Jozef Hertecant

722 total citations
7 papers, 120 citations indexed

About

Jozef Hertecant is a scholar working on Clinical Biochemistry, Genetics and Molecular Biology. According to data from OpenAlex, Jozef Hertecant has authored 7 papers receiving a total of 120 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Clinical Biochemistry, 4 papers in Genetics and 2 papers in Molecular Biology. Recurrent topics in Jozef Hertecant's work include Metabolism and Genetic Disorders (4 papers), Neonatal Health and Biochemistry (2 papers) and Moyamoya disease diagnosis and treatment (1 paper). Jozef Hertecant is often cited by papers focused on Metabolism and Genetic Disorders (4 papers), Neonatal Health and Biochemistry (2 papers) and Moyamoya disease diagnosis and treatment (1 paper). Jozef Hertecant collaborates with scholars based in United Arab Emirates, Netherlands and Norway. Jozef Hertecant's co-authors include Hesham Osman, Dimah Saade, Aisha Al‐Shamsi, Fatma Al‐Jasmi, Abdul‐Kader Souid, Bassam R. Ali, Ayman W. El‐Hattab, Jehan Suleiman, Dirk J. Lefeber and Annemiek M. J. van Wegberg and has published in prestigious journals such as Nutrients, Molecular Genetics and Metabolism and Journal of Inherited Metabolic Disease.

In The Last Decade

Jozef Hertecant

6 papers receiving 118 citations

Peers

Jozef Hertecant

CB

MB

GENET

PPCH

RHEUM

Naomi Meeks United States

Ghunwa Nakouzi United States

Corinne Gemperle-Britschgi Switzerland

Melis Köse Türkiye

Celia Medrano Spain

Germaine Pierre United Kingdom

Cynthia LeMons United States

Patrícia Janeiro Portugal

Ulrich A. Schatz Germany

Samia Pichard France

Naomi Meeks United States

Jozef Hertecant

64 ×1.0

CB

86 ×1.4

MB

50 ×1.4

GENET

36 ×1.6

PPCH

13 ×0.7

RHEUM

Citations per year, relative to Jozef Hertecant Jozef Hertecant (= 1×) peers Naomi Meeks

Countries citing papers authored by Jozef Hertecant

Since Specialization

Citations

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

Fields of papers citing papers by Jozef Hertecant

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jozef Hertecant

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

All Works

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7 of 7 papers shown

1.

Alawadhi, Hussain, et al.. (2021). Delayed presentation of late-onset glutamic aciduria type II: A disease of infancy presenting in an adult. Ibnosina Journal of Medicine and Biomedical Sciences. 13(3). 148–152.

2.

Conte, Federica, Éva Morava, Nurulamin Abu Bakar, et al.. (2020). Phosphoglucomutase-1 deficiency: Early presentation, metabolic management and detection in neonatal blood spots. Molecular Genetics and Metabolism. 131(1-2). 135–146. 19 indexed citations

3.

Vliet, Danique van, Annemiek M. J. van Wegberg, Kirsten Ahring, et al.. (2019). Untreated PKU Patients without Intellectual Disability: What Do They Teach Us?. Nutrients. 11(11). 2572–2572. 20 indexed citations

4.

Hertecant, Jozef, et al.. (2018). West syndrome, developmental and epileptic encephalopathy, and severe CNS disorder associated with WWOX mutations. Epileptic Disorders. 20(5). 401–412. 15 indexed citations

5.

Al‐Jasmi, Fatma, et al.. (2015). Inborn Errors of Metabolism in the United Arab Emirates: Disorders Detected by Newborn Screening (2011–2014). JIMD Reports. 28. 127–135. 23 indexed citations

6.

Osman, Hesham, et al.. (2014). Expanding the comprehensive national neonatal screening programme in the United Arab Emirates from 1995 to 2011. Eastern Mediterranean Health Journal. 20(1). 17–23. 39 indexed citations

7.

Keenan, Catherine M., et al.. (2002). Lipoprotein lipase deficiency and transient diabetes mellitus in a neonate. Journal of Inherited Metabolic Disease. 25(5). 413–414. 4 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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