Eric Karlins

5.9k total citations
17 papers, 648 citations indexed

About

Eric Karlins is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Eric Karlins has authored 17 papers receiving a total of 648 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Genetics and 5 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Eric Karlins's work include Genetic Associations and Epidemiology (3 papers), Epigenetics and DNA Methylation (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Eric Karlins is often cited by papers focused on Genetic Associations and Epidemiology (3 papers), Epigenetics and DNA Methylation (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Eric Karlins collaborates with scholars based in United States, United Kingdom and New Zealand. Eric Karlins's co-authors include Elaine A. Ostrander, Brennan Decker, Erika M. Kwon, Heidi G. Parker, Danielle M. Karyadi, Brian W. Davis, Janet L. Stanford, Howard Andrews, Ruth Ottman and Karen Marder and has published in prestigious journals such as Neurology, Genome Research and The American Journal of Human Genetics.

In The Last Decade

Eric Karlins

17 papers receiving 633 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eric Karlins United States 12 266 214 185 171 90 17 648
Katarina Truvé Sweden 15 258 1.0× 167 0.8× 57 0.3× 48 0.3× 56 0.6× 17 542
Tomoyuki Furuta Japan 18 290 1.1× 363 1.7× 64 0.3× 62 0.4× 44 0.5× 44 980
Zhongyou Li United States 13 297 1.1× 150 0.7× 42 0.2× 70 0.4× 74 0.8× 20 569
Bishwanath Chatterjee United States 20 781 2.9× 290 1.4× 225 1.2× 22 0.1× 99 1.1× 50 1.1k
Daniela Balzereit Germany 6 663 2.5× 180 0.8× 29 0.2× 109 0.6× 128 1.4× 6 898
Nanae Izumi Japan 10 615 2.3× 51 0.2× 29 0.2× 90 0.5× 69 0.8× 21 959
Lily Shen Australia 9 887 3.3× 39 0.2× 37 0.2× 126 0.7× 77 0.9× 13 1.1k
Günter Assum Germany 17 450 1.7× 215 1.0× 102 0.6× 227 1.3× 53 0.6× 33 819
Jason A. Watts United States 12 862 3.2× 144 0.7× 29 0.2× 34 0.2× 87 1.0× 21 1.0k
Shu Wu United States 13 241 0.9× 97 0.5× 27 0.1× 36 0.2× 36 0.4× 25 515

Countries citing papers authored by Eric Karlins

Since Specialization
Citations

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

Fields of papers citing papers by Eric Karlins

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eric Karlins

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

All Works

17 of 17 papers shown
1.
Karlins, Eric, Xiaoping Sun, Daniel Veltri, et al.. (2024). Prevalence and impact of the KIT M541L variant in patients with mastocytosis. Oncotarget. 15(1). 521–531. 3 indexed citations
2.
Kiely, Maeve, Lap Ah Tse, Hela Koka, et al.. (2020). Age-related DNA methylation in paired normal and tumour breast tissue in Chinese breast cancer patients. Epigenetics. 16(6). 677–691. 9 indexed citations
3.
Webster, Timothy H., Madeline Couse, Bruno M. Grande, et al.. (2019). Identifying, understanding, and correcting technical artifacts on the sex chromosomes in next-generation sequencing data. GigaScience. 8(7). 48 indexed citations
4.
Webster, Timothy H., Madeline Couse, Bruno M. Grande, et al.. (2019). XYalign: Version 1.1.6. Zenodo (CERN European Organization for Nuclear Research). 1 indexed citations
5.
Dagnall, Casey, Lindsay M. Morton, Belynda Hicks, et al.. (2018). Successful use of whole genome amplified DNA from multiple source types for high-density Illumina SNP microarrays. BMC Genomics. 19(1). 182–182. 19 indexed citations
6.
Andrade, Kelvin C. de, Douglas R. Stewart, Eric Karlins, et al.. (2017). Higher-than-expected population prevalence of potentially pathogenic germlineTP53variants in individuals unselected for cancer history. Human Mutation. 38(12). 1723–1730. 36 indexed citations
7.
Decker, Brennan, Danielle M. Karyadi, Brian W. Davis, et al.. (2016). Biallelic BRCA2 Mutations Shape the Somatic Mutational Landscape of Aggressive Prostate Tumors. The American Journal of Human Genetics. 98(5). 818–829. 27 indexed citations
8.
9.
Wiencke, John K., et al.. (2016). Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome - eScholarship. 2 indexed citations
10.
Decker, Brennan, Heidi G. Parker, Deepika Dhawan, et al.. (2015). Homologous Mutation to Human BRAF V600E Is Common in Naturally Occurring Canine Bladder Cancer—Evidence for a Relevant Model System and Urine-Based Diagnostic Test. Molecular Cancer Research. 13(6). 993–1002. 100 indexed citations
11.
Decker, Brennan, Brian W. Davis, Maud Rimbault, et al.. (2015). Comparison against 186 canid whole-genome sequences reveals survival strategies of an ancient clonally transmissible canine tumor. Genome Research. 25(11). 1646–1655. 43 indexed citations
12.
Karyadi, Danielle M., Eric Karlins, Brennan Decker, et al.. (2013). A Copy Number Variant at the KITLG Locus Likely Confers Risk for Canine Squamous Cell Carcinoma of the Digit. PLoS Genetics. 9(3). e1003409–e1003409. 56 indexed citations
13.
Allen‐Brady, Kristina, James M. Farnham, Nicola J. Camp, et al.. (2009). No evidence of BRCA2 mutations in chromosome 13q-linked Utah high-risk prostate cancer pedigrees. BMC Research Notes. 2(1). 94–94. 3 indexed citations
14.
FitzGerald, Liesel M., Eric Karlins, Danielle M. Karyadi, et al.. (2008). Association of FGFR4 genetic polymorphisms with prostate cancer risk and prognosis. Prostate Cancer and Prostatic Diseases. 12(2). 192–197. 24 indexed citations
15.
Agalliu, Ilir, Eric Karlins, Erika M. Kwon, et al.. (2007). Rare germline mutations in the BRCA2 gene are associated with early-onset prostate cancer. British Journal of Cancer. 97(6). 826–831. 73 indexed citations
16.
Clark, Lorraine N., Eric Karlins, Yuanjia Wang, et al.. (2006). Case-Control Study of the Parkin Gene in Early-Onset Parkinson Disease. Archives of Neurology. 63(4). 548–548. 67 indexed citations
17.
Clark, Lorraine N., Eric Karlins, Helen Mejia‐Santana, et al.. (2006). Frequency of LRRK2 mutations in early- and late-onset Parkinson disease. Neurology. 67(10). 1786–1791. 126 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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