Jeffrey M. Kidd

20.8k total citations · 2 hit papers
63 papers, 4.7k citations indexed

About

Jeffrey M. Kidd is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Jeffrey M. Kidd has authored 63 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 41 papers in Genetics and 28 papers in Plant Science. Recurrent topics in Jeffrey M. Kidd's work include Chromosomal and Genetic Variations (28 papers), Genomics and Phylogenetic Studies (27 papers) and Genomic variations and chromosomal abnormalities (17 papers). Jeffrey M. Kidd is often cited by papers focused on Chromosomal and Genetic Variations (28 papers), Genomics and Phylogenetic Studies (27 papers) and Genomic variations and chromosomal abnormalities (17 papers). Jeffrey M. Kidd collaborates with scholars based in United States, Spain and Italy. Jeffrey M. Kidd's co-authors include Evan E. Eichler, Maika Malig, Carlos D. Bustamante, Francesca Antonacci, Can Alkan, Tomàs Marquès‐Bonet, Sarah B. Emery, John V. Moran, Rajinder Kaul and Tera L. Newman and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Jeffrey M. Kidd

61 papers receiving 4.6k 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.

Personalized copy number and segmental duplication maps using next-generation sequencing

2009 505 citations Can Alkan, Jeffrey M. Kidd et al. profile →
Hunter-gatherer genomic diversity suggests a southern African origin for modern humans

2011 260 citations Brenna M. Henn, Christopher R. Gignoux et al. Proceedings of the National Academy of Sciences profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jeffrey M. Kidd United States	33	2.8k	2.7k	1.5k	348	223	63	4.7k
Simon Myers United Kingdom	35	3.8k 1.4×	5.5k 2.0×	1.3k 0.9×	369 1.1×	293 1.3×	43	8.2k
Jinchuan Xing United States	42	3.1k 1.1×	2.5k 0.9×	1.8k 1.2×	468 1.3×	109 0.5×	106	5.5k
Tomàs Marquès‐Bonet Spain	46	3.5k 1.3×	3.3k 1.2×	1.3k 0.8×	405 1.2×	357 1.6×	144	6.3k
W. Scott Watkins United States	40	2.5k 0.9×	2.9k 1.1×	851 0.6×	154 0.4×	204 0.9×	78	5.2k
Rita Neumann United Kingdom	26	2.5k 0.9×	2.0k 0.7×	859 0.6×	305 0.9×	191 0.9×	46	4.0k
Brian L. Browning United States	31	2.4k 0.9×	6.8k 2.5×	2.0k 1.3×	820 2.4×	380 1.7×	62	9.0k
Sharon R. Browning United States	29	2.5k 0.9×	7.4k 2.8×	2.0k 1.3×	807 2.3×	293 1.3×	77	9.6k
Ryan E. Mills United States	30	3.9k 1.4×	1.9k 0.7×	1.5k 1.0×	390 1.1×	215 1.0×	52	5.3k
Adam R. Boyko United States	35	1.9k 0.7×	3.9k 1.5×	1.3k 0.8×	178 0.5×	166 0.7×	60	6.1k
Jeffrey D. Wall United States	45	2.4k 0.9×	4.6k 1.7×	932 0.6×	163 0.5×	225 1.0×	89	6.7k

Countries citing papers authored by Jeffrey M. Kidd

Since Specialization

Citations

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

Fields of papers citing papers by Jeffrey M. Kidd

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jeffrey M. Kidd. 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 Jeffrey M. Kidd. The network helps show where Jeffrey M. Kidd may publish in the future.

Co-authorship network of co-authors of Jeffrey M. Kidd

This figure shows the co-authorship network connecting the top 25 collaborators of Jeffrey M. Kidd. A scholar is included among the top collaborators of Jeffrey M. Kidd 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 Jeffrey M. Kidd. Jeffrey M. Kidd 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

Kidd, Jeffrey M., et al.. (2024). Duplications and Retrogenes Are Numerous and Widespread in Modern Canine Genomic Assemblies. Genome Biology and Evolution. 16(7). 3 indexed citations

Meadows, Jennifer R. S., et al.. (2024). Characterization of Nuclear Mitochondrial Insertions in Canine Genome Assemblies. Genes. 15(10). 1318–1318. 1 indexed citations

Moldovan, John B., Huira C. Kopera, Ying Liu, et al.. (2024). Variable patterns of retrotransposition in different HeLa strains provide mechanistic insights into SINE RNA mobilization processes. Nucleic Acids Research. 52(13). 7761–7779. 2 indexed citations

Kidd, Jeffrey M., et al.. (2024). A Variant-Centric Analysis of Allele Sharing in Dogs and Wolves. Genes. 15(9). 1168–1168.

Jagannathan, Vidhya, Christophe Hitte, Jeffrey M. Kidd, et al.. (2021). Dog10K_Boxer_Tasha_1.0: A Long-Read Assembly of the Dog Reference Genome. Genes. 12(6). 847–847. 29 indexed citations

Pendleton, Amanda L., Aurélien J. Doucet, Thomas Derrien, et al.. (2021). Long-read assembly of a Great Dane genome highlights the contribution of GC-rich sequence and mobile elements to canine genomes. Proceedings of the National Academy of Sciences. 118(11). 31 indexed citations

Goubert, Clément, Jainy Thomas, Lindsay M. Payer, et al.. (2020). TypeTE: a tool to genotype mobile element insertions from whole genome resequencing data. Nucleic Acids Research. 48(6). e36–e36. 12 indexed citations

Li, Jing, Zhenxin Fan, Amanda L. Pendleton, et al.. (2020). Genomic Copy Number Variation Study of Nine Macaca Species Provides New Insights into Their Genetic Divergence, Adaptation, and Biomedical Application. Genome Biology and Evolution. 12(12). 2211–2230. 8 indexed citations

Read, David F., Kalyani Pyaram, Feng Yang, et al.. (2019). Stable integrant-specific differences in bimodal HIV-1 expression patterns revealed by high-throughput analysis. PLoS Pathogens. 15(10). e1007903–e1007903. 3 indexed citations

10.

Dietschi, Elisabeth, Ulrich Rytz, Peter Schawalder, et al.. (2019). An ADAMTS3 missense variant is associated with Norwich Terrier upper airway syndrome. PLoS Genetics. 15(5). e1008102–e1008102. 15 indexed citations

11.

Pendleton, Amanda L., et al.. (2019). Origin and recent expansion of an endogenous gammaretroviral lineage in domestic and wild canids. Retrovirology. 16(1). 6–6. 9 indexed citations

12.

Song, Shiya, Elżbieta Śliwerska, Sarah B. Emery, & Jeffrey M. Kidd. (2016). Modeling Human Population Separation History Using Physically Phased Genomes. Genetics. 205(1). 385–395. 33 indexed citations

13.

Henn, Brenna M., Laura R. Botigué, Stephan Peischl, et al.. (2015). Distance from sub-Saharan Africa predicts mutational load in diverse human genomes. Proceedings of the National Academy of Sciences. 113(4). 162 indexed citations

14.

Dayama, Gargi, Sarah B. Emery, Jeffrey M. Kidd, & Ryan E. Mills. (2014). The genomic landscape of polymorphic human nuclear mitochondrial insertions. Nucleic Acids Research. 42(20). 12640–12649. 127 indexed citations

15.

Martin, Alicia R., Helio A. Costa, Tuuli Lappalainen, et al.. (2014). Transcriptome Sequencing from Diverse Human Populations Reveals Differentiated Regulatory Architecture. PLoS Genetics. 10(8). e1004549–e1004549. 36 indexed citations

16.

Henn, Brenna M., Christopher R. Gignoux, Matthew J. Jobin, et al.. (2011). Hunter-gatherer genomic diversity suggests a southern African origin for modern humans. Proceedings of the National Academy of Sciences. 108(13). 5154–5162. 260 indexed citations breakdown →

17.

Ventura, Mario, Claudia Rita Catacchio, Can Alkan, et al.. (2011). Gorilla genome structural variation reveals evolutionary parallelisms with chimpanzee. Genome Research. 21(10). 1640–1649. 55 indexed citations

18.

Beck, Christine R., Catriona Macfarlane, Maika Malig, et al.. (2010). LINE-1 Retrotransposition Activity in Human Genomes. Cell. 141(7). 1159–1170. 437 indexed citations

19.

Antonacci, Francesca, Jeffrey M. Kidd, Tomàs Marquès‐Bonet, et al.. (2009). Characterization of six human disease-associated inversion polymorphisms. Human Molecular Genetics. 18(14). 2555–2566. 94 indexed citations

20.

Bailey, Jeffrey A., Jeffrey M. Kidd, & Evan E. Eichler. (2008). Human copy number polymorphic genes. Cytogenetic and Genome Research. 123(1-4). 234–243. 32 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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