Patricia Dickson

MedicineChemistryBiochemistry, 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 3%percentile

1.1Author 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.

From karyotypes to precision genomics in 9p deletion and duplication syndromes

Human Genetics and Genomics Advances(2021)10.1016/j.xhgg.2021.100081

Top 24%

0.827DataRank

Top 24%25 citations

Jeffrey K. Ng, Victoria Tate, Ying‐Chen Claire Hou, Yang Cao, Lucinda Antonacci-Fulton +8 more

Papers

Driven by 33 papers — median percentile 59. Top paper: “From karyotypes to precision genomics in 9p deletion and duplication syndromes”.

From karyotypes to precision genomics in 9p deletion and duplication syndromes

Human Genetics and Genomics Advances(2021)10.1016/j.xhgg.2021.100081

Top 24%

0.827DataRank

Top 24%25 citations

Jeffrey K. Ng, Victoria Tate, Ying‐Chen Claire Hou, Yang Cao, Lucinda Antonacci-Fulton +8 more

Neuronal ceroid lipofuscinosis: underlying mechanisms and emerging therapeutic targets

Nature Reviews Neurology(2025)10.1038/s41582-025-01132-4

N/A

0.342DataRank · unranked

8 citations

Keigo Takahashi, Patricia Dickson, Marco Sardiello, Mark S. Sands, Jonathan D. Cooper +1 more

Whole-genome sequencing reveals individual and cohort level insights into chromosome 9p syndromes

Genome Medicine(2025)10.1186/s13073-025-01563-0

Top 58%

0.269DataRank

Top 58%5 citations

Eleanor I. Sams, Rachel Slaugh, Sandra Crocker, Emily Cordova Hurtado, Sophia Tracy +66 more

A phase 1/2 open label nonrandomized clinical trial of intravenous 2-hydroxypropyl-β-cyclodextrin for acute liver disease in infants with Niemann-Pick C1

Molecular Genetics and Metabolism Reports(2021)10.1016/j.ymgmr.2021.100772

N/A

0DataRank · unranked

12 citations

Laura Linneman, Sofia E. Luna, Barbara B. Warner, Yumirle P. Turmelle, Sakil Kulkarni +8 more

Neuropathology of murine Sanfilippo D syndrome

Molecular Genetics and Metabolism(2021)10.1016/j.ymgme.2021.11.010

N/A

0DataRank · unranked

8 citations

Steven Q. Le, Shih‐hsin Kan, Matthew J. Jansen, Patricia Dickson, Jonathan D. Cooper +1 more

Biochemical evaluation of intracerebroventricular rhNAGLU-IGF2 enzyme replacement therapy in neonatal mice with Sanfilippo B syndrome

Molecular Genetics and Metabolism(2021)10.1016/j.ymgme.2021.03.013

N/A

0DataRank · unranked

7 citations

Ibrahim Elsharkawi, Steven Q. Le, Heather Prill, Linley Mangini, Jonathan D. Cooper +5 more

A GH89 human α-N-acetylglucosaminidase (hNAGLU) homologue from gut microbe Bacteroides thetaiotaomicron capable of hydrolyzing heparosan oligosaccharides

AMB Express(2021)10.1186/s13568-021-01253-1

N/A

0DataRank · unranked

1 citations

Xiaoxiao Yang, Hai Yu, Lan Na, Tamashree Ghosh, John B. McArthur +4 more

Recombinant NAGLU-IGF2 prevents physical and neurological disease and improves survival in Sanfilippo B syndrome

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.08.06.455469

N/A

0DataRank · unranked

1 citations

Shih‐hsin Kan, Marie S. Roberts, Joshua T. Dearborn, Rui Wang, Shan Li +15 more

Cross-species efficacy of enzyme replacement therapy for CLN1 disease in mice and sheep

Journal of Clinical Investigation(2022)10.1172/jci163107

N/A

0DataRank · unranked

19 citations

Samantha L. Eaton, Sophie H. Wang, Elizabeth M. Eultgen, Keigo Takahashi, Steven Q. Le +25 more

Diagnostic yield of exome sequencing in congenital vertical talus

European Journal of Medical Genetics(2022)10.1016/j.ejmg.2022.104514

N/A

0DataRank · unranked

6 citations

Wu‐Lin Charng, Patricia Dickson, Matthew B. Dobbs, Christina A. Gurnett, Naeimeh Tayebi

Impaired mitophagy in Sanfilippo a mice causes hypertriglyceridemia and brown adipose tissue activation

Journal of Biological Chemistry(2022)10.1016/j.jbc.2022.102159

N/A

0DataRank · unranked

5 citations

William C. Lamanna, Chrissa A. Dwyer, Daniel R. Sandoval, Ariane Pessentheiner, Norah Al-Azzam +13 more

Brain transplantation of genetically corrected Sanfilippo type B neural stem cells induces partial cross-correction of the disease

Molecular Therapy — Methods & Clinical Development(2022)10.1016/j.omtm.2022.10.013

N/A

0DataRank · unranked

5 citations

Don Clarke, Shih‐hsin Kan, Steven Q. Le, Valentina Sanghez, Anna Luzzi +6 more

Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy

Genetics in Medicine(2023)10.1016/j.gim.2023.100897

N/A

0DataRank · unranked

10 citations

Kelly Schoch, Rebecca Ganetzky, Peter G. Kranz, Neal Sondheimer, M. Louise Markert +92 more

Genomics Research with Undiagnosed Children: Ethical Challenges at the Boundaries of Research and Clinical Care

The Journal of Pediatrics(2023)10.1016/j.jpeds.2023.113537

N/A

0DataRank · unranked

7 citations

Jennifer L. Young, Charis Tang, Kevin Mintz, Sawyer Lucas-Griffin, AudreyStephannie Maghiro +95 more

Intra-Articular AAV9 α-l-Iduronidase Gene Replacement in the Canine Model of Mucopolysaccharidosis Type I

Advances in Cell and Gene Therapy(2023)10.1155/2023/7419017

N/A

0DataRank · unranked

1 citations

Shih‐hsin Kan, Haoyue Zhang, Jodi D. Smith, Afshin Aminian, Elizabeth Snella +5 more

Characterization of early markers of disease progression in the mouse model of Mucopolysaccharidosis IIIB

Research Square(2023)10.21203/rs.3.rs-3381843/v1

N/A

0DataRank · unranked

0 citations

Amanda Titus, Kate M Reardon, Sara Conyers, Joseph D. Dougherty, Xia Ge +5 more

Case report: ocular manifestations of a gain-of-function mutation in CLCN6 , a newly diagnosed disease

Ophthalmic Genetics(2023)10.1080/13816810.2023.2291683

N/A

0DataRank · unranked

0 citations

Sameera Nadimpalli, Sudhi P. Kurup, F. Sessions Cole, Russell Huang, Kathleen Sisco +7 more

Combining angiotensin receptor blockade and enzyme replacement therapy for vascular disease in mucopolysaccharidosis type I

Molecular Genetics and Metabolism Reports(2023)10.1016/j.ymgmr.2023.101036

N/A

0DataRank · unranked

0 citations

Moin Vera, Steven Q. Le, Shih‐hsin Kan, Quang D. Bui, Patricia Dickson +1 more

Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder

Genetics in Medicine(2024)10.1016/j.gim.2024.101166

N/A

0DataRank · unranked

11 citations

Nicole Legro, Dustin Baldridge, Jimann Shin, Angela Bowman, Berrak Uğur +89 more

Characterization of early markers of disease in the mouse model of mucopolysaccharidosis IIIB

Journal of Neurodevelopmental Disorders(2024)10.1186/s11689-024-09534-z

N/A

0DataRank · unranked

3 citations

Amanda Titus, Kate M Reardon, Sara Conyers, Joseph D. Dougherty, Xia Ge +5 more

LUSTR: a new customizable tool for calling genome-wide germline and somatic short tandem repeat variants

BMC Genomics(2024)10.1186/s12864-023-09935-9

N/A

0DataRank · unranked

0 citations

Camilo Toro, David R. Adams, Undiagnosed Diseases Network, Maria T. Acosta, Margaret P Adam +95 more

GABAergic interneurons contribute to the fatal seizure phenotype of CLN2 disease mice

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.03.29.587276

N/A

0DataRank · unranked

0 citations

Nicholas Rensing, Elizabeth M. Eultgen, Sophie H. Wang, Hemanth R. Nelvagal, Steven Q. Le +8 more

Atypical free sialic acid storage disorder associated with tissue specific mosaicism of SLC17A5

Molecular Genetics and Metabolism(2024)10.1016/j.ymgme.2024.109004

N/A

0DataRank · unranked

0 citations

Daniel Wegner, Alexander J. Paul, William Buchser, Robert G. Schmidt, Jai Prakash Sharma +14 more

Gene therapy ameliorates bowel dysmotility and enteric neuron degeneration and extends survival in lysosomal storage disorder mouse models

Science Translational Medicine(2025)10.1126/scitranslmed.adj1445

N/A

0DataRank · unranked

17 citations

Matthew J. Jansen, Letitia L. Williams, Sophie H. Wang, Elizabeth M. Eultgen, Keigo Takahashi +17 more

Protocol to measure endogenous GlcNAc-1-phosphotransferase activity in SK-MEL-30 cells

STAR Protocols(2025)10.1016/j.xpro.2025.103935

N/A

0DataRank · unranked

1 citations

Danielle Henn, Yang Xi, Ming Li, Patricia Dickson, Balraj Doray

Age-sensitive response of systemic AAV-mediated gene therapy in a newly characterized feline model of mucolipidosis II

Molecular Therapy(2025)10.1016/j.ymthe.2025.04.030

N/A

0DataRank · unranked

1 citations

Jessica Bagel, Charles Shyng, Patricia M. O’Donnell, Keiko Miyadera, Jennifer Srnak +10 more

Antibodies to recombinant human alpha-L-iduronidase prevent disease correction in cortical bone in MPS I mice

Molecular Therapy — Methods & Clinical Development(2025)10.1016/j.omtm.2024.101405

N/A

0DataRank · unranked

0 citations

Steven Q. Le, Shih‐hsin Kan, Quang D. Bui, Michael D. Brodt, Patricia Dickson +1 more

Subtle Cellular Phenotypes Inform Pathological and Benign Genetic Mutants in the Iduronidase-2 Sulfatase Gene

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.04.17.649412

N/A

0DataRank · unranked

0 citations

Serena N Elia, Steven Q. Le, Sarah Hurt, Balraj Doray, Jason Waligorski +4 more

DE NOVO VARIANTS IN THE POLY(RC)-BINDING PROTEIN GENE PCBP1 CAUSE A NEURODEVELOPMENTAL DISORDER

medRxiv(2025)10.64898/2025.12.11.25341975

N/A

0DataRank · unranked

0 citations

Thomas Besnard, Florence Desprez, Benjamin Cogné, Laura Do Souto Ferreira, Virginie Vignard +43 more

Phenotypic expansion of KMT2D‐related disorder: Beyond Kabuki syndrome

American Journal of Medical Genetics Part A(2020)10.1002/ajmg.a.61518

N/A

0DataRank · unranked

37 citations

Rebecca C. Spillmann, Daniel Wegner, Jennifer Wambach, Frances V. White, Kathleen Sisco +6 more

Phenotypic expansion of CALM1/2 -associated disorders to include neurologic phenotypes without arrhythmia

Human Molecular Genetics(2025)10.1093/hmg/ddaf195

N/A

0DataRank · unranked

0 citations

Rebecca C. Spillmann, David A. Wenger, Maria Giovanna Tedesco, Malene Brohus, Antonio Novelli +24 more

Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

Genetics in Medicine(2021)10.1038/s41436-021-01232-8

N/A

0DataRank · unranked

49 citations

Rebecca C. Spillmann, Harley T. Kurata, Shawn M. Lamothe, Jasmine Maghera, Rami Abou Jamra +92 more

Mucopolysaccharidoses type I gene therapy

Journal of Inherited Metabolic Disease(2021)10.1002/jimd.12414

N/A

0DataRank · unranked

14 citations

Patricia Dickson, David T. Curiel, Sarah Hurt

Patricia Dickson

Indexed papers

Top data-sharing exemplar

Papers