# Klaudia Walter

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/klaudia-walter/

## Facts

| Field | Value |
| --- | --- |
| Citations | 87,302 |
| Field | Genetic Associations and Epidemiology |
| h-index | 54 |
| i10-index | 78 |
| Last Known Institution | Wellcome Sanger Institute |
| OpenAlex ID | https://openalex.org/A5009265821 |
| ORCID iD | https://orcid.org/0000-0003-4448-0301 |
| Works | 149 |

## Researcher papers

- [An integrated map of genetic variation from 1,092 human genomes](https://scholariq.org/papers/an-integrated-map-of-genetic-variation-from-1-092-human-genomes/)
- [A map of human genome variation from population-scale sequencing](https://scholariq.org/papers/a-map-of-human-genome-variation-from-population-scale-sequencing-2/)
- [A reference panel of 64,976 haplotypes for genotype imputation](https://scholariq.org/papers/a-reference-panel-of-64-976-haplotypes-for-genotype-imputation/)
- [An integrated map of structural variation in 2,504 human genomes](https://scholariq.org/papers/an-integrated-map-of-structural-variation-in-2-504-human-genomes/)
- [The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease](https://scholariq.org/papers/the-allelic-landscape-of-human-blood-cell-trait-variation-and-links-to-common/)
- [A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes](https://scholariq.org/papers/a-systematic-survey-of-loss-of-function-variants-in-human-protein-coding-genes/)
- [Mapping copy number variation by population-scale genome sequencing](https://scholariq.org/papers/mapping-copy-number-variation-by-population-scale-genome-sequencing/)
- [Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel](https://scholariq.org/papers/integrating-sequence-and-array-data-to-create-an-improved-1000-genomes-project/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Genomics and Chromatin Dynamics](https://scholariq.org/topics/genomics-and-chromatin-dynamics/)
- [Genetic Mapping and Diversity in Plants and Animals](https://scholariq.org/topics/genetic-mapping-and-diversity-in-plants-and-animals/)

## Researcher university

- [Wellcome Sanger Institute](https://scholariq.org/institutions/wellcome-sanger-institute/)

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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.