Maria Blazo

983 total citations
13 papers, 386 citations indexed

About

Maria Blazo is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Maria Blazo has authored 13 papers receiving a total of 386 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Surgery. Recurrent topics in Maria Blazo's work include Connective tissue disorders research (3 papers), Genomics and Rare Diseases (2 papers) and Mitochondrial Function and Pathology (2 papers). Maria Blazo is often cited by papers focused on Connective tissue disorders research (3 papers), Genomics and Rare Diseases (2 papers) and Mitochondrial Function and Pathology (2 papers). Maria Blazo collaborates with scholars based in United States, Netherlands and Mexico. Maria Blazo's co-authors include Richard A. Lewis, Sharon E. Plon, Murali Chintagumpala, Charles W. McCluggage, Fernando Scaglia, Hidehiro Takei, Ross Tonini, Lee‐Jun Wong, Christian P. Schaaf and Brendan Lee and has published in prestigious journals such as SHILAP Revista de lepidopterología, Developmental Biology and Journal of Bone and Mineral Research.

In The Last Decade

Maria Blazo

13 papers receiving 381 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Maria Blazo United States	8	170	140	99	91	89	13	386
Ruth A. Heim United States	13	111 0.7×	155 1.1×	57 0.6×	117 1.3×	50 0.6×	21	643
R. Tsuburaya Japan	9	72 0.4×	180 1.3×	271 2.7×	26 0.3×	141 1.6×	19	434
Yalda Nilipour Iran	12	41 0.2×	219 1.6×	51 0.5×	68 0.7×	90 1.0×	61	426
Akatsuki Kubota Japan	11	80 0.5×	215 1.5×	70 0.7×	26 0.3×	44 0.5×	35	442
Jeffrey B. Sherman United States	8	82 0.5×	128 0.9×	224 2.3×	63 0.7×	247 2.8×	9	446
Yawen Zhao China	10	46 0.3×	135 1.0×	132 1.3×	21 0.2×	76 0.9×	45	331
Peyker Temız Türkiye	9	146 0.9×	185 1.3×	196 2.0×	30 0.3×	64 0.7×	51	497
Teresa Giugliano Italy	12	110 0.6×	189 1.4×	37 0.4×	94 1.0×	47 0.5×	21	339
Osvaldo H. Perurena United States	6	123 0.7×	122 0.9×	356 3.6×	39 0.4×	218 2.4×	8	483
Cecilie F. Rustad Norway	11	170 1.0×	210 1.5×	111 1.1×	116 1.3×	84 0.9×	18	491

Countries citing papers authored by Maria Blazo

Since Specialization

Citations

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

Fields of papers citing papers by Maria Blazo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maria Blazo

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Blazo. A scholar is included among the top collaborators of Maria Blazo 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 Blazo. Maria Blazo 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:

13 of 13 papers shown

Blazo, Maria, et al.. (2016). Long QT Manifested as Giant and Inverted T Waves With a SCN5A Mutation. Journal of Cardiovascular Electrophysiology. 27(12). 1490–1491. 1 indexed citations

Jain, Mahim, et al.. (2015). Catel–Manzke syndrome: Further delineation of the phenotype associated with pathogenic variants in TGDS. SHILAP Revista de lepidopterología. 4. 89–91. 7 indexed citations

Liu, Yang, Yixin Jin, Jieli Li, et al.. (2013). Inactivation of Cdc42 in neural crest cells causes craniofacial and cardiovascular morphogenesis defects. Developmental Biology. 383(2). 239–252. 40 indexed citations

Shapiro, Jay R., Caressa Lietman, Monica Grover, et al.. (2013). Phenotypic Variability of Osteogenesis Imperfecta Type V Caused by an IFITM 5 Mutation. Journal of Bone and Mineral Research. 28(7). 1523–1530. 61 indexed citations

Liu, Yang, Yixin Jin, Jieli Li, et al.. (2013). Abstract 12728: Inactivation of Cdc42 in Neural Crest Cells Causes Craniofacial and Cardiovascular Morphogenesis Defects. 128. 1 indexed citations

Hernández, Andrés, Erwin Brosens, Hitisha P. Zaveri, et al.. (2012). Contribution of LPP copy number and sequence changes to esophageal atresia, tracheoesophageal fistula, and VACTERL association. American Journal of Medical Genetics Part A. 158A(7). 1785–1787. 8 indexed citations

Eble, Tanya N., Sandesh C.S. Nagamani, Luis M. Franco, et al.. (2012). The practice of adult genetics: A 7‐year experience from a single center. American Journal of Medical Genetics Part A. 161(1). 89–93. 5 indexed citations

Schaaf, Christian P., Maria Blazo, Richard A. Lewis, et al.. (2011). Early-onset severe neuromuscular phenotype associated with compound heterozygosity for OPA1 mutations. Molecular Genetics and Metabolism. 103(4). 383–387. 56 indexed citations

Breman, Amy M., Frank J. Probst, Maria Blazo, et al.. (2011). Identification of complex chromosome 18 rearrangements by FISH and array CGH in two patients with apparent isochromosome 18q. American Journal of Medical Genetics Part A. 155(6). 1465–1468. 1 indexed citations

10.

Blazo, Maria, et al.. (2009). Pheochromocytoma and Von Hippel–Lindau in Pregnancy. American Journal of Perinatology. 27(3). 257–263. 7 indexed citations

11.

Brunetti‐Pierri, Nicola, Stephen B. Doty, John Hicks, et al.. (2008). Generalized metabolic bone disease in Neurofibromatosis type I. Molecular Genetics and Metabolism. 94(1). 105–111. 86 indexed citations

12.

Blazo, Maria, et al.. (2004). Outcomes of systematic screening for optic pathway tumors in children with Neurofibromatosis Type 1. American Journal of Medical Genetics Part A. 127A(3). 224–229. 84 indexed citations

13.

Moretti, Paolo, Maria Blazo, Dawna L. Armstrong, et al.. (2003). Spinocerebellar ataxia type 2 (SCA2) presenting with ophthalmoplegia and developmental delay in infancy. American Journal of Medical Genetics Part A. 124A(4). 392–396. 29 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