Donna M. Lehman

5.6k total citations
52 papers, 1.8k citations indexed

About

Donna M. Lehman is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Donna M. Lehman has authored 52 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 23 papers in Genetics and 7 papers in Epidemiology. Recurrent topics in Donna M. Lehman's work include Genetic Associations and Epidemiology (14 papers), Genetic Mapping and Diversity in Plants and Animals (6 papers) and Peroxisome Proliferator-Activated Receptors (5 papers). Donna M. Lehman is often cited by papers focused on Genetic Associations and Epidemiology (14 papers), Genetic Mapping and Diversity in Plants and Animals (6 papers) and Peroxisome Proliferator-Activated Receptors (5 papers). Donna M. Lehman collaborates with scholars based in United States, Australia and Mexico. Donna M. Lehman's co-authors include John Blangero, Ravindranath Duggirala, P. T. Magee, K. J. Kwon-Chung, Michael P. Stern, Rector Arya, Robin J. Leach, Thomas D. Dyer, Nancy Ransom and Stuart J. McKinnon and has published in prestigious journals such as Nature Communications, Blood and PLoS ONE.

In The Last Decade

Donna M. Lehman

50 papers receiving 1.8k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Donna M. Lehman United States 24 899 528 296 191 190 52 1.8k
Florian C. Kurschus Germany 26 831 0.9× 157 0.3× 67 0.2× 85 0.4× 122 0.6× 47 3.1k
John Lin United States 24 605 0.7× 117 0.2× 216 0.7× 179 0.9× 55 0.3× 73 2.0k
M. Scott Harris United States 22 1.3k 1.4× 284 0.5× 57 0.2× 234 1.2× 83 0.4× 64 2.2k
Timothy R. Hughes United Kingdom 25 786 0.9× 68 0.1× 182 0.6× 136 0.7× 63 0.3× 63 1.9k
William Jia Canada 29 1.2k 1.3× 656 1.2× 53 0.2× 65 0.3× 43 0.2× 96 2.3k
Catherine Bruyns Belgium 20 517 0.6× 132 0.3× 106 0.4× 146 0.8× 44 0.2× 53 2.0k
Michał Krawczyk Poland 21 715 0.8× 114 0.2× 70 0.2× 70 0.4× 55 0.3× 43 1.6k
Harvey R. Kaslow United States 26 1.0k 1.1× 295 0.6× 33 0.1× 182 1.0× 114 0.6× 50 1.9k
Kazuko Uno Japan 25 673 0.7× 108 0.2× 47 0.2× 104 0.5× 63 0.3× 100 2.2k
Isabel Sastre Spain 22 617 0.7× 198 0.4× 34 0.1× 128 0.7× 91 0.5× 51 1.7k

Countries citing papers authored by Donna M. Lehman

Since Specialization
Citations

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

Fields of papers citing papers by Donna M. Lehman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Donna M. Lehman

This figure shows the co-authorship network connecting the top 25 collaborators of Donna M. Lehman. A scholar is included among the top collaborators of Donna M. Lehman 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 Donna M. Lehman. Donna M. Lehman 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.
Joslin, Amelia C., Débora R. Sobreira, Grace Hansen, et al.. (2021). A functional genomics pipeline identifies pleiotropy and cross-tissue effects within obesity-associated GWAS loci. Nature Communications. 12(1). 5253–5253. 25 indexed citations
2.
López-Alvarenga, Juan Carlos, Geetha Chittoor, Solomon F.D. Paul, et al.. (2020). Acanthosis nigricans as a composite marker of cardiometabolic risk and its complex association with obesity and insulin resistance in Mexican American children. PLoS ONE. 15(10). e0240467–e0240467. 8 indexed citations
3.
Kos, Mark Z., Nicholas B. Blackburn, Juan M. Peralta, et al.. (2020). Genotype phasing in pedigrees using whole-genome sequence data. European Journal of Human Genetics. 28(6). 790–803. 3 indexed citations
4.
Mummidi, Srinivas, Joselín Hernández-Ruiz, Vidya S. Farook, et al.. (2019). 1337-P: Prediction of Insulin Sensitivity Using Serum Carotenoid Concentrations and Pediatric Metabolic Index in Mexican-American Children. Diabetes. 68(Supplement_1).
5.
Ramstetter, Monica D., Sushila Shenoy, Thomas D. Dyer, et al.. (2018). Inferring Identical-by-Descent Sharing of Sample Ancestors Promotes High-Resolution Relative Detection. The American Journal of Human Genetics. 103(1). 30–44. 23 indexed citations
6.
Ramstetter, Monica D., Thomas D. Dyer, Donna M. Lehman, et al.. (2017). Benchmarking Relatedness Inference Methods with Genome-Wide Data from Thousands of Relatives. Genetics. 207(1). 75–82. 56 indexed citations
7.
Wang, Chen-Pin, Donna M. Lehman, John G. Kuhn, et al.. (2016). Metformin for Reducing Racial/Ethnic Difference in Prostate Cancer Incidence for Men with Type II Diabetes. Cancer Prevention Research. 9(10). 779–787. 20 indexed citations
8.
Chittoor, Geetha, Jack W. Kent, Marcio Almeida, et al.. (2016). GWAS and transcriptional analysis prioritize ITPR1 and CNTN4 for a serum uric acid 3p26 QTL in Mexican Americans. BMC Genomics. 17(1). 276–276. 13 indexed citations
9.
Wang, Han, et al.. (2015). Improvement of Cell Survival During Human Pluripotent Stem Cell Definitive Endoderm Differentiation. Stem Cells and Development. 24(21). 2536–2546. 24 indexed citations
10.
Almeida, Marcio, Joanne E. Curran, Matthew P. Johnson, et al.. (2015). Effects of copy number variable regions on local gene expression in white blood cells of Mexican Americans. European Journal of Human Genetics. 23(9). 1229–1235. 6 indexed citations
11.
Lehman, Donna M., et al.. (2014). Imputation in families using a heuristic phasing approach. BMC Proceedings. 8(S1). S16–S16. 2 indexed citations
12.
Almasy, Laura, Thomas D. Dyer, Juan M. Peralta, et al.. (2014). Data for Genetic Analysis Workshop 18: human whole genome sequence, blood pressure, and simulated phenotypes in extended pedigrees. BMC Proceedings. 8(S1). S2–S2. 62 indexed citations
13.
Gelfond, Jonathan, Yao Li, Javier Castro‐Hernández, et al.. (2013). Validation of copy number variants associated with prostate cancer risk and prognosis. Urologic Oncology Seminars and Original Investigations. 32(1). 44.e15–44.e20. 2 indexed citations
14.
Lehman, Donna M., Carlos Lorenzo, Javier Hernández, & Chen-Pin Wang. (2012). Statin Use as a Moderator of Metformin Effect on Risk for Prostate Cancer Among Type 2 Diabetic Patients. Diabetes Care. 35(5). 1002–1007. 49 indexed citations
15.
Farook, Vidya S., Sobha Puppala, Jennifer L. Schneider, et al.. (2012). Metabolic Syndrome Is Linked to Chromosome 7q21 and Associated With Genetic Variants in CD36 and GNAT3 in Mexican Americans. Obesity. 20(10). 2083–2092. 25 indexed citations
16.
Beuten, Joke, Indrani Halder, Sharon P. Fowler, et al.. (2011). Wide Disparity in Genetic Admixture Among Mexican Americans from San Antonio, TX. Annals of Human Genetics. 75(4). 529–538. 17 indexed citations
17.
Lehman, Donna M., Robin J. Leach, Teresa L. Johnson‐Pais, et al.. (2006). Evaluation of Tight Junction Protein 1 Encoding Zona Occludens 1 as a Candidate Gene for Albuminuria in a Mexican American Population. Experimental and Clinical Endocrinology & Diabetes. 114(8). 432–437. 13 indexed citations
18.
Rincon-Choles, Hernan, Farook Thameem, Donna M. Lehman, et al.. (2005). Genetic Basis of Diabetic Nephropathy. American Journal of Therapeutics. 12(6). 555–561. 10 indexed citations
19.
Lehman, Donna M., W.E. Sponsel, Robert F. Stratton, et al.. (2001). Genetic mapping of a novel X-linked recessive colobomatous microphthalmia. American Journal of Medical Genetics. 101(2). 114–119. 16 indexed citations
20.
Cody, Jannine D., et al.. (1999). Haplosufficiency of the melanocortin-4 receptor gene in individuals with deletions of 18q. Human Genetics. 105(5). 424–427. 23 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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