| Survival of human lymphoma cells requires B-cell receptor engagement by self-antigens RM Young, T Wu, R Schmitz, M Dawood, W Xiao, JD Phelan, W Xu, ... Proceedings of the National Academy of Sciences 112 (44), 13447-13454, 2015 | 182 | 2015 |
| Centers for Mendelian Genomics: A decade of facilitating gene discovery SM Baxter, JE Posey, NJ Lake, N Sobreira, JX Chong, S Buyske, EE Blue, ... Genetics in Medicine 24 (4), 784-797, 2022 | 47 | 2022 |
| High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population T Mitani, S Isikay, A Gezdirici, EY Gulec, J Punetha, JM Fatih, I Herman, ... The American Journal of Human Genetics 108 (10), 1981-2005, 2021 | 46 | 2021 |
| Exome variant discrepancies due to reference-genome differences H Li, M Dawood, MM Khayat, JR Farek, SN Jhangiani, ZM Khan, T Mitani, ... The American Journal of Human Genetics 108 (7), 1239-1250, 2021 | 41 | 2021 |
| Beyond the exome: what’s next in diagnostic testing for Mendelian conditions MH Wojcik, CM Reuter, S Marwaha, M Mahmoud, MH Duyzend, ... The American Journal of Human Genetics 110 (8), 1229-1248, 2023 | 26 | 2023 |
| Novel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome: WNT signaling perturbation and phenotypic variability C Zhang, A Jolly, BJ Shayota, JF Mazzeu, H Du, M Dawood, PC Soper, ... Human Genetics and Genomics Advances 3 (1), 2022 | 25 | 2022 |
| Quantitative dissection of multilocus pathogenic variation in an Egyptian infant with severe neurodevelopmental disorder resulting from multiple molecular diagnoses I Herman, A Jolly, H Du, M Dawood, GMH Abdel‐Salam, D Marafi, ... American Journal of Medical Genetics Part A 188 (3), 735-750, 2022 | 14 | 2022 |
| Determination of molecular structures of HIV envelope glycoproteins using cryo-electron tomography and automated sub-tomogram averaging JR Meyerson, TA White, D Bliss, A Moran, A Bartesaghi, MJ Borgnia, ... JoVE (Journal of Visualized Experiments), e2770, 2011 | 14 | 2011 |
| Phenotypic and mutational spectrum of ROR2‐related Robinow syndrome AR Lima, BM Ferreira, C Zhang, A Jolly, H Du, JJ White, M Dawood, ... Human Mutation 43 (7), 900-918, 2022 | 11 | 2022 |
| AHDC1 missense mutations in Xia-Gibbs syndrome MM Khayat, J Hu, Y Jiang, H Li, V Chander, M Dawood, AW Hansen, S Li, ... Human Genetics and Genomics Advances 2 (4), 2021 | 8 | 2021 |
| The multiple de novo copy number variant (MdnCNV) phenomenon presents with peri-zygotic DNA mutational signatures and multilocus pathogenic variation H Du, A Jolly, CM Grochowski, B Yuan, M Dawood, SN Jhangiani, H Li, ... Genome Medicine 14 (1), 122, 2022 | 6 | 2022 |
| Shrewd AKT regulation to survive M Dawood, GB Mills, Z Ding Oncoscience 1 (2), 113, 2014 | 6 | 2014 |
| Long read sequencing and expression studies of AHDC1 deletions in Xia‐Gibbs syndrome reveal a novel genetic regulatory mechanism V Chander, M Mahmoud, J Hu, Z Dardas, CM Grochowski, M Dawood, ... Human Mutation 43 (12), 2033-2053, 2022 | 5 | 2022 |
| Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease DG Calame, T Guo, C Wang, L Garrett, A Jolly, M Dawood, A Kurolap, ... The American Journal of Human Genetics 110 (8), 1394-1413, 2023 | 4 | 2023 |
| An international virtual hackathon to build tools for the analysis of structural variants within species ranging from coronaviruses to vertebrates AM Mc Cartney, M Mahmoud, M Jochum, DP Agustinho, B Zorman, ... F1000Research 10, 2021 | 4 | 2021 |
| Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-Küster-Hauser syndrome A Jolly, H Du, C Borel, N Chen, S Zhao, CM Grochowski, R Duan, ... Human Genetics and Genomics Advances 4 (3), 2023 | 2 | 2023 |
| RNA Sequencing in B-Cell Lymphomas DW Huang, M Dawood, CA Johnson, R Schmitz Lymphoma, 283-303, 2019 | 2 | 2019 |
| NODAL variants are associated with a continuum of laterality defects from simple D-transposition of the great arteries to heterotaxy Z Dardas, JM Fatih, A Jolly, M Dawood, H Du, CM Grochowski, EG Jones, ... Genome Medicine 16 (1), 53, 2024 | | 2024 |
| Defining and Reducing Variant Classification Disparities M Dawood, S Fayer, S Pendyala, M Post, D Kalra, K Patterson, E Venner, ... medRxiv, 2024.04. 11.24305690, 2024 | | 2024 |
| O01: Using multiplexed functional data to reduce the VUS burden in populations underrepresented in genomic medicine M Dawood, S Fayer, M Post, D Kalra, K Patterson, E Venner, L Muffley, ... Genetics in Medicine Open 2, 2024 | | 2024 |
James LupskiBaylor College of MedicineVerified email at bcm.edu
