Klaudia Walter

69.0k total citations · 1 hit paper
29 papers, 1.7k citations indexed

About

Klaudia Walter is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Klaudia Walter has authored 29 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 13 papers in Molecular Biology and 5 papers in Rheumatology. Recurrent topics in Klaudia Walter's work include Genetic Associations and Epidemiology (10 papers), Genomics and Rare Diseases (6 papers) and Genomics and Chromatin Dynamics (6 papers). Klaudia Walter is often cited by papers focused on Genetic Associations and Epidemiology (10 papers), Genomics and Rare Diseases (6 papers) and Genomics and Chromatin Dynamics (6 papers). Klaudia Walter collaborates with scholars based in United Kingdom, United States and Germany. Klaudia Walter's co-authors include Nicole Soranzo, Walter R. Gilks, Lorenzo Bomba, Greg Elgar, Tanya Vavouri, Irina Abnizova, Sarah Smith, Phil Snell, Martin Goodson and Debbie K. Goode and has published in prestigious journals such as Nature Genetics, Bioinformatics and The Journal of Immunology.

In The Last Decade

Klaudia Walter

28 papers receiving 1.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Highly Conserved Non-Coding Sequences Are Associated with Vertebrate Development

2004 723 citations Adam Woolfe, Martin Goodson et al. PLoS Biology profile →

Peers

Klaudia Walter

GENET

PARAS

Malek Djabali France

Christelle Le Dantec France

Hidehito Inagaki Japan

Allerdien Visser Netherlands

Su Wen Qian United States

Michael Cheeseman United Kingdom

Mireia Jordà Spain

Nader Ghebranious United States

C. Lacroix France

David M. Reynolds United States

Malek Djabali France

Klaudia Walter

1.3k ×1.2

311 ×0.5

GENET

103 ×0.4

96 ×0.6

PARAS

111 ×1.0

Citations per year, relative to Klaudia Walter Klaudia Walter (= 1×) peers Malek Djabali

Countries citing papers authored by Klaudia Walter

Since Specialization

Citations

This map shows the geographic impact of Klaudia Walter's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Klaudia Walter with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Klaudia Walter more than expected).

Fields of papers citing papers by Klaudia Walter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Klaudia Walter. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Klaudia Walter. The network helps show where Klaudia Walter may publish in the future.

Co-authorship network of co-authors of Klaudia Walter

This figure shows the co-authorship network connecting the top 25 collaborators of Klaudia Walter. A scholar is included among the top collaborators of Klaudia Walter based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Klaudia Walter. Klaudia Walter is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Walter, Klaudia, Qin Huang, Juha Karjalainen, et al.. (2025). Widespread recessive effects on common diseases in a cohort of 44,000 British Pakistanis and Bangladeshis with high autozygosity. The American Journal of Human Genetics. 112(6). 1316–1329.

Guo, Jing, Klaudia Walter, Pedro M. Quirós, et al.. (2024). Inherited polygenic effects on common hematological traits influence clonal selection on JAK2V617F and the development of myeloproliferative neoplasms. Nature Genetics. 56(2). 273–280. 10 indexed citations

Kundu, Kousik, Manuel Tardáguila, Alice Mann, et al.. (2022). Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for 12 immune-mediated diseases. Nature Genetics. 54(3). 251–262. 31 indexed citations

Bell, Joshua A., David A. Hughes, Laura J. Corbin, et al.. (2021). Effects of adiposity on the human plasma proteome: observational and Mendelian randomisation estimates. International Journal of Obesity. 45(10). 2221–2229. 26 indexed citations

Riveros-Mckay, Fernando, Clare Oliver‐Williams, Savita Karthikeyan, et al.. (2020). The influence of rare variants in circulating metabolic biomarkers. PLoS Genetics. 16(3). e1008605–e1008605. 8 indexed citations

Iotchkova, Valentina, Graham R. S. Ritchie, Matthias Geihs, et al.. (2019). GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signals. Nature Genetics. 51(2). 343–353. 94 indexed citations

Süveges, Dániel, Klaudia Walter, Kousik Kundu, et al.. (2019). Population‐wide copy number variation calling using variant call format files from 6,898 individuals. Genetic Epidemiology. 44(1). 79–89. 3 indexed citations

Panoutsopoulou, Kalliope & Klaudia Walter. (2018). Quality Control of Common and Rare Variants. Methods in molecular biology. 1793. 25–36. 8 indexed citations

Bomba, Lorenzo, Klaudia Walter, & Nicole Soranzo. (2017). The impact of rare and low-frequency genetic variants in common disease. Genome biology. 18(1). 77–77. 222 indexed citations

10.

Geihs, Matthias, Yan Yan, Klaudia Walter, et al.. (2015). An interactive genome browser of association results from the UK10K cohorts project. Bioinformatics. 31(24). 4029–4031. 8 indexed citations

11.

Xu, Changjiang, Ioanna Tachmazidou, Klaudia Walter, et al.. (2014). Estimating Genome‐Wide Significance for Whole‐Genome Sequencing Studies. Genetic Epidemiology. 38(4). 281–290. 50 indexed citations

12.

Vavouri, Tanya, Klaudia Walter, Walter R. Gilks, Ben Lehner, & Greg Elgar. (2007). Parallel evolution of conserved non-coding elements that target a common set of developmental regulatory genes from worms to humans. Genome biology. 8(2). R15–R15. 83 indexed citations

13.

Walter, Klaudia, Anthony J. C. Fulford, Rowena McBeath, et al.. (2006). Increased Human IgE Induced by Killing Schistosoma mansoni In Vivo Is Associated with Pretreatment Th2 Cytokine Responsiveness to Worm Antigens. The Journal of Immunology. 177(8). 5490–5498. 42 indexed citations

14.

Fitzsimmons, Colin M., Rowena McBeath, Sarah Joseph, et al.. (2006). Factors Affecting Human IgE and IgG Responses to Allergen-Like <i>Schistosoma mansoni </i>Antigens: Molecular Structure and Patterns of in vivo Exposure. International Archives of Allergy and Immunology. 142(1). 40–50. 56 indexed citations

15.

Edwards, Yvonne J. K., Klaudia Walter, Gayle K. McEwen, et al.. (2005). Characterisation of conserved non-coding sequences in vertebrate genomes using bioinformatics, statistics and functional studies. Comparative Biochemistry and Physiology Part D Genomics and Proteomics. 1(1). 46–58. 6 indexed citations

16.

Walter, Klaudia, Irina Abnizova, Greg Elgar, & Walter R. Gilks. (2005). Striking nucleotide frequency pattern at the borders of highly conserved vertebrate non-coding sequences. Trends in Genetics. 21(8). 436–440. 26 indexed citations

17.

Abnizova, Irina, René te Boekhorst, Klaudia Walter, & Walter R. Gilks. (2005). Some statistical properties of regulatory DNA sequences, and their use in predicting regulatory regions in the Drosophila genome: the fluffy-tail test. BMC Bioinformatics. 6(1). 109–109. 26 indexed citations

18.

Woolfe, Adam, Martin Goodson, Debbie K. Goode, et al.. (2004). Highly Conserved Non-Coding Sequences Are Associated with Vertebrate Development. PLoS Biology. 3(1). e7–e7. 723 indexed citations breakdown →

19.

Wichmann, I., M. Montes-Cano, N. Respaldiza, et al.. (2003). Clinical Significance of Anti-Multiple Nuclear Dots/Sp100 Autoantibodies. Scandinavian Journal of Gastroenterology. 38(9). 996–999. 21 indexed citations

20.

González‐Escribano, M.F., et al.. (1998). Distribution of HLA class II alleles among Spanish patients with pemphigus vulgaris. Tissue Antigens. 52(3). 275–278. 56 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact