# Howard Trachtman

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/howard-trachtman/

## Facts

| Field | Value |
| --- | --- |
| Citations | 19,442 |
| Field | Renal Diseases and Glomerulopathies |
| h-index | 68 |
| i10-index | 246 |
| Last Known Institution | University of Michigan |
| OpenAlex ID | https://openalex.org/A5029482359 |
| ORCID iD | 0000-0001-7447-9489 |
| Works | 511 |

## Researcher papers

Showing 12 of 22.

- [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/)
- [APOL1 Genetic Variants in Focal Segmental Glomerulosclerosis and HIV-Associated Nephropathy](https://scholariq.org/papers/apol1-genetic-variants-in-focal-segmental-glomerulosclerosis-and-hiv-associated/)
- [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/)
- [MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis](https://scholariq.org/papers/myh9-is-a-major-effect-risk-gene-for-focal-segmental-glomerulosclerosis/)
- [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/)
- [Soluble Urokinase Receptor and Chronic Kidney Disease](https://scholariq.org/papers/soluble-urokinase-receptor-and-chronic-kidney-disease/)
- [Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism](https://scholariq.org/papers/recurrent-gain-of-function-mutation-in-calcium-channel-cacna1h-causes-early/)
- [Design of the Nephrotic Syndrome Study Network (NEPTUNE) to evaluate primary glomerular nephropathy by a multidisciplinary approach](https://scholariq.org/papers/design-of-the-nephrotic-syndrome-study-network-neptune-to-evaluate-primary/)
- [Urolithiasis in Pediatric Patients: A Single Center Study of Incidence, Clinical Presentation and Outcome](https://scholariq.org/papers/urolithiasis-in-pediatric-patients-a-single-center-study-of-incidence-clinical/)
- [Management of Childhood Onset Nephrotic Syndrome](https://scholariq.org/papers/management-of-childhood-onset-nephrotic-syndrome/)
- [Efficacy and safety of sparsentan versus irbesartan in patients with IgA nephropathy (PROTECT): 2-year results from a randomised, active-controlled, phase 3 trial](https://scholariq.org/papers/efficacy-and-safety-of-sparsentan-versus-irbesartan-in-patients-with-iga/)
- [IPNA clinical practice recommendations for the diagnosis and management of children with steroid-sensitive nephrotic syndrome](https://scholariq.org/papers/ipna-clinical-practice-recommendations-for-the-diagnosis-and-management-of-2/)

## Researcher topics

- [Renal Diseases and Glomerulopathies](https://scholariq.org/topics/renal-diseases-and-glomerulopathies/)
- [Chronic Kidney Disease and Diabetes](https://scholariq.org/topics/chronic-kidney-disease-and-diabetes/)
- [Vasculitis and related conditions](https://scholariq.org/topics/vasculitis-and-related-conditions/)
- [Complement system in diseases](https://scholariq.org/topics/complement-system-in-diseases/)
- [Pediatric Urology and Nephrology Studies](https://scholariq.org/topics/pediatric-urology-and-nephrology-studies/)

## Researcher university

- [University of Michigan](https://scholariq.org/institutions/university-of-michigan/)

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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.