Mohammad K. Eldomery

2.2k citations
34 papers · 1.6k · h-index 18

Impact in

  • Genetics top 5%
    • Genomics and Rare Diseases
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities

Papers in

    • Genomics and Rare Diseases 9
    • Genetics and Neurodevelopmental Disorders 5
    • Genomic variations and chromosomal abnormalities 4
    • Congenital heart defects research 4
    • Mitochondrial Function and Pathology 3

Mohammad K. Eldomery

28 papers receiving 1.6k citations

Peers

Mohammad K. Eldomery
Comparison fields: 5 of 86
  • Genetics 679
  • Clinical Biochemistry 91
  • Molecular Biology 802
  • Immunology 219
  • Cancer Research 124
Replace Andreas Massouras with:
Andreas Massouras Switzerland
Niema Ibrahim Saudi Arabia
Samantha Penney United States
Maaike Vreeburg Netherlands
Véronique Bolduc United States
R. Marzella Italy
Prashant Sharma United States
Loydie Anne Jerome‐Majewska Canada
Birgit Susanne Budde Germany
Daniel R. Carvalho Brazil
Mohammad K. Eldomery relative to Andreas Massouras Switzerland Andreas Massouras's profile →
Citations per field
00.5×2×4×5.5×
Andreas Massouras · 1×
Citations per year

Countries citing papers authored by Mohammad K. Eldomery

Since Specialization
Citations

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

Fields of papers citing papers by Mohammad K. Eldomery

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mohammad K. Eldomery. 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 Mohammad K. Eldomery. The network helps show where Mohammad K. Eldomery may publish in the future.

Co-authors

The 25 scholars most cited alongside Mohammad K. Eldomery, 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 Mohammad K. Eldomery Line = papers co-authored together Mohammad K. Eldomery links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 34 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2016227
2 2017190
3 2016147
4 2016108
5 2016105
6 201674
7 201774
8 201665
9 201865
10 201865
11 201964
12 201763
13 201559
14 201658
15 202254
16 201654
17 201648
18 201629
19 202217
20 201614

About Mohammad K. Eldomery

Mohammad K. Eldomery is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Genetics and Hematology, having authored 34 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (9 papers), Genetics and Neurodevelopmental Disorders (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Congenital heart defects research (4 papers), Neuroblastoma Research and Treatments (3 papers), Mitochondrial Function and Pathology (3 papers), Genetic factors in colorectal cancer (3 papers) and Acute Myeloid Leukemia Research (3 papers). The work is most often cited by research in Genetics (679 citations), Clinical Biochemistry (91 citations), Molecular Biology (802 citations), Immunology (219 citations) and Cancer Research (124 citations). Mohammad K. Eldomery has collaborated with scholars based in United States, Netherlands and Germany. Frequent co-authors include Sean R. Williamson, Mehdi Nassiri, David J. Grignon, Khaleel I. Al‐Obaidy, Wael Sakr, Nilesh Gupta, Liang Cheng, Muhammad T. Idrees, Oudai Hassan and John N. Eble. Their work appears in journals such as The American Journal of Human Genetics, Genome Medicine, Haematologica, Genetics in Medicine and Leukemia.

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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