Saskia Koene

1.9k total citations
49 papers, 1.1k citations indexed

About

Saskia Koene is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Saskia Koene has authored 49 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 22 papers in Clinical Biochemistry and 12 papers in Genetics. Recurrent topics in Saskia Koene's work include Mitochondrial Function and Pathology (27 papers), Metabolism and Genetic Disorders (22 papers) and ATP Synthase and ATPases Research (11 papers). Saskia Koene is often cited by papers focused on Mitochondrial Function and Pathology (27 papers), Metabolism and Genetic Disorders (22 papers) and ATP Synthase and ATPases Research (11 papers). Saskia Koene collaborates with scholars based in Netherlands, United Kingdom and United States. Saskia Koene's co-authors include Jan Smeıtınk, Richard J. Rodenburg, Mirian C. H. Janssen, Paul de Laat, C.M. Verhaak, Werner J.H. Koopman, Peter H.G.M. Willems, Julien Beyrath, Éva Morava and Robert McFarland and has published in prestigious journals such as Neurology, Journal of Affective Disorders and Clinical Pharmacology & Therapeutics.

In The Last Decade

Saskia Koene

47 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Saskia Koene Netherlands	18	846	481	139	117	101	49	1.1k
Irina Anselm United States	16	810 1.0×	477 1.0×	122 0.9×	303 2.6×	108 1.1×	29	1.2k
Zarazuela Zolkipli United Kingdom	10	291 0.3×	145 0.3×	89 0.6×	67 0.6×	59 0.6×	13	604
Roser Pons Greece	21	644 0.8×	826 1.7×	261 1.9×	273 2.3×	322 3.2×	58	1.6k
Sara Petrillo Italy	18	730 0.9×	99 0.2×	128 0.9×	64 0.5×	292 2.9×	34	1.1k
James D. Clelland United States	16	236 0.3×	98 0.2×	98 0.7×	45 0.4×	46 0.5×	29	666
Tyler G. Demarest United States	19	607 0.7×	49 0.1×	336 2.4×	67 0.6×	116 1.1×	22	1.3k
Elizabeth Neal United Kingdom	13	336 0.4×	965 2.0×	1.4k 9.9×	189 1.6×	125 1.2×	20	1.6k
Ruby H. Schwartz United Kingdom	6	285 0.3×	816 1.7×	1.1k 8.2×	161 1.4×	111 1.1×	9	1.4k
Pierre Castelnau France	16	283 0.3×	61 0.1×	79 0.6×	94 0.8×	160 1.6×	50	826
Knut H. Lauritzen Norway	14	599 0.7×	67 0.1×	303 2.2×	42 0.4×	217 2.1×	20	1.0k

Countries citing papers authored by Saskia Koene

Since Specialization

Citations

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

Fields of papers citing papers by Saskia Koene

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Saskia Koene

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

Haeringen, Arie van, Lisenka E.L.M. Vissers, Emilia K. Bijlsma, et al.. (2023). Reanalysis of whole-exome sequencing (WES) data of children with neurodevelopmental disorders in a standard patient care context. European Journal of Pediatrics. 183(1). 345–355. 8 indexed citations

Koene, Saskia, Dagmar Berghuis, Angela Morgan, et al.. (2023). Clinical phenotype of FOXP1 syndrome: parent-reported medical signs and symptoms in 40 individuals. Journal of Medical Genetics. 61(4). 399–404. 4 indexed citations

Dooren, M. F. van, Augusta M.A. Lachmeijer, Virginie J. M. Verhoeven, et al.. (2023). Diagnostic Gene Panel Testing in (Non)-Syndromic Patients with Cleft Lip, Alveolus and/or Palate in the Netherlands. Molecular Syndromology. 14(4). 270–282. 3 indexed citations

Graff, Maud, Lonneke de Boer, Imelda J. M. de Groot, et al.. (2023). Using PRPP‐Assessment for measuring change in everyday activities by home‐based videos: An exploratory case series study in children with multiple disabilities. Australian Occupational Therapy Journal. 70(6). 644–660.

Groot, Imelda J. M. de, et al.. (2022). Perceive, Recall, Plan and Perform (PRPP)-Assessment Based on Parent-Provided Videos of Children with Mitochondrial Disorder: Action Design Research on Implementation Challenges. Physical & Occupational Therapy In Pediatrics. 43(1). 74–92. 4 indexed citations

Koene, Saskia, et al.. (2022). Sacral abnormalities including caudal appendage, skeletal dysplasia, and prenatal cardiomyopathy associated with a pathogenic TAB2 variant in a 3‐generation family. American Journal of Medical Genetics Part A. 188(12). 3510–3515. 2 indexed citations

Koene, Saskia, Jeroen Knijnenburg, Mariëtte J.V. Hoffer, et al.. (2022). Hearing loss, cleft palate, and congenital hip dysplasia in female carriers of an intragenic deletion of AMMECR1. American Journal of Medical Genetics Part A. 188(5). 1578–1582. 2 indexed citations

Koene, Saskia, Melissa Nott, Maria W. G. Nijhuis–van der Sanden, et al.. (2022). The reliability and validity of the perceive, recall, plan and perform assessment in children with a mitochondrial disorder. Disability and Rehabilitation. 45(14). 2354–2367. 4 indexed citations

Sanden, Maria W. G. Nijhuis–van der, et al.. (2021). Insight into Performance of Daily Activities in Real Life of A Child with Limited Physical, Cognitive and Communication Abilities: A Case Report. Journal of Occupational Therapy Schools & Early Intervention. 15(2). 205–217. 4 indexed citations

10.

Koene, Saskia, Cacha Peeters‐Scholte, Jeroen Knijnenburg, et al.. (2020). Intracerebral hemorrhage in a neonate with an intragenic COL4A2 duplication. American Journal of Medical Genetics Part A. 185(2). 571–574. 3 indexed citations

11.

Steultjens, Esther, et al.. (2019). The Perspectives and Values of Children with a Mitochondrial Disorder with Regard to Everyday Activities. Journal of Developmental and Physical Disabilities. 32(3). 509–534. 3 indexed citations

12.

Janssen, Mariska M. H. P., Edwin Spaans, Imelda J. M. de Groot, et al.. (2019). Natural variability of daily physical activity measured by accelerometry in children with a mitochondrial disease. Mitochondrion. 47. 30–37. 6 indexed citations

13.

Koene, Saskia, Niki M. Stolwijk, Maaike C. de Vries, et al.. (2018). Quantification of gait in children with mitochondrial disease. Journal of Inherited Metabolic Disease. 41(4). 731–740.

14.

Koene, Saskia, Enrico Bertini, Cecilia Jimenez‐Moreno, et al.. (2018). Outcome measures for children with mitochondrial disease: consensus recommendations for future studies from a Delphi‐based international workshop. Journal of Inherited Metabolic Disease. 41(6). 1267–1273. 21 indexed citations

15.

Koene, Saskia, et al.. (2017). Quantification of gait in mitochondrial m.3243A > G patients: a validation study. Orphanet Journal of Rare Diseases. 12(1). 91–91. 4 indexed citations

16.

Koene, Saskia, Edwin Spaans, Luc Van Bortel, et al.. (2017). KH176 under development for rare mitochondrial disease: a first in man randomized controlled clinical trial in healthy male volunteers. Orphanet Journal of Rare Diseases. 12(1). 163–163. 43 indexed citations

17.

Góraj, Bożena, et al.. (2016). Radboud Centre for Mitochondrial Medicine Pediatric MRI score. Mitochondrion. 32. 36–41. 2 indexed citations

18.

Verhaak, C.M., Paul de Laat, Saskia Koene, et al.. (2016). Quality of life, fatigue and mental health in patients with the m.3243A > G mutation and its correlates with genetic characteristics and disease manifestation. Orphanet Journal of Rare Diseases. 11(1). 25–25. 14 indexed citations

19.

Laat, Paul de, et al.. (2012). Clinical features and heteroplasmy in blood, urine and saliva in 34 Dutch families carrying the m.3243A > G mutation. Journal of Inherited Metabolic Disease. 35(6). 1059–1069. 105 indexed citations

20.

Koene, Saskia & Jan Smeıtınk. (2009). Mitochondrial medicine: entering the era of treatment. Journal of Internal Medicine. 265(2). 193–209. 57 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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