes, VR Perera, W Fenical, V Nizet, ME Hensler Marine drugs 9 (4), 680-689, 2011 | 34 | 2011 |
| Use of plasma metagenomic next-generation sequencing for pathogen identification in pediatric endocarditis RK To, N Ramchandar, A Gupta, A Pong, C Cannavino, J Foley, ... The Pediatric Infectious Disease Journal 40 (5), 486-488, 2021 | 28 | 2021 |
| Rapid whole-genome sequencing identifies a novel GABRA1 variant associated with West syndrome L Farnaes, SA Nahas, S Chowdhury, J Nelson, S Batalov, DM Dimmock, ... Molecular Case Studies 3 (5), a001776, 2017 | 28 | 2017 |
| Concomitant diagnosis of immune deficiency and Pseudomonas sepsis in a 19 month old with ecthyma gangrenosum by host whole-genome sequencing E Sanford, L Farnaes, S Batalov, M Bainbridge, S Laubach, HM Worthen, ... Molecular Case Studies 4 (6), a003244, 2018 | 24 | 2018 |
| Cost efficacy of rapid whole genome sequencing in the pediatric intensive care unit E Sanford Kobayashi, B Waldman, BM Engorn, K Perofsky, E Allred, ... Frontiers in pediatrics 9, 809536, 2022 | 23 | 2022 |
| Metagenomic next-generation sequencing for pathogen detection and transcriptomic analysis in pediatric central nervous system infections N Ramchandar, NG Coufal, AS Warden, B Briggs, T Schwarz, R Stinnett, ... Open Forum Infectious Diseases 8 (6), ofab104, 2021 | 21 | 2021 |
