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Genetic predisposition to longer telomere length and risk of childhood, adolescent and adult-onset ependymoma.
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- Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. N.PAG, doi. 10.1186/s40478-020-01038-w
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- Article
DNA methylation at birth in monozygotic twins discordant for pediatric acute lymphoblastic leukemia.
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- Nature Communications, 2022, v. 13, p. 1, doi. 10.1038/s41467-022-33677-z
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- Article
Epigenomic signature of major congenital heart defects in newborns with Down syndrome.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00540-1
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- Article
The genetic risk of acute lymphoblastic leukemia and its implications for children of Latin American origin.
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- Frontiers in Oncology, 2024, p. 1, doi. 10.3389/fonc.2023.1299355
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- Article
Ras-mutant cancers are sensitive to small molecule inhibition of V-type ATPases in mice.
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- Nature Biotechnology, 2022, v. 40, n. 12, p. 1834, doi. 10.1038/s41587-022-01386-z
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- Article
Variant to function mapping at single-cell resolution through network propagation.
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- Nature Biotechnology, 2022, v. 40, n. 11, p. 1644, doi. 10.1038/s41587-022-01341-y
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- Article
cnvHap: an integrative population and haplotype–based multiplatform model of SNPs and CNVs.
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- Nature Methods, 2010, v. 7, n. 7, p. 541, doi. 10.1038/nmeth.1466
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- Article
Genomic characterization of chronic lymphocytic leukemia (CLL) in radiation-exposed Chornobyl cleanup workers.
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- 2018
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- Publication type:
- journal article
Predisposing germline mutations in high hyperdiploid acute lymphoblastic leukemia in children.
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- Genes, Chromosomes & Cancer, 2019, v. 58, n. 10, p. 723, doi. 10.1002/gcc.22765
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- Article
Clinical characteristics of cytomegalovirus‐positive pediatric acute lymphoblastic leukemia at diagnosis.
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- American Journal of Hematology, 2022, v. 97, n. 6, p. E198, doi. 10.1002/ajh.26528
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- Article
Incorporation of DNA methylation quantitative trait loci (mQTLs) in epigenome-wide association analysis: application to birthweight effects in neonatal whole blood.
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- Clinical Epigenetics, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13148-022-01385-6
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- Publication type:
- Article
Somatic Mutation Allelic Ratio Test Using ddPCR (SMART-ddPCR): An Accurate Method for Assessment of Preferential Allelic Imbalance in Tumor DNA.
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- PLoS ONE, 2015, v. 10, n. 11, p. 1, doi. 10.1371/journal.pone.0143343
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- Article
Rare Genomic Structural Variants in Complex Disease: Lessons from the Replication of Associations with Obesity.
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- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0058048
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- Article
Small Deletion Variants Have Stable Breakpoints Commonly Associated with Alu Elements.
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- PLoS ONE, 2008, v. 3, n. 8, p. 1, doi. 10.1371/journal.pone.0003104
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- Publication type:
- Article
Increased burden of familial-associated early-onset cancer risk among minority Americans compared to non-Latino Whites.
- Published in:
- eLife, 2021, p. 1, doi. 10.7554/eLife.64793
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- Publication type:
- Article
Meta-Analysis of DNA Methylation Datasets Shows Aberrant DNA Methylation of Thyroid Development or Function Genes in Down Syndrome.
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- Thyroid, 2023, v. 33, n. 1, p. 53, doi. 10.1089/thy.2022.0320
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- Publication type:
- Article
European genetic ancestry associated with risk of childhood ependymoma.
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- Neuro-Oncology, 2020, v. 22, n. 11, p. 1637, doi. 10.1093/neuonc/noaa130
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- Publication type:
- Article
Germline cancer predisposition variants and pediatric glioma: a population-based study in California.
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- Neuro-Oncology, 2020, v. 22, n. 6, p. 864, doi. 10.1093/neuonc/noaa014
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- Publication type:
- Article
Germline genetic landscape of pediatric central nervous system tumors.
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- Neuro-Oncology, 2019, v. 21, n. 11, p. 1376, doi. 10.1093/neuonc/noz108
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- Publication type:
- Article
Associations between early‐life and in utero infections and cytomegalovirus‐positive acute lymphoblastic leukemia in children.
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- International Journal of Cancer, 2023, v. 152, n. 5, p. 845, doi. 10.1002/ijc.34292
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- Article
Investigation of the HIN200 Locus in UK SLE Families Identifies Novel Copy Number Variants.
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- Annals of Human Genetics, 2011, v. 75, n. 3, p. 383, doi. 10.1111/j.1469-1809.2011.00641.x
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- Article
Trends in Acute Lymphoblastic Leukemia Incidence in the United States by Race/Ethnicity From 2000 to 2016.
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- American Journal of Epidemiology, 2021, v. 190, n. 4, p. 519, doi. 10.1093/aje/kwaa215
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- Publication type:
- Article
History of Early Childhood Infections and Acute Lymphoblastic Leukemia Risk Among Children in a US Integrated Health-Care System.
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- American Journal of Epidemiology, 2020, v. 189, n. 10, p. 1076, doi. 10.1093/aje/kwaa062
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- Publication type:
- Article
Accurate Single-Nucleotide Polymorphism Allele Assignment in Trisomic or Duplicated Regions by Using a Single Base--Extension Assay with MALDI-TOF Mass Spectrometry.
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- Clinical Chemistry, 2011, v. 57, n. 8, p. 1188, doi. 10.1373/clinchem.2010.159558
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- Article
Common genetic variants associated with telomere length confer risk for neuroblastoma and other childhood cancers.
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- Carcinogenesis, 2016, v. 37, n. 6, p. 576, doi. 10.1093/carcin/bgw037
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- Publication type:
- Article
PDGFRα demarcates the cardiogenic clonogenic Sca1<sup>+</sup> stem/progenitor cell in adult murine myocardium.
- Published in:
- Nature Communications, 2015, v. 6, n. 5, p. 6930, doi. 10.1038/ncomms7930
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- Publication type:
- Article
Mitochondrial 1555 G>A variant as a potential risk factor for childhood glioblastoma.
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- Neuro-Oncology Advances, 2022, v. 4, n. 1, p. 1, doi. 10.1093/noajnl/vdac045
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- Publication type:
- Article
To ERV Is Human: A Phenotype-Wide Scan Linking Polymorphic Human Endogenous Retrovirus-K Insertions to Complex Phenotypes.
- Published in:
- Frontiers in Genetics, 2018, p. 1, doi. 10.3389/fgene.2018.00298
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- Article
Investigating DNA methylation as a mediator of genetic risk in childhood acute lymphoblastic leukemia.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 21, p. 3741, doi. 10.1093/hmg/ddac137
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- Publication type:
- Article
Imprinted expression of UBE3A in non-neuronal cells from a Prader–Willi syndrome patient with an atypical deletion.
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- Human Molecular Genetics, 2014, v. 23, n. 9, p. 2364, doi. 10.1093/hmg/ddt628
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- Article
Novel association approach for variable number tandem repeats (VNTRs) identifies DOCK5 as a susceptibility gene for severe obesity.
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- Human Molecular Genetics, 2012, v. 21, n. 16, p. 3727, doi. 10.1093/hmg/dds187
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- Article
BMI1 enhancer polymorphism underlies chromosome 10p12.31 association with childhood acute lymphoblastic leukemia.
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- International Journal of Cancer, 2018, v. 143, n. 11, p. 2647, doi. 10.1002/ijc.31622
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- Article
Cancer health disparities in racial/ethnic minorities in the United States.
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- 2021
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- Publication type:
- journal article
In Utero Origins of Acute Leukemia in Children.
- Published in:
- Biomedicines, 2024, v. 12, n. 1, p. 236, doi. 10.3390/biomedicines12010236
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- Article
GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-017-02596-9
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- Article
Chromosome 19p13.3 deletion in a patient with macrocephaly, obesity, mental retardation, and behavior problems.
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- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 5, p. 1192, doi. 10.1002/ajmg.a.33986
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- Article
Genetic determinants of childhood and adult height associated with osteosarcoma risk.
- Published in:
- 2018
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- Publication type:
- journal article
In utero and early-life exposure to thirdhand smoke causes profound changes to the immune system.
- Published in:
- Clinical Science, 2021, v. 135, n. 8, p. 1053, doi. 10.1042/CS20201498
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- Publication type:
- Article
Multi-ancestry genome-wide association study of 4069 children with glioma identifies 9p21.3 risk locus.
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- Neuro-Oncology, 2023, v. 25, n. 9, p. 1709, doi. 10.1093/neuonc/noad042
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- Publication type:
- Article
A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 17, p. 3257, doi. 10.1093/hmg/ddp263
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- Article
Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 23, p. 2783, doi. 10.1093/hmg/ddm208
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- Publication type:
- Article
Localized variation in ancestral admixture identifies pilocytic astrocytoma risk loci among Latino children.
- Published in:
- PLoS Genetics, 2022, v. 18, n. 9, p. 1, doi. 10.1371/journal.pgen.1010388
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- Publication type:
- Article
Accelerated epigenetic aging in newborns with Down syndrome.
- Published in:
- Aging Cell, 2022, v. 21, n. 7, p. 1, doi. 10.1111/acel.13652
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- Publication type:
- Article