# Jian Wang

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/jian-wang-4/

## Facts

| Field | Value |
| --- | --- |
| Citations | 6,241 |
| Field | Genomics and Rare Diseases |
| h-index | 40 |
| i10-index | 124 |
| Last Known Institution | Shanghai University |
| OpenAlex ID | https://openalex.org/A5100370569 |
| ORCID iD | 0000-0003-3391-5250 |
| Works | 268 |

## Researcher papers

- [A map of human genome variation from population-scale sequencing](https://scholariq.org/papers/a-map-of-human-genome-variation-from-population-scale-sequencing/)
- [Somatic Mutations in Cerebral Cortical Malformations](https://scholariq.org/papers/somatic-mutations-in-cerebral-cortical-malformations/)
- [Biallelic Mutations in CFAP43 and CFAP44 Cause Male Infertility with Multiple Morphological Abnormalities of the Sperm Flagella](https://scholariq.org/papers/biallelic-mutations-in-cfap43-and-cfap44-cause-male-infertility-with-multiple/)
- [VEGF: A modifier of the del22q11 (DiGeorge) syndrome?](https://scholariq.org/papers/vegf-a-modifier-of-the-del22q11-digeorge-syndrome/)
- [Targeted inactivation of the sodium‐calcium exchanger (Ncx1) results in the lack of a heartbeat and abnormal myofibrillar organization](https://scholariq.org/papers/targeted-inactivation-of-the-sodium-calcium-exchanger-ncx1-results-in-the-lack/)
- [Loss-of-function variants in endothelial lipase are a cause of elevated HDL cholesterol in humans](https://scholariq.org/papers/loss-of-function-variants-in-endothelial-lipase-are-a-cause-of-elevated-hdl/)
- [Prevalence and determinants of depressive and anxiety symptoms in adults with type 2 diabetes in China: a cross-sectional study](https://scholariq.org/papers/prevalence-and-determinants-of-depressive-and-anxiety-symptoms-in-adults-with/)
- [Boosting cartilage repair with silk fibroin-DNA hydrogel-based cartilage organoid precursor](https://scholariq.org/papers/boosting-cartilage-repair-with-silk-fibroin-dna-hydrogel-based-cartilage/)
- [Evaluation of three read-depth based CNV detection tools using whole-exome sequencing data](https://scholariq.org/papers/evaluation-of-three-read-depth-based-cnv-detection-tools-using-whole-exome/)
- [Grb10, a Positive, Stimulatory Signaling Adapter in Platelet-Derived Growth Factor BB-, Insulin-Like Growth Factor I-, and Insulin-Mediated Mitogenesis](https://scholariq.org/papers/grb10-a-positive-stimulatory-signaling-adapter-in-platelet-derived-growth-factor/)
- [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/)

## Researcher topics

- [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/)
- [Congenital heart defects research](https://scholariq.org/topics/congenital-heart-defects-research/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [RNA modifications and cancer](https://scholariq.org/topics/rna-modifications-and-cancer/)

## Researcher university

- [Shanghai University](https://scholariq.org/institutions/shanghai-university/)

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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.