Dashboard » Human Genomics » 2015

Human Genomics - 2015

34 articles | Last updated: 2025-12-03 14:12:57
Caucasian
0
White
0
European
1
Other
1
Article Title Cauc. White Euro. Other Phrases Used
T A T A T A T A
Integrative genomic analysis reveals functional diversification of APOBEC gene family in breast cancer
Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patients
Update of the human and mouse Fanconi anemia genes
Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments
Genomics is changing personal healthcare and medicine: the dawn of iPH (individualized preventive healthcare)
HDAC3 role in medication consumption in medication overuse headache patients: a pilot study
A survey of computational tools for downstream analysis of proteomic and other omic datasets
Cancer classification in the genomic era: five contemporary problems
Integrative DNA methylation and gene expression analysis to assess the universality of the CpG island methylator phenotype
Remotely acting SMCHD1 gene regulatory elements: in silico prediction and identification of potential regulatory variants in patients with FSHD
Eyeing the Cyr61/CTGF/NOV (CCN) group of genes in development and diseases: highlights of their structural likenesses and functional dissimilarities
MATWIN: bridging the gap between academic research and industry
Copy number alterations detected by whole-exome and whole-genome sequencing of esophageal adenocarcinoma
Trans-species polymorphism in humans and the great apes is generally maintained by balancing selection that modulates the host immune response
Performance evaluation of indel calling tools using real short-read data
Whole-genome sequencing targets drug-resistant bacterial infections
Predicting the combined effect of multiple genetic variants
Fine-scale population structure of Malays in Peninsular Malaysia and Singapore and implications for association studies
Utility and limitations of exome sequencing as a genetic diagnostic tool for conditions associated with pediatric sudden cardiac arrest/sudden cardiac death
Epigenetic inheritance and the missing heritability
SIRT1 affects DNA methylation of polycomb group protein target genes, a hotspot of the epigenetic shift observed in ageing
Genomics in the renal clinic - translating nephrogenetics for clinical practice
Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach
Success stories in genomic medicine from resource-limited countries
Clinical application of next-generation sequencing for Mendelian diseases
Is the genomic translational pipeline being disrupted?
Prediction of complex human diseases from pathway-focused candidate markers by joint estimation of marker effects: case of chronic fatigue syndrome
Complement regulator CD46: genetic variants and disease associations
Whole-exome sequencing identifies de novo mutation in the COL1A1 gene to underlie the severe osteogenesis imperfecta
Comparative sequence- and structure-inspired drug design for PilF protein of Neisseria meningitidis
Reviewer acknowledgement 2015
Evaluation of copy number variation and gene expression in neurofibromatosis type-1-associated malignant peripheral nerve sheath tumours
Rapid detection of genetic mutations in individual breast cancer patients by next-generation DNA sequencing
Self-reported race/ethnicity in the age of genomic research: its potential impact on understanding health disparities ✓ ✓ ✓ European ancestry; European Americans; African ancestry; African Americans; Latino; race; ethnicity; ancestry; biogeographical ancestry; an