Patrick Aubourg

12.5k citations
99 papers · 6.3k · 1 hit paper · h-index 45

Impact in

    • Metabolism and Genetic Disorders
  • Physiology top 0.5%
    • Adipose Tissue and Metabolism
    • Adenosine and Purinergic Signaling
    • Lysosomal Storage Disorders Research

Papers in

    • Peroxisome Proliferator-Activated Receptors 75
    • RNA regulation and disease 14
    • Adipose Tissue and Metabolism 24
    • Adenosine and Purinergic Signaling 11
    • Nitric Oxide and Endothelin Effects 5

Patrick Aubourg

98 papers receiving 6.0k citations

Patrick Aubourg's Hit Papers

Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters 1993 · 995 citations
9950+11+22Years since publication250500750

Peers

Patrick Aubourg
Comparison fields: 5 of 114
  • Clinical Biochemistry 1.9k
  • Physiology 344
  • Molecular Biology 5.0k
  • Physiology 1.6k
  • Biochemistry 488
Replace Nobuyuki Shimozawa with:
Nobuyuki Shimozawa Japan
H. W. Moser United States
Masaki Takiguchi Japan
Manuel Rojo France
Nancy J. Philp United States
Anu Jalanko Finland
Rodolfo Zunino Canada
Florian Sennlaub France
Andrew L. Markhard United States
Toya Ohashi Japan
Patrick Aubourg relative to Nobuyuki Shimozawa Japan Nobuyuki Shimozawa's profile →
Citations per field
00.5×3.8×
Nobuyuki Shimozawa · 1×
Citations per year

Countries citing papers authored by Patrick Aubourg

Since Specialization
Citations

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

Fields of papers citing papers by Patrick Aubourg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Patrick Aubourg, 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 Patrick Aubourg Line = papers co-authored together Patrick Aubourg links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 99 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters
Hit paper breakdown →
1993995
2 2012379
3 1990282
4 2004278
5 2000233
6 1994223
7 2012206
8 1993179
9 1999121
10 2010112
11 2009109
12 2010108
13 1990104
14 199799
15 201888
16 198687
17
Mutational and protein analysis of patients and heterozygous women with X-linked adrenoleukodystrophy.
199687
18 201286
19 201286
20 198776

About Patrick Aubourg

Patrick Aubourg is a scholar working on Molecular Biology, Physiology, Clinical Biochemistry, Physiology and Biochemistry, having authored 99 papers that have together received 6.3k indexed citations. Recurring topics across this work include Peroxisome Proliferator-Activated Receptors (75 papers), Metabolism and Genetic Disorders (32 papers), Adipose Tissue and Metabolism (24 papers), RNA regulation and disease (14 papers), Adenosine and Purinergic Signaling (11 papers), Eicosanoids and Hypertension Pharmacology (9 papers), Virus-based gene therapy research (7 papers) and Nitric Oxide and Endothelin Effects (5 papers). The work is most often cited by research in Clinical Biochemistry (1.9k citations), Physiology (344 citations), Molecular Biology (5.0k citations), Physiology (1.6k citations) and Biochemistry (488 citations). Patrick Aubourg has collaborated with scholars based in France, United States and Netherlands. Frequent co-authors include Jean‐Louis Mandel, Jean Mosser, Nathalie Cartier, Claude‐Olivier Sarde, Hugo W. Moser, Robert Feil, Stephan Kemp, Petra Kioschis, Annemarie Poustka and Ronald J. A. Wanders. Their work appears in journals such as Human Molecular Genetics, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, FEBS Letters, Journal of Inherited Metabolic Disease and Biochemical and Biophysical Research Communications.

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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