| Year |
Citation |
Score |
| 2025 |
Wagner J, Olson ND, McDaniel J, Harris L, Pinto BJ, Jáspez D, Muñoz-Barrera A, Rubio-Rodríguez LA, Lorenzo-Salazar JM, Flores C, Sahraeian SME, Narzisi G, Byrska-Bishop M, Evani US, Xiao C, et al. Small variant benchmark from a complete assembly of X and Y chromosomes. Nature Communications. 16: 497. PMID 39779690 DOI: 10.1038/s41467-024-55710-z |
0.745 |
|
| 2023 |
Singhal P, Guare L, Morse C, Lucas A, Byrska-Bishop M, Guerraty MA, Kim D, Ritchie MD, Verma A. DETECT: Feature extraction method for disease trajectory modeling in electronic health records. Amia Joint Summits On Translational Science Proceedings. Amia Joint Summits On Translational Science. 2023: 487-496. PMID 37350926 |
0.743 |
|
| 2022 |
Nam Y, Jung SH, Yun JS, Sriram V, Singhal P, Byrska-Bishop M, Verma A, Shin H, Park WY, Won HH, Kim D. Discovering comorbid diseases using an inter-disease interactivity network based on biobank-scale PheWAS data. Bioinformatics (Oxford, England). PMID 36571484 DOI: 10.1093/bioinformatics/btac822 |
0.748 |
|
| 2022 |
Humphrey J, Venkatesh S, Hasan R, Herb JT, de Paiva Lopes K, Küçükali F, Byrska-Bishop M, Evani US, Narzisi G, Fagegaltier D, Sleegers K, Phatnani H, Knowles DA, Fratta P, Raj T. Integrative transcriptomic analysis of the amyotrophic lateral sclerosis spinal cord implicates glial activation and suggests new risk genes. Nature Neuroscience. PMID 36482247 DOI: 10.1038/s41593-022-01205-3 |
0.708 |
|
| 2022 |
Wagner J, Olson ND, Harris L, Khan Z, Farek J, Mahmoud M, Stankovic A, Kovacevic V, Yoo B, Miller N, Rosenfeld JA, Ni B, Zarate S, Kirsche M, Aganezov S, ... ... Byrska-Bishop M, et al. Benchmarking challenging small variants with linked and long reads. Cell Genomics. 2. PMID 36452119 DOI: 10.1016/j.xgen.2022.100128 |
0.756 |
|
| 2022 |
Byrska-Bishop M, Evani US, Zhao X, Basile AO, Abel HJ, Regier AA, Corvelo A, Clarke WE, Musunuri R, Nagulapalli K, Fairley S, Runnels A, Winterkorn L, Lowy E, Germer S, et al. High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios. Cell. 185: 3426-3440.e19. PMID 36055201 DOI: 10.1016/j.cell.2022.08.004 |
0.784 |
|
| 2022 |
Sahajpal NS, Jill Lai CY, Hastie A, Mondal AK, Dehkordi SR, van der Made CI, Fedrigo O, Al-Ajli F, Jalnapurkar S, Byrska-Bishop M, Kanagal-Shamanna R, Levy B, Schieck M, Illig T, Bacanu SA, et al. Optical genome mapping identifies rare structural variations as predisposition factors associated with severe COVID-19. Iscience. 103760. PMID 35036860 DOI: 10.1016/j.isci.2022.103760 |
0.757 |
|
| 2021 |
Foox J, Tighe SW, Nicolet CM, Zook JM, Byrska-Bishop M, Clarke WE, Khayat MM, Mahmoud M, Laaguiby PK, Herbert ZT, Warner D, Grills GS, Jen J, Levy S, Xiang J, et al. Author Correction: Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study. Nature Biotechnology. PMID 34635840 DOI: 10.1038/s41587-021-01122-z |
0.722 |
|
| 2021 |
Foox J, Tighe SW, Nicolet CM, Zook JM, Byrska-Bishop M, Clarke WE, Khayat MM, Mahmoud M, Laaguiby PK, Herbert ZT, Warner D, Grills GS, Jen J, Levy S, Xiang J, et al. Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study. Nature Biotechnology. 39: 1129-1140. PMID 34504351 DOI: 10.1038/s41587-021-01049-5 |
0.746 |
|
| 2021 |
Wilfert AB, Turner TN, Murali SC, Hsieh P, Sulovari A, Wang T, Coe BP, Guo H, Hoekzema K, Bakken TE, Winterkorn LH, Evani US, Byrska-Bishop M, Earl RK, Bernier RA, et al. Recent ultra-rare inherited variants implicate new autism candidate risk genes. Nature Genetics. PMID 34312540 DOI: 10.1038/s41588-021-00899-8 |
0.743 |
|
| 2021 |
Padhi EM, Hayeck TJ, Cheng Z, Chatterjee S, Mannion BJ, Byrska-Bishop M, Willems M, Pinson L, Redon S, Benech C, Uguen K, Audebert-Bellanger S, Le Marechal C, Férec C, Efthymiou S, et al. Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism. Human Genomics. 15: 44. PMID 34256850 DOI: 10.1186/s40246-021-00342-3 |
0.74 |
|
| 2021 |
Ebert P, Audano PA, Zhu Q, Rodriguez-Martin B, Porubsky D, Bonder MJ, Sulovari A, Ebler J, Zhou W, Serra Mari R, Yilmaz F, Zhao X, Hsieh P, Lee J, Kumar S, ... ... Byrska-Bishop M, et al. Haplotype-resolved diverse human genomes and integrated analysis of structural variation. Science (New York, N.Y.). PMID 33632895 DOI: 10.1126/science.abf7117 |
0.79 |
|
| 2018 |
Verma A, Bang L, Miller JE, Zhang Y, Lee MTM, Zhang Y, Byrska-Bishop M, Carey DJ, Ritchie MD, Pendergrass SA, Kim D. Human-Disease Phenotype Map Derived from PheWAS across 38,682 Individuals. American Journal of Human Genetics. PMID 30598166 DOI: 10.1016/J.Ajhg.2018.11.006 |
0.74 |
|
| 2018 |
Basile AO, Byrska-Bishop M, Wallace J, Frase AT, Ritchie MD. Novel features and enhancements in BioBin, a tool for the biologically inspired binning and association analysis of rare variants. Bioinformatics (Oxford, England). 34: 527-529. PMID 28968757 DOI: 10.1093/Bioinformatics/Btx559 |
0.764 |
|
| 2016 |
Basile AO, Verma A, Byrska-Bishop M, Pendergrass SA, Darabos C, Lester Kirchner H. PATTERNS IN BIOMEDICAL DATA-HOW DO WE FIND THEM? Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 22: 177-183. PMID 27896973 |
0.722 |
|
| 2015 |
Byrska-Bishop M, VanDorn D, Campbell AE, Betensky M, Arca PR, Yao Y, Gadue P, Costa FF, Nemiroff RL, Blobel GA, French DL, Hardison RC, Weiss MJ, Chou ST. Pluripotent stem cells reveal erythroid-specific activities of the GATA1 N-terminus. The Journal of Clinical Investigation. 125: 993-1005. PMID 25621499 DOI: 10.1172/Jci75714 |
0.756 |
|
| 2015 |
Steinberg Shemer O, Byrska-Bishop M, Ulirsch JC, Abdulmalik O, Yao Y, Kim AR, Gadue P, Kingsley PD, French D, Hardison RC, Palis J, Sankaran VG, Weiss MJ. Temporally Distinct Developmental Waves of Erythropoiesis from Human Pluripotent Stem Cells Blood. 126: 1170-1170. DOI: 10.1182/Blood.V126.23.1170.1170 |
0.74 |
|
| 2012 |
Chou ST, Byrska-Bishop M, Tober JM, Yao Y, Vandorn D, Opalinska JB, Mills JA, Choi JK, Speck NA, Gadue P, Hardison RC, Nemiroff RL, French DL, Weiss MJ. Trisomy 21-associated defects in human primitive hematopoiesis revealed through induced pluripotent stem cells. Proceedings of the National Academy of Sciences of the United States of America. 109: 17573-8. PMID 23045704 DOI: 10.1073/Pnas.1211175109 |
0.735 |
|
| 2012 |
Huda S, Soh S, Pilans D, Byrska-Bishop M, Kim J, Wilk G, Borisy GG, Kandere-Grzybowska K, Grzybowski BA. Microtubule guidance tested through controlled cell geometry. Journal of Cell Science. 125: 5790-9. PMID 22992457 DOI: 10.1242/Jcs.110494 |
0.687 |
|
| 2012 |
Stamatoyannopoulos JA, Snyder M, Hardison R, Ren B, Gingeras T, Gilbert DM, Groudine M, Bender M, Kaul R, Canfield T, Giste E, Johnson A, Zhang M, Balasundaram G, ... ... Byrska-Bishop M, et al. An encyclopedia of mouse DNA elements (Mouse ENCODE). Genome Biology. 13: 418. PMID 22889292 DOI: 10.1186/Gb-2012-13-8-418 |
0.684 |
|
| 2012 |
Cheng H, Byrska-Bishop M, Zhang CT, Kastrup CJ, Hwang NS, Tai AK, Lee WW, Xu X, Nahrendorf M, Langer R, Anderson DG. Stem cell membrane engineering for cell rolling using peptide conjugation and tuning of cell-selectin interaction kinetics. Biomaterials. 33: 5004-12. PMID 22494889 DOI: 10.1016/J.Biomaterials.2012.03.065 |
0.689 |
|
| Show low-probability matches. |