Majed Dasouki

6.1k total citations
90 papers, 2.7k citations indexed

About

Majed Dasouki is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Majed Dasouki has authored 90 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Molecular Biology, 31 papers in Genetics and 15 papers in Physiology. Recurrent topics in Majed Dasouki's work include Genomic variations and chromosomal abnormalities (11 papers), Immunodeficiency and Autoimmune Disorders (11 papers) and Lysosomal Storage Disorders Research (10 papers). Majed Dasouki is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Immunodeficiency and Autoimmune Disorders (11 papers) and Lysosomal Storage Disorders Research (10 papers). Majed Dasouki collaborates with scholars based in United States, Saudi Arabia and Canada. Majed Dasouki's co-authors include Anas M. Abdel Rahman, Minnie Jacob, Andreas L. Lopata, Uttam Garg, Merlin G. Butler, Karine Hovanes, A. S. Najim Al-Din, Amar Mubaidin, Jennifer Roberts and Mason Barr and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Scientific Reports.

In The Last Decade

Majed Dasouki

89 papers receiving 2.6k citations

Peers

Countries citing papers authored by Majed Dasouki

Since Specialization

Citations

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

Fields of papers citing papers by Majed Dasouki

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Majed Dasouki

This figure shows the co-authorship network connecting the top 25 collaborators of Majed Dasouki. A scholar is included among the top collaborators of Majed Dasouki 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 Majed Dasouki. Majed Dasouki 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	Design of an innovative aptasensor for the detection of chemotherapeutic drug Fludarabine phosphate 2024 ·Scientific Reports ·(unknown), Amina Rhouati, Amani Chrouda, Dana Cialla‐May, Jürgen Popp, Saddam Muthana, Majed Dasouki, Mohammed Zourob	1
2	Role of gene therapy in Fanconi anemia 2021 ·Hematology/Oncology and Stem Cell Therapy ·(unknown), (unknown), Aric Parnes, Majed Dasouki, Syed Osman Ahmed, Shahrukh K. Hashmi	7
3	Molecular classification of blood and bleeding disorder genes 2021 ·npj Genomic Medicine ·Batoul Baz, Mohamed Abouelhoda, Tarek Owaidah, Majed Dasouki, Dorota Monies, Nada Al Tassan	2
4	Serum-Based Proteomics Profiling in Adult Patients with Cystic Fibrosis 2020 ·International Journal of Molecular Sciences ·Hicham Benabdelkamel, (unknown), Meshail Okla, Afshan Masood, (unknown), Ibrahim O. Alanazi, Assim A. Alfadda, Imran Nizami, Majed Dasouki, Anas M. Abdel Rahman	14
5	A genomics approach to male infertility 2020 ·Genetics in Medicine ·Naif Alhathal, Sateesh Maddirevula, Serdar Coşkun, (unknown), Mirna Assoum, T.J. Morris, (unknown), (unknown), (unknown), (unknown), Nour Ewida, Mashael Alqahtani, Niema Ibrahim, Firdous Abdulwahab, Waleed Altaweel, Majed Dasouki, Abdullah M. Assiri, (unknown), Fowzan S. Alkuraya	51
6	Metabolomics Distinguishes DOCK8 Deficiency from Atopic Dermatitis: Towards a Biomarker Discovery 2019 ·Metabolites ·Minnie Jacob, (unknown), Xian Luo, Hamoud Al‐Mousa, Rand Arnaout, Bandar Al‐Saud, Andreas L. Lopata, Liang Li, Majed Dasouki, Anas M. Abdel Rahman	19
7	High Incidence of Severe Combined Immunodeficiency Disease in Saudi Arabia Detected Through Combined T Cell Receptor Excision Circle and Next Generation Sequencing of Newborn Dried Blood Spots 2018 ·Frontiers in Immunology ·Hamoud Al‐Mousa, (unknown), (unknown), (unknown), Mohamed Abouelhoda, (unknown), Dorota Monies, Brian F. Meyer, Abbas Hawwari, Majed Dasouki	54
8	Metabolomics Based Profiling of Dexamethasone Side Effects in Rats 2018 ·Frontiers in Pharmacology ·(unknown), Karem H. Alzoubi, Minnie Jacob, Goran Matic, (unknown), Achraf Al Faraj, (unknown), Majed Dasouki, Anas M. Abdel Rahman	73
9	Safety and efficacy of alternative alglucosidase alfa regimens in Pompe disease 2014 ·Neuromuscular Disorders ·Laura E. Case, Carl Bjartmar, Claire Morgan, Robin Casey, Joel Charrow, John Clancy, Majed Dasouki, Stephanie DeArmey, Khan Nedd, (unknown), Heidi Peters, Dawn Phillips, Zachary Spigelman, Cynthia J. Tifft, Priya S. Kishnani	44
10	Flow cytometry biomarkers distinguish DOCK8 deficiency from severe atopic dermatitis 2014 ·Clinical Immunology ·Erin Janssen, Erdyni N. Tsitsikov, Waleed Al–Herz, Marie‐Paule Lefranc, André Mégarbané, Majed Dasouki, Francisco A. Bonilla, Talal A. Chatila, Lynda C. Schneider, Raif S. Geha	21
11	Exome sequencing reveals a thrombopoietin ligand mutation in a Micronesian family with autosomal recessive aplastic anemia 2013 ·Blood ·Majed Dasouki, Syed K. Rafi, (unknown), Nathan R. Wilson, Sunil Abhyankar, Brigitte Ganter, L. Mike Furness, Jianwen Fang, Rodrigo T. Calado, Irfan Saadi	40
12	Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services 2013 ·Gene ·Jennifer Roberts, Karine Hovanes, Majed Dasouki, Ann M. Manzardo, Merlin G. Butler	80
13	Pallido-pyramidal degeneration, supranuclear upgaze paresis and dementia: Kufor-Rakeb syndrome 2009 ·Acta Neurologica Scandinavica ·A. S. Najim Al-Din, (unknown), Amar Mubaidin, Majed Dasouki, (unknown)	127
14	DMD Trp3X nonsense mutation associated with a founder effect in North American families with mild Becker muscular dystrophy 2009 ·Neuromuscular Disorders ·Kevin M. Flanigan, Diane M. Dunn, Andrew von Niederhausern, Michael Howard, Jerry R. Mendell, Anne M. Connolly, Carol Saunders, Ann Modrcin, Majed Dasouki, Giacomo P. Comi, Roberto Del Bo, (unknown), Richard D. Jacobson, Richard S. Finkel, Līvija Medne, Robert B. Weiss	34
15	A 9‐year‐old male with a duplication of chromosome 3p25.3p26.2: Clinical report and gene expression analysis 2006 ·American Journal of Medical Genetics Part A ·Douglas C. Bittel, Nataliya Kibiryeva, Majed Dasouki, Joan H.M. Knoll, Merlin G. Butler	37
16	Germline PTEN Promoter Mutations and Deletions in Cowden/Bannayan-Riley-Ruvalcaba Syndrome Result in Aberrant PTEN Protein and Dysregulation of the Phosphoinositol-3-Kinase/Akt Pathway 2003 ·The American Journal of Human Genetics ·Xiao-Ping Zhou, Kristin Waite, Robert Pilarski, Heather Hampel, Magali Fernandez, (unknown), Majed Dasouki, Gerald L. Feldman, (unknown), Jennifer Ivanovich, Ellen Matloff, (unknown), Mary Ella Pierpont, Donna Russo, Najah T. Nassif, Charis Eng	199
17	Childhood hyperuricemia and acute renal failure resulting from a missense mutation in the HPRT gene 2002 ·American Journal of Medical Genetics ·Tarak Srivastava, John P. O’Neill, Majed Dasouki, Ari M. Simckes	20
18	Autosomal recessive ataxia, slow eye movements and psychomotor retardation 1994 ·Journal of the Neurological Sciences ·A. S. Najim Al-Din, (unknown), Majed Dasouki, (unknown), (unknown), Amar Mubaidin, (unknown)	4
19	Clarification of chromosomal abnormalities associated with sexual ambiguity by studies with Y-chromosomal DNA sequences 1988 ·Cytogenetic and Genome Research ·(unknown), Robert P. Erickson, Majed Dasouki, Thomas W. Glover, (unknown)	15
20	Occurrence of holoprosencephaly in chromosome 13 disorders cannot be explained by duplication/deficiency of a single locus 1986 ·American Journal of Medical Genetics ·Golder N. Wilson, Majed Dasouki, Mason Barr, John M. Opitz, James F. Reynolds	12

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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