Patrick Aubourg

12.4k total citations · 1 hit paper
96 papers, 5.8k citations indexed

About

Patrick Aubourg is a scholar working on Molecular Biology, Physiology and Clinical Biochemistry. According to data from OpenAlex, Patrick Aubourg has authored 96 papers receiving a total of 5.8k indexed citations (citations by other indexed papers that have themselves been cited), including 85 papers in Molecular Biology, 37 papers in Physiology and 32 papers in Clinical Biochemistry. Recurrent topics in Patrick Aubourg's work include Peroxisome Proliferator-Activated Receptors (73 papers), Metabolism and Genetic Disorders (32 papers) and Adipose Tissue and Metabolism (25 papers). Patrick Aubourg is often cited by papers focused on Peroxisome Proliferator-Activated Receptors (73 papers), Metabolism and Genetic Disorders (32 papers) and Adipose Tissue and Metabolism (25 papers). Patrick Aubourg collaborates with scholars based in France, United States and Netherlands. Patrick Aubourg's 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 Anne‐Marie Douar and has published in prestigious journals such as Nature, New England Journal of Medicine and The Lancet.

In The Last Decade

Patrick Aubourg

94 papers receiving 5.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters

1993 924 citations Jean Mosser, Claude‐Olivier Sarde et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Patrick Aubourg France	44	4.7k	2.0k	1.7k	514	499	96	5.8k
Nobuyuki Shimozawa Japan	38	4.2k 0.9×	1.1k 0.5×	1.2k 0.7×	266 0.5×	163 0.3×	217	5.3k
Masaki Takiguchi Japan	35	2.0k 0.4×	444 0.2×	801 0.5×	539 1.0×	362 0.7×	100	3.9k
Nancy J. Philp United States	42	4.0k 0.9×	220 0.1×	640 0.4×	315 0.6×	629 1.3×	93	5.9k
Tarun B. Patel United States	36	2.2k 0.5×	325 0.2×	506 0.3×	256 0.5×	401 0.8×	97	3.3k
Guy Las United States	14	2.7k 0.6×	561 0.3×	886 0.5×	162 0.3×	62 0.1×	17	3.6k
Anu Jalanko Finland	35	2.1k 0.4×	282 0.1×	2.0k 1.2×	64 0.1×	85 0.2×	88	3.8k
Roshni R. Singaraja Canada	48	5.8k 1.2×	132 0.1×	522 0.3×	297 0.6×	1.4k 2.7×	81	8.4k
Florian Sennlaub France	45	2.5k 0.5×	198 0.1×	451 0.3×	157 0.3×	268 0.5×	127	6.1k
Manuel Rojo France	28	3.8k 0.8×	904 0.5×	677 0.4×	73 0.1×	100 0.2×	47	4.6k
Andrew L. Markhard United States	11	4.1k 0.9×	135 0.1×	707 0.4×	163 0.3×	316 0.6×	15	5.4k

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-authorship network of co-authors of Patrick Aubourg

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

All Works

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20 of 20 papers shown

Raymond, Gerald V., Patrick Aubourg, Asif Paker, et al.. (2018). Survival and Functional Outcomes in Boys with Cerebral Adrenoleukodystrophy with and without Hematopoietic Stem Cell Transplantation. Biology of Blood and Marrow Transplantation. 25(3). 538–548. 82 indexed citations

Ofman, Rob, Inge M. E. Dijkstra, Eveline Verheij, et al.. (2016). CYP4F2 affects phenotypic outcome in adrenoleukodystrophy by modulating the clearance of very long-chain fatty acids. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1862(10). 1861–1870. 15 indexed citations

Engelen, Marc, Stephan Kemp, Marjolein Visser, et al.. (2012). X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and management. Orphanet Journal of Rare Diseases. 7(1). 51–51. 350 indexed citations

Schlüter, Agatha, Lluı́s Espinosa, Stéphane Fourcade, et al.. (2011). Functional genomic analysis unravels a metabolic-inflammatory interplay in adrenoleukodystrophy. Human Molecular Genetics. 21(5). 1062–1077. 60 indexed citations

Matsukawa, Takashi, Muriel Asheuer, Yuji Takahashi, et al.. (2010). Identification of novel SNPs of ABCD1, ABCD2, ABCD3, and ABCD4 genes in patients with X-linked adrenoleukodystrophy (ALD) based on comprehensive resequencing and association studies with ALD phenotypes. Neurogenetics. 12(1). 41–50. 21 indexed citations

Cartier, Nathalie, Salima Hacein‐Bey‐Abina, Christof von Kalle, et al.. (2010). Thérapie génique de l’adrénoleucodystrophie liée à l’X par transfert du gène dans les cellules souches hématopoïétiques à l’aide d’un vecteur lentiviral. Bulletin de l Académie Nationale de Médecine. 194(2). 255–268. 16 indexed citations

Sabbagh, Audrey, Éric Pasmant, Ingrid Laurendeau, et al.. (2009). Unravelling the genetic basis of variable clinical expression in neurofibromatosis 1. Human Molecular Genetics. 18(15). 2768–2778. 97 indexed citations

Colle, Marie‐Anne, Françoise Piguet, Sylvie Raoul, et al.. (2009). Efficient intracerebral delivery of AAV5 vector encoding human ARSA in non-human primate. Human Molecular Genetics. 19(1). 147–158. 58 indexed citations

Sevin, Caroline, Patrick Aubourg, & Nathalie Cartier. (2007). Enzyme, cell and gene‐based therapies for metachromatic leukodystrophy. Journal of Inherited Metabolic Disease. 30(2). 175–183. 57 indexed citations

10.

Sedel, F., Ayman Tourbah, Nicole Baumann, et al.. (2005). Leucoencéphalopathies génétiques de l’adulte. Revue Neurologique. 161(10). 916–931. 6 indexed citations

11.

Guimarães, Carla P., Pedro Domíngues, Patrick Aubourg, et al.. (2004). Mouse liver PMP70 and ALDP: homomeric interactions prevail in vivo. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1689(3). 235–243. 45 indexed citations

12.

Shapiro, Elsa, William Krivit, Lawrence A. Lockman, et al.. (2000). Long-term effect of bone-marrow transplantation for childhood-onset cerebral X-linked adrenoleukodystrophy. The Lancet. 356(9231). 713–718. 206 indexed citations

13.

Lannuzel, Annie, Patrick Aubourg, & Marc Tardieu. (1998). Excessive production of tumour necrosis factor α by peripheral blood mononuclear cells in X-linked adrenoleukodystrophy. European Journal of Paediatric Neurology. 2(1). 27–32. 16 indexed citations

14.

Troffer-Charlier, N., et al.. (1998). Mirror expression of adrenoleukodystrophy and adrenoleukodystrophy related genes in mouse tissues and human cell lines. European Journal of Cell Biology. 75(3). 254–264. 71 indexed citations

15.

Douar, Anne, Jean Mosser, Claude‐Olivier Sarde, et al.. (1994). X-linked adrenoleukodystrophy gene: identification of a candidate gene by positional cloning. Biomedicine & Pharmacotherapy. 48(5-6). 215–218. 6 indexed citations

16.

Fanen, Pascale, et al.. (1994). Identification of mutations in the putative ATP-binding domain of the adrenoleukodystrophy gene.. Journal of Clinical Investigation. 94(2). 516–520. 56 indexed citations

17.

Sarde, Claude‐Olivier, Jean Mosser, Petra Kioschis, et al.. (1994). Genomic Organization of the Adrenoleukodystrophy Gene. Genomics. 22(1). 13–20. 65 indexed citations

18.

Aubourg, Patrick, C. Adamsbaum, F. Rocchiccioli, et al.. (1993). A Two-Year Trial of Oleic and Erucic Acids (“Lorenzo's Oil”) as Treatment for Adrenomyeloneuropathy. New England Journal of Medicine. 329(11). 745–752. 166 indexed citations

19.

Aubourg, Patrick, et al.. (1986). Neonatal adrenoleukodystrophy.. Journal of Neurology Neurosurgery & Psychiatry. 49(1). 77–86. 46 indexed citations

20.

Roels, Frank, Bwee Tien Poll‐The, Patrick Aubourg, et al.. (1986). Cytochemistry of hepatic peroxisomes/their absence in Infantile Refsum's Disease (IRD) and their presence in Neonatal Adrenoleukodystrophy (NALD). European Journal of Cell Biology. 41. 1 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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