OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
SMPD1 expression profile and mutation landscape help decipher genotype–phenotype association and precision diagnosis for acid sphingomyelinase deficiency
Ruisong Wang, Ziyi Qin, Long Shuang Huang, et al.
Hereditas (2023) Vol. 160, Iss. 1
Open Access | Times Cited: 8
Ruisong Wang, Ziyi Qin, Long Shuang Huang, et al.
Hereditas (2023) Vol. 160, Iss. 1
Open Access | Times Cited: 8
Showing 8 citing articles:
The Genetic Basis, Lung Involvement, and Therapeutic Options in Niemann–Pick Disease: A Comprehensive Review
Claudio Tirelli, Ornella Rondinone, Marta Italia, et al.
Biomolecules (2024) Vol. 14, Iss. 2, pp. 211-211
Open Access | Times Cited: 8
Claudio Tirelli, Ornella Rondinone, Marta Italia, et al.
Biomolecules (2024) Vol. 14, Iss. 2, pp. 211-211
Open Access | Times Cited: 8
ASM variants in the spotlight: A structure-based atlas for unraveling pathogenic mechanisms in lysosomal acid sphingomyelinase
Simone Scrima, Matteo Lambrughi, Matteo Tiberti, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2024) Vol. 1870, Iss. 7, pp. 167260-167260
Open Access | Times Cited: 5
Simone Scrima, Matteo Lambrughi, Matteo Tiberti, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2024) Vol. 1870, Iss. 7, pp. 167260-167260
Open Access | Times Cited: 5
Perspective Chapter: Next-Generation Sequencing and Variant Cataloging for Screening and Diagnosis of Sphingolipidoses and Mucopolysaccharidoses
Irina Vlasova-St. Louis, Uri Barak, Svetlana F. Khaiboullina
IntechOpen eBooks (2025)
Closed Access
Irina Vlasova-St. Louis, Uri Barak, Svetlana F. Khaiboullina
IntechOpen eBooks (2025)
Closed Access
Natural disease course of chronic visceral acid sphingomyelinase deficiency in adults: A first step toward treatment criteria
Eline C. B. Eskes, Laura van Dussen, Marion M. Brands, et al.
Journal of Inherited Metabolic Disease (2024)
Open Access | Times Cited: 2
Eline C. B. Eskes, Laura van Dussen, Marion M. Brands, et al.
Journal of Inherited Metabolic Disease (2024)
Open Access | Times Cited: 2
ASM Variants in the Spotlight: A Structure-Based Atlas for Unraveling Pathogenic Mechanisms in Lysosomal Acid Sphingomyelinase
Simone Scrima, Matteo Lambrughi, Matteo Tiberti, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 2
Simone Scrima, Matteo Lambrughi, Matteo Tiberti, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 2
Allele frequency of pathogenic variants causing acid sphingomyelinase deficiency and Gaucher disease in the general Japanese population
Shuhei Sako, Kimihiko Oishi, Hiroyuki Ida, et al.
Human Genome Variation (2024) Vol. 11, Iss. 1
Open Access
Shuhei Sako, Kimihiko Oishi, Hiroyuki Ida, et al.
Human Genome Variation (2024) Vol. 11, Iss. 1
Open Access
Niemann-Pick Disease, Type A: Clinical Case of 5 Months Old Patient
Nataliya V. Zhurkova, Nato D. Vashakmadze, А. Н. Сурков, et al.
Вопросы современной педиатрии (2024) Vol. 23, Iss. 3, pp. 188-196
Open Access
Nataliya V. Zhurkova, Nato D. Vashakmadze, А. Н. Сурков, et al.
Вопросы современной педиатрии (2024) Vol. 23, Iss. 3, pp. 188-196
Open Access
The Niemann–Pick diseases
Edward H. Schuchman, Robert J. Desnick
Elsevier eBooks (2024), pp. 559-569
Closed Access
Edward H. Schuchman, Robert J. Desnick
Elsevier eBooks (2024), pp. 559-569
Closed Access
