Laura Vives

13.5k total citations · 2 hit papers
17 papers, 2.6k citations indexed

About

Laura Vives is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Laura Vives has authored 17 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 8 papers in Molecular Biology and 8 papers in Plant Science. Recurrent topics in Laura Vives's work include Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (8 papers) and Genomics and Rare Diseases (7 papers). Laura Vives is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (8 papers) and Genomics and Rare Diseases (7 papers). Laura Vives collaborates with scholars based in United States, Spain and Italy. Laura Vives's co-authors include Evan E. Eichler, Raphael Bernier, Carl Baker, Brian J. O’Roak, Jay Shendure, Santhosh Girirajan, Emre Karakoç, Mark J. Rieder, Sarah Ng and Jerrod J. Schwartz and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Communications.

In The Last Decade

Laura Vives

17 papers receiving 2.6k citations

Hit Papers

Exome sequencing in sporadic autism spectrum disorders id... 2011 2026 2016 2021 2011 2015 250 500 750
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.

  1. Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
    2011 806 citations Brian J. O’Roak, Pelagia Deriziotis et al. Nature Genetics profile →
  2. Excess of rare, inherited truncating mutations in autism
    2015 345 citations Niklas Krumm, Tychele N. Turner et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Laura Vives United States 15 1.9k 1.5k 730 333 203 17 2.6k
Michael Ronemus United States 12 1.1k 0.6× 1.1k 0.7× 836 1.1× 512 1.5× 122 0.6× 21 2.2k
Dag H. Yasui United States 32 1.9k 1.0× 2.4k 1.6× 792 1.1× 111 0.3× 225 1.1× 46 3.5k
Sharmila Banerjee‐Basu United States 21 1.2k 0.6× 1.6k 1.1× 820 1.1× 91 0.3× 201 1.0× 36 2.6k
Dalila Pinto United States 23 2.0k 1.1× 1.4k 0.9× 882 1.2× 182 0.5× 263 1.3× 46 3.1k
Irina Voineagu Australia 18 1.3k 0.7× 2.3k 1.5× 994 1.4× 158 0.5× 256 1.3× 34 3.3k
Martine Raynaud France 25 2.1k 1.1× 1.9k 1.2× 757 1.0× 143 0.4× 80 0.4× 57 3.0k
Niklas Krumm United States 12 1.3k 0.7× 871 0.6× 705 1.0× 72 0.2× 193 1.0× 23 2.0k
Melissa B. Ramocki United States 19 1.2k 0.7× 1.1k 0.7× 497 0.7× 157 0.5× 78 0.4× 29 1.9k
Alan Packer United States 17 975 0.5× 1.4k 1.0× 592 0.8× 103 0.3× 89 0.4× 25 2.4k
Bai-Lin Wu United States 21 1.4k 0.7× 1.0k 0.7× 646 0.9× 154 0.5× 55 0.3× 43 2.2k

Countries citing papers authored by Laura Vives

Since Specialization
Citations

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

Fields of papers citing papers by Laura Vives

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laura Vives

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

All Works

17 of 17 papers shown
1.
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
2.
Krumm, Niklas, Tychele N. Turner, Carl Baker, et al.. (2015). Excess of rare, inherited truncating mutations in autism. Nature Genetics. 47(6). 582–588. 345 indexed citations breakdown →
3.
O’Roak, Brian J., Holly A.F. Stessman, Evan A. Boyle, et al.. (2014). Recurrent de novo mutations implicate novel genes underlying simplex autism risk. Nature Communications. 5(1). 5595–5595. 223 indexed citations
4.
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
5.
Lorente-Galdós, Belén, Gabriel Santpere, Laura Vives, et al.. (2013). Accelerated exon evolution within primate segmental duplications. Genome biology. 14(1). R9–R9. 12 indexed citations
6.
Giannuzzi, Giuliana, John Huddleston, Francesca Antonacci, et al.. (2013). Hominoid fission of chromosome 14/15 and the role of segmental duplications. Genome Research. 23(11). 1763–1773. 10 indexed citations
7.
Krumm, Niklas, Brian J. O’Roak, Emre Karakoç, et al.. (2013). Transmission Disequilibrium of Small CNVs in Simplex Autism. The American Journal of Human Genetics. 93(4). 595–606. 65 indexed citations
8.
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
9.
Ventura, Mario, Claudia Rita Catacchio, Saba Sajjadian, et al.. (2012). The evolution of African great ape subtelomeric heterochromatin and the fusion of human chromosome 2. Genome Research. 22(6). 1036–1049. 29 indexed citations
10.
Campbell, Catarina D., Jessica X. Chong, Maika Malig, et al.. (2012). Estimating the human mutation rate using autozygosity in a founder population. Nature Genetics. 44(11). 1277–1281. 140 indexed citations
11.
Karakoç, Emre, Can Alkan, Brian J. O’Roak, et al.. (2011). Detection of structural variants and indels within exome data. Nature Methods. 9(2). 176–178. 82 indexed citations
12.
O’Roak, Brian J., Pelagia Deriziotis, Choli Lee, et al.. (2011). Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. Nature Genetics. 43(6). 585–589. 806 indexed citations breakdown →
13.
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
14.
Girirajan, Santhosh, Zoran Brkanac, Bradley P. Coe, et al.. (2011). Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes. PLoS Genetics. 7(11). e1002334–e1002334. 221 indexed citations
15.
Antonacci, Francesca, Jeffrey M. Kidd, Tomàs Marquès‐Bonet, et al.. (2010). A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk. Nature Genetics. 42(9). 745–750. 73 indexed citations
16.
Rodríguez, Jairo, et al.. (2008). Bivalent domains enforce transcriptional memory of DNA methylated genes in cancer cells. Proceedings of the National Academy of Sciences. 105(50). 19809–19814. 85 indexed citations
17.
Rodríguez, Jairo, Laura Vives, Mireia Jordà, et al.. (2007). Genome-wide tracking of unmethylated DNA Alu repeats in normal and cancer cells. Nucleic Acids Research. 36(3). 770–784. 83 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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