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:
Fetal therapies and trials for lysosomal storage diseases: a survey of attitudes of parents and patients
Marisa E. Schwab, Julia E. H. Brown, Billie R. Lianoglou, et al.
Orphanet Journal of Rare Diseases (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 13
Marisa E. Schwab, Julia E. H. Brown, Billie R. Lianoglou, et al.
Orphanet Journal of Rare Diseases (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 13
Showing 13 citing articles:
Prenatal Delivery of Enzyme Replacement Therapy to Fetuses Affected by Early‐Onset Lysosomal Storage Diseases
Beltran Borges, Emma Canepa, Irene J. Chang, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2025)
Closed Access | Times Cited: 1
Beltran Borges, Emma Canepa, Irene J. Chang, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2025)
Closed Access | Times Cited: 1
Fetal gene therapy
Simon N. Waddington, William H. Peranteau, Ahad A. Rahim, et al.
Journal of Inherited Metabolic Disease (2023) Vol. 47, Iss. 1, pp. 192-210
Open Access | Times Cited: 14
Simon N. Waddington, William H. Peranteau, Ahad A. Rahim, et al.
Journal of Inherited Metabolic Disease (2023) Vol. 47, Iss. 1, pp. 192-210
Open Access | Times Cited: 14
Advancing precision care in pregnancy through a treatable fetal findings list
Jennifer L. Cohen, Michael H. Duyzend, Sophia Adelson, et al.
The American Journal of Human Genetics (2025)
Closed Access
Jennifer L. Cohen, Michael H. Duyzend, Sophia Adelson, et al.
The American Journal of Human Genetics (2025)
Closed Access
Parental perception of treatment options for mucopolysaccharidosis: a survey to bridge the gap for personalized medicine
Anna‐Maria Wiesinger, Florian B. Lagler
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access
Anna‐Maria Wiesinger, Florian B. Lagler
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access
Ascending vaginal infection in mice induces preterm birth and neonatal morbidity
Ashley K. Boyle, Konstantina Tetorou, Natalie Suff, et al.
American Journal Of Pathology (2025)
Open Access
Ashley K. Boyle, Konstantina Tetorou, Natalie Suff, et al.
American Journal Of Pathology (2025)
Open Access
Intrauterine enzyme replacement therapies for lysosomal storage disorders: Current developments and promising future prospects
Akos Herzeg, Beltran Borges, Billie R. Lianoglou, et al.
Prenatal Diagnosis (2023) Vol. 43, Iss. 13, pp. 1638-1649
Open Access | Times Cited: 10
Akos Herzeg, Beltran Borges, Billie R. Lianoglou, et al.
Prenatal Diagnosis (2023) Vol. 43, Iss. 13, pp. 1638-1649
Open Access | Times Cited: 10
Factors affecting overall care experience for people living with rare conditions in the UK: exploratory analysis of a quantitative patient experience survey
Jennifer Jones, M Cruddas, Amy Simpson, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 2
Jennifer Jones, M Cruddas, Amy Simpson, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 2
Impact of prenatal genomics on clinical genetics practice
Roni Zemet, Ignatia B. Van den Veyver
Best Practice & Research Clinical Obstetrics & Gynaecology (2024) Vol. 97, pp. 102545-102545
Closed Access | Times Cited: 2
Roni Zemet, Ignatia B. Van den Veyver
Best Practice & Research Clinical Obstetrics & Gynaecology (2024) Vol. 97, pp. 102545-102545
Closed Access | Times Cited: 2
Prenatal Somatic Cell Gene Therapies: Charting a Path Toward Clinical Applications (Proceedings of the CERSI‐FDA Meeting)
Akos Herzeg, Graça Almeida‐Porada, R. Alta Charo, et al.
The Journal of Clinical Pharmacology (2022) Vol. 62, Iss. S1
Open Access | Times Cited: 10
Akos Herzeg, Graça Almeida‐Porada, R. Alta Charo, et al.
The Journal of Clinical Pharmacology (2022) Vol. 62, Iss. S1
Open Access | Times Cited: 10
Diagnosis and Emerging Treatment Strategies for Mucopolysaccharidosis VII (Sly Syndrome)
Fabiano de Oliveira Poswar, Johanna Henriques Nehm, Francyne Kubaski, et al.
Therapeutics and Clinical Risk Management (2022) Vol. Volume 18, pp. 1143-1155
Open Access | Times Cited: 10
Fabiano de Oliveira Poswar, Johanna Henriques Nehm, Francyne Kubaski, et al.
Therapeutics and Clinical Risk Management (2022) Vol. Volume 18, pp. 1143-1155
Open Access | Times Cited: 10
Outcome and etiology of fetal pleural effusion, fetal ascites and hydrops fetalis after fetal intervention: retrospective observational cohort from a single institution
Wan-Ju Wu, Gwo‐Chin Ma, Ting‐Yu Chang, et al.
Ultrasound in Obstetrics and Gynecology (2023) Vol. 63, Iss. 4, pp. 536-543
Closed Access | Times Cited: 5
Wan-Ju Wu, Gwo‐Chin Ma, Ting‐Yu Chang, et al.
Ultrasound in Obstetrics and Gynecology (2023) Vol. 63, Iss. 4, pp. 536-543
Closed Access | Times Cited: 5
From pathological mechanisms in Krabbe disease to cutting‐edge therapy: A comprehensive review
Imen Ketata, Emna Ellouz
Neuropathology (2024) Vol. 44, Iss. 4, pp. 255-277
Closed Access | Times Cited: 1
Imen Ketata, Emna Ellouz
Neuropathology (2024) Vol. 44, Iss. 4, pp. 255-277
Closed Access | Times Cited: 1
Acceptability of prenatal diagnosis and prenatal treatment of haemophilia using cell and gene therapies within US haemophilia community
Quan D. M. Pham, Sharon M. Thomson, Burk N. Schaible, et al.
Haemophilia (2023) Vol. 29, Iss. 4, pp. 1024-1031
Open Access | Times Cited: 1
Quan D. M. Pham, Sharon M. Thomson, Burk N. Schaible, et al.
Haemophilia (2023) Vol. 29, Iss. 4, pp. 1024-1031
Open Access | Times Cited: 1
