Susan Zeesman

1.9k total citations
19 papers, 608 citations indexed

About

Susan Zeesman is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Susan Zeesman has authored 19 papers receiving a total of 608 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 8 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Susan Zeesman's work include Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genomics and Rare Diseases (4 papers). Susan Zeesman is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genomics and Rare Diseases (4 papers). Susan Zeesman collaborates with scholars based in Canada, United States and France. Susan Zeesman's co-authors include Małgorzata J.M. Nowaczyk, Donald T. Whelan, Éléonore Eymard-Pierre, John M. Opitz, Anne Fogli, Charles R. Scriver, Pierre Labauge, Raphael Schiffmann, Carol L. Clow and Odile Boespflug‐Tanguy and has published in prestigious journals such as The American Journal of Human Genetics, The Journal of Pediatrics and Genetics in Medicine.

In The Last Decade

Susan Zeesman

18 papers receiving 553 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Susan Zeesman Canada 12 315 284 77 55 44 19 608
Pietro Palumbo Italy 15 314 1.0× 325 1.1× 61 0.8× 38 0.7× 21 0.5× 64 620
Damien Lederer Belgium 13 359 1.1× 518 1.8× 58 0.8× 53 1.0× 58 1.3× 25 771
Veronica J. Peschansky United States 9 663 2.1× 188 0.7× 39 0.5× 83 1.5× 32 0.7× 11 914
Maria Francesca Bedeschi Italy 16 264 0.8× 353 1.2× 212 2.8× 59 1.1× 53 1.2× 64 811
Kate Pope Australia 17 567 1.8× 392 1.4× 96 1.2× 31 0.6× 98 2.2× 28 867
Jan E. Dumon Belgium 14 498 1.6× 240 0.8× 90 1.2× 140 2.5× 42 1.0× 31 944
Purita Ramos United States 13 465 1.5× 371 1.3× 32 0.4× 49 0.9× 34 0.8× 14 880
Jeffrey C. Murray United States 14 209 0.7× 231 0.8× 60 0.8× 33 0.6× 11 0.3× 21 461
Nancy Detich Canada 7 834 2.6× 224 0.8× 169 2.2× 49 0.9× 29 0.7× 7 994
Gordana Raca United States 12 421 1.3× 235 0.8× 22 0.3× 29 0.5× 131 3.0× 28 667

Countries citing papers authored by Susan Zeesman

Since Specialization
Citations

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

Fields of papers citing papers by Susan Zeesman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Susan Zeesman

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

All Works

19 of 19 papers shown
1.
Tan, Christopher, Scott Topper, Daniela del Gaudio, et al.. (2015). Characterization of patients referred for non‐specific intellectual disability testing: the importance of autosomal genes for diagnosis. Clinical Genetics. 89(4). 478–483. 11 indexed citations
2.
Zeesman, Susan, M. Elizabeth McCready, Bekim Sadiković, & Małgorzata J.M. Nowaczyk. (2014). Prader–Willi syndrome and Tay–Sachs disease in association with mixed maternal uniparental isodisomy and heterodisomy 15 in a girl who also had isochromosome Xq. American Journal of Medical Genetics Part A. 167(1). 180–184. 18 indexed citations
3.
Speevak, Marsha, et al.. (2013). Further evidence that a 100 Kb critical region is responsible for developmental delay, seizures, and dysmorphic features in 1q43q44 deletion patients. American Journal of Medical Genetics Part A. 161(4). 913–915. 3 indexed citations
4.
Dauber, Andrew, Christelle Golzio, Francine M. Jodelka, et al.. (2013). SCRIB and PUF60 Are Primary Drivers of the Multisystemic Phenotypes of the 8q24.3 Copy-Number Variant. The American Journal of Human Genetics. 93(5). 798–811. 58 indexed citations
5.
Wang, David, Susan Zeesman, Mark A. Tarnopolsky, & Małgorzata J.M. Nowaczyk. (2013). Duplication of AKT3 as a cause of macrocephaly in duplication 1q43q44. American Journal of Medical Genetics Part A. 161(8). 2016–2019. 41 indexed citations
6.
Thompson, Brandi, Susan Zeesman, Ute Moog, et al.. (2013). Deletion of MAP2K2/MEK2: a novel mechanism for a RASopathy?. Clinical Genetics. 85(2). 138–146. 22 indexed citations
7.
Zeesman, Susan, Susanne Kjærgaard, Hanne Hove, et al.. (2012). Microdeletion in distal 17p13.1: A recognizable phenotype with microcephaly, distinctive facial features, and intellectual disability. American Journal of Medical Genetics Part A. 158A(8). 1832–1836. 9 indexed citations
8.
Zeesman, Susan, Małgorzata J.M. Nowaczyk, Ikuko Teshima, et al.. (2006). Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2. American Journal of Medical Genetics Part A. 140A(5). 509–514. 97 indexed citations
9.
Nowaczyk, Małgorzata J.M., Susan Zeesman, John S. Waye, & James D. Douketis. (2004). Incidence of Smith-Lemli-Opitz syndrome in Canada: Results of three-year population surveillance. The Journal of Pediatrics. 145(4). 530–535. 25 indexed citations
10.
Zeesman, Susan, Lonnie Zwaigenbaum, Donald T. Whelan, et al.. (2004). Paternal transmission of fragile X syndrome. American Journal of Medical Genetics Part A. 129A(2). 184–189. 35 indexed citations
11.
Potter, Murray, Susan Zeesman, Keiko Kobayashi, et al.. (2004). Pregnancy in a healthy woman with untreated citrullinemia. American Journal of Medical Genetics Part A. 129A(1). 77–82. 10 indexed citations
12.
Fogli, Anne, Diana Rodriguez, Éléonore Eymard-Pierre, et al.. (2003). Ovarian Failure Related to Eukaryotic Initiation Factor 2B Mutations. The American Journal of Human Genetics. 72(6). 1544–1550. 133 indexed citations
13.
Nowaczyk, Małgorzata J.M., Susan Zeesman, Donald T. Whelan, Victoria Wright, & Sally Feather. (2003). Oral‐facial‐digital syndrome VII is oral‐facial‐digital syndrome I: A clarification. American Journal of Medical Genetics Part A. 123A(2). 179–182. 9 indexed citations
14.
Nowaczyk, Małgorzata J.M., Susan Zeesman, April Kam, et al.. (2003). Boy with 47,XXY,del(15)(q11.2q13) karyotype and Prader–Willi syndrome: A new case and review of the literature. American Journal of Medical Genetics Part A. 125A(1). 73–76. 20 indexed citations
15.
Zeesman, Susan, Nancy Carson, & Donald T. Whelan. (2002). Paternal transmission of the congenital form of myotonic dystrophy type 1: A new case and review of the literature. American Journal of Medical Genetics. 107(3). 222–226. 25 indexed citations
16.
McGowan‐Jordan, Jean, Susan Zeesman, Donald T. Whelan, et al.. (2000). Detection of a de novo mutation in a family with SMA Type I: The importance of dosage testing. Genetics in Medicine. 2(1). 106–106.
17.
Rc, Polomeno, et al.. (1987). Autosomal recessive Duane's retraction syndrome.. PubMed. 22(7). 384–6. 8 indexed citations
18.
Rc, Polomeno, et al.. (1987). Norrie's disease in a French-Canadian kindred: attempt to detect carriers by DNA analysis.. PubMed. 22(1). 21–3. 5 indexed citations
19.
Zeesman, Susan, Carol L. Clow, Lola Cartier, et al.. (1984). A private view of heterozygosity: Eight‐year follow‐up study on carriers of the Tay‐Sachs gene detected by high school screening in montreal. American Journal of Medical Genetics. 18(4). 769–778. 79 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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