OpenAlex Citation Counts

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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:

Hermansky–Pudlak Syndrome
Wilfredo De Jesús Rojas, Lisa R. Young
Seminars in Respiratory and Critical Care Medicine (2020) Vol. 41, Iss. 02, pp. 238-246
Closed Access | Times Cited: 35

Showing 1-25 of 35 citing articles:

Genetic disorders of cellular trafficking
Ángeles García‐Cazorla, Alfonso Oyarzábal, Jean‐Marie Saudubray, et al.
Trends in Genetics (2022) Vol. 38, Iss. 7, pp. 724-751
Closed Access | Times Cited: 44

The biochemistry of melanogenesis: an insight into the function and mechanism of melanogenesis-related proteins
Feifei Wang, Wenjing Ma, Dongjie Fan, et al.
Frontiers in Molecular Biosciences (2024) Vol. 11
Open Access | Times Cited: 5

Hermansky–Pudlak syndrome pulmonary fibrosis: a rare inherited interstitial lung disease
Tadafumi Yokoyama, Bernadette R. Gochuico
European Respiratory Review (2021) Vol. 30, Iss. 159, pp. 200193-200193
Open Access | Times Cited: 31

The importance of genetic counselling and testing in inherited eye diseases: A population-based retrospective study
Michal Kaminer Abargel, Michal Macarov, Karen Hendler, et al.
PLoS ONE (2025) Vol. 20, Iss. 2, pp. e0318492-e0318492
Open Access

Re-Examining the Role of Pulmonary Lipids in the Pathogenesis of Pulmonary Fibrosis
Marissa O’Callaghan, Elizabeth J. Tarling, James P. Bridges, et al.
American Journal of Respiratory Cell and Molecular Biology (2024) Vol. 71, Iss. 4, pp. 407-419
Closed Access | Times Cited: 3

Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
Jahangir Khan, Saaim Asif, Shamsul Ghani, et al.
BMC Ophthalmology (2024) Vol. 24, Iss. 1
Open Access | Times Cited: 2

Impairment of Renal Function in Hermansky-Pudlak Syndrome
Tadafumi Yokoyama, Kevin O’Brien, Tesiya M Franklin, et al.
American Journal of Nephrology (2024), pp. 1-10
Closed Access | Times Cited: 2

The Genetics of Primary Ciliary Dyskinesia in Puerto Rico
W. De Jesus-Rojas, José Muñiz‐Hernández, Francisco Alvarado-Huerta, et al.
Diagnostics (2022) Vol. 12, Iss. 5, pp. 1127-1127
Open Access | Times Cited: 10

Prospective Study of the Phenotypic and Mutational Spectrum of Ocular Albinism and Oculocutaneous Albinism
Hwei Wuen Chan, Elena Schiff, Vijay Tailor, et al.
Genes (2021) Vol. 12, Iss. 4, pp. 508-508
Open Access | Times Cited: 14

Type II phosphatidylinositol 4-kinases function sequentially in cargo delivery from early endosomes to melanosomes
Yueyao Zhu, Shuixing Li, Alexa Jaume, et al.
The Journal of Cell Biology (2022) Vol. 221, Iss. 11
Open Access | Times Cited: 9

Current strategies and opportunities to manufacture cells for modeling human lungs
Ratna Varma, John P. Soleas, Thomas K. Waddell, et al.
Advanced Drug Delivery Reviews (2020) Vol. 161-162, pp. 90-109
Open Access | Times Cited: 9

Hermansky-Pudlak syndrome with early onset inflammatory bowel disease due to loss of dysbindin expression
Sagar Bhattad, Michael Libre, Joseph M. Choi, et al.
European Journal of Medical Genetics (2023) Vol. 66, Iss. 7, pp. 104786-104786
Closed Access | Times Cited: 2

Unraveling Hermansky–Pudlak syndrome type 7: a case report and comprehensive literature review on the identification of DTNBP1 variants
Rita Rodrigues, Rita Quental, Renato Silva, et al.
Ophthalmic Genetics (2023) Vol. 45, Iss. 3, pp. 262-266
Closed Access | Times Cited: 2

Delineating Novel and Known Pathogenic Variants in TYR, OCA2 and HPS-1 Genes in Eight Oculocutaneous Albinism (OCA) Pakistani Families
Muhammad Shakil, Abida Akbar, Nazish Mahmood Aisha, et al.
Genes (2022) Vol. 13, Iss. 3, pp. 503-503
Open Access | Times Cited: 3

Manifestations pulmonaires des maladies héréditaires du métabolisme
Wladimir Mauhin, Anaïs Brassier, Jonathan London, et al.
Revue des Maladies Respiratoires (2022) Vol. 39, Iss. 9, pp. 758-777
Closed Access | Times Cited: 3

Interdisciplinary approach to diagnosis of life-threatening form of albinism: Germanic-Pudlac syndrome case type 1
Anastasia M. Bobreshova, Sofya Ionova, В. В. Кадышев, et al.
Archives of Pediatrics and Pediatric Surgery (2024) Vol. 2, Iss. 1, pp. 148-154
Open Access

After an initial Hermansky–Pudlak syndrome clinical diagnosis, molecular testing reveals variants for oculocutaneous albinism type 1B: A case report
Joseline Serrano-González, Ingrid M. Montes‐Rodríguez, Jessicca Y. Renta, et al.
Molecular Genetics & Genomic Medicine (2024) Vol. 12, Iss. 7
Open Access

Hermansky-Pudlak Syndrome Pulmonary Fibrosis: an unusual pattern of fibrosis
Matthew Donnan, Samantha Ellis, Ian Glaspole
Respiratory Medicine Case Reports (2024) Vol. 52, pp. 102123-102123
Open Access

Pathogenesis and Therapy of Hermansky–Pudlak Syndrome (HPS)-Associated Pulmonary Fibrosis
Xiao Mei Hu, Zhixiao Wei, Yumeng Wu, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 20, pp. 11270-11270
Open Access

Masks of Albinism: Clinical Spectrum of Hermansky–Pudlak Syndrome
Anastasia M. Bobreshova, Sofya Ionova, В. В. Кадышев, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 20, pp. 11260-11260
Open Access

A case of Hermansky-Pudlak with dyspnea
Ali Hossein Samadi Takaldani, Nima Javanshir, Maryam Salimi, et al.
Oxford Medical Case Reports (2023) Vol. 2023, Iss. 2
Open Access | Times Cited: 1

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