Erik C. Thorland

10.9k total citations · 2 hit papers
61 papers, 4.2k citations indexed

About

Erik C. Thorland is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Erik C. Thorland has authored 61 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 31 papers in Genetics and 10 papers in Genetics. Recurrent topics in Erik C. Thorland's work include Genomic variations and chromosomal abnormalities (23 papers), Genomics and Rare Diseases (10 papers) and Epigenetics and DNA Methylation (9 papers). Erik C. Thorland is often cited by papers focused on Genomic variations and chromosomal abnormalities (23 papers), Genomics and Rare Diseases (10 papers) and Epigenetics and DNA Methylation (9 papers). Erik C. Thorland collaborates with scholars based in United States, China and United Kingdom. Erik C. Thorland's co-authors include Hutton M. Kearney, Sarah T. South, Kerry K. Brown, Fabiola Quintero‐Rivera, Jeremy C. Smith, Bobbie S. Gostout, Erin Rooney Riggs, Erica Andersen, Ankita Patel and Swaroop Aradhya and has published in prestigious journals such as Journal of Clinical Investigation, Blood and Neurology.

In The Last Decade

Erik C. Thorland

59 papers receiving 4.1k 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.

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 →
American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants

2011 643 citations Hutton M. Kearney, Erik C. Thorland 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						Papers	Cites
Erik C. Thorland United States	28	2.1k	1.8k	843	775	542	61	4.2k
Ying Qi China	23	1.8k 0.8×	1.9k 1.0×	399 0.5×	545 0.7×	328 0.6×	97	3.6k
Sarah T. South United States	28	2.4k 1.1×	2.0k 1.1×	1.2k 1.4×	263 0.3×	166 0.3×	82	4.3k
Koh-ichiro Yoshiura Japan	31	1.2k 0.6×	1.8k 1.0×	331 0.4×	255 0.3×	410 0.8×	159	3.4k
Corry M.R. Weemaes Netherlands	36	964 0.5×	3.2k 1.8×	271 0.3×	526 0.7×	823 1.5×	111	4.9k
Eric Seboun United States	12	1.3k 0.6×	1.8k 1.0×	176 0.2×	474 0.6×	294 0.5×	24	3.9k
Graham F. Kay Australia	33	2.6k 1.2×	4.6k 2.6×	305 0.4×	468 0.6×	604 1.1×	66	6.4k
Yoshihide Ueda Japan	29	742 0.3×	2.8k 1.6×	183 0.2×	1.2k 1.5×	579 1.1×	122	4.6k
Jian‐Min Chen France	41	1.8k 0.9×	2.5k 1.4×	207 0.2×	258 0.3×	1.4k 2.5×	196	5.8k
Derek A. Persons United States	37	1.8k 0.9×	2.9k 1.6×	311 0.4×	280 0.4×	754 1.4×	74	4.7k
Anya Tsalenko United States	24	1.3k 0.6×	2.1k 1.1×	169 0.2×	204 0.3×	268 0.5×	37	3.8k

Countries citing papers authored by Erik C. Thorland

Since Specialization

Citations

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

Fields of papers citing papers by Erik C. Thorland

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Erik C. Thorland. 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 Erik C. Thorland. The network helps show where Erik C. Thorland may publish in the future.

Co-authorship network of co-authors of Erik C. Thorland

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

All Works

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20 of 20 papers shown

Ding, Qiliang, J. Fine, Nicole L. Hoppman, et al.. (2024). Follow the LINE: A novel case of dilated cardiomyopathy caused by a LINE-1 insertion in the TTN gene. American Journal of Clinical Pathology. 163(4). 511–515.

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 →

Hoppman, Nicole L., Kandelaria M. Rumilla, Emily Lauer, Hutton M. Kearney, & Erik C. Thorland. (2018). Patterns of homozygosity in patients with uniparental disomy: detection rate and suggested reporting thresholds for SNP microarrays. Genetics in Medicine. 20(12). 1522–1527. 40 indexed citations

Lyon, Sarah, Darrel Waggoner, Sara Halbach, et al.. (2015). Syndromic craniosynostosis associated with microdeletion of chromosome 19p13.12–19p13.2. Genes & Diseases. 2(4). 347–352. 7 indexed citations

Dhamija, Radhika, John M. Graham, Nizar Smaoui, Erik C. Thorland, & Salman Kirmani. (2014). Novel de novo SPOCK1 mutation in a proband with developmental delay, microcephaly and agenesis of corpus callosum. European Journal of Medical Genetics. 57(4). 181–184. 20 indexed citations

Aypar, Umut, et al.. (2014). Does parent of origin matter? Methylation studies should be performed on patients with multiple copies of the Prader–Willi/Angelman syndrome critical region. American Journal of Medical Genetics Part A. 164(10). 2514–2520. 7 indexed citations

Banck, Michaela S., Rahul Kanwar, Amit Kulkarni, et al.. (2013). The genomic landscape of small intestine neuroendocrine tumors. Journal of Clinical Investigation. 123(6). 2502–2508. 208 indexed citations

Shearer, Brandon M., et al.. (2011). Reflex fluorescent in situ hybridization testing for unsuccessful product of conception cultures: A retrospective analysis of 5555 samples attempted by conventional cytogenetics and fluorescent in situ hybridization. Genetics in Medicine. 13(6). 545–552. 53 indexed citations

Kearney, Hutton M., Erik C. Thorland, Kerry K. Brown, Fabiola Quintero‐Rivera, & Sarah T. South. (2011). American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants. Genetics in Medicine. 13(7). 680–685. 643 indexed citations breakdown →

10.

Babovic, Nikola, Patricia S. Simmons, Christopher R. Moir, et al.. (2010). Mucinous cystadenoma of ovary in a patient with juvenile polyposis due to 10q23 microdeletion: Expansion of phenotype. American Journal of Medical Genetics Part A. 152A(10). 2623–2627. 9 indexed citations

11.

Thorland, Erik C., et al.. (2010). Hodgkin lymphoma in a young child contributing to a diagnosis of ataxia telangiectasia: review of the literature. Journal of Hematopathology. 3(2-3). 69–76. 1 indexed citations

12.

Mefford, Heather C, Gregory M. Cooper, Troy Zerr, et al.. (2009). A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease. Genome Research. 19(9). 1579–1585. 101 indexed citations

13.

Sekulić, Aleksandar, Paul Haluska, Arlo J. Miller, et al.. (2008). Malignant Melanoma in the 21st Century: The Emerging Molecular Landscape. Mayo Clinic Proceedings. 83(7). 825–846. 90 indexed citations

14.

Feldman, Andrew L., Mark E. Law, Anne J. Novak, et al.. (2008). Overexpression of Syk tyrosine kinase in peripheral T-cell lymphomas. Leukemia. 22(6). 1139–1143. 107 indexed citations

15.

Thorland, Erik C., Patrick R. Gonzales, Troy J. Gliem, Anne E. Wiktor, & Rhett P. Ketterling. (2007). Comprehensive validation of array comparative genomic hybridization platforms: how much is enough?. Genetics in Medicine. 9(9). 632–641. 8 indexed citations

16.

Wiktor, Anne E., Daniel L. Van Dyke, Rhett P. Ketterling, et al.. (2006). Preclinical validation of fluorescence in situ hybridization assays for clinical practice. Genetics in Medicine. 8(1). 16–23. 69 indexed citations

17.

Eklund, Erik A., Liangwu Sun, Samuel Yang, et al.. (2005). Congenital disorder of glycosylation Ic due to a de novo deletion and an hALG-6 mutation. Biochemical and Biophysical Research Communications. 339(3). 755–760. 13 indexed citations

18.

Ferber, Matthew J., Ileana Aderca, Andrew R. McGee, et al.. (2003). Integrations of the hepatitis B virus (HBV) and human papillomavirus (HPV) into the human telomerase reverse transcriptase (hTERT) gene in liver and cervical cancers. Oncogene. 22(24). 3813–3820. 171 indexed citations

19.

Morelli, Maria Cristina, Andrew J. Mungall, Erik C. Thorland, et al.. (2002). Cloning and characterization of the common fragile site FRA6F harboring a replicative senescence gene and frequently deleted in human tumors. Oncogene. 21(47). 7266–7276. 74 indexed citations

20.

Becker, Nicole A., Erik C. Thorland, Stacy R. Denison, Leslie A. Phillips, & Jeremy C. Smith. (2002). Evidence that instability within the FRA3B region extends four megabases. Oncogene. 21(57). 8713–8722. 52 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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