Adila Al‐Kindy

1.1k total citations
10 papers, 179 citations indexed

About

Adila Al‐Kindy is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Adila Al‐Kindy has authored 10 papers receiving a total of 179 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in Adila Al‐Kindy's work include Genomic variations and chromosomal abnormalities (5 papers), RNA modifications and cancer (2 papers) and Congenital heart defects research (2 papers). Adila Al‐Kindy is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), RNA modifications and cancer (2 papers) and Congenital heart defects research (2 papers). Adila Al‐Kindy collaborates with scholars based in Oman, France and Australia. Adila Al‐Kindy's co-authors include Nadia Chuzhanova, Usha Kini, D.N. Cooper, Meena Upadhyaya, Nobuhiko Okamoto, Hirotomo Saitsu, Noriko Miyake, Hirofumi Ohashi, Yoshinori Tsurusaki and Mitsuko Nakashima and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Autism and Developmental Disorders and Clinical Genetics.

In The Last Decade

Adila Al‐Kindy

10 papers receiving 174 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Adila Al‐Kindy Oman	5	119	72	45	39	19	10	179
Mohsin Malik Ireland	5	62 0.5×	19 0.3×	26 0.6×	42 1.1×	14 0.7×	6	153
Berardo Rinaldi Italy	7	99 0.8×	32 0.4×	10 0.2×	90 2.3×	8 0.4×	26	170
Juliane Eckhold Germany	8	116 1.0×	10 0.1×	16 0.4×	66 1.7×	23 1.2×	10	202
Heather Allewelt United States	7	66 0.6×	14 0.2×	27 0.6×	18 0.5×	30 1.6×	12	185
Joseph Hostyk United States	5	86 0.7×	17 0.2×	8 0.2×	85 2.2×	11 0.6×	7	177
Xiangzhi Zhou United States	4	124 1.0×	46 0.6×	42 0.9×	156 4.0×	5 0.3×	5	255
Milena Mariani Italy	9	165 1.4×	19 0.3×	5 0.1×	90 2.3×	13 0.7×	26	236
Mamiko Yamada Japan	9	111 0.9×	12 0.2×	7 0.2×	102 2.6×	14 0.7×	59	216
Jeannette Hoogeboom Netherlands	9	155 1.3×	33 0.5×	5 0.1×	201 5.2×	16 0.8×	13	325
Patrick L. Wilmot United States	10	95 0.8×	13 0.2×	19 0.4×	148 3.8×	11 0.6×	26	238

Countries citing papers authored by Adila Al‐Kindy

Since Specialization

Citations

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

Fields of papers citing papers by Adila Al‐Kindy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Adila Al‐Kindy. 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 Adila Al‐Kindy. The network helps show where Adila Al‐Kindy may publish in the future.

Co-authorship network of co-authors of Adila Al‐Kindy

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

All Works

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10 of 10 papers shown

Fasken, Milo B., Sara W. Leung, Adila Al‐Kindy, et al.. (2024). A biallelic variant of the RNA exosome gene, EXOSC4, associated with neurodevelopmental defects impairs RNA exosome function and translation. Journal of Biological Chemistry. 300(8). 107571–107571. 2 indexed citations

Al‐Kindy, Adila, et al.. (2019). Microphthalmos-anophthalmos-coloboma (MAC) spectrum in two brothers with Renpenning syndrome due to a truncating mutation in the polyglutamine tract binding protein 1 (PQBP1) gene. Ophthalmic Genetics. 40(6). 534–540. 2 indexed citations

Al‐Mamari, Watfa, et al.. (2015). De Novo Duplication of 7p21.1p22.2 in a Child with Autism Spectrum Disorder and Craniofacial Dysmorphism. Sultan Qaboos University medical journal. 15(3). e415–419. 3 indexed citations

Al‐Mamari, Watfa, Abeer Al‐Saegh, Adila Al‐Kindy, et al.. (2015). Diagnostic Yield of Chromosomal Microarray Analysis in a Cohort of Patients with Autism Spectrum Disorders from a Highly Consanguineous Population. Journal of Autism and Developmental Disorders. 45(8). 2323–2328. 9 indexed citations

Bruwer, Zandrè, et al.. (2014). Existing Challenges Associated with Offering Prenatal Genetic Diagnosis in an Arab Society in the Sultanate of Oman. Journal of Genetic Counseling. 23(6). 928–932. 4 indexed citations

Tsurusaki, Yoshinori, Nobuhiko Okamoto, Hirofumi Ohashi, et al.. (2013). Coffin–Siris syndrome is a SWI/SNF complex disorder. Clinical Genetics. 85(6). 548–554. 103 indexed citations

Al‐Kindy, Adila, et al.. (2013). Constitutional trisomy 8 mosaicism syndrome: case report and review.. PubMed. 2(4). 197–201. 7 indexed citations

Al‐Kindy, Adila, et al.. (2013). One in Three : Congenital Bent Bone Disease and Intermittent Hyperthermia in Three Siblings with Stuve-Wiedemann Syndrome. Sultan Qaboos University medical journal. 13(2). 301–305. 3 indexed citations

Al‐Kindy, Adila, et al.. (2013). A rare case of de novo mosaicism: Deletion 18p and isochromosome 18q syndrome.. PubMed. 2(3). 141–6. 1 indexed citations

10.

Al‐Kindy, Adila, Nadia Chuzhanova, Usha Kini, D.N. Cooper, & Meena Upadhyaya. (2012). Genotype-phenotype associations in neurofibromatosis type 1 (NF1): an increased risk of tumor complications in patients with NF1splice-site mutations?. Human Genomics. 6(1). 12–12. 45 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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