Other observed topics

genetic

Observed in 116 articles across 35 journals.

Steady

Latest share0.26%

Change vs baseline-0.08 pp

Months observed13

Latest monthJul 2026

Portfolio article share

Attention over this snapshot

13 monthly points

Journal breadth

Where it appears

Heart11
Journal of Medical Genetics11
BMJ Case Reports8
BMJ Open8
Gut7
Journal of Neurology, Neurosurgery & Psychiatry7
Lupus Science & Medicine7
BMJ Neurology Open5
British Journal of Ophthalmology5
Journal for ImmunoTherapy of Cancer4
Journal of Medical Ethics4
Archives of Disease in Childhood3

Co-occurrence

Explore nearby topics

Inspect the source signal

Article evidence

30 high-ranking examples

BMJ Oncology · 2026-07-20

Identification and management of genetic susceptibility to cancer: UK perspective

Phrase rank #2 · DOI 10.1136/bmjonc-2025-000849

Journal of Medical Genetics · 2026-01-20

Genetic and embryonic transcriptome analyses reveal the molecular and developmental basis of Mayer-Rokitansky-Küster-Hauser syndrome

Phrase rank #2 · DOI 10.1136/jmg-2025-110805

Journal of Neurology, Neurosurgery & Psychiatry · 2025-09-15

#8098 Genetic abnormalities in catatonia: a systematic review

Phrase rank #2 · DOI 10.1136/JNNP-2025-BNPA.23

BMJ Open Gastroenterology · 2025-09-14

Integrative genome-wide analysis unveils the genetic landscape of gallstone disease and highlights novel loci with therapeutic potential

Phrase rank #2 · DOI 10.1136/bmjgast-2025-001976

BMJ Case Reports · 2026-06-01

Gonadotropin-releasing hormone receptor mutation as a cause of pubertal delay

Phrase rank #4 · DOI 10.1136/bcr-2025-271583

JME Practical Bioethics · 2026-01-07

Autonomy, oppression and genetic enhancements

Phrase rank #4 · DOI 10.1136/jmepb-2025-000007

Heart · 2025-09-11

Synergistic effects of female-specific conditions and genetic risk on cardiometabolic disease: a cohort study

Phrase rank #4 · DOI 10.1136/heartjnl-2024-325355

Heart · 2025-08-13

1-030 Mainstream genetic testing in an ICC specialist centre: experience under national testing criteria

Phrase rank #4 · DOI 10.1136/heartjnl-2025-BCS.28

Gut · 2026-06-26

IDDF2026-ABS-0523 Genetic susceptibility to helicobacter pylori infection and its genetic association with gastric cancer

Phrase rank #5 · DOI 10.1136/gutjnl-2026-IDDF.159

Heart · 2026-06-09

238 Clinical utility of genetic testing in thoracic aortopathy: a five-year single-centre audit

Phrase rank #5 · DOI 10.1136/heartjnl-2026-BCS.16

BMJ Open Respiratory Research · 2026-05-07

O11 Using genetic and longitudinal data to understand the role of insomnia in the relationship between major depression and type 2 diabetes

Phrase rank #5 · DOI 10.1136/bmjresp-2026-BSS.11

Archives of Disease in Childhood - Fetal and Neonatal Edition · 2026-04-14

Diagnostic yield and imaging: aetiology correlations in prenatal intracranial haemorrhage–a retrospective cohort study

Phrase rank #5 · DOI 10.1136/archdischild-2025-330148

British Journal of Ophthalmology · 2026-03-20

Genetic associations of high myopia

Phrase rank #5 · DOI 10.1136/bjo-2025-327791

RMD Open · 2026-02-25

Tackling the diagnosis of HA20 in children: challenges of a highly variable clinical and genetic spectrum

Phrase rank #5 · DOI 10.1136/rmdopen-2025-006379

Journal of Medical Ethics · 2025-09-22

Genetic research and the collective good: participants as leaders to reconcile individual and public interests

Phrase rank #5 · DOI 10.1136/jme-2022-108867

Journal of Medical Ethics · 2025-08-20

Should newborn genetic testing for autism be introduced?

Phrase rank #5 · DOI 10.1136/jme-2024-110166

Heart · 2025-08-13

5-025 Mainstreaming genetic testing in a heart failure service

Phrase rank #5 · DOI 10.1136/heartjnl-2025-BCS.167

Heart · 2026-06-09

422 Mammalian epigenomic conservation of promoters and enhancers in the heart associates with trait-associated variation and impacts cardiomyocyte phenotypes

Phrase rank #6 · DOI 10.1136/heartjnl-2026-BCS.327

Journal of Neurology, Neurosurgery & Psychiatry · 2026-05-14

Genetic risk in a warming world

Phrase rank #6 · DOI 10.1136/jnnp-2025-338187

BMJ Mental Health · 2026-03-10

Sex differences in familial risk and genetic components of suicide attempts: a register-based cohort study in Sweden

Phrase rank #6 · DOI 10.1136/bmjment-2025-302082

Lupus Science & Medicine · 2026-03-01

PO:06:171 Clinical heterogeneity in systemic lupus erythematosus: exploring the impact of genetic risk profiles

Phrase rank #6 · DOI 10.1136/lupus-2026-el.233

BMJ Open · 2026-01-21

Weight-loss effects of macronutrient-based diets modified by genetic variants: a protocol for systematic review of randomised controlled trials

Phrase rank #6 · DOI 10.1136/bmjopen-2025-110935

Journal of Medical Genetics · 2025-12-25

Comprehensive genetic landscapes and clinical heterogeneity in nanophthalmos: new insights from a large Chinese cohort

Phrase rank #6 · DOI 10.1136/jmg-2025-110905

Occupational and Environmental Medicine · 2025-11-02

Gene–occupational exposure interactions in small airways obstruction in the UK Biobank: a cross-sectional study

Phrase rank #6 · DOI 10.1136/oemed-2025-110112

BMJ Neurology Open · 2025-10-23

CS16 Genetic testing in motor neuron disease: prevalence, implications, and emerging therapies

Phrase rank #6 · DOI 10.1136/bmjno-2025-ANZAN.24

BMJ Open · 2025-09-16

Genetic polymorphisms contributing to hearing loss in children treated with platinum agents: a systematic review and meta-analysis protocol

Phrase rank #6 · DOI 10.1136/bmjopen-2025-103735

Heart · 2026-06-09

197 Improving genetic testing pathways in idiopathic pulmonary arterial hypertension

Phrase rank #7 · DOI 10.1136/heartjnl-2026-BCS.86

Journal of Scleroderma and Related Disorders · 2026-06-05

P.046 Impact of genetic background on topoisomerase immunization in mouse model

Phrase rank #7 · DOI 10.1136/JSRD-2026-SSWC.98

Journal of Medical Genetics · 2026-04-29

Uterine serous carcinoma and germline genetic testing: patterns of referral, completion and pathogenic variant detection

Phrase rank #7 · DOI 10.1136/jmg-2025-111285

Heart · 2026-01-28

Comprehensive risk factor analysis of sick sinus syndrome: a genetic, sociodemographic, clinical and laboratory investigation using the UK Biobank data

Phrase rank #7 · DOI 10.1136/heartjnl-2025-327272