Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Mutations in the Gardos channel (KCNN4) are associated with hereditary xerocytosis
Edyta Glogowska, Kimberly Lezon-Geyda, Yelena Maksimova, et al.
Blood (2015) Vol. 126, Iss. 11, pp. 1281-1284
Open Access | Times Cited: 104

Showing 1-25 of 104 citing articles:

Squeezing for Life – Properties of Red Blood Cell Deformability
Rick Huisjes, Anna Bogdanova, Wouter W. van Solinge, et al.
Frontiers in Physiology (2018) Vol. 9
Open Access | Times Cited: 279
New insights on hereditary erythrocyte membrane defects
Immacolata Andolfo, Roberta Russo, Antonella Gambale, et al.
Haematologica (2016) Vol. 101, Iss. 11, pp. 1284-1294
Open Access | Times Cited: 174
Activation mechanism of a human SK-calmodulin channel complex elucidated by cryo-EM structures
Chia‐Hsueh Lee, Roderick MacKinnon
Science (2018) Vol. 360, Iss. 6388, pp. 508-513
Open Access | Times Cited: 162
Red Blood Cells: Chasing Interactions
Virginia Pretini, Mischa H. Koenen, Lars Kaestner, et al.
Frontiers in Physiology (2019) Vol. 10
Open Access | Times Cited: 146
Red cell membrane disorders
Jyothsna Narla, Narla Mohandas
International Journal of Laboratory Hematology (2017) Vol. 39, Iss. S1, pp. 47-52
Open Access | Times Cited: 139
Genetic Diseases of PIEZO1 and PIEZO2 Dysfunction
Seth L. Alper
Current topics in membranes (2017), pp. 97-134
Closed Access | Times Cited: 124
Novel mechanisms of PIEZO1 dysfunction in hereditary xerocytosis
Edyta Glogowska, Eve R. Schneider, Yelena Maksimova, et al.
Blood (2017) Vol. 130, Iss. 16, pp. 1845-1856
Open Access | Times Cited: 117
Disorders of erythrocyte hydration
Patrick G. Gallagher
Blood (2017) Vol. 130, Iss. 25, pp. 2699-2708
Open Access | Times Cited: 107
Red Blood Cell Passage of Small Capillaries Is Associated with Transient Ca2+-mediated Adaptations
Jens Danielczok, Emmanuel Terriac, Laura Hertz, et al.
Frontiers in Physiology (2017) Vol. 8
Open Access | Times Cited: 105
Clinical and biological features in PIEZO1-hereditary xerocytosis and Gardos channelopathy: a retrospective series of 126 patients
Véronique Picard, Corinne Guitton, Isabelle Thuret, et al.
Haematologica (2019) Vol. 104, Iss. 8, pp. 1554-1564
Open Access | Times Cited: 89
Pharmacology of Small- and Intermediate-Conductance Calcium-Activated Potassium Channels
Brandon M. Brown, Heesung Shim, Palle Christophersen, et al.
The Annual Review of Pharmacology and Toxicology (2019) Vol. 60, Iss. 1, pp. 219-240
Open Access | Times Cited: 88
Advances in understanding the pathogenesis of red cell membrane disorders
Achille Iolascon, Immacolata Andolfo, Roberta Russo
British Journal of Haematology (2019) Vol. 187, Iss. 1, pp. 13-24
Open Access | Times Cited: 81
Red cell membrane disorders: structure meets function
Mary Risinger, Theodosia A. Kalfa
Blood (2020) Vol. 136, Iss. 11, pp. 1250-1261
Open Access | Times Cited: 76
Ca2+-Sensitive Potassium Channels
Razan Orfali, Nora Al-Banyan
Molecules (2023) Vol. 28, Iss. 2, pp. 885-885
Open Access | Times Cited: 22
‘Gardos Channelopathy’: a variant of hereditary Stomatocytosis with complex molecular regulation
Elisa Fermo, Anna Bogdanova, Polina Petkova‐Kirova, et al.
Scientific Reports (2017) Vol. 7, Iss. 1
Open Access | Times Cited: 76
Osmotic gradient ektacytometry: A valuable screening test for hereditary spherocytosis and other red blood cell membrane disorders
Esther Llaudet‐Planas, Joan‐Lluis Vives Corrons, Valeria Rizzuto, et al.
International Journal of Laboratory Hematology (2017) Vol. 40, Iss. 1, pp. 94-102
Open Access | Times Cited: 72
Hereditary stomatocytosis: An underdiagnosed condition
Immacolata Andolfo, Roberta Russo, Antonella Gambale, et al.
American Journal of Hematology (2017) Vol. 93, Iss. 1, pp. 107-121
Open Access | Times Cited: 62
Calcium Channels and Calcium-Regulated Channels in Human Red Blood Cells
Lars Kaestner, Anna Bogdanova, Stéphane Égée
Advances in experimental medicine and biology (2019), pp. 625-648
Closed Access | Times Cited: 59
Trends in Piezo Channel Research Over the Past Decade: A Bibliometric Analysis
Jing Guo, Dongmei Gu, Tingting Zhao, et al.
Frontiers in Pharmacology (2021) Vol. 12
Open Access | Times Cited: 47
Signaling mechanisms in red blood cells: A view through the protein phosphorylation and deformability
Neslihan Cilek, Elif Uğurel, Evrim Goksel, et al.
Journal of Cellular Physiology (2023) Vol. 239, Iss. 3
Closed Access | Times Cited: 20
The Gárdos Channel and Piezo1 Revisited: Comparison between Reticulocytes and Mature Red Blood Cells
Polina Petkova‐Kirova, Nicoletta Murciano, Giulia Iacono, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 3, pp. 1416-1416
Open Access | Times Cited: 6
Insight into GATA1 transcriptional activity through interrogation of cis elements disrupted in human erythroid disorders
Aoi Wakabayashi, Jacob C. Ulirsch, Leif S. Ludwig, et al.
Proceedings of the National Academy of Sciences (2016) Vol. 113, Iss. 16, pp. 4434-4439
Open Access | Times Cited: 60
Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca2+-Activated K+ Channel SK3 Cause Zimmermann-Laband Syndrome
Christiane K. Bauer, Pauline E. Schneeberger, Fanny Kortüm, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 6, pp. 1139-1157
Open Access | Times Cited: 51
Genotype-phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patients
Immacolata Andolfo, Roberta Russo, Barbara Eleni Rosato, et al.
American Journal of Hematology (2018) Vol. 93, Iss. 12, pp. 1509-1517
Open Access | Times Cited: 50
Molecular diagnostic update in hereditary hemolytic anemia and neonatal hyperbilirubinemia
Anton Rets, Adam L. Clayton, Robert D. Christensen, et al.
International Journal of Laboratory Hematology (2019) Vol. 41, Iss. S1, pp. 95-101
Closed Access | Times Cited: 45
Page 1 - Next Page

Scroll to top