Edith Said

1.7k total citations
13 papers, 122 citations indexed

About

Edith Said is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Edith Said has authored 13 papers receiving a total of 122 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Edith Said's work include Genomics and Rare Diseases (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Prenatal Screening and Diagnostics (3 papers). Edith Said is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Prenatal Screening and Diagnostics (3 papers). Edith Said collaborates with scholars based in Malta, United States and Germany. Edith Said's co-authors include Roberto Galea, Caroline A. Sewry, Doriette Soler, Joris Vermeesch, J. P. Fryns, A. Cuschieri, Simona Pellacani, Federico Melani, Tiziana Pisano and Roser Urreizti and has published in prestigious journals such as SHILAP Revista de lepidopterología, European Journal of Human Genetics and European Journal of Surgical Oncology.

In The Last Decade

Edith Said

12 papers receiving 118 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Edith Said Malta	8	67	44	23	13	12	13	122
Hatice Mutlu Albayrak Türkiye	7	67 1.0×	41 0.9×	14 0.6×	19 1.5×	17 1.4×	26	147
Shahida Moosa South Africa	10	96 1.4×	91 2.1×	16 0.7×	6 0.5×	8 0.7×	29	169
Lea Velsher Canada	8	61 0.9×	91 2.1×	19 0.8×	4 0.3×	7 0.6×	18	181
Christopher Uy Canada	6	62 0.9×	29 0.7×	16 0.7×	16 1.2×	54 4.5×	14	238
Dominik S. Westphal Germany	7	82 1.2×	51 1.2×	15 0.7×	10 0.8×	22 1.8×	29	159
Cristina Skrypnyk Bahrain	8	95 1.4×	28 0.6×	8 0.3×	6 0.5×	8 0.7×	17	155
Christine Shieh United States	6	71 1.1×	78 1.8×	55 2.4×	6 0.5×	17 1.4×	12	178
Manisha Goyal India	8	48 0.7×	46 1.0×	16 0.7×	6 0.5×	5 0.4×	43	147
Jennifer Tarpinian United States	5	51 0.8×	55 1.3×	18 0.8×	6 0.5×	6 0.5×	5	117
María de la Luz Arenas‐Sordo Mexico	7	42 0.6×	44 1.0×	13 0.6×	3 0.2×	6 0.5×	21	109

Countries citing papers authored by Edith Said

Since Specialization

Citations

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

Fields of papers citing papers by Edith Said

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Edith Said

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

All Works

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13 of 13 papers shown

Said, Edith, et al.. (2024). Trophoblastic disease and choriocarcinoma. European Journal of Surgical Oncology. 51(4). 108727–108727.

Calleja‐Agius, Jean, et al.. (2024). Genotype-phenotype of autosomal dominant polycystic kidney disease in Malta. European Journal of Medical Genetics. 69. 104934–104934. 2 indexed citations

Maria, Beatrice De, Simona Balestrini, Davide Mei, et al.. (2021). Expanding the genetic and phenotypic spectrum of CHD2‐related disease: From early neurodevelopmental disorders to adult‐onset epilepsy. American Journal of Medical Genetics Part A. 188(2). 522–533. 15 indexed citations

Urreizti, Roser, K. Ulrich Mayer, Gilad D. Evrony, et al.. (2019). Correction: DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients. European Journal of Human Genetics. 28(1). 138–138. 1 indexed citations

Urreizti, Roser, Klaus Mayer, Gilad D. Evrony, et al.. (2019). DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients. European Journal of Human Genetics. 28(1). 64–75. 12 indexed citations

Galea, Roberto & Edith Said. (2018). Infantile Hypertrophic Pyloric Stenosis: An Epidemiological Review. Neonatal Network The Journal of Neonatal Nursing. 37(4). 197–204. 22 indexed citations

Said, Edith, Jessica X. Chong, Maja Hempel, et al.. (2017). Survival beyond the perinatal period expands the phenotypes caused by mutations in GLE1. American Journal of Medical Genetics Part A. 173(11). 3098–3103. 8 indexed citations

Said, Edith, et al.. (2017). DiGeorge phenotype in the absence of 22q11 deletion - a case report.. PubMed. 19(1). 8–9. 1 indexed citations

Said, Edith, et al.. (2015). A Case of True Hermaphroditism Presenting as a Testicular Tumour. SHILAP Revista de lepidopterología. 2015. 1–3. 7 indexed citations

10.

Said, Edith, A. Cuschieri, Joris Vermeesch, & J. P. Fryns. (2011). Toriello‐Carey syndrome with a 6Mb interstitial deletion at 22q12 detected by array CGH. American Journal of Medical Genetics Part A. 155(6). 1390–1392. 18 indexed citations

11.

Said, Edith, Doriette Soler, & Caroline A. Sewry. (2011). Vici syndrome—A rapidly progressive neurodegenerative disorder with hypopigmentation, immunodeficiency and myopathic changes on muscle biopsy. American Journal of Medical Genetics Part A. 158A(2). 440–444. 21 indexed citations

12.

Roche, Olivier, Carolina O. Jaliffa, Dominique Marchant, et al.. (2006). Eight previously unidentified mutations found in the OA1ocular albinism gene. BMC Medical Genetics. 7(1). 41–41. 13 indexed citations

13.

Cuschieri, A., Edith Said, & Jean Calleja‐Agius. (2004). DEFECT IN DORSO-VENTRAL PATTERNING, ASPLENIA, AND CONOTRUNCUS IN A SPONTANEOUSLY ABORTED FETUS. Fetal and Pediatric Pathology. 23(4). 265–274. 2 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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