Jacqueline Eason

5.7k total citations
10 papers, 321 citations indexed

About

Jacqueline Eason is a scholar working on Surgery, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jacqueline Eason has authored 10 papers receiving a total of 321 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Surgery, 4 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jacqueline Eason's work include Congenital heart defects research (4 papers), Prenatal Screening and Diagnostics (4 papers) and Fetal and Pediatric Neurological Disorders (3 papers). Jacqueline Eason is often cited by papers focused on Congenital heart defects research (4 papers), Prenatal Screening and Diagnostics (4 papers) and Fetal and Pediatric Neurological Disorders (3 papers). Jacqueline Eason collaborates with scholars based in United Kingdom, Australia and United States. Jacqueline Eason's co-authors include Mark Pope, J. David Brook, Javier T Granados-Riveron, Frances Bu’Lock, Michael P. Feneley, Richard P. Harvey, Diane Fatkin, Edwin P. Kirk, John A.L. Armour and Tushar K. Ghosh and has published in prestigious journals such as Human Molecular Genetics, Eye and JCI Insight.

In The Last Decade

Jacqueline Eason

9 papers receiving 320 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jacqueline Eason United Kingdom	4	246	157	89	71	49	10	321
Edward B. Clark United States	6	176 0.7×	106 0.7×	84 0.9×	23 0.3×	65 1.3×	6	337
Aho Ilgun Netherlands	6	196 0.8×	69 0.4×	82 0.9×	60 0.8×	30 0.6×	9	252
Elise Glen United Kingdom	4	146 0.6×	112 0.7×	31 0.3×	60 0.8×	57 1.2×	4	190
Silvia E. Racedo United States	9	198 0.8×	69 0.4×	11 0.1×	64 0.9×	48 1.0×	13	272
Ozanna Burnicka-Turek United States	4	168 0.7×	52 0.3×	32 0.4×	35 0.5×	17 0.3×	5	239
Lidia Ziółkowska Poland	11	138 0.6×	119 0.8×	224 2.5×	25 0.4×	77 1.6×	33	362
Luca Barbieri Italy	13	143 0.6×	35 0.2×	71 0.8×	51 0.7×	48 1.0×	20	350
Mary Goetsch United States	9	228 0.9×	124 0.8×	37 0.4×	76 1.1×	47 1.0×	16	345
Ulrike Lisewski Germany	7	161 0.7×	45 0.3×	187 2.1×	56 0.8×	4 0.1×	12	329
Kholiswa Ngumbela United States	5	181 0.7×	54 0.3×	335 3.8×	34 0.5×	45 0.9×	5	425

Countries citing papers authored by Jacqueline Eason

Since Specialization

Citations

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

Fields of papers citing papers by Jacqueline Eason

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jacqueline Eason

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

All Works

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10 of 10 papers shown

Li, Dong, Niels Mailand, Saskia Hoffmann, et al.. (2025). Quantitative hypermorphic FAM111A alleles cause autosomal recessive Kenny-Caffey syndrome type 2 and osteocraniostenosis. JCI Insight. 10(6).

Jones, Gabriela, Jacqueline Eason, Mark Hamilton, et al.. (2022). Traboulsi syndrome caused by mutations in ASPH: An autosomal recessive disorder with overlapping features of Marfan syndrome. European Journal of Medical Genetics. 65(10). 104572–104572. 10 indexed citations

Eason, Jacqueline, et al.. (2019). Association of unilateral lattice corneal dystrophy on slit lamp and bilateral confocal microscopy features with H572R mutation in the TGFBI gene. Eye. 33(12). 1973–1975. 3 indexed citations

Eason, Jacqueline, et al.. (2018). Prenatal diagnosis of genetic disorders. Obstetrics Gynaecology & Reproductive Medicine. 28(10). 308–313. 3 indexed citations

Hamilton, Mark & Jacqueline Eason. (2015). Prenatal diagnosis of genetic disorders. Obstetrics Gynaecology & Reproductive Medicine. 25(11). 307–313. 3 indexed citations

Wilsdon, Anna & Jacqueline Eason. (2013). Prenatal diagnosis of single gene disorders. Obstetrics Gynaecology & Reproductive Medicine. 23(1). 20–25. 2 indexed citations

Granados-Riveron, Javier T, Mark Pope, Frances Bu’Lock, et al.. (2011). Combined Mutation Screening of NKX2-5, GATA4, and TBX5 in Congenital Heart Disease: Multiple Heterozygosity and Novel Mutations. Congenital Heart Disease. 7(2). 151–159. 71 indexed citations

Granados-Riveron, Javier T, Tushar K. Ghosh, Mark Pope, et al.. (2010). α-Cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects. Human Molecular Genetics. 19(20). 4007–4016. 115 indexed citations

Eason, Jacqueline. (2010). Prenatal diagnosis of single gene disorders. Obstetrics Gynaecology & Reproductive Medicine. 20(5). 155–160. 2 indexed citations

10.

Matsson, Hans, Jacqueline Eason, Carol S. Bookwalter, et al.. (2007). Alpha-cardiac actin mutations produce atrial septal defects. Human Molecular Genetics. 17(2). 256–265. 112 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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