Erica Andersen

2.8k total citations · 1 hit paper
28 papers, 1.5k citations indexed

About

Erica Andersen is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Erica Andersen has authored 28 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Genetics and 5 papers in Cell Biology. Recurrent topics in Erica Andersen's work include Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (6 papers) and Zebrafish Biomedical Research Applications (4 papers). Erica Andersen is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (6 papers) and Zebrafish Biomedical Research Applications (4 papers). Erica Andersen collaborates with scholars based in United States, Austria and Lebanon. Erica Andersen's co-authors include Sarah T. South, Erik C. Thorland, Erin Rooney Riggs, Athena M. Cherry, Deborah Ritter, Daniel Pineda‐Alvarez, Gordana Raca, Swaroop Aradhya, Ankita Patel and Hutton M. Kearney and has published in prestigious journals such as SHILAP Revista de lepidopterología, Molecular and Cellular Biology and Development.

In The Last Decade

Erica Andersen

25 papers receiving 1.4k citations

Hit Papers

Technical standards for the interpretation and reporting ... 2019 2026 2021 2023 2019 250 500 750
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen)
    2019 879 citations Erin Rooney Riggs, Erica Andersen et al. Genetics in Medicine profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Erica Andersen United States 16 773 612 340 159 97 28 1.5k
Evica Rajcan‐Separovic Canada 24 770 1.0× 775 1.3× 386 1.1× 71 0.4× 106 1.1× 58 1.6k
Fabiola Quintero‐Rivera United States 16 907 1.2× 634 1.0× 357 1.1× 61 0.4× 68 0.7× 54 1.4k
Sibel Kantarci United States 15 1.0k 1.3× 821 1.3× 385 1.1× 126 0.8× 126 1.3× 23 1.8k
Gordana Raca United States 18 1.1k 1.4× 586 1.0× 490 1.4× 142 0.9× 150 1.5× 62 1.7k
Jeroen Knijnenburg Netherlands 22 578 0.7× 473 0.8× 201 0.6× 287 1.8× 111 1.1× 47 1.4k
Jayne Y. Hehir‐Kwa Netherlands 24 1.1k 1.4× 854 1.4× 378 1.1× 108 0.7× 217 2.2× 53 1.9k
Armand Bottani Switzerland 24 1.3k 1.7× 1.2k 2.0× 302 0.9× 154 1.0× 102 1.1× 62 2.2k
Andreas Dufke Germany 22 865 1.1× 695 1.1× 351 1.0× 109 0.7× 50 0.5× 60 1.4k
Sung‐Hae Kang United States 20 925 1.2× 737 1.2× 348 1.0× 60 0.4× 81 0.8× 30 1.4k
Pauline Terhal Netherlands 18 632 0.8× 574 0.9× 220 0.6× 70 0.4× 59 0.6× 28 1.0k

Countries citing papers authored by Erica Andersen

Since Specialization
Citations

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

Fields of papers citing papers by Erica Andersen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Erica Andersen

This figure shows the co-authorship network connecting the top 25 collaborators of Erica Andersen. A scholar is included among the top collaborators of Erica Andersen 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 Erica Andersen. Erica Andersen 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.
2.
Wen, Ting, Janice C. Palumbos, Betsy Ostrander, et al.. (2025). Vertical inheritance and unique differential phenotypes of reciprocal recombinant chromosome 18 within a multi-generation family. European Journal of Human Genetics. 34(1). 128–133.
3.
Hong, Bo, et al.. (2023). 7. AI-Based Algorithms for neoplastic metaphase cells boost efficiencies in the cytogenetics laboratory. Cancer Genetics. 278-279. 2–3. 1 indexed citations
4.
Zhao, Jian, et al.. (2023). P421: AI-assisted karyotyping improves efficiencies at scale in the cytogenetics laboratory. SHILAP Revista de lepidopterología. 1(1). 100468–100468. 3 indexed citations
5.
6.
Thaxton, Courtney, Marina T. DiStefano, Xi Luo, et al.. (2021). Utilizing ClinGen gene‐disease validity and dosage sensitivity curations to inform variant classification. Human Mutation. 43(8). 1031–1040. 26 indexed citations
7.
Gotway, Garrett, et al.. (2019). A Novel Homozygous Deletion within the <b><i>FRY</i></b> Gene Associated with Nonsyndromic Developmental Delay. Cytogenetic and Genome Research. 159(1). 19–25. 3 indexed citations
8.
Riggs, Erin Rooney, Erica Andersen, Athena M. Cherry, et al.. (2019). Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen). Genetics in Medicine. 22(2). 245–257. 879 indexed citations breakdown →
9.
Diamond, Steven, et al.. (2019). Pediatric acute myeloid leukemia with t(7;21)(p22;q22). Genes Chromosomes and Cancer. 58(8). 551–557. 8 indexed citations
10.
Zhou, Xiaolong, Abner Louissaint, Alexander T. Wenzel, et al.. (2018). Genomic Analyses Identify Recurrent Alterations in Immune Evasion Genes in Diffuse Large B-Cell Lymphoma, Leg Type. Journal of Investigative Dermatology. 138(11). 2365–2376. 51 indexed citations
11.
Herriges, John, Jillian R. Ozmore, John B. Moeschler, et al.. (2018). Identification of two 14q32 deletions involving DICER1 associated with the development of DICER1-related tumors. European Journal of Medical Genetics. 62(1). 9–14. 16 indexed citations
12.
Andersen, Erica, Christian N. Paxton, Dennis P. O’Malley, et al.. (2017). Genomic analysis of follicular dendritic cell sarcoma by molecular inversion probe array reveals tumor suppressor-driven biology. Modern Pathology. 30(9). 1321–1334. 22 indexed citations
13.
Paxton, Christian N., Dennis P. O’Malley, Andrew M. Bellizzi, et al.. (2017). Genetic evaluation of juvenile xanthogranuloma: genomic abnormalities are uncommon in solitary lesions, advanced cases may show more complexity. Modern Pathology. 30(9). 1234–1240. 21 indexed citations
14.
Andersen, Erica, Erin E. Baldwin, Sara Ellingwood, Rosemarie Smith, & Allen N. Lamb. (2014). Xq28 duplication overlapping the int22h‐1/int22h‐2 region and including RAB39B and CLIC2 in a family with intellectual and developmental disability. American Journal of Medical Genetics Part A. 164(7). 1795–1801. 31 indexed citations
15.
Andersen, Erica, John C. Carey, Dawn Earl, et al.. (2013). Deletions involving genes WHSC1 and LETM1 may be necessary, but are not sufficient to cause Wolf–Hirschhorn Syndrome. European Journal of Human Genetics. 22(4). 464–470. 30 indexed citations
16.
Wang, Liangjun, et al.. (2013). Elements of the Polycomb Repressor SU(Z)12 Needed for Histone H3-K27 Methylation, the Interface with E(Z), and In Vivo Function. Molecular and Cellular Biology. 33(24). 4844–4856. 26 indexed citations
17.
18.
Andersen, Erica, et al.. (2010). Live Imaging of Cell Motility and Actin Cytoskeleton of Individual Neurons and Neural Crest Cells in Zebrafish Embryos. Journal of Visualized Experiments. 18 indexed citations
19.
Wang, Liangjun, Erica Andersen, Judith Benes, et al.. (2006). Alternative ESC and ESC-Like Subunits of a Polycomb Group Histone Methyltransferase Complex Are Differentially Deployed during Drosophila Development. Molecular and Cellular Biology. 26(7). 2637–2647. 31 indexed citations
20.
Ketel, Carrie S., et al.. (2005). Subunit Contributions to Histone Methyltransferase Activities of Fly and Worm Polycomb Group Complexes. Molecular and Cellular Biology. 25(16). 6857–6868. 145 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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