A. L. Ludwig

592 total citations
9 papers, 457 citations indexed

About

A. L. Ludwig is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, A. L. Ludwig has authored 9 papers receiving a total of 457 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Genetics and 1 paper in Cognitive Neuroscience. Recurrent topics in A. L. Ludwig's work include Genetics and Neurodevelopmental Disorders (8 papers), RNA modifications and cancer (6 papers) and RNA regulation and disease (2 papers). A. L. Ludwig is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), RNA modifications and cancer (6 papers) and RNA regulation and disease (2 papers). A. L. Ludwig collaborates with scholars based in United States, Netherlands and India. A. L. Ludwig's co-authors include Paul J. Hagerman, Flora Tassone, Christine Iwahashi, Alexandra Beilina, Philip H. Schwartz, Thorsten Dieckmann, Michael Fry, Pnina Weisman-Shomer, Samer Khateb and Dolores Garcia-Arocena and has published in prestigious journals such as Nucleic Acids Research, Journal of Molecular Biology and Human Molecular Genetics.

In The Last Decade

A. L. Ludwig

9 papers receiving 454 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A. L. Ludwig United States 8 368 345 116 103 50 9 457
Kali Witherspoon United States 2 283 0.8× 446 1.3× 279 2.4× 35 0.3× 33 0.7× 2 568
Dolores Garcia-Arocena United States 8 480 1.3× 531 1.5× 198 1.7× 121 1.2× 89 1.8× 9 625
Nisha Raj United States 9 373 1.0× 181 0.5× 103 0.9× 43 0.4× 32 0.6× 13 473
Poornima Manavalan United States 5 326 0.9× 261 0.8× 139 1.2× 48 0.5× 20 0.4× 5 423
Doris Wöhrle Germany 6 425 1.2× 492 1.4× 193 1.7× 89 0.9× 21 0.4× 8 619
Marius F. Ifrim United States 9 323 0.9× 177 0.5× 49 0.4× 75 0.7× 64 1.3× 11 420
Bonnie Nijhof Netherlands 8 223 0.6× 209 0.6× 74 0.6× 77 0.7× 33 0.7× 11 391
Jean-Louis Mandel France 3 481 1.3× 588 1.7× 291 2.5× 48 0.5× 32 0.6× 4 660
Bernadette Van Roy Belgium 6 601 1.6× 687 2.0× 295 2.5× 96 0.9× 37 0.7× 10 837
Bettina Lipkowitz Germany 6 297 0.8× 168 0.5× 60 0.5× 40 0.4× 17 0.3× 6 383

Countries citing papers authored by A. L. Ludwig

Since Specialization
Citations

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

Fields of papers citing papers by A. L. Ludwig

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. L. Ludwig

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

All Works

9 of 9 papers shown
1.
Ludwig, A. L., Dalyir Pretto, Glòria Arqué, et al.. (2014). CNS expression of murine fragile X protein (FMRP) as a function of CGG-repeat size. Human Molecular Genetics. 23(12). 3228–3238. 57 indexed citations
2.
Ludwig, A. L., et al.. (2014). Expression of an expanded CGG-repeat RNA in a single pair of primary sensory neurons impairs olfactory adaptation in Caenorhabditis elegans. Human Molecular Genetics. 23(18). 4945–4959. 6 indexed citations
3.
Garcia-Arocena, Dolores, F. Tassone, A. L. Ludwig, et al.. (2011). CGG-repeat length threshold for FMR1 RNA pathogenesis in a cellular model for FXTAS. Human Molecular Genetics. 20(11). 2161–2170. 56 indexed citations
4.
Ludwig, A. L., John W.B. Hershey, & Paul J. Hagerman. (2011). Initiation of Translation of the FMR1 mRNA Occurs Predominantly through 5′-End-Dependent Ribosomal Scanning. Journal of Molecular Biology. 407(1). 21–34. 22 indexed citations
5.
Ludwig, A. L., et al.. (2009). Translation of the FMR1 mRNA is not influenced by AGG interruptions. Nucleic Acids Research. 37(20). 6896–6904. 18 indexed citations
6.
Garcia-Arocena, Dolores, Judith R. Brouwer, Flora Tassone, et al.. (2009). Fibroblast phenotype in male carriers of FMR1 premutation alleles. Human Molecular Genetics. 19(2). 299–312. 54 indexed citations
7.
Ludwig, A. L., et al.. (2007). Secondary Structure and Dynamics of the r(CGG) Repeat in the mRNA of the Fragile X Mental Retardation 1(FMR1)Gene. RNA Biology. 4(2). 93–100. 55 indexed citations
8.
Khateb, Samer, et al.. (2007). The tetraplex (CGG)n destabilizing proteins hnRNP A2 and CBF-A enhance the in vivo translation of fragile X premutation mRNA. Nucleic Acids Research. 35(17). 5775–5788. 64 indexed citations
9.
Iwahashi, Christine, Alexandra Beilina, A. L. Ludwig, et al.. (2005). Induction of inclusion formation and disruption of lamin A/C structure by premutation CGG-repeat RNA in human cultured neural cells. Human Molecular Genetics. 14(23). 3661–3671. 125 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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