Genetics and genomic medicine in Israel.

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

Who cites it

24 citing papers in PubMed.

1. The Genetic Landscape of Inherited Retinal Diseases in the Israeli Population.Investigative ophthalmology & visual science · 2026
   Article
2. More of the same? Israel's expanded carrier screening for cystic fibrosis.European journal of human genetics : EJHG · 2025
   Article
3. Predictors of short stature in Israeli children aged 6-7 years: a retrospective cohort study.Israel journal of health policy research · 2025
   Article
4. Non-Uptake of Newborn Screening in Planned Homebirth Is Associated with Preventive Health Practices for Infants: A Retrospective Case-Control Study.International journal of neonatal screening · 2025
   Article
5. Worldwide patterns and trends in ovarian cancer incidence by histological subtype: a population-based analysis from 1988 to 2017.EClinicalMedicine · 2025
   Article
6. Potential Founder Variants in COL4A4 Identified in Bukharian Jews Linked to Autosomal Dominant and Autosomal Recessive Alport Syndrome.Genes · 2023
   Article
7. Community data-driven approach to identify pathogenic founder variants for pan-ethnic carrier screening panels.Human genomics · 2023
   Article
8. Prevalence and spectrum of DNA mismatch repair gene variation in the general Chinese population.Journal of medical genetics · 2022
   Article
9. Diagnostic Yield and Economic Implications of Whole-Exome Sequencing for ASD Diagnosis in Israel.Genes · 2021
   Article
10. Recommendation of premarital genetic screening in the Syrian Jewish community based on mutation carrier frequencies within Syrian Jewish cohorts.Molecular genetics & genomic medicine · 2021
    Article
11. International trends in ovarian cancer incidence from 1973 to 2012.Archives of gynecology and obstetrics · 2021
    Article
12. A study of normal copy number variations in Israeli population.Human genetics · 2021
    Article
13. Regulating reproductive genetic services: dealing with spiral-shaped processes and techno-scientific imaginaries.Journal of assisted reproduction and genetics · 2021
    Article
14. Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1.Clinical genetics · 2020
    Article
15. The Israeli national population program of genetic carrier screening for reproductive purposes. How should it be continued?Israel journal of health policy research · 2019
    Article
16. The role of AGG interruptions in the FMR1 gene stability: A survey in ethnic groups with low and high rate of consanguinity.Molecular genetics & genomic medicine · 2019
    Article
17. Genetics of hearing loss in the Arab population of Northern Israel.European journal of human genetics : EJHG · 2018
    Article
18. Genomic medicine for kidney disease.Nature reviews. Nephrology · 2018
    Review
19. Looking back and looking forward.Molecular genetics & genomic medicine · 2018
    Article
20. International patterns and trends in ovarian cancer incidence, overall and by histologic subtype.International journal of cancer · 2017
    Article

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

Authors and funding

1 author.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.