Cheryl DeScipio

2.2k total citations
18 papers, 834 citations indexed

About

Cheryl DeScipio is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Cheryl DeScipio has authored 18 papers receiving a total of 834 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Pediatrics, Perinatology and Child Health, 11 papers in Genetics and 8 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Cheryl DeScipio's work include Prenatal Screening and Diagnostics (11 papers), Gestational Trophoblastic Disease Studies (8 papers) and Genomic variations and chromosomal abnormalities (6 papers). Cheryl DeScipio is often cited by papers focused on Prenatal Screening and Diagnostics (11 papers), Gestational Trophoblastic Disease Studies (8 papers) and Genomic variations and chromosomal abnormalities (6 papers). Cheryl DeScipio collaborates with scholars based in United States, Italy and Canada. Cheryl DeScipio's co-authors include Brigitte M. Ronnett, Dinah Yaeger, Ian D. Krantz, Kathleen M. Murphy, Maninder Kaur, Laird G. Jackson, Russell Vang, Marcella Devoto, Jennifer McCallum and Katie Beierl and has published in prestigious journals such as SHILAP Revista de lepidopterología, Diabetes and Annals of the New York Academy of Sciences.

In The Last Decade

Cheryl DeScipio

17 papers receiving 820 citations

Peers

Cheryl DeScipio

PPCH

PHEOH

GENET

SURGE

Manuel Viotti United States

Azzedine Aboura France

Véronique Satre France

Thue Bryndorf Denmark

Koen Theunis Belgium

Daniela Bettio Italy

Yoichi Sekita Japan

Didier Theophile France

David Humpherys United States

Afroditi Mertzanidou Belgium

Manuel Viotti United States

Cheryl DeScipio

609 ×1.5

PPCH

358 ×1.0

PHEOH

720 ×2.1

323 ×1.0

GENET

128 ×1.5

SURGE

Citations per year, relative to Cheryl DeScipio Cheryl DeScipio (= 1×) peers Manuel Viotti

Countries citing papers authored by Cheryl DeScipio

Since Specialization

Citations

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

Fields of papers citing papers by Cheryl DeScipio

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cheryl DeScipio

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

All Works

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18 of 18 papers shown

Murphy, Kathleen M., Cheryl DeScipio, Katie Beierl, et al.. (2015). Invasive Complete Hydatidiform Moles. International Journal of Gynecological Pathology. 35(2). 134–141. 15 indexed citations

Banet, Natalie, Cheryl DeScipio, Kathleen M. Murphy, et al.. (2013). Characteristics of hydatidiform moles: analysis of a prospective series with p57 immunohistochemistry and molecular genotyping. Modern Pathology. 27(2). 238–254. 92 indexed citations

DeScipio, Cheryl, Kathleen M. Murphy, Lisa Haley, et al.. (2013). Characterization of Androgenetic/Biparental Mosaic/Chimeric Conceptions, Including Those With a Molar Component. International Journal of Gynecological Pathology. 32(2). 199–214. 54 indexed citations

Henderson, Lindsay B., et al.. (2013). First Trimester Diagnosis of Holoprosencephaly Secondary to a Ring Chromosome 7. SHILAP Revista de lepidopterología. 2013. 1–3.

Gupta, Mamta, Russell Vang, Anna Yemelyanova, et al.. (2012). Diagnostic Reproducibility of Hydatidiform Moles. The American Journal of Surgical Pathology. 36(12). 1747–1760. 33 indexed citations

Vang, Russell, Mamta Gupta, Anna Yemelyanova, et al.. (2012). Diagnostic Reproducibility of Hydatidiform Moles. The American Journal of Surgical Pathology. 36(3). 443–453. 55 indexed citations

Ronnett, Brigitte M., Cheryl DeScipio, & Kathleen M. Murphy. (2011). Hydatidiform Moles. International Journal of Gynecological Pathology. 0(0). 101–116. 60 indexed citations

Murphy, Kathleen M., et al.. (2011). Tetraploid Partial Hydatidiform Mole. International Journal of Gynecological Pathology. 31(1). 73–79. 21 indexed citations

DeScipio, Cheryl, et al.. (2011). Diandric Triploid Hydatidiform Mole With Loss of Maternal Chromosome 11. The American Journal of Surgical Pathology. 35(10). 1586–1591. 28 indexed citations

10.

DeScipio, Cheryl, Nancy B. Spinner, Maninder Kaur, et al.. (2008). Fine‐mapping subtelomeric deletions and duplications by comparative genomic hybridization in 42 individuals. American Journal of Medical Genetics Part A. 146A(6). 730–739. 32 indexed citations

11.

Blankenhorn, Elizabeth P., et al.. (2007). Refinement of the Iddm4 Diabetes Susceptibility Locus Reveals TCRVβ4 as a Candidate Gene. Annals of the New York Academy of Sciences. 1103(1). 128–131. 11 indexed citations

12.

DeScipio, Cheryl. (2007). The 6p subtelomere deletion syndrome. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 145C(4). 377–382. 36 indexed citations

13.

DeScipio, Cheryl, Lori Schneider, Terri L. Young, et al.. (2005). Subtelomeric deletions of chromosome 6p: Molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher?Schinzel (3C) syndrome. American Journal of Medical Genetics Part A. 134A(1). 3–11. 54 indexed citations

14.

DeScipio, Cheryl, Maninder Kaur, Dinah Yaeger, et al.. (2005). Chromosome rearrangements in Cornelia de Lange syndrome (CdLS): Report of a der(3)t(3;12)(p25.3;p13.3) in two half sibs with features of CdLS and review of reported CdLS cases with chromosome rearrangements. American Journal of Medical Genetics Part A. 137A(3). 276–282. 25 indexed citations

15.

Kaur, Maninder, Cheryl DeScipio, Jennifer McCallum, et al.. (2005). Precocious sister chromatid separation (PSCS) in Cornelia de Lange syndrome. American Journal of Medical Genetics Part A. 138A(1). 27–31. 73 indexed citations

16.

Hornum, Lars, Cheryl DeScipio, Helle Markholst, et al.. (2004). Comparative mapping of rat Iddm4 to segments on HSA7 and MMU6. Mammalian Genome. 15(1). 53–61. 6 indexed citations

17.

Gillis, Lynette A., Jennifer McCallum, Maninder Kaur, et al.. (2004). NIPBL Mutational Analysis in 120 Individuals with Cornelia de Lange Syndrome and Evaluation of Genotype-Phenotype Correlations. The American Journal of Human Genetics. 75(4). 610–623. 213 indexed citations

18.

Mordes, John P., Jean Leif, Stephen J. Novak, et al.. (2002). Theiddm4Locus Segregates With Diabetes Susceptibility in Congenic WF.iddm4Rats. Diabetes. 51(11). 3254–3262. 26 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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