# Tingting Yu

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/tingting-yu/

## Facts

| Field | Value |
| --- | --- |
| Citations | 2,330 |
| Field | Genomics and Rare Diseases |
| h-index | 23 |
| i10-index | 60 |
| Last Known Institution | Shanghai Jiao Tong University |
| OpenAlex ID | https://openalex.org/A5015738756 |
| ORCID iD | 0000-0001-6030-9614 |
| Works | 147 |

## Researcher papers

- [Recent advances in targeting the “undruggable” proteins: from drug discovery to clinical trials](https://scholariq.org/papers/recent-advances-in-targeting-the-undruggable-proteins-from-drug-discovery-to/)
- [Exonic Deletions in AUTS2 Cause a Syndromic Form of Intellectual Disability and Suggest a Critical Role for the C Terminus](https://scholariq.org/papers/exonic-deletions-in-auts2-cause-a-syndromic-form-of-intellectual-disability-and/)
- [P2Y12 regulates microglia activation and excitatory synaptic transmission in spinal lamina II neurons during neuropathic pain in rodents](https://scholariq.org/papers/p2y12-regulates-microglia-activation-and-excitatory-synaptic-transmission-in/)
- [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/)
- [Proband-only medical exome sequencing as a cost-effective first-tier genetic diagnostic test for patients without prior molecular tests and clinical diagnosis in a developing country: the China experience](https://scholariq.org/papers/proband-only-medical-exome-sequencing-as-a-cost-effective-first-tier-genetic/)
- [Prevalence of precocious puberty among Chinese children: a school population-based study](https://scholariq.org/papers/prevalence-of-precocious-puberty-among-chinese-children-a-school-population/)
- [Exome sequencing identifies a de novo mutation of CTNNB1 gene in a patient mainly presented with retinal detachment, lens and vitreous opacities, microcephaly, and developmental delay](https://scholariq.org/papers/exome-sequencing-identifies-a-de-novo-mutation-of-ctnnb1-gene-in-a-patient/)
- [Description of the molecular and phenotypic spectrum of Wiedemann-Steiner syndrome in Chinese patients](https://scholariq.org/papers/description-of-the-molecular-and-phenotypic-spectrum-of-wiedemann-steiner/)
- [Novel pathogenic ACAN variants in non-syndromic short stature patients](https://scholariq.org/papers/novel-pathogenic-acan-variants-in-non-syndromic-short-stature-patients/)
- [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/)
- [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/)
- [Connective tissue disorders research](https://scholariq.org/topics/connective-tissue-disorders-research/)
- [Mitochondrial Function and Pathology](https://scholariq.org/topics/mitochondrial-function-and-pathology/)
- [Genetic Syndromes and Imprinting](https://scholariq.org/topics/genetic-syndromes-and-imprinting/)

## Researcher university

- [Shanghai Jiao Tong University](https://scholariq.org/institutions/shanghai-jiao-tong-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.