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Somatic CpG hypermutation is associated with mismatch repair deficiency in cancer.
- Published in:
- Molecular Systems Biology, 2024, v. 20, n. 9, p. 1006, doi. 10.1038/s44320-024-00054-5
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- Article
Personal receptor repertoires: olfaction as a model.
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- BMC Genomics, 2012, v. 13, n. 1, p. 414, doi. 10.1186/1471-2164-13-414
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- Article
Chromatin accessibility landscape of pediatric T‐lymphoblastic leukemia and human T‐cell precursors.
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- EMBO Molecular Medicine, 2020, v. 12, n. 9, p. 1, doi. 10.15252/emmm.202012104
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- Article
PDX models recapitulate the genetic and epigenetic landscape of pediatric T‐cell leukemia.
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- EMBO Molecular Medicine, 2018, v. 10, n. 12, p. N.PAG, doi. 10.15252/emmm.201809443
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- Publication type:
- Article
Mutation-Attention (MuAt): deep representation learning of somatic mutations for tumour typing and subtyping.
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- Genome Medicine, 2023, v. 15, n. 1, p. 1, doi. 10.1186/s13073-023-01204-4
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- Article
Genomic Variation and Its Impact on Gene Expression in Drosophila melanogaster.
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- PLoS Genetics, 2012, v. 8, n. 11, p. 1, doi. 10.1371/journal.pgen.1003055
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- Article
Reply to Li and Colleagues.
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- JNCI: Journal of the National Cancer Institute, 2023, v. 115, n. 6, p. 760, doi. 10.1093/jnci/djad057
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- Article
Reply to Evans and Woodward.
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- JNCI: Journal of the National Cancer Institute, 2023, v. 115, n. 2, p. 231, doi. 10.1093/jnci/djac224
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- Publication type:
- Article
Heterozygous BRCA1 and BRCA2 and Mismatch Repair Gene Pathogenic Variants in Children and Adolescents With Cancer.
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- JNCI: Journal of the National Cancer Institute, 2022, v. 114, n. 11, p. 1523, doi. 10.1093/jnci/djac151
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- Publication type:
- Article
Genomic and transcriptomic changes complement each other in the pathogenesis of sporadic Burkitt lymphoma.
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- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-08578-3
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- Article
Systematic Inference of Copy-Number Genotypes from Personal Genome Sequencing Data Reveals Extensive Olfactory Receptor Gene Content Diversity.
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- PLoS Computational Biology, 2010, v. 6, n. 11, p. 1, doi. 10.1371/journal.pcbi.1000988
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- Article
No correlation between NF1 mutation position and risk of optic pathway glioma in 77 unrelated NF1 patients.
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- Human Genetics, 2016, v. 135, n. 5, p. 469, doi. 10.1007/s00439-016-1646-x
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- Article
A leukemia-protective germline variant mediates chromatin module formation via transcription factor nucleation.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29625-6
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- Publication type:
- Article
Pan-cancer atlas of somatic core and linker histone mutations.
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- NPJ Genomic Medicine, 2023, v. 8, n. 1, p. 1, doi. 10.1038/s41525-023-00367-8
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- Article
Pan-cancer atlas of somatic core and linker histone mutations.
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- NPJ Genomic Medicine, 2023, v. 8, n. 1, p. 1, doi. 10.1038/s41525-023-00367-8
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- Publication type:
- Article
Identification and removal of low-complexity sites in allele-specific analysis of ChIP-seq data.
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- Bioinformatics, 2014, v. 30, n. 2, p. 165, doi. 10.1093/bioinformatics/btt667
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- Article
Author Correction: Butler enables rapid cloud-based analysis of thousands of human genomes.
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- 2023
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- Correction Notice
Publisher Correction: Butler enables rapid cloud-based analysis of thousands of human genomes.
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- 2023
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- Publication type:
- Correction Notice
Butler enables rapid cloud-based analysis of thousands of human genomes.
- Published in:
- Nature Biotechnology, 2020, v. 38, n. 3, p. 288, doi. 10.1038/s41587-019-0360-3
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- Publication type:
- Article
Rational combination platform trial design for children and young adults with diffuse midline glioma: A report from PNOC.
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- Neuro-Oncology, 2024, v. 26, p. S125, doi. 10.1093/neuonc/noad181
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- Article
Clinical outcome of pediatric medulloblastoma patients with Li–Fraumeni syndrome.
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- Neuro-Oncology, 2023, v. 25, n. 12, p. 2273, doi. 10.1093/neuonc/noad114
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- Article
Mechanisms of imipridones in targeting mitochondrial metabolism in cancer cells.
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- Neuro-Oncology, 2021, v. 23, n. 4, p. 542, doi. 10.1093/neuonc/noaa283
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- Article
MEDU-11. MOLECULAR CHARACTERIZATION OF ETMRs REVEALS A ROLE FOR R-LOOP MEDIATED CHROMOSOMAL INSTABILITY.
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- Neuro-Oncology, 2019, v. 21, p. ii105, doi. 10.1093/neuonc/noz036.170
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- Article
A common microdeletion affecting a hippocampus- and amygdala-specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders.
- Published in:
- Bipolar Disorders, 2014, v. 16, n. 7, p. 764, doi. 10.1111/bdi.12207
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- Article
A cell-based model system links chromothripsis with hyperploidy.
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- Molecular Systems Biology, 2015, v. 11, n. 9, p. n/a, doi. 10.15252/msb.20156505
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- Publication type:
- Article
A yeast one-hybrid and microfluidics-based pipeline to map mammalian gene regulatory networks.
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- Molecular Systems Biology, 2013, v. 9, n. 1, p. 1, doi. 10.1038/msb.2013.38
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- Publication type:
- Article