Terri M. King

2.8k total citations
46 papers, 1.9k citations indexed

About

Terri M. King is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Terri M. King has authored 46 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 18 papers in Genetics and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Terri M. King's work include Genetic Associations and Epidemiology (8 papers), Genetic Mapping and Diversity in Plants and Animals (6 papers) and Agriculture and Farm Safety (4 papers). Terri M. King is often cited by papers focused on Genetic Associations and Epidemiology (8 papers), Genetic Mapping and Diversity in Plants and Animals (6 papers) and Agriculture and Farm Safety (4 papers). Terri M. King collaborates with scholars based in United States, Italy and Germany. Terri M. King's co-authors include Dianna M. Milewicz, Christopher I. Amos, Jacqueline T. Hecht, Michael J. Gambello, Kit Sing Au, Hope Northrup, D. Kim Waller, Sylvia A. Frazier‐Bowers, Dongchuan Guo and David Aguilar and has published in prestigious journals such as American Journal of Clinical Nutrition, JNCI Journal of the National Cancer Institute and Journal of the American Society of Nephrology.

In The Last Decade

Terri M. King

45 papers receiving 1.9k citations

Peers

Terri M. King
Madelon Bracke Netherlands
Lina Shao United States
Madelon Bracke Netherlands
Terri M. King
Citations per year, relative to Terri M. King Terri M. King (= 1×) peers Madelon Bracke

Countries citing papers authored by Terri M. King

Since Specialization
Citations

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

Fields of papers citing papers by Terri M. King

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Terri M. King

This figure shows the co-authorship network connecting the top 25 collaborators of Terri M. King. A scholar is included among the top collaborators of Terri M. King 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 Terri M. King. Terri M. King 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.
Northrup, Hope, et al.. (2009). Expanded newborn screening in Texas: a survey and educational module addressing the knowledge of pediatric residents. Genetics in Medicine. 11(3). 163–168. 3 indexed citations
2.
Davidson, Christina M., Hope Northrup, Terri M. King, et al.. (2008). Genes in Glucose Metabolism and Association With Spina Bifida. Reproductive Sciences. 15(1). 51–58. 37 indexed citations
3.
Shankar, Suma P., John H. Fingert, Valério Carelli, et al.. (2008). Evidence for a Novel X-Linked Modifier Locus for Leber Hereditary Optic Neuropathy. Ophthalmic Genetics. 29(1). 17–24. 88 indexed citations
4.
Au, Kit Sing, E. Steve Roach, Lori Batchelor, et al.. (2007). Genotype/phenotype correlation in 325 individuals referred for a diagnosis of tuberous sclerosis complex in the United States. Genetics in Medicine. 9(2). 88–100. 296 indexed citations
5.
Daiger, Stephen P., Suma P. Shankar, Alice B. Schindler, et al.. (2007). Genetic Factors Modifying Clinical Expression of Autosomal Dominant RP. Advances in experimental medicine and biology. 572. 3–8. 9 indexed citations
6.
King, Terri M., Kit Sing Au, Christina M. Davidson, et al.. (2007). The Impact of BRCA1 on Spina Bifida Meningomyelocele Lesions. Annals of Human Genetics. 71(6). 719–728. 10 indexed citations
7.
Leichman, Joshua G., et al.. (2006). Association of plasma free fatty acids and left ventricular diastolic function in patients with clinically severe obesity. American Journal of Clinical Nutrition. 84(2). 336–341. 51 indexed citations
8.
Leichman, Joshua G., et al.. (2006). Association of plasma free fatty acids and left ventricular diastolic function in patients with clinically severe obesity1–3. American Journal of Clinical Nutrition. 84(2). 336–341. 54 indexed citations
9.
Leichman, Joshua G., David Aguilar, Terri M. King, et al.. (2006). Improvements in systemic metabolism, anthropometrics, and left ventricular geometry 3 months after bariatric surgery. Surgery for Obesity and Related Diseases. 2(6). 592–599. 48 indexed citations
10.
King, Terri M., et al.. (2005). DNA Pooling as a Tool for Case-Control Association Studies of Complex Traits. Genomics & Informatics. 3(1). 1–7.
11.
Shankar, Suma P., Valério Carelli, Terri M. King, et al.. (2005). Linkage Analysis of the X Chromosome in a Brazilian Family With Leber Hereditary Optic Neuropathy (LHON). Investigative Ophthalmology & Visual Science. 46(13). 663–663. 3 indexed citations
12.
Au, Kit Sing, Hope Northrup, Kelly A. Volcik, et al.. (2005). Promotor genotype of the platelet‐derived growth factor receptor‐α gene shows population stratification but not association with spina bifida meningomyelocele. American Journal of Medical Genetics Part A. 139A(3). 194–198. 17 indexed citations
13.
Shaw, Andrew, Ara A. Vaporciyan, Xifeng Wu, et al.. (2005). Inflammatory Gene Polymorphisms Influence Risk of Postoperative Morbidity After Lung Resection. The Annals of Thoracic Surgery. 79(5). 1704–1710. 25 indexed citations
14.
Mitchell, Braxton D., Wen‐Chi Hsueh, Terri M. King, et al.. (2001). Heritability of life span in the Old Order Amish. American Journal of Medical Genetics. 102(4). 346–352. 131 indexed citations
15.
Baur, Max P., Partha P. Majumder, Christopher I. Amos, et al.. (2001). International Genetic Epidemiology Society: Commentary on Darkness in El Dorado by Patrick Tierney. Genetic Epidemiology. 21(2). 81–104. 5 indexed citations
16.
Barnholtz‐Sloan, Jill S., Mariza de Andrade, Grier P. Page, et al.. (1999). Assessing linkage of monoamine oxidase B in a genome‐wide scan using a univariate variance components approach. Genetic Epidemiology. 17(S1). S49–54. 9 indexed citations
17.
King, Terri M., Terri H. Beaty, & Kung‐Yee Liang. (1996). Comparison of methods for survival analysis of dependent data. Genetic Epidemiology. 13(2). 139–158. 13 indexed citations
18.
Goldin, Lynn R., et al.. (1995). Use of exact and adjusted liability scores to detect genes affecting common traits. Genetic Epidemiology. 12(6). 765–769. 6 indexed citations
19.
King, Terri M., Jason Brandt, & Deborah A. Meyers. (1993). Effect of laboratory or clerical error on presymptomatic risk calculations for Huntington disease: A simulation study. American Journal of Medical Genetics. 46(2). 154–158. 2 indexed citations
20.
Maestri, Nancy E., et al.. (1992). Using recombinant chromosomes to map new markers. Cytogenetic and Genome Research. 59(2-3). 116–118. 2 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

Rankless by CCL
2026