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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.

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Showing 12 citing articles:

Mass Spectrometry as a First-Line Diagnostic Aid for Congenital Disorders of Glycosylation
Yoshinao Wada
Mass Spectrometry (2025) Vol. 14, Iss. 1, pp. A0169-A0169
Open Access | Times Cited: 1
Analysis of carbohydrates and glycoconjugates by matrix‐assisted laser desorption/ionization mass spectrometry: An update for 2019–2020
David J. Harvey
Mass Spectrometry Reviews (2022) Vol. 42, Iss. 5, pp. 1984-2206
Open Access | Times Cited: 24
Treatment Options in Congenital Disorders of Glycosylation
Julien H. Park, Thorsten Marquardt
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 25
Clinical and Molecular Features of Patients With Congenital Disorders of Glycosylation in Japan
Nobuhiko Okamoto, Machiko Kadoya, Yoshinao Wada
JIMD Reports (2025) Vol. 66, Iss. 3
Open Access
Targeted metabolomic evaluation of peripheral blood mononucleated cells from patients with PMM2-CDG
Renata Mangione, Lara Cirnigliaro, Miriam Wissam Saab, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
Genetic counseling for congenital disorders of glycosylation (CDG)
Tara Weixel, Lynne A. Wolfe, Ellen F. Macnamara
Journal of Genetic Counseling (2024) Vol. 33, Iss. 6, pp. 1358-1364
Open Access | Times Cited: 2
Normal transferrin glycosylation does not rule out severe ALG1 deficiency
Inez Bosnyák, Mustafa Sadek, Wasantha Ranatunga, et al.
JIMD Reports (2024) Vol. 65, Iss. 3, pp. 135-143
Open Access | Times Cited: 1
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
Siblings with MAN1B1-CDG Showing Novel Biochemical Profiles
Nobuhiko Okamoto, Tatsuyuki Ohto, Takashi Enokizono, et al.
Cells (2021) Vol. 10, Iss. 11, pp. 3117-3117
Open Access | Times Cited: 8
Apolipoprotein C‐III O‐glycoform profiling of 500 serum samples by matrix‐assisted laser desorption/ionization mass spectrometry for diagnosis of congenital disorders of glycosylation
Yoshinao Wada, Nobuhiko Okamoto
Journal of Mass Spectrometry (2020) Vol. 56, Iss. 4
Closed Access | Times Cited: 8
Novel ALG12 variants and hydronephrosis in siblings with impaired N-glycosylation
Takuya Hiraide, Yoshinao Wada, Tomoko Matsubayashi, et al.
Brain and Development (2021) Vol. 43, Iss. 9, pp. 945-951
Open Access | Times Cited: 5
A case of ALG11-congenital disorders of glycosylation diagnosed by post-mortem whole exome sequencing
Yuto Arai, Tohru Okanishi, Sotaro Kanai, et al.
Brain and Development (2022) Vol. 44, Iss. 10, pp. 732-736
Open Access | Times Cited: 2
Wrodzone zaburzenia glikozylacji białek – stale powiększająca się grupa chorób metabolicznych.
Anna Bogdańska, Anna Tylki‐Szymańska
Postępy Biochemii (2020)
Open Access | Times Cited: 1
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