There is nothing 'incidental' about unrelated findings

An Adult Presentation of KIF11-Related MCLID Syndrome: Case Report and 40-Year Follow-Up.

American journal of medical genetics. Part A·2026

Pathogenic variants in the cohesin loader subunit MAU2 underlie a distinct Cornelia de Lange Syndrome subtype.

Nature communications·2026

Functional Data Strengthen Clinical Validation of PhenoScore Phenotype-Guided AI for ANKRD11 Missense Variants.

Clinical genetics·2026

Generation of a male isogenic pair and a female isogenic pair(R83C) for studying NAA10-related syndrome as part of a large Ogden syndrome biobank.

Stem cell research·2026

Pathogenic variants in the cohesin loader subunit MAU2 lead to a new Cornelia de Lange Syndrome subtype.

medRxiv : the preprint server for health sciences·2025

Distinct patterns of de novo coding variants contribute to Tourette Syndrome etiology.

bioRxiv : the preprint server for biology·2025

A cost-effective conventional endpoint PCR assay for HLA-B*13:01 genotyping to guide personalized dapsone therapy in leprosy in low-resource settings.

Personalized medicine·2026

Association of microRNA SNP variations and SNP-SNP interactions with breast cancer in Yemeni women.

Personalized medicine·2026

Engineering innovations for precision medicine: sensors, AI biomarkers, and predictive interventions.

Personalized medicine·2026

CAUSAL artificial intelligence and data-driven decision intelligence in personalized medicine: a review of healthcare informatics systems.

Personalized medicine·2026

B‑cell activating factor gene polymorphisms rs9514828 and rs1041569 increase preeclampsia risk.

Personalized medicine·2026

The historical evolution, technological transformation, and future vision of personalized medicine: a narrative review.

Personalized medicine·2026

Identification of the Novel HLA-B*57:212 Allele by Next-Generation Sequencing.

HLA·2026

Characterisation of the Novel HLA-DRB3*01:127 Allele by Next-Generation Sequencing.

HLA·2026

Early-Onset TRNT1-Related SIFD Syndrome with an Additional Monoallelic C7 Variant: A Pediatric Case Report.

Diagnostics (Basel, Switzerland)·2026

Identification of the Novel HLA-DQB1*06:556 Allele by Next-Generation Sequencing.

HLA·2026

The HLA-A*24:02:190 Allele Identified by Next-Generation Sequencing and Confirmed by Nanopore Sequencing.

HLA·2026

Characterisation of the Novel HLA-DQB1*05:01:56 Allele Using Next-Generation Sequencing in a Chinese Cord Blood Donor.

HLA·2026

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There is nothing 'incidental' about unrelated findings

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An Adult Presentation of KIF11-Related MCLID Syndrome: Case Report and 40-Year Follow-Up.

Pathogenic variants in the cohesin loader subunit MAU2 underlie a distinct Cornelia de Lange Syndrome subtype.

Functional Data Strengthen Clinical Validation of PhenoScore Phenotype-Guided AI for ANKRD11 Missense Variants.

Generation of a male isogenic pair and a female isogenic pair(R83C) for studying NAA10-related syndrome as part of a large Ogden syndrome biobank.

Pathogenic variants in the cohesin loader subunit MAU2 lead to a new Cornelia de Lange Syndrome subtype.

Distinct patterns of de novo coding variants contribute to Tourette Syndrome etiology.

A cost-effective conventional endpoint PCR assay for HLA-B*13:01 genotyping to guide personalized dapsone therapy in leprosy in low-resource settings.

Association of microRNA SNP variations and SNP-SNP interactions with breast cancer in Yemeni women.

Engineering innovations for precision medicine: sensors, AI biomarkers, and predictive interventions.

CAUSAL artificial intelligence and data-driven decision intelligence in personalized medicine: a review of healthcare informatics systems.

B‑cell activating factor gene polymorphisms rs9514828 and rs1041569 increase preeclampsia risk.

The historical evolution, technological transformation, and future vision of personalized medicine: a narrative review.

Identification of the Novel HLA-B*57:212 Allele by Next-Generation Sequencing.

Characterisation of the Novel HLA-DRB3*01:127 Allele by Next-Generation Sequencing.

Early-Onset TRNT1-Related SIFD Syndrome with an Additional Monoallelic C7 Variant: A Pediatric Case Report.

Identification of the Novel HLA-DQB1*06:556 Allele by Next-Generation Sequencing.

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There is nothing 'incidental' about unrelated findings

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