L.I. Al-Gazali

2.6k total citations
60 papers, 1.5k citations indexed

About

L.I. Al-Gazali is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, L.I. Al-Gazali has authored 60 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 26 papers in Molecular Biology and 13 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in L.I. Al-Gazali's work include Connective tissue disorders research (11 papers), Genetic Syndromes and Imprinting (8 papers) and Metabolism and Genetic Disorders (7 papers). L.I. Al-Gazali is often cited by papers focused on Connective tissue disorders research (11 papers), Genetic Syndromes and Imprinting (8 papers) and Metabolism and Genetic Disorders (7 papers). L.I. Al-Gazali collaborates with scholars based in United Arab Emirates, United States and United Kingdom. L.I. Al-Gazali's co-authors include Adekunle Dawodu, László Sztriha, Yousef M. Abdulrazzaq, Michael Nork, P. DeBuse, Sophie Fletcher, Tarek Gaber, Abdülbari Bener, Maja Di Rocco and Céline Huber and has published in prestigious journals such as Neurology, The American Journal of Human Genetics and Developmental Medicine & Child Neurology.

In The Last Decade

L.I. Al-Gazali

60 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
L.I. Al-Gazali United Arab Emirates 22 691 553 231 207 201 60 1.5k
M. Le Merrer France 23 983 1.4× 919 1.7× 320 1.4× 142 0.7× 135 0.7× 93 1.8k
Christine Verellen‐Dumoulin Belgium 21 750 1.1× 818 1.5× 112 0.5× 133 0.6× 174 0.9× 38 1.8k
Abdelaziz Sefiani Morocco 21 964 1.4× 526 1.0× 141 0.6× 118 0.6× 142 0.7× 123 1.8k
Kathleen A. Leppig United States 23 662 1.0× 681 1.2× 95 0.4× 209 1.0× 124 0.6× 57 2.0k
Katta M. Girisha India 24 977 1.4× 866 1.6× 218 0.9× 171 0.8× 159 0.8× 196 1.9k
Hiroshi Kawame Japan 23 1.1k 1.6× 634 1.1× 139 0.6× 253 1.2× 194 1.0× 66 2.1k
Eul‐Ju Seo South Korea 24 796 1.2× 417 0.8× 98 0.4× 156 0.8× 224 1.1× 116 1.9k
Boris G. Kousseff United States 25 603 0.9× 785 1.4× 143 0.6× 276 1.3× 88 0.4× 83 1.6k
David J. Bunyan United Kingdom 23 991 1.4× 979 1.8× 107 0.5× 113 0.5× 216 1.1× 60 2.0k
Julie McGaughran Australia 25 822 1.2× 727 1.3× 128 0.6× 176 0.9× 343 1.7× 79 2.4k

Countries citing papers authored by L.I. Al-Gazali

Since Specialization
Citations

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

Fields of papers citing papers by L.I. Al-Gazali

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of L.I. Al-Gazali

This figure shows the co-authorship network connecting the top 25 collaborators of L.I. Al-Gazali. A scholar is included among the top collaborators of L.I. Al-Gazali 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 L.I. Al-Gazali. L.I. Al-Gazali 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.
Below, Jennifer E., Dawn Earl, Kathryn M. Shively, et al.. (2012). Whole-Genome Analysis Reveals that Mutations in Inositol Polyphosphate Phosphatase-like 1 Cause Opsismodysplasia. The American Journal of Human Genetics. 92(1). 137–143. 44 indexed citations
2.
Tükel, Turgut, Dražen Šošić, L.I. Al-Gazali, et al.. (2010). Homozygous Nonsense Mutations in TWIST2 Cause Setleis Syndrome. The American Journal of Human Genetics. 87(2). 289–296. 50 indexed citations
3.
Alazami, Anas M., Ranad Shaheen, Fatema Alzahrani, et al.. (2009). FREM1 Mutations Cause Bifid Nose, Renal Agenesis, and Anorectal Malformations Syndrome. The American Journal of Human Genetics. 85(3). 414–418. 64 indexed citations
4.
Dagoneau, Nathalie, Samuel Bellais, Patricia Blanchet, et al.. (2007). Mutations in Cytokine Receptor-Like Factor 1 (CRLF1) Account for Both Crisponi and Cold-Induced Sweating Syndromes. The American Journal of Human Genetics. 80(5). 966–970. 51 indexed citations
5.
Taban, Mehryar, et al.. (2007). Cohen syndrome: Report of nine cases and review of the literature, with emphasis on ophthalmic features. Journal of American Association for Pediatric Ophthalmology and Strabismus. 11(5). 431–437. 33 indexed citations
6.
Rizk, Diaa E. E., et al.. (2006). Sporadic Larsen Syndrome in a Preterm Female Originally Diagnosed as Positional Deformities Due to Oligohydramnios. American Journal of Perinatology. 23(1). 71–74. 4 indexed citations
7.
Al-Gazali, L.I.. (2005). Attitudes toward Genetic Counseling in the United Arab Emirates. Public Health Genomics. 8(1). 48–51. 23 indexed citations
8.
Dagoneau, Nathalie, Déborah Scheffer, Céline Huber, et al.. (2004). Null Leukemia Inhibitory Factor Receptor (LIFR) Mutations in Stüve-Wiedemann/Schwartz-Jampel Type 2 Syndrome. The American Journal of Human Genetics. 74(2). 298–305. 136 indexed citations
9.
Al-Gazali, L.I., et al.. (2004). „Body Stalk Anomaly” (dysplasia umbilico-fetalis) - Eine extrem seltene Entwicklungsfehlbildung. RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren. 176(5). 768–769. 3 indexed citations
10.
Al-Gazali, L.I., Jozef Hertecant, Rania A. Ahmed, Nazir Ahmad Khan, & R. Padmanabhan. (2003). Further delineation of Hennekam syndrome. Clinical Dysmorphology. 12(4). 227–232. 13 indexed citations
11.
Gururaj, Aithala, et al.. (2002). Are the strokes in moyamoya syndrome associated with Down syndrome due to protein C deficiency?. Brain and Development. 24(7). 719–722. 19 indexed citations
12.
Al-Gazali, L.I., et al.. (2002). An autosomal recessive syndrome of nasal anomalies associated with renal and anorectal malformations. Clinical Dysmorphology. 11(1). 33–38. 11 indexed citations
13.
Al-Gazali, L.I., et al.. (2001). Micromelic dwarfism ??? humerus, femur and tibia type. Clinical Dysmorphology. 10(1). 25–28. 3 indexed citations
14.
Al-Gazali, L.I., et al.. (2001). Gerodermia osteodysplastica and wrinkly skin syndrome: Are they the same?. American Journal of Medical Genetics. 101(3). 213–220. 30 indexed citations
15.
Al-Gazali, L.I., R. Padmanabhan, Stepan Melnyk, et al.. (2001). Abnormal folate metabolism and genetic polymorphism of the folate pathway in a child with Down syndrome and neural tube defect. American Journal of Medical Genetics. 103(2). 128–132. 68 indexed citations
16.
Sztriha, László, L.I. Al-Gazali, Ronald J. A. Wanders, et al.. (2000). Abnormal myelin formation in rhizomelic chondrodysplasia punctata type 2 (DHAPAT-deficiency). Developmental Medicine & Child Neurology. 42(7). 492–495. 23 indexed citations
17.
Sztriha, László, et al.. (1999). Joubert’s syndrome: new cases and review of clinicopathologic correlation. Pediatric Neurology. 20(4). 274–281. 34 indexed citations
18.
Al-Gazali, L.I., et al.. (1998). XK aprosencephaly. Clinical Dysmorphology. 7(2). 143–147. 3 indexed citations
19.
Al-Gazali, L.I., et al.. (1998). Autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia and distinctive facial appearance. Clinical Dysmorphology. 7(3). 177–184. 9 indexed citations
20.
Al-Gazali, L.I., et al.. (1996). Anterior encephalocele and anophthalmia. Clinical Dysmorphology. 5(1). 81–83. 3 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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