Diane Lucente

7.1k total citations
29 papers, 1.2k citations indexed

About

Diane Lucente is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Diane Lucente has authored 29 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 14 papers in Cellular and Molecular Neuroscience and 7 papers in Neurology. Recurrent topics in Diane Lucente's work include Genetic Neurodegenerative Diseases (9 papers), Neurological diseases and metabolism (6 papers) and Mitochondrial Function and Pathology (6 papers). Diane Lucente is often cited by papers focused on Genetic Neurodegenerative Diseases (9 papers), Neurological diseases and metabolism (6 papers) and Mitochondrial Function and Pathology (6 papers). Diane Lucente collaborates with scholars based in United States, United Kingdom and Israel. Diane Lucente's co-authors include James F. Gusella, Stephen J. Haggarty, Bradford C. Dickerson, M. Catarina Silva, Steven D. Sheridan, Debasis Patnaik, Tammy Gillis, Eric S. Fischer, Anat Blumenfeld and Katherine A. Donovan and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Diane Lucente

28 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Diane Lucente United States	15	748	361	235	196	143	29	1.2k
Rick A.C.M. Boonen Netherlands	11	683 0.9×	246 0.7×	170 0.7×	442 2.3×	83 0.6×	13	1.2k
Dongcheul Kang United States	11	753 1.0×	335 0.9×	359 1.5×	271 1.4×	74 0.5×	14	1.1k
Christine Laliberté Canada	16	435 0.6×	278 0.8×	130 0.6×	122 0.6×	111 0.8×	20	930
Yanmei Tao China	14	733 1.0×	466 1.3×	86 0.4×	107 0.5×	66 0.5×	20	1.2k
Jack Tseng United States	15	627 0.8×	774 2.1×	251 1.1×	149 0.8×	240 1.7×	31	1.4k
Guillermo López‐Doménech United Kingdom	18	1.1k 1.4×	366 1.0×	172 0.7×	208 1.1×	105 0.7×	21	1.5k
Miguel A. López‐Toledano United States	18	1.1k 1.5×	408 1.1×	136 0.6×	373 1.9×	70 0.5×	27	1.9k
Romina Combi Italy	19	496 0.7×	375 1.0×	150 0.6×	97 0.5×	77 0.5×	38	1.1k
Esther Sammler United Kingdom	15	512 0.7×	285 0.8×	116 0.5×	239 1.2×	464 3.2×	27	1.1k
David A. Rempe United States	16	559 0.7×	503 1.4×	67 0.3×	173 0.9×	116 0.8×	20	1.2k

Countries citing papers authored by Diane Lucente

Since Specialization

Citations

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

Fields of papers citing papers by Diane Lucente

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Diane Lucente

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Jenny, Kim, Kristiana Salmon, Ashley Crook, et al.. (2025). The Importance of Offering Genetic Counseling and Testing to All Persons Diagnosed With Frontotemporal Degeneration Spectrum Disorders. Neurology. 105(3). e213814–e213814.

Gao, Dadi, Kevin Correia, Jennie C. L. Roy, et al.. (2024). Splice modulators target PMS1 to reduce somatic expansion of the Huntington’s disease-associated CAG repeat. Nature Communications. 15(1). 3182–3182. 14 indexed citations

Pao, Ping‐Chieh, Jinsoo Seo, Audrey Lee, et al.. (2023). A Cdk5-derived peptide inhibits Cdk5/p25 activity and improves neurodegenerative phenotypes. Proceedings of the National Academy of Sciences. 120(16). e2217864120–e2217864120. 32 indexed citations

Nuttle, Xander, Benjamin Currall, Mariana Moysés‐Oliveira, et al.. (2023). Parallelized engineering of mutational models using piggyBac transposon delivery of CRISPR libraries. Cell Reports Methods. 4(1). 100672–100672. 1 indexed citations

Lee, Yejin, Douglas Barker, Kevin Correia, et al.. (2021). Mutations causing Lopes-Maciel-Rodan syndrome are huntingtin hypomorphs. Human Molecular Genetics. 30(3-4). 135–148. 20 indexed citations

Wong, Bonnie, et al.. (2021). Knowledge assessment and psychological impact of genetic counseling in people at risk for familial FTD. Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring. 13(1). e12225–e12225. 4 indexed citations

Silva, M. Catarina, Sharon Tentarelli, Ian Gurrell, et al.. (2020). Prolonged tau clearance and stress vulnerability rescue by pharmacological activation of autophagy in tauopathy neurons. Nature Communications. 11(1). 3258–3258. 102 indexed citations

Silva, M. Catarina, Fleur M. Ferguson, Quan-Ying Cai, et al.. (2019). Targeted degradation of aberrant tau in frontotemporal dementia patient-derived neuronal cell models. eLife. 8. 203 indexed citations

Chao, Michael J., Kyung‐Hee Kim, Diane Lucente, et al.. (2018). Population-specific genetic modification of Huntington's disease in Venezuela. PLoS Genetics. 14(5). e1007274–e1007274. 34 indexed citations

10.

Seo, Jinsoo, Oleg Kritskiy, L. Ashley Watson, et al.. (2017). Inhibition of p25/Cdk5 Attenuates Tauopathy in Mouse and iPSC Models of Frontotemporal Dementia. Journal of Neuroscience. 37(41). 9917–9924. 120 indexed citations

11.

Hennig, Krista M., Daniel M. Fass, Wen‐Ning Zhao, et al.. (2017). WNT/β-Catenin Pathway and Epigenetic Mechanisms Regulate the Pitt-Hopkins Syndrome and Schizophrenia Risk Gene TCF4. PubMed. 3(1). 53–71. 21 indexed citations

12.

Rodan, Lance H., Julie S. Cohen, Ali Fatemi, et al.. (2016). A novel neurodevelopmental disorder associated with compound heterozygous variants in the huntingtin gene. European Journal of Human Genetics. 24(12). 1826–1827. 45 indexed citations

13.

Shin, Aram, Tammy Gillis, Jayalakshmi Srinidhi Mysore, et al.. (2016). The HTT CAG-Expansion Mutation Determines Age at Death but Not Disease Duration in Huntington Disease. The American Journal of Human Genetics. 98(2). 287–298. 103 indexed citations

14.

Blumenfeld, Anat, Susan A. Slaugenhaupt, Christopher B. Liebert, et al.. (1999). Precise Genetic Mapping and Haplotype Analysis of the Familial Dysautonomia Gene on Human Chromosome 9q31. The American Journal of Human Genetics. 64(4). 1110–1118. 53 indexed citations

15.

Rutter, M., et al.. (1996). Assignment of the p60 Subunit of Chromatin Assembly Factor I to Chromosome 21q22.2. Genomics. 34(1). 148–150. 1 indexed citations

16.

Slaugenhaupt, Susan A., Anat Blumenfeld, Christopher B. Liebert, et al.. (1995). The human gene for neurotrophic tyrosine kinase receptor type 2 (NTRK2) is located on chromosome 9 but is not the familial dysautonomia gene. Genomics. 25(3). 730–732. 8 indexed citations

17.

Blumenfeld, Anat, Diane Lucente, James A. Trofatter, et al.. (1995). Peripherin gene is linked to keratin 18 gene on human chromosome 12. Somatic Cell and Molecular Genetics. 21(1). 83–88. 7 indexed citations

18.

Lucente, Diane, Sonia Samec, M. Rutter, et al.. (1995). Localization of 102 exons to a 2.5 Mb region involved in Down syndrome. Human Molecular Genetics. 4(8). 1305–1311. 36 indexed citations

19.

Blumenfeld, Anat, Susan Slaugenhaupt, Diane Lucente, et al.. (1993). The gene for familial dysautonomia is linked to chromosome 9 and shows strong linkage disequilibrium with D9S58. The Society for Neuroscience Abstracts. 19. 1463. 7 indexed citations

20.

Blumenfeld, Anat, Susan A. Slaugenhaupt, Felicia B. Axelrod, et al.. (1993). Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosis. Nature Genetics. 4(2). 160–164. 104 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.

Explore authors with similar magnitude of impact