Cheryl Shuman

5.3k total citations
70 papers, 2.4k citations indexed

About

Cheryl Shuman is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Cheryl Shuman has authored 70 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Genetics, 38 papers in Pediatrics, Perinatology and Child Health and 31 papers in Molecular Biology. Recurrent topics in Cheryl Shuman's work include Prenatal Screening and Diagnostics (29 papers), Genetic Syndromes and Imprinting (25 papers) and Epigenetics and DNA Methylation (19 papers). Cheryl Shuman is often cited by papers focused on Prenatal Screening and Diagnostics (29 papers), Genetic Syndromes and Imprinting (25 papers) and Epigenetics and DNA Methylation (19 papers). Cheryl Shuman collaborates with scholars based in Canada, United States and United Kingdom. Cheryl Shuman's co-authors include Rosanna Weksberg, Sanaa Choufani, J. Bruce Beckwith, David Chitayat, Peter N. Ray, Adam C. Smith, Stephen W. Scherer, Robin Z. Hayeems, Leslie Steele and Jeremy A. Squire and has published in prestigious journals such as SHILAP Revista de lepidopterología, Annals of Internal Medicine and Journal of the American Society of Nephrology.

In The Last Decade

Cheryl Shuman

69 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cheryl Shuman Canada 28 1.6k 1.2k 1.1k 213 180 70 2.4k
Philippe Backeljauw United States 28 1.4k 0.9× 1.2k 1.0× 542 0.5× 171 0.8× 449 2.5× 118 3.2k
Kirstine Stochholm Denmark 30 2.1k 1.3× 1.3k 1.0× 476 0.4× 146 0.7× 515 2.9× 84 3.6k
Anders Bojesen Denmark 28 2.1k 1.3× 1.8k 1.4× 253 0.2× 263 1.2× 201 1.1× 53 3.2k
Gioacchino Scarano Italy 25 838 0.5× 1.2k 1.0× 396 0.4× 154 0.7× 332 1.8× 83 2.3k
Hanan Hamamy Switzerland 23 678 0.4× 509 0.4× 521 0.5× 139 0.7× 149 0.8× 66 2.3k
Howard M. Saal United States 33 2.4k 1.5× 1.3k 1.0× 765 0.7× 395 1.9× 470 2.6× 114 4.2k
Erica A. Eugster United States 34 1.2k 0.8× 1.5k 1.2× 383 0.3× 420 2.0× 499 2.8× 195 4.2k
Wilma Oostdijk Netherlands 36 1.1k 0.7× 1.5k 1.2× 914 0.8× 459 2.2× 287 1.6× 121 3.7k
Joan M. Stoler United States 24 860 0.5× 514 0.4× 538 0.5× 115 0.5× 243 1.4× 63 1.9k
Brian Hon‐Yin Chung Hong Kong 26 1.3k 0.8× 1.0k 0.8× 414 0.4× 100 0.5× 210 1.2× 152 2.7k

Countries citing papers authored by Cheryl Shuman

Since Specialization
Citations

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

Fields of papers citing papers by Cheryl Shuman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cheryl Shuman

This figure shows the co-authorship network connecting the top 25 collaborators of Cheryl Shuman. A scholar is included among the top collaborators of Cheryl Shuman 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 Shuman. Cheryl Shuman 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.
Brzezinski, Jack, Sanaa Choufani, Rodrigo Romao, et al.. (2020). Clinically and biologically relevant subgroups of Wilms tumour defined by genomic and epigenomic analyses. British Journal of Cancer. 124(2). 437–446. 14 indexed citations
2.
Hayeems, Robin Z., Jasmin Bhawra, Kate Tsiplova, et al.. (2017). Care and cost consequences of pediatric whole genome sequencing compared to chromosome microarray. European Journal of Human Genetics. 25(12). 1303–1312. 27 indexed citations
3.
Anderson, James A., M. Stephen Meyn, Cheryl Shuman, et al.. (2016). Parents perspectives on whole genome sequencing for their children: qualified enthusiasm?. Journal of Medical Ethics. 43(8). 535–539. 60 indexed citations
4.
Shuman, Cheryl, et al.. (2015). Experience with genetic counseling: the adolescent perspective. Journal of Genetic Counseling. 25(3). 583–595. 19 indexed citations
5.
Fox, Edward, Jeanna McCuaig, Rochelle Demsky, et al.. (2015). The sooner the better: Genetic testing following ovarian cancer diagnosis. Gynecologic Oncology. 137(3). 423–429. 17 indexed citations
6.
Hayeems, Robin Z., Ny Hoang, Sébastien Chénier, et al.. (2014). Capturing the clinical utility of genomic testing: medical recommendations following pediatric microarray. European Journal of Human Genetics. 23(9). 1135–1141. 17 indexed citations
7.
Choufani, Sanaa, Cheryl Shuman, & Rosanna Weksberg. (2013). Molecular Findings in Beckwith–Wiedemann Syndrome. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 163(2). 131–140. 139 indexed citations
8.
Baskin, Berivan, Sanaa Choufani, Yi‐An Chen, et al.. (2013). High frequency of copy number variations (CNVs) in the chromosome 11p15 region in patients with Beckwith–Wiedemann syndrome. Human Genetics. 133(3). 321–330. 58 indexed citations
9.
Ferreira, José Carlos, Sanaa Choufani, Daria Grafodatskaya, et al.. (2011). WNT2promoter methylation in human placenta is associated with low birthweight percentile in the neonate. Epigenetics. 6(4). 440–449. 46 indexed citations
10.
Carroll, June, Andrea L. Rideout, Brenda J. Wilson, et al.. (2009). Genetic education for primary care providers. Canadian Family Physician. 55(12). 6 indexed citations
11.
Caulfield, Timothy, et al.. (2009). Direct‐to‐consumer genetic testing: good, bad or benign?. Clinical Genetics. 77(2). 101–105. 64 indexed citations
12.
Buchanan, Janet A., Andrew R. Carson, David Chitayat, et al.. (2009). The cycle of genome-directed medicine. Genome Medicine. 1(2). 16–16. 7 indexed citations
13.
Guo, Lin, Sanaa Choufani, José Carlos Ferreira, et al.. (2008). Altered gene expression and methylation of the human chromosome 11 imprinted region in small for gestational age (SGA) placentae. Developmental Biology. 320(1). 79–91. 128 indexed citations
14.
Weksberg, Rosanna, Cheryl Shuman, Louise Wilkins‐Haug, et al.. (2007). Workshop report: evaluation of genetic and epigenetic risks associated with assisted reproductive technologies and infertility. Fertility and Sterility. 88(1). 27–31. 5 indexed citations
15.
Smith, Adam C., Cheryl Shuman, Laurel L. Estabrooks, et al.. (2006). New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndrome. Cytogenetic and Genome Research. 113(1-4). 313–317. 23 indexed citations
16.
Nakabayashi, Kazuhiko, Bridget A. Fernandez, Ikuko Teshima, et al.. (2002). Molecular Genetic Studies of Human Chromosome 7 in Russell–Silver Syndrome. Genomics. 79(2). 186–196. 25 indexed citations
17.
Li, Madeline, Cheryl Shuman, Eva Maria Cutiongco, et al.. (2001). GPC3 mutation analysis in a spectrum of patients with overgrowth expands the phenotype of Simpson-Golabi-Behmel syndrome. American Journal of Medical Genetics. 102(2). 161–168. 87 indexed citations
18.
Smith, Adam C., Jeremy A. Squire, Paul S. Thorner, et al.. (2001). Association of Alveolar Rhabdomyosarcoma with the Beckwith-Wiedemann Syndrome. Pediatric and Developmental Pathology. 4(6). 550–558. 38 indexed citations
19.
Teshima, Ikuko, Erawati V. Bawle, Rosanna Weksberg, et al.. (2000). Analphoid 3qter markers. American Journal of Medical Genetics. 94(2). 113–119. 14 indexed citations
20.
Everman, David B., et al.. (2000). Serum α-fetoprotein levels in Beckwith-Wiedemann syndrome. The Journal of Pediatrics. 137(1). 123–127. 54 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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