# Gabriel C. Dworschak

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/gabriel-c-dworschak/

## Facts

| Field | Value |
| --- | --- |
| Citations | 1,649 |
| Field | Renal and related cancers |
| h-index | 21 |
| i10-index | 27 |
| OpenAlex ID | https://openalex.org/A5017101571 |
| ORCID iD | 0000-0003-0015-6964 |
| Works | 46 |

## Researcher papers

- [Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract](https://scholariq.org/papers/mutations-in-12-known-dominant-disease-causing-genes-clarify-many-congenital/)
- [Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans](https://scholariq.org/papers/single-gene-causes-of-congenital-anomalies-of-the-kidney-and-urinary-tract-cakut/)
- [Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association](https://scholariq.org/papers/whole-exome-resequencing-reveals-recessive-mutations-in-trap1-in-individuals/)
- [Mild Recessive Mutations in Six Fraser Syndrome–Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract](https://scholariq.org/papers/mild-recessive-mutations-in-six-fraser-syndrome-related-genes-cause-isolated/)
- [Mutations of the SLIT2–ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract](https://scholariq.org/papers/mutations-of-the-slit2-robo2-pathway-genes-slit2-and-srgap1-confer-risk-for/)
- [Increased psychosocial risk, depression and reduced quality of life living with autosomal dominant polycystic kidney disease](https://scholariq.org/papers/increased-psychosocial-risk-depression-and-reduced-quality-of-life-living-with/)
- [De novo 13q deletions in two patients with mild anorectal malformations as part of VATER/VACTERL and VATER/VACTERL‐like association and analysis of <i>EFNB2</i> in patients with anorectal malformations](https://scholariq.org/papers/de-novo-13q-deletions-in-two-patients-with-mild-anorectal-malformations-as-part/)
- [Clinical Effectiveness of Newborn Screening for Spinal Muscular Atrophy](https://scholariq.org/papers/clinical-effectiveness-of-newborn-screening-for-spinal-muscular-atrophy/)
- [Comprehensive review of the duplication 3q syndrome and report of a patient with Currarino syndrome and <i>de novo</i> duplication 3q26.32‐q27.2](https://scholariq.org/papers/comprehensive-review-of-the-duplication-3q-syndrome-and-report-of-a-patient-with/)
- [Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate<i>ZIC3</i>and<i>FOXF1</i>in Human VATER/VACTERL Association](https://scholariq.org/papers/targeted-resequencing-of-29-candidate-genes-and-mouse-expression-studies/)

## Researcher topics

- [Renal and related cancers](https://scholariq.org/topics/renal-and-related-cancers/)
- [Esophageal and GI Pathology](https://scholariq.org/topics/esophageal-and-gi-pathology/)
- [Urological Disorders and Treatments](https://scholariq.org/topics/urological-disorders-and-treatments/)
- [Congenital Diaphragmatic Hernia Studies](https://scholariq.org/topics/congenital-diaphragmatic-hernia-studies/)
- [Congenital gastrointestinal and neural anomalies](https://scholariq.org/topics/congenital-gastrointestinal-and-neural-anomalies/)

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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.