Mariam AlMulla

489 citations
9 papers · 372 · h-index 8

Impact in

    • Genomics and Rare Diseases
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Neurogenetic and Muscular Disorders Research
    • Metabolism and Genetic Disorders

Papers in

Mariam AlMulla

9 papers receiving 369 citations

Peers

Mariam AlMulla
Comparison fields: 5 of 61
  • Genetics 145
  • Genetics 53
  • Clinical Biochemistry 23
  • Cell Biology 33
  • Pediatrics, Perinatology and Child Health 33
Replace Abdulrahman Aldeeri with:
Abdulrahman Aldeeri Saudi Arabia
Aida I. Al Aqeel Saudi Arabia
Amali C. Mallawaarachchi Australia
Wafaa M. Eyaid Saudi Arabia
Paula W. Morris United States
Hamad Al‐Mojalli Saudi Arabia
Julie Wiedower United States
Renata Gaillyová Czechia
Francis Rossignol United States
Salah Baz Saudi Arabia
Mariam AlMulla relative to Abdulrahman Aldeeri Saudi Arabia Abdulrahman Aldeeri's profile →
Citations per field
00.5×2×2.6×
Abdulrahman Aldeeri · 1×
Citations per year

Countries citing papers authored by Mariam AlMulla

Since Specialization
Citations

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

Fields of papers citing papers by Mariam AlMulla

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 23 scholars most cited alongside Mariam AlMulla, 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 AlMulla Line = papers co-authored together Mariam AlMulla links everyone, so they are left out of the graph.

All Works

9 of 9 papers shown
#Work
1 2015165
2 201944
3 201944
4 202139
5 201821
6 202020
7 201919
8 202112
9 20208

About Mariam AlMulla

Mariam AlMulla is a scholar working on Genetics, Genetics, Clinical Biochemistry, Biochemistry and Neurology, having authored 9 papers that have together received 372 indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (3 papers), Genomics and Rare Diseases (3 papers), Autoimmune and Inflammatory Disorders Research (1 paper), RNA modifications and cancer (1 paper), RNA regulation and disease (1 paper), Neurological diseases and metabolism (1 paper), Metabolism and Genetic Disorders (1 paper) and Hereditary Neurological Disorders (1 paper). The work is most often cited by research in Genetics (145 citations), Genetics (53 citations), Clinical Biochemistry (23 citations), Cell Biology (33 citations) and Pediatrics, Perinatology and Child Health (33 citations). Mariam AlMulla has collaborated with scholars based in Qatar, Saudi Arabia and United States. Frequent co-authors include Rehab Ali, Noora Shahbeck, Mariam Al‐Mureikhi, Laila Mahmoud, Nader Izz Eddin Al-Dewik, Angus John Clarke, Abdulbari Bener, Fowzan Sami Alkuraya, Patrik Vitazka and Tawfeg Ben‐Omran. Their work appears in journals such as Human Genetics, Gene Therapy, The American Journal of Human Genetics, Journal of Inherited Metabolic Disease and American Journal of Medical Genetics Part A.

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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