Frontiers in Genetics | Statistical Genetics and Methodology

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Journal notices

p53 bound to DNA
p53 prevents cancer formation and acts as a guardian of the genome. Mutations in the p53 gene contribute to about half of the cases of human cancer. 3d rendering

Research Topic of the Month

Featuring recent ebook published in Rare Diseases Research and Diagnosis in Low - and Middle-Income Countries.

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Call for Submissions

Seeking contributions for Research Topic in Genomic Methods and Applications for Malaria Surveillance.

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Thank you to everyone who visited us at the American Society of Human Genetics meeting! It was a pleasure connecting with you all.

New Research Topic Published

Seeking contributions to our new published collection in "Nutrigenetics and Nutrigenomics in Livestock". Submit your research now!

Statistical Genetics and Methodology

Submit your research

Author guidelines

Editor guidelines

Peer review

Publishing fees

Journal notices

Trending Article

Research Topic of the Month

Call for Submissions

Conference Stand at the American Society of Human Genetics

New Research Topic Published

Editors

simon charles heath

saonli basu

thibaud boutin

alexandre bureau

Articles

Molecular Mechanisms of TTC21B Gene Mutations in Nephronophthisis Type 12 and Genetic Prevention through PGT

Identification and functional analysis of a novel CSNK2A1 frameshift variant in stillbirth

A novel dinucleotide variant at 5′ splice sites in the F8 gene causes exon 19 skipping in a Chinese family with hemophilia A

Mining for gene-environment and gene-gene interactions: parametric and non-parametric tests for detecting variance quantitative trait loci

Research Topics

Unraveling DNA Molecular Structures and Their Epigenetic Implications: Advances in Spectroscopic and Biophysical Approaches.

Moving towards haplotype-based analysis to accelerate genetic gains in both crops and livestock

Multi-Omics Insights into Autoimmune Diseases and Major Chronic Non-Communicable Diseases

Functional Study of Novel VUS (Variant of Uncertain Significance) Mutations in Single-gene Inherited Disease, Volume II