Howard Henderson

1.8k total citations
47 papers, 1.5k citations indexed

About

Howard Henderson is a scholar working on Endocrinology, Diabetes and Metabolism, Cardiology and Cardiovascular Medicine and Surgery. According to data from OpenAlex, Howard Henderson has authored 47 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Endocrinology, Diabetes and Metabolism, 19 papers in Cardiology and Cardiovascular Medicine and 17 papers in Surgery. Recurrent topics in Howard Henderson's work include Lipid metabolism and disorders (19 papers), Diabetes, Cardiovascular Risks, and Lipoproteins (18 papers) and Lipoproteins and Cardiovascular Health (12 papers). Howard Henderson is often cited by papers focused on Lipid metabolism and disorders (19 papers), Diabetes, Cardiovascular Risks, and Lipoproteins (18 papers) and Lipoproteins and Cardiovascular Health (12 papers). Howard Henderson collaborates with scholars based in South Africa, Canada and United States. Howard Henderson's co-authors include Michael R. Hayden, A. David Marais, John J.P. Kastelein, Séverine Gagné, Yuanhong Ma, Felicity Leisegang, John D. Brunzell, Miao Li, Susanne M. Clee and G M Berger and has published in prestigious journals such as New England Journal of Medicine, Journal of Clinical Investigation and PLoS ONE.

In The Last Decade

Howard Henderson

47 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Howard Henderson South Africa	26	743	659	543	356	224	47	1.5k
Steven R. Silberman United States	10	409 0.6×	706 1.1×	785 1.4×	733 2.1×	102 0.5×	10	1.8k
Carole L. Banka United States	20	158 0.2×	396 0.6×	564 1.0×	478 1.3×	185 0.8×	31	1.6k
Ilia V. Fuki United States	20	266 0.4×	451 0.7×	803 1.5×	747 2.1×	98 0.4×	27	1.7k
Joseph C. Obunike United States	17	352 0.5×	422 0.6×	307 0.6×	390 1.1×	55 0.2×	19	1.1k
Sarada C. Prasad United States	16	342 0.5×	603 0.9×	423 0.8×	490 1.4×	99 0.4×	33	1.4k
Stephen J. Demosky United States	22	161 0.2×	452 0.7×	1.0k 1.9×	723 2.0×	93 0.4×	37	1.7k
Margarita de la Llera Moya United States	10	162 0.2×	508 0.8×	1.1k 1.9×	627 1.8×	54 0.2×	13	1.6k
Karen O. Badellino United States	18	278 0.4×	347 0.5×	340 0.6×	145 0.4×	58 0.3×	22	969
V. Clavey France	18	162 0.2×	477 0.7×	663 1.2×	503 1.4×	57 0.3×	31	1.3k
P Lohse Germany	27	176 0.2×	295 0.4×	450 0.8×	586 1.6×	253 1.1×	57	1.4k

Countries citing papers authored by Howard Henderson

Since Specialization

Citations

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

Fields of papers citing papers by Howard Henderson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Howard Henderson

This figure shows the co-authorship network connecting the top 25 collaborators of Howard Henderson. A scholar is included among the top collaborators of Howard Henderson 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 Howard Henderson. Howard Henderson 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

Henderson, Howard, et al.. (2014). L-2 hydroxyglutaric aciduria in a South African Staffordshire Bull Terrier. Journal of the South African Veterinary Association. 85(1). 1042–1042. 3 indexed citations

Owen, E., Peter Berman, S. E. Olpin, et al.. (2010). Glutaric aciduria type 1 in South Africa—high incidence of glutaryl-CoA dehydrogenase deficiency in black South Africans. Molecular Genetics and Metabolism. 101(2-3). 178–182. 37 indexed citations

Wood, Kathryn J., Brian Eley, David Beatty, et al.. (2009). Polymorphic Variation in TIRAP Is Not Associated with Susceptibility to Childhood TB but May Determine Susceptibility to TBM in Some Ethnic Groups. PLoS ONE. 4(8). e6698–e6698. 29 indexed citations

Blom, Dirk, et al.. (2008). Severe Hypertriglyceridaemia as a result of Familial Chylomicronaemia. South African Medical Journal. 98(2). 105–108. 11 indexed citations

Wegner, Daniel, Christopher S. Carlson, Jennifer Wambach, et al.. (2008). Recombination as a mechanism for sporadic mutation in the surfactant protein‐C gene. Pediatric Pulmonology. 43(5). 443–450. 8 indexed citations

Roberts, Andrew, Andrew D. Thomas, Reinhard Würzner, et al.. (2007). Prevalence of mutations leading to complete C6 deficiency (C6Q0) in the Western Cape, South Africa and detection of novel mutations leading to C6Q0 in an Irish family. Molecular Immunology. 44(10). 2756–2760. 16 indexed citations

Marais, A. David, et al.. (2006). Autosomal recessive hypercholesterolaemia: Discrimination of ARH protein and LDLR function in the homozygous FH phenotype. Clinica Chimica Acta. 378(1-2). 33–37. 8 indexed citations

Young, Douglas, Brian Eley, Howard Henderson, et al.. (2003). Failure to Control Growth of Mycobacteria in Blood from Children Infected with Human Immunodeficiency Virus and Its Relationship to T Cell Function. The Journal of Infectious Diseases. 187(10). 1544–1551. 36 indexed citations

Eley, Brian, et al.. (2003). X-linked Hyper IgM (HIGM1) in an African kindred: the first report from South Africa. BMC Pediatrics. 3(1). 12–12. 3 indexed citations

10.

Wilmshurst, Jo M., Lindsay M. Reynolds, Ronald van Toorn, Felicity Leisegang, & Howard Henderson. (2002). Spinal muscular atrophy in black South Africans: concordance with the universal SMN1 genotype. Clinical Genetics. 62(2). 165–168. 8 indexed citations

11.

Clee, Susanne M., Nagat Bissada, Fudan Miao, et al.. (2000). Plasma and vessel wall lipoprotein lipase have different roles in atherosclerosis. Journal of Lipid Research. 41(4). 521–531. 86 indexed citations

12.

Henderson, Howard, Saskia M. Bijvoet, Taco Bruin, et al.. (1998). Ile225Thr loop mutation in thelipoprotein lipase (LPL) gene is a de novo event. American Journal of Medical Genetics. 78(4). 313–316. 13 indexed citations

13.

Kastelein, John J.P., David Hallman, Howard Henderson, et al.. (1998). The Asn9 variant of lipoprotein lipase is associated with the -93G promoter mutation and an increased risk of coronary artery disease. Clinical Genetics. 53(1). 27–33. 40 indexed citations

14.

Zhang, Hanfang, Howard Henderson, Séverine Gagné, et al.. (1996). Common sequence variants of lipoprotein lipase: standardized studies of in vitro expression and catalytic function. Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism. 1302(2). 159–166. 101 indexed citations

15.

Ma, Yuanhong, Saskia M. Bijvoet, Howard Henderson, et al.. (1992). A missense mutation (Asp250→Asn) in exon 6 of the human lipoprotein lipase gene causes chylomicronemia in patients of different ancestries. Genomics. 13(3). 649–653. 37 indexed citations

16.

Bruin, Taco, John J.P. Kastelein, D.E. van Diermen, et al.. (1992). A missense mutation Pro157Arg in lipoprotein lipase (LPL_Nijmegen) resulting in loss of catalytic activity. European Journal of Biochemistry. 208(2). 267–272. 13 indexed citations

17.

Henderson, Howard, Yuxuan Ma, María Victoria Monsalve, et al.. (1991). Amino acid substitution (Ile194----Thr) in exon 5 of the lipoprotein lipase gene causes lipoprotein lipase deficiency in three unrelated probands. Support for a multicentric origin.. Journal of Clinical Investigation. 87(6). 2005–2011. 65 indexed citations

18.

Ma, Yuanhong, Howard Henderson, M.R. Ven Murthy, et al.. (1991). A Mutation in the Human Lipoprotein Lipase Gene as the Most Common Cause of Familial Chylomicronemia in French Canadians. New England Journal of Medicine. 324(25). 1761–1766. 87 indexed citations

19.

Henderson, Howard, Maritha J. Kotze, & G M Berger. (1989). Multiple mutations underlying familial hypercholesterolemia in the South African population. Human Genetics. 83(1). 67–70. 2 indexed citations

20.

Henderson, Howard, G M Berger, & A. David Marais. (1988). A new LDL receptor gene deletion mutation in the South African population. Human Genetics. 80(4). 371–374. 16 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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