Engela Honey

561 total citations
25 papers, 168 citations indexed

About

Engela Honey is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Engela Honey has authored 25 papers receiving a total of 168 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Genetics. Recurrent topics in Engela Honey's work include Neurogenetic and Muscular Disorders Research (4 papers), Muscle Physiology and Disorders (2 papers) and Connective tissue disorders research (2 papers). Engela Honey is often cited by papers focused on Neurogenetic and Muscular Disorders Research (4 papers), Muscle Physiology and Disorders (2 papers) and Connective tissue disorders research (2 papers). Engela Honey collaborates with scholars based in South Africa, United States and Belgium. Engela Honey's co-authors include Lodewyk J. Mienie, Sumaiya Adam, Peter Beighton, Karen Fieggen, Detlef Knoll, Amanda Krause, Francois H. van der Westhuizen, Sam W. Moore, Christiaan F. Hoogendijk and Justyna A. Karolak and has published in prestigious journals such as Clinical Chemistry, AIDS and Journal of the Neurological Sciences.

In The Last Decade

Engela Honey

22 papers receiving 166 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Engela Honey South Africa	9	65	38	33	24	22	25	168
Lissette Estrella United States	5	39 0.6×	37 1.0×	9 0.3×	34 1.4×	64 2.9×	9	238
Juliana Teo Australia	6	103 1.6×	24 0.6×	8 0.2×	17 0.7×	9 0.4×	11	194
Dita Cebecauerová Czechia	8	68 1.0×	15 0.4×	33 1.0×	5 0.2×	12 0.5×	12	131
Michael Parfenov United States	7	98 1.5×	28 0.7×	29 0.9×	8 0.3×	30 1.4×	10	254
Olga Shamardina United Kingdom	3	56 0.9×	129 3.4×	8 0.2×	26 1.1×	9 0.4×	3	192
V. Doireau France	5	21 0.3×	11 0.3×	26 0.8×	29 1.2×	18 0.8×	12	179
María Caimari Spain	8	86 1.3×	113 3.0×	42 1.3×	8 0.3×	10 0.5×	14	232
Shunsuke Tamaru Japan	10	81 1.2×	23 0.6×	22 0.7×	39 1.6×	14 0.6×	25	241
Rita Valdéz Argentina	6	30 0.5×	46 1.2×	23 0.7×	4 0.2×	28 1.3×	10	171
Domenico Dell’Edera Italy	13	51 0.8×	46 1.2×	83 2.5×	5 0.2×	16 0.7×	39	363

Countries citing papers authored by Engela Honey

Since Specialization

Citations

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

Fields of papers citing papers by Engela Honey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Engela Honey

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

Honey, Engela, et al.. (2024). Maternally inherited diabetes and deafness with a variable presentation across three generations within a pedigree, South Africa. African Journal of Laboratory Medicine. 13(1). 2384–2384.

Honey, Engela, et al.. (2024). Mutation analysis and clinical profile of South African patients with Neurofibromatosis type 1 (NF1) phenotype. Frontiers in Genetics. 15. 1331278–1331278. 2 indexed citations

Spencer, Careni, et al.. (2024). Mutation profiling in South African patients with Cornelia de Lange syndrome phenotype. Molecular Genetics & Genomic Medicine. 12(1). e2342–e2342. 2 indexed citations

Laver, Thomas W., Matthew N. Wakeling, Richard Caswell, et al.. (2024). Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements. European Journal of Human Genetics. 32(7). 813–818. 2 indexed citations

Spencer, Careni, et al.. (2023). A feasible molecular diagnostic strategy for rare genetic disorders within resource-constrained environments. Journal of Community Genetics. 15(1). 39–48. 5 indexed citations

Honey, Engela, et al.. (2022). Parents’ perspectives on the use of children’s facial images for research and diagnosis: a survey. Journal of Community Genetics. 13(6). 641–654. 1 indexed citations

Joseph, Jessica, Engela Honey, Mansour Farahani, et al.. (2020). Pregnancy outcomes and birth defects from an antiretroviral drug safety study of women in South Africa and Zambia. UNC Libraries.

Karolak, Justyna A., Tomasz Gambin, Engela Honey, et al.. (2020). A de novo 2.2 Mb recurrent 17q23.1q23.2 deletion unmasks novel putative regulatory non-coding SNVs associated with lethal lung hypoplasia and pulmonary hypertension: a case report. BMC Medical Genomics. 13(1). 34–34. 11 indexed citations

Adam, Sumaiya, et al.. (2018). Pena-Shokeir syndrome: current management strategies and palliative care. The Application of Clinical Genetics. Volume 11. 111–120. 12 indexed citations

10.

Westhuizen, Francois H. van der, et al.. (2017). A novel mutation in ETFDH manifesting as severe neonatal-onset multiple acyl-CoA dehydrogenase deficiency. Journal of the Neurological Sciences. 384. 121–125. 17 indexed citations

11.

Beighton, Peter, Manogari Chetty, B Henderson, et al.. (2017). Osteogenesis imperfecta type 3 in South Africa: Causative mutations in FKBP10. South African Medical Journal. 107(5). 457–457. 12 indexed citations

12.

Spencer, Careni, et al.. (2017). Biallelic BRCA2 mutations in two black South African children with Fanconi anaemia. Familial Cancer. 16(3). 441–446. 8 indexed citations

13.

Honey, Engela. (2016). Spondyloepimetaphyseal dysplasia with joint laxity (Beighton type): A unique South African disorder. South African Medical Journal. 106(6). 54–54. 7 indexed citations

14.

Hoffman, Jodi D., et al.. (2015). Three new families with recurrent male miscarriages and hypercoiled umbilical cord. Clinical Dysmorphology. 24(3). 128–131. 4 indexed citations

15.

Moore, Sam W., Karen Fieggen, Engela Honey, & Monique G. Zaahl. (2015). Novel Zeb2 gene variation in the Mowat Wilson syndrome (MWS). Journal of Pediatric Surgery. 51(2). 268–271. 7 indexed citations

16.

Olckers, Antonel, et al.. (2012). Compound heterozygosity in a South African patient with Facioscapulohumeral muscular dystrophy. Neuromuscular Disorders. 22(8). 728–734. 2 indexed citations

17.

Honey, Engela, et al.. (2012). ALG6-CDG in South Africa: Genotype-Phenotype Description of Five Novel Patients. JIMD Reports. 8. 17–23. 12 indexed citations

18.

Hoogendijk, Christiaan F., J. J. M. Marx, Engela Honey, Etheresia Pretorius, & Arnold L. Christianson. (2006). Ultrastructural Investigation of Zimmermann-Laband Syndrome. Ultrastructural Pathology. 30(6). 423–426. 9 indexed citations

19.

Honey, Engela, et al.. (2003). Spondyloenchondromatosis with D-2-hydroxyglutaric aciduria: a report of a second patient with this unusual combination. Clinical Dysmorphology. 12(2). 95–99. 20 indexed citations

20.

Honey, Engela, et al.. (2000). Flap repair: an effective strategy for minimising sexual morbidity associated with the surgical management of vulval intra epithelial neoplasia.. PubMed. 45(2). 81–4. 17 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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