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:
Screening, patient identification, evaluation, and treatment in patients with Gaucher disease: Results from a Delphi consensus
Priya S. Kishnani, Walla Al‐Hertani, Manisha Balwani, et al.
Molecular Genetics and Metabolism (2021) Vol. 135, Iss. 2, pp. 154-162
Open Access | Times Cited: 23
Priya S. Kishnani, Walla Al‐Hertani, Manisha Balwani, et al.
Molecular Genetics and Metabolism (2021) Vol. 135, Iss. 2, pp. 154-162
Open Access | Times Cited: 23
Showing 23 citing articles:
The diagnosis and management of Gaucher disease in pediatric patients: Where do we go from here?
Neal J. Weinreb, Özlem Göker-Alpan, Priya S. Kishnani, et al.
Molecular Genetics and Metabolism (2022) Vol. 136, Iss. 1, pp. 4-21
Open Access | Times Cited: 44
Neal J. Weinreb, Özlem Göker-Alpan, Priya S. Kishnani, et al.
Molecular Genetics and Metabolism (2022) Vol. 136, Iss. 1, pp. 4-21
Open Access | Times Cited: 44
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
Challenges in Gaucher disease: Perspectives from an expert panel
Gregory A. Grabowski, Priya S. Kishnani, Roy N. Alcalay, et al.
Molecular Genetics and Metabolism (2025), pp. 109074-109074
Closed Access | Times Cited: 1
Gregory A. Grabowski, Priya S. Kishnani, Roy N. Alcalay, et al.
Molecular Genetics and Metabolism (2025), pp. 109074-109074
Closed Access | Times Cited: 1
Modern Clinical Guidelines for the Management of Patients with Gaucher Disease
И. В. Анисимова, Galina Baydakova, Baranov Aa, et al.
Педиатрическая фармакология (2025) Vol. 21, Iss. 6, pp. 551-568
Open Access
И. В. Анисимова, Galina Baydakova, Baranov Aa, et al.
Педиатрическая фармакология (2025) Vol. 21, Iss. 6, pp. 551-568
Open Access
Obstacles to Early Diagnosis of Gaucher Disease
Samantha Nishimura, Charis Ma, Ellen Sidransky, et al.
Therapeutics and Clinical Risk Management (2025) Vol. Volume 21, pp. 93-101
Open Access
Samantha Nishimura, Charis Ma, Ellen Sidransky, et al.
Therapeutics and Clinical Risk Management (2025) Vol. Volume 21, pp. 93-101
Open Access
Prospective Monitoring of Lyso-Gb1 on DBS Sample in Three Children Recognized at Newborn Screening for Gaucher Disease and Untreated
Cláudia Rossi, Daniela Trotta, Rossella Ferrante, et al.
Children (2025) Vol. 12, Iss. 3, pp. 350-350
Open Access
Cláudia Rossi, Daniela Trotta, Rossella Ferrante, et al.
Children (2025) Vol. 12, Iss. 3, pp. 350-350
Open Access
Newborn Screening for Gaucher Disease: The New Jersey Experience
Caitlin Menello, Shaney Pressley, Madeline Steffensen, et al.
International Journal of Neonatal Screening (2025) Vol. 11, Iss. 2, pp. 34-34
Open Access
Caitlin Menello, Shaney Pressley, Madeline Steffensen, et al.
International Journal of Neonatal Screening (2025) Vol. 11, Iss. 2, pp. 34-34
Open Access
Neuronopathic Gaucher disease: Rare in the West, common in the East
Özlem Göker-Alpan, Margarita M. Ivanova
Journal of Inherited Metabolic Disease (2024) Vol. 47, Iss. 5, pp. 917-934
Open Access | Times Cited: 3
Özlem Göker-Alpan, Margarita M. Ivanova
Journal of Inherited Metabolic Disease (2024) Vol. 47, Iss. 5, pp. 917-934
Open Access | Times Cited: 3
Consensus recommendations for the treatment and management of patients with Fabry disease on migalastat: a modified Delphi study
Daniel G. Bichet, Robert J. Hopkin, Patrício Aguiar, et al.
Frontiers in Medicine (2023) Vol. 10
Open Access | Times Cited: 8
Daniel G. Bichet, Robert J. Hopkin, Patrício Aguiar, et al.
Frontiers in Medicine (2023) Vol. 10
Open Access | Times Cited: 8
The budget impact of enzyme replacement therapy in type 1 Gaucher disease in the United States
Sepehr Farahbakhshian, Timothy J. Inocencio, Gregory W. Poorman, et al.
Journal of Medical Economics (2022) Vol. 25, Iss. 1, pp. 755-761
Open Access | Times Cited: 8
Sepehr Farahbakhshian, Timothy J. Inocencio, Gregory W. Poorman, et al.
Journal of Medical Economics (2022) Vol. 25, Iss. 1, pp. 755-761
Open Access | Times Cited: 8
Long‐term follow‐up of a patient with neonatal form of Gaucher disease
Vincenza Gragnaniello, Chiara Cazzorla, Daniela Gueraldi, et al.
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 7, pp. 1917-1922
Open Access | Times Cited: 4
Vincenza Gragnaniello, Chiara Cazzorla, Daniela Gueraldi, et al.
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 7, pp. 1917-1922
Open Access | Times Cited: 4
What should rheumatologists know about Gaucher disease and Fabry disease? Connecting the dots for an overview
Rafael Alves Cordeiro, Nilton Salles Rosa Neto, Henrique Ayres Mayrink Giardini
Advances in Rheumatology (2024) Vol. 64, Iss. 1
Open Access | Times Cited: 1
Rafael Alves Cordeiro, Nilton Salles Rosa Neto, Henrique Ayres Mayrink Giardini
Advances in Rheumatology (2024) Vol. 64, Iss. 1
Open Access | Times Cited: 1
Phenotypic consequences of GBA1 pathological variant R463C (p.R502C )
Emory Ryan, Samantha Nishimura, Grisel Lopez, et al.
American Journal of Medical Genetics Part A (2024) Vol. 194, Iss. 9
Closed Access | Times Cited: 1
Emory Ryan, Samantha Nishimura, Grisel Lopez, et al.
American Journal of Medical Genetics Part A (2024) Vol. 194, Iss. 9
Closed Access | Times Cited: 1
The Liver and Lysosomal Storage Diseases: From Pathophysiology to Clinical Presentation, Diagnostics, and Treatment
Patryk Lipiński, Anna Tylki‐Szymańska
Diagnostics (2024) Vol. 14, Iss. 12, pp. 1299-1299
Open Access | Times Cited: 1
Patryk Lipiński, Anna Tylki‐Szymańska
Diagnostics (2024) Vol. 14, Iss. 12, pp. 1299-1299
Open Access | Times Cited: 1
Management goals of type 1 Gaucher disease in South Africa: An expert Delphi consensus document on good clinical practice
Vernon Louw, Ilanca Fraser, Pilar Giraldo
PLoS ONE (2023) Vol. 18, Iss. 8, pp. e0290401-e0290401
Open Access | Times Cited: 3
Vernon Louw, Ilanca Fraser, Pilar Giraldo
PLoS ONE (2023) Vol. 18, Iss. 8, pp. e0290401-e0290401
Open Access | Times Cited: 3
Bone disease in early detected Gaucher Type I disease: A case report
Vincenza Gragnaniello, Alessandro P. Burlina, Renzo Manara, et al.
JIMD Reports (2022) Vol. 63, Iss. 5, pp. 414-419
Open Access | Times Cited: 5
Vincenza Gragnaniello, Alessandro P. Burlina, Renzo Manara, et al.
JIMD Reports (2022) Vol. 63, Iss. 5, pp. 414-419
Open Access | Times Cited: 5
Newborn Screening in Gaucher Disease: A Bright and Complicated Future
Emory Ryan, Tiffany Jong, Ellen Sidransky
OBM Genetics (2022) Vol. 06, Iss. 03, pp. 1-21
Open Access | Times Cited: 3
Emory Ryan, Tiffany Jong, Ellen Sidransky
OBM Genetics (2022) Vol. 06, Iss. 03, pp. 1-21
Open Access | Times Cited: 3
A retrospective and prospective observational study of MRI changes in bone in patients with type 1 Gaucher disease treated with velaglucerase alfa: the EIROS study.
Monia Bengherbia, Marc Berger, Bénédicte Hivert, et al.
Research Square (Research Square) (2024)
Open Access
Monia Bengherbia, Marc Berger, Bénédicte Hivert, et al.
Research Square (Research Square) (2024)
Open Access
A Real-World Investigation of MRI Changes in Bone in Patients with Type 1 Gaucher Disease Treated with Velaglucerase Alfa: The EIROS Study
Monia Bengherbia, Marc Berger, Bénédicte Hivert, et al.
Journal of Clinical Medicine (2024) Vol. 13, Iss. 10, pp. 2926-2926
Open Access
Monia Bengherbia, Marc Berger, Bénédicte Hivert, et al.
Journal of Clinical Medicine (2024) Vol. 13, Iss. 10, pp. 2926-2926
Open Access
Gaucher's disease in children: Case report from Afghanistan with literature review
Turyalai Hakimi, Omran Omar Amarkhil, Muhammad Arif Zamani, et al.
Global Pediatrics (2023) Vol. 5, pp. 100072-100072
Open Access | Times Cited: 1
Turyalai Hakimi, Omran Omar Amarkhil, Muhammad Arif Zamani, et al.
Global Pediatrics (2023) Vol. 5, pp. 100072-100072
Open Access | Times Cited: 1
Overview of Newborn Screening of Lysosomal Storage Diseases for Pediatric Care Providers
Ashley Lahr, Nadene Henderson, Lee Williams, et al.
OBM Genetics (2023) Vol. 07, Iss. 03, pp. 1-12
Open Access | Times Cited: 1
Ashley Lahr, Nadene Henderson, Lee Williams, et al.
OBM Genetics (2023) Vol. 07, Iss. 03, pp. 1-12
Open Access | Times Cited: 1
Incidence of Pulmonary and Respiratory Conditions in Gaucher Disease from 2000 to 2020: A Multi-institutional Cohort Study
Yu‐Nan Huang, Jing‐Yang Huang, WEN-LING LIAO, et al.
In Vivo (2023) Vol. 37, Iss. 5, pp. 2276-2283
Open Access
Yu‐Nan Huang, Jing‐Yang Huang, WEN-LING LIAO, et al.
In Vivo (2023) Vol. 37, Iss. 5, pp. 2276-2283
Open Access
Gaucher-kór és az ajánlott új diagnosztikai algoritmus
Ottó Csacsovszki, Hussain Alizadeh, Árpád Bátai, et al.
Hematológia–Transzfuziológia (2023) Vol. 56, Iss. 2, pp. 76-80
Closed Access
Ottó Csacsovszki, Hussain Alizadeh, Árpád Bátai, et al.
Hematológia–Transzfuziológia (2023) Vol. 56, Iss. 2, pp. 76-80
Closed Access
Eduardo Garrido, Anna A. Pendina, Mikhail Krapivin, et al.
OBM Genetics (2022) Vol. 6, Iss. 3
Open Access
