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:

A recurrent missense variant inSLC9A7causes nonsyndromic X-linked intellectual disability with alteration of Golgi acidification and aberrant glycosylation
Wujood Khayat, Anna Hackett, Marie Shaw, et al.
Human Molecular Genetics (2018) Vol. 28, Iss. 4, pp. 598-614
Open Access | Times Cited: 31

Showing 1-25 of 31 citing articles:

Congenital disorders of glycosylation
Irene J. Chang, Miao He, Christina Lam
Annals of Translational Medicine (2018) Vol. 6, Iss. 24, pp. 477-477
Open Access | Times Cited: 194
Aging activates escape of the silent X chromosome in the female mouse hippocampus
Margaret Gadek, Cayce K. Shaw, Samira Abdulai-Saiku, et al.
Science Advances (2025) Vol. 11, Iss. 10
Open Access | Times Cited: 8
Golgi pH, Ion and Redox Homeostasis: How Much Do They Really Matter?
Sakari Kellokumpu
Frontiers in Cell and Developmental Biology (2019) Vol. 7
Open Access | Times Cited: 119
Congenital disorders of glycosylation: Still “hot” in 2020
Nina Ondrušková, Anna Čechová, Hana Hansíková, et al.
Biochimica et Biophysica Acta (BBA) - General Subjects (2020) Vol. 1865, Iss. 1, pp. 129751-129751
Closed Access | Times Cited: 115
Determinants, maintenance, and function of organellar pH
Spencer A. Freeman, Sergio Grinstein, John Orlowski
Physiological Reviews (2022) Vol. 103, Iss. 1, pp. 515-606
Closed Access | Times Cited: 51
Role of the X Chromosome in Alzheimer Disease Genetics
Michaël E. Belloy, Yann Le Guen, Ilaria Stewart, et al.
JAMA Neurology (2024)
Closed Access | Times Cited: 11
Golgi Acidification by NHE7 Regulates Cytosolic pH Homeostasis in Pancreatic Cancer Cells
Koen M.O. Galenkamp, Paulina Sosicka, Michael Jung, et al.
Cancer Discovery (2020) Vol. 10, Iss. 6, pp. 822-835
Open Access | Times Cited: 45
Endocytic regulation of cellular ion homeostasis controls lysosome biogenesis
Tania López-Hernández, Dmytro Puchkov, Eberhard Krause, et al.
Nature Cell Biology (2020) Vol. 22, Iss. 7, pp. 815-827
Open Access | Times Cited: 45
Janus sword actions of chloroquine and hydroxychloroquine against COVID-19
Xuesong Chen, Jonathan D. Geiger
Cellular Signalling (2020) Vol. 73, pp. 109706-109706
Open Access | Times Cited: 45
Roles of Endomembrane Alkali Cation/Proton Exchangers in Synaptic Function and Neurodevelopmental Disorders
Andy Gao, Etienne Lourdin-De Filippis, John Orlowski, et al.
Frontiers in Physiology (2022) Vol. 13
Open Access | Times Cited: 22
Altered distribution and localization of organellar Na+/H+ exchangers in postmortem schizophrenia dorsolateral prefrontal cortex
Brandon S. Pruett, Anita Pinner, Pitna Kim, et al.
Translational Psychiatry (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 10
Non‐syndromic X linked intellectual disability: Current knowledge in light of the recent advances in molecular and functional studies
María‐Isabel Tejada, Nekane Ibarluzea
Clinical Genetics (2020) Vol. 97, Iss. 5, pp. 677-687
Closed Access | Times Cited: 26
ATP6V0C variants impair V-ATPase function causing a neurodevelopmental disorder often associated with epilepsy
Kari A. Mattison, Gilles Tossing, Fred Mulroe, et al.
Brain (2022) Vol. 146, Iss. 4, pp. 1357-1372
Open Access | Times Cited: 16
X‐Linked intellectual disability update 2022
Charles E. Schwartz, Raymond J. Louie, Annick Toutain, et al.
American Journal of Medical Genetics Part A (2022) Vol. 191, Iss. 1, pp. 144-159
Closed Access | Times Cited: 16
A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction
Bobby Ng, Paulina Sosicka, François Fenaille, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 6, pp. 1040-1052
Open Access | Times Cited: 14
A new pH sensor localized in the Golgi apparatus of Saccharomyces cerevisiae reveals unexpected roles of Vph1p and Stv1p isoforms
Antoine Deschamps, Anne-Sophie Colinet, Olga Zimmermannová, et al.
Scientific Reports (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 14
Expanding the phenotype of X‐linked SSR4–CDG: Connective tissue implications
Claudia Castiglioni, François Feillet, Christine Barnérias, et al.
Human Mutation (2020) Vol. 42, Iss. 2, pp. 142-149
Open Access | Times Cited: 13
Monoallelic loss-of-function BMP2 variants result in BMP2-related skeletal dysplasia spectrum
Jessica Priestley, Ashish R. Deshwar, Harsha Murthy, et al.
Genetics in Medicine (2023) Vol. 25, Iss. 8, pp. 100863-100863
Open Access | Times Cited: 4
The Golgi as a “Proton Sink” in Cancer
Koen M.O. Galenkamp, Cosimo Commisso
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 10
Golgi pH and Ion Homeostasis in Health and Disease
Elham Khosrowabadi, Sakari Kellokumpu
Reviews of physiology, biochemistry and pharmacology (2020), pp. 1-23
Closed Access | Times Cited: 10
Are the Clinical Presentations (Phenotypes) of Gitelman’s and Bartter’s Syndromes Gene Mutations Driven by Their Effects on Intracellular pH, Their “pH” Enotype?
Lorenzo A. Calò, Paul A. Davis
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 16, pp. 5660-5660
Open Access | Times Cited: 8
De novo variants in GATAD2A in individuals with a neurodevelopmental disorder: GATAD2A-related neurodevelopmental disorder
Elizabeth A. Werren, Alba Guxholli, Natasha Jones, et al.
Human Genetics and Genomics Advances (2023) Vol. 4, Iss. 3, pp. 100198-100198
Open Access | Times Cited: 2
RNA sequencing reveals deep intronic CEP120 variant: A report of the diagnostic odyssey for two siblings with Joubert syndrome type 31
Aren E. Marshall, Gabrielle Lemire, Yijing Liang, et al.
American Journal of Medical Genetics Part A (2023) Vol. 194, Iss. 4
Closed Access | Times Cited: 2
Congenital disorders of N-linked Glycosylation
Marc C. Patterson
Elsevier eBooks (2024), pp. 827-846
Closed Access
Characterization of Freshly Isolated Human Peripheral Blood B Cells, Monocytes, CD4+ and CD8+ T Cells, and Skin Mast Cells by Quantitative Transcriptomics
Srinivas Akula, Perla Abigail Alvarado‐Vázquez, Erika Haide Mendez Enriquez, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 23, pp. 13050-13050
Open Access
Page 1 - Next Page

Scroll to top