Nancy J. Mendelsohn

4.8k total citations
51 papers, 2.1k citations indexed

About

Nancy J. Mendelsohn is a scholar working on Physiology, Genetics and Rheumatology. According to data from OpenAlex, Nancy J. Mendelsohn has authored 51 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Physiology, 19 papers in Genetics and 16 papers in Rheumatology. Recurrent topics in Nancy J. Mendelsohn's work include Lysosomal Storage Disorders Research (19 papers), Glycogen Storage Diseases and Myoclonus (11 papers) and Trypanosoma species research and implications (10 papers). Nancy J. Mendelsohn is often cited by papers focused on Lysosomal Storage Disorders Research (19 papers), Glycogen Storage Diseases and Myoclonus (11 papers) and Trypanosoma species research and implications (10 papers). Nancy J. Mendelsohn collaborates with scholars based in United States, Brazil and United Kingdom. Nancy J. Mendelsohn's co-authors include G. Bradley Schaefer, Roberto Giugliani, Simon Jones, Priya S. Kishnani, Paul Harmatz, Mary Ella Pierpont, Amy E. Roberts, Rossella Parini, Barbara K. Burton and Erica Tworog‐Dube and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and The American Journal of Cardiology.

In The Last Decade

Nancy J. Mendelsohn

50 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nancy J. Mendelsohn United States 26 859 651 650 471 422 51 2.1k
Richard P. Morse United States 19 319 0.4× 427 0.7× 679 1.0× 121 0.3× 255 0.6× 36 1.8k
J. Wahlström Sweden 33 556 0.6× 648 1.0× 627 1.0× 76 0.2× 274 0.6× 91 2.6k
Cynthia M. Powell United States 28 1.2k 1.4× 953 1.5× 176 0.3× 299 0.6× 109 0.3× 79 2.5k
Kim L. McBride United States 30 807 0.9× 1.3k 2.0× 266 0.4× 298 0.6× 88 0.2× 108 2.7k
Kenzo Takeshita Japan 21 223 0.3× 433 0.7× 225 0.3× 131 0.3× 121 0.3× 110 1.4k
Julie Hoover‐Fong United States 29 1.3k 1.5× 813 1.2× 174 0.3× 86 0.2× 419 1.0× 95 2.5k
Stephen R. Braddock United States 25 538 0.6× 525 0.8× 199 0.3× 84 0.2× 195 0.5× 71 1.7k
Giovanni Sorge Italy 22 553 0.6× 486 0.7× 207 0.3× 60 0.1× 135 0.3× 75 1.3k
Joan M. Stoler United States 24 860 1.0× 514 0.8× 106 0.2× 115 0.2× 140 0.3× 63 1.9k
Hong Pan China 25 529 0.6× 1.1k 1.7× 182 0.3× 171 0.4× 42 0.1× 123 2.0k

Countries citing papers authored by Nancy J. Mendelsohn

Since Specialization
Citations

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

Fields of papers citing papers by Nancy J. Mendelsohn

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nancy J. Mendelsohn. 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 Nancy J. Mendelsohn. The network helps show where Nancy J. Mendelsohn may publish in the future.

Co-authorship network of co-authors of Nancy J. Mendelsohn

This figure shows the co-authorship network connecting the top 25 collaborators of Nancy J. Mendelsohn. A scholar is included among the top collaborators of Nancy J. Mendelsohn 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 Nancy J. Mendelsohn. Nancy J. Mendelsohn 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.
Fıçıcıoğlu, Can, et al.. (2017). Intrafamilial variability in the clinical presentation of mucopolysaccharidosis type II: data from the Hunter Outcome Survey (HOS). Molecular Genetics and Metabolism. 120(1-2). S46–S46.
2.
Muenzer, Joseph, Simon Jones, Anna Tylki‐Szymańska, et al.. (2017). Ten years of the Hunter Outcome Survey (HOS): insights, achievements, and lessons learned from a global patient registry. Orphanet Journal of Rare Diseases. 12(1). 82–82. 47 indexed citations
3.
Bendel, Anne, et al.. (2016). LG-55CASE REPORT OF AN OPTIC PATHWAY GLIOMA IN A PATIENT WITH LEGIUS SYNDROME. Neuro-Oncology. 18(suppl 3). iii91.2–iii91. 1 indexed citations
4.
Hendriksz, Christian J., Joseph Muenzer, Adeline Vanderver, et al.. (2015). Levels of glycosaminoglycans in the cerebrospinal fluid of healthy young adults, surrogate-normal children, and Hunter syndrome patients with and without cognitive impairment. SHILAP Revista de lepidopterología. 5. 103–106. 27 indexed citations
5.
Tu, Yaqin, Ping Yang, Jia Yang, et al.. (2014). Clinical and genetic characteristics for the Urofacial Syndrome (UFS).. PubMed. 7(5). 1842–8. 8 indexed citations
6.
Jones, Simon, Rossella Parini, Paul Harmatz, et al.. (2013). The effect of idursulfase on growth in patients with Hunter syndrome: Data from the Hunter Outcome Survey (HOS). Molecular Genetics and Metabolism. 109(1). 41–48. 52 indexed citations
7.
Pyott, Shawna M., Thao Tran, Dru F. Leistritz, et al.. (2013). WNT1 Mutations in Families Affected by Moderately Severe and Progressive Recessive Osteogenesis Imperfecta. The American Journal of Human Genetics. 92(4). 590–597. 170 indexed citations
8.
Parini, Rossella, Simon W. Jones, Paul Harmatz, et al.. (2013). The natural history of growth in patients with Hunter syndrome: Data from the Hunter Outcome Survey (HOS). Molecular Genetics and Metabolism. 108(2). S72–S72. 1 indexed citations
9.
Mendelsohn, Nancy J., Timothy C. Wood, Rebecca Olson, et al.. (2013). Spondyloepiphyseal Dysplasias and Bilateral Legg-Calvé-Perthes Disease: Diagnostic Considerations for Mucopolysaccharidoses. JIMD Reports. 11. 125–132. 16 indexed citations
10.
Kishnani, Priya S., et al.. (2012). The new era of Pompe disease: Advances in the detection, understanding of the phenotypic spectrum, pathophysiology, and management. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 160C(1). 1–7. 55 indexed citations
11.
Wood, Timothy C., Olaf A. Bodamer, Maira Graeff Burin, et al.. (2012). Expert recommendations for the laboratory diagnosis of MPS VI. Molecular Genetics and Metabolism. 106(1). 73–82. 33 indexed citations
12.
Lakdawala, Neal K., Birgit Funke, Samantha Baxter, et al.. (2012). Genetic Testing for Dilated Cardiomyopathy in Clinical Practice. Journal of Cardiac Failure. 18(4). 296–303. 116 indexed citations
13.
Theisen, Aaron, Lea Velsher, Erawati V. Bawle, et al.. (2011). Duplication of the STS region in males is a benign copy‐number variant. American Journal of Medical Genetics Part A. 155(8). 1972–1975. 17 indexed citations
14.
Mendelsohn, Nancy J., Paul Harmatz, Olaf A. Bodamer, et al.. (2010). Importance of surgical history in diagnosing mucopolysaccharidosis type II (Hunter syndrome): Data from the Hunter Outcome Survey. Genetics in Medicine. 12(12). 816–822. 57 indexed citations
15.
Dolan, Michelle, Nancy J. Mendelsohn, Mary Ella Pierpont, et al.. (2010). A novel microdeletion/microduplication syndrome of 19p13.13. Genetics in Medicine. 12(8). 503–511. 33 indexed citations
16.
Schaefer, G. Bradley & Nancy J. Mendelsohn. (2008). Genetics evaluation for the etiologic diagnosis of autism spectrum disorders. Genetics in Medicine. 10(1). 4–12. 125 indexed citations
17.
Lussky, Richard C., et al.. (2005). Validity of Hospital Discharge Data for Identifying Infants with Cardiac Defects. Journal of Perinatology. 25(11). 737–742. 97 indexed citations
18.
Schimmenti, Lisa A., Rodney R. Higgins, Nancy J. Mendelsohn, et al.. (1995). Monosomy 9p24→pter and trisomy 5q31→qter: Case report and review of two cases. American Journal of Medical Genetics. 57(1). 52–56. 9 indexed citations
19.
20.
Whelan, Alison, et al.. (1993). Expression and Characterization of Human Mutant (Glutamic Acid304) Medium-Chain Acyl-Coenzyme A Dehydrogenase in Mammalian Cells. Pediatric Research. 34(5). 694–697. 7 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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