# Molecular Genetics & Genomic Medicine

**Type:** Journals  
**Canonical URL:** https://scholariq.org/journals/molecular-genetics-and-genomic-medicine/

## Facts

| Field | Value |
| --- | --- |
| APC (USD) | 2,700 |
| Citations | 33,382 |
| h-index | 58 |
| Homepage | https://onlinelibrary.wiley.com/journal/23249269 |
| Open Access | true |
| ISSN-L | 2324-9269 |
| ISSNs | 2324-9269 |
| OpenAlex ID | https://openalex.org/S2764373787 |
| Publisher | Wiley |
| Works | 2,886 |

## Journal papers

- [Current status of beta‐thalassemia and its treatment strategies](https://scholariq.org/papers/current-status-of-beta-thalassemia-and-its-treatment-strategies/)
- [Integrated bioinformatics analysis of key genes involved in progress of colon cancer](https://scholariq.org/papers/integrated-bioinformatics-analysis-of-key-genes-involved-in-progress-of-colon/)
- [Evaluation of copy number variant detection from panel‐based next‐generation sequencing data](https://scholariq.org/papers/evaluation-of-copy-number-variant-detection-from-panel-based-next-generation/)
- [Homozygous <i>GDF2</i> nonsense mutations result in a loss of circulating BMP9 and BMP10 and are associated with either PAH or an “HHT‐like” syndrome in children](https://scholariq.org/papers/homozygous-i-gdf2-i-nonsense-mutations-result-in-a-loss-of-circulating-bmp9-and/)
- [Genotype–phenotype investigation of 35 patients from 11 unrelated families with camptodactyly–arthropathy–coxa vara–pericarditis (<scp>CACP</scp>) syndrome](https://scholariq.org/papers/genotype-phenotype-investigation-of-35-patients-from-11-unrelated-families-with/)
- [A novel lncRNA‐mediated <i>trans</i>‐regulatory mechanism in the development of cleft palate in mouse](https://scholariq.org/papers/a-novel-lncrna-mediated-i-trans-i-regulatory-mechanism-in-the-development-of/)
- [Increased frequency of FBN1 frameshift and nonsense mutations in Marfan syndrome patients with aortic dissection](https://scholariq.org/papers/increased-frequency-of-fbn1-frameshift-and-nonsense-mutations-in-marfan-syndrome/)
- [Medical genetics and genomic medicine in Nigeria](https://scholariq.org/papers/medical-genetics-and-genomic-medicine-in-nigeria/)
- [Clinical and genetic analysis of lipoprotein glomerulopathy patients caused by <i>APOE</i> mutations](https://scholariq.org/papers/clinical-and-genetic-analysis-of-lipoprotein-glomerulopathy-patients-caused-by-i/)
- [Clinical and molecular characterization of five Chinese patients with autosomal recessive osteopetrosis](https://scholariq.org/papers/clinical-and-molecular-characterization-of-five-chinese-patients-with-autosomal/)

## Journal top topics

Showing 8 of 25.

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Connective tissue disorders research](https://scholariq.org/topics/connective-tissue-disorders-research/)
- [BRCA gene mutations in cancer](https://scholariq.org/topics/brca-gene-mutations-in-cancer/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Prenatal Screening and Diagnostics](https://scholariq.org/topics/prenatal-screening-and-diagnostics/)
- [Congenital heart defects research](https://scholariq.org/topics/congenital-heart-defects-research/)
- [Genetic Syndromes and Imprinting](https://scholariq.org/topics/genetic-syndromes-and-imprinting/)

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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.