# Donald W. Bowden

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/donald-w-bowden/

## Facts

| Field | Value |
| --- | --- |
| Citations | 57,230 |
| Field | Genetic Associations and Epidemiology |
| h-index | 100 |
| i10-index | 447 |
| OpenAlex ID | https://openalex.org/A5059764563 |
| ORCID iD | https://orcid.org/0000-0003-4861-8005 |
| Works | 648 |

## Researcher papers

- [The mutational constraint spectrum quantified from variation in 141,456 humans](https://scholariq.org/papers/the-mutational-constraint-spectrum-quantified-from-variation-in-141-456-humans/)
- [Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program](https://scholariq.org/papers/sequencing-of-53-831-diverse-genomes-from-the-nhlbi-topmed-program/)
- [Association of Trypanolytic ApoL1 Variants with Kidney Disease in African Americans](https://scholariq.org/papers/association-of-trypanolytic-apol1-variants-with-kidney-disease-in-african/)
- [Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps](https://scholariq.org/papers/fine-mapping-type-2-diabetes-loci-to-single-variant-resolution-using-high/)
- [Inherited causes of clonal haematopoiesis in 97,691 whole genomes](https://scholariq.org/papers/inherited-causes-of-clonal-haematopoiesis-in-97-691-whole-genomes/)
- [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/)
- [Rare and low-frequency coding variants alter human adult height](https://scholariq.org/papers/rare-and-low-frequency-coding-variants-alter-human-adult-height/)
- [Genetic diversity fuels gene discovery for tobacco and alcohol use](https://scholariq.org/papers/genetic-diversity-fuels-gene-discovery-for-tobacco-and-alcohol-use/)
- [Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity](https://scholariq.org/papers/protein-altering-variants-associated-with-body-mass-index-implicate-pathways/)
- [Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility](https://scholariq.org/papers/low-frequency-and-rare-exome-chip-variants-associate-with-fasting-glucose-and/)
- [Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND)](https://scholariq.org/papers/genome-wide-association-and-trans-ethnic-meta-analysis-for-advanced-diabetic/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Chronic Kidney Disease and Diabetes](https://scholariq.org/topics/chronic-kidney-disease-and-diabetes/)
- [Renal Diseases and Glomerulopathies](https://scholariq.org/topics/renal-diseases-and-glomerulopathies/)
- [Adipokines, Inflammation, and Metabolic Diseases](https://scholariq.org/topics/adipokines-inflammation-and-metabolic-diseases/)
- [Pancreatic function and diabetes](https://scholariq.org/topics/pancreatic-function-and-diabetes/)

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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.