Amanda Lindy

1.2k total citations
13 papers, 517 citations indexed

About

Amanda Lindy is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Amanda Lindy has authored 13 papers receiving a total of 517 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Amanda Lindy's work include Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Amanda Lindy is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Amanda Lindy collaborates with scholars based in United States, Germany and Belgium. Amanda Lindy's co-authors include Dianalee McKnight, Gabriele Richard, Elizabeth Butler, Kyle Retterer, Tracy Brandt, Anita Shanmugham, Costin Leu, Sameer M. Zuberi, Eduardo Pérez‐Palma and Andreas Brunklaus and has published in prestigious journals such as Nature Communications, Brain and Development.

In The Last Decade

Amanda Lindy

11 papers receiving 507 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Amanda Lindy United States 8 328 225 146 65 43 13 517
Maéva Langouët United States 8 226 0.7× 253 1.1× 164 1.1× 114 1.8× 25 0.6× 9 462
Shino Shimada Japan 15 318 1.0× 315 1.4× 43 0.3× 68 1.0× 6 0.1× 36 545
Saeko Ishida Japan 12 337 1.0× 402 1.8× 195 1.3× 191 2.9× 4 0.1× 20 719
Simone Brusco Italy 6 118 0.4× 235 1.0× 105 0.7× 156 2.4× 8 0.2× 9 377
Tetsushi Yamagata Japan 12 276 0.8× 448 2.0× 196 1.3× 221 3.4× 6 0.1× 14 736
Tara Newcomb United States 10 116 0.4× 263 1.2× 37 0.3× 119 1.8× 7 0.2× 12 454
Ippei Okada Japan 4 255 0.8× 210 0.9× 122 0.8× 120 1.8× 5 0.1× 5 444
Édouard Henrion Canada 7 328 1.0× 355 1.6× 36 0.2× 96 1.5× 5 0.1× 9 572
Nick Jacobsen United Kingdom 11 573 1.7× 463 2.1× 62 0.4× 64 1.0× 7 0.2× 11 840
Marta A. Bayly Australia 9 399 1.2× 181 0.8× 140 1.0× 74 1.1× 2 0.0× 11 588

Countries citing papers authored by Amanda Lindy

Since Specialization
Citations

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

Fields of papers citing papers by Amanda Lindy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amanda Lindy

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

All Works

13 of 13 papers shown
1.
Budnik, Nikita, Siwei Chen, David Báez-Nieto, et al.. (2025). Characterization of the functional and clinical impacts of CACNA1A missense variants found in neurodevelopmental disorders. Science Translational Medicine. 17(828). eadr0024–eadr0024.
2.
Vanoye, Carlos G., Reshma R. Desai, Zhigang Ji, et al.. (2022). High-throughput evaluation of epilepsy-associated KCNQ2 variants reveals functional and pharmacological heterogeneity. JCI Insight. 7(5). 28 indexed citations
3.
Pérez‐Palma, Eduardo, Joseph D. Symonds, Amanda Lindy, et al.. (2020). A catalogue of new incidence estimates of monogenic neurodevelopmental disorders caused by de novo variants. Brain. 143(4). 1099–1105. 76 indexed citations
4.
Evans, Perry, Chao Wu, Amanda Lindy, et al.. (2019). Genetic variant pathogenicity prediction trained using disease-specific clinical sequencing data sets. Genome Research. 29(7). 1144–1151. 16 indexed citations
5.
Lindy, Amanda, Elizabeth Butler, Anita Shanmugham, et al.. (2018). Diagnostic outcomes for genetic testing of 70 genes in 8565 patients with epilepsy and neurodevelopmental disorders. Epilepsia. 59(5). 1062–1071. 190 indexed citations
6.
Lindy, Amanda, et al.. (2017). High frequency of mosaic pathogenic variants in genes causing epilepsy-related neurodevelopmental disorders. Genetics in Medicine. 20(4). 403–410. 119 indexed citations
7.
Millan, Francisca, Dianalee McKnight, Julie Scuffins, et al.. (2017). EXOME SEQUENCING OFFERS A COMPREHENSIVE GENETIC EVALUATION AND HIGH DIAGNOSTIC RATE FOR ATAXIA-RELATED DISORDERS (S17.004). Neurology. 88(16_supplement).
8.
9.
Lindy, Amanda, Monica J. Basehore, Michael J. Friez, et al.. (2016). Identification of a novel insertion mutation in FGFR3 that causes thanatophoric dysplasia type 1. American Journal of Medical Genetics Part A. 170(6). 1573–1579. 7 indexed citations
10.
Lindy, Amanda, et al.. (2014). Truncating mutations in LRP4 lead to a prenatal lethal form of Cenani–Lenz syndrome. American Journal of Medical Genetics Part A. 164(9). 2391–2397. 18 indexed citations
11.
Lindy, Amanda, Puja K. Parekh, Patrick Kanju, et al.. (2014). TRPV channel-mediated calcium transients in nociceptor neurons are dispensable for avoidance behaviour. Nature Communications. 5(1). 4734–4734. 15 indexed citations
12.
Leung, Doris G., Harold A. Taylor, Amanda Lindy, Monica J. Basehore, & Andrew L. Mammen. (2013). A Case of Progressive Quadriceps Weakness and Elevated Creatine Kinase Level Mimicking Inclusion Body Myositis. Arthritis Care & Research. 66(2). 328–333. 4 indexed citations
13.
Foehr, Marisa L., Amanda Lindy, Nirav M. Amin, et al.. (2006). An antagonistic role for theC. elegansSchnurri homolog SMA-9 in modulating TGFβ signaling during mesodermal patterning. Development. 133(15). 2887–2896. 43 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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