Yanara Marincevic-Zuniga
Projektkoordinator vid Institutionen för medicinska vetenskaper; SNP&SEQ-teknologiplattformen
- Mobiltelefon:
- 070-167 93 65
- E-post:
- yanara.marincevic_zuniga@medsci.uu.se
- Besöksadress:
- BMC, Husargatan 3
752 37 Uppsala - Postadress:
- Molekylär Medicin, Box 1432, BMC
751 44 Uppsala
Publikationer
Senaste publikationer
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A multiomic characterization of the leukemia cell line REH using short- and long-read sequencing
Ingår i Life Science Alliance, 2024
- DOI för A multiomic characterization of the leukemia cell line REH using short- and long-read sequencing
- Ladda ner fulltext (pdf) av A multiomic characterization of the leukemia cell line REH using short- and long-read sequencing
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Multimodal classification of molecular subtypes in pediatric acute lymphoblastic leukemia
Ingår i npj Precision Oncology, 2023
- DOI för Multimodal classification of molecular subtypes in pediatric acute lymphoblastic leukemia
- Ladda ner fulltext (pdf) av Multimodal classification of molecular subtypes in pediatric acute lymphoblastic leukemia
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Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH
Ingår i BMC Research Notes, 2023
- DOI för Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH
- Ladda ner fulltext (pdf) av Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH
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Ingår i PLOS Genetics, 2022
- DOI för Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative
- Ladda ner fulltext (pdf) av Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative
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Comparison of EM-seq and PBAT methylome library methods for low-input DNA
Ingår i Epigenetics, s. 1195-1204, 2022
- DOI för Comparison of EM-seq and PBAT methylome library methods for low-input DNA
- Ladda ner fulltext (pdf) av Comparison of EM-seq and PBAT methylome library methods for low-input DNA
Alla publikationer
Artiklar i tidskrift
-
A multiomic characterization of the leukemia cell line REH using short- and long-read sequencing
Ingår i Life Science Alliance, 2024
- DOI för A multiomic characterization of the leukemia cell line REH using short- and long-read sequencing
- Ladda ner fulltext (pdf) av A multiomic characterization of the leukemia cell line REH using short- and long-read sequencing
-
Multimodal classification of molecular subtypes in pediatric acute lymphoblastic leukemia
Ingår i npj Precision Oncology, 2023
- DOI för Multimodal classification of molecular subtypes in pediatric acute lymphoblastic leukemia
- Ladda ner fulltext (pdf) av Multimodal classification of molecular subtypes in pediatric acute lymphoblastic leukemia
-
Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH
Ingår i BMC Research Notes, 2023
- DOI för Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH
- Ladda ner fulltext (pdf) av Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH
-
Ingår i PLOS Genetics, 2022
- DOI för Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative
- Ladda ner fulltext (pdf) av Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative
-
Comparison of EM-seq and PBAT methylome library methods for low-input DNA
Ingår i Epigenetics, s. 1195-1204, 2022
- DOI för Comparison of EM-seq and PBAT methylome library methods for low-input DNA
- Ladda ner fulltext (pdf) av Comparison of EM-seq and PBAT methylome library methods for low-input DNA
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Ingår i Cancer Medicine, s. 3997-4003, 2021
- DOI för RAG1 co-expression signature identifies ETV6-RUNX1-like B-cell precursor acute lymphoblastic leukemia in children
- Ladda ner fulltext (pdf) av RAG1 co-expression signature identifies ETV6-RUNX1-like B-cell precursor acute lymphoblastic leukemia in children
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Ingår i Scientific Reports, 2021
- DOI för Mutational patterns and clonal evolution from diagnosis to relapse in pediatric acute lymphoblastic leukemia
- Ladda ner fulltext (pdf) av Mutational patterns and clonal evolution from diagnosis to relapse in pediatric acute lymphoblastic leukemia
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The proliferative history shapes the DNA methylome of B-cell tumors and predicts clinical outcome
Ingår i Nature Cancer, s. 1066-1081, 2020
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Ingår i Scientific Reports, 2020
- DOI för Refined detection and phasing of structural aberrations in pediatric acute lymphoblastic leukemia by linked-read whole-genome sequencing
- Ladda ner fulltext (pdf) av Refined detection and phasing of structural aberrations in pediatric acute lymphoblastic leukemia by linked-read whole-genome sequencing
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Ingår i Leukemia and Lymphoma, s. 604-613, 2020
- DOI för Overexpression of chromatin remodeling and tyrosine kinase genes in iAMP21-positive acute lymphoblastic leukemia
- Ladda ner fulltext (pdf) av Overexpression of chromatin remodeling and tyrosine kinase genes in iAMP21-positive acute lymphoblastic leukemia
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Clinicopathological features and prognostic value of SOX11 in childhood acute lymphoblastic leukemia
Ingår i Scientific Reports, 2020
- DOI för Clinicopathological features and prognostic value of SOX11 in childhood acute lymphoblastic leukemia
- Ladda ner fulltext (pdf) av Clinicopathological features and prognostic value of SOX11 in childhood acute lymphoblastic leukemia
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Ingår i Journal of Hematology & Oncology, 2017
- DOI för Transcriptome sequencing in pediatric acute lymphoblastic leukemia identifies fusion genes associated with distinct DNA methylation profiles
- Ladda ner fulltext (pdf) av Transcriptome sequencing in pediatric acute lymphoblastic leukemia identifies fusion genes associated with distinct DNA methylation profiles
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PAX5-ESRRB is a recurrent fusion gene in B-cell precursor pediatric acute lymphoblastic leukemia
Ingår i Haematologica, 2016