M. Ryan Corces

18.7k total citations · 8 hit papers
42 papers, 6.9k citations indexed

About

M. Ryan Corces is a scholar working on Molecular Biology, Hematology and Cancer Research. According to data from OpenAlex, M. Ryan Corces has authored 42 papers receiving a total of 6.9k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 18 papers in Hematology and 16 papers in Cancer Research. Recurrent topics in M. Ryan Corces's work include Acute Myeloid Leukemia Research (18 papers), Cancer Genomics and Diagnostics (14 papers) and Single-cell and spatial transcriptomics (9 papers). M. Ryan Corces is often cited by papers focused on Acute Myeloid Leukemia Research (18 papers), Cancer Genomics and Diagnostics (14 papers) and Single-cell and spatial transcriptomics (9 papers). M. Ryan Corces collaborates with scholars based in United States, India and Germany. M. Ryan Corces's co-authors include Ravindra Majeti, Howard Y. Chang, William J. Greenleaf, Irving L. Weissman, Wan‐Jen Hong, Bruno C. Medeiros, Jeffrey M. Granja, Ryan A. Flynn, Steven M. Chan and Jason D. Buenrostro and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

M. Ryan Corces

39 papers receiving 6.8k citations

Hit Papers

5 papers align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A long noncoding RNA maintains active chromatin to coordinate homeotic gene expression

2011 1.6k citations M. Ryan Corces, Ryan A. Flynn et al. Nature profile →
Lineage-specific and single-cell chromatin accessibility charts human hematopoiesis and leukemia evolution

2016 656 citations M. Ryan Corces, Jason D. Buenrostro et al. Nature Genetics profile →
ArchR is a scalable software package for integrative single-cell chromatin accessibility analysis

2021 561 citations Jeffrey M. Granja, M. Ryan Corces et al. Nature Genetics profile →
Clonal Evolution of Preleukemic Hematopoietic Stem Cells Precedes Human Acute Myeloid Leukemia

2012 522 citations M. Ryan Corces, Stephen R. Quake et al. profile →
Preleukemic mutations in human acute myeloid leukemia affect epigenetic regulators and persist in remission

2014 494 citations M. Ryan Corces, Wan‐Jen Hong et al. profile →
Isocitrate dehydrogenase 1 and 2 mutations induce BCL-2 dependence in acute myeloid leukemia

2015 418 citations Steven M. Chan, Danièl Thomas et al. Nature Medicine profile →
Integrated Single-Cell Analysis Maps the Continuous Regulatory Landscape of Human Hematopoietic Differentiation

2018 397 citations Jason D. Buenrostro, M. Ryan Corces et al. profile →
Chromatin accessibility profiling by ATAC-seq

2022 240 citations Fiorella C. Grandi, Hailey Modi et al. Nature Protocols profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
M. Ryan Corces United States	28	5.1k	2.4k	1.8k	909	525	42	6.9k
Dirk Heckl Germany	21	5.6k 1.1×	650 0.3×	1.2k 0.6×	872 1.0×	464 0.9×	48	7.0k
Stephen M. Jane Australia	43	4.1k 0.8×	508 0.2×	787 0.4×	1.0k 1.1×	770 1.5×	148	6.2k
Naoki Takeda Japan	38	4.8k 0.9×	656 0.3×	424 0.2×	936 1.0×	260 0.5×	97	7.4k
Peter Laslo United States	17	7.4k 1.4×	1.3k 0.6×	558 0.3×	2.0k 2.2×	219 0.4×	20	9.9k
H. Leighton Grimes United States	51	4.4k 0.9×	1.1k 0.5×	1.6k 0.9×	3.0k 3.3×	483 0.9×	141	8.3k
Beijing Wu United States	10	4.8k 0.9×	1.0k 0.4×	340 0.2×	1.1k 1.2×	133 0.3×	10	5.8k
Marella de Bruijn United Kingdom	37	3.6k 0.7×	443 0.2×	1.9k 1.1×	2.9k 3.2×	628 1.2×	67	7.2k
Malek Faham United States	27	1.5k 0.3×	748 0.3×	682 0.4×	706 0.8×	435 0.8×	92	4.2k
Elena Vigorito United Kingdom	33	3.4k 0.7×	2.6k 1.1×	292 0.2×	2.1k 2.3×	355 0.7×	55	5.6k
Lidia Larizza Italy	43	3.7k 0.7×	573 0.2×	578 0.3×	577 0.6×	413 0.8×	271	6.3k

Countries citing papers authored by M. Ryan Corces

Since Specialization

Citations

This map shows the geographic impact of M. Ryan Corces's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by M. Ryan Corces with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Ryan Corces more than expected).

Fields of papers citing papers by M. Ryan Corces

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. Ryan Corces. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by M. Ryan Corces. The network helps show where M. Ryan Corces may publish in the future.

Co-authorship network of co-authors of M. Ryan Corces

This figure shows the co-authorship network connecting the top 25 collaborators of M. Ryan Corces. A scholar is included among the top collaborators of M. Ryan Corces based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with M. Ryan Corces. M. Ryan Corces is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Liu, Hao, Zhirui Hu, Shahram Oveisgharan, et al.. (2025). Human brain vascular multi-omics elucidates disease-risk associations. Neuron. 113(19). 3143–3161.e5.

Hasegawa, Kazuteru, Yang Zhao, Alina Garbuzov, et al.. (2024). Clonal inactivation of TERT impairs stem cell competition. Nature. 632(8023). 201–208. 6 indexed citations

Azizi, Armon, Caleb A. Lareau, Asiri Ediriwickrema, et al.. (2024). Convergent epigenetic evolution drives relapse in acute myeloid leukemia. eLife. 13. 14 indexed citations

Phongpreecha, Thanaphong, Fiorella C. Grandi, Lei Xue, et al.. (2023). Whole genome deconvolution unveils Alzheimer’s resilient epigenetic signature. Nature Communications. 14(1). 4947–4947. 13 indexed citations

Grandi, Fiorella C., Hailey Modi, Lucas Kampman, & M. Ryan Corces. (2022). Chromatin accessibility profiling by ATAC-seq. Nature Protocols. 17(6). 1518–1552. 240 indexed citations breakdown →

Corces, M. Ryan, et al.. (2022). Deep learning approaches for noncoding variant prioritization in neurodegenerative diseases. Frontiers in Aging Neuroscience. 14. 1027224–1027224. 7 indexed citations

Granja, Jeffrey M., M. Ryan Corces, Sarah E. Pierce, et al.. (2021). ArchR is a scalable software package for integrative single-cell chromatin accessibility analysis. Nature Genetics. 53(3). 403–411. 561 indexed citations breakdown →

Holden, Stephanie S., Fiorella C. Grandi, Bryan Higashikubo, et al.. (2021). Complement factor C1q mediates sleep spindle loss and epileptic spikes after mild brain injury. Science. 373(6560). eabj2685–eabj2685. 73 indexed citations

Romine, Kyle A., Tamilla Nechiporuk, Daniel Bottomly, et al.. (2021). Monocytic Differentiation and AHR Signaling as Primary Nodes of BET Inhibitor Response in Acute Myeloid Leukemia. Blood Cancer Discovery. 2(5). 518–531. 22 indexed citations

10.

Smith, Jason P., M. Ryan Corces, Jin Xu, et al.. (2021). PEPATAC: an optimized pipeline for ATAC-seq data analysis with serial alignments. NAR Genomics and Bioinformatics. 3(4). lqab101–lqab101. 37 indexed citations

11.

Pierce, Sarah E., Jeffrey M. Granja, M. Ryan Corces, et al.. (2021). LKB1 inactivation modulates chromatin accessibility to drive metastatic progression. Nature Cell Biology. 23(8). 915–924. 34 indexed citations

12.

Corces, M. Ryan, Anna Shcherbina, Soumya Kundu, et al.. (2020). Single-cell epigenomic analyses implicate candidate causal variants at inherited risk loci for Alzheimer’s and Parkinson’s diseases. Nature Genetics. 52(11). 1158–1168. 198 indexed citations

13.

Mumbach, Maxwell R., Jeffrey M. Granja, Ryan A. Flynn, et al.. (2019). HiChIRP reveals RNA-associated chromosome conformation. Nature Methods. 16(6). 489–492. 64 indexed citations

14.

Xu, Jin, Ulrike Litzenburger, Yanyan Qi, et al.. (2019). Single-cell lineage tracing by endogenous mutations enriched in transposase accessible mitochondrial DNA. eLife. 8. 95 indexed citations

15.

Mumbach, Maxwell R., Jeffrey M. Granja, Ryan A. Flynn, et al.. (2019). HiChIRP: RNA-centric chromatin conformation. Protocol Exchange. 1 indexed citations

16.

McKeown, Michael R., M. Ryan Corces, Matthew L. Eaton, et al.. (2017). Superenhancer Analysis Defines Novel Epigenomic Subtypes of Non-APL AML, Including an RARα Dependency Targetable by SY-1425, a Potent and Selective RARα Agonist. Cancer Discovery. 7(10). 1136–1153. 89 indexed citations

17.

Wapinski, Orly L., Qian Yi Lee, Albert C. Chen, et al.. (2017). Rapid Chromatin Switch in the Direct Reprogramming of Fibroblasts to Neurons. Cell Reports. 20(13). 3236–3247. 95 indexed citations

18.

Chao, Mark P., Andrew J. Gentles, Feng Lan, et al.. (2017). Human AML-iPSCs Reacquire Leukemic Properties after Differentiation and Model Clonal Variation of Disease. Cell stem cell. 20(3). 329–344.e7. 90 indexed citations

19.

Chan, Steven M., Danièl Thomas, M. Ryan Corces, et al.. (2015). Isocitrate dehydrogenase 1 and 2 mutations induce BCL-2 dependence in acute myeloid leukemia. Nature Medicine. 21(2). 178–184. 418 indexed citations breakdown →

20.

Mazumdar, Claire, Ying Shen, Feifei Zhao, et al.. (2015). Leukemia-Associated Cohesin Mutants Dominantly Enforce Stem Cell Programs and Impair Human Hematopoietic Progenitor Differentiation. Cell stem cell. 17(6). 675–688. 141 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact