Stephen B. Montgomery

Biochemistry, 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

51.7Author DataRank

Indexed papers

10in 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 10 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 global reference for human genetic variation

Nature(2015)10.1038/nature15393

Top 1%

10.6DataRank

Top 1%20166 citations

Gonçalo R. Abecasis, Richard M. Durbin, Panagiotis Deloukas, Aravinda Chakravarti, Peter Donnelly +516 more

Papers

Driven by 80 papers — median percentile 95. Top paper: “A global reference for human genetic variation”.

A global reference for human genetic variation

Nature(2015)10.1038/nature15393

Top 1%

10.6DataRank

Top 1%20166 citations

Gonçalo R. Abecasis, Richard M. Durbin, Panagiotis Deloukas, Aravinda Chakravarti, Peter Donnelly +516 more

Cell type–specific genetic regulation of gene expression across human tissues

Science(2020)10.1126/science.aaz8528

N/A

10.3DataRank · unranked

596 citations

François Aguet, Meritxell Oliva, Manuel Muñoz-Aguirre, Silva Kasela, Valentin Wucher +77 more

Genetic effects on gene expression across human tissues

Nature(2017)10.1038/nature24277

Top 1%

10.1DataRank

Top 1%4706 citations

Barbara E. Engelhardt, Stephen B. Montgomery, Sara Mostafavi, Ayellet V. Segrè, Hailei Zhang +227 more

A map of human genome variation from population-scale sequencing

Nature(2010)10.1038/nature09534

Top 2%

9.1DataRank

Top 2%8109 citations

Min Hu, Yuan Chen, Matthew N. Bainbridge, Richard M. Durbin, Si Quang Le +319 more

The impact of sex on gene expression across human tissues

Science(2020)10.1126/science.aba3066

N/A

9.0DataRank · unranked

727 citations

Manuel Muñoz-Aguirre, Sarah Kim-Hellmuth, Valentin Wucher, Ariel DH Gewirtz, Daniel J. Cotter +72 more

Determinants of telomere length across human tissues

Science(2020)10.1126/science.aaz6876

N/A

8.6DataRank · unranked

501 citations

Farzana Jasmine, Lin Chen, Meytal Chernoff, Tong Lin, Dayana Delgado +90 more

The GTEx Consortium atlas of genetic regulatory effects across human tissues

Science(2020)10.1126/science.aaz1776

Top 2%

8.0DataRank

Top 2%5930 citations

Shankara Anand, Kristin G. Ardlie, Stacey Gabriel, Gad Getz, Aaron Graubert +95 more

A Quantitative Proteome Map of the Human Body

Cell(2020)10.1016/j.cell.2020.08.036

Top 4%

5.1DataRank

Top 4%487 citations

Meng Wang, Shin Lin, Ruiqi Jian, Xiao Li, Joanne Chan +95 more

Transcriptomic signatures across human tissues identify functional rare genetic variation

Science(2020)10.1126/science.aaz5900

N/A

5.0DataRank · unranked

166 citations

Benjamin J. Strober, Jonah Einson, Nathan S. Abell, François Aguet, Alvaro N. Barbeira +183 more

Systematic functional regulatory assessment of disease-associated variants

Proceedings of the National Academy of Sciences(2013)10.1073/pnas.1219099110

N/A

3.7DataRank · unranked

95 citations

Joel T. Dudley, Kimberly R. Kukurba, Rong Chen, Atul Janardhan Butte, Stephen B. Montgomery +2 more

Temporal dynamics of the multi-omic response to endurance exercise training

Nature(2024)10.1038/s41586-023-06877-w

Top 7%

3.4DataRank

Top 7%248 citations

Primary authors, Lead Analysts, David Amar, Nicole R. Gay, Pierre M. Jean Beltran +95 more

A vast resource of allelic expression data spanning human tissues

Genome Biology(2020)10.1186/s13059-020-02122-z

Top 8%

2.7DataRank

Top 8%147 citations

François Aguet, Pejman Mohammadi, Kristin G. Ardlie, Anthony Philippakis, Leanne Haggerty +159 more

High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation

Genome Research(2024)10.1101/gr.279273.124

Top 13%

1.7DataRank

Top 13%78 citations

Sophia B Gibson, Nikhita Damaraju, Miranda Pg Zalusky, Kendra Hoekzema, David Twesigomwe +42 more

A lymphocyte chemoaffinity axis for lung, non-intestinal mucosae and CNS

Nature(2024)10.1038/s41586-024-08043-2

N/A

1.1DataRank · unranked

34 citations

Menglan Xiang, Yuhan Bi, Serena Tan, Kevin Brulois, Aiman Ayesha +16 more

A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes

Science(2012)10.1126/science.1215040

N/A

1.1DataRank · unranked

1321 citations

Suganthi Balasubramanian, Michael G. FitzGerald, Ni Huang, James Morris, Fred R. Hirsch +54 more

Organ aging signatures in the plasma proteome track health and disease

Nature(2023)10.1038/s41586-023-06802-1

N/A

0.957DataRank · unranked

588 citations

Jarod Rutledge, Daniel Nachun, Róbert Pálovics, Olamide Abiose, Patricia Moran‐Losada +31 more

Molecular Choreography of Acute Exercise

Cell(2020)10.1016/j.cell.2020.04.043

N/A

0.929DataRank · unranked

488 citations

Si Wu, Kegan Moneghetti, Daniel Hornburg, Sara Ahadi, Ming‐Shian Tsai +27 more

Molecular adaptations in response to exercise training are associated with tissue-specific transcriptomic and epigenomic signatures

Cell Genomics(2024)10.1016/j.xgen.2023.100421

N/A

0.928DataRank · unranked

38 citations

Hanna Pinças, Gregory R. Smith, Elena Zaslavsky, Yongchao Ge, Mary Anne S. Amper +75 more

Single-cell epigenomic analyses implicate candidate causal variants at inherited risk loci for Alzheimer’s and Parkinson’s diseases

Nature Genetics(2020)10.1038/s41588-020-00721-x

N/A

0.895DataRank · unranked

388 citations

Anna Shcherbina, Soumya Kundu, Michael J. Gloudemans, Laure Frésard, Jeffrey M. Granja +13 more

Effect of predicted protein-truncating genetic variants on the human transcriptome

Science(2015)10.1126/science.1261877

N/A

0.877DataRank · unranked

345 citations

Matti Pirinen, Donald F. Conrad, Monkol Lek, Emily K. Tsang, Konrad J. Karczewski +206 more

Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease

Cell(2021)10.1016/j.cell.2021.03.050

N/A

0.804DataRank · unranked

212 citations

Daniel C. Nachun, Nicole M. Ferraro, Michael J. Gloudemans, Abhiram S. Rao, Craig Smail +168 more

Multiple causal variants underlie genetic associations in humans

Science(2022)10.1126/science.abj5117

N/A

0.801DataRank · unranked

208 citations

Marianne K. DeGorter, Michael J. Gloudemans, Emily Greenwald, Kevin S. Smith, Zihuai He +2 more

Impact of admixture and ancestry on eQTL analysis and GWAS colocalization in GTEx

Genome biology(2020)10.1186/s13059-020-02113-0

N/A

0.724DataRank · unranked

124 citations

Michael J. Gloudemans, Margaret L. Antonio, Nathan S. Abell, Brunilda Balliu, YoSon Park +14 more

The Somatic Mosaicism across Human Tissues Network

Nature(2025)10.1038/s41586-025-09096-7

N/A

0.672DataRank · unranked

43 citations

Ji Won Oh, Yujin Angelina Choi, Nam Seop Lim, Boxun Zhao, Adam Voshall +365 more

Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics

Nature Genetics(2021)10.1038/s41588-021-00800-7

N/A

0.650DataRank · unranked

75 citations

Craig Smail, Michael J. Gloudemans, Laure Frésard, David Jakubosky, Matteo D’Antonio +22 more

The mitochondrial multi-omic response to exercise training across rat tissues

Cell Metabolism(2024)10.1016/j.cmet.2023.12.021

N/A

0.650DataRank · unranked

75 citations

Nicole R. Gay, David Jimenez‐Morales, Pierre M. Jean Beltran, Megan E. Ramaker, Archana N. Raja +95 more

TOWARDS TRANSCRIPTOMICS AS A PRIMARY TOOL FOR RARE DISEASE INVESTIGATION

Molecular Case Studies(2022)10.1101/mcs.a006198

N/A

0.553DataRank · unranked

39 citations

Jonathan A. Bernstein, Matthew T. Wheeler, Stephen B. Montgomery

The functional impact of rare variation across the regulatory cascade

Cell Genomics(2023)10.1016/j.xgen.2023.100401

N/A

0.526DataRank · unranked

15 citations

Nicole M. Ferraro, Benjamin J. Strober, François Aguet, Silva Kasela, Marios Arvanitis +33 more

An integrated approach to identify environmental modulators of genetic risk factors for complex traits

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.08.014

N/A

0.524DataRank · unranked

32 citations

Ivan Carcamo‐Orive, Michael J. Gloudemans, Daniel Nachun, Matthew G. Durrant, Steven Gazal +7 more

Integration of rare expression outlier-associated variants improves polygenic risk prediction

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.04.015

N/A

0.524DataRank · unranked

32 citations

Nicole M. Ferraro, Qin Hui, Matthew G. Durrant, Matthew Aguirre, Yosuke Tanigawa +14 more

Transcriptomics and chromatin accessibility in multiple African population samples

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.11.04.564839

Top 38%

0.505DataRank

Top 38%13 citations

Pagé C. Goddard, Emre Karakoç, Soumya Kundu, Stephanie M. Yan, Daniel Nachun +27 more

Methylation differences in Alzheimer’s disease neuropathologic change in the aged human brain

Acta Neuropathologica Communications(2022)10.1186/s40478-022-01470-0

N/A

0.494DataRank · unranked

26 citations

Tiffany Y. Eulalio, Eddie Fox, Koya Yakabi, Syed Bukhari, Claudia H. Kawas +7 more

Molecular Transducers of Physical Activity Consortium (MoTrPAC): human studies design and protocol

Journal of Applied Physiology(2024)10.1152/japplphysiol.00102.2024

Top 40%

0.483DataRank

Top 40%21 citations

John M. Jakicic, Wendy M. Kohrt, Joseph A. Houmard, Michael E. Miller, Shlomit Radom‐Aizik +89 more

Integrative analyses highlight functional regulatory variants associated with neuropsychiatric diseases

Nature Genetics(2023)10.1038/s41588-023-01533-5

N/A

0.470DataRank · unranked

22 citations

David L. Reynolds, Cheen Euong Ang, Yingfei Liu, Yang Zhao, Laura K. Donohue +23 more

Integration of transcriptomics and long-read genomics prioritizes structural variants in rare disease

Genome Research(2025)10.1101/gr.279323.124

N/A

0.425DataRank · unranked

11 citations

Bohan Ni, Chloe Reuter, John E. Gorzynski, Sarah Fazal, Devon Bonner +13 more

GREGoR: accelerating genomics for rare diseases

Nature(2025)10.1038/s41586-025-09613-8

N/A

0.416DataRank · unranked

15 citations

Ben Heavner, Marsha M. Wheeler, Rachel A. Ungar, Jonathan LoTempio, Laurens Wiel +94 more

Single-cell epigenomic identification of inherited risk loci in Alzheimer’s and Parkinson’s disease

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.01.06.896159

N/A

0.406DataRank · unranked

14 citations

Anna Shcherbina, Soumya Kundu, Michael J. Gloudemans, Laure Frésard, Jeffrey M. Granja +12 more

Detection and analysis of complex structural variation in human genomes across populations and in brains of donors with psychiatric disorders

Cell(2024)10.1016/j.cell.2024.09.014

N/A

0.399DataRank · unranked

8 citations

Joseph G. Arthur, Hanmin Guo, Taeyoung Kim, Yi‐Ling Huang, Reenal Pattni +32 more

Functional analysis of cancer-associated germline risk variants

Nature Genetics(2025)10.1038/s41588-024-02070-5

N/A

0.385DataRank · unranked

12 citations

Poornima H. Neela, Suhas Srinivasan, Zurab Siprashvili, Ronald L. Shanderson, Audrey W. Hong +22 more

De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders

medRxiv(2024)10.1101/2024.04.07.24305438

N/A

0.360DataRank · unranked

10 citations

Ruebena Dawes, Hyung Chul Kim, Sarah L. Stenton, Susan Walker, Alicia Ljungdahl +92 more

Integration of transcriptomics and long-read genomics prioritizes structural variants in rare disease

medRxiv(2024)10.1101/2024.03.22.24304565

N/A

0.321DataRank · unranked

5 citations

Bohan Ni, Chloe Reuter, John E. Gorzynski, Sarah Fazal, Devon Bonner +13 more

Integrated single-cell multiome analysis reveals muscle fiber-type gene regulatory circuitry modulated by endurance exercise

Genome Research(2025)10.1101/gr.280051.124

N/A

0.312DataRank · unranked

7 citations

Gregory R. Smith, Zidong Zhang, Xi Chen, Toby L. Chambers, Frederique Ruf-Zamojski +13 more

Integration of genetic colocalizations with physiological and pharmacological perturbations identifies cardiometabolic disease genes

medRxiv(2021)10.1101/2021.09.28.21264208

N/A

0.269DataRank · unranked

5 citations

Brunilda Balliu, Daniel Nachun, Matthew G. Durrant, Erik Ingelsson, Martin Wabitsch +5 more

Beyond the exome: what's next in diagnostic testing for Mendelian conditions

arXiv (Cornell University)(2023)10.48550/arxiv.2301.07363

N/A

0.269DataRank · unranked

5 citations

Chloe Reuter, Shruti Marwaha, Medhat Mahmoud, Michael Duyzend, Hayk Barseghyan +19 more

Integrated single-cell multiome analysis reveals muscle fiber-type gene regulatory circuitry modulated by endurance exercise

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.09.26.558914

N/A

0.269DataRank · unranked

5 citations

Gregory R. Smith, Zidong Zhang, Xi Chen, Toby L. Chambers, Frederique Ruf-Zamojski +13 more

Integration of rare large-effect expression variants improves polygenic risk prediction

medRxiv(2020)10.1101/2020.12.02.20242990

N/A

0.241DataRank · unranked

4 citations

Nicole M. Ferraro, Matthew G. Durrant, Abhiram Rao, Matthew Aguirre, Xin Li +12 more

Chromatin accessibility changes induced by the microbial metabolite butyrate reveal possible mechanisms of anti-cancer effects

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.30.437582

N/A

0.208DataRank · unranked

3 citations

Brayon J. Fremin, Abhiram Rao, Emily S. Cribas, Stephen B. Montgomery, Ami S. Bhatt +1 more

Molecular Choreography of Acute Exercise

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.01.13.905349

N/A

0.165DataRank · unranked

2 citations

Si Wu, Kegan Moneghetti, Daniel Hornburg, Sara Ahadi, Ming‐Shian Tsai +27 more

An integrated approach to identify environmental modulators of genetic risk factors for complex traits

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.02.23.432608

N/A

0.104DataRank · unranked

1 citations

Ivan Carcamo‐Orive, Michael J. Gloudemans, Daniel Nachun, Matthew G. Durrant, Steven Gazal +7 more

Interactions Between Dietary Metabolites and Regulatory Risk Variants for Human Colon Cancer

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.09.05.674475

N/A

0DataRank · unranked

0 citations

Robin M. Meyers, Evin M. Padhi, Laura N. Kellman, Yang Zhao, Soumya Kundu +8 more

Properties of structural variants and short tandem repeats associated with gene expression and complex traits

Nature Communications(2020)10.1038/s41467-020-16482-4

N/A

0DataRank · unranked

138 citations

Matteo D’Antonio, Marc Jan Bonder, Craig Smail, Margaret K. R. Donovan, William W. Greenwald +15 more

Evaluating the Genomic Parameters Governing rAAV-Mediated Homologous Recombination

Molecular Therapy(2020)10.1016/j.ymthe.2020.11.025

N/A

0DataRank · unranked

13 citations

Matthew Tiffany, Nicole M. Ferraro, Nathan S. Abell, Stephen B. Montgomery, Mark A. Kay +1 more

Discovery and quality analysis of a comprehensive set of structural variants and short tandem repeats

Nature Communications(2020)10.1038/s41467-020-16481-5

N/A

0DataRank · unranked

37 citations

Erin N. Smith, Matteo D’Antonio, Marc Jan Bonder, William W. Greenwald, Agnieszka D’Antonio‐Chronowska +14 more

Genome-wide functional screen of 3′UTR variants uncovers causal variants for human disease and evolution

Cell(2021)10.1016/j.cell.2021.08.025

N/A

0DataRank · unranked

188 citations

James R. Xue, Steven K. Reilly, Jacob C. Ulirsch, Kalki Kukreja, Joe R. Davis +11 more

Identification of putative causal loci in whole-genome sequencing data via knockoff statistics

Nature Communications(2021)10.1038/s41467-021-22889-4

N/A

0DataRank · unranked

42 citations

Linxi Liu, Chen Wang, Yann Le Guen, Justin Lee, Stephanie M. Gogarten +8 more

Nonsense-mediated decay is highly stable across individuals and tissues

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.06.008

N/A

0DataRank · unranked

44 citations

Daniel Nachun, Tiffany Y. Eulalio, Nicole M. Ferraro, Craig Smail, Manuel A. Rivas +2 more

Functional and structural analysis of cytokine-selective IL6ST defects that cause recessive hyper-IgE syndrome

Journal of Allergy and Clinical Immunology(2021)10.1016/j.jaci.2021.02.044

N/A

0DataRank · unranked

33 citations

Diane B. Zastrow, Riley D. Metcalfe, Lisa Gartner, Freia Krause, Craig J. Morton +23 more

The role of Sp140 revealed in IgE and mast cell responses in Collaborative Cross mice

JCI Insight(2021)10.1172/jci.insight.146572

N/A

0DataRank · unranked

14 citations

Xin Li, Yuki Nakamura, Danyue Dong, Kaori Mukai, Mindy Tsai +3 more

Multiple Causal Variants Underlie Genetic Associations in Humans

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.05.24.445471

N/A

0DataRank · unranked

12 citations

Marianne K. DeGorter, Michael J. Gloudemans, Emily Greenwald, Kevin S. Smith, Zihuai He +2 more

Nonsense-mediated decay is highly stable across individuals and tissues

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.02.03.429654

N/A

0DataRank · unranked

6 citations

Daniel Nachun, Tiffany Y. Eulalio, Nicole M. Ferraro, Craig Smail, Manuel A. Rivas +2 more

Identification of putative causal loci in whole-genome sequencing data via knockoff statistics

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.08.434451

N/A

0DataRank · unranked

4 citations

Linxi Liu, Chen Wang, Yann Le Guen, Justin Lee, Stephanie M. Gogarten +8 more

Deep learning-assisted genome-wide characterization of massively parallel reporter assays

Nucleic Acids Research(2022)10.1093/nar/gkac990

N/A

0DataRank · unranked

5 citations

Aaron Sossin, Nathan S. Abell, Stephen B. Montgomery, Zihuai He, Fred Lu

Africa-specific human genetic variation near CHD1L associates with HIV-1 load

Nature(2023)10.1038/s41586-023-06370-4

N/A

0DataRank · unranked

27 citations

Immacolata Porreca, Gennaro Iaconis, Hoi Ping Mok, Subhankar Mukhopadhyay, Emre Karakoç +66 more

RNAget: an API to securely retrieve RNA quantifications

Bioinformatics(2023)10.1093/bioinformatics/btad126

N/A

0DataRank · unranked

4 citations

Emilio Palumbo, Jeremy Adams, David Bujold, Guillaume Bourque, Jared L. Nedzel +58 more

The mitochondrial multi-omic response to exercise training across tissues

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.13.523698

N/A

0DataRank · unranked

12 citations

Nicole R. Gay, David Jimenez‐Morales, Pierre M. Jean Beltran, Megan E. Ramaker, Archana N. Raja +24 more

P643: Transcriptome sequencing increases yield of Mendelian disease diagnosis

Genetics in Medicine Open(2023)10.1016/j.gimo.2023.100708

N/A

0DataRank · unranked

0 citations

Rachel Ungar, Pagé C. Goddard, Jennefer N. Kohler, Chloe Reuter, Shruti Marwaha +4 more

RNA Sequencing in Disease Diagnosis

Annual Review of Genomics and Human Genetics(2024)10.1146/annurev-genom-021623-121812

N/A

0DataRank · unranked

29 citations

Stephen B. Montgomery, Craig Smail

Impact of genome build on RNA-seq interpretation and diagnostics

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.05.005

N/A

0DataRank · unranked

13 citations

Pagé C. Goddard, Tanner Jensen, Fabien Degalez, Kevin S. Smith, Christopher Jin +5 more

Impact of genome build on RNA-seq interpretation and diagnostics

medRxiv(2024)10.1101/2024.01.11.24301165

N/A

0DataRank · unranked

0 citations

Pagé C. Goddard, Tanner Jensen, Fabien Degalez, Kevin S. Smith, Christopher Jin +6 more

regionalpcs : improved discovery of DNA methylation associations with complex traits

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.05.01.590171

N/A

0DataRank · unranked

0 citations

Min Sun, Olivier Gevaert, Michael D. Greicius, Thomas J. Montine, Daniel Nachun +2 more

Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa

UNC Libraries(2024)10.17615/k3wp-sy78

N/A

0DataRank · unranked

0 citations

D.N. Cooper, A.P. Reiner, A.P. Morris, Eric Young, Cristina Pomilla +52 more

Transcriptome-wide outlier approach identifies individuals with minor spliceopathies

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.08.018

N/A

0DataRank · unranked

17 citations

Rodrigo Mendez, Rachel A. Ungar, Devon Bonner, Dena R. Matalon, Gabrielle Lemire +19 more

regionalpcs improve discovery of DNA methylation associations with complex traits

Nature Communications(2025)10.1038/s41467-024-55698-6

N/A

0DataRank · unranked

7 citations

Min Sun, Olivier Gevaert, Michael D. Greicius, Thomas J. Montine, Daniel Nachun +2 more

Transcriptomic signatures of rare variant impacts across sex and the X chromosome

Human Genetics and Genomics Advances(2025)10.1016/j.xhgg.2025.100463

N/A

0DataRank · unranked

2 citations

Taibo Li, Nikolai G. Vetr, Nicole Ersaro, Alexis Battle, Stephen B. Montgomery +1 more

Toward optimizing diversifying base editors for high-throughput mutational scanning studies

Nucleic Acids Research(2025)10.1093/nar/gkaf620

N/A

0DataRank · unranked

1 citations

Nathan S. Abell, Amy Li, Aradhana, Josh Tycko, Alisa Truong +3 more

Transcriptome-wide outlier approach identifies individuals with minor spliceopathies

medRxiv(2025)10.1101/2025.01.02.24318941

N/A

0DataRank · unranked

10 citations

Rodrigo Mendez, Rachel A. Ungar, Devon Bonner, Dena R. Matalon, Gabrielle Lemire +20 more

Mapping the regulatory effects of common and rare non-coding variants across cellular and developmental contexts in the brain and heart

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.02.18.638922

N/A

0DataRank · unranked

6 citations

Soumya Kundu, Evin M. Padhi, Salil Deshpande, Austin Wang, E. Robb +9 more

Focus on single gene effects limits discovery and interpretation of complex trait-associated variants

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.06.06.658175

N/A

0DataRank · unranked

1 citations

Tami Gjorgjieva, Stephen B. Montgomery, Kathryn A Lawrence

Functional impact of rare variants and sex across the X-chromosome and autosomes

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.01.23.634570

N/A

0DataRank · unranked

0 citations

Taibo Li, Nikolai G. Vetr, Nicole M. Ferraro, Alexis Battle, Stephen B. Montgomery +1 more

DragonRNA: Generality of DNA-primed RNA-extension activities by DNA-directed RNA polymerases

Nucleic Acids Research(2025)10.1093/nar/gkaf236

N/A

0DataRank · unranked

0 citations

Drew Galls, Joon Park, Nimit Jain, Stephen B. Montgomery, Bijoyita Roy +3 more

Stephen B. Montgomery

Indexed papers

Top data-sharing exemplar

Papers