A. Birve

637 total citations
5 papers, 306 citations indexed

About

A. Birve is a scholar working on Neurology, Genetics and Molecular Biology. According to data from OpenAlex, A. Birve has authored 5 papers receiving a total of 306 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Neurology, 3 papers in Genetics and 1 paper in Molecular Biology. Recurrent topics in A. Birve's work include Amyotrophic Lateral Sclerosis Research (5 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Parkinson's Disease Mechanisms and Treatments (2 papers). A. Birve is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (5 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Parkinson's Disease Mechanisms and Treatments (2 papers). A. Birve collaborates with scholars based in Sweden, Germany and Austria. A. Birve's co-authors include Peter M. Andersen, Stefan L. Marklund, Johan Bergh, Per Zetterström, Thomas Brännström, Karin Forsberg, Karin S. Graffmo, P. M. Andersen, Leonard H. van den Berg and Jan H. Veldink and has published in prestigious journals such as Neurology, Human Molecular Genetics and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

A. Birve

5 papers receiving 303 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A. Birve Sweden	5	261	173	123	55	53	5	306
Philip McGoldrick United Kingdom	4	292 1.1×	215 1.2×	186 1.5×	49 0.9×	35 0.7×	5	356
Tao Qiao United States	6	228 0.9×	150 0.9×	152 1.2×	47 0.9×	32 0.6×	7	310
Johan Bergh Sweden	4	276 1.1×	142 0.8×	132 1.1×	60 1.1×	51 1.0×	4	316
Olubunmi Abel United Kingdom	5	312 1.2×	172 1.0×	133 1.1×	101 1.8×	52 1.0×	6	379
N. Siddique United States	6	326 1.2×	197 1.1×	143 1.2×	108 2.0×	53 1.0×	8	399
Eleonora Maestri Italy	8	259 1.0×	171 1.0×	67 0.5×	56 1.0×	45 0.8×	8	290
Meike Michaelsen Germany	6	295 1.1×	164 0.9×	223 1.8×	54 1.0×	62 1.2×	6	370
Daniel Farny Germany	6	243 0.9×	131 0.8×	190 1.5×	47 0.9×	57 1.1×	6	320
Aurélie Leclerc United States	5	257 1.0×	162 0.9×	170 1.4×	64 1.2×	32 0.6×	5	334
Helena Ederle Germany	4	255 1.0×	156 0.9×	258 2.1×	36 0.7×	34 0.6×	4	370

Countries citing papers authored by A. Birve

Since Specialization

Citations

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

Fields of papers citing papers by A. Birve

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

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

All Works

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5 of 5 papers shown

1.

Eschbach, J. W., Birgit Schwalenstöcker, Selma M. Soyal, et al.. (2013). PGC-1 is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis. Human Molecular Genetics. 22(17). 3477–3484. 69 indexed citations

2.

Graffmo, Karin S., Karin Forsberg, Johan Bergh, et al.. (2012). Expression of wild-type human superoxide dismutase-1 in mice causes amyotrophic lateral sclerosis. Human Molecular Genetics. 22(1). 51–60. 117 indexed citations

3.

Waibel, Stefan, Manuela Neumann, Angela Rosenbohm, et al.. (2012). Truncating mutations in FUS/TLS give rise to a more aggressive ALS‐phenotype than missense mutations: a clinico‐genetic study in Germany. European Journal of Neurology. 20(3). 540–546. 48 indexed citations

4.

Goris, An, Robin Lemmens, Michael A. van Es, et al.. (2010). Tau levels do not influence human ALS or motor neuron degeneration in the SOD1 ^G93A mouse. Neurology. 74(21). 1687–1693. 14 indexed citations

5.

Es, Michael A. van, et al.. (2009). Large-scale SOD1 mutation screening provides evidence for genetic heterogeneity in amyotrophic lateral sclerosis. Journal of Neurology Neurosurgery & Psychiatry. 81(5). 562–566. 58 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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