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Daniela Nachmanson
Daniela Nachmanson
Bioinformatics Scientist, TwinStrand Biosciences
Verified email at eng.ucsd.edu
Title
Cited by
Cited by
Year
Ultra-sensitive TP53 sequencing for cancer detection reveals progressive clonal selection in normal tissue over a century of human lifespan
JJ Salk, K Loubet-Senear, E Maritschnegg, CC Valentine, LN Williams, ...
Cell Reports 28 (1), 132-144. e3, 2019
742019
Targeted genome fragmentation with CRISPR/Cas9 enables fast and efficient enrichment of small genomic regions and ultra-accurate sequencing with low DNA input (CRISPR-DS)
D Nachmanson, S Lian, EK Schmidt, MJ Hipp, KT Baker, Y Zhang, ...
Genome Research 28 (10), 1589-1599, 2018
462018
Inhibition of mTOR signaling and clinical activity of metformin in oral premalignant lesions
JS Gutkind, AA Molinolo, X Wu, Z Wang, D Nachmanson, O Harismendy, ...
JCI insight 6 (17), 2021
392021
Targeted deletion of AKAP7 in dentate granule cells impairs spatial discrimination
BW Jones, J Deem, TJ Younts, M Weisenhaus, CA Sanford, MC Slack, ...
Elife 5, e20695, 2016
352016
Mitochondrial DNA mutations are associated with ulcerative colitis preneoplasia but tend to be negatively selected in cancer
KT Baker, D Nachmanson, S Kumar, MJ Emond, C Ussakli, TA Brentnall, ...
Molecular Cancer Research 17 (2), 488-498, 2019
302019
The breast pre-cancer atlas illustrates the molecular and micro-environmental diversity of ductal carcinoma in situ
D Nachmanson, A Officer, H Mori, J Gordon, MF Evans, J Steward, H Yao, ...
NPJ Breast Cancer 8 (1), 6, 2022
162022
Characterization of TP53 mutations in Pap test DNA of women with and without serous ovarian carcinoma
JD Krimmel-Morrison, TS Ghezelayagh, S Lian, Y Zhang, J Fredrickson, ...
Gynecologic oncology 156 (2), 407-414, 2020
112020
Whole-genome CRISPR screening identifies PI3K/AKT as a downstream component of the oncogenic GNAQ–focal adhesion kinase signaling circuitry
N Arang, S Lubrano, DC Rigiracciolo, D Nachmanson, SM Lippman, ...
Journal of Biological Chemistry 299 (2), 2023
62023
Prevalence of cancer susceptibility variants in patients with multiple Lynch syndrome related cancers
YY Choi, SJ Shin, JE Lee, L Madlensky, ST Lee, JS Park, JH Jo, H Kim, ...
Scientific reports 11 (1), 14807, 2021
62021
Methods for targeted nucleic acid sequence enrichment with applications to error corrected nucleic acid sequencing
SR Kennedy, M Hipp, E Schmidt, RA Risques, D Nachmanson
US Patent 11,479,807, 2022
42022
Mutational profiling of micro-dissected pre-malignant lesions from archived specimens
D Nachmanson, J Steward, H Yao, A Officer, E Jeong, TJ O’Keefe, ...
BMC Medical Genomics 13, 1-15, 2020
42020
Adopting duplex sequencing technology for genetic toxicity testing: A proof-of-concept mutagenesis experiment with N-ethyl-N-nitrosourea (ENU)-exposed rats
SL Smith-Roe, CA Hobbs, V Hull, JT Auman, L Recio, MA Streicker, ...
Mutation Research/Genetic Toxicology and Environmental Mutagenesis 891, 503669, 2023
32023
Targeted genome fragmentation with CRISPR/Cas9 improves hybridization capture, reduces PCR bias, and enables efficient high-accuracy sequencing of small targets
D Nachmanson, S Lian, EK Schmidt, MJ Hipp, KT Baker, Y Zhang, ...
bioRxiv, 207027, 2017
32017
Accurate genome-wide genotyping from archival tissue to explore the contribution of common genetic variants to pre-cancer outcomes
D Nachmanson, M Pagadala, J Steward, C Cheung, LK Bruce, NQ Lee, ...
Journal of Translational Medicine 20 (1), 623, 2022
22022
PolyG-DS: An ultrasensitive polyguanine tract–profiling method to detect clonal expansions and trace cell lineage
Y Zhang, BF Kohrn, M Yang, D Nachmanson, TR Soong, IH Lee, Y Tao, ...
Proceedings of the National Academy of Sciences 118 (31), e2023373118, 2021
22021
CRISPR-DS: an efficient, low DNA input method for ultra-accurate sequencing
D Nachmanson, S Lian, EK Schmidt, MJ Hipp, KT Baker, Y Zhang, ...
bioRxiv, 207027, 2017
22017
Integrated Molecular Characterization of Intraductal Papillary Mucinous Neoplasms: An NCI Cancer Moonshot Precancer Atlas Pilot Project
A Semaan, V Bernard, J Wong, Y Makino, DB Swartzlander, ...
Cancer Research Communications 3 (10), 2062-2073, 2023
12023
Accurate genome-wide germline profiling from decade-old archival tissue DNA reveals the contribution of common variants to precancer disease outcome
D Nachmanson, M Pagadala, J Steward, C Cheung, LK Bruce, NQ Lee, ...
medRxiv, 2022.03. 31.22273116, 2022
12022
Ultra-sensitive sequencing for cancer detection reveals progressive clonal selection in normal tissue over a century of human lifespan
JJ Salk, K Loubet-Senear, E Maritschnegg, CC Valentine, LN Williams, ...
bioRxiv, 457291, 2018
12018
Frequency and spectrum of mutations in human sperm measured using duplex sequencing correlate with trio-based de novo mutation analyses
J Axelsson, D LeBlanc, H Shojaeisaadi, MJ Meier, DM Fitzgerald, ...
medRxiv, 2024.02. 13.24302689, 2024
2024
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