Moeenaldeen AlSayed

1.7k total citations
49 papers, 737 citations indexed

About

Moeenaldeen AlSayed is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Moeenaldeen AlSayed has authored 49 papers receiving a total of 737 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 18 papers in Physiology and 17 papers in Genetics. Recurrent topics in Moeenaldeen AlSayed's work include Lysosomal Storage Disorders Research (12 papers), Metabolism and Genetic Disorders (11 papers) and Mitochondrial Function and Pathology (7 papers). Moeenaldeen AlSayed is often cited by papers focused on Lysosomal Storage Disorders Research (12 papers), Metabolism and Genetic Disorders (11 papers) and Mitochondrial Function and Pathology (7 papers). Moeenaldeen AlSayed collaborates with scholars based in Saudi Arabia, United Kingdom and Italy. Moeenaldeen AlSayed's co-authors include Faiqa Imtiaz, Khushnooda Ramzan, Roberto Giugliani, Brian F. Meyer, Rossella Parini, Christian J. Hendriksz, Julian Raiman, Paul Harmatz, Nicole L. Miller and Derralynn Hughes and has published in prestigious journals such as The American Journal of Human Genetics, Gene and Cells.

In The Last Decade

Moeenaldeen AlSayed

43 papers receiving 727 citations

Peers

Countries citing papers authored by Moeenaldeen AlSayed

Since Specialization

Citations

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

Fields of papers citing papers by Moeenaldeen AlSayed

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Moeenaldeen AlSayed

This figure shows the co-authorship network connecting the top 25 collaborators of Moeenaldeen AlSayed. A scholar is included among the top collaborators of Moeenaldeen AlSayed 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 Moeenaldeen AlSayed. Moeenaldeen AlSayed 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	Natural history of SPTBN4-related neurodevelopmental disorder with hypotonia, neuropathy, and deafness 2025 ·Orphanet Journal of Rare Diseases ·(unknown), Mohammad A. Al–Muhaizea, (unknown), (unknown), (unknown), (unknown), Anoud Albader, (unknown), Rawan Almass, Albandary AlBakheet, Tarfa Al‐Sheddi, Eman Alobeid, Maha Al‐Rasheed, Ali Al‐Odaib, Hamad Alzaidan, Moeenaldeen AlSayed, Namik Kaya	0
2	Consensus-based expert recommendations on the management of MPS IVa and VI in Saudi Arabia 2024 ·Orphanet Journal of Rare Diseases ·Moeenaldeen AlSayed, (unknown), (unknown), (unknown), Nouriya Al‐Sannaa, (unknown), Maha Faden	2
3	Expanding the allelic spectrum of ELOVL4‐related autosomal recessive neuro‐ichthyosis 2023 ·Molecular Genetics & Genomic Medicine ·(unknown), (unknown), Haya H. Al‐Balool, Alice Gardham, Emma Wakeling, Harry G. Leitch, Moeenaldeen AlSayed, (unknown), (unknown), Antonio Romito, Kapil Kampe, Sacha Ferdinandusse, (unknown), (unknown), (unknown), Lailá Bastaki, Frédéric M. Vaz, Aida M. Bertoli‐Avella, Dana Marafi	4
4	A Novel Homozygous Founder Variant of RTN4IP1 in Two Consanguineous Saudi Families 2022 ·Cells ·Mazhor Aldosary, Maysoon Alsagob, (unknown), (unknown), Stefan T. Arold, (unknown), (unknown), Rawan Almass, Albandary AlBakheet, (unknown), Alya Qari, Mysoon M. Al‐Ansari, Monika Oláhová, Saif Alshahrani, Moeenaldeen AlSayed, Dilek Çolak, Robert W. Taylor, Mohammed Al‐Owain, Namik Kaya	0
5	Optimising the diagnosis and referral of achondroplasia in Europe: European Achondroplasia Forum best practice recommendations 2022 ·Orphanet Journal of Rare Diseases ·Valérie Cormier‐Daire, Moeenaldeen AlSayed, (unknown), (unknown), Tawfeg Ben‐Omran, Silvio Boero, Svein O. Fredwall, Cathérine Garel, Encarna Guillén‐Navarro, Melita Irving, (unknown), Mohamad Maghnie, Geert Mortier, Sérgio B. Sousa, Klaus Mohnike	6
6	Optimising care and follow-up of adults with achondroplasia 2022 ·Orphanet Journal of Rare Diseases ·Svein O. Fredwall, (unknown), Moeenaldeen AlSayed, (unknown), Tawfeg Ben‐Omran, Silvio Boero, Valérie Cormier‐Daire, Encarna Guillén‐Navarro, Melita Irving, (unknown), Mohamad Maghnie, Klaus Mohnike, Geert Mortier, Sérgio B. Sousa, Michael Wright	6
7	The first European consensus on principles of management for achondroplasia 2021 ·Orphanet Journal of Rare Diseases ·Valérie Cormier‐Daire, Moeenaldeen AlSayed, Tawfeg Ben‐Omran, Sérgio B. Sousa, Silvio Boero, Svein O. Fredwall, Encarna Guillén‐Navarro, Melita Irving, (unknown), Mohamad Maghnie, Geert Mortier, (unknown), Klaus Mohnike	28
8	The neuroimaging findings of monocarboxylate transporter 1 deficiency 2020 ·Neuroradiology ·(unknown), R. Medlej, Raashda A. Sulaiman, Moeenaldeen AlSayed	3
9	Recessive, Deleterious Variants in SMG8 Expand the Role of Nonsense-Mediated Decay in Developmental Disorders in Humans 2020 ·The American Journal of Human Genetics ·Fatema Alzahrani, Hiroyuki Kuwahara, (unknown), Mohammed Al‐Owain, (unknown), Moeenaldeen AlSayed, Mohammed Mahnashi, (unknown), Maha Alnemer, Mohamed H. Al‐Hamed, Gabrielle Lemire, Kym M. Boycott, Mais Hashem, Wenkai Han, Almundher Al‐Maawali, (unknown), Khalid Al‐Thihli, Xin Gao, Fowzan S. Alkuraya	19
10	Homozygous loss‐of‐function variants of TASP1 , a gene encoding an activator of the histone methyltransferases KMT2A and KMT2D, cause a syndrome of developmental delay, happy demeanor, distinctive facial features, and congenital anomalies 2019 ·Human Mutation ·Jehan Suleiman, Korbinian M. Riedhammer, (unknown), (unknown), Laurie Werner, Mirjana Gušić, (unknown), Hessa S. Alsaif, (unknown), Nabil Moghrabi, (unknown), Moeenaldeen AlSayed, Weimin Bi, Srirangan Sampath, Fowzan S. Alkuraya, Ayman W. El‐Hattab	9
11	Spectrum of mutations underlying Propionic acidemia and further insight into a genotype-phenotype correlation for the common mutation in Saudi Arabia 2019 ·Molecular Genetics and Metabolism Reports ·Mohamed H. Al‐Hamed, Faiqa Imtiaz, Zuhair N. Al‐Hassnan, Mohammed Al‐Owain, Hamad Alzaidan, Mohamed Al‐Amoudi, Eissa Faqeih, Majid Alfadhel, Ali Alasmari, Mohammed M. Saleh, Fuad Al Mutairi, Nabil Moghrabi, Moeenaldeen AlSayed	12
12	Mucopolysaccharidoses: overview of neuroimaging manifestations 2018 ·Pediatric Radiology ·(unknown), Moeenaldeen AlSayed	24
13	Impact of long-term elosulfase alfa on activities of daily living in patients with Morquio A syndrome in an open-label, multi-center, phase 3 extension study 2017 ·Molecular Genetics and Metabolism ·Christian J. Hendriksz, Rossella Parini, Moeenaldeen AlSayed, Julian Raiman, Roberto Giugliani, John J. Mitchell, Barbara K. Burton, Norberto Guelbert, Fiona Stewart, Derralynn Hughes, Robert Matousek, Sara M. Hawley, Celeste Decker, Paul Harmatz	22
14	Mitochondrial Neurogastrointestinal Encephalomyopathy Treated with Stem Cell Transplantation 2015 ·Hematology/Oncology and Stem Cell Therapy ·(unknown), (unknown), (unknown), Moeenaldeen AlSayed, Hazzaa Alzahrani	12
15	Multi-domain impact of elosulfase alfa in Morquio A syndrome in the pivotal phase III trial 2014 ·Molecular Genetics and Metabolism ·Christian J. Hendriksz, (unknown), Paul Harmatz, Eugen Mengel, Nathalie Guffon, Vassili Valayannopoulos, Rossella Parini, Derralynn Hughes, Gregory M. Pastores, Heather Lau, Moeenaldeen AlSayed, Julian Raiman, Kehu Yang, Matthew E. Mealiffe, Christine Haller	62
16	Spectrum of Mutations in 60 Saudi Patients with Mut Methylmalonic Acidemia 2014 ·JIMD Reports ·Faiqa Imtiaz, (unknown), (unknown), Mohamed H. Al‐Hamed, (unknown), Zuhair N. Al‐Hassnan, Mohammed Al‐Owain, Hamad Alzaidan, Zuhair Rahbeeni, Alya Qari, Eissa Faqeih, Ali Alasmari, (unknown), Majid Alfadhel, Wafaa Eyaid, Mohamed S. Rashed, Moeenaldeen AlSayed	5
17	Mutations in NALCN Cause an Autosomal-Recessive Syndrome with Severe Hypotonia, Speech Impairment, and Cognitive Delay 2013 ·The American Journal of Human Genetics ·Moeenaldeen AlSayed, Hamad Alzaidan, Albandary AlBakheet, (unknown), (unknown), Yusra Alyafee, Mazhor Aldosary, Alya Qari, Tarfa Al‐Sheddi, (unknown), (unknown), (unknown), Hindi Al‐Hindi, (unknown), Dilek Çolak, Namik Kaya	69
18	Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan disease 2008 ·Genetics in Medicine ·Namik Kaya, Faiqa Imtiaz, Dilek Çolak, Moeenaldeen AlSayed, Ali Al‐Odaib, (unknown), Bashayer Al‐Mubarak, Mohammad Al-Owain, Hesham Aldhalaan, Aziza Chedrawi, Zuhair N. Al‐Hassnan, Serdar Coşkun, Nadia Sakati, Pinar T. Ozand, Brian F. Meyer	17
19	Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3) 2008 ·European Journal of Human Genetics ·Osama Alsmadi, Brian F. Meyer, Fowzan S. Alkuraya, Salma M. Wakil, Fadi Alkayal, Haya Al‐Saud, Khushnooda Ramzan, Moeenaldeen AlSayed	32
20	Mutations underlying 3-Hydroxy-3-Methylglutaryl CoA Lyase deficiency in the Saudi population 2006 ·BMC Medical Genetics ·Moeenaldeen AlSayed, Faiqa Imtiaz, Osama Alsmadi, (unknown), Brian F. Meyer	14

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