William J. Rhead

6.7k total citations
111 papers, 4.5k citations indexed

About

William J. Rhead is a scholar working on Clinical Biochemistry, Molecular Biology and Physiology. According to data from OpenAlex, William J. Rhead has authored 111 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 71 papers in Clinical Biochemistry, 60 papers in Molecular Biology and 36 papers in Physiology. Recurrent topics in William J. Rhead's work include Metabolism and Genetic Disorders (71 papers), Mitochondrial Function and Pathology (23 papers) and Diet and metabolism studies (23 papers). William J. Rhead is often cited by papers focused on Metabolism and Genetic Disorders (71 papers), Mitochondrial Function and Pathology (23 papers) and Diet and metabolism studies (23 papers). William J. Rhead collaborates with scholars based in United States, Canada and Germany. William J. Rhead's co-authors include Brad A. Amendt, Kay Tanaka, Anne Moon, G. N. Schrauzer, Susan A. Berry, Gregory M. Enns, Saul W. Brusilow, Philip A. Wood, Ada Hamosh and Gerard T. Berry and has published in prestigious journals such as Science, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

William J. Rhead

108 papers receiving 4.3k citations

Peers

Countries citing papers authored by William J. Rhead

Since Specialization

Citations

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

Fields of papers citing papers by William J. Rhead

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of William J. Rhead. A scholar is included among the top collaborators of William J. Rhead 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 William J. Rhead. William J. Rhead 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

#	Work	Indexed citations
1	Long-term safety and efficacy of glycerol phenylbutyrate for the management of urea cycle disorder patients 2019 ·Molecular Genetics and Metabolism ·George A. Díaz, Andreas Schulze, Nicola Longo, William J. Rhead, Annette Feigenbaum, Derek A. Wong, J. Lawrence Merritt, William Berquist, Renata C. Gallagher, Dennis Bartholomew, Shawn E. McCandless, Wendy E. Smith, Cary O. Harding, Roberto Zori, Uta Lichter‐Konecki, Jerry Vockley, (unknown), Thomas Vescio, Robert J. Holt, Susan A. Berry	10
2	Glycerol phenylbutyrate treatment in children with urea cycle disorders: Pooled analysis of short and long-term ammonia control and outcomes 2014 ·Molecular Genetics and Metabolism ·Susan A. Berry, Uta Lichter‐Konecki, George A. Díaz, Shawn E. McCandless, William J. Rhead, Wendy E. Smith, Cynthia LeMons, Sandesh C.S. Nagamani, Dion F. Coakley, Masoud Mokhtarani, Bruce F. Scharschmidt, Brendan Lee	27
3	Pancreatic insufficiency in Toriello–Carey syndrome: Report of a second patient 2012 ·American Journal of Medical Genetics Part A ·Khalil El‐Chammas, (unknown), Regan Veith, Neha Sekhri, William J. Rhead, Helga V. Toriello, Praveen S. Goday	3
4	Phase 2 comparison of a novel ammonia scavenging agent with sodium phenylbutyrate in patients with urea cycle disorders: Safety, pharmacokinetics and ammonia control 2010 ·Molecular Genetics and Metabolism ·Brendan Lee, William J. Rhead, George A. Díaz, Bruce F. Scharschmidt, Asad Mian, Oleg A. Shchelochkov, Jean‐Francois Marier, Martin Béliveau, (unknown), Klara Dickinson	72
5	Agalsidase Alfa and Kidney Dysfunction in Fabry Disease 2009 ·Journal of the American Society of Nephrology ·Michael L. West, Kathy Nicholls, Atul Mehta, Joe T.R. Clarke, Robert D. Steiner, Michael Beck, Bruce A. Barshop, William J. Rhead, (unknown), Markus Ries, Raphael Schiffmann	119
6	Identification of Urine Organic Acids for the Detection of Inborn Errors of Metabolism Using Urease and Gas Chromatography-Mass Spectrometry (GC-MS) 2009 ·Methods in molecular biology ·Stanley F. Lo, (unknown), William J. Rhead	8
7	Transient multiple acyl-CoA dehydrogenation deficiency in a newborn female caused by maternal riboflavin deficiency 2007 ·Molecular Genetics and Metabolism ·Mary Anne D. Chiong, Keow Giak Sim, Kevin Carpenter, William J. Rhead, Gladys Ho, Rikke Katrine Jentoft Olsen, John Christodoulou	33
8	Rescue from neonatal death in the murine model of hereditary tyrosinemia by glutathione monoethylester and vitamin C treatment 2007 ·Molecular Genetics and Metabolism ·(unknown), Rossana Jorquera, (unknown), Anne Bergeron, Milton J. Finegold, William J. Rhead, Robert M. Tanguay	8
9	Urea Cycle Disorders: Clinical Presentation Outside the Newborn Period 2005 ·Critical Care Clinics ·Wendy E. Smith, Priya S. Kishnani, Brendan Lee, Rani H. Singh, William J. Rhead, Lisa Sniderman King, Michael C. Smith, Marshall Summar	66
10	Ascorbate decreases Fabry cerebral hyperperfusion suggesting a reactive oxygen species abnormality: An arterial spin tagging study 2004 ·Journal of Magnetic Resonance Imaging ·David F. Moore, (unknown), Marie‐Luise Brennan, Surya Gupta, Bruce A. Barshop, Robert D. Steiner, William J. Rhead, Roscoe O. Brady, Stanley L. Hazen, Raphael Schiffmann	65
11	Genitopatellar syndrome: Expanding the phenotype 2003 ·American Journal of Medical Genetics Part A ·(unknown), William J. Rhead, Steven R. Leuthner, Mark Lubinsky	10
12	Carbohydrate-deficient glycoprotein syndrome type 1 with profound thrombocytopenia and normal phosphomannomutase and phosphomannose isomerase activities 1998 ·The Journal of Pediatrics ·Michael J. Acarregui, T. Neville George, William J. Rhead	19
13	Purification of human very-long-chain acyl-coenzyme A dehydrogenase and characterization of its deficiency in seven patients. 1995 ·Journal of Clinical Investigation ·Toshifumi Aoyama, Masayoshi Souri, (unknown), Takehiko Kamijo, Seiji Yamaguchi, Richard I. Kelley, William J. Rhead, Katsuji Uetake, Kay Tanaka, T. Hashimoto	135
14	Formation of a novel arachidonic acid metabolite in peroxisomes 1995 ·Prostaglandins Leukotrienes and Essential Fatty Acids ·Joel Gordon, (unknown), William J. Rhead, Paul A. Watkins, Arthur A. Spector	6
15	Glutaric acidemia type II. Heterogeneity in beta-oxidation flux, polypeptide synthesis, and complementary DNA mutations in the alpha subunit of electron transfer flavoprotein in eight patients. 1992 ·Journal of Clinical Investigation ·E Fréneaux, Val C. Sheffield, (unknown), (unknown), William J. Rhead	44
16	Defect in fatty acid oxidation: Laboratory and pathologic findings in a patient 1991 ·Pediatric Neurology ·James H. Tonsgard, Janet K. Stephens, William J. Rhead, Duna Penn, Allen L. Horwitz, Barbara S. Kirschner, Peter F. Whitington, Stuart Berger, Marjorie E. Tripp	5
17	Identification of a common mutation in patients with medium-chain acyl-CoA dehydrogenase deficiency 1990 ·Biochemical and Biophysical Research Communications ·Yoichi Matsubara, Kuniaki Narisawa, Shigeaki Miyabayashi, Keiya Tada, Paul M. Coates, C. Bachmann, Louis J. Elsas, R. J. Pollitt, William J. Rhead, Charles R. Roe	97
18	Peroxisomal L-Pipecolic Acid Oxidation Is Deficient in Liver from Zellweger Syndrome Patients 1989 ·Pediatric Research ·Stephanie J. Mihalik, Hugo W. Moser, Paul A. Watkins, David M. Danks, A. Poulos, William J. Rhead	35
19	Short-chain acyl-coenzyme A dehydrogenase deficiency. Clinical and biochemical studies in two patients. 1987 ·Journal of Clinical Investigation ·Brad A. Amendt, Carol L. Greene, Lawrence Sweetman, (unknown), (unknown), Anne Moon, (unknown), William J. Rhead	133
20	Abetalipoproteinemia 1984 ·Ophthalmologica ·(unknown), William J. Rhead, (unknown)	9

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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