Stephen Laderman

1.1k total citations
4 papers, 783 citations indexed

About

Stephen Laderman is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Stephen Laderman has authored 4 papers receiving a total of 783 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Plant Science. Recurrent topics in Stephen Laderman's work include Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers) and Chromosomal and Genetic Variations (2 papers). Stephen Laderman is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers) and Chromosomal and Genetic Variations (2 papers). Stephen Laderman collaborates with scholars based in United States, Russia and South Korea. Stephen Laderman's co-authors include Laurakay Bruhn, Amir Ben‐Dor, Nick Sampas, Peter Tsang, Zohar Yakhini, N. Alice Yamada, Anya Tsalenko, Michael T. Barrett, Kristin Baird and Paul S. Meltzer and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Stephen Laderman

4 papers receiving 766 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stephen Laderman United States	4	541	436	211	126	107	4	783
D. C. Burford United Kingdom	6	394 0.7×	324 0.7×	210 1.0×	70 0.6×	83 0.8×	6	583
Jiangzhen Li United States	8	751 1.4×	418 1.0×	217 1.0×	294 2.3×	126 1.2×	8	946
Merete Bugge Denmark	10	584 1.1×	935 2.1×	107 0.5×	146 1.2×	71 0.7×	15	1.2k
Anne W. Higgins United States	11	360 0.7×	529 1.2×	409 1.9×	143 1.1×	36 0.3×	17	885
James Tepperberg United States	15	532 1.0×	362 0.8×	149 0.7×	284 2.3×	84 0.8×	28	889
Anita S. Kulharya United States	14	452 0.8×	509 1.2×	106 0.5×	147 1.2×	60 0.6×	31	843
Franck Court France	19	416 0.8×	888 2.0×	87 0.4×	257 2.0×	196 1.8×	37	1.0k
Christa M. Lese United States	8	438 0.8×	313 0.7×	168 0.8×	157 1.2×	50 0.5×	12	598
Judith A. Fantes United Kingdom	14	302 0.6×	611 1.4×	272 1.3×	43 0.3×	68 0.6×	28	843
E. Redeker Netherlands	17	284 0.5×	571 1.3×	91 0.4×	77 0.6×	48 0.4×	29	808

Countries citing papers authored by Stephen Laderman

Since Specialization

Citations

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

Fields of papers citing papers by Stephen Laderman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephen Laderman

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

All Works

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4 of 4 papers shown

1.

Lee, Ho‐Young, R.E. Haurwitz, Alex Apffel, et al.. (2013). RNA–protein analysis using a conditional CRISPR nuclease. Proceedings of the National Academy of Sciences. 110(14). 5416–5421. 65 indexed citations

2.

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

3.

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

4.

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

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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