Rosario I. Corona

MedicineBiochemistry, 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 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 32 papers. Top paper: “Reprogramming of the FOXA1 cistrome in treatment-emergent neuroendocrine prostate cancer”.

Reprogramming of the FOXA1 cistrome in treatment-emergent neuroendocrine prostate cancer

Nature Communications(2021)10.1038/s41467-021-22139-7

N/A

0.773DataRank · unranked

172 citations

David Y. Takeda, Ji-Heui Seo, Justin H. Hwang, Sheng-Yu Ku, Rand Arafeh +36 more

Molecular Subclasses of Clear Cell Ovarian Carcinoma and Their Impact on Disease Behavior and Outcomes

Clinical Cancer Research(2022)10.1158/1078-0432.ccr-21-3817

N/A

0.697DataRank · unranked

103 citations

Denise Chen, Rosario I. Corona, Zhuxuan Fu, Rajmohan Murali, Martin Köbel +33 more

Large-scale mutational analysis identifies UNC93B1 variants that drive TLR-mediated autoimmunity in mice and humans

The Journal of Experimental Medicine(2024)10.1084/jem.20232005

N/A

0.553DataRank · unranked

39 citations

Julian A. Yano, John Huizar, Leianna C. Slayden, Madeleine A. Weiss, Elizabeth A Turcotte +93 more

Epigenomic charting and functional annotation of risk loci in renal cell carcinoma

Nature Communications(2023)10.1038/s41467-023-35833-5

N/A

0.538DataRank · unranked

35 citations

Sarah Abou Alaiwi, Sylvan C. Baca, Elio Adib, Rosario I. Corona, Ji-Heui Seo +31 more

Single-cell Transcriptomics Identifies Gene Expression Networks Driving Differentiation and Tumorigenesis in the Human Fallopian Tube

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.28.119933

N/A

0.436DataRank · unranked

6 citations

Xianzhi Lin, Forough Abbasi, Robbin Nameki, Marcela Haro, Claire Olingy +13 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

0.360DataRank · unranked

10 citations

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

De novo variants in MRTFB have gain-of-function activity in Drosophila and are associated with a novel neurodevelopmental phenotype with dysmorphic features

Genetics in Medicine(2023)10.1016/j.gim.2023.100833

N/A

0.359DataRank · unranked

6 citations

Jung-Wan Mok, Oguz Kanca, Sharayu Jangam, Cynthia J. Tifft, Ellen F. Macnamara +95 more

De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.06.012

N/A

0.345DataRank · unranked

9 citations

Rossella Venditti, Evangelos A. Theodorou, Lauren C. Briere, Marion Rosello, Alfonsina Tirozzi +94 more

PAX8 orchestrates an angiogenic program through interaction with SOX17

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.09.09.290387

N/A

0.345DataRank · unranked

9 citations

Marilyn A. Mitchell, Cristina Arruza, Priyanka Rawat, Simone Sidoli, Robbin Nameki +11 more

De novo variants in DENND5B cause a neurodevelopmental disorder

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.02.001

N/A

0.345DataRank · unranked

9 citations

Valeria Tomati, Matteo P. Ferla, Mariateresa Lena, Julie S. Cohen, Ali Fatemi +94 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

0.312DataRank · unranked

7 citations

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

Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations

Nature Communications(2025)10.1038/s41467-025-61712-2

N/A

0.269DataRank · unranked

5 citations

Mikhail A. Moldovan, Rebecca Reimers, Daniel Traviglia, Xinyun Li, Danielle Barnum +95 more

De novo variants in RYBP are associated with a severe neurodevelopmental disorder and congenital anomalies

Genetics in Medicine(2025)10.1016/j.gim.2025.101369

N/A

0.269DataRank · unranked

5 citations

Lindsay C. Burrage, Sharayu Jangam, Jill A. Rosenfeld, Sandra von Hardenberg, Anke K. Bergmann +92 more

chromMAGMA: regulatory element-centric interrogation of risk variants

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.01.21.477270

N/A

0.104DataRank · unranked

1 citations

Anamay Shetty, Eileen Dareng, Jonathan P. Tyrer, Xianzhi Lin, Paul D.P. Pharoah +4 more

Enriched phenotypes in rare variant carriers suggest pathogenic mechanisms in rare disease patients

BioData Mining(2025)10.1186/s13040-024-00418-5

N/A

0.104DataRank · unranked

1 citations

Undiagnosed Diseases Network, Maria T. Acosta, David R. Adams, Ben Afzali, Ali Al-Beshri +95 more

DNA binding and transposition activity of the Sleeping Beauty transposase: role of structural stability of the primary DNA-binding domain

Nucleic Acids Research(2024)10.1093/nar/gkae1188

N/A

0.104DataRank · unranked

1 citations

Gage O. Leighton, Chenbo Yan, Maria E. Arango, Janna Lustig, Rosario I. Corona +5 more

Rare germline genetic variation in PAX8 transcription factor binding sites and susceptibility to epithelial ovarian cancer

American Journal of Epidemiology(2024)10.1093/aje/kwae301

N/A

0.104DataRank · unranked

1 citations

Michelle L. Johnson Jones, Ed Dicks, Amber de Vries, Pei-Chen Peng, Kate Lawrenson +8 more

Rewiring of master transcription factor cistromes during high-grade serous ovarian cancer development

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.04.11.536378

N/A

0DataRank · unranked

6 citations

Heidi Chang, Pak Yu, Forough Abbasi, Xianzhi Lin, Jessica Reddy +7 more

Ovarian Cancer Risk Variants Are Enriched in Histotype-Specific Enhancers and Disrupt Transcription Factor Binding Sites

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.08.021

N/A

0DataRank · unranked

27 citations

Pei-Chen Peng, Simon G. Coetzee, Jonathan P. Tyrer, Alberto Luiz P. Reyes, Rosario I. Corona +14 more

Single-cell transcriptomics identifies gene expression networks driving differentiation and tumorigenesis in the human fallopian tube

Cell Reports(2021)10.1016/j.celrep.2021.108978

N/A

0DataRank · unranked

115 citations

Xianzhi Lin, Forough Abbasi, Robbin Nameki, Marcela Haro, Claire Olingy +13 more

A multi-level investigation of the genetic relationship between endometriosis and ovarian cancer histotypes

medRxiv(2021)10.1101/2021.06.28.21259290

N/A

0DataRank · unranked

8 citations

Rosario I. Corona, Pik Fang Kho, Paul D.P. Pharoah, Ji-Heui Seo, Matthew L. Freedman +12 more

A multi-level investigation of the genetic relationship between endometriosis and ovarian cancer histotypes

Cell Reports Medicine(2022)10.1016/j.xcrm.2022.100542

N/A

0DataRank · unranked

60 citations

Rosario I. Corona, Pik Fang Kho, Paul D.P. Pharoah, Ji-Heui Seo, Matthew L. Freedman +12 more

chromMAGMA: regulatory element-centric interrogation of risk variants

Life Science Alliance(2022)10.26508/lsa.202201446

N/A

0DataRank · unranked

3 citations

Anamay Shetty, Eileen Dareng, Jonathan P. Tyrer, Xianzhi Lin, Paul D.P. Pharoah +4 more

Transcription factors in epithelial ovarian cancer: histotype-specific drivers and novel therapeutic targets

Pharmacology & Therapeutics(2020)10.1016/j.pharmthera.2020.107722

N/A

0DataRank · unranked

60 citations

Heidi Chang, Jessica Reddy, Rosario I. Corona, Kate Lawrenson, Robbin Nameki

Rewiring of master transcription factor cistromes during high-grade serous ovarian cancer development

eLife(2023)10.7554/elife.86360.1

N/A

0DataRank · unranked

1 citations

Heidi Chang, Pak Yu, Forough Abbasi, Xianzhi Lin, Jessica Reddy +7 more

Rewiring of master transcription factor cistromes during high-grade serous ovarian cancer development

eLife(2023)10.7554/elife.86360

N/A

0DataRank · unranked

0 citations

Heidi Chang, Pak Yu, Forough Abbasi, Xianzhi Lin, Jessica Reddy +7 more

Genetic variants in DDX53 contribute to autism spectrum disorder associated with the Xp22.11 locus

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.11.003

N/A

0DataRank · unranked

10 citations

Clarrisa A. Bradley, Jennifer Howe, Brett Trost, Nelson Bautista Salazar, Carole Shum +29 more

The spectrum of heart defects in the TRAF7 -related multiple congenital anomalies-intellectual disability syndrome

Proceedings of the National Academy of Sciences(2024)10.1073/pnas.2317601121

N/A

0DataRank · unranked

4 citations

Chiara De Luca, Francesco Brancati, Rossana Sanchez Russo, Dong Li, Elizabeth Bhoj +29 more

Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.02.13.580158

N/A

0DataRank · unranked

3 citations

Mikhail A. Moldovan, Rebecca Reimers, Daniel Traviglia, Xinyun Li, Danielle Barnum +14 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

The Undiagnosed Diseases Network: Characteristics of solvable applicants and diagnostic suggestions for nonaccepted ones

Genetics in Medicine(2024)10.1016/j.gim.2024.101203

N/A

0DataRank · unranked

0 citations

Laura Findley, Weihong Ni, Janet S. Sinsheimer, Francesca Cole, Cecilia Esteves +94 more

DNA binding and transposition activity of the Sleeping Beauty transposase: role of structural stability of the primary DNA-binding domain

UNC Libraries(2024)10.17615/1kzj-5t96

N/A

0DataRank · unranked

0 citations

Jun-tao Guo, Maria E. Arango, Yuri E. Nesmelov, Venkatesh Ranjan, Irina V. Nesmelova +5 more