Dominique Roland

1.5k total citations
16 papers, 610 citations indexed

About

Dominique Roland is a scholar working on Physiology, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Dominique Roland has authored 16 papers receiving a total of 610 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Physiology, 5 papers in Molecular Biology and 4 papers in Clinical Biochemistry. Recurrent topics in Dominique Roland's work include Metabolism and Genetic Disorders (4 papers), Mitochondrial Function and Pathology (3 papers) and Sleep and related disorders (3 papers). Dominique Roland is often cited by papers focused on Metabolism and Genetic Disorders (4 papers), Mitochondrial Function and Pathology (3 papers) and Sleep and related disorders (3 papers). Dominique Roland collaborates with scholars based in Belgium, United States and France. Dominique Roland's co-authors include K. S. Polonsky, Eve Van Cauter, John D Blackman, Samuel Refetoff, Jean‐Paul Spire, Lionel Van Maldergem, Jeppe Sturis, F. Dehout, M. M. Byrne and Bénédicte Guillaume and has published in prestigious journals such as Journal of Clinical Investigation, The Journal of Clinical Endocrinology & Metabolism and American Journal of Physiology-Endocrinology and Metabolism.

In The Last Decade

Dominique Roland

16 papers receiving 592 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dominique Roland Belgium 11 257 215 145 120 99 16 610
Tasneem Ansari United States 5 335 1.3× 307 1.4× 58 0.4× 143 1.2× 28 0.3× 7 569
Mohammad A. Ghatei United Kingdom 8 149 0.6× 225 1.0× 98 0.7× 164 1.4× 150 1.5× 8 605
Asha Seth United Kingdom 11 226 0.9× 398 1.9× 62 0.4× 152 1.3× 125 1.3× 15 687
Werner Kern Germany 13 111 0.4× 171 0.8× 73 0.5× 38 0.3× 80 0.8× 17 513
Dyan Sellayah United Kingdom 11 335 1.3× 215 1.0× 104 0.7× 222 1.9× 163 1.6× 19 756
Marjolein A. Wijngaarden Netherlands 9 167 0.6× 74 0.3× 23 0.2× 201 1.7× 108 1.1× 12 499
Carolina Villegas‐Montoya United States 8 418 1.6× 464 2.2× 44 0.3× 131 1.1× 31 0.3× 8 721
G. Esposti Italy 15 121 0.5× 349 1.6× 43 0.3× 69 0.6× 66 0.7× 22 550
Nabilah I. Chowdhury Canada 15 142 0.6× 66 0.3× 14 0.1× 180 1.5× 69 0.7× 21 685
Peter S. Cunningham United Kingdom 11 213 0.8× 361 1.7× 64 0.4× 62 0.5× 115 1.2× 16 499

Countries citing papers authored by Dominique Roland

Since Specialization
Citations

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

Fields of papers citing papers by Dominique Roland

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dominique Roland

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

All Works

16 of 16 papers shown
1.
Mercier, Nathalie, et al.. (2024). A new case of sodium‐dependent multivitamin transporter defect occurring as a life‐threatening condition responsive to early vitamin supplementation and literature review. Molecular Genetics & Genomic Medicine. 12(2). e2388–e2388. 4 indexed citations
2.
Mercier, Nathalie, et al.. (2024). Mitochondrial HMG-CoA synthase deficiency. Molecular Genetics and Metabolism. 144(1). 109007–109007. 2 indexed citations
3.
Beckers, Dominique, et al.. (2020). A Novel Phenotype Combining Primary Ovarian Insufficiency Growth Retardation and Pilomatricomas With MCM8 Mutation. The Journal of Clinical Endocrinology & Metabolism. 105(6). 1973–1982. 23 indexed citations
4.
Chaussenot, Annabelle, Gérard Besson, Foudil Lamari, et al.. (2019). Cholic acid as a treatment for cerebrotendinous xanthomatosis in adults. Journal of Neurology. 266(8). 2043–2050. 30 indexed citations
5.
Fontaine, Monique, Anne‐Frédérique Dessein, Karine Mention-Mulliez, et al.. (2018). Fluxomic assay-assisted diagnosis orientation in a cohort of 11 patients with myopathic form of CPT2 deficiency. Molecular Genetics and Metabolism. 123(4). 441–448. 11 indexed citations
6.
Roland, Dominique, Gilbert Briand, Jòseph Vamecq, et al.. (2017). Coupled brain and urine spectroscopy - in vivo metabolomic characterization of HMG-CoA lyase deficiency in 5 patients. Molecular Genetics and Metabolism. 121(2). 111–118. 11 indexed citations
7.
Benoît, Valérie, Monique Cordonnier, Françoise Meire, et al.. (2013). Uncommon Leber “Plus” Disease Associated With Mitochondrial Mutation m.11778G>A in a Premature Child. Journal of Child Neurology. 29(8). NP18–NP23. 5 indexed citations
8.
Dehout, F., et al.. (2006). Successful pregnancy in a patient with Fabry disease receiving enzyme replacement therapy. Digital Access to Libraries. 95. 137–138. 5 indexed citations
9.
Dehout, F., et al.. (2004). Relief of gastrointestinal symptoms under enzyme replacement therapy in patients with Fabry disease. Journal of Inherited Metabolic Disease. 27(4). 499–505. 50 indexed citations
10.
Maldergem, Lionel Van, Ann B. Moser, Marie Vincent, et al.. (2004). Orthotopic liver transplantation from a living‐related donor in an infant with a peroxisome biogenesis defect of the infantile Refsum disease type. Journal of Inherited Metabolic Disease. 28(4). 593–600. 23 indexed citations
11.
Wuyts, Wim, Dominique Roland, Hermann‐Josef Lüdecke, et al.. (2002). Multiple exostoses, mental retardation, hypertrichosis, and brain abnormalities in a boy with a de novo 8q24 submicroscopic interstitial deletion. American Journal of Medical Genetics. 113(4). 326–332. 29 indexed citations
12.
Roland, Dominique, Pascale Hilbert, F. Dehout, Yves Pirson, & Lionel Van Maldergem. (2002). Fabry disease in Belgium: ascertainment of 12 families. Acta Paediatrica. 91(s439). 115–115. 1 indexed citations
13.
Frank, Samuel, Dominique Roland, Jeppe Sturis, et al.. (1995). Effects of aging on glucose regulation during wakefulness and sleep. American Journal of Physiology-Endocrinology and Metabolism. 269(6). E1006–E1016. 28 indexed citations
14.
Cauter, Eve Van, K. S. Polonsky, John D Blackman, et al.. (1994). Abnormal temporal patterns of glucose tolerance in obesity: relationship to sleep-related growth hormone secretion and circadian cortisol rhythmicity.. The Journal of Clinical Endocrinology & Metabolism. 79(6). 1797–1805. 49 indexed citations
15.
O’Meara, N., Jeppe Sturis, John D Blackman, et al.. (1993). Analytical problems in detecting rapid insulin secretory pulses in normal humans. American Journal of Physiology-Endocrinology and Metabolism. 264(2). E231–E238. 13 indexed citations
16.
Cauter, Eve Van, John D Blackman, Dominique Roland, et al.. (1991). Modulation of glucose regulation and insulin secretion by circadian rhythmicity and sleep.. Journal of Clinical Investigation. 88(3). 934–942. 326 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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