# Nicholas Katsanis

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/nicholas-katsanis/

## Facts

| Field | Value |
| --- | --- |
| Citations | 46,419 |
| Field | Genetic and Kidney Cyst Diseases |
| h-index | 113 |
| i10-index | 287 |
| Last Known Institution | FORTH Institute of Molecular Biology and Biotechnology |
| OpenAlex ID | https://openalex.org/A5041321997 |
| ORCID iD | https://orcid.org/0000-0002-2480-0171 |
| Works | 484 |

## Researcher papers

Showing 12 of 15.

- [A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants](https://scholariq.org/papers/a-large-genome-wide-association-study-of-age-related-macular-degeneration/)
- [Ciliopathies](https://scholariq.org/papers/ciliopathies/)
- [Comparative Genomics Identifies a Flagellar and Basal Body Proteome that Includes the BBS5 Human Disease Gene](https://scholariq.org/papers/comparative-genomics-identifies-a-flagellar-and-basal-body-proteome-that/)
- [Genetic variants near <i>TIMP3</i> and high-density lipoprotein–associated loci influence susceptibility to age-related macular degeneration](https://scholariq.org/papers/genetic-variants-near-i-timp3-i-and-high-density-lipoprotein-associated-loci/)
- [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/)
- [Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling](https://scholariq.org/papers/exome-capture-reveals-znf423-and-cep164-mutations-linking-renal-ciliopathies-to/)
- [TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum](https://scholariq.org/papers/ttc21b-contributes-both-causal-and-modifying-alleles-across-the-ciliopathy/)
- [Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy](https://scholariq.org/papers/candidate-exome-capture-identifies-mutation-of-sdccag8-as-the-cause-of-a-retinal/)
- [A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies](https://scholariq.org/papers/a-common-allele-in-rpgrip1l-is-a-modifier-of-retinal-degeneration-in/)
- [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/)
- [Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy](https://scholariq.org/papers/exome-sequence-analysis-suggests-that-genetic-burden-contributes-to-phenotypic/)
- [Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans](https://scholariq.org/papers/defects-in-the-ift-b-component-ift172-cause-jeune-and-mainzer-saldino-syndromes/)

## Researcher topics

- [Genetic and Kidney Cyst Diseases](https://scholariq.org/topics/genetic-and-kidney-cyst-diseases/)
- [Genetic Syndromes and Imprinting](https://scholariq.org/topics/genetic-syndromes-and-imprinting/)
- [Hedgehog Signaling Pathway Studies](https://scholariq.org/topics/hedgehog-signaling-pathway-studies/)
- [Renal and related cancers](https://scholariq.org/topics/renal-and-related-cancers/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)

## Researcher university

- [FORTH Institute of Molecular Biology and Biotechnology](https://scholariq.org/institutions/forth-institute-of-molecular-biology-and-biotechnology/)

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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.