J. William Higgins

2.3k total citations · 1 hit paper
20 papers, 1.5k citations indexed

About

J. William Higgins is a scholar working on Oncology, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, J. William Higgins has authored 20 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Oncology, 7 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in J. William Higgins's work include Drug Transport and Resistance Mechanisms (10 papers), Pharmacogenetics and Drug Metabolism (7 papers) and Pharmacological Effects and Toxicity Studies (7 papers). J. William Higgins is often cited by papers focused on Drug Transport and Resistance Mechanisms (10 papers), Pharmacogenetics and Drug Metabolism (7 papers) and Pharmacological Effects and Toxicity Studies (7 papers). J. William Higgins collaborates with scholars based in United States, United Kingdom and Canada. J. William Higgins's co-authors include Maciej J. Zamek‐Gliszczynski, Jing Bao, Ewan E. Morrison, Jacquelyn Bond, Alice Ke, C. Geoffrey Woods, Christopher Bennett, Emma Roberts, Sharon C. Presnell and Stephen D. Hall and has published in prestigious journals such as Nature Genetics, Nature Materials and PLoS ONE.

In The Last Decade

J. William Higgins

19 papers receiving 1.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Cellular extrusion bioprinting improves kidney organoid reproducibility and conformation

2020 310 citations Kynan T. Lawlor, Jessica M. Vanslambrouck et al. Nature Materials profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
J. William Higgins United States	14	728	448	344	304	235	20	1.5k
Guy Makin United Kingdom	23	969 1.3×	537 1.2×	150 0.4×	101 0.3×	133 0.6×	49	1.8k
Robert D. Bruno United States	20	450 0.6×	508 1.1×	99 0.3×	439 1.4×	207 0.9×	34	1.4k
Jung‐Hwa Oh South Korea	21	866 1.2×	223 0.5×	80 0.2×	156 0.5×	166 0.7×	69	1.4k
Hae‐Yun Jung South Korea	20	823 1.1×	505 1.1×	186 0.5×	75 0.2×	65 0.3×	31	1.5k
Judith Hagenbuchner Austria	21	980 1.3×	182 0.4×	107 0.3×	118 0.4×	38 0.2×	38	1.4k
Jiangchao Li China	22	963 1.3×	368 0.8×	90 0.3×	52 0.2×	48 0.2×	72	1.6k
Xuejian Zhao China	25	868 1.2×	408 0.9×	141 0.4×	259 0.9×	150 0.6×	62	1.7k
Vivi Kasim China	24	1.3k 1.8×	253 0.6×	137 0.4×	99 0.3×	104 0.4×	62	1.9k
Nicolas Germain France	20	519 0.7×	160 0.4×	45 0.1×	87 0.3×	68 0.3×	41	1.4k
Houjie Liang China	29	1.2k 1.7×	711 1.6×	174 0.5×	175 0.6×	97 0.4×	73	2.4k

Countries citing papers authored by J. William Higgins

Since Specialization

Citations

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

Fields of papers citing papers by J. William Higgins

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J. William Higgins. 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 J. William Higgins. The network helps show where J. William Higgins may publish in the future.

Co-authorship network of co-authors of J. William Higgins

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

All Works

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20 of 20 papers shown

Murphy, Keith E., J. William Higgins, Sara Brin Rosenthal, et al.. (2024). Induction of MASH in three-dimensional bioprinted human liver tissue. PLoS ONE. 19(12). e0312615–e0312615. 1 indexed citations

Martin, Heather L., J. William Higgins, Anna A. Tang, et al.. (2023). Affimer-mediated locking of p21-activated kinase 5 in an intermediate activation state results in kinase inhibition. Cell Reports. 42(10). 113184–113184. 3 indexed citations

Coe, Kevin J., Mark Feinstein, J. William Higgins, et al.. (2022). Characterization of JNJ-2482272 [4-(4-Methyl-2-(4-(Trifluoromethyl)Phenyl)Thiazole-5-yl) Pyrimidine-2-Amine] As a Strong Aryl Hydrocarbon Receptor Activator in Rat and Human. Drug Metabolism and Disposition. 50(8). 1064–1076. 2 indexed citations

Lawlor, Kynan T., Jessica M. Vanslambrouck, J. William Higgins, et al.. (2020). Cellular extrusion bioprinting improves kidney organoid reproducibility and conformation. Nature Materials. 20(2). 260–271. 310 indexed citations breakdown →

King, Shelby M., et al.. (2017). 3D Proximal Tubule Tissues Recapitulate Key Aspects of Renal Physiology to Enable Nephrotoxicity Testing. Frontiers in Physiology. 8. 123–123. 93 indexed citations

Posada, Maria M., Ellen A. Cannady, Christopher D. Payne, et al.. (2017). Prediction of Transporter‐Mediated Drug‐Drug Interactions for Baricitinib. Clinical and Translational Science. 10(6). 509–519. 55 indexed citations

King, Shelby M., et al.. (2016). A three-dimensional (3D) bioprinted model of the renal proximal tubule for evaluation of drug-induced nephrotoxicity. Toxicology Letters. 258. S288–S288. 1 indexed citations

Martin, Heather L., Matthew Adams, J. William Higgins, et al.. (2014). High-Content, High-Throughput Screening for the Identification of Cytotoxic Compounds Based on Cell Morphology and Cell Proliferation Markers. PLoS ONE. 9(2). e88338–e88338. 55 indexed citations

Higgins, J. William, Alice Ke, & Maciej J. Zamek‐Gliszczynski. (2014). Clinical CYP3A Inhibitor Alternatives to Ketoconazole, Clarithromycin and Itraconazole, Are Not Transported into the Liver by Hepatic Organic Anion Transporting Polypeptides and Organic Cation Transporter 1. Drug Metabolism and Disposition. 42(11). 1780–1784. 16 indexed citations

10.

Ke, Alice, et al.. (2014). Itraconazole and Clarithromycin as Ketoconazole Alternatives for Clinical CYP3A Inhibition Studies. Clinical Pharmacology & Therapeutics. 95(5). 473–476. 50 indexed citations

11.

Posada, Maria M., James A. Bacon, Karen Schneck, et al.. (2014). Prediction of Renal Transporter Mediated Drug-Drug Interactions for Pemetrexed Using Physiologically Based Pharmacokinetic Modeling. Drug Metabolism and Disposition. 43(3). 325–334. 54 indexed citations

12.

Adams, Matthew, Victoria Cookson, J. William Higgins, et al.. (2013). A High-Throughput Assay to Identify Modifiers of Premature Chromosome Condensation. SLAS DISCOVERY. 19(1). 176–183. 8 indexed citations

13.

Zamek‐Gliszczynski, Maciej J., Jing Bao, Jeffrey S. Day, & J. William Higgins. (2013). Metformin Sinusoidal Efflux from the Liver Is Consistent with Negligible Biliary Excretion and Absence of Enterohepatic Cycling. Drug Metabolism and Disposition. 41(11). 1967–1971. 23 indexed citations

14.

Higgins, J. William, Jing Bao, Alice Ke, et al.. (2013). Utility of Oatp1a/1b-Knockout and OATP1B1/3-Humanized Mice in the Study of OATP-Mediated Pharmacokinetics and Tissue Distribution: Case Studies with Pravastatin, Atorvastatin, Simvastatin, and Carboxydichlorofluorescein. Drug Metabolism and Disposition. 42(1). 182–192. 75 indexed citations

15.

Higgins, J. William, et al.. (2012). Ablation of Both Organic Cation Transporter (Oct)1 and Oct2 Alters Metformin Pharmacokinetics but Has No Effect on Tissue Drug Exposure and Pharmacodynamics. Drug Metabolism and Disposition. 40(6). 1170–1177. 88 indexed citations

16.

Zamek‐Gliszczynski, Maciej J., et al.. (2012). Characterization of SAGE Mdr1a (P-gp), Bcrp, and Mrp2 Knockout Rats Using Loperamide, Paclitaxel, Sulfasalazine, and Carboxydichlorofluorescein Pharmacokinetics. Drug Metabolism and Disposition. 40(9). 1825–1833. 81 indexed citations

17.

Higgins, J. William, Carol Midgley, Sandra Bell, et al.. (2010). Human ASPM participates in spindle organisation, spindle orientation and cytokinesis. BMC Cell Biology. 11(1). 85–85. 95 indexed citations

18.

Gannon, Michael K., Stephanie M. Bennett, Tip W. Loo, et al.. (2009). Rhodamine Inhibitors of P-Glycoprotein: An Amide/Thioamide “Switch” for ATPase Activity. Journal of Medicinal Chemistry. 52(10). 3328–3341. 54 indexed citations

19.

Sawada, Geri A., et al.. (2008). Chalcogenopyrylium dyes as inhibitors/modulators of P-glycoprotein in multidrug-resistant cells. Bioorganic & Medicinal Chemistry. 16(22). 9745–9756. 13 indexed citations

20.

Bond, Jacquelyn, Emma Roberts, Kelly Springell, et al.. (2005). A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size. Nature Genetics. 37(4). 353–355. 423 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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