Emad Muhammad

429 total citations
12 papers, 297 citations indexed

About

Emad Muhammad is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Infectious Diseases. According to data from OpenAlex, Emad Muhammad has authored 12 papers receiving a total of 297 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Cardiology and Cardiovascular Medicine and 2 papers in Infectious Diseases. Recurrent topics in Emad Muhammad's work include Cardiomyopathy and Myosin Studies (5 papers), SARS-CoV-2 and COVID-19 Research (2 papers) and Mitochondrial Function and Pathology (2 papers). Emad Muhammad is often cited by papers focused on Cardiomyopathy and Myosin Studies (5 papers), SARS-CoV-2 and COVID-19 Research (2 papers) and Mitochondrial Function and Pathology (2 papers). Emad Muhammad collaborates with scholars based in Israel, United States and Germany. Emad Muhammad's co-authors include Ruti Parvari, Val C. Sheffield, Aviva Levitas, Esther Manor, Vered Chalifa‐Caspi, John C. Beck, Ann Saada, Yoram Etzion, Rivka Ofir and Eli Hershkovitz and has published in prestigious journals such as The Journal of Physiology, Human Molecular Genetics and PLoS Genetics.

In The Last Decade

Emad Muhammad

11 papers receiving 292 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Emad Muhammad Israel	8	199	85	32	31	29	12	297
I‐Fen Cheng Germany	6	262 1.3×	75 0.9×	64 2.0×	29 0.9×	25 0.9×	10	364
Madhurima Saha Bangladesh	11	250 1.3×	35 0.4×	23 0.7×	9 0.3×	26 0.9×	33	352
Wu Deng United States	11	154 0.8×	68 0.8×	17 0.5×	19 0.6×	29 1.0×	18	294
Sean McGee United States	5	194 1.0×	168 2.0×	18 0.6×	18 0.6×	21 0.7×	5	446
Tricia T Nguyen United States	5	146 0.7×	72 0.8×	20 0.6×	75 2.4×	57 2.0×	5	318
Vi T. Tang United States	10	196 1.0×	155 1.8×	22 0.7×	24 0.8×	64 2.2×	19	406
Rana Chakrabarti Canada	5	146 0.7×	17 0.2×	15 0.5×	39 1.3×	41 1.4×	7	227
Jae-Hong Ko South Korea	10	276 1.4×	50 0.6×	14 0.4×	86 2.8×	11 0.4×	13	367
Shu Su China	8	138 0.7×	26 0.3×	31 1.0×	36 1.2×	26 0.9×	26	280

Countries citing papers authored by Emad Muhammad

Since Specialization

Citations

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

Fields of papers citing papers by Emad Muhammad

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emad Muhammad

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

All Works

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12 of 12 papers shown

Stein, Nili, et al.. (2025). Efficacy and safety of direct oral anticoagulants in patients with venous thrombosis and inherited thrombophilia. International Journal of Medical Sciences. 22(13). 3182–3190.

Muhammad, Emad, et al.. (2022). Specific antibody response of 14 patients with common variable immunodeficiency to 3 BNT162b2 messenger RNA coronavirus disease 2019 vaccinations. Annals of Allergy Asthma & Immunology. 129(1). 108–109. 2 indexed citations

Muhammad, Emad, et al.. (2021). Specific antibody response of patients with common variable immunodeficiency to BNT162b2 coronavirus disease 2019 vaccination. Annals of Allergy Asthma & Immunology. 127(4). 501–503. 15 indexed citations

Cassel, Aliza, Nurit Rosenberg, Emad Muhammad, et al.. (2021). Novel mutation in coagulation factor VII (Carmel mutation): Identification and characterization. Research and Practice in Thrombosis and Haemostasis. 5(4). e12407–e12407. 4 indexed citations

Levitas, Aviva, Emad Muhammad, Yuan Zhang, et al.. (2020). A Novel Recessive Mutation in SPEG Causes Early Onset Dilated Cardiomyopathy. PLoS Genetics. 16(9). e1009000–e1009000. 21 indexed citations

Etzion, Sharon, Sigal Elyagon, Emad Muhammad, et al.. (2018). DOCK10 is vital for normal cardiac function under neurohormonal activation. Journal of Molecular and Cellular Cardiology. 120. 18–18. 1 indexed citations

Muhammad, Emad, Aviva Levitas, Alex Braiman, et al.. (2015). PLEKHM2mutation leads to abnormal localization of lysosomes, impaired autophagy flux and associates with recessive dilated cardiomyopathy and left ventricular noncompaction. Human Molecular Genetics. 24(25). 7227–7240. 58 indexed citations

Levitas, Aviva, Yuval Konstantino, Emad Muhammad, et al.. (2015). D117N in Cypher/ZASP may not be a causative mutation for dilated cardiomyopathy and ventricular arrhythmias. European Journal of Human Genetics. 24(5). 666–671. 8 indexed citations

Hong, Jeong Hee, Emad Muhammad, Changyu Zheng, et al.. (2015). Essential role of carbonic anhydrase XII in secretory gland fluid and HCO₃⁻ secretion revealed by disease causing human mutation. The Journal of Physiology. 593(24). 5299–5312. 33 indexed citations

10.

Muhammad, Emad, Orit Reish, Yusuke Ohno, et al.. (2013). Congenital myopathy is caused by mutation of HACD1. Human Molecular Genetics. 22(25). 5229–5236. 41 indexed citations

11.

Levitas, Aviva, Emad Muhammad, Ann Saada, et al.. (2010). Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenase. European Journal of Human Genetics. 18(10). 1160–1165. 89 indexed citations

12.

Muhammad, Emad, Galit Parvari, Aaron Hanukoglu, et al.. (2010). Autosomal recessive hyponatremia due to isolated salt wasting in sweat associated with a mutation in the active site of Carbonic Anhydrase 12. Human Genetics. 129(4). 397–405. 25 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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