Cathleen Lutz

ORCID: 0000-0003-2502-1900

MedicineBiochemistry, Genetics and Molecular BiologyNeuroscience

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 3%percentile

1.0Author 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 comprehensive atlas of AAV tropism in the mouse

Molecular Therapy(2025)10.1016/j.ymthe.2025.01.041

Top 27%

0.752DataRank

Top 27%39 citations

Kathy J. Snow, Jote Bulcha, Aaron R. Cox, Alexa Martinez, M. Cecilia Ljungberg +21 more

Papers

Driven by 59 papers — median percentile 58. Top paper: “A platform for experimental precision medicine: The extended BXD mouse family”.

A platform for experimental precision medicine: The extended BXD mouse family

Cell Systems(2021)10.1016/j.cels.2020.12.002

N/A

0.801DataRank · unranked

207 citations

Danny Arends, Pjotr Prins, Megan K. Mulligan, Suheeta Roy, Evan G. Williams +11 more

A comprehensive atlas of AAV tropism in the mouse

Molecular Therapy(2025)10.1016/j.ymthe.2025.01.041

Top 27%

0.752DataRank

Top 27%39 citations

Kathy J. Snow, Jote Bulcha, Aaron R. Cox, Alexa Martinez, M. Cecilia Ljungberg +21 more

Loss of Tmem106b exacerbates FTLD pathologies and causes motor deficits in progranulin‐deficient mice

EMBO Reports(2020)10.15252/embr.202050197

N/A

0.635DataRank · unranked

68 citations

Mieu Brooks, Peizhou Jiang, Shunsuke Koga, Aamir Zuberi, Matthew Baker +11 more

Into the Wild: A novel wild-derived inbred strain resource expands the genomic and phenotypic diversity of laboratory mouse models

PLoS Genetics(2024)10.1371/journal.pgen.1011228

N/A

0.606DataRank · unranked

23 citations

Daniel M. Gatti, Mallory A. Ballinger, Dana Lin, Megan Phifer‐Rixey, Michael J. Sheehan +10 more

A Drosophila screen identifies NKCC1 as a modifier of NGLY1 deficiency

eLife(2020)10.7554/elife.57831

N/A

0.568DataRank · unranked

43 citations

Katie G Owings, Emily Coelho, Gaëlle Mercenne, John M. Pleinis, Raghavendran Partha +7 more

Neurobehavioral deficits of mice expressing a low level of G127V mutant frataxin

Neurobiology of Disease(2023)10.1016/j.nbd.2023.105996

N/A

0.373DataRank · unranked

11 citations

Robbie L. Conley, Aamir Zuberi, Cathleen Lutz, Terry Gemelli, Марек Напиерала +2 more

Loss of Pex1 in Inner Ear Hair Cells Contributes to Cochlear Synaptopathy and Hearing Loss

Cells(2022)10.3390/cells11243982

N/A

0.330DataRank · unranked

8 citations

Thibault Peineau, Aamir Zuberi, Cathleen Lutz, Gwenaëlle S. G. Géléoc, Stéphanie A. Mauriac

The mutant mouse resource and research center (MMRRC) consortium: the US-based public mouse repository system

Mammalian Genome(2024)10.1007/s00335-024-10070-3

Top 57%

0.284DataRank

Top 57%4 citations

James M. Amos-Landgraf, Renee Araiza, Jennifer Brennan, C. H. Carlson, Dominic J. Ciavatta +12 more

Alternating hemiplegia of childhood associated mutations in Atp1a3 reveal diverse neurological alterations in mice

Neurobiology of Disease(2025)10.1016/j.nbd.2025.106954

N/A

0.224DataRank · unranked

3 citations

Georgii Krivoshein, Scott I. Adamson, Elena Arystarkhova, Laura Anderson, John Szwec +16 more

Phenotype Distinctions in Mice Deficient in the Neuron-Specific α3 Subunit of Na,K-ATPase:Atp1a3tm1Ling/+andAtp1a3+/D801Y

eNeuro(2024)10.1523/eneuro.0101-24.2024

N/A

0.165DataRank · unranked

2 citations

Elena Arystarkhova, Amanda N. Sacino, Margit V. Szabari, Cathleen Lutz, Markus Terrey +7 more

In-utero rescue of neurological dysfunction in a mouse model of Wiedemann-Steiner syndrome

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.07.19.604339

N/A

0.104DataRank · unranked

1 citations

Kimberley Jade Anderson, Andrew Brinn, Katheryn P. Franklin, Juan Ouyang, Ásbjörg Ósk Snorradóttir +5 more

AAV9-mediated FIG4 delivery prolongs life span in Charcot-Marie-Tooth disease type 4J mouse model

Journal of Clinical Investigation(2021)10.1172/jci137159

N/A

0DataRank · unranked

33 citations

Rachel M. Bailey, Crystal Davis, Tara Murphy, Jenn Cook, Randy Walls +7 more

Efficient in vivo neuronal genome editing in the mouse brain using nanocapsules containing CRISPR-Cas9 ribonucleoproteins

Biomaterials(2022)10.1016/j.biomaterials.2022.121959

N/A

0DataRank · unranked

33 citations

Yuyuan Wang, Samuel S. Neuman, Kathy J. Snow, Stephen A. Murray, Cathleen Lutz +14 more

Promoting validation and cross-phylogenetic integration in model organism research

Disease Models & Mechanisms(2022)10.1242/dmm.049600

N/A

0DataRank · unranked

13 citations

Rebecca D. Burdine, Mary E. Dickinson, Stephen C. Ekker, Alex Y. Lin, K. C. Kent Lloyd +13 more

New mouse models with hypomorphic SUMF1 variants mimic attenuated forms of multiple sulfatase deficiency

Journal of Inherited Metabolic Disease(2022)10.1002/jimd.12577

N/A

0DataRank · unranked

8 citations

Maximiliano Presa, Sergio Attanasio, Vincenzo Cacace, Martina Sofia, Aamir Zuberi +9 more

An Integrated Approach to Studying Rare Neuromuscular Diseases Using Animal and Human Cell-Based Models

Frontiers in Cell and Developmental Biology(2022)10.3389/fcell.2021.801819

N/A

0DataRank · unranked

3 citations

Cathleen Lutz, Stephen A. Murray, Robert W. Burgess, Timothy J. Hines

Stathmin-2 loss leads to neurofilament-dependent axonal collapse driving motor and sensory denervation

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.12.11.519794

N/A

0DataRank · unranked

9 citations

Mariana Bravo‐Hernández, Maximiliano Presa, Michael W. Baughn, Ze’ev Melamed, Melinda S. Beccari +19 more

Efficient in vivo neuronal genome editing in the mouse brain using nanocapsules containing CRISPR-Cas9 ribonucleoproteins

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.07.24.501299

N/A

0DataRank · unranked

3 citations

Yuyuan Wang, Samuel S. Neuman, Kathy J. Snow, Stephen A. Murray, Cathleen Lutz +13 more

Focused ultrasound-mediated brain genome editing

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.12.10.519924

N/A

0DataRank · unranked

1 citations

Robin Ji, Joyce K. Zhou, Kathy J. Snow, Nancy Kwon, Ethan Saville +18 more

Mechanism of STMN2 cryptic splice-polyadenylation and its correction for TDP-43 proteinopathies

Science(2023)10.1126/science.abq5622

N/A

0DataRank · unranked

253 citations

Ze’ev Melamed, Jone López‐Erauskin, Melinda S. Beccari, Karen Ling, Aamir Zuberi +19 more

Stathmin-2 loss leads to neurofilament-dependent axonal collapse driving motor and sensory denervation

Nature Neuroscience(2023)10.1038/s41593-023-01496-0

N/A

0DataRank · unranked

49 citations

Mariana Bravo‐Hernández, Maximiliano Presa, Michael W. Baughn, Ze’ev Melamed, Melinda S. Beccari +21 more

Focused ultrasound–mediated brain genome editing

Proceedings of the National Academy of Sciences(2023)10.1073/pnas.2302910120

N/A

0DataRank · unranked

33 citations

Robin Ji, Joyce K. Zhou, Kathy J. Snow, Nancy Kwon, Ethan Saville +18 more

MATR3 P154S knock-in mice do not exhibit motor, muscle or neuropathologic features of ALS

Biochemical and Biophysical Research Communications(2023)10.1016/j.bbrc.2023.01.032

N/A

0DataRank · unranked

4 citations

Nicole Houchins, Vinisha Venugopal, Aamir Zuberi, Cathleen Lutz, Bessie Meechooveet +4 more

Loss of Endothelial TDP-43 Leads to Blood Brain Barrier Defects in Mouse Models of Amyotrophic Lateral Sclerosis and Frontotemporal Dementia

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.12.13.571184

N/A

0DataRank · unranked

13 citations

Amy L. Kimble, Jordan D. Tyburski, Nathan K. Leclair, Aamir Zuberi, Melissa Murphy +7 more

Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microglia

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.06.01.541136

N/A

0DataRank · unranked

4 citations

Del Hayden Gadd, Michelle Mosqueda, Jianjun Zhong, Jonathan Jung, Shankaracharya +15 more

Focused ultrasound-mediated brain genome editing

Research Square(2023)10.21203/rs.3.rs-2365576/v1

N/A

0DataRank · unranked

0 citations

Yeh‐Hsing Lao, Robin Ji, Joyce K. Zhou, Kathy J. Snow, Nancy Kwon +18 more

Gain-of-function mutations of TRPV4 acting in endothelial cells drive blood-CNS barrier breakdown and motor neuron degeneration in mice

Science Translational Medicine(2024)10.1126/scitranslmed.adk1358

N/A

0DataRank · unranked

26 citations

Anna M. Bagnell, Jonathan Alevy, Elvia Mena Avila, Ljubica Mihaljević, Pamela C. Saavedra-Rivera +12 more

Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microglia

Nature Communications(2024)10.1038/s41467-024-46695-w

N/A

0DataRank · unranked

23 citations

Jonathan Jung, Del Hayden Gadd, Michelle Mosqueda, Jianjun Zhong, Shankaracharya +19 more

Improving laboratory animal genetic reporting: LAG-R guidelines

Nature Communications(2024)10.1038/s41467-024-49439-y

N/A

0DataRank · unranked

18 citations

James M. Amos-Landgraf, Fernando Benavides, Marie‐Christine Birling, Steve D. M. Brown, Elizabeth C. Bryda +49 more

Impaired axon initial segment structure and function in a model of ARHGEF9 developmental and epileptic encephalopathy

Proceedings of the National Academy of Sciences(2024)10.1073/pnas.2400709121

N/A

0DataRank · unranked

4 citations

Damian J. Williams, Jia Jie Teoh, Divyalakshmi Soundararajan, Aamir Zuberi, Cathleen Lutz +3 more

Characterization of Collaborative Cross mouse founder strain CAST/EiJ as a novel model for lethal COVID-19

Scientific Reports(2024)10.1038/s41598-024-77087-1

N/A

0DataRank · unranked

3 citations

Debra K. Duso, Naga Rama Kothapalli, Tricia Hart, Sean Casey, Tres Cookenham +19 more

Hematopoietic stem cell gene therapy improves outcomes in a clinically relevant mouse model of multiple sulfatase deficiency

Molecular Therapy(2024)10.1016/j.ymthe.2024.08.015

N/A

0DataRank · unranked

3 citations

Lucas Tricoli, Xinying Hong, Parith Wongkittichote, Carlo Castruccio Castracani, Amaliris Guerra +11 more

Valine and Inflammation Drive Epilepsy in a Mouse Model of ECHS1 Deficiency

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.06.13.598697

N/A

0DataRank · unranked

4 citations

Aamir Zuberi, Xiaorong Fu, Shawn C. Burgess, Cathleen Lutz, Rachel M. Bailey +1 more

Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy

eLife(2024)10.7554/elife.91204

N/A

0DataRank · unranked

3 citations

Emma C. Thompson, Anuraag Madabushi, Kristen Park, Heun Soh, Nissi Varghese +20 more

Characterization of Collaborative Cross mouse founder strain CAST/EiJ as a novel model for lethal COVID-19

Research Square(2024)10.21203/rs.3.rs-4675061/v1

N/A

0DataRank · unranked

1 citations

Debra K. Duso, Naga Rama Kothapalli, Tricia Hart, Sean Casey, Tres Cookenham +18 more

Association of cerebellar inflammation and neurodegeneration in a novel spinocerebellar ataxia type 13 mouse model

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.10.28.620701

N/A

0DataRank · unranked

1 citations

Jennifer White, Swati Khare, Michael Wu, Aamir Zuberi, Ming Gao +6 more

Alternating hemiplegia of childhood associated mutations in Atp1a3 reveal diverse neurological alterations in mice

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.12.24.630241

N/A

0DataRank · unranked

1 citations

Georgii Krivoshein, Scott I. Adamson, Elena Arystarkhova, Laura Anderson, John Szwec +16 more

Reviewer #1 (Public Review): Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy

(2024)10.7554/elife.91204.1.sa2

N/A

0DataRank · unranked

0 citations

Emma C. Thompson, Anuraag Madabushi, Heun Soh, Nissi Varghese, Carlos G. Vanoye +20 more

Hematopoietic stem cell gene therapy improves outcomes in a clinically relevant mouse model of Multiple Sulfatase Deficiency

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.03.08.584099

N/A

0DataRank · unranked

0 citations

Lucas Tricoli, Xinying Hong, Parith Wongkittichote, Carlo Castruccio Castracani, Amaliris Guerra +11 more

Bone marrow transplantation increases sulfatase activity in somatic tissues in a multiple sulfatase deficiency mouse model

Communications Medicine(2024)10.1038/s43856-024-00648-y

N/A

0DataRank · unranked

0 citations

Vi Pham, Somdatta Ray, Pierre-Alexandre Piec, Jennifer D. Ryan, Timothy Billings +6 more

Patient-Specific In Vivo Gene Editing to Treat a Rare Genetic Disease

New England Journal of Medicine(2025)10.1056/nejmoa2504747

N/A

0DataRank · unranked

294 citations

Sarah Grandinette, Xiao Wang, Taylor R. Hudson, Kevin Briseno, Anne Marie Berry +40 more

In vivo prime editing rescues alternating hemiplegia of childhood in mice

Cell(2025)10.1016/j.cell.2025.06.038

N/A

0DataRank · unranked

33 citations

Markus Terrey, Holt A. Sakai, Christine Q. Simmons, Elena Arystarkhova, Natalia S. Morsci +14 more

Amyotrophic lateral sclerosis and frontotemporal dementia mutation reduces endothelial TDP-43 and causes blood-brain barrier defects

Science Advances(2025)10.1126/sciadv.ads0505

N/A

0DataRank · unranked

15 citations

Amy L. Kimble, Emily N. Burrage, Stephen B. Helming, Jordan D. Tyburski, Nathan K. Leclair +10 more

Genetic Deletion of Sarm1 in Mouse Models of Three Neurological Diseases

Journal of the Peripheral Nervous System(2025)10.1111/jns.70052

N/A

0DataRank · unranked

3 citations

Markus Terrey, Maximiliano Presa, Jennifer Ryan, Sara Perkins, Vicki Kennedy +3 more

Preclinical use of a clinically-relevant scAAV9/SUMF1 vector for the treatment of multiple sulfatase deficiency

Communications Medicine(2025)10.1038/s43856-025-00734-9

N/A

0DataRank · unranked

2 citations

Rachel M. Bailey, Somdatta Ray, Lauren Bailey, Saurabh Tata, Tara Murphy +5 more

Synaptic dysregulation in a mouse model of GRIN2D developmental and epileptic encephalopathy

Brain(2025)10.1093/brain/awaf125

N/A

0DataRank · unranked

5 citations

Jane Simko, Chad R. Camp, Christine J. Liu, Wanqi Wang, Damian J. Williams +23 more

Development of an AAV-based gene therapy for the ocular phenotype of Friedreich’s ataxia

Molecular Therapy(2025)10.1016/j.ymthe.2025.10.048

N/A

0DataRank · unranked

1 citations

Siddhant Gupte, Emily Xu, Kaitlyn R. Calabro, Hannah Friend, Sean M. Crosson +10 more

Content and Performance of the MiniMUGA Genotyping Array: A New Tool To Improve Rigor and Reproducibility in Mouse Research

Genetics(2020)10.1534/genetics.120.303596

N/A

0DataRank · unranked

112 citations

Matthew W Blanchard, Ralph S. Baric, Timothy A. Bell, Jennifer Brennan, Gudrun A. Brockmann +64 more

In utero rescue of neurological dysfunction in a mouse model of Wiedemann-Steiner syndrome

JCI Insight(2025)10.1172/jci.insight.187039

N/A

0DataRank · unranked

2 citations

Kimberley Jade Anderson, Katrín Möller, Stefán Pétursson, Andrew Brinn, Katheryn P. Franklin +7 more

The Loss of TBK1 Kinase Activity in Motor Neurons or in All Cell Types Differentially Impacts ALS Disease Progression in SOD1 Mice

Neuron(2020)10.1016/j.neuron.2020.03.005

N/A

0DataRank · unranked

109 citations

Esther Kaunga, Junqiang Ye, Daniele Canzio, Sean O’Keeffe, Noam D. Rudnick +4 more

Reduced GABAergic Neuron Excitability, Altered Synaptic Connectivity, and Seizures in a KCNT1 Gain-of-Function Mouse Model of Childhood Epilepsy

Cell Reports(2020)10.1016/j.celrep.2020.108303

N/A

0DataRank · unranked

91 citations

Sophie Colombo, William F. Tobin, Sabrina Petri, Erin R. Cullen, Soledad Domínguez +13 more

Modelling and treating GRIN2A developmental and epileptic encephalopathy in mice

Brain(2020)10.1093/brain/awaa147

N/A

0DataRank · unranked

83 citations

Christopher D. Bostick, Heather E. Olson, Jurrian Peters, Chad R. Camp, Daniel Krizay +21 more

Loss of TMEM106B leads to myelination deficits: implications for frontotemporal dementia treatment strategies

Brain(2020)10.1093/brain/awaa141

N/A

0DataRank · unranked

79 citations

Alexandra M. Nicholson, Yingxue Ren, Mieu Brooks, Peizhou Jiang, Aamir Zuberi +17 more

Regulation of BMP4/Dpp retrotranslocation and signaling by deglycosylation

eLife(2020)10.7554/elife.55596

N/A

0DataRank · unranked

51 citations

Joshua Adams, Shinya Matsuda, Maximiliano Presa, Ashutosh Pandey, Seung Yeop Han +9 more

Mitochondrial damage and senescence phenotype of cells derived from a novel frataxin G127V point mutation mouse model of Friedreich's ataxia

Disease Models & Mechanisms(2020)10.1242/dmm.045229

N/A

0DataRank · unranked

17 citations

Balu K. Chacko, Robbie L. Conley, Xiaosen Ouyang, Jianhua Zhang, Victor Darley‐Usmar +5 more

Dominant mutations of the Notch ligand Jagged1 cause peripheral neuropathy

Journal of Clinical Investigation(2020)10.1172/jci128152

N/A

0DataRank · unranked

24 citations

William W. Motley, Janel O. Johnson, William H. Aisenberg, Katherine Marshall, Katy Barwick +16 more

The paradoxical effects of K + channel gain-of-function are mediated by GABAergic neuron hypoexcitability and hyperconnectivity

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.03.05.978841

N/A

0DataRank · unranked

2 citations

Sophie Colombo, William F. Tobin, Sabrina Petri, Erin R. Cullen, Soledad Domínguez +13 more

A Drosophila natural variation screen identifies NKCC1 as a substrate of NGLY1 deglycosylation and a modifier of NGLY1 deficiency

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.04.13.039651

N/A

0DataRank · unranked

1 citations

Katie G Owings, Emily Coelho, Gaëlle Mercenne, John M. Pleinis, Aamir Zuberi +6 more

The NIH Somatic Cell Genome Editing program

Nature(2021)10.1038/s41586-021-03191-1

N/A

0DataRank · unranked

132 citations

Erik J. Sontheimer, Philip J. Brooks, Melinda R. Dwinell, Charles A. Gersbach, David R. Liu +70 more

Cathleen Lutz

Indexed papers

Top data-sharing exemplar

Papers