Xylena Reed

Also affiliated with National Institute of Neurological Disorders and Stroke, Institute on Aging, National Institute on Aging

MedicineNeuroscienceBiochemistry, 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

1.2Author 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.

The Foundational Data Initiative for Parkinson Disease: Enabling efficient translation from genetic maps to mechanism

Cell Genomics(2023)10.1016/j.xgen.2023.100261

Top 17%

1.2DataRank

Top 17%54 citations

Xylena Reed, Vikas Bansal, Elizabeth Hutchins, Melanie M. Cobb, Michelle G. Webb +37 more

Papers

Driven by 28 papers — median percentile 83. Top paper: “Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets”.

Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets

JAMA Neurology(2021)10.1001/jamaneurol.2020.5257

N/A

4.5DataRank · unranked

205 citations

David Zhang, Sebastian Guelfi, Claudia Manzoni, Leon Hubbard, Regina Hertfelder Reynolds +85 more

The Foundational Data Initiative for Parkinson Disease: Enabling efficient translation from genetic maps to mechanism

Cell Genomics(2023)10.1016/j.xgen.2023.100261

Top 17%

1.2DataRank

Top 17%54 citations

Xylena Reed, Vikas Bansal, Elizabeth Hutchins, Melanie M. Cobb, Michelle G. Webb +37 more

Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome

Nature Communications(2021)10.1038/s41467-021-26280-1

N/A

0.808DataRank · unranked

217 citations

Demis A. Kia, Mona M. Almramhi, Sara Bandres-Ciga, Chris Finan, Alastair J. Noyce +170 more

Association of a common genetic variant with Parkinson’s disease is mediated by microglia

Science Translational Medicine(2022)10.1126/scitranslmed.abp8869

N/A

0.688DataRank · unranked

97 citations

Alexandra Beilina, Xylena Reed, Alice Kaganovich, Andrew Singleton, Cornelis Blauwendraat +3 more

Association of a Common Genetic Variant with Parkinson’s Disease is Propagated through Microglia

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.01.15.426824

N/A

0.588DataRank · unranked

10 citations

Alexandra Beilina, Xylena Reed, Andrew Singleton, Cornelis Blauwendraat, J. Raphael Gibbs +2 more

Coding and Noncoding Variation in LRRK2 and Parkinson's Disease Risk

Movement Disorders(2021)10.1002/mds.28787

N/A

0.561DataRank · unranked

41 citations

Xylena Reed, Rebekah G. Langston, Mike A. Nalls, Ziv Gan‐Or, Mark Cookson +4 more

African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1

Nature Structural & Molecular Biology(2024)10.1038/s41594-024-01423-2

N/A

0.425DataRank · unranked

16 citations

Peter Wild Crea, Daniel M. Ramos, Emil K. Gustavsson, Mandy Radefeldt, Andrey Damianov +36 more

An ANXA11 P93S variant dysregulates TDP-43 and causes corticobasal syndrome

Research Square(2023)10.21203/rs.3.rs-3462973/v1

N/A

0.312DataRank · unranked

7 citations

Veronica H. Ryan, James Hawrot, Sydney Lawton, Daniel M. Ramos, Yue Qi +16 more

Human brain single nucleus cell type enrichments in neurodegenerative diseases

Research Square(2023)10.21203/rs.3.rs-3390225/v1

N/A

0.208DataRank · unranked

3 citations

Cory A. Weller, Nicholas L. Johnson, Hampton L. Leonard, Andrew Singleton, Xylena Reed +3 more

Haplotype-Resolved DNA Methylation at the APOE Locus identifies Allele-Specific Epigenetic Signatures Relevant to Alzheimer’s Disease Risk

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.07.01.662592

N/A

0.104DataRank · unranked

1 citations

Melissa Meredith, Abraham Moller, Cory A. Weller, Kensuke Daida, Alexis Ayuketah +18 more

Characterizing a complex CT-rich haplotype in intron 4 of SNCA using large-scale targeted amplicon long-read sequencing

npj Parkinson s Disease(2024)10.1038/s41531-024-00749-4

N/A

0.104DataRank · unranked

1 citations

Kensuke Daida, Francis P. Grenn, Laksh Malik, Abigail Miano‐Burkhardt, Mary B. Makarious +17 more

Genome-wide Association Identifies Novel Etiological Insights Associated with Parkinson’s Disease in African and African Admixed Populations

medRxiv(2023)10.1101/2023.05.05.23289529

N/A

0DataRank · unranked

18 citations

Sara Bandrés‐Ciga, Mary B. Makarious, Oluwadamilola O. Ojo, Peter Wild Crea, Oladunni Abiodun +74 more

An ANXA11 P93S variant dysregulates TDP‐43 and causes corticobasal syndrome

Alzheimer s & Dementia(2024)10.1002/alz.13915

N/A

0DataRank · unranked

18 citations

Veronica H. Ryan, James Hawrot, Sydney Lawton, Daniel M. Ramos, Yue Qi +16 more

A SINE-VNTR-Alu at the LRIG2 locus is associated with proximal and distal gene expression in CRISPR and population models

Scientific Reports(2024)10.1038/s41598-023-50307-w

N/A

0DataRank · unranked

3 citations

Ben Middlehurst, Max A. M. Cadogan, Xylena Reed, Kimberley J. Billingsley, Vivien J. Bubb +2 more

African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1

medRxiv(2024)10.1101/2024.02.20.24302827

N/A

0DataRank · unranked

1 citations

Peter Wild Crea, Daniel M. Ramos, Emil K. Gustavsson, Mandy Radefeldt, Mary B. Makarious +33 more

Characterization of DNA methylation in PBMCs and donor-matched iPSCs shows methylation is reset during stem cell reprogramming

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.12.13.627515

N/A

0DataRank · unranked

1 citations

Cory A. Weller, Sara Sáez-Atiénzar, Alexandra Beilina, Sultana Solaiman, Makayla Portley +10 more

Long-Read epigenetic clocks identify improved brain aging predictions

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.09.30.679553

N/A

0DataRank · unranked

1 citations

Mary B. Makarious, Melissa Meredith, Abraham Moller, Melissa Grant‐Peters, Amy R. Hicks +13 more

Genome‐Wide Analysis of Structural Variants in Parkinson Disease

Annals of Neurology(2023)10.1002/ana.26608

N/A

0DataRank · unranked

37 citations

Jinhui Ding, Pilar Álvarez Jerez, Anastasia Illarionova, Kristin Levine, Francis P. Grenn +35 more

The Parkinson’s Disease GWAS Locus Browser

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.04.01.020404

N/A

0DataRank · unranked

3 citations

Jonggeol J. Kim, Mary B. Makarious, Hirotaka Iwaki, Anastasia Illarionova, Kajsa Brolin +18 more

Generation of fourteen isogenic cell lines for Parkinson’s disease-associated leucine-rich repeat kinase (LRRK2)

Stem Cell Research(2021)10.1016/j.scr.2021.102354

N/A

0DataRank · unranked

19 citations

Rebekah G. Langston, Dorien Rosen, Xylena Reed, Mark Cookson, Aleksandra Beylina

Advancing Personalized Medicine in Common Forms of Parkinson’s Disease through Genetics: Current Therapeutics and the Future of Individualized Management

Journal of Personalized Medicine(2021)10.3390/jpm11030169

N/A

0DataRank · unranked

12 citations

Artur Francisco Schumacher Schuh, Jing Hu, Sara Bandrés‐Ciga, Xylena Reed

Transcriptional signatures in iPSC-derived neurons are reproducible across labs when differentiation protocols are closely matched

Stem Cell Research(2021)10.1016/j.scr.2021.102558

N/A

0DataRank · unranked

10 citations

Melanie M. Cobb, Gaia Skinbinski, Dorien A. Roosen, Alice Kaganovich, Jinhui Ding +3 more

LRRK2 coding variants and the risk of Parkinson’s disease

medRxiv(2021)10.1101/2021.04.22.21255928

N/A

0DataRank · unranked

1 citations

Xylena Reed, Rebekah G. Langston, Mike A. Nalls, Ziv Gan‐Or, Mark Cookson +4 more

Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study

The Lancet Neurology(2023)10.1016/s1474-4422(23)00283-1

N/A

0DataRank · unranked

157 citations

Sara Bandrés‐Ciga, Mary B. Makarious, Oluwadamilola O. Ojo, Peter Wild Crea, Oladunni Abiodun +72 more

Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation

Nature Methods(2023)10.1038/s41592-023-01993-x

N/A

0DataRank · unranked

143 citations

Kimberley J. Billingsley, Mira Mastoras, Melissa Meredith, Jean Monlong, Ryan Lorig-Roach +25 more

Inhibition of p38α MAPK restores neuronal p38γ MAPK and ameliorates synaptic degeneration in a mouse model of DLB/PD

Science Translational Medicine(2023)10.1126/scitranslmed.abq6089

N/A

0DataRank · unranked

40 citations

Changyoun Kim, Somin Kwon, Marcell Szabo, Liam Horan-Portelance, Cody J. Peer +10 more

The Parkinson's Disease Genome‐Wide Association Study Locus Browser

Movement Disorders(2020)10.1002/mds.28197

N/A

0DataRank · unranked

104 citations

Jonggeol J. Kim, Mary B. Makarious, Hirotaka Iwaki, Anastasia Illarionova, Kajsa Brolin +20 more

Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.12.523790

N/A

0DataRank · unranked

31 citations

Kimberley J. Billingsley, Mira Mastoras, Melissa Meredith, Jean Monlong, Ryan Lorig-Roach +25 more

Xylena Reed

Indexed papers

Top data-sharing exemplar

Papers