Julie A. Sharp

2.1k total citations
63 papers, 1.4k citations indexed

About

Julie A. Sharp is a scholar working on Nutrition and Dietetics, Molecular Biology and Genetics. According to data from OpenAlex, Julie A. Sharp has authored 63 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Nutrition and Dietetics, 22 papers in Molecular Biology and 21 papers in Genetics. Recurrent topics in Julie A. Sharp's work include Infant Nutrition and Health (25 papers), Animal Genetics and Reproduction (18 papers) and Antimicrobial Peptides and Activities (9 papers). Julie A. Sharp is often cited by papers focused on Infant Nutrition and Health (25 papers), Animal Genetics and Reproduction (18 papers) and Antimicrobial Peptides and Activities (9 papers). Julie A. Sharp collaborates with scholars based in Australia, India and United States. Julie A. Sharp's co-authors include Kevin R. Nicholas, Christophe Lefèvre, Alex Andrianopoulos, Meryl A. Davis, Michael J. Hynes, Erik W. Thompson, Xungai Wang, Esfandiar Pakdel, Sima Kashi and Vengamanaidu Modepalli and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Chemical Engineering Journal.

In The Last Decade

Julie A. Sharp

61 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Julie A. Sharp Australia 22 562 281 275 138 119 63 1.4k
Marek Haftek France 35 821 1.5× 280 1.0× 116 0.4× 125 0.9× 99 0.8× 154 4.0k
Mark O. Clements United Kingdom 24 1.2k 2.2× 497 1.8× 107 0.4× 144 1.0× 229 1.9× 39 2.3k
Bruce J. Shenker United States 39 1.4k 2.5× 509 1.8× 246 0.9× 114 0.8× 218 1.8× 85 4.3k
Jolon M. Dyer New Zealand 30 990 1.8× 187 0.7× 180 0.7× 123 0.9× 140 1.2× 105 2.6k
Bow Ho Singapore 36 989 1.8× 350 1.2× 126 0.5× 64 0.5× 166 1.4× 73 3.3k
Koji Kawata Japan 19 493 0.9× 141 0.5× 79 0.3× 100 0.7× 210 1.8× 33 1.7k
Lina Liu China 20 775 1.4× 164 0.6× 60 0.2× 129 0.9× 218 1.8× 98 1.9k
Xiaojuan Cao China 22 640 1.1× 261 0.9× 92 0.3× 95 0.7× 153 1.3× 111 2.3k
Yi Wen United States 33 1.4k 2.5× 146 0.5× 146 0.5× 60 0.4× 364 3.1× 91 3.1k
Yutaka Shimizu Japan 33 1.4k 2.5× 166 0.6× 95 0.3× 150 1.1× 106 0.9× 159 3.7k

Countries citing papers authored by Julie A. Sharp

Since Specialization
Citations

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

Fields of papers citing papers by Julie A. Sharp

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Julie A. Sharp. 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 Julie A. Sharp. The network helps show where Julie A. Sharp may publish in the future.

Co-authorship network of co-authors of Julie A. Sharp

This figure shows the co-authorship network connecting the top 25 collaborators of Julie A. Sharp. A scholar is included among the top collaborators of Julie A. Sharp 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 Julie A. Sharp. Julie A. Sharp 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.
Usman, Ken Aldren S., Ahmed O. Rashed, James W. Maina, et al.. (2024). Biocompatible MXene-reinforced molecularly imprinted membranes for simultaneous filtration and acetaminophen capture. Separation and Purification Technology. 348. 127663–127663. 12 indexed citations
2.
Tardy, Blaise L., James W. Maina, Julie A. Sharp, et al.. (2024). Fouling during hemodialysis – Influence of module design and membrane surface chemistry. SHILAP Revista de lepidopterología. 4. 100100–100100. 8 indexed citations
3.
Lefèvre, Christophe, et al.. (2021). Insulin regulates human mammosphere development and function. Cell and Tissue Research. 384(2). 333–352. 9 indexed citations
4.
Nicholas, Kevin R., Vengamanaidu Modepalli, Lyn A. Hinds, et al.. (2019). Guiding Development of the Neonate: Lessons from Mammalia. Nestlé Nutrition Institute Workshop series. 90. 203–215.
5.
Parveen, Sadiya, et al.. (2019). Structural and mechanistic insights into EchAMP: A antimicrobial protein from the Echidna milk. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1861(6). 1260–1274. 3 indexed citations
6.
7.
Sharp, Julie A., et al.. (2016). Analysis of human breast milk cells: gene expression profiles during pregnancy, lactation, involution, and mastitic infection. Functional & Integrative Genomics. 16(3). 297–321. 32 indexed citations
8.
Modepalli, Vengamanaidu, Lyn A. Hinds, Julie A. Sharp, Christophe Lefèvre, & Kevin R. Nicholas. (2015). Role of marsupial tammar wallaby milk in lung maturation of pouch young. BMC Developmental Biology. 15(1). 16–16. 8 indexed citations
9.
Sharp, Julie A., et al.. (2014). Bioactive Functions of Milk Proteins: a Comparative Genomics Approach. Journal of Mammary Gland Biology and Neoplasia. 19(3-4). 289–302. 20 indexed citations
10.
Kumar, Amit, et al.. (2013). Lactating fur seal case study suggests miR21 may contribute to mammary gland involution evasion during off-shore lactation via regulation of PTEN. Deakin Research Online (Deakin University). 1(1). 5–8.
11.
Kumar, Satish, Peggy Rismiller, Stewart C. Nicol, et al.. (2013). Identification and Functional Characterization of a Novel Monotreme- Specific Antibacterial Protein Expressed during Lactation. PLoS ONE. 8(1). e53686–e53686. 42 indexed citations
12.
Sharp, Julie A., et al.. (2011). WFDC2 is differentially expressed in the mammary gland of the tammar wallaby and provides immune protection to the mammary gland and the developing pouch young. Developmental & Comparative Immunology. 36(3). 584–590. 21 indexed citations
13.
Maksimovic, Jovana, Julie A. Sharp, Kevin R. Nicholas, Benjamin G. Cocks, & Keith W. Savin. (2010). Conservation of the ST6Gal I gene and its expression in the mammary gland. Glycobiology. 21(4). 467–481. 8 indexed citations
14.
Brennan, A. J., Julie A. Sharp, Christophe Lefèvre, & Kevin R. Nicholas. (2008). Uncoupling the mechanisms that facilitate cell survival in hormone-deprived bovine mammary explants. Journal of Molecular Endocrinology. 41(3). 103–116. 9 indexed citations
15.
Brennan, A. J., et al.. (2008). A population of mammary epithelial cells do not require hormones or growth factors to survive. Journal of Endocrinology. 196(3). 483–496. 7 indexed citations
16.
Sharp, Julie A., Christophe Lefèvre, A. J. Brennan, & Kevin R. Nicholas. (2007). The Fur Seal—a Model Lactation Phenotype to Explore Molecular Factors Involved in the Initiation of Apoptosis at Involution. Journal of Mammary Gland Biology and Neoplasia. 12(1). 47–58. 8 indexed citations
17.
18.
Tester, Angus M., et al.. (2002). Correlation between extent of osteolytic damage and metastatic burden of human breast cancer metastasis in nude mice: Real-time PCR quantitation. Clinical & Experimental Metastasis. 19(5). 377–383. 12 indexed citations
19.
Sharp, Julie A., et al.. (2002). Doxycycline-Inducible Expression of SPARC/ Osteonectin/ BM40 in MDA-MB-231 Human Breast Cancer Cells Results in Growth Inhibition. Breast Cancer Research and Treatment. 75(1). 73–85. 73 indexed citations
20.
Papagiannopoulos, Peter, et al.. (1996). ThehapC gene ofAspergillus nidulans is involved in the expression of CCAAT-containing promoters. Molecular and General Genetics MGG. 251(4). 412–421. 58 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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