Evelyne Vanneste

1.8k total citations · 1 hit paper
20 papers, 1.3k citations indexed

About

Evelyne Vanneste is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Evelyne Vanneste has authored 20 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 13 papers in Pediatrics, Perinatology and Child Health and 9 papers in Molecular Biology. Recurrent topics in Evelyne Vanneste's work include Genomic variations and chromosomal abnormalities (14 papers), Prenatal Screening and Diagnostics (13 papers) and Cancer Genomics and Diagnostics (6 papers). Evelyne Vanneste is often cited by papers focused on Genomic variations and chromosomal abnormalities (14 papers), Prenatal Screening and Diagnostics (13 papers) and Cancer Genomics and Diagnostics (6 papers). Evelyne Vanneste collaborates with scholars based in Belgium, United States and France. Evelyne Vanneste's co-authors include Joris Vermeesch, Thierry Voet, Yves Moreau, Sophie Debrock, Cindy Melotte, Thomas D’Hooghe, Peter Könings, Jean‐Pierre Fryns, Michèle Ampe and Geert Verbeke and has published in prestigious journals such as Nucleic Acids Research, Nature Medicine and Nature Protocols.

In The Last Decade

Evelyne Vanneste

20 papers receiving 1.2k 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.

Chromosome instability is common in human cleavage-stage embryos

2009 601 citations Evelyne Vanneste, Thierry Voet et al. Nature Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Evelyne Vanneste Belgium	13	759	555	532	348	169	20	1.3k
Michèle Ampe Belgium	4	336 0.4×	278 0.5×	286 0.5×	173 0.5×	93 0.6×	7	663
Masoud Zamani Esteki Netherlands	13	350 0.5×	290 0.5×	286 0.5×	185 0.5×	103 0.6×	34	727
Anıl Biricik Italy	18	1.2k 1.6×	614 1.1×	315 0.6×	468 1.3×	87 0.5×	41	1.5k
Jing Fu China	17	419 0.6×	286 0.5×	505 0.9×	749 2.2×	39 0.2×	43	1.1k
Avirachan T. Tharapel United States	19	881 1.2×	976 1.8×	443 0.8×	125 0.4×	274 1.6×	61	1.5k
Jingly F. Weier United States	12	259 0.3×	191 0.3×	312 0.6×	63 0.2×	90 0.5×	36	675
Hiroki Umehara Japan	12	251 0.3×	415 0.7×	1000 1.9×	203 0.6×	27 0.2×	17	1.2k
Diane M. Worrad United States	12	111 0.1×	373 0.7×	1.0k 1.9×	439 1.3×	71 0.4×	13	1.2k
I. Findlay United Kingdom	16	412 0.5×	267 0.5×	244 0.5×	98 0.3×	51 0.3×	34	684
M.C. Magli United States	25	2.0k 2.6×	739 1.3×	536 1.0×	1.4k 4.0×	103 0.6×	50	2.5k

Countries citing papers authored by Evelyne Vanneste

Since Specialization

Citations

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

Fields of papers citing papers by Evelyne Vanneste

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Evelyne Vanneste

This figure shows the co-authorship network connecting the top 25 collaborators of Evelyne Vanneste. A scholar is included among the top collaborators of Evelyne Vanneste 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 Evelyne Vanneste. Evelyne Vanneste 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

Vanneste, Evelyne, et al.. (2014). Lightning related fatalities in livestock: Veterinary expertise and the added value of lightning location data. The Veterinary Journal. 203(1). 103–108. 7 indexed citations

Aa, Niels van der, Jie Cheng, Ligia Mateiu, et al.. (2013). Genome-wide copy number profiling of single cells in S-phase reveals DNA-replication domains. Nucleic Acids Research. 41(6). e66–e66. 61 indexed citations

Vanneste, Evelyne, Thierry Voet, Michèle Ampe, et al.. (2012). Chromosome Instability Is Common in Human Cleavage-Stage Embryos. Obstetrical & Gynecological Survey. 67(12). 787–788. 1 indexed citations

Mertzanidou, Afroditi, L. Wilton, Jun‐Hu Cheng, et al.. (2012). Microarray analysis reveals abnormal chromosomal complements in over 70% of 14 normally developing human embryos. Human Reproduction. 28(1). 256–264. 151 indexed citations

Könings, Peter, Evelyne Vanneste, Michèle Ampe, et al.. (2012). Microarray analysis of copy number variation in single cells. Nature Protocols. 7(2). 281–310. 23 indexed citations

Vanneste, Evelyne. (2012). New array approaches to explore single cells genomes. Frontiers in Genetics. 3. 44–44. 13 indexed citations

Vanneste, Evelyne, Niels van der Aa, Thierry Voet, & Joris Vermeesch. (2012). Aneuploidy and Copy Number Variation in Early Human Development. Seminars in Reproductive Medicine. 30(4). 302–308. 10 indexed citations

Cheng, Jie, Evelyne Vanneste, Peter Könings, et al.. (2011). Single-cell copy number variation detection. Genome biology. 12(8). R80–R80. 29 indexed citations

Voet, Thierry, Evelyne Vanneste, Niels van der Aa, et al.. (2011). Breakage-fusion-bridge cycles leading to inv dup del occur in human cleavage stage embryos. Human Mutation. 32(7). 783–793. 51 indexed citations

10.

Vanneste, Evelyne, Cindy Melotte, Thierry Voet, et al.. (2011). PGD for a complex chromosomal rearrangement by array comparative genomic hybridization. Human Reproduction. 26(4). 941–949. 38 indexed citations

11.

Voet, Thierry, Evelyne Vanneste, & Joris Vermeesch. (2011). The Human Cleavage Stage Embryo Is a Cradle of Chromosomal Rearrangements. Cytogenetic and Genome Research. 133(2-4). 160–168. 40 indexed citations

12.

Vanneste, Evelyne, Cindy Melotte, C. Staessen, et al.. (2010). Genome-wide single cell array analysis for preimplantation genetic diagnosis of a complex chromosomal rearrangement carrier. European Journal of Human Genetics. 18. 27–27. 2 indexed citations

13.

Robberecht, Caroline, Evelyne Vanneste, A. Pexsters, et al.. (2010). Somatic Genomic Variations in Early Human Prenatal Development. Current Genomics. 11(6). 397–401. 12 indexed citations

14.

Ampe, Michèle, Geert Verbeke, Evelyne Vanneste, & Joris Vermeesch. (2010). Analysis of array CGH data for the detection of single-cell chromosomal imbalances. 11(2). 224–244. 2 indexed citations

15.

Voet, Thierry, Evelyne Vanneste, Hilde Peeters, et al.. (2009). Haplotyping of single human cells. Chromosome Research. 17. 106–106. 1 indexed citations

16.

Vanneste, Evelyne, Thierry Voet, Cindy Melotte, et al.. (2009). What next for preimplantation genetic screening? High mitotic chromosome instability rate provides the biological basis for the low success rate. Human Reproduction. 24(11). 2679–2682. 84 indexed citations

17.

Vanneste, Evelyne, Cindy Melotte, Sophie Debrock, et al.. (2009). Preimplantation genetic diagnosis using fluorescent in situ hybridization for cancer predisposition syndromes caused by microdeletions. Human Reproduction. 24(6). 1522–1528. 20 indexed citations

18.

Vanneste, Evelyne, Thierry Voet, Cédric Le Caignec, et al.. (2009). Chromosome instability is common in human cleavage-stage embryos. Nature Medicine. 15(5). 577–583. 601 indexed citations breakdown →

19.

Debrock, Sophie, Cindy Melotte, Carl Spiessens, et al.. (2009). Preimplantation genetic screening for aneuploidy of embryos after in vitro fertilization in women aged at least 35 years: a prospective randomized trial. Fertility and Sterility. 93(2). 364–373. 102 indexed citations

20.

Debrock, Sophie, Cindy Melotte, Joris Vermeesch, et al.. (2007). Preimplantation genetic screening (PGS) for aneuploidy in embryos after in vitro fertilization (IVF) does not improve reproductive outcome in women over 35: a prospective controlled randomized study. Fertility and Sterility. 88. S237–S237. 11 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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