Works matching IS 14739542 AND DT 2015 AND VI 9
Results: 42
Integrative genomic analysis reveals functional diversification of APOBEC gene family in breast cancer.
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- Human Genomics, 2015, v. 9, p. 1, doi. 10.1186/s40246-015-0056-9
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- Article
Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patients.
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- Human Genomics, 2015, v. 9, p. 1, doi. 10.1186/s40246-015-0055-x
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Update of the human and mouse Fanconi anemia genes.
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- Human Genomics, 2015, v. 9, p. 1, doi. 10.1186/s40246-015-0054-y
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Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments.
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- Human Genomics, 2015, v. 9, p. 1, doi. 10.1186/s40246-015-0053-z
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- Article
HDAC3 role in medication consumption in medication overuse headache patients: a pilot study.
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- Human Genomics, 2015, v. 9, p. 1, doi. 10.1186/s40246-015-0051-1
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Genomics is changing personal healthcare and medicine: the dawn of iPH (individualized preventive healthcare).
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- Human Genomics, 2015, v. 9, p. 1, doi. 10.1186/s40246-015-0052-0
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A survey of computational tools for downstream analysis of proteomic and other omic datasets.
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- Human Genomics, 2015, v. 9, p. 1, doi. 10.1186/s40246-015-0050-2
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Cancer classification in the genomic era: five contemporary problems.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0049-8
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Integrative DNA methylation and gene expression analysis to assess the universality of the CpG island methylator phenotype.
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- Human Genomics, 2015, v. 9, p. 1, doi. 10.1186/s40246-015-0048-9
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Remotely acting SMCHD1 gene regulatory elements: in silico prediction and identification of potential regulatory variants in patients with FSHD.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0047-x
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Eyeing the Cyr61/CTGF/NOV (CCN) group of genes in development and diseases: highlights of their structural likenesses and functional dissimilarities.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0046-y
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MATWIN: bridging the gap between academic research and industry.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0045-z
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Copy number alterations detected by whole-exome and whole-genome sequencing of esophageal adenocarcinoma.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0044-0
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Trans-species polymorphism in humans and the great apes is generally maintained by balancing selection that modulates the host immune response.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0043-1
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Performance evaluation of indel calling tools using real short-read data.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0042-2
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Whole-genome sequencing targets drug-resistant bacterial infections.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0037-z
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Performance evaluation of indel calling tools using real short-read data.
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- Human Genomics, 2015, v. 9, n. 1, p. 20, doi. 10.1186/s40246-015-0042-2
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Epigenetic inheritance and the missing heritability.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0041-3
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Predicting the combined effect of multiple genetic variants.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0040-4
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Fine-scale population structure of Malays in Peninsular Malaysia and Singapore and implications for association studies.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0039-x
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- Article
Utility and limitations of exome sequencing as a genetic diagnostic tool for conditions associated with pediatric sudden cardiac arrest/sudden cardiac death.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0038-y
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Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0034-2
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Epigenetic inheritance and the missing heritability.
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- Human Genomics, 2015, v. 9, n. 1, p. 17, doi. 10.1186/s40246-015-0041-3
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Is the genomic translational pipeline being disrupted?
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0032-4
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- Article
Utility and limitations of exome sequencing as a genetic diagnostic tool for conditions associated with pediatric sudden cardiac arrest/sudden cardiac death
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- Human Genomics, 2015, v. 9, n. 1, p. 15, doi. 10.1186/s40246-015-0038-y
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- Article
SIRT1 affects DNA methylation of polycomb group protein target genes, a hotspot of the epigenetic shift observed in ageing.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0036-0
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Genomics in the renal clinic - translating nephrogenetics for clinical practice.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0035-1
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Genomics in the renal clinic - translating nephrogenetics for clinical practice
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- Human Genomics, 2015, v. 9, n. 1, p. 13, doi. 10.1186/s40246-015-0035-1
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- Article
Fine-scale population structure of Malays in Peninsular Malaysia and Singapore and implications for association studies.
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- Human Genomics, 2015, v. 9, n. 1, p. 16, doi. 10.1186/s40246-015-0039-x
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- Article
Clinical application of next-generation sequencing for Mendelian diseases.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0031-5
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Prediction of complex human diseases from pathway-focused candidate markers by joint estimation of marker effects: case of chronic fatigue syndrome.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0030-6
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Complement regulator CD46: genetic variants and disease associations.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0029-z
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Success stories in genomic medicine from resource-limited countries.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0033-3
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Whole-exome sequencing identifies de novo mutation in the COL1A1 gene to underlie the severe osteogenesis imperfecta.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0028-0
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- Article
Comparative sequence- and structure-inspired drug design for PilF protein of Neisseria meningitidis.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0027-1
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Comparative sequence- and structure-inspired drug design for PilF protein of Neisseria meningitidis.
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- Human Genomics, 2015, v. 9, p. 1, doi. 10.1186/s40246-015-0027-1
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Reviewer acknowledgement 2015.
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- Human Genomics, 2015, v. 9, n. 1, p. 4, doi. 10.1186/s40246-015-0026-2
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Evaluation of copy number variation and gene expression in neurofibromatosis type-1-associated malignant peripheral nerve sheath tumours.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0025-3
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Rapid detection of genetic mutations in individual breast cancer patients by next-generation DNA sequencing.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0024-4
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Rapid detection of genetic mutations in individual breast cancer patients by next-generation DNA sequencing.
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- Human Genomics, 2015, v. 9, n. 2, p. 1, doi. 10.1186/s40246-015-0024-4
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Self-reported race/ethnicity in the age of genomic research: its potential impact on understanding health disparities.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-014-0023-x
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- Article
Self-reported race/ethnicity in the age of genomic research: its potential impact on understanding health disparities.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-014-0023-x
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- Article