David Skaar

1.5k total citations
34 papers, 1.1k citations indexed

About

David Skaar is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, David Skaar has authored 34 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 19 papers in Genetics and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in David Skaar's work include Epigenetics and DNA Methylation (17 papers), Genetic Syndromes and Imprinting (15 papers) and Prenatal Screening and Diagnostics (6 papers). David Skaar is often cited by papers focused on Epigenetics and DNA Methylation (17 papers), Genetic Syndromes and Imprinting (15 papers) and Prenatal Screening and Diagnostics (6 papers). David Skaar collaborates with scholars based in United States, United Kingdom and Tanzania. David Skaar's co-authors include Cathrine Hoyo, Randy L. Jirtle, Susan K. Murphy, Thomas L. Kieft, Carleton S. White, John A. Craig, Samuel R. Loftin, Richard Aguilar, Arno L. Greenleaf and Rachel L. Maguire and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and Molecular Cell.

In The Last Decade

David Skaar

34 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David Skaar United States 16 451 278 230 212 136 34 1.1k
Kate Griffiths United Kingdom 23 311 0.7× 251 0.9× 151 0.7× 88 0.4× 17 0.1× 99 2.2k
Jana P. Lim United States 15 742 1.6× 170 0.6× 127 0.6× 35 0.2× 96 0.7× 17 1.3k
Thea M. Edwards United States 18 232 0.5× 182 0.7× 115 0.5× 615 2.9× 8 0.1× 38 1.5k
Louise C. Ross United Kingdom 14 1.1k 2.5× 40 0.1× 118 0.5× 33 0.2× 24 0.2× 27 2.1k
John D. McKenzie Australia 14 164 0.4× 68 0.2× 51 0.2× 52 0.2× 19 0.1× 37 1.5k
Ingrid Sadler‐Riggleman United States 27 1.3k 2.8× 516 1.9× 391 1.7× 365 1.7× 37 0.3× 39 2.2k
R.L. Buschbom United States 20 69 0.2× 103 0.4× 44 0.2× 297 1.4× 13 0.1× 70 1.7k
Hans Jürgen Hahn Germany 22 148 0.3× 112 0.4× 52 0.2× 58 0.3× 19 0.1× 86 1.4k
Kimberly A. Miller United States 21 445 1.0× 380 1.4× 80 0.3× 17 0.1× 10 0.1× 57 1.8k
F Girard France 23 321 0.7× 173 0.6× 57 0.2× 30 0.1× 15 0.1× 85 1.7k

Countries citing papers authored by David Skaar

Since Specialization
Citations

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

Fields of papers citing papers by David Skaar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Skaar

This figure shows the co-authorship network connecting the top 25 collaborators of David Skaar. A scholar is included among the top collaborators of David Skaar 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 David Skaar. David Skaar 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.
Dwaraka, Varun B., Dereje D. Jima, David Skaar, et al.. (2024). Creation and validation of the first infinium DNA methylation array for the human imprintome. SHILAP Revista de lepidopterología. 4(1). 3 indexed citations
2.
Skaar, David, Dereje D. Jima, Andy Liu, et al.. (2024). DNA methylation of imprint control regions associated with Alzheimer’s disease in non-Hispanic Blacks and non-Hispanic Whites. Clinical Epigenetics. 16(1). 58–58. 4 indexed citations
3.
Vidal, Adriana C., Yukun Liu, Susan K. Murphy, et al.. (2023). AHRR Hypomethylation mediates the association between maternal smoking and metabolic profiles in children. Hepatology Communications. 7(10). 2 indexed citations
4.
Jima, Dereje D., David Skaar, Antonio Planchart, et al.. (2022). Genomic map of candidate human imprint control regions: the imprintome. Epigenetics. 17(13). 1920–1943. 34 indexed citations
5.
Skaar, David, Eric C. Dietze, Jackelyn A. Alva-Ornelas, et al.. (2021). Epigenetic Dysregulation of KCNK9 Imprinting and Triple-Negative Breast Cancer. Cancers. 13(23). 6031–6031. 4 indexed citations
6.
Bosire, Claire, Adriana C. Vidal, Jennifer S. Smith, et al.. (2021). Association between PEG3 DNA methylation and high-grade cervical intraepithelial neoplasia. Infectious Agents and Cancer. 16(1). 42–42. 3 indexed citations
7.
Maguire, Rachel L., John S. House, Terrence K. Allen, et al.. (2020). Associations between maternal obesity, gestational cytokine levels and child obesity in the NEST cohort. Pediatric Obesity. 16(7). e12763–e12763. 16 indexed citations
8.
Dietrich, Kim N., Kim M. Cecil, David Skaar, et al.. (2020). Lead Exposure during Early Human Development and DNA Methylation of Imprinted Gene Regulatory Elements in Adulthood. UNC Libraries. 1 indexed citations
9.
Cowley, Michael, David Skaar, Dereje D. Jima, et al.. (2018). Effects of Cadmium Exposure on DNA Methylation at Imprinting Control Regions and Genome-Wide in Mothers and Newborn Children. Environmental Health Perspectives. 126(3). 37003–37003. 59 indexed citations
10.
Vidal, Adriana C., David Skaar, Rachel L. Maguire, et al.. (2015). IL-10, IL-15, IL-17, and GMCSF levels in cervical cancer tissue of Tanzanian women infected with HPV16/18 vs. non-HPV16/18 genotypes. Infectious Agents and Cancer. 10(1). 10–10. 21 indexed citations
11.
Li, Yue, Changchun Xie, Susan K. Murphy, et al.. (2015). Lead Exposure during Early Human Development and DNA Methylation of Imprinted Gene Regulatory Elements in Adulthood. Environmental Health Perspectives. 124(5). 666–673. 52 indexed citations
12.
Vidal, Adriana C., Thomas H. Darrah, Avner Vengosh, et al.. (2015). Maternal cadmium, iron and zinc levels, DNA methylation and birth weight. BMC Pharmacology and Toxicology. 16(1). 20–20. 94 indexed citations
13.
Hoyo, Cathrine, Susan K. Murphy, Joellen M. Schildkraut, et al.. (2012). IGF2RGenetic Variants, Circulating IGF2 Concentrations and Colon Cancer Risk in African Americans and Whites. Disease Markers. 32(2). 133–141. 15 indexed citations
14.
Skaar, David, Yulong Li, Adriana Bernal, et al.. (2012). The Human Imprintome: Regulatory Mechanisms, Methods of Ascertainment, and Roles in Disease Susceptibility. ILAR Journal. 53(3-4). 341–358. 59 indexed citations
15.
Hoyo, Cathrine, Susan K. Murphy, Joellen M. Schildkraut, et al.. (2012). IGF2R genetic variants, circulating IGF2 concentrations and colon cancer risk in African Americans and Whites.. SHILAP Revista de lepidopterología. 32(2). 133–41. 15 indexed citations
16.
Zhang, Aiping, David Skaar, Yue Li, et al.. (2011). Novel retrotransposed imprinted locus identified at human 6p25. Nucleic Acids Research. 39(13). 5388–5400. 19 indexed citations
17.
Cukier, Holly N., David Skaar, Ioanna Konidari, et al.. (2009). Identification of chromosome 7 inversion breakpoints in an autistic family narrows candidate region for autism susceptibility. Autism Research. 2(5). 258–266. 11 indexed citations
18.
Ashley‐Koch, Allison E., James Jaworski, Hao Mei, et al.. (2007). Investigation of potential gene–gene interactions between apoe and reln contributing to autism risk. Psychiatric Genetics. 17(4). 221–226. 33 indexed citations
19.
Skaar, David, Yujun Shao, J.L. Haines, et al.. (2004). Analysis of the RELN gene as a genetic risk factor for autism. Molecular Psychiatry. 10(6). 563–571. 145 indexed citations
20.
Skaar, David & Arno L. Greenleaf. (2002). The RNA Polymerase II CTD Kinase CTDK-I Affects Pre-mRNA 3′ Cleavage/Polyadenylation through the Processing Component Pti1p. Molecular Cell. 10(6). 1429–1439. 45 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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