Gajja S. Salomons

11.9k total citations
219 papers, 6.9k citations indexed

About

Gajja S. Salomons is a scholar working on Clinical Biochemistry, Molecular Biology and Cell Biology. According to data from OpenAlex, Gajja S. Salomons has authored 219 papers receiving a total of 6.9k indexed citations (citations by other indexed papers that have themselves been cited), including 130 papers in Clinical Biochemistry, 101 papers in Molecular Biology and 71 papers in Cell Biology. Recurrent topics in Gajja S. Salomons's work include Metabolism and Genetic Disorders (130 papers), Muscle metabolism and nutrition (70 papers) and Biochemical and Molecular Research (32 papers). Gajja S. Salomons is often cited by papers focused on Metabolism and Genetic Disorders (130 papers), Muscle metabolism and nutrition (70 papers) and Biochemical and Molecular Research (32 papers). Gajja S. Salomons collaborates with scholars based in Netherlands, United States and Canada. Gajja S. Salomons's co-authors include Cornelis Jakobs, Nanda M. Verhoeven, Eduard A. Struys, Marjo S. van der Knaap, Ton J. deGrauw, C. Jakobs, Silvy J.M. van Dooren, Kim M. Cecil, Lígia S. Almeida and William S. Ball and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

Gajja S. Salomons

216 papers receiving 6.8k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gajja S. Salomons Netherlands	45	3.3k	2.8k	2.2k	1.1k	927	219	6.9k
Éva Morava United States	47	5.3k 1.6×	1.7k 0.6×	863 0.4×	1.4k 1.2×	578 0.6×	312	7.6k
Michèl A.A.P. Willemsen Netherlands	41	2.8k 0.9×	1.2k 0.4×	682 0.3×	734 0.6×	396 0.4×	199	5.7k
Richard I. Kelley United States	55	7.4k 2.2×	2.3k 0.8×	741 0.3×	809 0.7×	416 0.4×	143	10.1k
Bwee Tien Poll‐The Netherlands	48	6.0k 1.8×	2.8k 1.0×	382 0.2×	1.8k 1.6×	711 0.8×	225	8.6k
Fernando Scaglia United States	50	4.8k 1.5×	3.0k 1.0×	377 0.2×	1.0k 0.9×	495 0.5×	168	7.1k
Kurt Ullrich Germany	39	2.4k 0.7×	2.5k 0.9×	576 0.3×	2.1k 1.8×	1.7k 1.8×	166	5.5k
Antònia Ribes Spain	38	2.5k 0.8×	2.1k 0.8×	435 0.2×	586 0.5×	558 0.6×	175	3.9k
Barbara Plecko Austria	37	2.3k 0.7×	1.9k 0.7×	329 0.1×	984 0.9×	597 0.6×	138	4.6k
Takeyori Saheki Japan	47	3.4k 1.0×	4.8k 1.7×	344 0.2×	1.5k 1.3×	552 0.6×	219	7.4k
Eduardo Bonilla United States	49	6.9k 2.1×	3.5k 1.2×	778 0.4×	943 0.8×	882 1.0×	127	9.0k

Countries citing papers authored by Gajja S. Salomons

Since Specialization

Citations

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

Fields of papers citing papers by Gajja S. Salomons

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gajja S. Salomons. 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 Gajja S. Salomons. The network helps show where Gajja S. Salomons may publish in the future.

Co-authorship network of co-authors of Gajja S. Salomons

This figure shows the co-authorship network connecting the top 25 collaborators of Gajja S. Salomons. A scholar is included among the top collaborators of Gajja S. Salomons 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 Gajja S. Salomons. Gajja S. Salomons 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

Schomakers, Bauke V., Peter T. Simpson, Michel van Weeghel, et al.. (2025). Integrated multi-omics mapping of mitochondrial dysfunction and substrate preference in Barth syndrome cardiac tissue. EMBO Molecular Medicine. 17(11). 3227–3246.

Mendes, Marisa I., Nicole I. Wolf, Joëlle Rudinger‐Thirion, et al.. (2024). Simultaneous determination of cytosolic aminoacyl-tRNA synthetase activities by LC–MS/MS. Nucleic Acids Research. 52(22). e107–e107. 1 indexed citations

Bergner, Caroline G., Inge M. E. Dijkstra, Irene C. Huffnagel, et al.. (2024). Lipidomic biomarkers in plasma correlate with disease severity in adrenoleukodystrophy. SHILAP Revista de lepidopterología. 4(1). 175–175. 9 indexed citations

Vaz, Frédéric M., Jan B. van Klinken, Henk van Lenthe, et al.. (2024). Discovery of novel diagnostic biomarkers for Sjögren-Larsson syndrome by untargeted lipidomics. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1869(2). 159447–159447. 3 indexed citations

Kuilenburg, André B. P., Angelique Sijben, Thijs H. Oude Munnink, et al.. (2024). Lethal Capecitabine Toxicity in Patients With Complete Dihydropyrimidine Dehydrogenase Deficiency Due to Ultra-Rare DPYD Variants. JCO Precision Oncology. 8(8). e2300599–e2300599. 1 indexed citations

Dane, Adrie, et al.. (2024). Four-dimensional lipidomics profiling in X-linked adrenoleukodystrophy using trapped ion mobility mass spectrometry. Journal of Lipid Research. 65(6). 100567–100567. 2 indexed citations

Schene, Imre F., Marisa I. Mendes, Desirée E.C. Smith, et al.. (2024). Isoleucine-to-valine substitutions support cellular physiology during isoleucine deprivation. Nucleic Acids Research. 53(1). 1 indexed citations

Ravel, Jean‐Marie, Natacha Dreumont, Desirée E.C. Smith, et al.. (2021). A bi‐allelic loss‐of‐function SARS1 variant in children with neurodevelopmental delay, deafness, cardiomyopathy, and decompensation during fever. Human Mutation. 42(12). 1576–1583. 6 indexed citations

Wasim, Muhammad, Haq Nawaz Khan, Hina Ayesha, et al.. (2021). Identification of three novel pathogenic mutations in cystathionine beta-synthase gene of Pakistani intellectually disabled patients. Journal of Pediatric Endocrinology and Metabolism. 0(0). 325–332. 7 indexed citations

10.

Abily-Donval, Lénaïg, Alice Goldenberg, Gajja S. Salomons, et al.. (2021). Heterogenous Clinical Landscape in a Consanguineous Malonic Aciduria Family. International Journal of Molecular Sciences. 22(23). 12633–12633. 5 indexed citations

11.

Lenz, Dominic, Mirjam Stahl, Elias Seidl, et al.. (2020). Rescue of respiratory failure in pulmonary alveolar proteinosis due to pathogenic MARS1 variants. Pediatric Pulmonology. 55(11). 3057–3066. 19 indexed citations

12.

Williams, Monique, Vassili Valayannopoulos, Ruqaiah Altassan, et al.. (2018). Clinical, biochemical, and molecular overview of transaldolase deficiency and evaluation of the endocrine function: update of 34 patients. Journal of Inherited Metabolic Disease. 2 indexed citations

13.

Thurm, Audrey, Precilla D’Souza, Owen M. Rennert, et al.. (2016). Creatine Transporter Deficiency. Journal of Developmental & Behavioral Pediatrics. 37(4). 322–326. 10 indexed citations

14.

Jaeger, Bregje, N. G. G. M. Abeling, Gajja S. Salomons, et al.. (2016). Pyridoxine responsive epilepsy caused by a novel homozygous PNPO mutation. Molecular Genetics and Metabolism Reports. 6. 60–63. 26 indexed citations

15.

Patel, Jaina, Peixiang Wang, Berge A. Minassian, et al.. (2015). Estimated carrier frequency of creatine transporter deficiency in females in the general population using functional characterization of novel missense variants in the SLC6A8 gene. Gene. 565(2). 187–191. 28 indexed citations

16.

Nota, Benjamin, Joseph Ndika, Jiddeke M. van de Kamp, et al.. (2014). RNA Sequencing of Creatine Transporter (SLC6A8) Deficient Fibroblasts Reveals Impairment of the Extracellular Matrix. Human Mutation. 35(9). 1128–1135. 9 indexed citations

17.

Oliveira, Renata L. de, Paula Garcia, Isabel Fineza, et al.. (2013). Pyridoxine‐dependent epilepsy due to antiquitin deficiency: achieving a favourable outcome. Epileptic Disorders. 15(4). 400–406. 18 indexed citations

18.

Ndika, Joseph, et al.. (2013). Cloning and characterization of the promoter regions from the parent and paralogous creatine transporter genes. Gene. 533(2). 488–493. 6 indexed citations

19.

Käll, Kerstin, Gajja S. Salomons, Inga Talvik, et al.. (2009). The screening of SLC6A8 deficiency among Estonian families with X‐linked mental retardation. Journal of Inherited Metabolic Disease. 33(S3). 5–11. 39 indexed citations

20.

Mancardi, Maria Margherita, Ubaldo Caruso, Maria Cristina Schiaffino, et al.. (2007). Severe Epilepsy in X‐Linked Creatine Transporter Defect (CRTR‐D). Epilepsia. 48(6). 1211–1213. 35 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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