Diane Lucente

7.1k citations

29 papers · 1.2k indexed · h-index 15

Impact in

Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
Neurology top 10%

Papers in ⓘ

Molecular Biology 19
- Mitochondrial Function and Pathology 6
- Genomics and Chromatin Dynamics 3
Cellular and Molecular Neuroscience 14
- Genetic Neurodegenerative Diseases 9
- Hereditary Neurological Disorders 5

Co-authors: James F. Gusella (16 shared papers)Stephen J. Haggarty (6 shared papers)Bradford C. Dickerson (8 shared papers)M. Catarina Silva (4 shared papers)Steven D. Sheridan (3 shared papers)Tammy Gillis (4 shared papers)Debasis Patnaik (2 shared papers)Quan-Ying Cai (1 shared paper)
Journals: Proceedings of the National Academy of Sciences (3 papers)Nature Communications (2 papers)Human Molecular Genetics (2 papers)The American Journal of Human Genetics (2 papers)Genomics (2 papers)
Partner nations: United States United Kingdom Israel

In The Last Decade

Diane Lucente

28 papers receiving 1.2k citations

Peers

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-authors

The 25 scholars most cited alongside Diane Lucente, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Diane Lucente Line = papers co-authored together Diane Lucente links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 29 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors Proceedings of the National Academy of Sciences ·Aarathi Sugathan, Marta Biagioli, Christelle Golzio, Serkan Erdin, Ian Blumenthal, Poornima Manavalan, Ashok Ragavendran, Harrison Brand, Diane Lucente, Judith H. Miles, Steven D. Sheridan, Alexei Stortchevoi, Manolis Kellis, Stephen J. Haggarty, Nicholas Katsanis, James F. Gusella, Michael E. Talkowski	2014	227
2	Targeted degradation of aberrant tau in frontotemporal dementia patient-derived neuronal cell models eLife ·M. Catarina Silva, Fleur M. Ferguson, Quan-Ying Cai, Katherine A. Donovan, Ghata Nandi, Debasis Patnaik, Tinghu Zhang, Hai‐Tsang Huang, Diane Lucente, Bradford C. Dickerson, Timothy J. Mitchison, Eric S. Fischer, Nathanael S. Gray, Stephen J. Haggarty	2019	203
3	Inhibition of p25/Cdk5 Attenuates Tauopathy in Mouse and iPSC Models of Frontotemporal Dementia Journal of Neuroscience ·Jinsoo Seo, Oleg Kritskiy, L. Ashley Watson, Scarlett J. Barker, Dilip Dey, Waseem Raja, Yuan-Ta Lin, Tak Ko, Sukhee Cho, Jay Penney, M. Catarina Silva, Steven D. Sheridan, Diane Lucente, James F. Gusella, Bradford C. Dickerson, Stephen J. Haggarty, Li‐Huei Tsai	2017	120
4	Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosis Nature Genetics ·Anat Blumenfeld, Susan A. Slaugenhaupt, Felicia B. Axelrod, Diane Lucente, Channa Maayan, Christopher B. Liebert, Laurie J. Ozelius, James A. Trofatter, Jonathan L. Haines, Xandra O. Breakefield, James F. Gusella	1993	104
5	The HTT CAG-Expansion Mutation Determines Age at Death but Not Disease Duration in Huntington Disease The American Journal of Human Genetics ·Jae Whan Keum, Aram Shin, Tammy Gillis, Jayalakshmi Srinidhi Mysore, Kawther Abu Elneel, Diane Lucente, Tiffany C. Hadzi, Peter Holmans, Lesley Jones, Michael Orth, Seung Kwak, Marcy E. MacDonald, James F. Gusella, Jong‐Min Lee	2016	103
6	Prolonged tau clearance and stress vulnerability rescue by pharmacological activation of autophagy in tauopathy neurons Nature Communications ·M. Catarina Silva, Ghata Nandi, Sharon Tentarelli, Ian Gurrell, Tanguy Jamier, Diane Lucente, Bradford C. Dickerson, Dean G. Brown, Nicholas J. Brandon, Stephen J. Haggarty	2020	102
7	Precise Genetic Mapping and Haplotype Analysis of the Familial Dysautonomia Gene on Human Chromosome 9q31 The American Journal of Human Genetics ·Anat Blumenfeld, Susan A. Slaugenhaupt, Christopher B. Liebert, Violeta Temper, Channa Maayan, Sandra Gill, Diane Lucente, Maria Idelson, Kathy MacCormack, Mary Anne Monahan, James Mull, Maire Leyne, Marc L. Mendillo, Taryn A. Schiripo, Esther Mishori, Xandra O. Breakefield, Felicia B. Axelrod, James F. Gusella	1999	53
8	A novel neurodevelopmental disorder associated with compound heterozygous variants in the huntingtin gene European Journal of Human Genetics ·Lance H. Rodan, Julie S. Cohen, Ali Fatemi, Tammy Gillis, Diane Lucente, James F. Gusella, Jonathan Picker	2016	45
9	Localization of 102 exons to a 2.5 Mb region involved in Down syndrome Human Molecular Genetics ·Diane Lucente, H.M. Chen, Deborah Shea, Sonia Samec, M. Rutter, Roman Chrast, Colette Rossier, Alan Buckler, Stylianos E. Antonarakis, Mary Kay McCormick	1995	36
10	Population-specific genetic modification of Huntington's disease in Venezuela PLoS Genetics ·Michael J. Chao, Kyung‐Hee Kim, Jun Wan Shin, Diane Lucente, Vanessa C. Wheeler, Hong Li, Jared C. Roach, Leroy Hood, Nancy S. Wexler, Laura Bannach Jardim, Peter Holmans, Lesley Jones, Michael Orth, Seung Kwak, Marcy E. MacDonald, James F. Gusella, Jong‐Min Lee	2018	34
11	A Cdk5-derived peptide inhibits Cdk5/p25 activity and improves neurodegenerative phenotypes Proceedings of the National Academy of Sciences ·Ping‐Chieh Pao, Jinsoo Seo, Audrey Lee, Oleg Kritskiy, Debasis Patnaik, Jay Penney, Ravikiran M. Raju, Ute Geigenmuller, M. Catarina Silva, Diane Lucente, James F. Gusella, Bradford C. Dickerson, Anjanet Loon, Margaret X. Yu, Michael Bula, Melody Yu, Stephen J. Haggarty, Li‐Huei Tsai	2023	32
12	WNT/β-Catenin Pathway and Epigenetic Mechanisms Regulate the Pitt-Hopkins Syndrome and Schizophrenia Risk Gene TCF4 PubMed ·Krista M. Hennig, Daniel M. Fass, Wen‐Ning Zhao, Steven D. Sheridan, Ting Fu, Serkan Erdin, Alexei Stortchevoi, Diane Lucente, Jannine D. Cody, David A. Sweetser, James F. Gusella, Michael E. Talkowski, Stephen J. Haggarty	2017	21
13	Mutations causing Lopes-Maciel-Rodan syndrome are huntingtin hypomorphs Human Molecular Genetics ·Roy Jung, Yejin Lee, Douglas Barker, Kevin Correia, Baehyun Shin, Jacob M. Loupe, Ryan L. Collins, Diane Lucente, Jayla Ruliera, Tammy Gillis, Jayalakshmi Srinidhi Mysore, Lance H. Rodan, Jonathan Picker, Jong‐Min Lee, David Howland, Ramee Lee, Seung Kwak, Marcy E. MacDonald, James F. Gusella, Ihn Sik Seong	2021	20
14	Diagnostic Evaluation and Monitoring of Patients With Posterior Cortical Atrophy Neurodegenerative Disease Management ·Bonnie Wong, Diane Lucente, Julie MacLean, Jaya Padmanabhan, Megan Quimby, Katherine D. Brandt, Deepti Putcha, Janet C. Sherman, Matthew P. Frosch, Scott McGinnis, Bradford C. Dickerson	2019	19
15	Splice modulators target PMS1 to reduce somatic expansion of the Huntington’s disease-associated CAG repeat Nature Communications ·Zachariah L. McLean, Dadi Gao, Kevin Correia, Jennie C. L. Roy, Shota Shibata, Iris N. Farnum, Zoe Valdepenas-Mellor, Marina Kovalenko, Manasa Rapuru, Elisabetta Morini, Jayla Ruliera, Tammy Gillis, Diane Lucente, Benjamin P. Kleinstiver, Jong‐Min Lee, Marcy E. MacDonald, Vanessa C. Wheeler, Ricardo Mouro Pinto, James F. Gusella	2024	14
16	The human gene for neurotrophic tyrosine kinase receptor type 2 (NTRK2) is located on chromosome 9 but is not the familial dysautonomia gene Genomics ·Susan A. Slaugenhaupt, Anat Blumenfeld, Christopher B. Liebert, James Mull, Diane Lucente, Marianne Monahan, Xandra O. Breakefield, Channa Maayan, Luis F. Parada, Felicia B. Axelrod, James F. Gusella	1995	8
17	The gene for familial dysautonomia is linked to chromosome 9 and shows strong linkage disequilibrium with D9S58 The Society for Neuroscience Abstracts ·Anat Blumenfeld, Susan Slaugenhaupt, Diane Lucente, Felicia B. Axelrod, Christopher B. Liebert, Channa Maayan, Marianne Monahan, James A. Trofatter, J. L. Haines, X. O. Breakefield, James F. Gusella	1993	7
18	Peripherin gene is linked to keratin 18 gene on human chromosome 12 Somatic Cell and Molecular Genetics ·Anat Blumenfeld, Diane Lucente, James A. Trofatter, Terry J. Lerner, Susan A. Slaugenhaupt, Christopher B. Liebert, Marianne Monahan, Jonathan L. Haines, James F. Gusella, Xandra O. Breakefield, Linda M. Parysek	1995	7
19	A 63-Year-Old Man With Progressive Visual Symptoms JAMA Neurology ·Sara Mitchell, Diane Lucente, Mykol Larvie, M. I. Cobos, Matthew P. Frosch, Bradford C. Dickerson	2016	7
20	Posttranscriptional regulation of FAN1 by miR-124-3p at rs3512 underlies onset-delaying genetic modification in Huntington’s disease Proceedings of the National Academy of Sciences ·Kyung‐Hee Kim, Eun Pyo Hong, Yukyeong Lee, Zachariah L. McLean, Emanuela Elezi, Ramee Lee, Seung Kwak, Branduff McAllister, Thomas H. Massey, S. V. Lobanov, Peter Holmans, Michael Orth, Marc Ciosi, Darren G. Monckton, Jeffrey D. Long, Diane Lucente, Vanessa C. Wheeler, Marcy E. MacDonald, James F. Gusella, Jong‐Min Lee	2024	5

About Diane Lucente

Diane Lucente is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Neurology, Neurology and Cell Biology, having authored 29 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (9 papers), Neurological diseases and metabolism (6 papers), Mitochondrial Function and Pathology (6 papers), Hereditary Neurological Disorders (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Alzheimer's disease research and treatments (3 papers), Amyotrophic Lateral Sclerosis Research (3 papers) and Genomics and Chromatin Dynamics (3 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (361 citations), Neurology (114 citations), Developmental Neuroscience (54 citations), Molecular Biology (748 citations) and Neurology (143 citations). Diane Lucente has collaborated with scholars based in United States, United Kingdom and Israel. Frequent co-authors include James F. Gusella, Stephen J. Haggarty, Bradford C. Dickerson, M. Catarina Silva, Steven D. Sheridan, Tammy Gillis, Debasis Patnaik, Quan-Ying Cai, Christopher B. Liebert and Michael E. Talkowski. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Communications, Human Molecular Genetics, The American Journal of Human Genetics and Genomics.

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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