# Journal of Human Genetics

**Type:** Journals  
**Canonical URL:** https://scholariq.org/journals/journal-of-human-genetics/

## Facts

| Field | Value |
| --- | --- |
| Open Access | false |
| ISSN-L | 1434-5161 |
| ISSNs | 1434-5161,1435-232X |
| OpenAlex ID | https://openalex.org/S31156748 |
| Publisher | Springer Nature |

## Journal papers

Showing 12 of 14.

- [Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction](https://scholariq.org/papers/identification-of-a-novel-non-coding-rna-miat-that-confers-risk-of-myocardial/)
- [Recent trends in microRNA research into breast cancer with particular focus on the associations between microRNAs and intrinsic subtypes](https://scholariq.org/papers/recent-trends-in-microrna-research-into-breast-cancer-with-particular-focus-on/)
- [Association of VKORC1 and CYP2C9 polymorphisms with warfarin dose requirements in Japanese patients](https://scholariq.org/papers/association-of-vkorc1-and-cyp2c9-polymorphisms-with-warfarin-dose-requirements/)
- [Identification of six novel MYH9 mutations and genotype–phenotype relationships in autosomal dominant macrothrombocytopenia with leukocyte inclusions](https://scholariq.org/papers/identification-of-six-novel-myh9-mutations-and-genotype-phenotype-relationships/)
- [Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations](https://scholariq.org/papers/genetic-causes-of-nonsyndromic-hearing-loss-in-iran-in-comparison-with-other/)
- [Nationwide survey on cerebrotendinous xanthomatosis in Japan](https://scholariq.org/papers/nationwide-survey-on-cerebrotendinous-xanthomatosis-in-japan/)
- [Molecular epidemiology, genotype–phenotype correlation and BH4 responsiveness in Spanish patients with phenylketonuria](https://scholariq.org/papers/molecular-epidemiology-genotype-phenotype-correlation-and-bh4-responsiveness-in/)
- [Association of genetic polymorphisms in MDM2, PTEN and P53 with risk of esophageal squamous cell carcinoma](https://scholariq.org/papers/association-of-genetic-polymorphisms-in-mdm2-pten-and-p53-with-risk-of/)
- [Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms](https://scholariq.org/papers/denaturing-high-performance-liquid-chromatography-screening-of-the-long-qt/)
- [Molecular diagnose of a large hearing loss population from China by targeted genome sequencing](https://scholariq.org/papers/molecular-diagnose-of-a-large-hearing-loss-population-from-china-by-targeted/)
- [Association studies of TNFSF4, TNFAIP3 and FAM167A-BLK polymorphisms with primary Sjogren’s syndrome in Han Chinese](https://scholariq.org/papers/association-studies-of-tnfsf4-tnfaip3-and-fam167a-blk-polymorphisms-with-primary/)
- [Whole-exome sequencing reveals known and novel variants in a cohort of intracranial vertebral–basilar artery dissection (IVAD)](https://scholariq.org/papers/whole-exome-sequencing-reveals-known-and-novel-variants-in-a-cohort-of/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.