Bert Dorland

451 total citations
11 papers, 347 citations indexed

About

Bert Dorland is a scholar working on Molecular Biology, Clinical Biochemistry and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Bert Dorland has authored 11 papers receiving a total of 347 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Clinical Biochemistry and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Bert Dorland's work include Metabolism and Genetic Disorders (7 papers), Amino Acid Enzymes and Metabolism (2 papers) and Glycosylation and Glycoproteins Research (2 papers). Bert Dorland is often cited by papers focused on Metabolism and Genetic Disorders (7 papers), Amino Acid Enzymes and Metabolism (2 papers) and Glycosylation and Glycoproteins Research (2 papers). Bert Dorland collaborates with scholars based in Netherlands, Germany and France. Bert Dorland's co-authors include S. Schweitzer, C. Jakobs, Tom J. de Koning, Christian Körner, J. G. M. Huijmans, Ruud Berger, Monique G.M. de Sain–van der Velden, Eric Rappaport, Berthil H.C.M.T. Prinsen and Ludwig Lehle and has published in prestigious journals such as Journal of the American Society of Nephrology, The American Journal of Human Genetics and Neuropsychopharmacology.

In The Last Decade

Bert Dorland

10 papers receiving 343 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bert Dorland Netherlands	8	220	93	67	50	46	11	347
Rebecca Mardach United States	11	193 0.9×	164 1.8×	100 1.5×	40 0.8×	82 1.8×	17	351
Didem Demirbas United States	12	221 1.0×	121 1.3×	29 0.4×	44 0.9×	18 0.4×	23	375
Serap Sivri Türkiye	11	120 0.5×	182 2.0×	145 2.2×	43 0.9×	28 0.6×	53	342
Anke Schumann Germany	11	179 0.8×	149 1.6×	75 1.1×	64 1.3×	19 0.4×	32	379
Vladimı́r Bzdúch Slovakia	8	103 0.5×	65 0.7×	83 1.2×	39 0.8×	18 0.4×	28	259
John J. Noonan United States	11	175 0.8×	86 0.9×	44 0.7×	59 1.2×	23 0.5×	17	470
Norma Spécola Argentina	11	154 0.7×	206 2.2×	181 2.7×	49 1.0×	32 0.7×	19	376
Mercedes Casado Spain	12	164 0.7×	101 1.1×	45 0.7×	46 0.9×	14 0.3×	25	332
Nawal Makhseed Kuwait	12	167 0.8×	104 1.1×	53 0.8×	38 0.8×	15 0.3×	18	303
Bing-Zhi Yang United States	13	232 1.1×	159 1.7×	160 2.4×	68 1.4×	39 0.8×	18	445

Countries citing papers authored by Bert Dorland

Since Specialization

Citations

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

Fields of papers citing papers by Bert Dorland

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bert Dorland

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

All Works

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11 of 11 papers shown

Veiga‐da‐Cunha, Maria, Nanda M. Verhoeven‐Duif, Tom J. de Koning, et al.. (2012). Mutations in the AGXT2L2 gene cause phosphohydroxylysinuria. Journal of Inherited Metabolic Disease. 36(6). 961–966. 3 indexed citations

Keularts, I., Piet Leroy, M. Estela Rubio‐Gozalbo, et al.. (2010). Fatal cerebral edema associated with serine deficiency in CSF. Journal of Inherited Metabolic Disease. 33(S3). 181–185. 5 indexed citations

Vorstman, Jacob, Bruce I. Turetsky, Bert Dorland, et al.. (2008). Proline Affects Brain Function in 22q11DS Children with the Low Activity COMT158 Allele. Neuropsychopharmacology. 34(3). 739–746. 80 indexed citations

Westermann, C.M., Bert Dorland, Monique G. de Sain-van der Velden, et al.. (2008). Plasma acylcarnitine and fatty acid profiles during exercise and training in Standardbreds. American Journal of Veterinary Research. 69(11). 1469–1475. 12 indexed citations

Ham, Maria van der, Berthil H.C.M.T. Prinsen, J. G. M. Huijmans, et al.. (2006). Quantification of free and total sialic acid excretion by LC–MS/MS. Journal of Chromatography B. 848(2). 251–257. 53 indexed citations

Reijngoud, Dirk‐Jan, et al.. (2005). RESPIRATORY INSUFFICIENCY AS FIRST PRESENTATION OF MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY (MADD). Journal of Inherited Metabolic Disease. 28. 115–115.

Schwarz, Markus, Christian Thiel, Bert Dorland, et al.. (2004). Deficiency of GDP-Man:GlcNAc2-PP-Dolichol Mannosyltransferase Causes Congenital Disorder of Glycosylation Type Ik. The American Journal of Human Genetics. 74(3). 472–481. 59 indexed citations

Spronsen, Francjan J. van, Margreet Th.E. Bink‐Boelkens, Dirk‐Jan Reijngoud, et al.. (2004). Ventricular Fibrillation Without Overt Cardiomyopathy as First Presentation of Organic Cation Transporter 2‐Deficiency in Adolescence. Pacing and Clinical Electrophysiology. 27(5). 675–676. 22 indexed citations

Vos, Ingrid H. C., Ton J. Rabelink, Bert Dorland, et al.. (2001). L-Arginine Supplementation Improves Function and Reduces Inflammation in Renal Allografts. Journal of the American Society of Nephrology. 12(2). 361–367. 39 indexed citations

10.

Jakobs, C., S. Schweitzer, & Bert Dorland. (1995). Galactitol in galactosemia. European Journal of Pediatrics. 154(S2). S50–S52. 36 indexed citations

11.

Bakker, H. D., H.R. Scholte, Coby Van den Bogert, et al.. (1993). Deficiency of the Adenine Nucleotide Translocator in Muscle of a Patient with Myopathy and Lactic Acidosis: A New Mitochondrial Defect. Pediatric Research. 33(4). 412–417. 38 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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