# Shrikant Mane

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/shrikant-mane/

## Facts

| Field | Value |
| --- | --- |
| Citations | 56,167 |
| Field | Genomics and Rare Diseases |
| h-index | 88 |
| i10-index | 205 |
| Last Known Institution | University of Iowa |
| OpenAlex ID | https://openalex.org/A5054738149 |
| ORCID iD | https://orcid.org/0000-0002-3267-5139 |
| Works | 297 |

## Researcher papers

Showing 12 of 15.

- [Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci](https://scholariq.org/papers/insights-into-autism-spectrum-disorder-genomic-architecture-and-biology-from-71/)
- [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 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/)
- [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/)
- [Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations](https://scholariq.org/papers/whole-exome-sequencing-identifies-recessive-wdr62-mutations-in-severe-brain/)
- [Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome](https://scholariq.org/papers/recessive-mutations-in-dgke-cause-atypical-hemolytic-uremic-syndrome/)
- [Early Assessment of Lung Cancer Immunotherapy Response via Circulating Tumor DNA](https://scholariq.org/papers/early-assessment-of-lung-cancer-immunotherapy-response-via-circulating-tumor-dna/)
- [Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome](https://scholariq.org/papers/whole-exome-sequencing-of-patients-with-steroid-resistant-nephrotic-syndrome/)
- [Insights into genetics, human biology and disease gleaned from family based genomic studies](https://scholariq.org/papers/insights-into-genetics-human-biology-and-disease-gleaned-from-family-based/)
- [Isolated polycystic liver disease genes define effectors of polycystin-1 function](https://scholariq.org/papers/isolated-polycystic-liver-disease-genes-define-effectors-of-polycystin-1/)

## Researcher topics

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Renal and related cancers](https://scholariq.org/topics/renal-and-related-cancers/)
- [Renal Diseases and Glomerulopathies](https://scholariq.org/topics/renal-diseases-and-glomerulopathies/)
- [Genetic and Kidney Cyst Diseases](https://scholariq.org/topics/genetic-and-kidney-cyst-diseases/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)

## Researcher university

- [University of Iowa](https://scholariq.org/institutions/university-of-iowa/)

---
Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.