| Resistance to linezolid: characterization of mutations in rRNA and comparison of their occurrences in vancomycin-resistant enterococci J Prystowsky, F Siddiqui, J Chosay, DL Shinabarger, J Millichap, ... Antimicrobial agents and chemotherapy 45 (7), 2154-2156, 2001 | 380 | 2001 |
| Intracellular targets of moxifloxacin: a comparison with other fluoroquinolones E Pestova, JJ Millichap, GA Noskin, LR Peterson Journal of Antimicrobial Chemotherapy 45 (5), 583-590, 2000 | 337 | 2000 |
| Progress in understanding and treating SCN2A-mediated disorders SJ Sanders, AJ Campbell, JR Cottrell, RS Moller, FF Wagner, ... Trends in neurosciences 41 (7), 442-456, 2018 | 250 | 2018 |
| Role of viral infections in the etiology of febrile seizures JG Millichap, JJ Millichap Pediatric neurology 35 (3), 165-172, 2006 | 244 | 2006 |
| GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects K Platzer, H Yuan, H Schütz, A Winschel, W Chen, C Hu, H Kusumoto, ... Journal of medical genetics 54 (7), 460-470, 2017 | 221 | 2017 |
| KCNQ2 encephalopathy: Features, mutational hot spots, and ezogabine treatment of 11 patients JJ Millichap, KL Park, T Tsuchida, B Ben-Zeev, L Carmant, R Flamini, ... Neurology: Genetics 2 (5), e96, 2016 | 205 | 2016 |
| Response to treatment in a prospective national infantile spasms cohort KG Knupp, J Coryell, KC Nickels, N Ryan, E Leister, T Loddenkemper, ... Annals of neurology 79 (3), 475-484, 2016 | 198 | 2016 |
| The 2010 revised classification of seizures and epilepsy AT Berg, JJ Millichap Continuum: Lifelong Learning in Neurology 19 (3), 571-597, 2013 | 168 | 2013 |
| Mechanistic insight into NMDA receptor dysregulation by rare variants in the GluN2A and GluN2B agonist binding domains SA Swanger, W Chen, G Wells, PB Burger, A Tankovic, S Bhattacharya, ... The American Journal of Human Genetics 99 (6), 1261-1280, 2016 | 155 | 2016 |
| The incidence and significance of periictal apnea in epileptic seizures N Lacuey, B Zonjy, JP Hampson, MRS Rani, A Zaremba, RK Sainju, ... Epilepsia 59 (3), 573-582, 2018 | 129 | 2018 |
| Defining the phenotypic spectrum of SLC6A1 mutations KM Johannesen, E Gardella, T Linnankivi, C Courage, A de Saint Martin, ... Epilepsia 59 (2), 389-402, 2018 | 119 | 2018 |
| A Convenient Assay for Estimating the Possible Involvement of Efflux of Fluoroquinolones by Streptococcus pneumoniae andStaphylococcus aureus: Evidence for … R Beyer, E Pestova, JJ Millichap, V Stosor, GA Noskin, LR Peterson Antimicrobial agents and chemotherapy 44 (3), 798-801, 2000 | 115 | 2000 |
| Autonomic epileptic seizures, autonomic effects of seizures, and SUDEP B Moseley, L Bateman, JJ Millichap, E Wirrell, CP Panayiotopoulos Epilepsy & Behavior 26 (3), 375-385, 2013 | 103 | 2013 |
| Infantile spasms and encephalopathy without preceding neonatal seizures caused by KCNQ2 R198Q, a gain‐of‐function variant JJ Millichap, F Miceli, M De Maria, C Keator, N Joshi, B Tran, ... Epilepsia 58 (1), e10-e15, 2017 | 94 | 2017 |
| Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort with childhood epilepsy R Truty, N Patil, R Sankar, J Sullivan, J Millichap, G Carvill, A Entezam, ... Epilepsia open 4 (3), 397-408, 2019 | 89 | 2019 |
| Hypsarrhythmia assessment exhibits poor interrater reliability: a threat to clinical trial validity SA Hussain, G Kwong, JJ Millichap, JR Mytinger, N Ryan, JH Matsumoto, ... Epilepsia 56 (1), 77-81, 2015 | 86 | 2015 |
| Response to second treatment after initial failed treatment in a multicenter prospective infantile spasms cohort KG Knupp, E Leister, J Coryell, KC Nickels, N Ryan, E Juarez‐Colunga, ... Epilepsia 57 (11), 1834-1842, 2016 | 64 | 2016 |
| Child Neurology: Dravet syndrome: when to suspect the diagnosis JJ Millichap, S Koh, LC Laux, DR Nordli Jr Neurology 73 (13), e59-e62, 2009 | 64 | 2009 |
| Improving the inter-rater agreement of hypsarrhythmia using a simplified EEG grading scale for children with infantile spasms JR Mytinger, SA Hussain, MP Islam, JJ Millichap, AD Patel, NR Ryan, ... Epilepsy research 116, 93-98, 2015 | 61 | 2015 |
| Novel de novo EEF1A2 missense mutations causing epilepsy and intellectual disability WWK Lam, JJ Millichap, DC Soares, R Chin, A McLellan, DR FitzPatrick, ... Molecular genetics & genomic medicine 4 (4), 465-474, 2016 | 60 | 2016 |
J. Gordon MillichapPediatric Neurologist, Lurie Children's Hospital; Professor Emeritus, Northwestern UniversityVerified email at northwestern.edu
