Leonard Prouty

507 total citations
17 papers, 401 citations indexed

About

Leonard Prouty is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Leonard Prouty has authored 17 papers receiving a total of 401 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 8 papers in Molecular Biology and 3 papers in Surgery. Recurrent topics in Leonard Prouty's work include Genomic variations and chromosomal abnormalities (3 papers), Chromosomal and Genetic Variations (3 papers) and Acute Myeloid Leukemia Research (2 papers). Leonard Prouty is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Chromosomal and Genetic Variations (3 papers) and Acute Myeloid Leukemia Research (2 papers). Leonard Prouty collaborates with scholars based in United States. Leonard Prouty's co-authors include Jian Liang, Kerry Blanchard, Briana J. Williams, Mark A. Dayton, Alan R. Mootnick, William S. Pollitzer, Philip D. Buchanan, Sushil K. Jain, Charles E. Schwartz and Roger E. Stevenson and has published in prestigious journals such as Blood, Free Radical Biology and Medicine and Journal of Cellular Biochemistry.

In The Last Decade

Leonard Prouty

17 papers receiving 380 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Leonard Prouty United States	11	191	157	48	46	39	17	401
Sharon Bain Australia	12	85 0.4×	154 1.0×	9 0.2×	33 0.7×	38 1.0×	13	417
P. H. Saldanha Brazil	12	128 0.7×	138 0.9×	12 0.3×	7 0.2×	31 0.8×	42	447
Sandy Goodburn United Kingdom	9	294 1.5×	277 1.8×	8 0.2×	12 0.3×	12 0.3×	12	650
Oswaldo Frota‐Pessoa Brazil	14	290 1.5×	235 1.5×	15 0.3×	10 0.2×	5 0.1×	65	711
E. Hosoi Japan	11	41 0.2×	60 0.4×	13 0.3×	18 0.4×	15 0.4×	21	324
J. Schmidtke Germany	11	192 1.0×	242 1.5×	7 0.1×	19 0.4×	9 0.2×	33	455
A Mayerová Germany	12	183 1.0×	199 1.3×	17 0.4×	11 0.2×	6 0.2×	33	545
Saurav Guha United States	18	324 1.7×	330 2.1×	19 0.4×	58 1.3×	4 0.1×	29	725
Liza Chang United States	10	212 1.1×	82 0.5×	10 0.2×	14 0.3×	61 1.6×	13	395
A L Jørgensen Denmark	11	476 2.5×	294 1.9×	8 0.2×	54 1.2×	20 0.5×	23	630

Countries citing papers authored by Leonard Prouty

Since Specialization

Citations

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

Fields of papers citing papers by Leonard Prouty

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Leonard Prouty. 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 Leonard Prouty. The network helps show where Leonard Prouty may publish in the future.

Co-authorship network of co-authors of Leonard Prouty

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

All Works

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17 of 17 papers shown

1.

Prouty, Leonard, et al.. (2017). Case Report of Proliferative Peripheral Retinopathy in Two Familial Lissencephaly Infants with Miller–Dieker Syndrome. Journal of Pediatric Genetics. 7(2). 86–91. 2 indexed citations

2.

Alexander, J. Steven, et al.. (2013). Venous endothelial injury in central nervous system diseases. BMC Medicine. 11(1). 219–219. 18 indexed citations

3.

Prouty, Leonard, et al.. (2004). Protective effects of 17β-estradiol and trivalent chromium on interleukin-6 secretion, oxidative stress, and adhesion of monocytes: Relevance to heart disease in postmenopausal women. Free Radical Biology and Medicine. 37(11). 1730–1735. 22 indexed citations

4.

Kannan, Krishnaswamy, et al.. (2004). Progesterone, but not 17β-estradiol, increases TNF-α secretion in U937 monocytes. Cytokine. 26(3). 102–105. 31 indexed citations

5.

Chen, Harold, et al.. (1999). Uniparental isodisomy resulting from 46,XX,i(1p),i(1q) in a woman with short stature, ptosis, micro/retrognathia, myopathy, deafness, and sterility. American Journal of Medical Genetics. 82(3). 215–218. 17 indexed citations

6.

Asamoah, Alexander, et al.. (1998). A case of insertional translocation involving chromosomes 2 and 4. Clinical Genetics. 53(2). 142–146. 2 indexed citations

7.

Liang, Jian, Leonard Prouty, Briana J. Williams, Mark A. Dayton, & Kerry Blanchard. (1998). Acute Mixed Lineage Leukemia With an inv(8)(p11q13) Resulting in Fusion of the Genes for MOZ and TIF2. Blood. 92(6). 2118–2122. 116 indexed citations

8.

Liang, Jian, Leonard Prouty, Briana J. Williams, Mark A. Dayton, & Kerry Blanchard. (1998). Acute Mixed Lineage Leukemia With an inv(8)(p11q13) Resulting in Fusion of the Genes for MOZ and TIF2. Blood. 92(6). 2118–2122. 14 indexed citations

9.

Wolfe, Steven A., et al.. (1994). Primate testicular histone H1t genes are highly conserved and the human H1t gene is located on chromosome 6. Journal of Cellular Biochemistry. 54(2). 219–230. 20 indexed citations

10.

Prouty, Leonard, et al.. (1989). Non‐mosaic trisomy 20 in amniotic fluid cultures with minor anomalies in the fetus. Clinical Genetics. 35(4). 233–236. 6 indexed citations

11.

Schwartz, Charles E., Mary C. Phelan, Gordon H. Wilkes, et al.. (1988). Fragile X syndrome: Incidence, clinical and cytogenetic findings in the black and white populations of South Carolina. American Journal of Medical Genetics. 30(1-2). 641–654. 17 indexed citations

12.

Prouty, Leonard, R. Curtis Rogers, Roger E. Stevenson, et al.. (1988). Fragile X syndrome: Growth, development, and intellectual function. American Journal of Medical Genetics. 30(1-2). 123–142. 50 indexed citations

13.

Phelan, Mary C., Leonard Prouty, Roger E. Stevenson, et al.. (1988). The parental origin and mechanism of formation of three dicentric X chromosomes. Human Genetics. 80(1). 81–84. 9 indexed citations

14.

Prouty, Leonard, et al.. (1987). Oligohydramnios sequence (Potter's syndrome): case clustering in northeastern Tennessee.. PubMed. 80(5). 585–92. 4 indexed citations

15.

Prouty, Leonard, et al.. (1987). Consumer costs for genetic services. American Journal of Medical Genetics. 26(3). 521–530. 5 indexed citations

16.

Prouty, Leonard, Philip D. Buchanan, William S. Pollitzer, & Alan R. Mootnick. (1983). Taxonomic note: Bunopithecus: A genus‐level taxon for the hoolock gibbon (Hylobates hoolock). American Journal of Primatology. 5(1). 83–87. 27 indexed citations

17.

Prouty, Leonard, Philip D. Buchanan, William S. Pollitzer, & Alan R. Mootnick. (1983). A presumptive new hylobatid subgenus with 38 chromosomes. Cytogenetic and Genome Research. 35(2). 141–142. 41 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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