# Richard P. Lifton

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/richard-p-lifton/

## Facts

| Field | Value |
| --- | --- |
| Citations | 95,540 |
| Field | Ion Transport and Channel Regulation |
| h-index | 150 |
| i10-index | 410 |
| Last Known Institution | Rockefeller University |
| OpenAlex ID | https://openalex.org/A5047765832 |
| ORCID iD | https://orcid.org/0000-0002-5745-5984 |
| Works | 578 |

## Researcher papers

Showing 12 of 27.

- [Autoantibodies against type I IFNs in patients with life-threatening COVID-19](https://scholariq.org/papers/autoantibodies-against-type-i-ifns-in-patients-with-life-threatening-covid-19/)
- [Molecular Mechanisms of Human Hypertension](https://scholariq.org/papers/molecular-mechanisms-of-human-hypertension/)
- [Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism](https://scholariq.org/papers/multiple-recurrent-de-novo-cnvs-including-duplications-of-the-7q11-23-williams/)
- [Genomic Analysis of Non- <i>NF2</i> Meningiomas Reveals Mutations in <i>TRAF7</i> , <i>KLF4</i> , <i>AKT1</i> , and <i>SMO</i>](https://scholariq.org/papers/genomic-analysis-of-non-i-nf2-i-meningiomas-reveals-mutations-in-i-traf7-i-i/)
- [Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III](https://scholariq.org/papers/mutations-in-the-chloride-channel-gene-clcnkb-cause-bartter-s-syndrome-type-iii/)
- [Genetic heterogeneity of Barter's syndrome revealed by mutations in the K+ channel, ROMK](https://scholariq.org/papers/genetic-heterogeneity-of-barter-s-syndrome-revealed-by-mutations-in-the-k/)
- [Impaired HLA Class I Antigen Processing and Presentation as a Mechanism of Acquired Resistance to Immune Checkpoint Inhibitors in Lung Cancer](https://scholariq.org/papers/impaired-hla-class-i-antigen-processing-and-presentation-as-a-mechanism-of/)
- [A Single-Gene Cause in 29.5% of Cases of Steroid-Resistant Nephrotic Syndrome](https://scholariq.org/papers/a-single-gene-cause-in-29-5-of-cases-of-steroid-resistant-nephrotic-syndrome/)
- [Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities](https://scholariq.org/papers/mutations-in-kelch-like-3-and-cullin-3-cause-hypertension-and-electrolyte/)
- [Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens](https://scholariq.org/papers/discovery-of-new-risk-loci-for-iga-nephropathy-implicates-genes-involved-in/)
- [Genome-wide association study identifies susceptibility loci for IgA nephropathy](https://scholariq.org/papers/genome-wide-association-study-identifies-susceptibility-loci-for-iga-nephropathy/)
- [Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism](https://scholariq.org/papers/somatic-and-germline-cacna1d-calcium-channel-mutations-in-aldosterone-producing/)

## Researcher topics

- [Ion Transport and Channel Regulation](https://scholariq.org/topics/ion-transport-and-channel-regulation/)
- [Hormonal Regulation and Hypertension](https://scholariq.org/topics/hormonal-regulation-and-hypertension/)
- [Renal Diseases and Glomerulopathies](https://scholariq.org/topics/renal-diseases-and-glomerulopathies/)
- [Ion channel regulation and function](https://scholariq.org/topics/ion-channel-regulation-and-function/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)

## Researcher university

- [Rockefeller University](https://scholariq.org/institutions/rockefeller-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.