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10021 results

Full text 2026

Successful experience with high-risk and family screening for Fabry disease in Ninghai County, Zhejiang Province, Eastern China: genotype‒phenotype analysis of the GLA IVS4 + 919G > A variant

Ge Z, Mao J, Dai Z, et al.

BACKGROUND: Fabry disease is a rare and non-specific disease that is difficult and expensive to diagnose. This study aimed to investigate the clinical phenotypes and genetic characteristics of patients with Fabry disease characterised by the …

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Bioinformatics
Full text 2026

Pembrolizumab and Paclitaxel in Patients with HR+/HER2- Breast Cancer with HER2-Enriched or Basal-like Subtypes

Conte B, Brasó-Maristany F, Pascual T, et al.

<h4>Purpose</h4>Hormone receptor-positive (HR+), HER2-negative (HER2-) metastatic breast cancer (mBC) is biologically distinct from early-stage disease, with a higher prevalence of genomically defined nonluminal subtypes, particularly the HER2-enriched (HER2-E) and basal-like subtypes. These tumors are highly …

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Bioinformatics
Full text 2026

Genetic-epigenetic interactions (meQTLs) in orofacial clefts etiology

Petrin AL, Machado-Paula LA, Keen HL, et al.

Understanding how genetic variants influence disease risk through molecular mechanisms remains a central challenge in complex disease genetics. Nonsyndromic orofacial clefts (OFCs) exemplify this challenge, with most risk loci residing in non-coding regions. We hypothesized …

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Epigenetics
Full text 2026

Single-cell RNA sequencing of leukocytes at the maternal-fetal interface in physiological and pathological Nodal-deficient pregnancies

Yull S, Pacis A, Girardet L, et al.

Leukocytes at the maternal-fetal interface have critical functions during pregnancy in the prevention of maternal reactivity towards fetal alloantigens, suppression of excess inflammation and promotion of placental angiogenesis. Failed maternal immune adaptations to pregnancy can …

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Single-Cell Transcriptomics
Full text 2025

Relational work in implementation: a qualitative analysis of intra- and inter- professional strategies leveraged in genomic multidisciplinary teams

Do TT, Martyn M, McEwen A, et al.

<h4>Background</h4>Relationships are foundational to successful implementation of innovations in healthcare. In genomic medicine, multidisciplinary teams with good communication are most effective to provide safe genomic care; however, working together could be challenging due to the …

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Bioinformatics
Full text 2026

A Cross-Tissue Multiomics Analysis Reveals the Protective Role of TGFBR3 in Postmenopausal Osteoporosis

Liu Y, Xie C, Yang K, et al.

<h4>Background</h4>Postmenopausal osteoporosis (PMO) develops as a result of pathological cross-tissue interactions. However, current experimental paradigms are constrained by their single-tissue focus, hindering efforts to discover systemwide regulatory genes.<h4>Objective</h4>We aimed to discover conserved genetic regulators of …

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Bioinformatics Single-Cell Transcriptomics
Full text 2026

Phenotypic spectrum of 11p15.5 duplications: parent-of-origin and copy number variant size shape outcomes from Silver-Russell to Beckwith-Wiedemann syndromes

Wang C, Zhang H, Wang M, et al.

BACKGROUND: Genomic imprinting at the 11p15.5 region is critically involved in fetal growth regulation. Disturbances in this region are primarily associated with two opposing growth disorders: Silver-Russell syndrome (SRS, growth restriction) and Beckwith-Wiedemann syndrome (BWS, …

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Structural Variants