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Ewa A Bergmann (Grabowska)
Ewa A Bergmann (Grabowska)
Manager, Bioinformatics at Illumina
Verified email at illumina.com
Title
Cited by
Cited by
Year
The contribution of de novo coding mutations to autism spectrum disorder
I Iossifov, BJ O’roak, SJ Sanders, M Ronemus, N Krumm, D Levy, ...
Nature 515 (7526), 216, 2014
20132014
De novo gene disruptions in children on the autistic spectrum
I Iossifov, M Ronemus, D Levy, Z Wang, I Hakker, J Rosenbaum, ...
Neuron 74 (2), 285-299, 2012
14432012
Indel variant analysis of short-read sequencing data with Scalpel
H Fang, EA Bergmann, K Arora, V Vacic, MC Zody, I Iossifov, JA O'Rawe, ...
Nature Protocols 11 (12), 2529-2548, 2016
842016
Genome-wide somatic variant calling using localized colored de Bruijn graphs
G Narzisi, A Corvelo, K Arora, EA Bergmann, M Shah, R Musunuri, ...
Communications Biology 1 (1), 20, 2018
712018
Genome-wide somatic variant calling using localized colored de Bruijn graphs
G Narzisi, A Corvelo, K Arora, EA Bergmann, M Shah, R Musunuri, ...
Communications Biology 1 (1), 20, 2018
712018
Conpair: concordance and contamination estimator for matched tumor–normal pairs
EA Bergmann, BJ Chen, K Arora, V Vacic, MC Zody
Bioinformatics 32 (20), 3196-3198, 2016
492016
Comparing sequencing assays and human-machine analyses in actionable genomics for glioblastoma
KO Wrzeszczynski, MO Frank, T Koyama, K Rhrissorrakrai, N Robine, ...
Neurology Genetics 3 (4), e164, 2017
382017
State MW, Wigler M
I Iossifov, BJ O'Roak, SJ Sanders, M Ronemus, N Krumm, D Levy, ...
The contribution of de novo coding mutations to autism spectrum disorder …, 2014
252014
A family with 3460G> A and 11778G> A mutations and haplogroup analysis of Polish Leber hereditary optic neuropathy patients
K Tonska, M Kurzawa, AM Ambroziak, M Korwin-Rujna, JP Szaflik, ...
Mitochondrion 8 (5-6), 383-388, 2008
242008
Integrative genetic analysis of mouse and human AML identifies cooperating disease alleles
MA Hatlen, K Arora, V Vacic, EA Grabowska, W Liao, B Riley-Gillis, ...
Journal of Experimental Medicine 213 (1), 25-34, 2016
232016
Correction to: Sequencing and curation strategies for identifying candidate glioblastoma treatments
MO Frank, T Koyama, K Rhrissorrakrai, N Robine, F Utro, AK Emde, ...
BMC medical genomics 12 (1), 1-1, 2019
72019
Sequencing and curation strategies for identifying candidate glioblastoma treatments
MO Frank, T Koyama, K Rhrissorrakrai, N Robine, F Utro, AK Emde, ...
BMC Medical Genomics 12 (1), 56, 2019
72019
Lancet: genome-wide somatic variant calling using localized colored DeBruijn graphs
G Narzisi, A Corvelo, K Arora, E Bergmann, M Shah, R Musunuri, ...
bioRxiv, 196311, 2017
52017
NYGC glioblastoma clinical outcomes pilot study: Discovering therapeutic potential in glioblastoma through integrative genomics
KO Wrzeszczynski, N Robine, V Vacic, AK Emde, BJ Chen, W Liao, ...
Cancer Research 76 (14 Supplement), 4497-4497, 2016
12016
RNA-Seq in the NYGC GBM Clinical Outcomes Pilot Study
BJR Chen, N Robine, K Wrzeszczynski, V Vacic, AK Emde, K Arora, ...
Cancer Research 76 (14 Supplement), 4498-4498, 2016
2016
Mutations References
I Iossifov, M Ronemus, D Levy, Z Wang, I Hakker, J Rosenbaum, ...
Neuron 74 (2), 285-99, 2012
2012
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