Sacha Ferdinandusse

Also affiliated with University of Amsterdam

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 6 papers. Top paper: “Nutritional ketosis improves exercise metabolism in patients with very long‐chain acyl‐CoA dehydrogenase deficiency”.

Nutritional ketosis improves exercise metabolism in patients with very long‐chain acyl‐CoA dehydrogenase deficiency

Journal of Inherited Metabolic Disease(2020)10.1002/jimd.12217

N/A

1.4DataRank · unranked

39 citations

Gepke Visser, Kieran Clarke, Sacha Ferdinandusse, Ferdinand H. de Haan, Riekelt H. Houtkooper +15 more

An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

Genetics in Medicine(2020)10.1038/s41436-020-01027-3

N/A

0DataRank · unranked

49 citations

Kirsty McWalter, Heleen te Brinke, Lodewijk IJlst, Petra M. Mooijer, Jos P.N. Ruiter +95 more

Medical nutrition therapy in patients with HIBCH and ECHS1 defects: Clinical and biochemical response to low valine diet

Molecular Genetics and Metabolism Reports(2020)10.1016/j.ymgmr.2020.100617

N/A

0DataRank · unranked

29 citations

Mary Sowa, Mariella Simon, Maija Steenari, Janette Skaar, Shaya S. Eftekharian +4 more

ECHS1 disease in two unrelated families of Samoan descent: Common variant ‐ rare disorder

American Journal of Medical Genetics Part A(2020)10.1002/ajmg.a.61936

N/A

0DataRank · unranked

27 citations

Shaya S. Eftekharian, Sacha Ferdinandusse, Sha Tang, Take Naseri, Muagututi‘a Sefuiva Reupena +12 more

International Recommendations for the Diagnosis and Management of Patients With Adrenoleukodystrophy

Neurology(2022)10.1212/wnl.0000000000201374

N/A

0DataRank · unranked

142 citations

Wouter J. C. van Ballegoij, Eric J. Mallack, Keith Van Haren, Wolfgang Köhler, Ettore Salsano +23 more

Novel SUCLG1 Variants in a Patient with Fatal Neonatal Onset Succinyl-Coa Ligase Deficiency

Journal of Pediatric Genetics(2025)10.53391/2146-460x.1009

N/A

0DataRank · unranked

0 citations

Lauren Culbertson, Cary O. Harding, Cori Feist, Johan L.K. Van Hove, Marisa W. Friederich +6 more