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:
Current and Novel Therapeutical Approaches of Classical Homocystinuria in Childhood With Special Focus on Enzyme Replacement Therapy, Liver-Directed Therapy and Gene Therapy
Stefan Bittmann, Gloria Villalon, Elena Moschüring-Alieva, et al.
Journal of Clinical Medicine Research (2023) Vol. 15, Iss. 2, pp. 76-83
Open Access | Times Cited: 7
Stefan Bittmann, Gloria Villalon, Elena Moschüring-Alieva, et al.
Journal of Clinical Medicine Research (2023) Vol. 15, Iss. 2, pp. 76-83
Open Access | Times Cited: 7
Showing 7 citing articles:
The live biotherapeutic SYNB1353 decreases plasma methionine via directed degradation in animal models and healthy volunteers
Mylène Perreault, Jillian Means, Erik Gerson, et al.
Cell Host & Microbe (2024) Vol. 32, Iss. 3, pp. 382-395.e10
Open Access | Times Cited: 16
Mylène Perreault, Jillian Means, Erik Gerson, et al.
Cell Host & Microbe (2024) Vol. 32, Iss. 3, pp. 382-395.e10
Open Access | Times Cited: 16
High clinical burden of classical homocystinuria in the United States: a retrospective analysis
Mahim Jain, Mehul Shah, Kamlesh M. Thakker, et al.
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access
Mahim Jain, Mehul Shah, Kamlesh M. Thakker, et al.
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access
An orally administered enzyme therapeutic for homocystinuria that suppresses homocysteine by metabolizing methionine in the gastrointestinal tract
Kristen J. Skvorak, Vesna Mitchell, Leann Teadt, et al.
Molecular Genetics and Metabolism (2023) Vol. 139, Iss. 4, pp. 107653-107653
Open Access | Times Cited: 6
Kristen J. Skvorak, Vesna Mitchell, Leann Teadt, et al.
Molecular Genetics and Metabolism (2023) Vol. 139, Iss. 4, pp. 107653-107653
Open Access | Times Cited: 6
The treatment of biochemical genetic diseases: From substrate reduction to nucleic acid therapies
E. Naomi Vos, Didem Demirbas, Matthew Mangel, et al.
Molecular Genetics and Metabolism (2023) Vol. 140, Iss. 3, pp. 107693-107693
Closed Access | Times Cited: 4
E. Naomi Vos, Didem Demirbas, Matthew Mangel, et al.
Molecular Genetics and Metabolism (2023) Vol. 140, Iss. 3, pp. 107693-107693
Closed Access | Times Cited: 4
Methionine gamma lyase: Structure-activity relationships and therapeutic applications
Samanta Raboni, Serena Faggiano, Stefano Bettati, et al.
Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics (2023) Vol. 1872, Iss. 3, pp. 140991-140991
Open Access | Times Cited: 3
Samanta Raboni, Serena Faggiano, Stefano Bettati, et al.
Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics (2023) Vol. 1872, Iss. 3, pp. 140991-140991
Open Access | Times Cited: 3
Clinical, biochemical and molecular characteristics of classic homocystinuria in Saudi Arabia and the impact of newborn screening on prevention of the complications: A tertiary center experience
Ahmed Sarar Mohamed, Talal Alanzi, Amal Alhashem, et al.
JIMD Reports (2024) Vol. 66, Iss. 1
Open Access
Ahmed Sarar Mohamed, Talal Alanzi, Amal Alhashem, et al.
JIMD Reports (2024) Vol. 66, Iss. 1
Open Access
Hereditary Amino Acid Metabolism Disorders and Urea Cycle Disorders: to Practicing Physician
Nataliya V. Zhurkova, Nato D. Vashakmadze, Nataliya S. Sergienko, et al.
Вопросы современной педиатрии (2024) Vol. 22, Iss. 6, pp. 560-571
Open Access
Nataliya V. Zhurkova, Nato D. Vashakmadze, Nataliya S. Sergienko, et al.
Вопросы современной педиатрии (2024) Vol. 22, Iss. 6, pp. 560-571
Open Access
