Nick Sampas

3.2k total citations
7 papers, 1.5k citations indexed

About

Nick Sampas is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Nick Sampas has authored 7 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Plant Science. Recurrent topics in Nick Sampas's work include Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (4 papers) and Chromosomal and Genetic Variations (3 papers). Nick Sampas is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (4 papers) and Chromosomal and Genetic Variations (3 papers). Nick Sampas collaborates with scholars based in United States, Italy and South Korea. Nick Sampas's co-authors include Laurakay Bruhn, Anya Tsalenko, Peter Tsang, Amir Ben‐Dor, Zohar Yakhini, Maika Malig, Stephen Laderman, Peter H. Sudmant, Can Alkan and Francesca Antonacci and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Methods.

In The Last Decade

Nick Sampas

7 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nick Sampas United States	7	977	856	424	183	170	7	1.5k
Elena Prigmore United Kingdom	18	758 0.8×	742 0.9×	225 0.5×	164 0.9×	131 0.8×	27	1.4k
Joan Alexander United States	6	1.7k 1.7×	1.1k 1.3×	684 1.6×	262 1.4×	295 1.7×	8	2.1k
Rhea U. Vallente United States	11	1.5k 1.5×	1.4k 1.7×	1.1k 2.6×	203 1.1×	131 0.8×	23	2.2k
Bert H.J. Eussen Netherlands	12	572 0.6×	1.7k 2.0×	355 0.8×	93 0.5×	138 0.8×	23	2.2k
Jayne Y. Hehir‐Kwa Netherlands	24	1.1k 1.1×	854 1.0×	221 0.5×	378 2.1×	217 1.3×	53	1.9k
Sandrine Caburet France	23	686 0.7×	1.3k 1.5×	229 0.5×	98 0.5×	141 0.8×	39	1.9k
P Maraschio Italy	25	1.1k 1.1×	1.0k 1.2×	480 1.1×	263 1.4×	97 0.6×	73	1.7k
Marc Listewnik United States	5	1.7k 1.8×	1.1k 1.3×	586 1.4×	337 1.8×	256 1.5×	5	2.2k
Marjorie Withers United States	17	1.1k 1.2×	925 1.1×	412 1.0×	150 0.8×	51 0.3×	23	1.6k
Marguerite Prieur France	22	740 0.8×	789 0.9×	233 0.5×	171 0.9×	245 1.4×	33	1.5k

Countries citing papers authored by Nick Sampas

Since Specialization

Citations

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

Fields of papers citing papers by Nick Sampas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nick Sampas

This figure shows the co-authorship network connecting the top 25 collaborators of Nick Sampas. A scholar is included among the top collaborators of Nick Sampas 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 Nick Sampas. Nick Sampas 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:

7 of 7 papers shown

1.

Campbell, Catarina D., Nick Sampas, Anya Tsalenko, et al.. (2011). Population-Genetic Properties of Differentiated Human Copy-Number Polymorphisms. The American Journal of Human Genetics. 88(3). 317–332. 64 indexed citations

2.

Kidd, Jeffrey M., Nick Sampas, Francesca Antonacci, et al.. (2010). Characterization of missing human genome sequences and copy-number polymorphic insertions. Nature Methods. 7(5). 365–371. 97 indexed citations

3.

Sudmant, Peter H., Jacob O. Kitzman, Francesca Antonacci, et al.. (2010). Diversity of Human Copy Number Variation and Multicopy Genes. Science. 330(6004). 641–646. 483 indexed citations

4.

Perry, George H., Amir Ben‐Dor, Anya Tsalenko, et al.. (2008). The Fine-Scale and Complex Architecture of Human Copy-Number Variation. The American Journal of Human Genetics. 82(3). 685–695. 266 indexed citations

5.

Smith, Adam J. de, Anya Tsalenko, Nick Sampas, et al.. (2007). Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases. Human Molecular Genetics. 16(23). 2783–2794. 176 indexed citations

6.

Barrett, Michael T., Amir Ben‐Dor, Nick Sampas, et al.. (2004). Comparative genomic hybridization using oligonucleotide microarrays and total genomic DNA. Proceedings of the National Academy of Sciences. 101(51). 17765–17770. 276 indexed citations

7.

Ho, Michael, Eugene Yang, George R. Matcuk, et al.. (2003). Identification of endothelial cell genes by combined database mining and microarray analysis. Physiological Genomics. 13(3). 249–262. 99 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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