Epidemiology, cancer genetics and microarrays: making correct inferences, using appropriate designs

Incidence Rates of Melanoma and Lung Cancer Are Generally Low in the Lynch Syndromes and Vary Across path_MMR Variants: A Prospective Lynch Syndrome Database Report.

Cancers·2026

Is health a basic human right or a commodity? Travelling the difficult road towards equity of outcomes.

The New Zealand medical journal·2026

Subsequent primary cancer risks for non-hereditary colorectal cancer survivors.

EClinicalMedicine·2026

Associations of epidemiologic risk factors with Fusobacterium nucleatum and bacterial alpha diversity in the colorectal tumor-associated microbiota.

Cancer causes & control : CCC·2026

Genetic risk factors modulate the association between physical activity and colorectal cancer.

BMC medicine·2026

Nurse endoscopists: a rational response to rising rates of young-onset colorectal cancer in Aotearoa New Zealand.

The New Zealand medical journal·2025

'Tango' or 'tangle' in transcriptional condensates.

Trends in genetics : TIG·2026

A categorization of spatial transcriptomics methods for cell-cell communication analysis.

Trends in genetics : TIG·2026

Rethinking evidence for epigenetic inheritance in human research.

Trends in genetics : TIG·2026

Everything, everywhere: FSHD as a model for complex genetic disease.

Trends in genetics : TIG·2026

Post-transcriptional regulation of allele-specific expression.

Trends in genetics : TIG·2026

B chromosomes put the 'super' in supernumerary.

Trends in genetics : TIG·2026

Unveiling the Immune Mechanisms of Hypertension With Single-Cell Transcriptome-Wide Mendelian Randomization.

FASEB journal : official publication of the Federation of American Societies for Experimental Biology·2026

Case Report: Functional validation of a PKD1 c.7489 + 5G>A variant in an ADPKD family.

Frontiers in genetics·2026

An analysis of intestinal morphology and incretin-producing cells after sleeve gastrectomy in male mice.

Journal of molecular endocrinology·2026

MRI-based assessment of fetal brain gyrification: Reliability across two methods.

Neuroimage. Reports·2026

Transcriptome-wide splicing analysis reveals HuR-regulated post-transcriptional programs in osteocytes.

iScience·2026

Structural variants contribute substantially to complex trait heritability.

Research square·2026

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Epidemiology, cancer genetics and microarrays: making correct inferences, using appropriate designs

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Incidence Rates of Melanoma and Lung Cancer Are Generally Low in the Lynch Syndromes and Vary Across path_MMR Variants: A Prospective Lynch Syndrome Database Report.

Is health a basic human right or a commodity? Travelling the difficult road towards equity of outcomes.

Subsequent primary cancer risks for non-hereditary colorectal cancer survivors.

Associations of epidemiologic risk factors with Fusobacterium nucleatum and bacterial alpha diversity in the colorectal tumor-associated microbiota.

Genetic risk factors modulate the association between physical activity and colorectal cancer.

Nurse endoscopists: a rational response to rising rates of young-onset colorectal cancer in Aotearoa New Zealand.

'Tango' or 'tangle' in transcriptional condensates.

A categorization of spatial transcriptomics methods for cell-cell communication analysis.

Rethinking evidence for epigenetic inheritance in human research.

Everything, everywhere: FSHD as a model for complex genetic disease.

Post-transcriptional regulation of allele-specific expression.

B chromosomes put the 'super' in supernumerary.

Unveiling the Immune Mechanisms of Hypertension With Single-Cell Transcriptome-Wide Mendelian Randomization.

Case Report: Functional validation of a PKD1 c.7489 + 5G>A variant in an ADPKD family.

An analysis of intestinal morphology and incretin-producing cells after sleeve gastrectomy in male mice.

MRI-based assessment of fetal brain gyrification: Reliability across two methods.

Transcriptome-wide splicing analysis reveals HuR-regulated post-transcriptional programs in osteocytes.

Structural variants contribute substantially to complex trait heritability.

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Epidemiology, cancer genetics and microarrays: making correct inferences, using appropriate designs

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