Cheryl Cytrynbaum

7.8k total citations
36 papers, 991 citations indexed

About

Cheryl Cytrynbaum is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Cheryl Cytrynbaum has authored 36 papers receiving a total of 991 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 21 papers in Genetics and 10 papers in Cognitive Neuroscience. Recurrent topics in Cheryl Cytrynbaum's work include Congenital heart defects research (9 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Autism Spectrum Disorder Research (9 papers). Cheryl Cytrynbaum is often cited by papers focused on Congenital heart defects research (9 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Autism Spectrum Disorder Research (9 papers). Cheryl Cytrynbaum collaborates with scholars based in Canada, United States and Belgium. Cheryl Cytrynbaum's co-authors include Rosanna Weksberg, Stephen W. Scherer, Sanaa Choufani, Russell Schachar, Andrea Shugar, Leona Fishman, Ikuko Teshima, Jacqueline Siegel‐Bartelt, Paul Arnold and Cheryl Shuman and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

Cheryl Cytrynbaum

32 papers receiving 950 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 Cytrynbaum Canada 16 636 435 207 149 126 36 991
Paula Goldenberg United States 11 571 0.9× 307 0.7× 370 1.8× 173 1.2× 76 0.6× 24 957
Karlene Coleman United States 13 643 1.0× 330 0.8× 422 2.0× 263 1.8× 106 0.8× 19 873
Julie S. Cohen United States 22 617 1.0× 578 1.3× 84 0.4× 78 0.5× 76 0.6× 44 1.4k
Oana Caluseriu Canada 14 583 0.9× 389 0.9× 208 1.0× 138 0.9× 67 0.5× 37 876
Nathalie Van der Aa Belgium 19 412 0.6× 388 0.9× 98 0.5× 99 0.7× 92 0.7× 26 809
Géraldine Viot France 21 674 1.1× 647 1.5× 121 0.6× 109 0.7× 41 0.3× 56 1.4k
Sophie Dahoun Switzerland 14 371 0.6× 271 0.6× 104 0.5× 113 0.8× 64 0.5× 26 629
Shay Ben‐Shachar Israel 18 592 0.9× 700 1.6× 103 0.5× 46 0.3× 238 1.9× 41 1.0k
Theresa A. Grebe United States 16 449 0.7× 458 1.1× 36 0.2× 71 0.5× 102 0.8× 34 879
Mei Baker United States 20 418 0.7× 620 1.4× 154 0.7× 327 2.2× 285 2.3× 58 1.4k

Countries citing papers authored by Cheryl Cytrynbaum

Since Specialization
Citations

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

Fields of papers citing papers by Cheryl Cytrynbaum

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cheryl Cytrynbaum

This figure shows the co-authorship network connecting the top 25 collaborators of Cheryl Cytrynbaum. A scholar is included among the top collaborators of Cheryl Cytrynbaum 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 Cytrynbaum. Cheryl Cytrynbaum 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
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Awamleh, Zain, Sanaa Choufani, Cheryl Cytrynbaum, et al.. (2022). ANKRD11 pathogenic variants and 16q24.3 microdeletions share an altered DNA methylation signature in patients with KBG syndrome. Human Molecular Genetics. 32(9). 1429–1438. 7 indexed citations
4.
Chater‐Diehl, Eric, Sarah J. Goodman, Cheryl Cytrynbaum, et al.. (2021). Anatomy of DNA methylation signatures: Emerging insights and applications. The American Journal of Human Genetics. 108(8). 1359–1366. 29 indexed citations
5.
Chan, Ada J. S., Cheryl Cytrynbaum, Ny Hoang, et al.. (2019). Expanding the neurodevelopmental phenotypes of individuals with de novo KMT2A variants. npj Genomic Medicine. 4(1). 9–9. 29 indexed citations
6.
Butcher, Darci T., Andrei L. Turinsky, Cheryl Cytrynbaum, et al.. (2019). Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants. Clinical Epigenetics. 11(1). 103–103. 43 indexed citations
7.
Walker, Susan, Matthew J. Gazzellone, Barbara Kellam, et al.. (2018). Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesity. European Journal of Human Genetics. 26(11). 1588–1596. 19 indexed citations
8.
Hoang, Ny, Cheryl Cytrynbaum, & Stephen W. Scherer. (2017). Communicating complex genomic information: A counselling approach derived from research experience with Autism Spectrum Disorder. Patient Education and Counseling. 101(2). 352–361. 26 indexed citations
9.
Cytrynbaum, Cheryl, Karen Chong, Vickie Hannig, et al.. (2016). Genomic imbalance in the centromeric 11p15 imprinting center in three families: Further evidence of a role for IC2 as a cause of Russell–Silver syndrome. American Journal of Medical Genetics Part A. 170(10). 2731–2739. 14 indexed citations
10.
Shugar, Andrea, et al.. (2015). An increased prevalence of thyroid disease in children with 22q11.2 deletion syndrome. American Journal of Medical Genetics Part A. 167(7). 1560–1564. 15 indexed citations
11.
Fung, Wai Lun Alan, Nancy J. Butcher, Gregory Costain, et al.. (2015). Practical guidelines for managing adults with 22q11.2 deletion syndrome. Genetics in Medicine. 17(8). 599–609. 194 indexed citations
12.
Inbar‐Feigenberg, Michal, Sanaa Choufani, Cheryl Cytrynbaum, et al.. (2012). Mosaicism for genome‐wide paternal uniparental disomy with features of multiple imprinting disorders: Diagnostic and management issues. American Journal of Medical Genetics Part A. 161(1). 13–20. 46 indexed citations
13.
Baskin, Berivan, Adam C. Smith, Andrea Shugar, et al.. (2007). Molecular diagnosis of 22q11.2 deletion and duplication by multiplex ligation dependent probe amplification. American Journal of Medical Genetics Part A. 143A(24). 2924–2930. 39 indexed citations
14.
Zampino, Giuseppe, Francesca Pantaleoni, Claudio Carta, et al.. (2006). Diversity, parental germline origin, and phenotypic spectrum of de novoHRASmissense changes in Costello syndrome. Human Mutation. 28(3). 265–272. 99 indexed citations
15.
White, Susan M., J. M. Graham, Bronwyn Kerr, et al.. (2005). The adult phenotype in Costello syndrome. American Journal of Medical Genetics Part A. 136A(2). 128–135. 60 indexed citations
16.
Cytrynbaum, Cheryl, et al.. (2005). Advances in overgrowth syndromes: clinical classification to molecular delineation in Sotos syndrome and Beckwith-Wiedemann syndrome. Current Opinion in Pediatrics. 17(6). 740–746. 12 indexed citations
17.
Graham, John M., Briedgeen Kerr, Karen W. Gripp, et al.. (2005). Adult phenotype in Costello syndrome (Am J Med Genet 136A: 128–135, 2005). American Journal of Medical Genetics Part A. 139A(1). 55–55. 1 indexed citations
18.
Hopyan, Talar, Maureen Dennis, Rosanna Weksberg, & Cheryl Cytrynbaum. (2001). Music Skills and the Expressive Interpretation of Music in Children with Williams-Beuren Syndrome: Pitch, Rhythm, Melodic Imagery, Phrasing, and Musical Affect. Child Neuropsychology. 7(1). 42–53. 52 indexed citations
19.
Arnold, Paul, Jacqueline Siegel‐Bartelt, Cheryl Cytrynbaum, Ikuko Teshima, & Russell Schachar. (2001). Velo‐cardio‐facial syndrome: Implications of microdeletion 22q11 for schizophrenia and mood disorders. American Journal of Medical Genetics. 105(4). 354–362. 75 indexed citations
20.
Metcalfe, Kay, Leslie Smoot, Pascal McKeown, et al.. (2000). Elastin: mutational spectrum in supravalvular aortic stenosis. European Journal of Human Genetics. 8(12). 955–963. 110 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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