Mariam AlMulla

468 total citations
7 papers, 280 citations indexed

About

Mariam AlMulla is a scholar working on Genetics, Genetics and Molecular Biology. According to data from OpenAlex, Mariam AlMulla has authored 7 papers receiving a total of 280 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 3 papers in Genetics and 2 papers in Molecular Biology. Recurrent topics in Mariam AlMulla's work include Genomics and Rare Diseases (3 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Mariam AlMulla is often cited by papers focused on Genomics and Rare Diseases (3 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Mariam AlMulla collaborates with scholars based in Qatar, Saudi Arabia and Türkiye. Mariam AlMulla's co-authors include Rehab Ali, Noora Shahbeck, Mariam Al‐Mureikhi, Nader Al‐Dewik, Laila Mahmoud, Fowzan S. Alkuraya, Abdulbari Bener, Angus Clarke, Patrik Vitazka and Zafar Nawaz and has published in prestigious journals such as Gene Therapy, Human Genetics and American Journal of Medical Genetics Part A.

In The Last Decade

Mariam AlMulla

7 papers receiving 278 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mariam AlMulla Qatar	7	125	92	44	32	31	7	280
Naama Orenstein Israel	10	123 1.0×	103 1.1×	30 0.7×	28 0.9×	31 1.0×	31	311
Maya Chopra United States	11	174 1.4×	151 1.6×	24 0.5×	14 0.4×	51 1.6×	25	406
Selwa A.F. Al-Hazzaa Saudi Arabia	10	71 0.6×	112 1.2×	41 0.9×	22 0.7×	13 0.4×	27	365
Ruolan Guo China	11	120 1.0×	158 1.7×	28 0.6×	31 1.0×	62 2.0×	41	332
Simone Pizzi Italy	11	123 1.0×	185 2.0×	45 1.0×	15 0.5×	18 0.6×	31	313
Christopher Chun Yu Mak Hong Kong	13	240 1.9×	192 2.1×	33 0.8×	29 0.9×	61 2.0×	30	466
Elisa Biamino Italy	13	204 1.6×	188 2.0×	18 0.4×	57 1.8×	24 0.8×	25	456
Dhanya Lakshmi Narayanan India	10	88 0.7×	135 1.5×	17 0.4×	19 0.6×	22 0.7×	42	261
Frances Elmslie United Kingdom	10	99 0.8×	117 1.3×	26 0.6×	22 0.7×	43 1.4×	16	291
Eyby Leon United States	9	104 0.8×	263 2.9×	24 0.5×	22 0.7×	32 1.0×	29	379

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-authorship network of co-authors of Mariam AlMulla

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

All Works

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7 of 7 papers shown

1.

Ibrahim, Khalid, Mahmoud F. Elsaid, Mariam AlMulla, et al.. (2021). Gene therapy for spinal muscular atrophy: the Qatari experience. Gene Therapy. 28(10-11). 676–680. 32 indexed citations

2.

Ali, Rehab, Nader Al‐Dewik, Laila Mahmoud, et al.. (2021). Expanding on the phenotypic spectrum ofWoodhouse‐Sakatisyndrome due to founder pathogenic variant inDCAF17: Report of 58 additional patients from Qatar and literature review. American Journal of Medical Genetics Part A. 188(1). 116–129. 8 indexed citations

3.

Al‐Mureikhi, Mariam, Noora Shahbeck, Rehab Ali, et al.. (2020). A founder RAB27A variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families. American Journal of Medical Genetics Part A. 182(11). 2570–2580. 8 indexed citations

4.

Al‐Dewik, Nader, Mariam Al‐Mureikhi, Rehab Ali, et al.. (2019). Clinical exome sequencing in 509 Middle Eastern families with suspected Mendelian diseases: The Qatari experience. American Journal of Medical Genetics Part A. 179(6). 927–935. 32 indexed citations

5.

Bener, Abdulbari, Mariam AlMulla, & Angus Clarke. (2019). Premarital screening and genetic counseling program: Studies from an endogamous population. International Journal of Applied and Basic Medical Research. 9(1). 20–20. 40 indexed citations

6.

Al‐Dewik, Nader, Mariam Al‐Mureikhi, Noora Shahbeck, et al.. (2018). Clinical genetics and genomic medicine in Qatar. Molecular Genetics & Genomic Medicine. 6(5). 702–712. 20 indexed citations

7.

Al‐Dewik, Nader, Mariam Al‐Mureikhi, Rehab Ali, et al.. (2015). High diagnostic yield of clinical exome sequencing in Middle Eastern patients with Mendelian disorders. Human Genetics. 134(9). 967–980. 140 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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