Kathryn Roeder

Biochemistry, 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 4%percentile

0.765Author DataRank

Indexed papers

4in 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 4 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.

Cross-ancestry atlas of gene, isoform, and splicing regulation in the developing human brain

Science(2024)10.1126/science.adh0829

Top 26%

0.765DataRank

Top 26%50 citations

Michael Margolis, Rujia Dai, Pan Zhang, Pawel F. Przytycki, Daniel Vo +95 more

Papers

Driven by 24 papers — median percentile 74. Top paper: “Discovery of target genes and pathways at GWAS loci by pooled single-cell CRISPR screens”.

Discovery of target genes and pathways at GWAS loci by pooled single-cell CRISPR screens

Science(2023)10.1126/science.adh7699

N/A

5.2DataRank · unranked

207 citations

Christina M. Caragine, Zharko Daniloski, Júlia Domingo, Timothy Barry, Lu Lu +11 more

Functional impact of global rare copy number variation in autism spectrum disorders

Nature(2010)10.1038/nature09146

N/A

1.1DataRank · unranked

2044 citations

Alistair T. Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan +204 more

Patterns and rates of exonic de novo mutations in autism spectrum disorders

Nature(2012)10.1038/nature11011

N/A

1.1DataRank · unranked

1794 citations

Yan Kou, Li Liu, Avi Ma’ayan, Kaitlin E. Samocha, Aniko Sabo +60 more

A framework for the interpretation of de novo mutation in human disease

Nature Genetics(2014)10.1038/ng.3050

N/A

1.1DataRank · unranked

1119 citations

Elise B Robinson, Stephan J. Sanders, Christine Stevens, Aniko Sabo, Lauren M. McGrath +25 more

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

Nature Genetics(2022)10.1038/s41588-022-01104-0

N/A

0.969DataRank · unranked

638 citations

F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong +112 more

APOE and TREM2 regulate amyloid-responsive microglia in Alzheimer’s disease

Acta Neuropathologica(2020)10.1007/s00401-020-02200-3

N/A

0.847DataRank · unranked

283 citations

Kui Wang, Gang Hu, Xuran Wang, Zhen Miao, Joshua A. Azevedo +7 more

Cross-ancestry atlas of gene, isoform, and splicing regulation in the developing human brain

Science(2024)10.1126/science.adh0829

Top 26%

0.765DataRank

Top 26%50 citations

Michael Margolis, Rujia Dai, Pan Zhang, Pawel F. Przytycki, Daniel Vo +95 more

Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

10.1101/2021.12.20.21267194

N/A

0.538DataRank · unranked

35 citations

F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong +60 more

Spatiotemporal and genetic regulation of A-to-I editing throughout human brain development

Cell Reports(2022)10.1016/j.celrep.2022.111585

N/A

0.520DataRank · unranked

31 citations

Xuanjia Fan, Laura Sloofman, Lindsay Liang, Enrico Mossotto, Kendall Moore +11 more

Neurobiological Clusters Are Associated With Trajectories of Overall Psychopathology in Youth

Biological Psychiatry Cognitive Neuroscience and Neuroimaging(2023)10.1016/j.bpsc.2023.04.007

N/A

0.333DataRank · unranked

5 citations

Rebecca A. Hayes, Kathryn Roeder, Maria Jalbrzikowski, Catherine Wang

The genetic architecture of obsessive-compulsive disorder: alleles across the frequency spectrum contribute liability to OCD

medRxiv10.1101/2021.01.26.21250409

N/A

0.233DataRank · unranked

3 citations

Lambertus Klei, Manuel Mattheisen, Matthew W. Halvorsen, Abraham Reichenberg, Kathryn Roeder +15 more

Cell Type Hierarchy Reconstruction via Reconciliation of Multi-resolution Cluster Tree

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.02.06.430067

N/A

0DataRank · unranked

7 citations

Brie Wamsley, Andrew Elkins, Daniel Geschwind, Yuting Wei, Kathryn Roeder +1 more

Gradient-based sparse principal component analysis with extensions to online learning

Biometrika(2022)10.1093/biomet/asac041

N/A

0DataRank · unranked

9 citations

Jing Lei, Kathryn Roeder, Yixuan Qiu

Cell type hierarchy reconstruction via reconciliation of multi-resolution cluster tree

Nucleic Acids Research(2021)10.1093/nar/gkab481

N/A

0DataRank · unranked

24 citations

Brie Wamsley, Andrew Elkins, Daniel H. Geschwind, Yuting Wei, Kathryn Roeder +1 more

Delineating Additional Risk Factors

View(2023)10.7551/mitpress/15380.003.0006

N/A

0DataRank · unranked

0 citations

Joshua A. Gordon, Till F. M. Andlauer, Lukoye Atwoli, Na Cai, Thomas Lehner +3 more

Bayesian estimation of cell type–specific gene expression with prior derived from single-cell data

Genome Research(2021)10.1101/gr.268722.120

N/A

0DataRank · unranked

115 citations

Kathryn Roeder, Bernie Devlin, Jiebiao Wang

Robust differential expression testing for single-cell CRISPR screens at low multiplicity of infection

Genome biology(2024)10.1186/s13059-024-03254-2

N/A

0DataRank · unranked

23 citations

Kaishu Mason, Kathryn Roeder, Eugene Katsevich, Timothy Barry

Exponential family measurement error models for single-cell CRISPR screens

Biostatistics(2024)10.1093/biostatistics/kxae010

N/A

0DataRank · unranked

12 citations

Kathryn Roeder, Eugene Katsevich, Timothy Barry

Evaluating and improving health equity and fairness of polygenic scores

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100280

N/A

0DataRank · unranked

3 citations

Geyu Zhou, Lambertus Klei, Peng Liu, Alexandra Chouldechova, Hongyu Zhao +4 more

Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populations

medRxiv(2025)10.1101/2024.12.27.24319460

N/A

0DataRank · unranked

3 citations

Seulgi Jung, F. Kyle Satterstrom, Jack Fu, Tess Levy, Laura G Sloofman +49 more

Gene expression elucidates functional impact of polygenic risk for schizophrenia

UNC Libraries(2020)10.17615/k6wj-s665

N/A

0DataRank · unranked

0 citations

Edwin C. Oh, Eli A. Stahl, David A. Bennett, Nicholas Katsanis, Tymor Hamamsy +53 more

Identification of cell-type-specific marker genes from co-expression patterns in tissue samples

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.07.373043

N/A

0DataRank · unranked

1 citations

Jiebiao Wang, Jing Lei, Kathryn Roeder, Yixuan Qiu

Identification of cell-type-specific marker genes from co-expression patterns in tissue samples

Bioinformatics(2021)10.1093/bioinformatics/btab257

N/A

0DataRank · unranked

36 citations

Jiebiao Wang, Jing Lei, Kathryn Roeder, Yixuan Qiu

Discovery of target genes and pathways of blood trait loci using pooled CRISPR screens and single cell RNA sequencing

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.04.07.438882

N/A

0DataRank · unranked

20 citations

Zharko Daniloski, Júlia Domingo, Timothy Barry, Marcello Ziosi, Dafni A. Glinos +8 more

Kathryn Roeder

Indexed papers

Top data-sharing exemplar

Papers