Rocio Moran

2.0k total citations
27 papers, 854 citations indexed

About

Rocio Moran is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Molecular Biology. According to data from OpenAlex, Rocio Moran has authored 27 papers receiving a total of 854 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 9 papers in Pulmonary and Respiratory Medicine and 7 papers in Molecular Biology. Recurrent topics in Rocio Moran's work include Connective tissue disorders research (7 papers), Aortic Disease and Treatment Approaches (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Rocio Moran is often cited by papers focused on Connective tissue disorders research (7 papers), Aortic Disease and Treatment Approaches (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Rocio Moran collaborates with scholars based in United States, Israel and Australia. Rocio Moran's co-authors include Christina Rigelsky, Carol A. Burke, Brandie Heald, Jill A. Rosenfeld, Elias I. Traboulsi, Qingping Yao, Min Shen, Charis Eng, Neil Friedman and Margaret O’Malley and has published in prestigious journals such as Molecular Cell, Circulation Research and Science Advances.

In The Last Decade

Rocio Moran

26 papers receiving 819 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rocio Moran United States 16 378 324 307 128 117 27 854
Qihua Fu China 18 227 0.6× 595 1.8× 129 0.4× 80 0.6× 75 0.6× 105 922
Xuan Chi United States 14 212 0.6× 969 3.0× 252 0.8× 220 1.7× 53 0.5× 26 1.2k
Olaug K. Rødningen Norway 20 310 0.8× 410 1.3× 110 0.4× 243 1.9× 42 0.4× 50 949
Astrid Golla Germany 15 333 0.9× 317 1.0× 75 0.2× 105 0.8× 117 1.0× 25 806
Yi Dai China 17 142 0.4× 348 1.1× 140 0.5× 37 0.3× 64 0.5× 50 958
Francesca Romana Lepri Italy 18 429 1.1× 608 1.9× 85 0.3× 74 0.6× 58 0.5× 62 972
Inge B. Mathijssen Netherlands 17 192 0.5× 379 1.2× 101 0.3× 143 1.1× 84 0.7× 30 740
Lori A. Reed United States 7 176 0.5× 833 2.6× 229 0.7× 150 1.2× 107 0.9× 8 1.0k
Brad Angle United States 18 527 1.4× 444 1.4× 107 0.3× 191 1.5× 21 0.2× 33 1000
Martine Blayau France 18 404 1.1× 649 2.0× 234 0.8× 118 0.9× 25 0.2× 44 1.1k

Countries citing papers authored by Rocio Moran

Since Specialization
Citations

This map shows the geographic impact of Rocio Moran'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 Rocio Moran with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rocio Moran more than expected).

Fields of papers citing papers by Rocio Moran

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rocio Moran. 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 Rocio Moran. The network helps show where Rocio Moran may publish in the future.

Co-authorship network of co-authors of Rocio Moran

This figure shows the co-authorship network connecting the top 25 collaborators of Rocio Moran. A scholar is included among the top collaborators of Rocio Moran 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 Rocio Moran. Rocio Moran is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Bar, A., Rocio Moran, Netta Mendelson Cohen, et al.. (2025). Pregnancy and postpartum dynamics revealed by millions of lab tests. Science Advances. 11(13). eadr7922–eadr7922. 4 indexed citations
2.
Elitt, Matthew S., Joan Tamburro, Rocio Moran, & Elias I. Traboulsi. (2020). Cutis marmorata telangiectatica congenita: a focus on its diagnosis, ophthalmic anomalies, and possible etiologic factors. Ophthalmic Genetics. 41(2). 101–107. 6 indexed citations
3.
Raina, Rupesh, Rajshekhar Chakraborty, Sandeep Mahajan, et al.. (2020). Renal cystic diseases during the perinatal and neonatal period. Journal of Neonatal-Perinatal Medicine. 14(2). 163–176.
4.
Guo, Dongchuan, Ellen S. Regalado, Limin Gong, et al.. (2016). LOX Mutations Predispose to Thoracic Aortic Aneurysms and Dissections. Circulation Research. 118(6). 928–934. 156 indexed citations
5.
Heald, Brandie, Christina Rigelsky, Rocio Moran, et al.. (2015). Prevalence of thoracic aortopathy in patients with juvenile Polyposis Syndrome‐Hereditary Hemorrhagic Telangiectasia due to SMAD4. American Journal of Medical Genetics Part A. 167(8). 1758–1762. 62 indexed citations
6.
Hao, Yi-Heng, Michael D. Fountain, Klementina Fon Tacer, et al.. (2015). USP7 Acts as a Molecular Rheostat to Promote WASH-Dependent Endosomal Protein Recycling and Is Mutated in a Human Neurodevelopmental Disorder. Molecular Cell. 59(6). 956–969. 149 indexed citations
7.
Moran, Rocio, et al.. (2015). Evolving Approaches to Genetic Evaluation of Specific Cardiomyopathies. Current Heart Failure Reports. 12(6). 339–349. 12 indexed citations
8.
Yao, Qingping, Min Shen, Christine McDonald, et al.. (2015). NOD2-associated autoinflammatory disease: a large cohort study. Lara D. Veeken. 54(10). 1904–1912. 49 indexed citations
9.
Shen, Min, Rocio Moran, Kenneth J. Tomecki, & Qingping Yao. (2015). Granulomatous disease associated with NOD2 sequence variants and familial camptodactyly: An intermediate form of NOD2-associated diseases?. Seminars in Arthritis and Rheumatism. 45(3). 357–360. 15 indexed citations
10.
Greenberg, Roy K., et al.. (2013). Treatment of a patient with vertebral and subclavian aneurysms in the setting of a TGFBR2 mutation. Journal of Vascular Surgery. 57(4). 1116–1119. 4 indexed citations
11.
Brown, Chase R., Roy K. Greenberg, Tara M. Mastracci, et al.. (2013). Family history of aortic disease predicts disease patterns and progression and is a significant influence on management strategies for patients and their relatives. Journal of Vascular Surgery. 58(3). 573–581. 20 indexed citations
12.
Svensson, Lars G., Eugene H. Blackstone, Lillian H. Batizy, et al.. (2012). Midterm Results of David Reimplantation in Patients With Connective Tissue Disorder. The Annals of Thoracic Surgery. 95(2). 555–562. 30 indexed citations
13.
Teng, Kathryn, et al.. (2012). Building an innovative model for personalized healthcare. Cleveland Clinic Journal of Medicine. 79(4 suppl 1). S1–S9. 11 indexed citations
14.
Moran, Rocio, André B. P. Kuilenburg, John A. Duley, et al.. (2012). Phosphoribosylpyrophosphate synthetase superactivity and recurrent infections is caused by a p.Val142Leu mutation in PRS‐I. American Journal of Medical Genetics Part A. 158A(2). 455–460. 22 indexed citations
15.
Mester, Jessica L., Allison Schreiber, & Rocio Moran. (2012). Genetic counselors: Your partners in clinical practice. Cleveland Clinic Journal of Medicine. 79(8). 560–568. 12 indexed citations
16.
Rosenfeld, Jill A., Brad Angle, Valerie Banks, et al.. (2011). Distinctive phenotype in 9 patients with deletion of chromosome 1q24‐q25. American Journal of Medical Genetics Part A. 155(6). 1336–1351. 29 indexed citations
17.
Balasubramanian, Meena, Kath Smith, Lina Basel‐Vanagaite, et al.. (2011). Case series: 2q33.1 microdeletion syndrome—further delineation of the phenotype. Journal of Medical Genetics. 48(5). 290–298. 64 indexed citations
18.
McGowan, Michelle L., Christopher J. Burant, Rocio Moran, & Ruth M. Farrell. (2009). Patient education and informed consent for preimplantation genetic diagnosis: Health literacy for genetics and assisted reproductive technology. Genetics in Medicine. 11(9). 640–645. 11 indexed citations
19.
Heur, Martin, et al.. (2008). The Value of Keratometry and Central Corneal Thickness Measurements in the Clinical Diagnosis of Marfan Syndrome. American Journal of Ophthalmology. 145(6). 997–1001.e1. 48 indexed citations
20.
Heald, Brandie, Rocio Moran, Mira Milas, Carol A. Burke, & Charis Eng. (2007). Familial adenomatous polyposis in a patient with unexplained mental retardation. Nature Clinical Practice Neurology. 3(12). 694–700. 38 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

Breakdown of academic impact, for papers by Qihua Fu Breakdown of academic impact, for papers by Xuan Chi Breakdown of academic impact, for papers by Olaug K. Rødningen Breakdown of academic impact, for papers by Astrid Golla Breakdown of academic impact, for papers by Yi Dai Breakdown of academic impact, for papers by Francesca Romana Lepri Breakdown of academic impact, for papers by Inge B. Mathijssen Breakdown of academic impact, for papers by Lori A. Reed Breakdown of academic impact, for papers by Brad Angle Breakdown of academic impact, for papers by Martine Blayau
Rankless by CCL
2026