Diane Lucente

Also affiliated with Massachusetts General Hospital

NeuroscienceMedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 1%percentile

7.4Author DataRank

Indexed papers

2in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 2 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

A cross-disorder dosage sensitivity map of the human genome

Cell(2022)10.1016/j.cell.2022.06.036

Top 5%

4.7DataRank

Top 5%367 citations

Joseph Glessner, Eleonora Porcu, Maarja Lepamets, Rhonda Brandon, Christopher Lauricella +46 more

Papers

Driven by 28 papers — median percentile 94. Top paper: “A cross-disorder dosage sensitivity map of the human genome”.

A cross-disorder dosage sensitivity map of the human genome

Cell(2022)10.1016/j.cell.2022.06.036

Top 5%

4.7DataRank

Top 5%367 citations

Joseph Glessner, Eleonora Porcu, Maarja Lepamets, Rhonda Brandon, Christopher Lauricella +46 more

Utility of the global CDR® plus NACC FTLD rating and development of scoring rules: Data from the ARTFL/LEFFTDS Consortium

Alzheimer s & Dementia(2020)10.1002/alz.12033

Top 8%

2.6DataRank

Top 8%169 citations

Danielle Brushaber, Jeremy A. Syrjanen, Walter K. Kremers, Julie A. Fields, Leah K. Forsberg +80 more

A cross-disorder dosage sensitivity map of the human genome

medRxiv(2021)10.1101/2021.01.26.21250098

N/A

2.0DataRank · unranked

54 citations

Joseph Glessner, Eleonora Porcu, Lisa‐Marie Niestroj, Jacob C. Ulirsch, Georgios Kellaris +28 more

Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.07.010

N/A

1.4DataRank · unranked

57 citations

Elise Valkanas, Jessica L. Giordano, Harold Z. Wang, Benjamin B Currall, Kathryn O’Keefe +40 more

Mutations causing Lopes-Maciel-Rodan syndrome are huntingtin hypomorphs

Human Molecular Genetics(2021)10.1093/hmg/ddaa283

N/A

1.2DataRank · unranked

38 citations

Yejin Lee, Douglas Barker, Kevin Correia, Baehyun Shin, Jacob M. Loupe +15 more

Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal models

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.09.015

N/A

0.963DataRank · unranked

33 citations

Rachita Yadav, Eva D’haene, Philip M. Boone, Serkan Erdin, Dadi Gao +18 more

Prolonged tau clearance and stress vulnerability rescue by pharmacological activation of autophagy in tauopathy neurons

Nature Communications(2020)10.1038/s41467-020-16984-1

N/A

0.762DataRank · unranked

160 citations

Ghata Nandi, Sharon Tentarelli, Ian Gurrell, Tanguy Jamier, Diane Lucente +5 more

Patterns of CAG repeat instability in the central nervous system and periphery in Huntington’s disease and in spinocerebellar ataxia type 1

Human Molecular Genetics(2020)10.1093/hmg/ddaa139

N/A

0.742DataRank · unranked

140 citations

Larissa Arning, James V. Giordano, Pedram Razghandi, Marissa A Andrew, Tammy Gillis +19 more

Genetic modifiers of Huntington disease differentially influence motor and cognitive domains

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.03.004

N/A

0.721DataRank · unranked

121 citations

Yuan Huang, Michael Orth, Tammy Gillis, Jacqueline Siciliano, Eunpyo Hong +23 more

Comprehensive cross-sectional and longitudinal analyses of plasma neurofilament light across FTD spectrum disorders

Cell Reports Medicine(2022)10.1016/j.xcrm.2022.100607

N/A

0.641DataRank · unranked

71 citations

Michael G. Heckman, Launia J. White, Austin M. Veire, Otto Pedraza, Alexander R. Burch +77 more

A Cdk5-derived peptide inhibits Cdk5/p25 activity and improves neurodegenerative phenotypes

Proceedings of the National Academy of Sciences(2023)10.1073/pnas.2217864120

N/A

0.617DataRank · unranked

60 citations

Jinsoo Seo, Audrey Lee, Oleg Kritskiy, Debasis Patnaik, Jay Penney +13 more

ASLPrep: a platform for processing of arterial spin labeled MRI and quantification of regional brain perfusion

Nature Methods(2022)10.1038/s41592-022-01458-7

N/A

0.590DataRank · unranked

50 citations

Maxwell A. Bertolero, Sudipto Dolui, Matthew Cieslak, Kristin Murtha, Erica B. Baller +94 more

Genetic modifiers of somatic expansion and clinical phenotypes in Huntington’s disease highlight shared and tissue-specific effects

Nature Genetics(2025)10.1038/s41588-025-02191-5

N/A

0.578DataRank · unranked

46 citations

Jong-Min Lee, Zachariah L. McLean, Kevin Correia, Jun Wan Shin, Sujin Lee +38 more

Systematic evaluation of genome sequencing for the assessment of fetal structural anomalies

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.08.12.248526

N/A

0.385DataRank · unranked

12 citations

Elise Valkanas, Jessica L. Giordano, Harold Z. Wang, Benjamin B Currall, Kathryn O’Keefe +40 more

FAN1 nuclease activity affects CAG expansion and age at onset of Huntington’s disease

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.04.13.439716

N/A

0DataRank · unranked

3 citations

Jasmine Donaldson, Caroline S. Binda, Sophie Powell, Uroosa Chughtai, Gareth Edwards +29 more

Association Analysis of Chromosome X to Identify Genetic Modifiers of Huntington’s Disease

Journal of Huntington s Disease(2021)10.3233/jhd-210485

N/A

0DataRank · unranked

8 citations

Michael J. Chao, Thomas H. Massey, Branduff McAllister, S. V. Lobanov, Lesley Jones +12 more

Genetic modifiers of Huntington’s disease differentially influence motor and cognitive domains

medRxiv(2022)10.1101/2022.01.03.22268687

N/A

0DataRank · unranked

1 citations

Yuan Huang, Michael Orth, Tammy Gillis, Jacqueline Siciliano, Eunpyo Hong +23 more

Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal models

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.02.15.480098

N/A

0DataRank · unranked

0 citations

Rachita Yadav, Eva D’haene, Philip M. Boone, Serkan Erdin, Dadi Gao +15 more

SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome

UNC Libraries(2020)10.17615/tdb3-bx52

N/A

0DataRank · unranked

0 citations

Hemant Bengani, Joseph A. Marsh, Angela M. Kaindl, Koh-ichiro Yoshiura, Katharina Steindl +73 more

Parallelized engineering of mutational models using piggyBac transposon delivery of CRISPR libraries

Cell Reports Methods(2023)10.1016/j.crmeth.2023.100672

N/A

0DataRank · unranked

4 citations

Nicholas D. Burt, Benjamin B Currall, Mariana Moysés‐Oliveira, Kiana Mohajeri, Riya Bhavsar +6 more

PMS1 as a target for splice modulation to prevent somatic CAG repeat expansion in Huntington’s disease

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.07.25.550489

N/A

0DataRank · unranked

2 citations

Dadi Gao, Kevin Correia, Jennie C. L. Roy, Shota Shibata, Iris N. Farnum +13 more

Resolution of ring chromosomes, Robertsonian translocations, and complex structural variants from long-read sequencing and telomere-to-telomere assembly

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.09.07.555775

N/A

0DataRank · unranked

0 citations

Philip M. Boone, Yongqing Huang, Kiran Garimella, Kar‐Tong Tan, Bianca Russell +13 more

Resolution of ring chromosomes, Robertsonian translocations, and complex structural variants from long-read sequencing and telomere-to-telomere assembly

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.10.006

N/A

0DataRank · unranked

23 citations

Philip M. Boone, Yongqing Huang, Kiran Garimella, Kar‐Tong Tan, Bianca Russell +17 more

Modification of Huntington’s disease by short tandem repeats

Brain Communications(2024)10.1093/braincomms/fcae016

N/A

0DataRank · unranked

12 citations

Eliana Marisa Ramos, N. Ahmad Aziz, Thomas H. Massey, Branduff McAllister, S. V. Lobanov +16 more

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(2024)10.1073/pnas.2322924121

N/A

0DataRank · unranked

10 citations

Eun Pyo Hong, Yukyeong Lee, Zachariah L. McLean, Emanuela Elezi, Ramee Lee +15 more

Exome sequencing of individuals with Huntington’s disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset

Nature Neuroscience(2022)10.1038/s41593-022-01033-5

N/A

0DataRank · unranked

92 citations

Jasmine Donaldson, Caroline S. Binda, Sophie Powell, Uroosa Chughtai, Gareth Edwards +29 more

Huntington’s disease LIG1 modifier variant increases ligase fidelity and suppresses somatic CAG repeat expansion

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.07.15.664798

N/A

0DataRank · unranked

0 citations

Wonju Kim, David H. Beier, Yejin Lee, Marina Kovalenko, Faaiza Saif +17 more

Temporal order of clinical and biomarker changes in familial frontotemporal dementia

Nature Medicine(2022)10.1038/s41591-022-01942-9

N/A

0DataRank · unranked

138 citations

Melanie Quintana, Barbara Wendelberger, Hilary W. Heuer, Lucy L. Russell, Yann Cobigo +95 more

Diane Lucente

Indexed papers

Top data-sharing exemplar

Papers