Mais Hashem

854 total citations
3 papers, 77 citations indexed

About

Mais Hashem is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Mais Hashem has authored 3 papers receiving a total of 77 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Molecular Biology and 1 paper in Cellular and Molecular Neuroscience. Recurrent topics in Mais Hashem's work include Genetics and Neurodevelopmental Disorders (2 papers), Genetic Syndromes and Imprinting (1 paper) and Genomics and Rare Diseases (1 paper). Mais Hashem is often cited by papers focused on Genetics and Neurodevelopmental Disorders (2 papers), Genetic Syndromes and Imprinting (1 paper) and Genomics and Rare Diseases (1 paper). Mais Hashem collaborates with scholars based in United States, Saudi Arabia and Qatar. Mais Hashem's co-authors include Fowzan S. Alkuraya, Ranad Shaheen, Mohammed Zain Seidahmed, Kristina Palmer, Tarfa Alshidi, Leslie O. Goodwin, Stephen A. Murray, Mohamed Abouelhoda, Tawfeg Ben‐Omran and Salma M. Wakil and has published in prestigious journals such as The American Journal of Human Genetics and American Journal of Medical Genetics Part A.

In The Last Decade

Mais Hashem

3 papers receiving 76 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mais Hashem United States	3	64	32	7	6	6	3	77
Eleina England United States	6	54 0.8×	43 1.3×	6 0.9×	7 1.2×	3 0.5×	10	87
Olin Blodgett United States	2	54 0.8×	16 0.5×	3 0.4×	6 1.0×	5 0.8×	2	78
Mark Mundt United States	4	54 0.8×	37 1.2×	7 1.0×	7 1.2×	7 1.2×	5	102
Nurit Assia Batzir Israel	5	58 0.9×	43 1.3×	8 1.1×	6 1.0×	4 0.7×	9	92
Ali Abdullah Alfaiz Switzerland	5	108 1.7×	33 1.0×	6 0.9×	18 3.0×	9 1.5×	6	138
Anna de Burca United Kingdom	3	39 0.6×	36 1.1×	6 0.9×	3 0.5×	3 0.5×	3	56
Muhsin Elmas Türkiye	6	47 0.7×	32 1.0×	9 1.3×	11 1.8×	4 0.7×	25	89
Norine Voisin Switzerland	6	71 1.1×	40 1.3×	7 1.0×	12 2.0×	5 0.8×	7	97
Eric Bartell United States	3	62 1.0×	35 1.1×	4 0.6×	3 0.5×	10 1.7×	4	94
Joseph Porrmann Germany	7	69 1.1×	56 1.8×	3 0.4×	5 0.8×	15 2.5×	9	110

Countries citing papers authored by Mais Hashem

Since Specialization

Citations

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

Fields of papers citing papers by Mais Hashem

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mais Hashem

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

All Works

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3 of 3 papers shown

1.

Shamseldin, Hanan E., Turki H. Albatti, Mais Hashem, et al.. (2021). PLXNA2 as a candidate gene in patients with intellectual disability. American Journal of Medical Genetics Part A. 185(12). 3859–3865. 9 indexed citations

2.

Shaheen, Ranad, Nan Jiang, Fatema Alzahrani, et al.. (2019). Bi-allelic Mutations in FAM149B1 Cause Abnormal Primary Cilium and a Range of Ciliopathy Phenotypes in Humans. The American Journal of Human Genetics. 104(4). 731–737. 21 indexed citations

3.

Shaheen, Ranad, Shams Anazi, Tawfeg Ben‐Omran, et al.. (2016). Mutations in SMG9, Encoding an Essential Component of Nonsense-Mediated Decay Machinery, Cause a Multiple Congenital Anomaly Syndrome in Humans and Mice. The American Journal of Human Genetics. 98(4). 643–652. 47 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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