Maria Celeste M. Ramirez

1.2k total citations
12 papers, 572 citations indexed

About

Maria Celeste M. Ramirez is a scholar working on Molecular Biology, Virology and Genetics. According to data from OpenAlex, Maria Celeste M. Ramirez has authored 12 papers receiving a total of 572 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Virology and 3 papers in Genetics. Recurrent topics in Maria Celeste M. Ramirez's work include Bacillus and Francisella bacterial research (6 papers), Poxvirus research and outbreaks (4 papers) and Rabies epidemiology and control (3 papers). Maria Celeste M. Ramirez is often cited by papers focused on Bacillus and Francisella bacterial research (6 papers), Poxvirus research and outbreaks (4 papers) and Rabies epidemiology and control (3 papers). Maria Celeste M. Ramirez collaborates with scholars based in United States, Switzerland and Germany. Maria Celeste M. Ramirez's co-authors include John A. Martignetti, Analisa DiFeo, Oonagh Dowling, Goutham Narla, Marc Glucksman, Luisa Bonafé, Joseph A. Madri, Valerie Grum‐Tokars, Mone Zaidi and Etsuko Abe and has published in prestigious journals such as PEDIATRICS, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Maria Celeste M. Ramirez

12 papers receiving 562 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Maria Celeste M. Ramirez United States	11	333	107	101	95	82	12	572
Jason G. Cyster United States	6	217 0.7×	40 0.4×	73 0.7×	32 0.3×	455 5.5×	6	1.1k
Luciano Castiello United States	17	270 0.8×	55 0.5×	73 0.7×	23 0.2×	302 3.7×	30	842
F. Michael Pope United Kingdom	13	300 0.9×	48 0.4×	466 4.6×	21 0.2×	72 0.9×	32	805
Pierre Rollini Switzerland	16	285 0.9×	72 0.7×	223 2.2×	26 0.3×	63 0.8×	22	960
Patricia Klinger Germany	11	202 0.6×	76 0.7×	74 0.7×	58 0.6×	77 0.9×	16	531
Dan P. Hartmann United States	10	134 0.4×	61 0.6×	63 0.6×	32 0.3×	186 2.3×	12	543
Yoshiaki Sohma Japan	12	359 1.1×	21 0.2×	55 0.5×	34 0.4×	147 1.8×	18	1.6k
Gilles Marodon France	21	212 0.6×	33 0.3×	240 2.4×	101 1.1×	215 2.6×	43	1.3k
Stéphanie Fabre France	13	485 1.5×	71 0.7×	82 0.8×	26 0.3×	247 3.0×	22	1.2k
Mario Pujato United States	11	250 0.8×	55 0.5×	86 0.9×	30 0.3×	111 1.4×	20	594

Countries citing papers authored by Maria Celeste M. Ramirez

Since Specialization

Citations

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

Fields of papers citing papers by Maria Celeste M. Ramirez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maria Celeste M. Ramirez. 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 Maria Celeste M. Ramirez. The network helps show where Maria Celeste M. Ramirez may publish in the future.

Co-authorship network of co-authors of Maria Celeste M. Ramirez

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

All Works

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12 of 12 papers shown

Camacho‐Vanegas, Olga, Sandra Catalina Camacho, Jacob E. Till, et al.. (2012). Primate Genome Gain and Loss: A Bone Dysplasia, Muscular Dystrophy, and Bone Cancer Syndrome Resulting from Mutated Retroviral-Derived MTAP Transcripts. The American Journal of Human Genetics. 90(4). 614–627. 23 indexed citations

Varón, Daniel, David Loewenstein, Elizabeth Potter, et al.. (2011). Minimal Atrophy of the Entorhinal Cortex and Hippocampus: Progression of Cognitive Impairment. Dementia and Geriatric Cognitive Disorders. 31(4). 276–283. 31 indexed citations

Lausch, Ekkehart, Nicolas Guex, Laurence Abrami, et al.. (2011). Hyaline Fibromatosis Syndrome inducing mutations in the ectodomain of anthrax toxin receptor 2 can be rescued by proteasome inhibitors. EMBO Molecular Medicine. 3(4). 208–221. 44 indexed citations

Radbill, Brian, Ritu Gupta, Maria Celeste M. Ramirez, et al.. (2010). Loss of Matrix Metalloproteinase-2 Amplifies Murine Toxin-Induced Liver Fibrosis by Upregulating Collagen I Expression. Digestive Diseases and Sciences. 56(2). 406–416. 63 indexed citations

Abrami, Laurence, et al.. (2009). Systemic hyalinosis mutations in the CMG2 ectodomain leading to loss of function through retention in the endoplasmic reticulum. Human Mutation. 30(4). 583–589. 23 indexed citations

Chen, Elaine, Maria Celeste M. Ramirez, Valerie Grum‐Tokars, et al.. (2008). Infantile systemic hyalinosis: Case report and review of the literature. Journal of the American Academy of Dermatology. 58(2). 303–307. 25 indexed citations

Antaya, Richard J., Mariana M. Cajaiba, Joseph A. Madri, et al.. (2007). Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis Overlap Associated With a Novel Mutation in Capillary Morphogenesis Protein-2 Gene. American Journal of Dermatopathology. 29(1). 99–103. 19 indexed citations

Phadke, Shubha R., Maria Celeste M. Ramirez, Analisa DiFeo, John A. Martignetti, & Katta M. Girisha. (2007). Torg–Winchester syndrome: lack of efficacy of pamidronate therapy. Clinical Dysmorphology. 16(2). 95–100. 8 indexed citations

Mosig, Rebecca, Oonagh Dowling, Analisa DiFeo, et al.. (2007). Loss of MMP-2 disrupts skeletal and craniofacial development and results in decreased bone mineralization, joint erosion and defects in osteoblast and osteoclast growth. Human Molecular Genetics. 16(9). 1113–1123. 172 indexed citations

10.

Shieh, Joseph T.C., John A. Martignetti, Maria Celeste M. Ramirez, et al.. (2006). Systemic Hyalinosis: A Distinctive Early Childhood–Onset Disorder Characterized by Mutations in the Anthrax Toxin Receptor 2 Gene (ANTRX2). PEDIATRICS. 118(5). e1485–e1492. 20 indexed citations

11.

Bishop, David F., Annika Johansson, Robert Phelps, et al.. (2006). Uroporphyrinogen III Synthase Knock-In Mice Have the Human Congenital Erythropoietic Porphyria Phenotype, Including the Characteristic Light-Induced Cutaneous Lesions. The American Journal of Human Genetics. 78(4). 645–658. 17 indexed citations

12.

Dowling, Oonagh, Analisa DiFeo, Maria Celeste M. Ramirez, et al.. (2003). Mutations in Capillary Morphogenesis Gene-2 Result in the Allelic Disorders Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis. The American Journal of Human Genetics. 73(4). 957–966. 127 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.

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