| Excess of rare, inherited truncating mutations in autism N Krumm, TN Turner, C Baker, L Vives, K Mohajeri, K Witherspoon, ... Nature genetics 47 (6), 582-588, 2015 | 626 | 2015 |
| Evolution and diversity of copy number variation in the great ape lineage PH Sudmant, J Huddleston, CR Catacchio, M Malig, LDW Hillier, C Baker, ... Genome research 23 (9), 1373-1382, 2013 | 175 | 2013 |
| A cross-disorder dosage sensitivity map of the human genome RL Collins, JT Glessner, E Porcu, M Lepamets, R Brandon, C Lauricella, ... Cell 185 (16), 3041-3055. e25, 2022 | 153 | 2022 |
| Transmission disequilibrium of small CNVs in simplex autism N Krumm, BJ O’Roak, E Karakoc, K Mohajeri, B Nelson, L Vives, ... The American Journal of Human Genetics 93 (4), 595-606, 2013 | 118 | 2013 |
| Genome-wide association study and admixture mapping reveal new loci associated with total IgE levels in Latinos M Pino-Yanes, CR Gignoux, JM Galanter, AM Levin, CD Campbell, C Eng, ... Journal of Allergy and Clinical Immunology 135 (6), 1502-1510, 2015 | 61 | 2015 |
| Whole-genome sequencing of individuals from a founder population identifies candidate genes for asthma CD Campbell, K Mohajeri, M Malig, F Hormozdiari, B Nelson, G Du, ... PloS one 9 (8), e104396, 2014 | 42 | 2014 |
| Interchromosomal core duplicons drive both evolutionary instability and disease susceptibility of the Chromosome 8p23. 1 region K Mohajeri, S Cantsilieris, J Huddleston, BJ Nelson, BP Coe, ... Genome research 26 (11), 1453-1467, 2016 | 40 | 2016 |
| Fine-mapping of nuclear compartments using ultra-deep Hi-C shows that active promoter and enhancer elements localize in the active A compartment even when adjacent sequences do not H Gu, H Harris, M Olshansky, Y Eliaz, A Krishna, A Kalluchi, M Jacobs, ... BioRxiv, 2021 | 28 | 2021 |
| Tissue and cell-type specific molecular and functional signatures of 16p11. 2 reciprocal genomic disorder across mouse brain and human neuronal models DJC Tai, P Razaz, S Erdin, D Gao, J Wang, X Nuttle, CE de Esch, ... bioRxiv, 2022 | 15 | 2022 |
| Biallelic mutation of FBXL7 suggests a novel form of Hennekam syndrome PM Boone, S Paterson, K Mohajeri, W Zhu, CA Genetti, DJC Tai, N Nori, ... American Journal of Medical Genetics Part A 182 (1), 189-194, 2020 | 15 | 2020 |
| Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal models K Mohajeri, R Yadav, E D'haene, PM Boone, S Erdin, D Gao, ... The American Journal of Human Genetics 109 (11), 2049-2067, 2022 | 11 | 2022 |
| Parallelized engineering of mutational models using piggyBac transposon delivery of CRISPR libraries X Nuttle, ND Burt, B Currall, M Moysés-Oliveira, K Mohajeri, R Yadav, ... BioRxiv, 2020 | 3* | 2020 |
| Mechanistic dissection of direct MEF2C disruption and long-range regulatory alterations within the chromosome 5q14. 3 locus as strong effect drivers of neurodevelopmental disorders K Mohajeri Harvard University, 2022 | | 2022 |
| Phenotype-Conscious Models of Cohesin and CTCF Loss of Function P Boone, K Mohajeri, J Lemanski, R Collins, C De Esch, MM Oliveira, ... ANNALS OF NEUROLOGY 90, S195-S196, 2021 | | 2021 |
| Mechanistic dissection of chromatin topology disruption in the 5q14. 3 MEF2C locus as an indirect driver of neurodevelopmental disorders K Mohajeri, E D'haene, R Yadav, H Gu, B Menten, A Presser Aiden, ... 53rd European Society of Human Genetics (ESHG) Conference 28 (Suppl. 1), 35-35, 2020 | | 2020 |
| Whole-genome sequencing of individuals from a founder population identifies candidate genes for asthma E Burchard, CD Campbell, K Mohajeri, M Malig, F Hormozdiari, B Nelson, ... | | 2014 |
