Integrated multiomics revealed adenosine signaling predict immunotherapy response and regulate tumor ecosystem of melanoma

2024-9-15

Reply to correspondence by Deora et al. in Human Genomics 18, article no.: 52 (2024): critical insights on “Association of the C allele of rs479200 in the EGLN1 gene with COVID‑19 severity in Indian population: a novel finding”

2024-9-12

The effect of family structure on the still-missing heritability and genomic prediction accuracy of type 2 diabetes

2024-9-11

AI-derived comparative assessment of the performance of pathogenicity prediction tools on missense variants of breast cancer genes

2024-9-11

Association of novel DNAH11 variants with asthenoteratozoospermia lead to male infertility

2024-9-11

Multi-regional genomic and transcriptomic characterization of a melanoma-associated oral cavity cancer provide evidence for CASP8 alteration-mediated field cancerization

2024-9-7

Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype

2024-9-4

The T-cell repertoire of Spanish patients with COVID-19 as a strategy to link T-cell characteristics to the severity of the disease

2024-9-4

Polygenic risk score portability for common diseases across genetically diverse populations

2024-9-2

Characterizing PFAS hazards and risks: a human population-based in vitro cardiotoxicity assessment strategy

2024-9-2

Biological and clinical relevance of correlated expression levels of coding and long noncoding RNAs in HPV16 positive cervical cancers

2024-8-29

Variant Impact Predictor database (VIPdb), version 2: trends from three decades of genetic variant impact predictors

2024-8-28

Rapid discrimination between deleterious and benign missense mutations in the CAGI 6 experiment

2024-8-27

Shaping the future of kidney genetics in Australia: proceedings from the KidGen policy implementation workshop 2023

2024-8-17

Assessing the contribution of genes involved in monogenic bone disorders to the etiology of atypical femoral fractures

2024-8-15

Public perceptions of international genetic information sharing for biomedical research in China: a case study of the social media debate on the article “A Pangenome Reference of 36 Chinese Populations” published in Nature

2024-8-7

Genome-wide association study and meta-analysis of phytosterols identifies a novel locus for serum levels of campesterol

2024-8-1

Clinical outcomes of patients with mut-type methylmalonic acidemia identified through expanded newborn screening in China

2024-7-29

A qualitative approach to assess the opinion of physicians about the challenges and prospects of pharmacogenomic testing implementation in clinical practice in Greece

2024-7-19

Targeted panel sequencing of pharmacogenes and oncodrivers in colorectal cancer patients reveals genes with prognostic significance

2024-7-19

Genetic distance and ancestry proportion modify the association between maternal genetic risk score of type 2 diabetes and fetal growth

2024-7-19

Identification of novel immune-related signatures for keloid diagnosis and treatment: insights from integrated bulk RNA-seq and scRNA-seq analysis

2024-7-16

Post-implantation analysis of genomic variations in the progeny from developing fetus to birth

2024-7-15

Pharmacogenetics in Italy: current landscape and future prospects

2024-7-10

An investigation of the molecular characterization of the tripartite motif (TRIM) family and primary validation of TRIM31 in gastric cancer

2024-7-9

Association of lipid-lowering drugs with risk of sarcopenia: a drug target mendelian randomization study and meta-analysis

2024-7-3

The cuproptosis-related signature predicts the prognosis and immune microenvironments of primary diffuse gliomas: a comprehensive analysis

2024-7-2

A novel variant in GAS2 is associated with autosomal dominant nonsyndromic hearing impairment in a Chinese family

2024-7-2

Unveiling the molecular landscape of cognitive aging: insights from polygenic risk scores, DNA methylation, and gene expression

2024-7-2

EU surveys insights: analytical tools, future directions, and the essential requirement for reference materials in wastewater monitoring of SARS-CoV-2, antimicrobial resistance and beyond

2024-6-27

Elucidating the role of liver enzymes as markers and regulators in ovarian cancer: a synergistic approach using Mendelian randomization, single-cell analysis, and clinical evidence

2024-6-24

Polygenic subtype identified in ACCORD trial displays a favorable type 2 diabetes phenotype in the UKBiobank population

2024-6-22

Bayesian-frequentist hybrid inference framework for single cell RNA-seq analyses

2024-6-20

Germline mutations of breast cancer susceptibility genes through expanded genetic analysis in unselected Colombian patients

2024-6-18

Growth characteristics of HCT116 xenografts lacking asparagine synthetase vary according to sex

2024-6-17

Application of mendelian randomization in ocular diseases: a review

2024-6-17

Comprehensive bioinformatics analysis of human cytomegalovirus pathway genes in pan-cancer

2024-6-17

Next-generation sequencing profiling of miRNAs in individuals with 22q11.2 deletion syndrome revealed altered expression of miR-185-5p

2024-6-13

Systematic analysis of IGF2BP family members in non-small-cell lung cancer

2024-6-12

Shared genetic effect of kidney function on bipolar and major depressive disorders: a large-scale genome-wide cross-trait analysis

2024-6-11

Development of novel lysosome-related signatures and their potential target drugs based on bulk RNA-seq and scRNA-seq for diabetic foot ulcers

2024-6-11

Trace amine associated receptor 1: predicted effects of single nucleotide variants on structure-function in geographically diverse populations

2024-6-11

Genetic analysis of 106 sporadic cases with hearing loss in the UAE population

2024-6-7

Deep learning-based pathway-centric approach to characterize recurrent hepatocellular carcinoma after liver transplantation

2024-6-5

Sperm epigenetics and male infertility: unraveling the molecular puzzle

2024-6-4

Mendelian randomization evidence based on European ancestry for the causal effects of leukocyte telomere length on prostate cancer

2024-6-3

Pan-cancer analysis of CDKN2A alterations identifies a subset of gastric cancer with a cold tumor immune microenvironment

2024-5-31

Assessment of nucleic acid extraction protocols for antibiotic resistance genes (ARGs) quantification in aircraft wastewater

2024-5-30

Evolutionary and functional analyses of LRP5 in archaic and extant modern humans

2024-5-27

Critical insights on “Association of the C allele of rs479200 in the EGLN1 gene with COVID‑19 severity in Indian population: a novel finding”

2024-5-24