BMC Medical Genomics View Homepage


Ontology type: schema:Periodical      Open Access: True


Journal Info

START YEAR

2008

PUBLISHER

BioMed Central

LANGUAGE

en

HOMEPAGE

http://bmcmedgenomics.biomedcentral.com/

Recent publications latest 20 shown

  • 2019-12 Familial Xp11.22 microdeletion including SHROOM4 and CLCN5 is associated with intellectual disability, short stature, microcephaly and Dent disease: a case report
  • 2019-12 Long contiguous stretches of homozygosity detected by chromosomal microarrays (CMA) in patients with neurodevelopmental disorders in the South of Brazil
  • 2019-12 Glucocorticoid-driven transcriptomes in human airway epithelial cells: commonalities, differences and functional insight from cell lines and primary cells
  • 2019-12 Identification of sequence variants associated with severe microtia-astresia by targeted sequencing
  • 2019-12 Transcriptomic analysis of fetal membranes reveals pathways involved in preterm birth
  • 2019-12 Chromosome (re)positioning in spermatozoa of fathers and sons – carriers of reciprocal chromosome translocation (RCT)
  • 2019-12 Identification of biomarkers for amyotrophic lateral sclerosis by comprehensive analysis of exosomal mRNAs in human cerebrospinal fluid
  • 2019-12 Meta-analysis of gene expression profiles in long-term non-progressors infected with HIV-1
  • 2019-03 Prioritization of genes involved in endothelial cell apoptosis by their implication in lymphedema using an analysis of associative gene networks with ANDSystem
  • 2019-03 FTO haplotyping underlines high obesity risk for European populations
  • 2019-03 Interrelation of chemerin and TNF-α with mtDNA copy number in adipose tissues and blood cells in obese patients with and without type 2 diabetes
  • 2019-03 Design and analysis of stably integrated reporters for inducible transgene expression in human T cells and CAR NK-cell lines
  • 2019-03 Genotype-phenotype correlations in FSHD
  • 2019-03 Identification of potential biomarkers related to glioma survival by gene expression profile analysis
  • 2019-01 Context-sensitive network analysis identifies food metabolites associated with Alzheimer’s disease: an exploratory study
  • 2019-01 Identification of exon skipping events associated with Alzheimer’s disease in the human hippocampus
  • 2019-01 Selecting precise reference normal tissue samples for cancer research using a deep learning approach
  • 2018-12 Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction
  • 2018-12 Chromosomal microarray analysis in developmental delay and intellectual disability with comorbid conditions
  • 2018-12 Patient with multiple acyl-CoA dehydrogenase deficiency disease and ETFDH mutations benefits from riboflavin therapy: a case report
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