Genetic analysis
View article: Supplementary Figure from Clonal Hematopoiesis and Mosaicism Revealed by a Multi-Tissue Analysis of Constitutional <i>TP53</i> Status
Supplementary Figure from Clonal Hematopoiesis and Mosaicism Revealed by a Multi-Tissue Analysis of Constitutional <i>TP53</i> Status Open
Supplementary Figure from Clonal Hematopoiesis and Mosaicism Revealed by a Multi-Tissue Analysis of Constitutional TP53 Status
View article: Supplementary Figure from Overview of Research on Germline Genetic Variation in Immune Genes and Cancer Outcomes
Supplementary Figure from Overview of Research on Germline Genetic Variation in Immune Genes and Cancer Outcomes Open
Supplementary Figure from Overview of Research on Germline Genetic Variation in Immune Genes and Cancer Outcomes
View article: Supplementary Table S4 from Genetic Susceptibility to Nonalcoholic Fatty Liver Disease and Risk for Pancreatic Cancer: Mendelian Randomization
Supplementary Table S4 from Genetic Susceptibility to Nonalcoholic Fatty Liver Disease and Risk for Pancreatic Cancer: Mendelian Randomization Open
Supplementary Table S4 shows results of univariate analysis for 17 imaging and biopsy validated SNPs in the PanScan sample
View article: Genetic Diversity of Rice Bacterial Leaf Blight Pathogen, Xanthomonas oryzae pv. oryzae in Godavari Zone of Andhra Pradesh, India
Genetic Diversity of Rice Bacterial Leaf Blight Pathogen, Xanthomonas oryzae pv. oryzae in Godavari Zone of Andhra Pradesh, India Open
Bacterial leaf blight (BLB), caused by Xanthomonas oryzae pv. oryzae (Xoo), is one of the major biotic constraints limiting yields in paddy in Andhra Pradesh. The present study was conducted at ANGRAU – Regional Agricultural Research Stati…
View article: Supplementary Figure from Overview of Research on Germline Genetic Variation in Immune Genes and Cancer Outcomes
Supplementary Figure from Overview of Research on Germline Genetic Variation in Immune Genes and Cancer Outcomes Open
Supplementary Figure from Overview of Research on Germline Genetic Variation in Immune Genes and Cancer Outcomes
View article: What genetic tests are used to diagnose hereditary spastic paraplegia?
What genetic tests are used to diagnose hereditary spastic paraplegia? Open
Genetic testing for hereditary spastic paraplegia involves analyzing specific genes depending on the subtype and inheritance pattern, utilizing modern sequencing technologies such as NGS and WES.
View article: Supplementary Figure from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility
Supplementary Figure from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility Open
Supplementary Figure from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility
View article: Supplementary Figure from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility
Supplementary Figure from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility Open
Supplementary Figure from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility
View article: Supplementary Table S2 from Genetic Susceptibility to Nonalcoholic Fatty Liver Disease and Risk for Pancreatic Cancer: Mendelian Randomization
Supplementary Table S2 from Genetic Susceptibility to Nonalcoholic Fatty Liver Disease and Risk for Pancreatic Cancer: Mendelian Randomization Open
Supplementary Table S2 shows results of univariate analysis for 22 imaging-defined nonalcoholic fatty liver disease SNPs in the PanScan sample
View article: Supplementary Figure from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility
Supplementary Figure from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility Open
Supplementary Figure from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility
View article: Presence of <i>Listeria</i> spp., including pathogenic <i>Listeria monocytogenes</i> and <i>Listeria ivanovii</i>, on fresh vegetables in the markets of Abidjan (Cote d’Ivoire)
Presence of <i>Listeria</i> spp., including pathogenic <i>Listeria monocytogenes</i> and <i>Listeria ivanovii</i>, on fresh vegetables in the markets of Abidjan (Cote d’Ivoire) Open
Listeria monocytogenes is a pathogenic bacterium that can contaminate various food products and is the causative agent of listeriosis, a severe and life-threatening foodborne illness. This study aimed to assess the occurrence of Listeria s…
View article: Data from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility
Data from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility Open
Background:Neuroblastoma is rarer in African American (AA) children compared with American children of European descent. AA children affected with neuroblastoma, however, more frequently develop the high-risk form of the disease.Methods:We…
View article: Evaluation of clinical, analytical, and genotyping performance of Hex L1 real-time PCR coupled with high-resolution melting curve analysis for fowl adenovirus outbreak investigation in Morocco
Evaluation of clinical, analytical, and genotyping performance of Hex L1 real-time PCR coupled with high-resolution melting curve analysis for fowl adenovirus outbreak investigation in Morocco Open
Fowl adenoviruses (FAdVs) are widespread viruses in poultry populations, responsible for several severe diseases, including Inclusion Body Hepatitis (IBH), Adenoviral Gizzard Erosion (AGE), and Hepatitis-Hydropericardium Syndrome (HHP). Th…
View article: Supplementary Figure from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility
Supplementary Figure from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility Open
Supplementary Figure from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility
View article: Supplementary Figure from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility
Supplementary Figure from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility Open
Supplementary Figure from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility
View article: Supplementary Figure from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility
Supplementary Figure from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility Open
Supplementary Figure from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility
View article: Supplementary Table S8 from Genetic Susceptibility to Nonalcoholic Fatty Liver Disease and Risk for Pancreatic Cancer: Mendelian Randomization
Supplementary Table S8 from Genetic Susceptibility to Nonalcoholic Fatty Liver Disease and Risk for Pancreatic Cancer: Mendelian Randomization Open
Supplementary Table S8 shows results of univariate analysis for 17 imaging and biopsy validated SNPs in the PanC4 sample
View article: Supplementary Figure from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility
Supplementary Figure from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility Open
Supplementary Figure from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility
View article: Supplementary Table 1 from Genetic Predictors for Fecal Propionate and Butyrate-Producing Microbiome Pathway Are Not Associated with Colorectal Cancer Risk: A Mendelian Randomization Analysis
Supplementary Table 1 from Genetic Predictors for Fecal Propionate and Butyrate-Producing Microbiome Pathway Are Not Associated with Colorectal Cancer Risk: A Mendelian Randomization Analysis Open
Supplementary Table 1 shows the power calculation for the associations of PWY-5022 and propionate with CRC risk.
View article: Supplementary Table S6 from Genetic Susceptibility to Nonalcoholic Fatty Liver Disease and Risk for Pancreatic Cancer: Mendelian Randomization
Supplementary Table S6 from Genetic Susceptibility to Nonalcoholic Fatty Liver Disease and Risk for Pancreatic Cancer: Mendelian Randomization Open
Supplementary Table S6 shows results of univariate analysis for 22 imaging defined nonalcoholic fatty liver disease SNPs in the PanC4 sample
View article: What genetic tests are used to diagnose hereditary spastic paraplegia?
What genetic tests are used to diagnose hereditary spastic paraplegia? Open
Genetic testing for hereditary spastic paraplegia involves analyzing specific genes depending on the subtype and inheritance pattern, utilizing modern sequencing technologies such as NGS and WES.
View article: A new tandem repeat-based genotyping scheme for the global surveillance of Xanthomonas citri pv. mangiferaeindicae, an understudied bacterial pathogen of major importance to mango and cashew production
A new tandem repeat-based genotyping scheme for the global surveillance of Xanthomonas citri pv. mangiferaeindicae, an understudied bacterial pathogen of major importance to mango and cashew production Open
Bacterial canker, caused by Xanthomonas citri pv. mangiferaeindicae ( Xcm ), is a disease that has a devastating impact on mango and cashew industries in many regions. Yet, despite its agricultural importance for these Anacardiaceae specie…
View article: Infantile‐Onset Ascending Hereditary Spastic Paraplegia due to a Homozygous <scp> <i>ALS2</i> </scp> Exons 24–25 Deletion: Expanding the Genotypic <scp> <i>Spectrum</i> </scp>
Infantile‐Onset Ascending Hereditary Spastic Paraplegia due to a Homozygous <span> <i>ALS2</i> </span> Exons 24–25 Deletion: Expanding the Genotypic <span> <i>Spectrum</i> </span> Open
We describe a novel homozygous intragenic deletion in the ALS2 gene in an 8‐year‐old boy with Infantile‐onset Ascending Hereditary Spastic Paraplegia (IAHSP) and oculomotor apraxia, thereby contributing to the expanding genetic landscape o…
View article: Supplementary table from Overview of Research on Germline Genetic Variation in Immune Genes and Cancer Outcomes
Supplementary table from Overview of Research on Germline Genetic Variation in Immune Genes and Cancer Outcomes Open
Supplementary table from Overview of Research on Germline Genetic Variation in Immune Genes and Cancer Outcomes
View article: Clinical and molecular genetic analysis of a Chinese patient with Cockayne syndrome caused by ERCC8 gene synonymous variant at splicing site and exon 1 deletion
Clinical and molecular genetic analysis of a Chinese patient with Cockayne syndrome caused by ERCC8 gene synonymous variant at splicing site and exon 1 deletion Open
Background Cockayne Syndrome (CS) is a rare autosomal recessive genetic disease, mainly caused by ERCC8 and ERCC6 gene defect. However, many of its molecular characteristics remain unclear. In this study, molecular genetic analysis was per…
View article: Supplementary Table S3 from Genetic Susceptibility to Nonalcoholic Fatty Liver Disease and Risk for Pancreatic Cancer: Mendelian Randomization
Supplementary Table S3 from Genetic Susceptibility to Nonalcoholic Fatty Liver Disease and Risk for Pancreatic Cancer: Mendelian Randomization Open
Supplementary Table S3 shows results of univariate analysis for 36 biopsy-confirmed nonalcoholic fatty liver disease SNPs in the PanScan sample
View article: Data from Overview of Research on Germline Genetic Variation in Immune Genes and Cancer Outcomes
Data from Overview of Research on Germline Genetic Variation in Immune Genes and Cancer Outcomes Open
Since the late 19th century, the immune system has been known to play a role in cancer risk, initiation, and progression. Genome-wide association studies (GWAS) have identified hundreds of genetic risk loci for autoimmune and inflammatory …
View article: Supplementary Data from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility
Supplementary Data from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility Open
Supplementary Data from Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma Susceptibility
View article: Phylogenomic analysis and genetic mechanisms of antifungal resistance in clinical isolates of <i>Candida glabrata</i> ( <i>Nakaseomyces glabratus</i> ) from across Canada, 2013–2020
Phylogenomic analysis and genetic mechanisms of antifungal resistance in clinical isolates of <i>Candida glabrata</i> ( <i>Nakaseomyces glabratus</i> ) from across Canada, 2013–2020 Open
Candida glabrata ( Nakaseomyces glabratus ) is an important cause of invasive fungal infections and may exhibit reduced susceptibility toward antifungal drugs. Here, we used whole-genome sequencing to investigate the genomic phylogeny and …
View article: Supplementary Table S7 from Genetic Susceptibility to Nonalcoholic Fatty Liver Disease and Risk for Pancreatic Cancer: Mendelian Randomization
Supplementary Table S7 from Genetic Susceptibility to Nonalcoholic Fatty Liver Disease and Risk for Pancreatic Cancer: Mendelian Randomization Open
Supplementary Table S7 shows results of univariate analysis for 36 biopsy-confirmed nonalcoholic fatty liver disease SNPs in the PanC4 sample