Mariam Al Eissa

5.3k citations
2 papers · 14 · h-index 2

Impact in

    • Williams Syndrome Research
    • Genomics and Rare Diseases
    • Genetic Associations and Epidemiology
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders

Papers in

    • Genomics and Rare Diseases 2
    • Genetic Associations and Epidemiology 1
    • Genetics and Neurodevelopmental Disorders 1
    • Metabolism and Genetic Disorders 1

Mariam Al Eissa

2 papers receiving 14 citations

Peers

Mariam Al Eissa
Comparison fields: 5 of 12
  • Developmental Neuroscience 2
  • Genetics 8
  • Clinical Biochemistry 1
  • Cancer Research 2
  • Ophthalmology 1
Replace Kimberley Gamet with:
Kimberley Gamet New Zealand
E.G. Holliday Australia
Shawn Leonard United States
Mingyang Shi Japan
Tian Wu Hong Kong
Dihong Zhou United States
Chang Bum Hong South Korea
Allison Faber Brazil
Mattias Frånberg Sweden
Wenwen Li Denmark
Mariam Al Eissa relative to Kimberley Gamet New Zealand Kimberley Gamet's profile →
Citations per field
00.5×1.5×
Kimberley Gamet · 1×
Citations per year

Countries citing papers authored by Mariam Al Eissa

Since Specialization
Citations

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

Fields of papers citing papers by Mariam Al Eissa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mariam Al Eissa. 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 Mariam Al Eissa. The network helps show where Mariam Al Eissa may publish in the future.

Co-authors

The 12 scholars most cited alongside Mariam Al Eissa, 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 Mariam Al Eissa Line = papers co-authored together Mariam Al Eissa links everyone, so they are left out of the graph.

All Works

About Mariam Al Eissa

Mariam Al Eissa is a scholar working on Genetics, Clinical Biochemistry, Rheumatology, Infectious Diseases and Organic Chemistry, having authored 2 papers that have together received 14 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (2 papers), Metabolism and Genetic Disorders (1 paper), Folate and B Vitamins Research (1 paper), Genetic Associations and Epidemiology (1 paper) and Genetics and Neurodevelopmental Disorders (1 paper). The work is most often cited by research in Developmental Neuroscience (2 citations), Genetics (8 citations), Clinical Biochemistry (1 citation), Cancer Research (2 citations) and Ophthalmology (1 citation). Mariam Al Eissa has collaborated with scholars based in United Kingdom and Saudi Arabia. Frequent co-authors include Nicholas Bass, Andrew McQuillin, Sally I. Sharp, Ahmed Alfares, Niamh L. O’Brien, Majid Alfadhel, Alessia Fiorentino, Abdulrahman Alswaid, David Curtis and Lamia Alsubaie. Their work appears in journals such as Schizophrenia Research and SHILAP Revista de lepidopterología.

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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