Ilse J. Anderson

627 total citations
11 papers, 304 citations indexed

About

Ilse J. Anderson is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ilse J. Anderson has authored 11 papers receiving a total of 304 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ilse J. Anderson's work include Genetic Syndromes and Imprinting (2 papers), RNA modifications and cancer (2 papers) and Mitochondrial Function and Pathology (2 papers). Ilse J. Anderson is often cited by papers focused on Genetic Syndromes and Imprinting (2 papers), RNA modifications and cancer (2 papers) and Mitochondrial Function and Pathology (2 papers). Ilse J. Anderson collaborates with scholars based in United States, Canada and Japan. Ilse J. Anderson's co-authors include Petros Tsipouras, Robert B. Goldberg, William B. Upholt, Robert W. Marion, David Whiteman, Nicholas T. Potter, Michaël Meyer, Andrew W. Zimmerman, Bryan Williams and Cheryl R. Greenberg and has published in prestigious journals such as Annals of Neurology, Human Molecular Genetics and The Journal of Pediatrics.

In The Last Decade

Ilse J. Anderson

11 papers receiving 303 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ilse J. Anderson United States 7 165 164 52 44 43 11 304
Esther Nibbeling Netherlands 10 107 0.6× 191 1.2× 65 1.3× 29 0.7× 116 2.7× 15 408
Linda Manwaring United States 8 175 1.1× 136 0.8× 31 0.6× 18 0.4× 17 0.4× 15 374
Kei Shioda Japan 14 82 0.5× 274 1.7× 40 0.8× 11 0.3× 74 1.7× 25 517
Kathryn Friend Australia 12 320 1.9× 375 2.3× 57 1.1× 8 0.2× 68 1.6× 16 521
Sinan Çomu Türkiye 8 87 0.5× 165 1.0× 11 0.2× 23 0.5× 91 2.1× 15 404
Eric Noé France 8 119 0.7× 168 1.0× 11 0.2× 18 0.4× 83 1.9× 10 354
Catherine Bove United States 9 71 0.4× 86 0.5× 22 0.4× 77 1.8× 14 0.3× 12 441
Mefford Hc 6 90 0.5× 163 1.0× 19 0.4× 6 0.1× 35 0.8× 239 337
Joan E. Pellegrino United States 11 215 1.3× 256 1.6× 116 2.2× 5 0.1× 65 1.5× 19 492
Sietske H. Kevelam Netherlands 10 83 0.5× 283 1.7× 19 0.4× 8 0.2× 32 0.7× 11 473

Countries citing papers authored by Ilse J. Anderson

Since Specialization
Citations

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

Fields of papers citing papers by Ilse J. Anderson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ilse J. Anderson

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

All Works

11 of 11 papers shown
1.
Sengupta, Nivedita, Carlos R. Ferreira, Joshua G. Pemberton, et al.. (2022). De novo loss‐of‐function variant in PTDSS1 is associated with developmental delay. American Journal of Medical Genetics Part A. 188(6). 1739–1745. 5 indexed citations
2.
Anderson, Ilse J., et al.. (2020). Genetic evaluation including exome sequencing of two patients with Gomez‐Lopez‐Hernandez syndrome: Case reports and review of the literature. American Journal of Medical Genetics Part A. 182(4). 623–627. 5 indexed citations
3.
Shore, Eileen M., et al.. (2017). The congenital great toe malformation of fibrodysplasia ossificans progressiva? - A close call. European Journal of Medical Genetics. 60(7). 399–402. 12 indexed citations
4.
Tanaka, Akemi, Megan T. Cho, Rebecca Willaert, et al.. (2017). De novo variants in EBF3 are associated with hypotonia, developmental delay, intellectual disability, and autism. Molecular Case Studies. 3(6). a002097–a002097. 23 indexed citations
5.
Potter, Nicholas T., Christopher A. Miller, & Ilse J. Anderson. (2000). Mutation detection in an equivocal case of Friedreich’s ataxia. Pediatric Neurology. 22(5). 413–415. 6 indexed citations
6.
Potter, Nicholas T., et al.. (1995). Molecular and clinical findings in a family with dentatorubral‐pallidoluysian atrophy. Annals of Neurology. 37(2). 273–277. 41 indexed citations
7.
Weksberg, Rosanna, Ikuko Teshima, Bryan Williams, et al.. (1993). Molecular characterization of cytogenetic alterations associated with the Beckwith — Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted. Human Molecular Genetics. 2(5). 549–556. 76 indexed citations
8.
Potter, Nicholas T., et al.. (1992). Use of a molecular genetic approach to diagnosing the fragile X genotype. The Journal of Pediatrics. 121(3). 385–390. 2 indexed citations
9.
Chitayat, David, Catherine Meunier, Kathy Hodgkinson, et al.. (1991). Mucolipidosis type IV: Clinical manifestations and natural history. American Journal of Medical Genetics. 41(3). 313–318. 46 indexed citations
10.
Anderson, Ilse J., et al.. (1990). Spondyloepiphyseal dysplasia, mild autosomal dominant type is not due to primary defects of type II collagen. American Journal of Medical Genetics. 37(2). 272–276. 27 indexed citations
11.
Anderson, Ilse J., Robert B. Goldberg, Robert W. Marion, William B. Upholt, & Petros Tsipouras. (1990). Spondyloepiphyseal dysplasia congenita: genetic linkage to type II collagen (COL2AI).. PubMed. 46(5). 896–901. 61 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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