# Human Molecular Genetics

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

## Facts

| Field | Value |
| --- | --- |
| Open Access | false |
| ISSN-L | 0964-6906 |
| ISSNs | 0964-6906,1460-2083 |
| OpenAlex ID | https://openalex.org/S166515463 |
| Publisher | Oxford University Press |

## Journal papers

Showing 12 of 61.

- [DNA methylation differences after exposure to prenatal famine are common and timing- and sex-specific](https://scholariq.org/papers/dna-methylation-differences-after-exposure-to-prenatal-famine-are-common-and/)
- [Accumulation of Krebs cycle intermediates and over-expression of HIF1α in tumours which result from germline FH and SDH mutations](https://scholariq.org/papers/accumulation-of-krebs-cycle-intermediates-and-over-expression-of-hif1-in-tumours/)
- [Non-coding genetic variants in human disease: Figure 1.](https://scholariq.org/papers/non-coding-genetic-variants-in-human-disease-figure-1/)
- [A genome-wide scan for common alleles affecting risk for autism](https://scholariq.org/papers/a-genome-wide-scan-for-common-alleles-affecting-risk-for-autism/)
- [Disruption of the neurexin 1 gene is associated with schizophrenia](https://scholariq.org/papers/disruption-of-the-neurexin-1-gene-is-associated-with-schizophrenia/)
- [Mutations in the Gene Encoding KRIT1, a Krev-1/rap1a Binding Protein, Cause Cerebral Cavernous Malformations (CCM1)](https://scholariq.org/papers/mutations-in-the-gene-encoding-krit1-a-krev-1-rap1a-binding-protein-cause/)
- [Somatic mutations of the von Hippel — Lindau disease tumour suppressor gene in non-familial clear cell renal carcinoma](https://scholariq.org/papers/somatic-mutations-of-the-von-hippel-lindau-disease-tumour-suppressor-gene-in-non/)
- [In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouse](https://scholariq.org/papers/in-frame-deletion-in-a-novel-centrosomal-ciliary-protein-cep290-nphp6-perturbs/)
- [Individual common variants exert weak effects on the risk for autism spectrum disorders](https://scholariq.org/papers/individual-common-variants-exert-weak-effects-on-the-risk-for-autism-spectrum/)
- [Lowering of Pkd1 expression is sufficient to cause polycystic kidney disease](https://scholariq.org/papers/lowering-of-pkd1-expression-is-sufficient-to-cause-polycystic-kidney-disease/)
- [Single base polymorphism at −511 in the human interleukin-1β gene (IL1β)](https://scholariq.org/papers/single-base-polymorphism-at-511-in-the-human-interleukin-1-gene-il1/)
- [Evidence of novel neuronal functions of dysbindin, a susceptibility gene for schizophrenia](https://scholariq.org/papers/evidence-of-novel-neuronal-functions-of-dysbindin-a-susceptibility-gene-for/)

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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.