Katie B. Williams
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- Metabolism and Genetic Disorders 3
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- Parathyroid Disorders and Treatments 3
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- Genomics and Rare Diseases 3
- BRCA gene mutations in cancer 2
- Genetic Syndromes and Imprinting 1
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- CRISPR and Genetic Engineering 2
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- Bone health and treatments 1
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- Neonatal and fetal brain pathology 1
- Co-authors
- Hector F. DeLucaKevin A. StraussKarlla W. BrigattiMillie YoungErik G. PuffenbergerKavita PraveenJohn D. OvertonCora Taylor
- Journals
- PEDIATRICS (1 paper)Journal of Bone and Mineral Research (1 paper)The Journal of Pediatrics (1 paper)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Katie B. Williams
13 papers receiving 145 citations
Peers
Comparison fields: 5 of 52
- Clinical Biochemistry 28
- Nephrology 22
- Genetics 60
- Nutrition and Dietetics 25
- Cell Biology 20
Countries citing papers authored by Katie B. Williams
This map shows the geographic impact of Katie B. Williams'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 Katie B. Williams with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Katie B. Williams more than expected).
Fields of papers citing papers by Katie B. Williams
This network shows the impact of papers produced by Katie B. Williams. 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 Katie B. Williams. The network helps show where Katie B. Williams may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Katie B. Williams, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2022 | 4 | |
| 2 | 2022 | 1 | |
| 3 | 2022 | 6 | |
| 4 | 2022 | 13 | |
| 5 | 2021 | 3 | |
| 6 | 2020 | 11 | |
| 7 | 2020 | 30 | |
| 8 | 2019 | 1 | |
| 9 | 2017 | 36 | |
| 10 | 2017 | 6 | |
| 11 | 2008 | 2 | |
| 12 | 2008 | 4 | |
| 13 | 2007 | 31 |
About Katie B. Williams
Katie B. Williams is a scholar working on Clinical Biochemistry, Nephrology and Genetics, having authored 13 papers that have together received 148 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (3 papers), Metabolism and Genetic Disorders (3 papers), Parathyroid Disorders and Treatments (3 papers), BRCA gene mutations in cancer (2 papers), CRISPR and Genetic Engineering (2 papers), Genetic Syndromes and Imprinting (1 paper), Bone health and treatments (1 paper) and Neonatal and fetal brain pathology (1 paper). The work is most often cited by research in Clinical Biochemistry (28 citations), Nephrology (22 citations) and Genetics (60 citations). Katie B. Williams has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Hector F. DeLuca, Kevin A. Strauss, Karlla W. Brigatti, Millie Young, Erik G. Puffenberger, Kavita Praveen, John D. Overton, Cora Taylor, Scott Mellis and Mei Baker. Their work appears in journals such as PEDIATRICS, Journal of Bone and Mineral Research and The Journal of Pediatrics.
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.