Maciej Adamowicz

1.6k total citations
14 papers, 471 citations indexed

About

Maciej Adamowicz is a scholar working on Molecular Biology, Organic Chemistry and Physiology. According to data from OpenAlex, Maciej Adamowicz has authored 14 papers receiving a total of 471 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 4 papers in Organic Chemistry and 4 papers in Physiology. Recurrent topics in Maciej Adamowicz's work include Glycosylation and Glycoproteins Research (11 papers), Carbohydrate Chemistry and Synthesis (4 papers) and Galectins and Cancer Biology (3 papers). Maciej Adamowicz is often cited by papers focused on Glycosylation and Glycoproteins Research (11 papers), Carbohydrate Chemistry and Synthesis (4 papers) and Galectins and Cancer Biology (3 papers). Maciej Adamowicz collaborates with scholars based in Poland, Netherlands and Germany. Maciej Adamowicz's co-authors include Ron A. Wevers, Dirk J. Lefeber, Éva Morava, Ewa Pronicka, Jolanta Sykut‐Cegielska, Jaak Jaeken, Christian Körner, Karin Huijben, Emile Van Schaftingen and Maïlys Guillard and has published in prestigious journals such as PEDIATRICS, Human Molecular Genetics and Clinical Chemistry.

In The Last Decade

Maciej Adamowicz

14 papers receiving 464 citations

Peers

Maciej Adamowicz
Marianne Grüneberg Germany
Nina Ondrušková Czechia
Christina Lam United States
Julien H. Park Germany
M. Girós Spain
Gülden Gökçay Türkiye
Maud Chasseraud France
Kiyoto Sakata Japan
Vicki L. Nebes United States
Cynthia L. Toth United States
Marianne Grüneberg Germany
Maciej Adamowicz
Citations per year, relative to Maciej Adamowicz Maciej Adamowicz (= 1×) peers Marianne Grüneberg

Countries citing papers authored by Maciej Adamowicz

Since Specialization
Citations

This map shows the geographic impact of Maciej Adamowicz's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Maciej Adamowicz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Maciej Adamowicz more than expected).

Fields of papers citing papers by Maciej Adamowicz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maciej Adamowicz. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Maciej Adamowicz. The network helps show where Maciej Adamowicz may publish in the future.

Co-authorship network of co-authors of Maciej Adamowicz

This figure shows the co-authorship network connecting the top 25 collaborators of Maciej Adamowicz. A scholar is included among the top collaborators of Maciej Adamowicz based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Maciej Adamowicz. Maciej Adamowicz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

14 of 14 papers shown
1.
Socha, Piotr, Pietro Vajro, Dirk J. Lefeber, Maciej Adamowicz, & Stuart Tanner. (2014). Search for rare liver diseases: The case of glycosylation defects mimicking Wilson Disease ->. Clinics and Research in Hepatology and Gastroenterology. 38(4). 403–406. 8 indexed citations
2.
Funke, Simone, Thatjana Gardeitchik, Saskia B. Wortmann, et al.. (2013). Perinatal and early infantile symptoms in congenital disorders of glycosylation. American Journal of Medical Genetics Part A. 161(3). 578–584. 30 indexed citations
3.
Timal, Sharita, Alexander Hoischen, Ludwig Lehle, et al.. (2012). Gene identification in the congenital disorders of glycosylation type I by whole-exome sequencing. Human Molecular Genetics. 21(19). 4151–4161. 122 indexed citations
4.
Morava, Éva, Julia Vodopiutz, Dirk J. Lefeber, et al.. (2012). Defining the Phenotype in Congenital Disorder of Glycosylation Due to ALG1 Mutations. PEDIATRICS. 130(4). e1034–e1039. 26 indexed citations
5.
Guillard, Maïlys, Éva Morava, Floris L. van Delft, et al.. (2011). Plasma N-Glycan Profiling by Mass Spectrometry for Congenital Disorders of Glycosylation Type II. Clinical Chemistry. 57(4). 593–602. 49 indexed citations
6.
Jamroz, Ewa, Dariusz Adamek, Justyna Paprocka, et al.. (2009). CDG Type Ia and Congenital Cytomegalovirus Infection: Two Coexisting Conditions. Journal of Child Neurology. 24(1). 13–18. 4 indexed citations
7.
Guillard, Maïlys, Dirk J. Lefeber, Jolanta Sykut‐Cegielska, et al.. (2008). Pericardial and abdominal fluid accumulation in Congenital Disorder of Glycosylation type Ia. Molecular Genetics and Metabolism. 94(4). 481–484. 39 indexed citations
8.
Sturiale, Luisa, Rita Barone, Angelo Palmigiano, et al.. (2008). Multiplexed glycoproteomic analysis of glycosylation disorders by sequential yolk immunoglobulins immunoseparation and MALDI‐TOF MS. PROTEOMICS. 8(18). 3822–3832. 40 indexed citations
9.
Schollen, Els, Liesbeth Keldermans, François Foulquier, et al.. (2007). Characterization of two unusual truncating PMM2 mutations in two CDG-Ia patients. Molecular Genetics and Metabolism. 90(4). 408–413. 34 indexed citations
10.
11.
Wopereis, Suzan, Éva Morava, Stephanie Grünewald, et al.. (2005). Patients with unsolved congenital disorders of glycosylation type II can be subdivided in six distinct biochemical groups. Glycobiology. 15(12). 1312–1319. 23 indexed citations
12.
13.
Jaeken, Jaak, Michel Pirard, Maciej Adamowicz, Ewa Pronicka, & Emile Van Schaftingen. (1996). Inhibition of Phosphomannose Isomerase by Fructose 1-Phosphate: An Explanation for Defective N-Glycosylation in Hereditary Fructose Intolerance. Pediatric Research. 40(5). 764–766. 52 indexed citations
14.
Adamowicz, Maciej & Ewa Pronicka. (1996). Carbohydrate deficient glycoprotein syndrome – like transferrin isoelectric focusing pattern in untreated fructosaemia. European Journal of Pediatrics. 155(4). 347–347. 2 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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