Sherly Pardo

1.2k total citations
8 papers, 187 citations indexed

About

Sherly Pardo is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, Sherly Pardo has authored 8 papers receiving a total of 187 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Pathology and Forensic Medicine and 3 papers in Genetics. Recurrent topics in Sherly Pardo's work include Muscle Physiology and Disorders (3 papers), Genetic factors in colorectal cancer (3 papers) and BRCA gene mutations in cancer (2 papers). Sherly Pardo is often cited by papers focused on Muscle Physiology and Disorders (3 papers), Genetic factors in colorectal cancer (3 papers) and BRCA gene mutations in cancer (2 papers). Sherly Pardo collaborates with scholars based in Puerto Rico, United States and Slovenia. Sherly Pardo's co-authors include Amartya Basu, Donald A. Fischman, Julyann Pérez‐Mayoral, María González‐Pons, Marcia Cruz‐Correa, Julie Dutil, Miguel Echenique, Manisha Balwani, Claude Sansaricq and Kimiyo Raymond and has published in prestigious journals such as Journal of Cell Science, Journal of Inherited Metabolic Disease and American Journal of Medical Genetics Part A.

In The Last Decade

Sherly Pardo

8 papers receiving 186 citations

Peers

Sherly Pardo

MB

GENET

CCM

PFM

ONCOL

Yael Wilnai United States

Stacey Hume Canada

Sahar Elouej Tunisia

Noa Ruhrman‐Shahar Israel

Bo Lv China

Lidia Kasprzak Canada

Pouria Mashouri Canada

Saliha Yılmaz Türkiye

Imma Rost Germany

Nihir Patel United States

Yael Wilnai United States

Sherly Pardo

94 ×1.1

MB

85 ×1.6

GENET

23 ×0.4

CCM

10 ×0.4

PFM

12 ×0.5

ONCOL

Citations per year, relative to Sherly Pardo Sherly Pardo (= 1×) peers Yael Wilnai

Countries citing papers authored by Sherly Pardo

Since Specialization

Citations

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

Fields of papers citing papers by Sherly Pardo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sherly Pardo

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

8 of 8 papers shown

1.

Cruz‐Correa, Marcia, Julyann Pérez‐Mayoral, Julie Dutil, et al.. (2017). Hereditary cancer syndromes in Latino populations: genetic characterization and surveillance guidelines. Hereditary Cancer in Clinical Practice. 15(1). 3–3. 24 indexed citations

2.

Cruz‐Correa, Marcia, Julyann Pérez‐Mayoral, Julie Dutil, et al.. (2016). Clinical Cancer Genetics Disparities among Latinos. Journal of Genetic Counseling. 26(3). 379–386. 40 indexed citations

3.

Conde, José G., et al.. (2016). Prevalence and Genetic Profile of Duchene and Becker Muscular Dystrophy in Puerto Rico. Journal of Neuromuscular Diseases. 3(2). 261–266. 9 indexed citations

4.

Cruz‐Correa, Marcia, Julyann Pérez‐Mayoral, María González‐Pons, et al.. (2015). Clinical characterization and mutation spectrum in Caribbean Hispanic families with Lynch syndrome. Familial Cancer. 14(3). 415–425. 13 indexed citations

5.

Pardo, Sherly, et al.. (2015). Limb-Girdle Muscular Dystrophy Type 2A Resulting From c.C479G and c.G1818A Mutations in the Calpain-3 Gene. Journal of Clinical Neuromuscular Disease. 17(2). 59–62. 1 indexed citations

6.

Pardo, Sherly, Netta M. Blitman, Bokyung Kim Han, et al.. (2007). Multiple hemangiomas in a patient with a t(3q;4p) translocation: An infrequent association with Wolf–Hirschhorn syndrome. American Journal of Medical Genetics Part A. 146A(2). 219–224. 4 indexed citations

7.

Sansaricq, Claude, Sherly Pardo, Manisha Balwani, Marie Grace, & Kimiyo Raymond. (2006). Biochemical and molecular diagnosis of lipoamide dehydrogenase deficiency in a North American Ashkenazi Jewish family. Journal of Inherited Metabolic Disease. 29(1). 203–204. 15 indexed citations

8.

Pardo, Sherly, et al.. (1999). Identification of the A-band localization domain of myosin binding proteins C and H (MyBP-C, MyBP-H) in skeletal muscle. Journal of Cell Science. 112(1). 69–79. 81 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