Mohamad Saad

4.3k total citations
33 papers, 413 citations indexed

About

Mohamad Saad is a scholar working on Genetics, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Mohamad Saad has authored 33 papers receiving a total of 413 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 14 papers in Molecular Biology and 6 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Mohamad Saad's work include Genetic Associations and Epidemiology (16 papers), Epigenetics and DNA Methylation (6 papers) and Genetic and phenotypic traits in livestock (4 papers). Mohamad Saad is often cited by papers focused on Genetic Associations and Epidemiology (16 papers), Epigenetics and DNA Methylation (6 papers) and Genetic and phenotypic traits in livestock (4 papers). Mohamad Saad collaborates with scholars based in Qatar, United States and Lebanon. Mohamad Saad's co-authors include Ellen M. Wijsman, Éva Forgács, Ming Wei, Michael I. Lerman, Farida Latif, Anton Maximov, Ilya Bezprozvanny, John D. Minna, Yoshitaka Sekido and Boning Gao and has published in prestigious journals such as Journal of Biological Chemistry, Bioinformatics and Journal of the American College of Cardiology.

In The Last Decade

Mohamad Saad

31 papers receiving 405 citations

Peers

Countries citing papers authored by Mohamad Saad

Since Specialization

Citations

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

Fields of papers citing papers by Mohamad Saad

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mohamad Saad

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Genome‐Wide Association Study for Resting Electrocardiogram in the Qatari Population Identifies 6 Novel Genes and Validates Novel Polygenic Risk Scores 2025 ·Journal of the American Heart Association ·(unknown), (unknown), Khalid Kunji, Atlas Khan, (unknown), Mohammed Bashir, (unknown), Ayman Al Haj Zen, Krzysztof Kiryluk, Georges Nemer, Akl C. Fahed, Mohamad Saad	1
2	A multi-ancestry genome-wide association study and evaluation of polygenic scores of LDL-C levels 2025 ·Journal of Lipid Research ·Umm‐Kulthum Ismail Umlai, Salman M. Toor, Yasser Al‐Sarraj, (unknown), (unknown), Ehsan Ullah, Khalid Kunji, Ayman El‐Menyar, (unknown), Amin Jayyousi, Mohamad Saad, Nadeem Qureshi, Jassim Al Suwaidi, Omar Albagha	1
3	Correlations between Resting Electrocardiogram Findings and Disease Profiles: Insights from the Qatar Biobank Cohort 2024 ·Journal of Clinical Medicine ·Fatima Qafoud, Khalid Kunji, (unknown), Asma Althani, Amar M Salam, Jassim Al Suwaidi, Dawood Darbar, Nidal Asaad, Mohamad Saad	2
4	Genetic Susceptibility to Arrhythmia Phenotypes in a Middle Eastern Cohort of 14,259 Whole-Genome Sequenced Individuals 2024 ·Journal of Clinical Medicine ·Fatima Qafoud, (unknown), Khalid Kunji, Asma Althani, Amar M Salam, Jassim Al Suwaidi, Nidal Asaad, Dawood Darbar, Mohamad Saad	1
5	Validation of Polygenic Risk Scores for Coronary Heart Disease in a Middle Eastern Cohort Using Whole Genome Sequencing 2022 ·Circulation Genomic and Precision Medicine ·Mohamad Saad, Ayman El‐Menyar, Khalid Kunji, Ehsan Ullah, Jassim Al Suwaidi, Iftikhar J. Kullo	9
6	Untargeted Metabolomics Profiling Reveals Perturbations in Arginine-NO Metabolism in Middle Eastern Patients with Coronary Heart Disease 2022 ·Metabolites ·Ehsan Ullah, Ayman El‐Menyar, Khalid Kunji, (unknown), (unknown), (unknown), Maryam Al‐Nesf, (unknown), (unknown), Vidya Mohamed‐Ali, Mohamad Saad, Jassim Al Suwaidi	5
7	Including diverse and admixed populations in genetic epidemiology research 2022 ·Genetic Epidemiology ·Amke Caliebe, Fasil Tekola‐Ayele, Burcu F. Darst, Xuexia Wang, Yeunjoo E. Song, Jiang Gui, Ronnie Sebro, David J. Balding, Mohamad Saad, Marie‐Pierre Dubé	26
8	Analytic pipelines to assess the relationship between immune response and germline genetics in human tumors 2022 ·STAR Protocols ·Rosalyn W. Sayaman, Mohamad Saad, (unknown), Donglei Hu, Khalid Kunji, Jessica Roelands, Denise M. Wolf, Scott Huntsman, Michele Ceccarelli, Vésteinn Thórsson, Elad Ziv, Davide Bedognetti	1
9	METABOLOMICS REVEALS PERTURBATIONS IN ARGININE-NO METABOLISM, PURINE BIOSYNTHESIS AND CELLULAR ENERGY CHARGE IN PATIENTS WITH CORONARY HEART DISEASE 2021 ·Journal of the American College of Cardiology ·Ehsan Ullah, Ayman El‐Menyar, Khalid Kunji, (unknown), (unknown), Nedhal Al-Tamimi, Maryam Al‐Nesf, (unknown), (unknown), Vidya Mohamed‐Ali, Mohamad Saad, Jassim Al Suwaidi	1
10	WHOLE GENOME SEQUENCING OF A MIDDLE EASTERN COHORT REPLICATES KNOWN LOCI FOR CORONARY HEART DISEASE AND IDENTIFIES POTENTIAL NOVEL ONES 2021 ·Journal of the American College of Cardiology ·Khalid Kunji, Ayman El‐Menyar, Ehsan Ullah, Iftikhar Kullo, Mohamad Saad, Jassim Al Suwaidi	1
11	Distribution of Primary Brain Tumor Subtypes in Lebanon: A Multicenter Eleven-Year Study of 695 Patients 2021 ·Cureus ·Saïd El Hage, (unknown), Sanaa Nabha, (unknown), Mohamad Saad	4
12	Prognostic impact of adenylyl cyclase-associated protein 2 (CAP2) in glioma: A clinicopathological study 2020 ·Heliyon ·(unknown), Hisham F. Bahmad, Youssef Fares, (unknown), Mohamad Saad, Hayat Harati, Sanaa Nabha	5
13	Genetic Variation in CCL5 Signaling Genes and Triple Negative Breast Cancer: Susceptibility and Prognosis Implications 2019 ·Frontiers in Oncology ·Jingxuan Shan, (unknown), Younes Mokrab, Mohamad Saad, (unknown), Rosalyn W. Sayaman, Elad Ziv, Noureddine Bouaouina, (unknown), Sallouha Gabbouj, Jessica Roelands, Xiaojing Ma, Davide Bedognetti, Lotfi Chouchane	13
14	Comparison and assessment of family- and population-based genotype imputation methods in large pedigrees 2018 ·Genome Research ·Ehsan Ullah, Raghvendra Mall, Mostafa Abbas, Khalid Kunji, Alejandro Q. Nato, Halima Bensmail, Ellen M. Wijsman, Mohamad Saad	16
15	Prognostic values of the mRNA expression of natural killer receptor ligands and their association with clinicopathological features in breast cancer patients 2018 ·Oncotarget ·(unknown), (unknown), (unknown), Mohamad Saad, (unknown)	6
16	Post-traumatic stress disorder in adult victims of cluster munitions in Lebanon: a 10-year longitudinal study 2017 ·BMJ Open ·Jawad Fares, (unknown), Mohamad Saad, Hayat Harati, Sanaa Nabha, (unknown), (unknown), (unknown), Youssef Fares	26
17	Identity-by-descent estimation with population- and pedigree-based imputation in admixed family data 2016 ·BMC Proceedings ·Mohamad Saad, Alejandro Q. Nato, (unknown), Steven M. Lewis, Lisa Brown, Elizabeth Blue, Timothy A. Thornton, E. A. Thompson, Ellen M. Wijsman	3
18	Single-marker and multi-marker mixed models for polygenic score analysis in family-based data 2014 ·BMC Proceedings ·(unknown), Mohamad Saad, Andrés Legarra, María Martínez	0
19	Genetic comorbidities in Parkinson's disease 2013 ·Human Molecular Genetics ·Michael A. Nalls, Mohamad Saad, Alastair J. Noyce, Margaux F. Keller, Anette Schrag, JP Bestwick, Bryan J. Traynor, J. Raphael Gibbs, D. G. Hernandez, Mark Cookson, Huw R. Morris, N. Williams, Thomas Gasser, Peter Heutink, Nicholas Wood, John Hardy, María Martínez, A. B. Singleton	48
20	Comparative study of statistical methods for detecting association with rare variants in exome-resequencing data 2011 ·BMC Proceedings ·Mohamad Saad, Aude Saint Pierre, (unknown), (unknown), María Martínez	5

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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