Corinne De Laet

4.0k total citations
26 papers, 631 citations indexed

About

Corinne De Laet is a scholar working on Clinical Biochemistry, Physiology and Molecular Biology. According to data from OpenAlex, Corinne De Laet has authored 26 papers receiving a total of 631 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Clinical Biochemistry, 11 papers in Physiology and 8 papers in Molecular Biology. Recurrent topics in Corinne De Laet's work include Metabolism and Genetic Disorders (12 papers), Diet and metabolism studies (7 papers) and Amino Acid Enzymes and Metabolism (4 papers). Corinne De Laet is often cited by papers focused on Metabolism and Genetic Disorders (12 papers), Diet and metabolism studies (7 papers) and Amino Acid Enzymes and Metabolism (4 papers). Corinne De Laet collaborates with scholars based in Belgium, Italy and France. Corinne De Laet's co-authors include Patrick McKiernan, Carlo Dionisi‐Vici, Hélène Ogier de Baulny, Lidia Monti, Guillem Pintos‐Morell, Ute Spiekerkötter, James V. Leonard, Grant A. Mitchell, Philippe Goyens and Daniel Brasseur and has published in prestigious journals such as Journal of Biological Chemistry, American Journal of Clinical Nutrition and Clinical Chemistry.

In The Last Decade

Corinne De Laet

25 papers receiving 618 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Corinne De Laet Belgium 14 321 185 154 146 139 26 631
Laurie Bernstein United States 12 370 1.2× 199 1.1× 335 2.2× 148 1.0× 57 0.4× 32 717
Ertuğrul Kıykım Türkiye 11 137 0.4× 233 1.3× 117 0.8× 56 0.4× 40 0.3× 64 531
Carla Cuthbert United States 13 249 0.8× 161 0.9× 56 0.4× 111 0.8× 47 0.3× 24 529
Roger R. Lenke United States 8 364 1.1× 151 0.8× 124 0.8× 164 1.1× 41 0.3× 16 602
Trine Tangeraas Norway 13 138 0.4× 167 0.9× 41 0.3× 89 0.6× 28 0.2× 33 543
J. McConnell United Kingdom 11 231 0.7× 121 0.7× 183 1.2× 43 0.3× 47 0.3× 15 516
Stephen W. D’Souza United Kingdom 19 59 0.2× 197 1.1× 94 0.6× 112 0.8× 70 0.5× 27 1.1k
J. W. Sparks United States 19 147 0.5× 145 0.8× 151 1.0× 46 0.3× 40 0.3× 25 1.0k
Raquel Yahyaoui Spain 11 119 0.4× 125 0.7× 64 0.4× 60 0.4× 31 0.2× 37 447
J. P. Farriaux France 14 110 0.3× 137 0.7× 128 0.8× 36 0.2× 14 0.1× 55 606

Countries citing papers authored by Corinne De Laet

Since Specialization
Citations

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

Fields of papers citing papers by Corinne De Laet

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Corinne De Laet. 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 Corinne De Laet. The network helps show where Corinne De Laet may publish in the future.

Co-authorship network of co-authors of Corinne De Laet

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

All Works

20 of 20 papers shown
1.
2.
Laeremans, Hilde, François Boemer, Sandrine Marie, et al.. (2024). Impact of newborn screening for fatty acid oxidation disorders on neurological outcome: A Belgian retrospective and multicentric study. European Journal of Paediatric Neurology. 49. 60–65. 1 indexed citations
3.
Laet, Corinne De, et al.. (2021). Acquired Zinc Deficiency Mimicking Acrodermatitis Enteropathica in a Breast-Fed Premature Infant. Pediatric Reports. 13(3). 444–449. 6 indexed citations
4.
Spiekerkoetter, Ute, María L. Couce, Anibh M. Das, et al.. (2021). Long-term safety and outcomes in hereditary tyrosinaemia type 1 with nitisinone treatment: a 15-year non-interventional, multicentre study. The Lancet Diabetes & Endocrinology. 9(7). 427–435. 22 indexed citations
5.
Dain, Elena, et al.. (2019). Nutritional status of neurologically impaired children: Impact on comorbidity. Archives de Pédiatrie. 27(2). 95–103. 31 indexed citations
6.
Laet, Corinne De, Shancy Rooze, Ariane Willems, et al.. (2019). Shoshin Beriberi and Severe Accidental Hypothermia as Causes of Heart Failure in a 6-Year-Old Child: A Case Report and Brief Review of Literature. Frontiers in Pediatrics. 7. 119–119. 7 indexed citations
7.
Robert, Martine, et al.. (2018). Evaluation of nutritional care of hospitalized children in a tertiary pediatric hospital. Clinical Nutrition ESPEN. 25. 157–162. 11 indexed citations
8.
Burda, Patricie, Corinne Sagné, David Coelho, et al.. (2017). Clinical or ATPase domain mutations in ABCD4 disrupt the interaction between the vitamin B12-trafficking proteins ABCD4 and LMBD1. Journal of Biological Chemistry. 292(28). 11980–11991. 24 indexed citations
9.
Muntau, Ania C., Alberto Burlina, François Eyskens, et al.. (2017). Efficacy, safety and population pharmacokinetics of sapropterin in PKU patients <4 years: results from the SPARK open-label, multicentre, randomized phase IIIb trial. Orphanet Journal of Rare Diseases. 12(1). 47–47. 29 indexed citations
10.
Jahja, Rianne, Stephan C. J. Huijbregts, Anne Daly, et al.. (2016). Neurocognitive outcome in tyrosinemia type 1 patients compared to healthy controls. Orphanet Journal of Rare Diseases. 11(1). 87–87. 54 indexed citations
11.
Grodecká, Lucie, Sara Seneca, Katrien Stouffs, et al.. (2016). Detailed molecular characterization of a novel IDS exonic mutation associated with multiple pseudoexon activation. Journal of Molecular Medicine. 95(3). 299–309. 5 indexed citations
12.
Dewulf, Joseph P., Catherine Barréa, Marie‐Françoise Vincent, et al.. (2016). Evidence of a wide spectrum of cardiac involvement due to ACAD9 mutations: Report on nine patients. Molecular Genetics and Metabolism. 118(3). 185–189. 24 indexed citations
13.
Laet, Corinne De, Carlo Dionisi‐Vici, James V. Leonard, et al.. (2013). Recommendations for the management of tyrosinaemia type 1. Orphanet Journal of Rare Diseases. 8(1). 8–8. 151 indexed citations
14.
Huybrechts, Sophie, Corinne De Laet, Patrick Bontems, et al.. (2011). Deficiency of Subunit 6 of the Conserved Oligomeric Golgi Complex (COG6-CDG): Second Patient, Different Phenotype. JIMD Reports. 4. 103–108. 31 indexed citations
15.
Quentin, Christine, Sophie Huybrechts, Laurence Rozen, et al.. (2011). Vitamin B12 deficiency in a 9-month-old boy. European Journal of Pediatrics. 171(1). 193–195. 18 indexed citations
16.
Schiff, Manuel, Pierre Broué, B. Chabrol, et al.. (2011). Heterogeneity of follow‐up procedures in French and Belgian patients with treated hereditary tyrosinemia type 1: results of a questionnaire and proposed guidelines. Journal of Inherited Metabolic Disease. 35(5). 823–829. 19 indexed citations
17.
Bourdoux, Pierre, et al.. (2005). Age-Related Variations in Acylcarnitine and Free Carnitine Concentrations Measured by Tandem Mass Spectrometry. Clinical Chemistry. 51(4). 745–752. 45 indexed citations
18.
Tiège, Xavier De, et al.. (2004). Postinfectious immune-mediated encephalitis after pediatric herpes simplex encephalitis. Brain and Development. 27(4). 304–307. 34 indexed citations
19.
Goyens, Philippe, et al.. (2001). Diagnosis of methylmalonic aciduria (MMA) by neonatal screening using tandem mass spectrometry (MS/MS). Journal of Inherited Metabolic Disease. 24. 7–7. 2 indexed citations
20.
Laet, Corinne De, Jean-Claude Wautrecht, Daniel Brasseur, et al.. (1999). Plasma homocysteine concentrations in a Belgian school-age population. American Journal of Clinical Nutrition. 69(5). 968–972. 85 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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