Elizabeth Nickerson

22.9k total citations · 1 hit paper
13 papers, 1.9k citations indexed

About

Elizabeth Nickerson is a scholar working on Molecular Biology, Developmental Neuroscience and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Elizabeth Nickerson has authored 13 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 4 papers in Developmental Neuroscience and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Elizabeth Nickerson's work include Williams Syndrome Research (4 papers), Genomics and Phylogenetic Studies (2 papers) and Trauma and Emergency Care Studies (1 paper). Elizabeth Nickerson is often cited by papers focused on Williams Syndrome Research (4 papers), Genomics and Phylogenetic Studies (2 papers) and Trauma and Emergency Care Studies (1 paper). Elizabeth Nickerson collaborates with scholars based in United States, United Kingdom and Kuwait. Elizabeth Nickerson's co-authors include Chris Mungall, Todd Harris, Suzanna Lewis, Shengqiang Shu, Marco Mangone, Michael Caudy, Allen Day, Lincoln Stein, Jason Stajich and Lisa G. Shaffer and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Genome Research and The American Journal of Human Genetics.

In The Last Decade

Elizabeth Nickerson

13 papers receiving 1.8k citations

Hit Papers

align trajectories

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.

The Generic Genome Browser: A Building Block for a Model Organism System Database

2002 848 citations Lincoln Stein, Chris Mungall et al. Genome Research profile →

Peers

Elizabeth Nickerson

MB

GENET

PS

DN

CR

Shaun Mahony United States

Ian H. Maxwell United States

John S. Hawkins United States

A. Zantema Netherlands

M. Wintzerith France

Kornel Labun Norway

Bryan Zeitler United States

Elizabeth S. Egan United States

Isao Ishida Japan

Hideaki Tagami Japan

Shaun Mahony United States

Elizabeth Nickerson

2.2k ×1.6

MB

355 ×0.8

GENET

302 ×0.9

PS

113 ×0.6

DN

172 ×1.3

CR

Citations per year, relative to Elizabeth Nickerson Elizabeth Nickerson (= 1×) peers Shaun Mahony

Countries citing papers authored by Elizabeth Nickerson

Since Specialization

Citations

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

Fields of papers citing papers by Elizabeth Nickerson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elizabeth Nickerson

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

All Works

Sort: Min cites: Since: Top N: Style:

13 of 13 papers shown

1.

Nickerson, Elizabeth, Verity Bennett, Aideen Naughton, et al.. (2020). Head computed tomography in suspected physical abuse: time to rethink?. Archives of Disease in Childhood. 106(5). 461–466. 3 indexed citations

2.

Kemp, Alison, Elizabeth Nickerson, László Trefán, et al.. (2016). Selecting children for head CT following head injury. Archives of Disease in Childhood. 101(10). 929–934. 12 indexed citations

3.

Akizu, Naiara, Tawfeg Ben‐Omran, Lailá Bastaki, et al.. (2013). Whole-Exome Sequencing Identifies Mutated C12orf57 in Recessive Corpus Callosum Hypoplasia. The American Journal of Human Genetics. 92(3). 392–400. 19 indexed citations

4.

Martínez, Fernando J., Jeong Ho Lee, Ji Eun Lee, et al.. (2012). Whole exome sequencing identifies a splicing mutation in NSUN2 as a cause of a Dubowitz-like syndrome. Journal of Medical Genetics. 49(6). 380–385. 183 indexed citations

5.

Thomas, Reji Koshy, Heidi Greulich, Janice Lee, et al.. (2005). Detection of Oncogenic Mutations in the EGFR Gene in Lung Adenocarcinoma with Differential Sensitivity to EGFR Tyrosine Kinase Inhibitors. Cold Spring Harbor Symposia on Quantitative Biology. 70(0). 73–81. 27 indexed citations

6.

Stein, Lincoln, Chris Mungall, Shengqiang Shu, et al.. (2002). The Generic Genome Browser: A Building Block for a Model Organism System Database. Genome Research. 12(10). 1599–1610. 848 indexed citations breakdown →

7.

Wu, Yuanqing, Elizabeth Nickerson, Lisa G. Shaffer, Kim M. Keppler‐Noreuil, & Ann Muilenburg. (1999). A case of Williams syndrome with a large, visible cytogenetic deletion. Journal of Medical Genetics. 36(12). 931–932. 15 indexed citations

8.

Nickerson, Elizabeth & David L. Nelson. (1998). Molecular Definition of Pericentric Inversion Breakpoints Occurring during the Evolution of Humans and Chimpanzees. Genomics. 50(3). 368–372. 73 indexed citations

9.

Sutton, V. Reid, Elizabeth Nickerson, James R. Lupski, et al.. (1998). Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental origin. American Journal of Medical Genetics. 78(1). 82–89. 77 indexed citations

10.

Takematsu, Hiromu, Sandra Diaz, Jane Iber, et al.. (1998). A mutation in human CMP-sialic acid hydroxylase occurred after theHomo-Pandivergence. Proceedings of the National Academy of Sciences. 95(20). 11751–11756. 449 indexed citations

11.

Grady, Deborah, Elizabeth Nickerson, John D. McPherson, et al.. (1996). The Generation and Regional Localization of 303 New Chromosome 5 Sequence-Tagged Sites. Genomics. 32(1). 91–96. 6 indexed citations

12.

Nickerson, Elizabeth, et al.. (1995). Deletions of the elastin gene at 7q11.23 occur in approximately 90% of patients with Williams syndrome.. PubMed. 56(5). 1156–61. 176 indexed citations

13.

Greenberg, Frank, et al.. (1994). Deletions of the elastin gene in Williams Syndrome. The American Journal of Human Genetics. 55. 2 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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