Katie B. Williams

431 total citations
13 papers, 148 citations indexed

About

Katie B. Williams is a scholar working on Genetics, Molecular Biology and Nephrology. According to data from OpenAlex, Katie B. Williams has authored 13 papers receiving a total of 148 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 5 papers in Molecular Biology and 3 papers in Nephrology. Recurrent topics in Katie B. Williams's work include Genomics and Rare Diseases (3 papers), Metabolism and Genetic Disorders (3 papers) and Parathyroid Disorders and Treatments (3 papers). Katie B. Williams is often cited by papers focused on Genomics and Rare Diseases (3 papers), Metabolism and Genetic Disorders (3 papers) and Parathyroid Disorders and Treatments (3 papers). Katie B. Williams collaborates with scholars based in United States, United Kingdom and Canada. Katie B. Williams's 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 and has published in prestigious journals such as PEDIATRICS, Journal of Bone and Mineral Research and The Journal of Pediatrics.

In The Last Decade

Katie B. Williams

13 papers receiving 145 citations

Peers

Countries citing papers authored by Katie B. Williams

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 of co-authors of Katie B. Williams

This figure shows the co-authorship network connecting the top 25 collaborators of Katie B. Williams. A scholar is included among the top collaborators of Katie B. Williams 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 Katie B. Williams. Katie B. Williams is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

#	Work	Indexed citations
1	Clinical characterization of familial hypercholesterolemia due to an amish founder mutation in Apolipoprotein B 2022 ·BMC Cardiovascular Disorders ·Katie B. Williams, Michael Horst, Millie Young, (unknown), Erik G. Puffenberger, Karlla W. Brigatti, Claudia Gonzaga‐Jauregui, Alan R. Shuldiner, Samuel S. Gidding, Kevin A. Strauss, Devyani Chowdhury	4
2	Telemedicine in the Amish and Mennonite communities of Wisconsin 2022 ·Journal of Community Genetics ·Sara Zoran, (unknown), Qianqian Zhao, Anne Bradford Harris, Katie B. Williams, (unknown)	1
3	Cross-sectional survey on genetic testing utilization and perceptions in Wisconsin Amish and Mennonite communities 2022 ·Journal of Community Genetics ·Katie B. Williams, Michael Lasarev, Mei Baker, Christine M. Seroogy	6
4	Evidence that the Ser192Tyr/Arg402Gln in cis Tyrosinase gene haplotype is a disease-causing allele in oculocutaneous albinism type 1B (OCA1B) 2022 ·npj Genomic Medicine ·Siying Lin, (unknown), (unknown), Katie B. Williams, Helena Lee, N. Simon Thomas, Jonathan L A Callaway, (unknown), J. Arjuna Ratnayaka, Diana Baralle, (unknown), (unknown), (unknown), Gaurav V. Harlalka, Sarah Ennis, Harold E. Cross, Olivia Wenger, Andrew H. Crosby, Emma L. Baple, Jay Self	13
5	Newborn Pulse Oximetry for Infants Born Out-of-Hospital 2021 ·PEDIATRICS ·Katie B. Williams, Michael Horst, (unknown), (unknown), (unknown), Devyani Chowdhury	3
6	No association between SCN9A and monogenic human epilepsy disorders 2020 ·PLoS Genetics ·James Fasham, (unknown), Jamie Harrison, (unknown), Katie B. Williams, (unknown), (unknown), Harold E. Cross, Andrew H. Crosby, Emma L. Baple	11
7	Glutaric acidemia type 1: Treatment and outcome of 168 patients over three decades 2020 ·Molecular Genetics and Metabolism ·Kevin A. Strauss, Katie B. Williams, (unknown), (unknown), (unknown), Millie Young, (unknown), Christine Hendrickson, (unknown), Cora Taylor, Barbara Haas‐Givler, (unknown), Stephanie A. Chopko, Erik G. Puffenberger, Karlla W. Brigatti, Freeman Miller, D. Holmes Morton	30
8	Neonatal Metabolic Crises 2019 ·Clinics in Perinatology ·Katie B. Williams, Patrice K. Held, (unknown)	1
9	Genomic diagnostics within a medically underserved population: efficacy and implications 2017 ·Genetics in Medicine ·Kevin A. Strauss, Claudia Gonzaga‐Jauregui, Karlla W. Brigatti, Katie B. Williams, Alejandra King, Cristopher V. Van Hout, (unknown), Millie Young, Kavita Praveen, (unknown), (unknown), Aris Baras, Jeffrey G. Reid, John D. Overton, Frederick E. Dewey, Robert N. Jinks, (unknown), Scott Mellis, Alan R. Shuldiner, Erik G. Puffenberger	36
10	Management of Congenital Heart Disease Associated with Ellis-van Creveld Short-rib Thoracic Dysplasia 2017 ·The Journal of Pediatrics ·Devyani Chowdhury, Katie B. Williams, Aaron Chidekel, Christian Pizarro, (unknown), Millie Young, Christine Hendrickson, (unknown), Portia A. Kreiger, Erik G. Puffenberger, Kevin A. Strauss	6
11	Diaminobutane (DAB) Dendrimers Are Potent Binders of Oral Phosphate 2008 ·Journal of Bone and Mineral Research ·Katie B. Williams, (unknown), Julia B. Zella, Hector F. DeLuca	2
12	2-Methylene-19-nor-20(S)-1α-hydroxy-bishomopregnacalciferol [20(S)-2MbisP], an analog of vitamin D3 [1,25(OH)2D3], does not stimulate intestinal phosphate absorption at levels previously shown to suppress parathyroid hormone 2008 ·Steroids ·Katie B. Williams, Hector F. DeLuca	4
13	Characterization of intestinal phosphate absorption using a novel in vivo method 2007 ·American Journal of Physiology-Endocrinology and Metabolism ·Katie B. Williams, Hector F. DeLuca	31

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.

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