G. Harton

4.9k total citations
55 papers, 3.1k citations indexed

About

G. Harton is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, G. Harton has authored 55 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Pediatrics, Perinatology and Child Health, 25 papers in Genetics and 9 papers in Molecular Biology. Recurrent topics in G. Harton's work include Prenatal Screening and Diagnostics (46 papers), Assisted Reproductive Technology and Twin Pregnancy (17 papers) and Genomic variations and chromosomal abnormalities (12 papers). G. Harton is often cited by papers focused on Prenatal Screening and Diagnostics (46 papers), Assisted Reproductive Technology and Twin Pregnancy (17 papers) and Genomic variations and chromosomal abnormalities (12 papers). G. Harton collaborates with scholars based in United States, United Kingdom and France. G. Harton's co-authors include Joyce Harper, Céline Moutou, Joanne Traeger‐Synodinos, L. Wilton, V. Goossens, Martine De Rycke, Alan R. Thornhill, Sioban SenGupta, Helen G. Tempest and Joep Geraedts and has published in prestigious journals such as Neurology, Human Reproduction and Fertility and Sterility.

In The Last Decade

G. Harton

54 papers receiving 2.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
G. Harton United States 30 2.4k 1.1k 790 616 518 55 3.1k
Francesco Fiorentino Italy 30 2.5k 1.0× 1.1k 1.0× 1.0k 1.3× 548 0.9× 462 0.9× 58 2.9k
Céline Moutou France 32 2.1k 0.9× 1.0k 0.9× 738 0.9× 1.1k 1.7× 562 1.1× 55 3.3k
L. Wilton Australia 29 2.5k 1.0× 1.2k 1.1× 1.1k 1.4× 731 1.2× 704 1.4× 50 3.4k
Edith Coonen Netherlands 33 2.8k 1.2× 1.2k 1.1× 1.3k 1.7× 825 1.3× 777 1.5× 69 3.5k
Anver Kuliev United States 36 3.0k 1.2× 1.4k 1.3× 907 1.1× 1.1k 1.8× 396 0.8× 165 4.1k
Martine De Rycke Belgium 43 3.0k 1.2× 1.4k 1.3× 1.2k 1.5× 1.9k 3.0× 666 1.3× 96 4.8k
I. Liebærs Belgium 35 1.7k 0.7× 1.2k 1.1× 1.0k 1.3× 1.5k 2.5× 1.3k 2.4× 81 3.9k
Paul N. Scriven United Kingdom 24 1.5k 0.6× 964 0.9× 379 0.5× 378 0.6× 216 0.4× 52 2.0k
Yury Verlinsky United States 41 3.9k 1.6× 1.7k 1.6× 1.2k 1.5× 1.5k 2.5× 526 1.0× 161 5.2k
N. J. Leschot Netherlands 28 1.2k 0.5× 899 0.8× 433 0.5× 702 1.1× 186 0.4× 94 2.3k

Countries citing papers authored by G. Harton

Since Specialization
Citations

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

Fields of papers citing papers by G. Harton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G. Harton

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

All Works

20 of 20 papers shown
1.
Dang, Duc-Anh, et al.. (2020). Development and clinical application of a preimplantation genetic testing for monogenic disease (PGT-M) for beta thalassemia in Vietnam. Journal of Assisted Reproduction and Genetics. 38(2). 365–374. 8 indexed citations
2.
Cinnioğlu, Cengiz, et al.. (2018). Aneuploidy Screening using Next Generation Sequencing. Methods in molecular biology. 1885. 85–102. 4 indexed citations
3.
Vera-Rodríguez, María, et al.. (2017). Embryonic mosaicism: defining prevalence in terms of clinical relevance. Fertility and Sterility. 107(3). e14–e14. 6 indexed citations
4.
Harton, G., Cengiz Cinnioğlu, & Francesco Fiorentino. (2017). Current experience concerning mosaic embryos diagnosed during preimplantation genetic screening. Fertility and Sterility. 107(5). 1113–1119. 31 indexed citations
5.
Girardet, Anne, Stéphanie Plaza, Martine De Rycke, et al.. (2015). The improvement of the best practice guidelines for preimplantation genetic diagnosis of cystic fibrosis: toward an international consensus. European Journal of Human Genetics. 24(4). 469–478. 24 indexed citations
6.
Harton, G., S. Munné, M. Surrey, et al.. (2014). Diminished Effect of Maternal Age on Implantation After Preimplantation Genetic Diagnosis With Array Comparative Genomic Hybridization. Obstetrical & Gynecological Survey. 69(12). 744–745. 2 indexed citations
7.
Dreesen, Jos, Aspasia Destouni, Georgia Kourlaba, et al.. (2013). Evaluation of PCR-based preimplantation genetic diagnosis applied to monogenic diseases: a collaborative ESHRE PGD consortium study. European Journal of Human Genetics. 22(8). 1012–1018. 48 indexed citations
8.
Deans, Zandra C., Francesco Fiorentino, Anıl Biricik, et al.. (2012). The experience of 3 years of external quality assessment of preimplantation genetic diagnosis for cystic fibrosis. European Journal of Human Genetics. 21(8). 800–806. 10 indexed citations
9.
Harton, G. & Helen G. Tempest. (2011). Chromosomal disorders and male infertility. Asian Journal of Andrology. 14(1). 32–39. 123 indexed citations
10.
Harton, G., Peter Braude, Alison Lashwood, et al.. (2010). ESHRE PGD consortium best practice guidelines for organization of a PGD centre for PGD/preimplantation genetic screening. Human Reproduction. 26(1). 14–24. 96 indexed citations
11.
Harper, Joyce & G. Harton. (2010). The use of arrays in preimplantation genetic diagnosis and screening. Fertility and Sterility. 94(4). 1173–1177. 90 indexed citations
12.
Harper, James, V. Goossens, G. Harton, & J. P. M. Geraedts. (2010). Session 09: PGD & PGS Session. Human Reproduction. 25(Supplement 1). i17–i18. 1 indexed citations
13.
14.
Harper, J, Edith Coonen, Martine De Rycke, et al.. (2010). What next for preimplantation genetic screening (PGS)? A position statement from the ESHRE PGD Consortium steering committee . Human Reproduction. 25(4). 821–823. 127 indexed citations
15.
Harton, G., Martine De Rycke, Francesco Fiorentino, et al.. (2010). ESHRE PGD consortium best practice guidelines for amplification-based PGD. Human Reproduction. 26(1). 33–40. 174 indexed citations
16.
Handyside, Alan H., G. Harton, B Mariani, et al.. (2009). Karyomapping: a universal method for genome wide analysis of genetic disease based on mapping crossovers between parental haplotypes. Journal of Medical Genetics. 47(10). 651–658. 282 indexed citations
17.
Goossens, V., G. Harton, Céline Moutou, et al.. (2008). ESHRE PGD Consortium data collection VIII: cycles from January to December 2005 with pregnancy follow-up to October 2006. Human Reproduction. 23(12). 2629–2645. 63 indexed citations
18.
Sermon, Karen, A. Michiels, G. Harton, et al.. (2006). ESHRE PGD Consortium data collection VI: cycles from January to December 2003 with pregnancy follow-up to October 2004. Human Reproduction. 22(2). 323–336. 78 indexed citations
19.
Stern, H., et al.. (2002). Non‐disclosing preimplantation genetic diagnosis for Huntington disease. Prenatal Diagnosis. 22(6). 503–507. 34 indexed citations
20.
Huffman, J.L., Jianfeng Wu, Frances T. Palmer, et al.. (1995). Diagnosing and preventing inherited disease: Nucleated erythrocytes in maternal blood: quantity and quality of fetal cells in enriched populations. Human Reproduction. 10(9). 2510–2515. 42 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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