Year |
Citation |
Score |
2024 |
Nazeen S, Wang X, Zielinski D, Lam I, Hallacli E, Xu P, Ethier E, Strom R, Zanella CA, Nithianandam V, Ritter D, Henderson A, Saurat N, Afroz J, Nutter-Upham A, et al. Deep sequencing of proteotoxicity modifier genes uncovers a Presenilin-2/beta-amyloid-actin genetic risk module shared among alpha-synucleinopathies. Biorxiv : the Preprint Server For Biology. PMID 38496508 DOI: 10.1101/2024.03.03.583145 |
0.579 |
|
2021 |
Jones KM, Cook-Deegan R, Rotimi CN, Callier SL, Bentley AR, Stevens H, Phillips KA, Jansen JP, Weyant CF, Roberts DE, Zielinski D, Erlich Y, Garrison NA, Carroll SR, Ossorio PN, et al. Complicated legacies: The human genome at 20. Science (New York, N.Y.). 371: 564-569. PMID 33542123 DOI: 10.1126/science.abg5266 |
0.624 |
|
2018 |
Yuan J, Gordon A, Speyer D, Aufrichtig R, Zielinski D, Pickrell J, Erlich Y. DNA.Land is a framework to collect genomes and phenomes in the era of abundant genetic information. Nature Genetics. PMID 29374253 DOI: 10.1038/S41588-017-0021-8 |
0.677 |
|
2017 |
Willems T, Zielinski D, Yuan J, Gordon A, Gymrek M, Erlich Y. Genome-wide profiling of heritable and de novo STR variations. Nature Methods. PMID 28436466 DOI: 10.1038/Nmeth.4267 |
0.586 |
|
2017 |
Erlich Y, Zielinski D. DNA Fountain enables a robust and efficient storage architecture. Science (New York, N.Y.). 355: 950-954. PMID 28254941 DOI: 10.1126/Science.Aaj2038 |
0.596 |
|
2016 |
Nida H, Blum S, Zielinski D, Srivastava DA, Elbaum R, Xin Z, Erlich Y, Fridman E, Shental N. Highly efficient de novo mutant identification in a Sorghum bicolor TILLING population using the ComSeq approach. The Plant Journal : For Cell and Molecular Biology. PMID 26959378 DOI: 10.1111/Tpj.13161 |
0.639 |
|
2014 |
Zielinski D, Gordon A, Zaks BL, Erlich Y. iPipet: sample handling using a tablet. Nature Methods. 11: 784-5. PMID 25075904 DOI: 10.1038/Nmeth.3028 |
0.544 |
|
2014 |
Zielinski D, Markus B, Sheikh M, Gymrek M, Chu C, Zaks M, Srinivasan B, Hoffman JD, Aizenbud D, Erlich Y. OTX2 duplication is implicated in hemifacial microsomia. Plos One. 9: e96788. PMID 24816892 DOI: 10.1371/Journal.Pone.0096788 |
0.686 |
|
2012 |
Zielinski D, Gymrek M, Erlich Y. Back to the family: a renewed approach to rare variant studies. Genome Medicine. 4: 97. PMID 23253160 DOI: 10.1186/Gm398 |
0.674 |
|
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