Aurélien Macé

3.3k citations
41 papers · 2.4k · 1 hit paper · h-index 23

Impact in

    • Tuberculosis Research and Epidemiology
    • SARS-CoV-2 detection and testing
  • Genetics top 2%
    • Genomic variations and chromosomal abnormalities
    • Genetic Associations and Epidemiology
    • Genetics and Neurodevelopmental Disorders
    • Genomics and Rare Diseases

Papers in

    • Tuberculosis Research and Epidemiology 11
    • SARS-CoV-2 detection and testing 6
    • Genomic variations and chromosomal abnormalities 11
    • Genetic Associations and Epidemiology 4

Aurélien Macé

38 papers receiving 2.3k citations

Aurélien Macé's Hit Papers

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders 2018 · 320 citations
3200+2+5Years since publication100200300

Peers

Aurélien Macé
Comparison fields: 5 of 106
  • Infectious Diseases 678
  • Genetics 979
  • Biological Psychiatry 27
  • Nephrology 73
  • Endocrine and Autonomic Systems 41
Replace Venu Pothula with:
Venu Pothula United States
Nayia Petousi United Kingdom
Melissa Garcia United States
Khoa Manh Dinh Denmark
Diana Carli Italy
Diego Real de Asúa Spain
Akinori Hoshika Japan
Ignacio Málaga Spain
Artika P. Nath Australia
Elena Andreucci Italy
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Citations per field
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Citations per year

Countries citing papers authored by Aurélien Macé

Since Specialization
Citations

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

Fields of papers citing papers by Aurélien Macé

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Aurélien Macé, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Aurélien Macé Line = papers co-authored together Aurélien Macé links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 41 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders
Hit paper breakdown →
2018320
2 2012240
3 2021203
4 2015190
5 2019176
6 2013155
7 2015149
8 202178
9 201575
10 201466
11 201766
12 202062
13 201960
14 201351
15 201851
16 202249
17 201545
18 201945
19 201339
20 201735

About Aurélien Macé

Aurélien Macé is a scholar working on Infectious Diseases, Genetics, Hepatology, Nephrology and Applied Microbiology and Biotechnology, having authored 41 papers that have together received 2.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Tuberculosis Research and Epidemiology (11 papers), SARS-CoV-2 detection and testing (6 papers), Genetic Associations and Epidemiology (4 papers), Sepsis Diagnosis and Treatment (2 papers), Hepatitis C virus research (2 papers), Electronic Health Records Systems (1 paper) and Magnesium in Health and Disease (1 paper). The work is most often cited by research in Infectious Diseases (678 citations), Genetics (979 citations), Biological Psychiatry (27 citations), Nephrology (73 citations) and Endocrine and Autonomic Systems (41 citations). Aurélien Macé has collaborated with scholars based in Switzerland, United States and Germany. Frequent co-authors include Claudia Maria Denkinger, Stefano Ongarello, Zoltán Kutalik, Armand Valsesia, Jilian A. Sacks, Sergio Carmona, Stephani Schmitz, Nira R. Pollock, Lukas E. Brümmer and Stephan Katzenschlager. Their work appears in journals such as PLoS Medicine, Nature Communications, BMJ Global Health, The American Journal of Human Genetics and PLoS Genetics.

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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