A. Dürr

1.9k total citations · 1 hit paper
12 papers, 963 citations indexed

About

A. Dürr is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, A. Dürr has authored 12 papers receiving a total of 963 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Cellular and Molecular Neuroscience, 5 papers in Molecular Biology and 5 papers in Neurology. Recurrent topics in A. Dürr's work include Genetic Neurodegenerative Diseases (7 papers), Neurological diseases and metabolism (5 papers) and Mitochondrial Function and Pathology (5 papers). A. Dürr is often cited by papers focused on Genetic Neurodegenerative Diseases (7 papers), Neurological diseases and metabolism (5 papers) and Mitochondrial Function and Pathology (5 papers). A. Dürr collaborates with scholars based in France, Italy and United Kingdom. A. Dürr's co-authors include Patricio Fernández‐Silva, Alessandro Filla, Marina Mora, Sonia Ciarmatori, Massimo Zeviani, R. Marconi, Andrea Ballabio, Maurizio De Fusco, Giuseppe De Michele and Giorgio Casari and has published in prestigious journals such as Cell, Neurology and Human Molecular Genetics.

In The Last Decade

A. Dürr

12 papers receiving 942 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.

Spastic Paraplegia and OXPHOS Impairment Caused by Mutations in Paraplegin, a Nuclear-Encoded Mitochondrial Metalloprotease

1998 586 citations Giorgio Casari, Maurizio De Fusco et al. Cell profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A. Dürr France	9	600	580	274	273	134	12	963
Hamid Azzedine France	17	715 1.2×	528 0.9×	342 1.2×	238 0.9×	41 0.3×	24	1.1k
G Fabrizi Italy	14	347 0.6×	323 0.6×	140 0.5×	192 0.7×	77 0.6×	23	706
Emeline Mundwiller France	13	316 0.5×	391 0.7×	170 0.6×	104 0.4×	52 0.4×	16	738
Andrzej Kochański Poland	14	490 0.8×	287 0.5×	184 0.7×	143 0.5×	22 0.2×	73	706
Marie‐Josée Dicaire Canada	16	379 0.6×	556 1.0×	82 0.3×	92 0.3×	42 0.3×	24	733
Paola Saveri Italy	14	433 0.7×	257 0.4×	127 0.5×	174 0.6×	22 0.2×	23	597
Tarik Hamadouche France	15	410 0.7×	221 0.4×	177 0.6×	178 0.7×	19 0.1×	19	630
Francesca Maltecca Italy	14	408 0.7×	644 1.1×	77 0.3×	121 0.4×	102 0.8×	25	727
Gerard W. Hensels Netherlands	12	663 1.1×	349 0.6×	273 1.0×	253 0.9×	27 0.2×	12	923
Vincenzo Lupo Spain	17	363 0.6×	328 0.6×	175 0.6×	94 0.3×	20 0.1×	34	633

Countries citing papers authored by A. Dürr

Since Specialization

Citations

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

Fields of papers citing papers by A. Dürr

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Dürr

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

All Works

Sort: Min cites: Since: Top N: Style:

12 of 12 papers shown

1.

Bauer, Peter, Giovanni Stévanin, Christian Beetz, et al.. (2010). Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindreds. Journal of Neurology Neurosurgery & Psychiatry. 81(11). 1229–1232. 36 indexed citations

2.

Schüle, Rebecca, Marina de Nadai Bonin Gomes, A. Dürr, et al.. (2009). Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24. Neurology. 72(22). 1893–1898. 15 indexed citations

3.

Gilman, Sid, Gregor K. Wenning, David J. Brooks, et al.. (2008). Second consensus statement on the diagnosis of multiple system atrophy. UCL Discovery (University College London). 6 indexed citations

4.

Anheim, Mathieu, Denys Chaigne, Marie Fleury, et al.. (2008). Ataxie spastique autosomique récessive de Charlevoix-Saguenay : étude d’une famille et revue de la littérature. Revue Neurologique. 164(4). 363–368. 16 indexed citations

5.

Stévanin, Giovanni, Caroline Paternotte, Paula Coutinho, et al.. (2007). A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21. Neurology. 68(21). 1837–1840. 21 indexed citations

6.

Charles, Perrine, A. Camuzat, N. Benammar, et al.. (2007). Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?. Neurology. 69(21). 1970–1975. 110 indexed citations

7.

Depienne, Christel, Chantal Tallaksen, Sandrine Poëa‐Guyon, et al.. (2006). Gene symbol: PRPF31. Disease: Retinitis pigmentosa. Accession #Hs0514.. PubMed. 118(6). 776–776. 1 indexed citations

8.

Ber, Isabelle Le, F. Clot, Laurent Vercueil, et al.. (2006). Predominant dystonia with marked cerebellar atrophy. Neurology. 67(10). 1769–1773. 60 indexed citations

9.

Ber, Isabelle Le, G. Saïd, Patrik Michel, et al.. (2005). Amyotrophie de type Charcot-Marie-Tooth associée à une ataxie cérébelleuse autosomique récessive révélatrice d’une mutation du gène de l’aprataxine. Revue Neurologique. 161(3). 331–336. 3 indexed citations

10.

Martínez, María, Alexis Brice, Jenny Vaughan, et al.. (2004). Genome-wide scan linkage analysis for Parkinson’s disease: the European genetic study of Parkinson’s disease. Journal of Medical Genetics. 41(12). 900–907. 33 indexed citations

11.

Stévanin, Giovanni, Paola Giunti, Gilles David, et al.. (1998). De Novo Expansion of Intermediate Alleles in Spinocerebellar Ataxia 7. Human Molecular Genetics. 7(11). 1809–1813. 76 indexed citations

12.

Casari, Giorgio, Maurizio De Fusco, Sonia Ciarmatori, et al.. (1998). Spastic Paraplegia and OXPHOS Impairment Caused by Mutations in Paraplegin, a Nuclear-Encoded Mitochondrial Metalloprotease. Cell. 93(6). 973–983. 586 indexed citations breakdown →

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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