Karyn Meltz Steinberg

5.2k total citations · 1 hit paper
22 papers, 2.1k citations indexed

About

Karyn Meltz Steinberg is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Karyn Meltz Steinberg has authored 22 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 13 papers in Genetics and 8 papers in Plant Science. Recurrent topics in Karyn Meltz Steinberg's work include Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (7 papers) and Genomics and Phylogenetic Studies (7 papers). Karyn Meltz Steinberg is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (7 papers) and Genomics and Phylogenetic Studies (7 papers). Karyn Meltz Steinberg collaborates with scholars based in United States, Canada and Australia. Karyn Meltz Steinberg's co-authors include Richard K. Wilson, Elaine R. Mardis, Daniel C. Koboldt, David E. Larson, Michael E. Zwick, Bruce R. Levin, David J. Cutler, David T. Okou, Evan E. Eichler and Thomas J. Albert and has published in prestigious journals such as Cell, Nature Genetics and Analytical Chemistry.

In The Last Decade

Karyn Meltz Steinberg

22 papers receiving 2.0k 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.

The Next-Generation Sequencing Revolution and Its Impact on Genomics

2013 665 citations Daniel C. Koboldt, Karyn Meltz Steinberg et al. Cell profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Karyn Meltz Steinberg United States	17	1.3k	826	341	262	210	22	2.1k
Sandro J. de Souza Brazil	29	2.2k 1.8×	358 0.4×	275 0.8×	374 1.4×	239 1.1×	118	2.9k
Michael F. Berger United States	25	2.9k 2.3×	563 0.7×	295 0.9×	231 0.9×	213 1.0×	44	3.6k
Frédéric Schütz Switzerland	24	1.8k 1.4×	612 0.7×	339 1.0×	561 2.1×	146 0.7×	38	3.2k
Ramesh Ramakrishnan United States	23	1.2k 0.9×	684 0.8×	142 0.4×	229 0.9×	144 0.7×	38	2.3k
Martin G. Reese United States	20	2.9k 2.3×	1.4k 1.7×	324 1.0×	257 1.0×	234 1.1×	25	4.4k
Nicholas R. Pannunzio United States	14	2.0k 1.6×	350 0.4×	339 1.0×	189 0.7×	164 0.8×	26	2.5k
John Smith United Kingdom	15	2.0k 1.6×	759 0.9×	371 1.1×	325 1.2×	307 1.5×	22	3.5k
Elizabeth Nickerson United States	10	1.3k 1.1×	454 0.5×	338 1.0×	131 0.5×	126 0.6×	13	1.9k
Fátima Gebauer Spain	34	3.5k 2.8×	634 0.8×	209 0.6×	577 2.2×	259 1.2×	76	4.7k
Namshin Kim South Korea	34	1.5k 1.2×	677 0.8×	860 2.5×	486 1.9×	195 0.9×	91	2.9k

Countries citing papers authored by Karyn Meltz Steinberg

Since Specialization

Citations

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

Fields of papers citing papers by Karyn Meltz Steinberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Karyn Meltz Steinberg. 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 Karyn Meltz Steinberg. The network helps show where Karyn Meltz Steinberg may publish in the future.

Co-authorship network of co-authors of Karyn Meltz Steinberg

This figure shows the co-authorship network connecting the top 25 collaborators of Karyn Meltz Steinberg. A scholar is included among the top collaborators of Karyn Meltz Steinberg 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 Karyn Meltz Steinberg. Karyn Meltz Steinberg 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

Solanki, Kaushal, Melissa Kelly, Karyn Meltz Steinberg, et al.. (2024). Genotype-First Analysis in an Unselected Health System–Based Population and Phenotypic Severity of COL4A5 Variants. Journal of the American Society of Nephrology. 36(6). 1138–1151. 2 indexed citations

Steinberg, Karyn Meltz, Valérie Schneider, Can Alkan, et al.. (2017). Building and Improving Reference Genome Assemblies. Proceedings of the IEEE. 1–14. 9 indexed citations

Huddleston, John, Mark Chaisson, Karyn Meltz Steinberg, et al.. (2016). Discovery and genotyping of structural variation from long-read haploid genome sequence data. Genome Research. 27(5). 677–685. 235 indexed citations

Steinberg, Karyn Meltz, T. Nicholas, Daniel C. Koboldt, et al.. (2015). Whole genome analyses reveal no pathogenetic single nucleotide or structural differences between monozygotic twins discordant for amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 16(5-6). 385–392. 19 indexed citations

Steinberg, Karyn Meltz, Bing Yu, Daniel C. Koboldt, Elaine R. Mardis, & Roger Pamphlett. (2015). Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS. Scientific Reports. 5(1). 9124–9124. 45 indexed citations

Koboldt, Daniel C., David E. Larson, Lori S. Sullivan, et al.. (2014). Exome-Based Mapping and Variant Prioritization for Inherited Mendelian Disorders. The American Journal of Human Genetics. 94(3). 373–384. 30 indexed citations

Steinberg, Karyn Meltz, Valérie Schneider, Tina A. Graves-Lindsay, et al.. (2014). Single haplotype assembly of the human genome from a hydatidiform mole. Genome Research. 24(12). 2066–2076. 75 indexed citations

Watson, Corey T., Karyn Meltz Steinberg, Tina Graves, et al.. (2014). Sequencing of the human IG light chain loci from a hydatidiform mole BAC library reveals locus-specific signatures of genetic diversity. Genes and Immunity. 16(1). 24–34. 27 indexed citations

Antonacci, Francesca, Megan Y. Dennis, John Huddleston, et al.. (2014). Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability. Nature Genetics. 46(12). 1293–1302. 86 indexed citations

10.

Watson, Corey T., Karyn Meltz Steinberg, John Huddleston, et al.. (2013). Complete Haplotype Sequence of the Human Immunoglobulin Heavy-Chain Variable, Diversity, and Joining Genes and Characterization of Allelic and Copy-Number Variation. The American Journal of Human Genetics. 92(4). 530–546. 154 indexed citations

11.

Koboldt, Daniel C., Karyn Meltz Steinberg, David E. Larson, Richard K. Wilson, & Elaine R. Mardis. (2013). The Next-Generation Sequencing Revolution and Its Impact on Genomics. Cell. 155(1). 27–38. 665 indexed citations breakdown →

12.

Steinberg, Karyn Meltz, et al.. (2012). Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorder. Molecular Autism. 3(1). 8–8. 21 indexed citations

13.

Itsara, Andy, Lisenka E.L.M. Vissers, Karyn Meltz Steinberg, et al.. (2012). Resolving the Breakpoints of the 17q21.31 Microdeletion Syndrome with Next-Generation Sequencing. The American Journal of Human Genetics. 90(4). 599–613. 16 indexed citations

14.

Steinberg, Karyn Meltz, Francesca Antonacci, Peter H. Sudmant, et al.. (2012). Structural diversity and African origin of the 17q21.31 inversion polymorphism. Nature Genetics. 44(8). 872–880. 88 indexed citations

15.

Mueller, Michael, Amy L. Roberts, Zhou Zhang, et al.. (2012). Genomic Pathology of SLE-Associated Copy-Number Variation at the FCGR2C/FCGR3B/FCGR2B Locus. The American Journal of Human Genetics. 92(1). 28–40. 46 indexed citations

16.

Shetty, Amol C., Prashanth Athri, Kajari Mondal, et al.. (2010). SeqAnt: A web service to rapidly identify and annotate DNA sequence variations. BMC Bioinformatics. 11(1). 471–471. 27 indexed citations

17.

Okou, David T., Adam E. Locke, Karyn Meltz Steinberg, et al.. (2009). Combining Microarray‐based Genomic Selection (MGS) with the Illumina Genome Analyzer Platform to Sequence Diploid Target Regions. Annals of Human Genetics. 73(5). 502–513. 17 indexed citations

18.

Steinberg, Karyn Meltz, David T. Okou, & Michael E. Zwick. (2008). Applying Rapid Genome Sequencing Technologies To Characterize Pathogen Genomes. Analytical Chemistry. 80(3). 520–528. 16 indexed citations

19.

Okou, David T., Karyn Meltz Steinberg, Christina M. Middle, et al.. (2007). Microarray-based genomic selection for high-throughput resequencing. Nature Methods. 4(11). 907–909. 276 indexed citations

20.

Steinberg, Karyn Meltz & Bruce R. Levin. (2007). Grazing protozoa and the evolution of the Escherichia coli O157:H7 Shiga toxin-encoding prophage. Proceedings of the Royal Society B Biological Sciences. 274(1621). 1921–1929. 119 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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