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Search results (130)

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Interpretation of Survival Outcomes in Multicancer Early Detection Testing Requires Caution

Houlston R. et al, (2026), JCO Precision Oncology, 10

Science Outreach: Providing an Authentic Independent Research Opportunity in Materials Science to School Students.

Garrido N. et al, (2026), Journal of chemical education, 103, 2986 - 2994

Contralateral breast cancer risks for BRCA1, BRCA2, PALB2, CHEK2, and ATM pathogenic variant carriers in two large cohort studies.

Allen I. et al, (2026), BJC reports, 4

Vibrotactile positional therapy for the treatment of positional obstructive sleep apnoea: a multicentre, randomised controlled trial

Kelly JL. et al, (2026), Thorax, 81, 370 - 379

Lung ventilation and the physiology of breathing

Phyu SL. and Turnbull CD., (2026), Surgery (Oxford), 44, 167 - 174

Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline PALB2 sequence variants.

Richardson ME. et al, (2026), American journal of human genetics

Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline ATM sequence variants.

Richardson ME. et al, (2026), American journal of human genetics

Association of Y-chromosomal gr/gr deletions with testicular germ cell tumor: whole-genome analysis of 198,306 individuals.

Choi S. et al, (2026)

Novel drinkable oxygen nanobubbles: a pilot randomised, double-blind, cross-over trial on patients with pulmonary fibrosis

Sheth M. et al, (2026), BMJ Innovations, 12, 51 - 56

The Testicular Cancer Consortium (TECAC): Filling Knowledge Gaps in the Genetic Etiology of Testicular Germ Cell Tumors.

Kanetsky PA. et al, (2026), Andrology

Quantifying evidence for phenotypic specificity (PP4) for syndromic phenotypes: Large-scale integration of rare germline FH variants from diagnostic laboratory testing for HLRCC and renal cancer.

Allen S. et al, (2025), Genetics in medicine : official journal of the American College of Medical Genetics, 27

APC I1307K and clinical management: insights from UK Biobank association analysis of colorectal and other cancer risks in Ashkenazi and non-Ashkenazi whites.

Allen S. et al, (2025), Journal of medical genetics, 62, 767 - 771

Availability of benign missense variant "truthsets" for validation of functional assays: Current status and a systematic approach.

Rowlands CF. et al, (2025), American journal of human genetics, 112, 2281 - 2294

Proposed framework for triage of putative germline variants detected via tumour genomic testing in UK oncology practice.

McVeigh TP. et al, (2025), Journal of medical genetics, 62, 709 - 719

Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline PALB2 sequence variants.

Richardson ME. et al, (2025), American journal of human genetics, 112, 2266 - 2280

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