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GenomicsNHLBI and NIDDK Sponsored GWAS in Benign Ethnic Neutropenia/Leukopenia (BEN) in African-Americans (age >45 yrs old) from the REGARDS

Benign ethnic neutropenia (BEN) is a clinical condition more commonly observed in African-Americans. It is characterized by a relative reduction in neutrophil count by about 1000 cells per microliter, leading to a decrease in total leukocyte count by similar decrement. Previous reports of this co...

phs000507.v1.p1 | EGA
TranscriptomicsCharacterization of an Entamoeba histolytica High-Mobility-Group Box Protein Induced during Intestinal Infection
The unicellular eukaryote Entamoeba histolytica is a human parasite that causes amebic dysentery and liver abscess. A genome-wide analysis of gene expression modulated by intestinal colonization and invasion identified an up-regulated transcript that encoded a putative high-mobility-group box (HMGB)...
ORGANISM(S): Entamoeba histolytica 
2008-11-19 | E-GEOD-12204 | biostudies-arrayexpress
UnknownEtiology of oncogenic fusions in 5,190 childhood cancers and its clinical and therapeutic implication.
Not available
S-EPMC10076316 | biostudies-literature
UnknownDiscovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing.
Not available
S-EPMC5282828 | biostudies-literature
UnknownExcessive burden of lysosomal storage disorder gene variants in Parkinson's disease.
Not available
S-EPMC5841393 | biostudies-literature
UnknownSusceptibility loci for pigmentation and melanoma in relation to Parkinson's disease.
Not available
S-EPMC3961492 | biostudies-literature
UnknownUse of support vector machines for disease risk prediction in genome-wide association studies: concerns and opportunities.
Not available
S-EPMC5968822 | biostudies-literature
UnknownUnbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease.
Not available
S-EPMC3932908 | biostudies-literature
UnknownA two-stage meta-analysis identifies several new loci for Parkinson's disease.
Not available
S-EPMC3128098 | biostudies-literature
UnknownImputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.
Not available
S-EPMC3696507 | biostudies-literature
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