Annette Abel

1.6k total citations · 1 hit paper
8 papers, 1.2k citations indexed

About

Annette Abel is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Genetics. According to data from OpenAlex, Annette Abel has authored 8 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Cellular and Molecular Neuroscience, 4 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Annette Abel's work include Hereditary Neurological Disorders (5 papers), Neurogenetic and Muscular Disorders Research (4 papers) and Neurological diseases and metabolism (3 papers). Annette Abel is often cited by papers focused on Hereditary Neurological Disorders (5 papers), Neurogenetic and Muscular Disorders Research (4 papers) and Neurological diseases and metabolism (3 papers). Annette Abel collaborates with scholars based in United States, France and Australia. Annette Abel's co-authors include Kenneth H. Fischbeck, Imke Puls, Craig L. Bennett, Bruce A. Rabin, David R. Cornblath, Ian P. Blair, John W. Griffin, Klaus Wagner, Vincent Timmerman and Michaela Auer‐Grumbach and has published in prestigious journals such as Philosophical Transactions of the Royal Society B Biological Sciences, Annals of the New York Academy of Sciences and The American Journal of Human Genetics.

In The Last Decade

Annette Abel

8 papers receiving 1.2k 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.

DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4)

2004 602 citations Craig L. Bennett, Ian P. Blair et al. The American Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Annette Abel United States	8	668	483	475	375	270	8	1.2k
Ines Dierick Belgium	9	677 1.0×	453 0.9×	460 1.0×	362 1.0×	278 1.0×	14	1.2k
Mayana Zatz Brazil	6	504 0.8×	523 1.1×	245 0.5×	334 0.9×	154 0.6×	9	961
Nicholas J. Kramer United States	11	715 1.1×	688 1.4×	264 0.6×	307 0.8×	101 0.4×	13	1.2k
Tammy Reid United States	9	745 1.1×	714 1.5×	425 0.9×	421 1.1×	97 0.4×	10	1.2k
SungWon Song United States	7	495 0.7×	568 1.2×	211 0.4×	352 0.9×	230 0.9×	8	1.0k
Kevin Drenner United States	9	514 0.8×	528 1.1×	143 0.3×	345 0.9×	103 0.4×	12	881
Yalda Sedaghat Canada	7	736 1.1×	698 1.4×	152 0.3×	439 1.2×	81 0.3×	10	1.1k
Giulia Bisogni Italy	15	372 0.6×	481 1.0×	135 0.3×	304 0.8×	122 0.5×	37	742
Véronique Belzil Canada	22	772 1.2×	996 2.1×	264 0.6×	653 1.7×	257 1.0×	29	1.5k
Susan Middleton United Kingdom	3	341 0.5×	525 1.1×	183 0.4×	307 0.8×	164 0.6×	4	811

Countries citing papers authored by Annette Abel

Since Specialization

Citations

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

Fields of papers citing papers by Annette Abel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Annette Abel

This figure shows the co-authorship network connecting the top 25 collaborators of Annette Abel. A scholar is included among the top collaborators of Annette Abel 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 Annette Abel. Annette Abel 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.

Scherer, Steven S., Linda Jo Bone, Suzanne M. Deschênes, et al.. (2007). The Role of the Gap Junction Protein Connexin32 in the Pathogenesis of X‐Linked Charcot‐Marie‐Tooth Disease. Novartis Foundation symposium. 219. 175–187. 10 indexed citations

2.

Bennett, Craig L., Ian P. Blair, Imke Puls, et al.. (2004). DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4). The American Journal of Human Genetics. 74(6). 1128–1135. 602 indexed citations breakdown →

3.

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

4.

Antonellis, Anthony, Rachel E. Ellsworth, Nyamkhishig Sambuughin, et al.. (2003). Glycyl tRNA Synthetase Mutations in Charcot-Marie-Tooth Disease Type 2D and Distal Spinal Muscular Atrophy Type V. The American Journal of Human Genetics. 72(5). 1293–1299. 420 indexed citations

5.

Blair, Ian P., Craig L. Bennett, Annette Abel, et al.. (2000). A gene for autosomal dominant juvenile amyotrophic lateral sclerosis (ALS4 ) localizes to a 500-kb interval on chromosome 9q34. Neurogenetics. 3(1). 1–6. 29 indexed citations

6.

Fischbeck, Kenneth H., Annette Abel, Grace Lin, & Steven S. Scherer. (1999). X‐linked Charcot‐Marie‐Tooth Disease and Connexin32. Annals of the New York Academy of Sciences. 883(1). 36–41. 16 indexed citations

7.

Abel, Annette, et al.. (1999). Studies in Transgenic Mice Indicate a Loss of Connexin32 Function in X-Linked Charcot-Marie-Tooth Disease. Journal of Neuropathology & Experimental Neurology. 58(7). 702–710. 30 indexed citations

8.

Fischbeck, Kenneth H., Andrew P. Lieberman, Christine K. Bailey, Annette Abel, & Diane E. Merry. (1999). Androgen receptor mutation in Kennedy'sdisease. Philosophical Transactions of the Royal Society B Biological Sciences. 354(1386). 1075–1078. 34 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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