Gerrit Smit

12.5k total citations · 1 hit paper
163 papers, 8.5k citations indexed

About

Gerrit Smit is a scholar working on Rheumatology, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Gerrit Smit has authored 163 papers receiving a total of 8.5k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Rheumatology, 52 papers in Molecular Biology and 36 papers in Clinical Biochemistry. Recurrent topics in Gerrit Smit's work include Glycogen Storage Diseases and Myoclonus (49 papers), Metabolism and Genetic Disorders (34 papers) and Lysosomal Storage Disorders Research (25 papers). Gerrit Smit is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (49 papers), Metabolism and Genetic Disorders (34 papers) and Lysosomal Storage Disorders Research (25 papers). Gerrit Smit collaborates with scholars based in Netherlands, United States and France. Gerrit Smit's co-authors include Wim Engels, Bart Smit, Jan W. Kijne, Jan Wouters, Eman Ayad, Ben Lugtenberg, Gepke Visser, M.A.J.S. van Boekel, E. Koen Bekedam and Henk A. Schols and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Blood.

In The Last Decade

Gerrit Smit

161 papers receiving 8.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Flavour formation by lactic acid bacteria and biochemical flavour profiling of cheese products

2005 672 citations Gerrit Smit, Bart Smit et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gerrit Smit Netherlands	50	3.0k	2.7k	2.1k	1.5k	1.3k	163	8.5k
Jie Yin China	55	4.6k 1.6×	1.1k 0.4×	254 0.1×	1.8k 1.2×	996 0.8×	244	9.6k
James D. House Canada	45	1.1k 0.4×	1.7k 0.6×	949 0.4×	441 0.3×	1.6k 1.2×	208	6.2k
Wenkai Ren China	50	3.8k 1.3×	764 0.3×	376 0.2×	1.4k 0.9×	888 0.7×	144	8.2k
Arne Dahlqvist Sweden	43	2.6k 0.9×	703 0.3×	285 0.1×	1.4k 0.9×	2.7k 2.1×	155	9.8k
Hamid M. Said United States	46	2.4k 0.8×	263 0.1×	1.8k 0.8×	1.3k 0.9×	1.8k 1.4×	241	7.9k
‬Min Du United States	69	6.3k 2.1×	1.3k 0.5×	235 0.1×	4.6k 3.0×	1.7k 1.3×	406	15.2k
Bie Tan China	52	3.8k 1.3×	982 0.4×	131 0.1×	1.9k 1.2×	1.2k 0.9×	227	9.9k
Pradeep K. Dudeja United States	51	4.4k 1.5×	534 0.2×	298 0.1×	1.3k 0.8×	1.2k 0.9×	293	8.5k
Mei‐chin Yin Taiwan	51	2.3k 0.8×	771 0.3×	143 0.1×	937 0.6×	483 0.4×	129	6.5k
Qing Gu China	47	3.8k 1.3×	1.9k 0.7×	135 0.1×	441 0.3×	1.1k 0.8×	380	8.6k

Countries citing papers authored by Gerrit Smit

Since Specialization

Citations

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

Fields of papers citing papers by Gerrit Smit

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gerrit Smit

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

Derks, Terry G. J., et al.. (2014). From genome to phenome—Simple inborn errors of metabolism as complex traits. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1842(10). 2021–2029. 7 indexed citations

Roland, Wibke S. U., Robin J. Gouka, Harry Gruppen, et al.. (2014). 6-Methoxyflavanones as Bitter Taste Receptor Blockers for hTAS2R39. PLoS ONE. 9(4). e94451–e94451. 97 indexed citations

Smit, Gerrit, et al.. (2013). In vitro and in vivo consequences of variant medium-chain acyl-CoA dehydrogenase genotypes. Orphanet Journal of Rare Diseases. 8(1). 43–43. 18 indexed citations

Derks, Terry G. J., et al.. (2013). Dietary treatment of glycogen storage disease type Ia: Uncooked cornstarch and/or continuous nocturnal gastric drip-feeding?. Molecular Genetics and Metabolism. 109(1). 1–2. 20 indexed citations

Smit, Gerrit, Maaike de Vries, Johannis B.C. de Klerk, et al.. (2012). Risk stratification by residual enzyme activity after newborn screening for medium-chain acyl-CoA dehyrogenase deficiency: data from a cohort study. Orphanet Journal of Rare Diseases. 7(1). 30–30. 24 indexed citations

Vos, Yvonne J., et al.. (2012). Mutation Analysis in Glycogen Storage Disease Type III Patients in the Netherlands: Novel Genotype-Phenotype Relationships and Five Novel Mutations in the AGL Gene. JIMD Reports. 7. 19–26. 13 indexed citations

Ebberink, Merel S., Janet Koster, Gepke Visser, et al.. (2012). A novel defect of peroxisome division due to a homozygous non-sense mutation in the PEX11β gene. Journal of Medical Genetics. 49(5). 307–313. 98 indexed citations

Kishnani, Priya S., Stephanie Austin, Pamela Arn, et al.. (2010). Glycogen Storage Disease Type III diagnosis and management guidelines. Genetics in Medicine. 12(7). 446–463. 197 indexed citations

Busch, Johanneke, et al.. (2009). Reviewing progress towards finding an acceptable natural flavour alternative to salt. Socio-Environmental Systems Modeling. 20(5). 66–68. 4 indexed citations

10.

Correia, Catherine E., Kaustuv Bhattacharya, Philip Lee, et al.. (2008). Use of modified cornstarch therapy to extend fasting in glycogen storage disease types Ia and Ib. American Journal of Clinical Nutrition. 88(5). 1272–1276. 66 indexed citations

11.

Sijens, Paul E., Gerrit Smit, Marinus A.J. Borgdorff, Peter Kappert, & Matthijs Oudkerk. (2006). Multiple voxel 1H MR spectroscopy of phosphorylase-b kinase deficient patients (GSD IXa) showing an accumulation of fat in the liver that resolves with aging. Journal of Hepatology. 45(6). 851–855. 13 indexed citations

12.

Smit, Ben, et al.. (2004). Development of a high throughput screening method to test flavour-forming capabilities of anaerobic micro-organisms. Journal of Applied Microbiology. 97(2). 306–313. 20 indexed citations

13.

Boelrijk, Alexandra E. M., et al.. (2003). The effect of co-solvent on the release of key flavours in alcoholic beverages; comparing in vivo with artificial mouth-MS Nose measurements. Socio-Environmental Systems Modeling. 204–207. 3 indexed citations

14.

Smit, Gerrit, Johan E. T. van Hylckama Vlieg, Bart Smit, Eman Ayad, & Wim Engels. (2002). Fermentative formation of flavour compounds by lactic acid bacteria. Australian Journal of Dairy Technology. 57(2). 61–68. 16 indexed citations

15.

Verheul, A., et al.. (2001). Enhanced flavour formation by combination of selected lactococci from industrial and artisanal origin with focus on completion of a metabolic pathway. Journal of Applied Microbiology. 90(1). 59–67. 72 indexed citations

16.

Verhoeven, Arthur J., et al.. (1999). A Convenient Diagnostic Function Test of Peripheral Blood Neutrophils in Glycogen Storage Disease Type Ib. Pediatric Research. 45(6). 881–885. 21 indexed citations

17.

Niezen‐Koning, Klary E., Ronald J. A. Wanders, Jos P.N. Ruiter, et al.. (1997). Succinyl-CoA:acetoacetate transferase deficiency: identification of a new patient with a neonatal onset and review of the literature. European Journal of Pediatrics. 156(11). 870–873. 28 indexed citations

18.

Hendrickx, Jan, Paul Coucke, Paul Bossuyt, et al.. (1993). X-linked liver glycogenosis: localization and isolation of a candidate gene. Human Molecular Genetics. 2(5). 583–589. 15 indexed citations

19.

Willems, P J, Jan Hendrickx, Bart Van Der Auwera, et al.. (1991). Mapping of the gene for X-linked liver glycogenosis due to phosphorylase kinase deficiency to human chromosome region Xp22. Genomics. 9(4). 565–569. 16 indexed citations

20.

Willems, Patrick J., et al.. (1987). Recurrence risk in the Angelman (“happy puppet”) syndrome. American Journal of Medical Genetics. 27(4). 773–780. 37 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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