André Mattman

3.2k total citations
80 papers, 1.9k citations indexed

About

André Mattman is a scholar working on Rheumatology, Surgery and Epidemiology. According to data from OpenAlex, André Mattman has authored 80 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Rheumatology, 15 papers in Surgery and 15 papers in Epidemiology. Recurrent topics in André Mattman's work include IgG4-Related and Inflammatory Diseases (13 papers), Neuroendocrine Tumor Research Advances (11 papers) and Metabolism and Genetic Disorders (10 papers). André Mattman is often cited by papers focused on IgG4-Related and Inflammatory Diseases (13 papers), Neuroendocrine Tumor Research Advances (11 papers) and Metabolism and Genetic Disorders (10 papers). André Mattman collaborates with scholars based in Canada, United States and Australia. André Mattman's co-authors include Luke Y. C. Chen, Mollie N. Carruthers, Scott A. Venners, Glenys M. Webster, Michael A. Seidman, Kristen C. Hoffbuhr, Scot C. Leary, Nancy G. Kennaway, Eric A. Shoubridge and Hana Antonická and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Scientific Reports.

In The Last Decade

André Mattman

77 papers receiving 1.8k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
André Mattman Canada 21 406 319 284 263 247 80 1.9k
Patrizia Pignatti Italy 30 400 1.0× 247 0.8× 389 1.4× 492 1.9× 216 0.9× 112 2.5k
Peter Taylor United Kingdom 28 600 1.5× 171 0.5× 52 0.2× 219 0.8× 420 1.7× 124 4.2k
Michel Fischbach France 34 437 1.1× 127 0.4× 392 1.4× 484 1.8× 182 0.7× 181 3.4k
Xiaolin Fan United States 16 246 0.6× 201 0.6× 366 1.3× 198 0.8× 113 0.5× 46 1.5k
Riccardo Masetti Italy 34 1.3k 3.3× 95 0.3× 1.2k 4.4× 281 1.1× 282 1.1× 147 3.2k
Anders Christensson Sweden 29 702 1.7× 650 2.0× 318 1.1× 147 0.6× 321 1.3× 104 5.0k
Mary R. Cahill Ireland 23 408 1.0× 125 0.4× 421 1.5× 157 0.6× 164 0.7× 84 1.6k
Yang Sun China 31 777 1.9× 121 0.4× 31 0.1× 133 0.5× 203 0.8× 138 2.7k
Yoshihide Fujigaki Japan 28 1.0k 2.5× 202 0.6× 121 0.4× 262 1.0× 217 0.9× 166 2.9k
Richard Lafayette United States 33 910 2.2× 331 1.0× 536 1.9× 538 2.0× 352 1.4× 156 4.5k

Countries citing papers authored by André Mattman

Since Specialization
Citations

This map shows the geographic impact of André Mattman'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 André Mattman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites André Mattman more than expected).

Fields of papers citing papers by André Mattman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by André Mattman. 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 André Mattman. The network helps show where André Mattman may publish in the future.

Co-authorship network of co-authors of André Mattman

This figure shows the co-authorship network connecting the top 25 collaborators of André Mattman. A scholar is included among the top collaborators of André Mattman 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 André Mattman. André Mattman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
McNicholas, Kathleen W., Lisa K. Peterson, Lusia Sepiashvili, et al.. (2025). Ferritin, C‐Reactive Protein, and Soluble CD25 Distinguish TAFRO From HLH. American Journal of Hematology. 100(12). 2421–2425. 1 indexed citations
2.
Mattman, André, Anthony K.-C. So, Howard J. Lim, et al.. (2025). Elevated CA19-9 in IgG4-related disease. Annals of Clinical Biochemistry International Journal of Laboratory Medicine. 63(2). 132–140.
3.
Ipsiroglu, O., Stefan Clemens, Alexander Mark Weber, et al.. (2024). Iron Deficiency and Sleep/Wake Behaviors: A Scoping Review of Clinical Practice Guidelines—How to Overcome the Current Conundrum?. Nutrients. 16(15). 2559–2559. 3 indexed citations
4.
Stukas, Sophie, Adi Zoref‐Lorenz, Kam Shojania, et al.. (2024). The role of C-reactive protein and ferritin in the diagnosis of HLH, adult-onset still’s disease, and COVID-19 cytokine storm. Scientific Reports. 14(1). 31306–31306. 7 indexed citations
5.
Wade, John, J. Antonio Aviña‐Zubieta, Audi Setiadi, et al.. (2024). CRP and sCD25 help distinguish between adult‐onset Still's disease and HLH. European Journal Of Haematology. 113(5). 576–583. 6 indexed citations
6.
Lee, Hyun, André Mattman, Zsuzsanna Hollander, et al.. (2022). The impact of IgG subclass deficiency on the risk of mortality in hospitalized patients with COPD. Respiratory Research. 23(1). 141–141. 7 indexed citations
7.
Estey, Mathew P., Tanya N. Nelson, Michelle Parker, et al.. (2021). Is the diagnostic rate for the common subtypes of A1AT deficiency consistent across two Canadian Provinces?. Clinical Biochemistry. 95. 84–88. 1 indexed citations
8.
Fung, Angela W.S., et al.. (2020). Clinical utility of serum IgG4 measurement. Clinica Chimica Acta. 506. 228–235. 15 indexed citations
9.
Tam, Andrea, Beheroze Sattha, Ian R. Mackenzie, et al.. (2018). A mitochondrial DNA D loop insertion detected almost exclusively in non-replicating tissues with maternal inheritance across three generations. Mitochondrion. 46. 298–301. 1 indexed citations
10.
Filho, Fernando Sergio Leitão, Seung Won, André Mattman, et al.. (2017). Serum IgG and risk of exacerbations and hospitalizations in chronic obstructive pulmonary disease. Journal of Allergy and Clinical Immunology. 140(4). 1164–1167.e6. 24 indexed citations
11.
Balasubramaniam, Shanti, Brandon Lewis, D M Mock, et al.. (2016). Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD). JIMD Reports. 33. 99–107. 16 indexed citations
12.
Leung, Janice M., Joseph C. Liu, Silvia Guillemi, et al.. (2014). The Determinants of Poor Respiratory Health Status in Adults Living with Human Immunodeficiency Virus Infection. AIDS Patient Care and STDs. 28(5). 240–247. 19 indexed citations
13.
Al‐Sarraf, Ahmad, et al.. (2012). Use of once-weekly statin in combination with ezetimibe in a patient with mitochondrial disease: Table 1. BMJ Case Reports. 2012. bcr1220115369–bcr1220115369. 2 indexed citations
14.
Lehman, Anna, André Mattman, Don D. Sin, et al.. (2012). Emphysema in an adult with galactosialidosis linked to a defect in primary elastic fiber assembly. Molecular Genetics and Metabolism. 106(1). 99–103. 15 indexed citations
15.
Yoshimitsu, Makoto, Koji Higuchi, Masaaki Miyata, et al.. (2011). Identification of novel mutations in the α-galactosidase A gene in patients with Fabry disease: Pitfalls of mutation analyses in patients with low α-galactosidase A activity. Journal of Cardiology. 57(3). 345–353. 15 indexed citations
16.
Kobelka, Christine, André Mattman, & Sylvie Langlois. (2009). An evaluation of the decision‐making process regarding amniocentesis following a screen‐positive maternal serum screen result. Prenatal Diagnosis. 29(5). 514–519. 22 indexed citations
17.
Langlois, Sylvie, et al.. (2009). Steroid sulfatase deficiency and contiguous gene deletion syndrome amongst pregnant patients with low serum unconjugated estriols. Prenatal Diagnosis. 29(10). 966–974. 18 indexed citations
18.
Brodkin, Elizabeth, et al.. (2006). Lead and mercury exposures: interpretation and action. Canadian Medical Association Journal. 176(1). 59–63. 95 indexed citations
19.
Waters, Paula J., Minesh Khashu, Yolanda Lillquist, et al.. (2005). Neonatal hyperphenylalaninemia, perinatal hemochromatosis, and renal tubulopathy: A unique patient or a novel metabolic disorder?. Molecular Genetics and Metabolism. 86. 148–152. 4 indexed citations
20.
Antonická, Hana, André Mattman, D. Moira Glerum, et al.. (2003). Mutations in COX15 Produce a Defect in the Mitochondrial Heme Biosynthetic Pathway, Causing Early-Onset Fatal Hypertrophic Cardiomyopathy. The American Journal of Human Genetics. 72(1). 101–114. 237 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Patrizia Pignatti Breakdown of academic impact, for papers by Peter Taylor Breakdown of academic impact, for papers by Michel Fischbach Breakdown of academic impact, for papers by Xiaolin Fan Breakdown of academic impact, for papers by Riccardo Masetti Breakdown of academic impact, for papers by Anders Christensson Breakdown of academic impact, for papers by Mary R. Cahill Breakdown of academic impact, for papers by Yang Sun Breakdown of academic impact, for papers by Yoshihide Fujigaki Breakdown of academic impact, for papers by Richard Lafayette
Rankless by CCL
2026