Laila Mahmoud

465 total citations
6 papers, 254 citations indexed

About

Laila Mahmoud is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Laila Mahmoud has authored 6 papers receiving a total of 254 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 2 papers in Molecular Biology and 1 paper in Cellular and Molecular Neuroscience. Recurrent topics in Laila Mahmoud's work include Genomics and Rare Diseases (3 papers), Genomic variations and chromosomal abnormalities (2 papers) and Cancer Genomics and Diagnostics (1 paper). Laila Mahmoud is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genomic variations and chromosomal abnormalities (2 papers) and Cancer Genomics and Diagnostics (1 paper). Laila Mahmoud collaborates with scholars based in Qatar, Saudi Arabia and Germany. Laila Mahmoud's co-authors include Noora Shahbeck, Rehab Ali, Mariam AlMulla, Nader Al‐Dewik, Mariam Al‐Mureikhi, Fowzan S. Alkuraya, Zafar Nawaz, Patrik Vitazka, Tawfeg Ben‐Omran and Shenela Lakhani and has published in prestigious journals such as Cell Reports, Human Genetics and American Journal of Medical Genetics Part A.

In The Last Decade

Laila Mahmoud

6 papers receiving 252 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Laila Mahmoud Qatar	6	136	100	35	31	26	6	254
Cristina Dias Portugal	11	143 1.1×	172 1.7×	30 0.9×	24 0.8×	23 0.9×	16	359
Julie A. Jurgens United States	11	124 0.9×	148 1.5×	38 1.1×	17 0.5×	32 1.2×	14	298
Saeed Al-Turki Saudi Arabia	4	102 0.8×	114 1.1×	36 1.0×	17 0.5×	21 0.8×	7	250
Arthur Sorlin France	8	86 0.6×	115 1.1×	18 0.5×	17 0.5×	16 0.6×	23	224
Taghreed Shuaib Saudi Arabia	9	74 0.5×	133 1.3×	27 0.8×	25 0.8×	14 0.5×	13	243
Mohammad Al-Owain Saudi Arabia	10	65 0.5×	170 1.7×	34 1.0×	41 1.3×	24 0.9×	15	264
Majdi Nagara Tunisia	10	140 1.0×	161 1.6×	37 1.1×	11 0.4×	19 0.7×	25	343
Mohammed Zain Seidahmed Saudi Arabia	12	227 1.7×	277 2.8×	26 0.7×	19 0.6×	65 2.5×	21	409
Amber Begtrup United States	9	104 0.8×	153 1.5×	16 0.5×	13 0.4×	16 0.6×	14	255
Shenela Lakhani United States	4	87 0.6×	77 0.8×	32 0.9×	12 0.4×	8 0.3×	6	185

Countries citing papers authored by Laila Mahmoud

Since Specialization

Citations

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

Fields of papers citing papers by Laila Mahmoud

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laila Mahmoud

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

All Works

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6 of 6 papers shown

1.

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

2.

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

3.

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

4.

Gramer, Gwendolyn, Ghassan Abdoh, Tawfeg Ben‐Omran, et al.. (2017). Newborn screening for remethylation disorders and vitamin B12 deficiency-evaluation of new strategies in cohorts from Qatar and Germany. World Journal of Pediatrics. 13(2). 136–143. 18 indexed citations

5.

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

6.

Shintani, Takafumi, Somayyeh Fahiminiya, Akihiro Fujikawa, et al.. (2015). Loss-of-Function Mutation in APC2 Causes Sotos Syndrome Features. Cell Reports. 10(9). 1585–1598. 36 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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