Alexandra D�rr

721 total citations
8 papers, 253 citations indexed

About

Alexandra D�rr is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Alexandra D�rr has authored 8 papers receiving a total of 253 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Cellular and Molecular Neuroscience, 5 papers in Neurology and 3 papers in Molecular Biology. Recurrent topics in Alexandra D�rr's work include Parkinson's Disease Mechanisms and Treatments (4 papers), Genetic Neurodegenerative Diseases (4 papers) and Neurological disorders and treatments (3 papers). Alexandra D�rr is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (4 papers), Genetic Neurodegenerative Diseases (4 papers) and Neurological disorders and treatments (3 papers). Alexandra D�rr collaborates with scholars based in France, United Kingdom and Netherlands. Alexandra D�rr's co-authors include Alexis Brice, Christopher A. Ross, Laure Jamot, Russell L. Margolis, A. Camuzat, Renu Saxena, Ishwar C. Verma, Hiroto Fujigasaki, Susan E. Holmes and Cecilia Zander and has published in prestigious journals such as Annals of Neurology, Movement Disorders and Muscle & Nerve.

In The Last Decade

Alexandra D�rr

8 papers receiving 246 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Alexandra D�rr France	8	193	124	122	58	21	8	253
Gia Tuong Tran Norway	7	104 0.5×	114 0.9×	210 1.7×	60 1.0×	9 0.4×	8	328
A. Tonelli Italy	6	140 0.7×	57 0.5×	108 0.9×	86 1.5×	27 1.3×	7	246
Elena Sánchez-Ferrero Spain	8	164 0.8×	86 0.7×	161 1.3×	101 1.7×	60 2.9×	10	313
Ichiro Kanazawa Japan	10	190 1.0×	113 0.9×	229 1.9×	16 0.3×	13 0.6×	15	328
Agnès Rastetter France	7	89 0.5×	109 0.9×	73 0.6×	42 0.7×	28 1.3×	9	271
Wai Yan Yau Australia	8	275 1.4×	112 0.9×	255 2.1×	50 0.9×	15 0.7×	15	390
Salima Assami Algeria	8	177 0.9×	106 0.9×	82 0.7×	111 1.9×	13 0.6×	8	268
Salvatore Rossi Italy	8	144 0.7×	67 0.5×	142 1.2×	16 0.3×	15 0.7×	25	201
Andrej Michalik Belgium	8	366 1.9×	84 0.7×	370 3.0×	39 0.7×	21 1.0×	11	463

Countries citing papers authored by Alexandra D�rr

Since Specialization

Citations

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

Fields of papers citing papers by Alexandra D�rr

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alexandra D�rr. 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 Alexandra D�rr. The network helps show where Alexandra D�rr may publish in the future.

Co-authorship network of co-authors of Alexandra D�rr

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

All Works

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8 of 8 papers shown

1.

Abel, Annette, Núria Fonknechten, Anne Höfer, et al.. (2004). Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A. Neurogenetics. 5(4). 239–243. 38 indexed citations

2.

Valente, Enza Maria, Francesco Brancati, Viviana Caputo, et al.. (2002). PARK6 is a common cause of familial parkinsonism. Neurological Sciences. 23(0). s117–s118. 32 indexed citations

3.

Bonifati, Vincenzo, Giuseppe De Michele, Alexandra D�rr, et al.. (2001). The parkin gene and its phenotype. Neurological Sciences. 22(1). 51–52. 26 indexed citations

4.

Fujigasaki, Hiroto, Ishwar C. Verma, A. Camuzat, et al.. (2001). SCA12 is a rare locus for autosomal dominant cerebellar ataxia: A study of an Indian family. Annals of Neurology. 49(1). 117–121. 72 indexed citations

5.

D�rr, Alexandra, Jean‐Pol Tassin, Marie Vidailhet, et al.. (2000). D2 dopamine receptor gene in myoclonic dystonia and essential myoclonus. Annals of Neurology. 48(1). 127–128. 10 indexed citations

6.

Kubis, Nathalie, Alexandra D�rr, Michel Gugenheim, et al.. (1999). Polyneuropathy in autosomal dominant cerebellar ataxias: Phenotype-genotype correlation. Muscle & Nerve. 22(6). 712–717. 38 indexed citations

7.

Brice, Alexis, Delphine Marez, Alexandra D�rr, et al.. (1999). CYP2D6 Polymorphism and Parkinson's disease susceptibility. Movement Disorders. 14(2). 230–236. 18 indexed citations

8.

Martin, Jean‐Jacques, Gilles David, Nicole Van Regemorter, et al.. (1997). Refinement of the locus for autosomal dominant cerebellar ataxia type II to chromosome 3p21.1-14.1. Human Genetics. 99(2). 225–232. 19 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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