# Structural Genomics Consortium

**Type:** Institutions  
**Canonical URL:** https://scholariq.org/institutions/structural-genomics-consortium/

## Facts

| Field | Value |
| --- | --- |
| Avg h-index | 94.5 |
| Citations | 360,491 |
| City | Toronto |
| Country | CA |
| Description | Structural Genomics Consortium is a research organisation in Toronto, CA. OpenAlex records 1,606 works and 360,491 citations for it. 413 researchers list it as their most recent affiliation. |
| Homepage | http://www.thesgc.org/ |
| OpenAlex ID | https://openalex.org/I2803004491 |
| Researchers | 413 |
| ROR ID | https://ror.org/04jzps455 |
| Type | nonprofit |
| Wikidata ID | https://www.wikidata.org/wiki/Q7624992 |
| Works | 1,606 |

## University papers

- [A common haplotype in the complement regulatory gene factor H ( <i>HF1/CFH</i> ) predisposes individuals to age-related macular degeneration](https://scholariq.org/papers/a-common-haplotype-in-the-complement-regulatory-gene-factor-h-i-hf1-cfh-i/)
- [Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways](https://scholariq.org/papers/exome-sequencing-in-amyotrophic-lateral-sclerosis-identifies-risk-genes-and/)
- [Diagnostic Utility of Exome Sequencing for Kidney Disease](https://scholariq.org/papers/diagnostic-utility-of-exome-sequencing-for-kidney-disease/)
- [Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis](https://scholariq.org/papers/mutations-in-the-profilin-1-gene-cause-familial-amyotrophic-lateral-sclerosis/)
- [Dating the Origin of the CCR5-Δ32 AIDS-Resistance Allele by the Coalescence of Haplotypes](https://scholariq.org/papers/dating-the-origin-of-the-ccr5-32-aids-resistance-allele-by-the-coalescence-of/)
- [Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene ( <i>LIPC</i> )](https://scholariq.org/papers/genome-wide-association-study-of-advanced-age-related-macular-degeneration/)
- [A Drosophila Genetic Resource of Mutants to Study Mechanisms Underlying Human Genetic Diseases](https://scholariq.org/papers/a-drosophila-genetic-resource-of-mutants-to-study-mechanisms-underlying-human/)
- [Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration](https://scholariq.org/papers/common-variants-near-frk-col10a1-and-vegfa-are-associated-with-advanced-age/)

## University top topics

Showing 8 of 25.

- [Epigenetics and DNA Methylation](https://scholariq.org/topics/epigenetics-and-dna-methylation/)
- [Cancer-related gene regulation](https://scholariq.org/topics/cancer-related-gene-regulation/)
- [Ubiquitin and proteasome pathways](https://scholariq.org/topics/ubiquitin-and-proteasome-pathways/)
- [RNA modifications and cancer](https://scholariq.org/topics/rna-modifications-and-cancer/)
- [Protein Degradation and Inhibitors](https://scholariq.org/topics/protein-degradation-and-inhibitors/)
- [Enzyme Structure and Function](https://scholariq.org/topics/enzyme-structure-and-function/)
- [RNA and protein synthesis mechanisms](https://scholariq.org/topics/rna-and-protein-synthesis-mechanisms/)
- [Genomics and Chromatin Dynamics](https://scholariq.org/topics/genomics-and-chromatin-dynamics/)

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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.