| Nucleosomal organization of telomere-specific chromatin in rat VL Makarov, S Lejnine, J Bedoyan, JP Langmore Cell 73 (4), 775-787, 1993 | 248 | 1993 |
| Surgical outcomes after breast cancer surgery: measuring acute lymphedema MA Kosir, C Rymal, P Koppolu, L Hryniuk, L Darga, W Du, V Rice, D Mood, ... Journal of Surgical Research 95 (2), 147-151, 2001 | 118 | 2001 |
| Mitochondrial Disease Sequence Data Resource (MSeqDR): a global grass-roots consortium to facilitate deposition, curation, annotation, and integrated analysis of genomic data … MJ Falk, L Shen, M Gonzalez, J Leipzig, MT Lott, APM Stassen, ... Molecular genetics and metabolism 114 (3), 388-396, 2015 | 90 | 2015 |
| Congenital diaphragmatic hernia: associated anomalies and antenatal diagnosis: Outcome-related variables at two Detroit hospitals JK Bedoyan, SC Blackwell, MC Treadwell, A Johnson, MD Klein Pediatric surgery international 20, 170-176, 2004 | 83 | 2004 |
| The impact of serotonin transporter (5-HTTLPR) genotype on the development of resting-state functional connectivity in children and adolescents: a preliminary report JL Wiggins, JK Bedoyan, SJ Peltier, S Ashinoff, M Carrasco, SJ Weng, ... Neuroimage 59 (3), 2760-2770, 2012 | 81 | 2012 |
| Clinical and biochemical characterization of four patients with mutations in ECHS1 S Ferdinandusse, MW Friederich, A Burlina, JPN Ruiter, CR Coughlin, ... Orphanet journal of rare diseases 10, 1-15, 2015 | 80 | 2015 |
| Consensus guidelines for management of hyperammonaemia in paediatric patients receiving continuous kidney replacement therapy R Raina, JK Bedoyan, U Lichter-Konecki, P Jouvet, S Picca, NA Mew, ... Nature Reviews Nephrology 16 (8), 471-482, 2020 | 75 | 2020 |
| Duplication 16p11. 2 in a child with infantile seizure disorder JK Bedoyan, RA Kumar, J Sudi, F Silverstein, T Ackley, RK Iyer, ... American Journal of Medical Genetics Part A 152 (6), 1567-1574, 2010 | 68 | 2010 |
| Leigh syndrome in a girl with a novel DLD mutation causing E3 deficiency SC Quinonez, SM Leber, DM Martin, JG Thoene, JK Bedoyan Pediatric neurology 48 (1), 67-72, 2013 | 62 | 2013 |
| Impact of diagnosis and therapy on cognitive function in urea cycle disorders R Posset, AL Gropman, SCS Nagamani, LC Burrage, JK Bedoyan, ... Annals of neurology 86 (1), 116-128, 2019 | 57 | 2019 |
| Branchiootorenal syndrome and oculoauriculovertebral spectrum features associated with duplication of SIX1, SIX6, and OTX2 resulting from a complex chromosomal rearrangement Z Ou, DM Martin, JK Bedoyan, ML Cooper, AC Chinault, P Stankiewicz, ... American Journal of Medical Genetics Part A 146 (19), 2480-2489, 2008 | 52 | 2008 |
| Mitochondrial diseases in North America: An analysis of the NAMDC Registry E Barca, Y Long, V Cooley, R Schoenaker, V Emmanuele, S DiMauro, ... Neurology: Genetics 6 (2), e402, 2020 | 47 | 2020 |
| Lethal neonatal case and review of primary short-chain enoyl-CoA hydratase (SCEH) deficiency associated with secondary lymphocyte pyruvate dehydrogenase complex (PDC) deficiency JK Bedoyan, SP Yang, S Ferdinandusse, RM Jack, A Miron, G Grahame, ... Molecular genetics and metabolism 120 (4), 342-349, 2017 | 40 | 2017 |
| Condensation of rat telomere-specific nucleosomal arrays containing unusually short DNA repeats and histone H1 JK Bedoyan, S Lejnine, VL Makarov, JP Langmore Journal of Biological Chemistry 271 (31), 18485-18493, 1996 | 40 | 1996 |
| DNA repair in a small yeast plasmid folded into chromatin MJ Smerdon, J Bedoyan, F Thoma Nucleic acids research 18 (8), 2045-2051, 1990 | 40 | 1990 |
| Early prediction of phenotypic severity in citrullinemia type 1 M Zielonka, S Kölker, F Gleich, N Stützenberger, SCS Nagamani, ... Annals of clinical and translational neurology 6 (9), 1858-1871, 2019 | 37 | 2019 |
| Age‐related effect of serotonin transporter genotype on amygdala and prefrontal cortex function in adolescence JL Wiggins, JK Bedoyan, M Carrasco, JR Swartz, DM Martin, CS Monk Human brain mapping 35 (2), 646-658, 2014 | 37 | 2014 |
| Transcription, nucleosome stability, and DNA repair in a yeast minichromosome. J Bedoyan, R Gupta, F Thoma, MJ Smerdon Journal of Biological Chemistry 267 (9), 5996-6005, 1992 | 37 | 1992 |
| Transmission of ring chromosome 13 from a mother to daughter with both having a 46, XX, r (13)(p13q34) karyotype JK Bedoyan, LA Flore, A Alkatib, SA Ebrahim, EV Bawle American Journal of Medical Genetics Part A 129 (3), 316-320, 2004 | 34 | 2004 |
| Novel SMC1A frameshift mutations in children with developmental delay and epilepsy JHR Goldstein, T Tim-Aroon, J Shieh, M Merrill, KK Deeb, S Zhang, ... European Journal of Medical Genetics 58 (10), 562-568, 2015 | 33 | 2015 |
