Found: 27
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KLF3 and PAX6 are candidate driver genes in late-stage, MSI-hypermutated endometrioid endometrial carcinomas.
- Published in:
- PLoS ONE, 2022, v. 17, n. 1, p. 1, doi. 10.1371/journal.pone.0251286
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- Article
Light whole genome sequence for SNP discoveryacross domestic cat breeds.
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- BMC Genomics, 2010, v. 11, p. 406, doi. 10.1186/1471-2164-11-406
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- Article
Effort required to finish shotgun-generated genome sequences differs significantly among vertebrates.
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- BMC Genomics, 2010, v. 11, p. 1
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- Publication type:
- Article
Evaluation of variant detection software for pooled next-generation sequence data.
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- BMC Bioinformatics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12859-015-0624-y
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- Publication type:
- Article
The Sleep Inbred Panel, a Collection of Inbred Drosophila melanogaster with Extreme Long and Short Sleep Duration.
- Published in:
- G3: Genes | Genomes | Genetics, 2018, v. 8, n. 9, p. 2865, doi. 10.1534/g3.118.200503
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- Article
Exome sequencing and SNP analysis detect novel compound heterozygosity in fatty acid hydroxylase-associated neurodegeneration.
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- European Journal of Human Genetics, 2012, v. 20, n. 4, p. 476, doi. 10.1038/ejhg.2011.222
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- Article
Exome sequencing of serous endometrial tumors identifies recurrent somatic mutations in chromatin-remodeling and ubiquitin ligase complex genes.
- Published in:
- Nature Genetics, 2012, v. 44, n. 12, p. 1310, doi. 10.1038/ng.2455
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- Article
Corrigendum: TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum.
- Published in:
- 2011
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- Publication type:
- Correction notice
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum.
- Published in:
- Nature Genetics, 2011, v. 43, n. 3, p. 189, doi. 10.1038/ng.756
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- Publication type:
- Article
Gene-Based Sequencing Identifies Lipid-Influencing Variants with Ethnicity-Specific Effects in African Americans.
- Published in:
- PLoS Genetics, 2014, v. 10, n. 3, p. 1, doi. 10.1371/journal.pgen.1004190
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- Publication type:
- Article
Mutational Signatures of De-Differentiation in Functional Non-Coding Regions of Melanoma Genomes.
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- PLoS Genetics, 2012, v. 8, n. 8, p. 1, doi. 10.1371/journal.pgen.1002871
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- Publication type:
- Article
Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases.
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- PLoS Genetics, 2011, v. 7, n. 10, p. 1, doi. 10.1371/journal.pgen.1002325
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- Publication type:
- Article
Predisposition to Cancer Caused by Genetic and Functional Defects of Mammalian Atad5.
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- PLoS Genetics, 2011, v. 7, n. 8, p. 1, doi. 10.1371/journal.pgen.1002245
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- Publication type:
- Article
Comparative clinical and genomic analysis of neurofibromatosis type 2-associated cranial and spinal meningiomas.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-69074-z
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- Article
Sequencing of Candidate Chromosome Instability Genes in Endometrial Cancers Reveals Somatic Mutations in <i>ESCO1</i>, <i>CHTF18</i>, and <i>MRE11A</i>.
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- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0063313
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- Publication type:
- Article
The FOXA2 transcription factor is frequently somatically mutated in uterine carcinosarcomas and carcinomas.
- Published in:
- 2018
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- Publication type:
- journal article
Somatic mutation profiles of clear cell endometrial tumors revealed by whole exome and targeted gene sequencing.
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- 2017
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- Publication type:
- journal article
Mutational analysis of the tyrosine kinome in serous and clear cell endometrial cancer uncovers rare somatic mutations in TNK2 and DDR1.
- Published in:
- 2014
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- Publication type:
- journal article
Shimmer: detection of genetic alterations in tumors using next-generation sequence data.
- Published in:
- Bioinformatics, 2013, v. 29, n. 12, p. 1498, doi. 10.1093/bioinformatics/btt183
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- Publication type:
- Article
Admixture mapping identifies genetic regions associated with blood pressure phenotypes in African Americans.
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- PLoS ONE, 2020, v. 15, n. 4, p. 1, doi. 10.1371/journal.pone.0232048
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- Publication type:
- Article
Mutational analysis of the tyrosine kinome in serous and clear cell endometrial cancer uncovers rare somatic mutations in TNK2 and DDR1.
- Published in:
- BMC Cancer, 2014, v. 14, n. 1, p. 1, doi. 10.1186/1471-2407-14-884
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- Publication type:
- Article
Mutational analysis of the tyrosine kinome in serous and clear cell endometrial cancer uncovers rare somatic mutations in TNK2 and DDR1.
- Published in:
- BMC Cancer, 2014, v. 14, p. 1, doi. 10.1186/1471-2407-14-884
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- Publication type:
- Article
Selection for long and short sleep duration in Drosophila melanogaster reveals the complex genetic network underlying natural variation in sleep.
- Published in:
- PLoS Genetics, 2017, v. 13, n. 12, p. 1, doi. 10.1371/journal.pgen.1007098
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- Publication type:
- Article
Author Correction: A robust benchmark for detection of germline large deletions and insertions.
- Published in:
- 2020
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- Publication type:
- Correction Notice
A robust benchmark for detection of germline large deletions and insertions.
- Published in:
- Nature Biotechnology, 2020, v. 38, n. 11, p. 1347, doi. 10.1038/s41587-020-0538-8
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- Publication type:
- Article
Low mutation burden and frequent loss of CDKN2A/B and SMARCA2, but not PRC2, define premalignant neurofibromatosis type 1–associated atypical neurofibromas.
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- Neuro-Oncology, 2019, v. 21, n. 8, p. 981, doi. 10.1093/neuonc/noz028
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- Publication type:
- Article
First insight into the somatic mutation burden of neurofibromatosis type 2-associated grade I and grade II meningiomas: a case report comprehensive genomic study of two cranial meningiomas with vastly different clinical presentation.
- Published in:
- 2017
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- Publication type:
- journal article