| Year |
Citation |
Score |
| 2020 |
Murdock DR, Dai H, Burrage LC, Rosenfeld JA, Ketkar S, Müller MF, Yépez VA, Gagneur J, Liu P, Chen S, Jain M, Zapata G, Bacino CA, Chao HT, Moretti P, et al. Transcriptome-directed analysis for Mendelian disease diagnosis overcomes limitations of conventional genomic testing. The Journal of Clinical Investigation. PMID 33001864 DOI: 10.1172/JCI141500 |
0.44 |
|
| 2020 |
Chen S, Jain M, Jhangiani S, Akdemir ZC, Campeau PM, Klein RF, Nielson C, Dai H, Muzny DM, Boerwinkle E, Gibbs RA, Orwoll ES, Lupski JR, Posey JE, Lee B. Genetic Burden Contributing to Extremely Low or High Bone Mineral Density in a Senior Male Population From the Osteoporotic Fractures in Men Study (MrOS). Jbmr Plus. 4: e10335. PMID 32161841 DOI: 10.1002/jbm4.10335 |
0.44 |
|
| 2019 |
Zhang J, Li J, Saucier JB, Feng Y, Jiang Y, Sinson J, McCombs AK, Schmitt ES, Peacock S, Chen S, Dai H, Ge X, Wang G, Shaw CA, Mei H, et al. Publisher Correction: Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA. Nature Medicine. PMID 30787481 DOI: 10.1038/s41591-019-0391-9 |
0.44 |
|
| 2019 |
Zhang J, Li J, Saucier JB, Feng Y, Jiang Y, Sinson J, McCombs AK, Schmitt ES, Peacock S, Chen S, Dai H, Ge X, Wang G, Shaw CA, Mei H, et al. Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA. Nature Medicine. PMID 30692697 DOI: 10.1038/s41591-018-0334-x |
0.44 |
|
| 2016 |
Dai H, Zhang VW, El-Hattab AW, Ficicioglu C, Shinawi M, Lines M, Schulze A, McNutt M, Gotway G, Tian X, Chen S, Wang J, Craigen WJ, Wong LJ. cprFBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndrome. Clinical Genetics. PMID 27743463 DOI: 10.1111/cge.12894 |
0.44 |
|
| 2015 |
Dai H, Ehrentraut S, Nagel S, Eberth S, Pommerenke C, Dirks WG, Geffers R, Kalavalapalli S, Kaufmann M, Meyer C, Faehnrich S, Chen S, Drexler HG, MacLeod RA. Genomic Landscape of Primary Mediastinal B-Cell Lymphoma Cell Lines. Plos One. 10: e0139663. PMID 26599546 DOI: 10.1371/journal.pone.0139663 |
0.44 |
|
| 2015 |
Mohamed NH, Liu M, Abdel-Mageed WM, Alwahibi LH, Dai H, Ismail MA, Badr G, Quinn RJ, Liu X, Zhang L, Shoreit AA. Cytotoxic cardenolides from the latex of Calotropis procera. Bioorganic & Medicinal Chemistry Letters. PMID 26323871 DOI: 10.1016/j.bmcl.2015.08.044 |
0.44 |
|
| 2015 |
Ping N, Qiu H, Wang Q, Dai H, Ruan C, Ehrentraut S, Drexler HG, MacLeod RA, Chen S. Establishment and genetic characterization of a novel mixed-phenotype acute leukemia cell line with EP300-ZNF384 fusion. Journal of Hematology & Oncology. 8: 100. PMID 26293203 DOI: 10.1186/s13045-015-0197-2 |
0.44 |
|
| 2011 |
Chen Y, Dai H, Chen S, Zhang L, Long M. Highly tissue specific expression of Sphinx supports its male courtship related role in Drosophila melanogaster. Plos One. 6: e18853. PMID 21541324 DOI: 10.1371/journal.pone.0018853 |
0.64 |
|
| 2008 |
Dai H, Chen Y, Chen S, Mao Q, Kennedy D, Landback P, Eyre-Walker A, Du W, Long M. The evolution of courtship behaviors through the origination of a new gene in Drosophila. Proceedings of the National Academy of Sciences of the United States of America. 105: 7478-83. PMID 18508971 DOI: 10.1073/pnas.0800693105 |
0.64 |
|
| 2006 |
Dai H, Yoshimatsu TF, Long M. Retrogene movement within- and between-chromosomes in the evolution of Drosophila genomes. Gene. 385: 96-102. PMID 17101240 DOI: 10.1016/j.gene.2006.04.033 |
0.64 |
|
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