Dima El‐Khechen

2.5k total citations
10 papers, 294 citations indexed

About

Dima El‐Khechen is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Dima El‐Khechen has authored 10 papers receiving a total of 294 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Dima El‐Khechen's work include Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetic factors in colorectal cancer (2 papers). Dima El‐Khechen is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetic factors in colorectal cancer (2 papers). Dima El‐Khechen collaborates with scholars based in United States, Australia and Israel. Dima El‐Khechen's co-authors include Kelly D. Farwell Hagman, Sha Tang, Mari Rossi, Zöe Powis, Mary Helen Black, Deepali N. Shinde, Kelly Radtke, Katherine L. Helbig, Erica D. Smith and Sourat Darabi and has published in prestigious journals such as Neurology, Mayo Clinic Proceedings and Human Mutation.

In The Last Decade

Dima El‐Khechen

10 papers receiving 292 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dima El‐Khechen United States 8 208 125 49 26 25 10 294
Mari Rossi United States 6 177 0.9× 101 0.8× 37 0.8× 10 0.4× 22 0.9× 7 257
Mariana Moysés‐Oliveira Brazil 11 206 1.0× 130 1.0× 29 0.6× 53 2.0× 6 0.2× 45 300
Frédérique Sloan‐Béna Switzerland 9 87 0.4× 123 1.0× 24 0.5× 30 1.2× 16 0.6× 23 263
Heidi Mateus Colombia 11 119 0.6× 165 1.3× 33 0.7× 31 1.2× 45 1.8× 32 362
Diane Hu‐Lince United States 7 144 0.7× 143 1.1× 24 0.5× 22 0.8× 9 0.4× 7 253
Vamsee Pillalamarri United States 9 222 1.1× 204 1.6× 22 0.4× 98 3.8× 15 0.6× 10 388
Avinash M. Veerappa India 10 112 0.5× 148 1.2× 17 0.3× 21 0.8× 12 0.5× 27 280
Radoslava Vazharova Bulgaria 7 103 0.5× 106 0.8× 21 0.4× 22 0.8× 25 1.0× 26 235
Devon Lamb Thrush United States 10 141 0.7× 218 1.7× 27 0.6× 26 1.0× 54 2.2× 19 334
Ganka Douglas United States 10 161 0.8× 228 1.8× 36 0.7× 45 1.7× 23 0.9× 13 336

Countries citing papers authored by Dima El‐Khechen

Since Specialization
Citations

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

Fields of papers citing papers by Dima El‐Khechen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dima El‐Khechen. 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 Dima El‐Khechen. The network helps show where Dima El‐Khechen may publish in the future.

Co-authorship network of co-authors of Dima El‐Khechen

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

All Works

10 of 10 papers shown
1.
El‐Khechen, Dima, et al.. (2021). Misattributed parentage identified through diagnostic exome sequencing: Frequency of detection and reporting practices. Journal of Genetic Counseling. 31(3). 631–640. 7 indexed citations
2.
Bayrak‐Toydemir, Pınar, Lora Jh Bean, Alicia Braxton, et al.. (2018). Misattributed parentage as an unanticipated finding during exome/genome sequencing: current clinical laboratory practices and an opportunity for standardization. Genetics in Medicine. 21(4). 861–866. 14 indexed citations
3.
Rossi, Mari, Dima El‐Khechen, Mary Helen Black, et al.. (2017). Outcomes of Diagnostic Exome Sequencing in Patients With Diagnosed or Suspected Autism Spectrum Disorders. Pediatric Neurology. 70. 34–43.e2. 64 indexed citations
4.
Smith, Erica D., Kelly Radtke, Mari Rossi, et al.. (2017). Classification of Genes: Standardized Clinical Validity Assessment of Gene-Disease Associations Aids Diagnostic Exome Analysis and Reclassifications. Human Mutation. 38(5). 600–608. 68 indexed citations
5.
Hagman, Kelly D. Farwell, Deepali N. Shinde, Cameron Mroske, et al.. (2016). Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseases. Genetics in Medicine. 19(2). 224–235. 34 indexed citations
6.
Tacik, Paweł, Audrey Strongosky, Daniel F. Broderick, et al.. (2015). Whole-Exome Sequencing as a Diagnostic Tool in a Family With Episodic Ataxia Type 1. Mayo Clinic Proceedings. 90(3). 366–371. 12 indexed citations
7.
Nagamani, Sandesh C.S., Ayelet Erez, Bruria Ben‐Zeev, et al.. (2012). Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders. European Journal of Human Genetics. 21(3). 343–346. 44 indexed citations
8.
El‐Khechen, Dima, et al.. (2010). A unique presentation of 22q13 deletion syndrome. Clinical Dysmorphology. 20(1). 53–54. 7 indexed citations
9.
Rosenfeld, Jill A., Yves Lacassie, Dima El‐Khechen, et al.. (2010). New cases and refinement of the critical region in the 1q41q42 microdeletion syndrome. European Journal of Medical Genetics. 54(1). 42–49. 27 indexed citations
10.
Kennerson, Marina, Garth A. Nicholson, Krzysztof Krajewski, et al.. (2009). X-linked distal hereditary motor neuropathy maps to the DSMAX locus on chromosome Xq13.1-q21. Neurology. 72(3). 246–252. 17 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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