Twenty-five years ago in Genetics: electrophoresis in the development of evolutionary genetics: milestone or millstone?

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics·2026

ZTTK Syndrome Expanding the Cardiac Phenotype: A Case of Shone's Complex With a Novel SON Variant and Focused Review of the Cardiac Manifestations in ZTTK Syndrome.

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Gonadal hormones and impulsivity facets: moderating roles of cortisol and anxiety.

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Diagnostic insights into Trisomy 21: a case of abnormal Inhibin A, beta-hCG, AFP, and ultrasound findings.

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Molecular Identification of HLA-DPB1*1651:01: A Novel Allele Discovered by Sequence Comparison of HLA-DPB1 Exon 2.

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Directions in evolutionary biology.

Locating regions of differential variability in DNA and protein sequences.

Nucleotide variation and conservation at the dpp locus, a gene controlling early development in Drosophila.

Detecting heterogeneity of substitution along DNA and protein sequences.

The detection of linkage disequilibrium in molecular sequence data.

Correlation between relatives for colorectal cancer mortality in familial adenomatous polyposis.

Epistasis and the changing fitness landscapes of SARS-CoV-2.

Genetic principles enabling the creation of bacteria-based therapeutics.

Discovery of a small peptide that increases yeast lifespan by enhancing the function of APCCdh1 in nondividing quiescent cells.

Screening for dual sgRNAs with comparable indel efficiencies enhances CRISPR-mediated large-fragment deletion.

Estimating cis and trans contributions to differences in gene regulation.

Genetic control of a multifunctional trait: The central role of a fatty acid synthase gene in regulating survival and sexual communication.

Extending the ATP9A-Related Phenotypic Spectrum: Indication of Schizophrenia Susceptibility.

ZTTK Syndrome Expanding the Cardiac Phenotype: A Case of Shone's Complex With a Novel SON Variant and Focused Review of the Cardiac Manifestations in ZTTK Syndrome.

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Molecular Identification of HLA-DPB1*1651:01: A Novel Allele Discovered by Sequence Comparison of HLA-DPB1 Exon 2.

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