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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:

Mass spectrometry of transferrin glycoforms to detect congenital disorders of glycosylation: Site‐specific profiles and pitfalls
Yoshinao Wada
PROTEOMICS (2016) Vol. 16, Iss. 24, pp. 3105-3110
Closed Access | Times Cited: 21

Showing 21 citing articles:

Combined integrin αvβ3 and lactoferrin receptor targeted docetaxel liposomes enhance the brain targeting effect and anti-glioma effect
Na Qi, Shangqian Zhang, Xiantai Zhou, et al.
Journal of Nanobiotechnology (2021) Vol. 19, Iss. 1
Open Access | Times Cited: 41
Metabolomics to Improve the Diagnostic Efficiency of Inborn Errors of Metabolism
Dylan Mordaunt, David J. Cox, Maria Fuller
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 4, pp. 1195-1195
Open Access | Times Cited: 41
Exploring Charge-Detection Mass Spectrometry on Chromatographic Time Scales
Lisa Strasser, Florian Füssl, Tomos E. Morgan, et al.
Analytical Chemistry (2023) Vol. 95, Iss. 40, pp. 15118-15124
Open Access | Times Cited: 16
Comparing Selected-Ion Collision Induced Unfolding with All Ion Unfolding Methods for Comprehensive Protein Conformational Characterization
Ashley Phetsanthad, Gongyu Li, Chae Kyung Jeon, et al.
Journal of the American Society for Mass Spectrometry (2022) Vol. 33, Iss. 6, pp. 944-951
Open Access | Times Cited: 18
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
A novel progress of drug delivery system for organelle targeting in tumour cells
Zhijing He, Yanan Zhang, Abdur Rauf Khan, et al.
Journal of drug targeting (2020) Vol. 29, Iss. 1, pp. 12-28
Closed Access | Times Cited: 24
ANALYSIS OF CARBOHYDRATES AND GLYCOCONJUGATES BY MATRIX‐ASSISTED LASER DESORPTION/IONIZATION MASS SPECTROMETRY: AN UPDATE FOR 2015–2016
David J. Harvey
Mass Spectrometry Reviews (2021) Vol. 40, Iss. 4, pp. 408-565
Open Access | Times Cited: 23
“Guide” of muscone modification enhanced brain‐targeting efficacy and anti‐glioma effect of lactoferrin modified DTX liposomes
Na Qi, Wenjuan Duan, Duan Gao, et al.
Bioengineering & Translational Medicine (2022) Vol. 8, Iss. 2
Open Access | Times Cited: 14
Phosphotyrosine profiling of human cerebrospinal fluid
Gajanan Sathe, Chan Hyun Na, Santosh Renuse, et al.
Clinical Proteomics (2018) Vol. 15, Iss. 1
Open Access | Times Cited: 23
Glycosylation and Characterization of Human Transferrin in an End-Stage Kidney Disease
Goran Miljuš, Ana Penezić, Lucia Pažitná, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 9, pp. 4625-4625
Open Access | Times Cited: 2
Sensitivity of transferrin isoform analysis for PMM2-CDG
Patrica L Hall, Kris Liedke, Coleman Turgeon, et al.
Molecular Genetics and Metabolism (2024) Vol. 143, Iss. 1-2, pp. 108564-108564
Closed Access | Times Cited: 2
L-Fucose treatment of FUT8-CDG
Julien H. Park, Janine Reunert, Miao He, et al.
Molecular Genetics and Metabolism Reports (2020) Vol. 25, pp. 100680-100680
Open Access | Times Cited: 18
Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry to Detect Diagnostic Glycopeptide Markers of Congenital Disorders of Glycosylation
Yoshinao Wada
Mass Spectrometry (2020) Vol. 9, Iss. 1, pp. A0084-A0084
Open Access | Times Cited: 12
Quantitative Assessment of Core Fucosylation for Congenital Disorders of Glycosylation
Yoshinao Wada, Machiko Kadoya
Mass Spectrometry (2024) Vol. 13, Iss. 1, pp. A0159-A0159
Open Access | Times Cited: 1
Correlation between chronological and physiological age of males from their multivariate urinary endogenous steroid profile and prostatic carcinoma-induced deviation
Eleonora Amante, Eugenio Alladio, Alberto Salomone, et al.
Steroids (2018) Vol. 139, pp. 10-17
Open Access | Times Cited: 9
Primary ovarian insufficiency in a female with phosphomannomutase-2 gene (<i>PMM2</i>) mutations for congenital disorder of glycosylation
Yohei Masunaga, M. Mochizuki, Machiko Kadoya, et al.
Endocrine Journal (2021) Vol. 68, Iss. 5, pp. 605-611
Open Access | Times Cited: 8
Electrospray Ionization Mass Spectrometry of Transferrin: Use of Quadrupole Mass Analyzers for Congenital Disorders of Glycosylation
Yoshinao Wada, Nobuhiko Okamoto
Mass Spectrometry (2022) Vol. 11, Iss. 1, pp. A0103-A0103
Open Access | Times Cited: 6
Diagnostic Potential of Transferrin Glycoforms—A Lectin‐Based Protein Microarray Approach
Ana Penezić, Martina Križáková, Goran Miljuš, et al.
PROTEOMICS - CLINICAL APPLICATIONS (2019) Vol. 13, Iss. 5
Closed Access | Times Cited: 7
High‐resolution capillary zone electrophoresis and mass spectrometry for distinction of undersialylated and hypoglycosylated transferrin glycoforms in body fluids
Jitka Caslavska, Christof Schild, Wolfgang Thormann
Journal of Separation Science (2019) Vol. 43, Iss. 1, pp. 241-257
Closed Access | Times Cited: 7
High‐resolution capillary zone electrophoresis for transferrin glycoform analysis associated with congenital disorders of glycosylation
Micha Tobler, Jitka Caslavska, Patricie Burda, et al.
Journal of Separation Science (2018) Vol. 41, Iss. 13, pp. 2808-2818
Open Access | Times Cited: 4
Abordagem diagnóstica de crianças com atraso do desenvolvimento e deficiência intelectual
Raquel Boy
Revista Hospital Universitário Pedro Ernesto (2016) Vol. 15, Iss. 2
Open Access
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