Mohammad Al-Haggar

475 total citations
47 papers, 330 citations indexed

About

Mohammad Al-Haggar is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Mohammad Al-Haggar has authored 47 papers receiving a total of 330 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 11 papers in Genetics and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Mohammad Al-Haggar's work include Neonatal Health and Biochemistry (4 papers), Glycogen Storage Diseases and Myoclonus (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Mohammad Al-Haggar is often cited by papers focused on Neonatal Health and Biochemistry (4 papers), Glycogen Storage Diseases and Myoclonus (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Mohammad Al-Haggar collaborates with scholars based in Egypt, United States and Japan. Mohammad Al-Haggar's co-authors include Youssef Al‐Tonbary, Ashraf Fouda, Rasha El‐Ashry, Hanan Azzam, Hassan I. El‐Sayyad, Sohier Yahia, Ali Al Kaissi, S. Ben Yahia, Ahmad Settin and Franz Grill and has published in prestigious journals such as SHILAP Revista de lepidopterología, Cells and Nutrition.

In The Last Decade

Mohammad Al-Haggar

39 papers receiving 310 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mohammad Al-Haggar Egypt 11 87 81 53 49 38 47 330
Fatih Kardaş Türkiye 11 87 1.0× 27 0.3× 34 0.6× 24 0.5× 50 1.3× 47 367
Kirsi Auro Finland 11 104 1.2× 31 0.4× 102 1.9× 29 0.6× 40 1.1× 17 431
Emmanuel Economou Greece 12 59 0.7× 134 1.7× 77 1.5× 51 1.0× 54 1.4× 33 547
Shiguo Liu China 12 155 1.8× 63 0.8× 26 0.5× 31 0.6× 40 1.1× 45 455
C W Lam Hong Kong 12 150 1.7× 90 1.1× 102 1.9× 17 0.3× 24 0.6× 28 440
Shinji Nomura Japan 11 74 0.9× 87 1.1× 16 0.3× 32 0.7× 60 1.6× 32 350
María Fernanda Garcés Colombia 16 81 0.9× 117 1.4× 24 0.5× 33 0.7× 44 1.2× 23 595
T.M. Mignot France 11 144 1.7× 167 2.1× 64 1.2× 49 1.0× 23 0.6× 17 533
Sali Usher Israel 11 70 0.8× 133 1.6× 40 0.8× 36 0.7× 22 0.6× 20 480
Harun Toy Türkiye 12 47 0.5× 80 1.0× 14 0.3× 67 1.4× 51 1.3× 28 413

Countries citing papers authored by Mohammad Al-Haggar

Since Specialization
Citations

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

Fields of papers citing papers by Mohammad Al-Haggar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mohammad Al-Haggar. 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 Mohammad Al-Haggar. The network helps show where Mohammad Al-Haggar may publish in the future.

Co-authorship network of co-authors of Mohammad Al-Haggar

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

All Works

20 of 20 papers shown
1.
Al-Haggar, Mohammad, et al.. (2023). Analysis of the association of NPHS2 and ACTN4 genes polymorphism with nephrotic syndrome in Egyptian children. Molecular Biology Reports. 50(5). 4481–4490.
2.
Al-Haggar, Mohammad, et al.. (2022). Recurrence pattern of non-syndromic familial congenital heart diseases among a large cohort of families from Egypt. BMC Pediatrics. 22(1). 607–607. 1 indexed citations
3.
Al-Haggar, Mohammad, et al.. (2020). Screening for the Most Common Mutations of CFTR Gene among Egyptian Children with Difficult-to-Treat Asthma. Journal of Pediatric Genetics. 9(3). 164–170. 2 indexed citations
4.
Al-Haggar, Mohammad, Ashraf Bakr, Paul Coucke, et al.. (2017). A novel fibrillin-1 mutation in an egyptian marfan family: A proband showing nephrotic syndrome due to focal segmental glomerulosclerosis. Saudi Journal of Kidney Diseases and Transplantation. 28(1). 141–141. 2 indexed citations
5.
Elbaz, Rizk, et al.. (2015). Overview on attention deficit hyperactivity disorder among children from Delta regions of Egypt (a 10 years-study). Journal of Pediatric Neurology. 4(1). 15–18. 4 indexed citations
6.
7.
Al-Haggar, Mohammad, et al.. (2014). Novel homozygousSLC29A3mutations among two unrelated Egyptian families with spectral features of H-syndrome. Pediatric Diabetes. 16(4). 305–316. 13 indexed citations
8.
El‐Sayyad, Hassan I., et al.. (2014). Effect of maternal diabetes and hypercholesterolemia on fetal liver of albino Wistar rats. Nutrition. 30(3). 326–336. 19 indexed citations
9.
Al-Haggar, Mohammad, et al.. (2013). Partial expression of ornithine transcarbamylase deficiency in an Egyptian female carrier. International Journal of Gynecology & Obstetrics. 124(2). 174–175.
10.
Al-Haggar, Mohammad. (2013). A Recent Experience in an Egyptian Medical Center: Strategies for the Clinical and Genetic Diagnoses of Nephropathic Cystinosis. British Journal of Medicine and Medical Research. 3(4). 1918–1928. 4 indexed citations
11.
Al-Haggar, Mohammad, et al.. (2013). Sporadic Fibrodysplasia Ossificans Progressiva in an Egyptian Infant with c.617G > A Mutation inACVR1Gene: A Case Report and Review of Literature. SHILAP Revista de lepidopterología. 2013. 1–8. 7 indexed citations
12.
Al-Haggar, Mohammad. (2012). Fanconi-Bickel syndrome as an example of marked allelic heterogeneity. World Journal of Nephrology. 1(3). 63–63. 8 indexed citations
13.
Al-Haggar, Mohammad, et al.. (2011). Fanconi Bickel Syndrome: Novel Mutations inGLUT 2Gene Causing a Distinguished Form of Renal Tubular Acidosis in Two Unrelated Egyptian Families. Case Reports in Nephrology. 2011. 1–5. 9 indexed citations
14.
Al-Haggar, Mohammad, et al.. (2010). p.R672C Mutation of MYH3 Gene in an Egyptian Infant Presented with Freeman-Sheldon Syndrome. The Indian Journal of Pediatrics. 78(1). 103–105. 12 indexed citations
15.
Al-Haggar, Mohammad, Ashraf Bakr, Toshihiro Tajima, et al.. (2009). Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: unusual clinical associations and novel claudin16 mutation in an Egyptian family. Clinical and Experimental Nephrology. 13(4). 288–294. 9 indexed citations
16.
Al-Haggar, Mohammad, et al.. (2008). Correlation of thyroid and growth hormones to chromosomal instability in Egyptian Fanconi anemia patients. The Indian Journal of Pediatrics. 75(7). 679–684. 1 indexed citations
17.
Settin, Ahmad, et al.. (2007). Prognostic cytogenetic markers in childhood acute lymphoblastic leukemia. The Indian Journal of Pediatrics. 74(3). 255–263. 12 indexed citations
18.
Al-Haggar, Mohammad, et al.. (2006). Soluble Adhesion Molecules in Juvenile Idiopathic Arthritis: Relation to Activity and Clinical Subtype. Journal of Medical Sciences(Faisalabad). 6(3). 474–479. 1 indexed citations
19.
Al-Haggar, Mohammad, et al.. (2006). Acute Painful Crises of Sickle Cell Disease in Egyptian Children: Predictors of Severity for a Preventive Strategy. International Journal of Hematology. 83(3). 224–228. 5 indexed citations
20.
Settin, Ahmad, et al.. (2006). Genetic Analysis of Rheumatic Fever among Egyptian Families: Consanguinity Pattern, Segregation Analysis and Blood Group Association. Journal of Medical Sciences(Faisalabad). 6(3). 359–366. 1 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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