Yearly Publication Trends - genetic variants

Year	Publication Count
2024	6897
2023	12820
2022	7726
2021	6359
2020	4795
2019	3092
2018	1953
2017	1844
2016	1560
2015	1297
2014	1262

Relevant Publications

Using GWAS and Machine Learning to Identify and Predict Genetic Variants Associated with Foodborne Bacteria Phenotypic Traits.

Issue Release: 2025

CRISPR-Mediated Viral Gene Knockout to Investigate Viral Evasion of Antiviral Innate Immunity.

Issue Release: 2025

Admixture mapping of cognitive function in diverse Hispanic and Latino adults: Results from the Hispanic Community Health Study/Study of Latinos.

Issue Release: 2024

Causal associations of gut microbiota and pulmonary tuberculosis: a two-sample Mendelian randomization study.

Issue Release: 2024

Allele-specific PCR with fluorescently labeled probes: criteria for selecting primers for genotyping.

Issue Release: 2024

Role of Vitamin D and Vitamin D Polymorphisms in COVID-19 Risk and Severity in Children: A Systematic Review.

Issue Release: 2024

[Clinical characteristics and genetic analysis of two children with X-linked Centronuclear myopathy due to variants of MTM1 gene].

Issue Release: 2024

Causal associations between the gut microbiota and multiple myeloma: a two-sample Mendelian randomization study.

Issue Release: 2024

PCCA variant rs16957301 is a novel AKI risk genotype-specific for patients who receive ICI treatment: Real-world evidence from All of Us cohort.

Issue Release: 2024

[Clinical characteristics and genetic analysis of a child with Neutral lipid storage disease with myopathy].

Issue Release: 2024

Variants in the Kallikrein Gene Family and Hypermobile Ehlers-Danlos Syndrome.

Issue Release: 2024

Association of genetic variants in soy isoflavones metabolism-related genes with lung cancer risk.

Issue Release: 2024

Investigating the role of killer cell immunoglobulin-like receptors and human leukocyte antigen genetic variants in hepatitis C virus infection.

Issue Release: 2024

Effectiveness of whole exome sequencing analyses in the molecular diagnosis of osteogenesis imperfecta.

Issue Release: 2024

Genetic Variations Affect Chemotherapy Outcomes: A Role of the Spindle-assembly Checkpoint.

Issue Release: 2024

Mapping of long interspersed element-1 (L1) insertions by TIPseq provides information about sub chromosomal genetic variation in human embryos.

Issue Release: 2024

Evolutionary variation in gene conversion at the avian MHC is explained by fluctuating selection, gene copy numbers and life history.

Issue Release: 2024

Understanding the genetic complexity of puberty timing across the allele frequency spectrum.

Issue Release: 2024

Unusual Voltage-Gated Sodium and Potassium Channelopathies Related to Epilepsy.

Issue Release: 2024

Concurrent of compound heterozygous variant of a novel in-frame deletion and the common hypomorphic haplotype in TBX6 and inherited 17q12 microdeletion in a fetus.

Issue Release: 2024

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