Katrina M. Dipple

6.2k total citations
66 papers, 1.9k citations indexed

About

Katrina M. Dipple is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Katrina M. Dipple has authored 66 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 19 papers in Genetics and 10 papers in Surgery. Recurrent topics in Katrina M. Dipple's work include Metabolism, Diabetes, and Cancer (13 papers), Peroxisome Proliferator-Activated Receptors (9 papers) and Adipose Tissue and Metabolism (9 papers). Katrina M. Dipple is often cited by papers focused on Metabolism, Diabetes, and Cancer (13 papers), Peroxisome Proliferator-Activated Receptors (9 papers) and Adipose Tissue and Metabolism (9 papers). Katrina M. Dipple collaborates with scholars based in United States, Canada and Japan. Katrina M. Dipple's co-authors include Edward R.B. McCabe, James C. Liao, Ganesh Sriram, David W. Crabb, Julián A. Martínez-Agosto, Lola Rahib, Fabiola Quintero‐Rivera, Nicole K. MacLennan, Steve Horvath and Mark J. Stewart and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Hepatology.

In The Last Decade

Katrina M. Dipple

64 papers receiving 1.8k citations

Peers

Katrina M. Dipple
Boqin Qiang China
Kathryn P. Burdon Australia
Georg Christoph Korenke Germany
Paldeep S. Atwal United States
Lindsay C. Burrage United States
Ruti Parvari Israel
Saskia B. Wortmann Netherlands
Jennifer J. Johnston United States
Gerald L. Feldman United States
Lee-Jun Wong United States
Boqin Qiang China
Katrina M. Dipple
Citations per year, relative to Katrina M. Dipple Katrina M. Dipple (= 1×) peers Boqin Qiang

Countries citing papers authored by Katrina M. Dipple

Since Specialization
Citations

This map shows the geographic impact of Katrina M. Dipple'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 Katrina M. Dipple with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Katrina M. Dipple more than expected).

Fields of papers citing papers by Katrina M. Dipple

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Katrina M. Dipple. 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 Katrina M. Dipple. The network helps show where Katrina M. Dipple may publish in the future.

Co-authorship network of co-authors of Katrina M. Dipple

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

All Works

20 of 20 papers shown
1.
German, Kendell, Gail Deutsch, Amanda S. Freed, et al.. (2019). Identification of a deletion containing TBX4 in a neonate with acinar dysplasia by rapid exome sequencing. American Journal of Medical Genetics Part A. 179(5). 842–845. 13 indexed citations
2.
McCabe, Edward R.B., et al.. (2015). Gestational diabetes associated with a novel mutation (378–379insTT) in the glycerol kinase gene. SHILAP Revista de lepidopterología. 4. 42–45. 4 indexed citations
3.
Quintero‐Rivera, Fabiola, et al.. (2014). Duodenal atresia in 17q12 microdeletion including HNF1B: A new associated malformation in this syndrome. American Journal of Medical Genetics Part A. 164(12). 3076–3082. 20 indexed citations
4.
Dipple, Katrina M., et al.. (2014). Development of catecholamine and cortisol stress responses in zebrafish. Molecular Genetics and Metabolism Reports. 1. 373–377. 21 indexed citations
5.
Amarillo, Ina, Katrina M. Dipple, & Fabiola Quintero‐Rivera. (2013). Familial Microdeletion of 17q24.3 Upstream of SOX9 Is Associated With Isolated Pierre Robin Sequence Due to Position Effect. American Journal of Medical Genetics Part A. 161(5). 1167–1172. 29 indexed citations
6.
7.
Ortube, Maria Carolina, Katrina M. Dipple, Yoshio Setoguchi, Henry K. Kawamoto, & Joseph L. Demer. (2010). Ocular Manifestations of Oblique Facial Clefts. Journal of Craniofacial Surgery. 21(5). 1630–1631. 9 indexed citations
8.
Tran, Linh M., Simon W. Beaven, Peter Tontonoz, et al.. (2009). Resistance to Diet-Induced Obesity in Mice with Synthetic Glyoxylate Shunt. Cell Metabolism. 9(6). 525–536. 27 indexed citations
9.
Rahib, Lola, et al.. (2009). Transcriptomic and network component analysis of glycerol kinase in skeletal muscle using a mouse model of glycerol kinase deficiency. Molecular Genetics and Metabolism. 96(3). 106–112. 16 indexed citations
10.
Sriram, Ganesh, et al.. (2007). Global metabolic effects of glycerol kinase overexpression in rat hepatoma cells. Molecular Genetics and Metabolism. 93(2). 145–159. 32 indexed citations
11.
Rahib, Lola, Nicole K. MacLennan, Steve Horvath, James C. Liao, & Katrina M. Dipple. (2007). Glycerol kinase deficiency alters expression of genes involved in lipid metabolism, carbohydrate metabolism, and insulin signaling. European Journal of Human Genetics. 15(6). 646–657. 51 indexed citations
12.
Sriram, Ganesh, Julián A. Martínez-Agosto, Edward R.B. McCabe, James C. Liao, & Katrina M. Dipple. (2005). Single-Gene Disorders: What Role Could Moonlighting Enzymes Play?. The American Journal of Human Genetics. 76(6). 911–924. 170 indexed citations
13.
14.
Cederbaum, Stephen D., Samantha Koo-McCoy, Ingrid Tein, et al.. (2002). Carnitine membrane transporter deficiency: a long-term follow up and OCTN2 mutation in the first documented case of primary carnitine deficiency. Molecular Genetics and Metabolism. 77(3). 195–201. 52 indexed citations
15.
Dipple, Katrina M. & Edward R.B. McCabe. (2000). Modifier Genes Convert “Simple” Mendelian Disorders to Complex Traits. Molecular Genetics and Metabolism. 71(1-2). 43–50. 201 indexed citations
16.
Dipple, Katrina M., Éric Vilain, Binquan Huang, et al.. (2000). AluY insertion (IVS4-52ins316alu) in the glycerol kinase gene from an individual with benign glycerol kinase deficiency. Human Mutation. 15(4). 316–323. 33 indexed citations
17.
18.
Stewart, Mark J., et al.. (1998). Binding and activation of the human aldehyde dehydrogenase 2 promoter by hepatocyte nuclear factor 4. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1399(2-3). 181–186. 29 indexed citations
19.
Dipple, Katrina M., et al.. (1993). Effects of thyroxine on the expression of alcohol dehydrogenase in rat liver and kidney. Hepatology. 17(4). 701–706. 4 indexed citations
20.
Crabb, David W., et al.. (1990). Endocrine Regulation and Methylation Patterns of Rat Class I Alcohol Dehydrogenase in Liver and Kidney. Advances in experimental medicine and biology. 284. 277–284. 4 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.

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