E Elian

409 citations
37 papers · 303 · h-index 11

Impact in

    • Genomic variations and chromosomal abnormalities
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genetic and rare skin diseases.

Papers in

    • Congenital Diaphragmatic Hernia Studies 5
    • Abdominal Trauma and Injuries 2
    • Sexual Differentiation and Disorders 3
    • RNA regulation and disease 2

E Elian

34 papers receiving 269 citations

Peers

E Elian
Comparison fields: 5 of 64
  • Genetics 109
  • Developmental Biology 7
  • Pediatrics, Perinatology and Child Health 48
  • Physiology 46
  • Surgery 65
Replace M. van Eygen with:
M. van Eygen Belgium
S Thieffry France
G. H. Newns United Kingdom
Burke Ec
B. A. Bharucha India
B. E. Walker Canada
M. Barr United States
A. Bou� France
Alex Russell Israel
Ralph E. Moloshok United States
E Elian relative to M. van Eygen Belgium M. van Eygen's profile →
Citations per field
00.5×1.5×
M. van Eygen · 1×
Citations per year

Countries citing papers authored by E Elian

Since Specialization
Citations

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

Fields of papers citing papers by E Elian

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside E Elian, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with E Elian Line = papers co-authored together E Elian links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 37 papers — load more, or switch the sort, to bring in the rest.

#Work
1 198133
2
The genetics of the aryl sulfatase A locus.
198132
3 198132
4 196127
5
Metachromatic leukodystrophy in the habbanite Jews: high frequency in a genetic isolate and screening for heterozygotes.
198022
6 198117
7 197915
8 197515
9 197212
10 197610
11 198110
12 19789
13 19568
14 19866
15
LH-RH and HCG studies in a Turner phenotype male (Noonan's syndrome). A case report.
19775
16 19755
17
Uveitis and ophthalmoplegia complicating chickenpox.
19785
18 19744
19 19774
20
Ultrastructural and functional studies of the platelets in patients with May-Hegglin anomaly.
19824

About E Elian

E Elian is a scholar working on Surgery, Molecular Biology, Pulmonary and Respiratory Medicine, Epidemiology and Genetics, having authored 37 papers that have together received 303 indexed citations. Recurring topics across this work include Congenital Diaphragmatic Hernia Studies (5 papers), Chromosomal and Genetic Variations (4 papers), Lysosomal Storage Disorders Research (3 papers), Sexual Differentiation and Disorders (3 papers), Herpesvirus Infections and Treatments (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Abdominal Trauma and Injuries (2 papers) and RNA regulation and disease (2 papers). The work is most often cited by research in Genetics (109 citations), Developmental Biology (7 citations), Pediatrics, Perinatology and Child Health (48 citations), Physiology (46 citations) and Surgery (65 citations). E Elian has collaborated with scholars based in Israel, United States and Italy. Frequent co-authors include Joël Zlotogora, I. Halbrecht, Yoram Barak, Gideon Bach, T. C. Iancu, Fiorella Shabtai, W. Hardy Hendren, Lea Sirota, Moshe Frydman and T. Schaap. Their work appears in journals such as Journal of Medical Genetics, Acta Paediatrica, Journal of Pediatric Ophthalmology & Strabismus, Clinical Genetics and PEDIATRICS.

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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