Ali Hellani

1.1k total citations
39 papers, 787 citations indexed

About

Ali Hellani is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ali Hellani has authored 39 papers receiving a total of 787 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 17 papers in Molecular Biology and 17 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ali Hellani's work include Prenatal Screening and Diagnostics (15 papers), Genomic variations and chromosomal abnormalities (12 papers) and Reproductive Biology and Fertility (4 papers). Ali Hellani is often cited by papers focused on Prenatal Screening and Diagnostics (15 papers), Genomic variations and chromosomal abnormalities (12 papers) and Reproductive Biology and Fertility (4 papers). Ali Hellani collaborates with scholars based in Saudi Arabia, United States and South Africa. Ali Hellani's co-authors include Khaled K. Abu‐Amero, Serdar Coşkun, Saad S. M. Hassan, Thomas M. Bosley, Pinar T. Ozand, Ali Al‐Odaib, Nadia Sakati, Moncef Benkhalifa, Ana González and José M Larruga and has published in prestigious journals such as Human Reproduction, Fertility and Sterility and Journal of the Neurological Sciences.

In The Last Decade

Ali Hellani

39 papers receiving 754 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Ali Hellani 333 311 286 164 86 39 787
Mira Malcov 345 1.0× 355 1.1× 483 1.7× 208 1.3× 118 1.4× 47 917
Jos Dreesen 314 0.9× 382 1.2× 372 1.3× 127 0.8× 78 0.9× 32 898
Azzedine Aboura 525 1.6× 258 0.8× 311 1.1× 100 0.6× 61 0.7× 40 767
J G Lesko 274 0.8× 308 1.0× 383 1.3× 62 0.4× 42 0.5× 15 805
Marie‐France Portnoï 574 1.7× 166 0.5× 446 1.6× 109 0.7× 111 1.3× 29 908
Ayala Aviram‐Goldring 429 1.3× 244 0.8× 411 1.4× 115 0.7× 184 2.1× 31 872
Giuliano Cottone 174 0.5× 350 1.1× 194 0.7× 146 0.9× 39 0.5× 16 615
Sylvie Jaillard 397 1.2× 148 0.5× 435 1.5× 123 0.8× 114 1.3× 54 802
J. O. Van Hemel 809 2.4× 356 1.1× 457 1.6× 107 0.7× 94 1.1× 38 1.1k
Véronique Satre 328 1.0× 114 0.4× 340 1.2× 204 1.2× 243 2.8× 34 775

Countries citing papers authored by Ali Hellani

Since Specialization
Citations

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

Fields of papers citing papers by Ali Hellani

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ali Hellani

This figure shows the co-authorship network connecting the top 25 collaborators of Ali Hellani. A scholar is included among the top collaborators of Ali Hellani 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 Ali Hellani. Ali Hellani 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.
2.
Abu‐Amero, Khaled K., Altaf A. Kondkar, Ali Hellani, Thomas M. Bosley, & Arif O. Khan. (2016). Chromosome 6 microdeletion in a patient with syndromic congenital cranial dysinnervation disorder. Neurosciences. 21(1). 72–74. 1 indexed citations
3.
Fakih, Michael, et al.. (2014). Morphokinetic analysis of cleavage stage embryos and its relationship to aneuploidy in a retrospective time-lapse imaging study. Journal of Assisted Reproduction and Genetics. 32(1). 69–75. 74 indexed citations
4.
Abu‐Amero, Khaled K., Altaf A. Kondkar, Ibrahim A. Alorainy, et al.. (2013). Partial Duplication of Chromosome 19 Associated with Syndromic Duane Retraction Syndrome. Ophthalmic Genetics. 36(1). 14–20. 5 indexed citations
5.
Abu‐Amero, Khaled K., Altaf A. Kondkar, Mustafa A. Salih, et al.. (2013). Ophthalmologic Observations in a Patient with Partial Mosaic Trisomy 8. Ophthalmic Genetics. 34(4). 249–253. 2 indexed citations
6.
Abu‐Amero, Khaled K., Altaf A. Kondkar, Ali Hellani, et al.. (2013). Nicotinic Receptor Mutation in a Mildly Dysmorphic Girl with Duane Retraction Syndrome. Ophthalmic Genetics. 36(2). 99–104. 3 indexed citations
7.
Abu‐Amero, Khaled K., et al.. (2010). Ophthalmologic abnormalities in a de novo terminal 6q deletion. Ophthalmic Genetics. 31(1). 1–11. 14 indexed citations
8.
Abu‐Amero, Khaled K., et al.. (2010). A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotype correlation. BMC Medical Genetics. 11(1). 135–135. 26 indexed citations
9.
Abu‐Amero, Khaled K., Ali Hellani, Mustafa A. Salih, et al.. (2010). Optic disk and white matter abnormalities in a patient with ade novo18p partial monosomy. Ophthalmic Genetics. 31(3). 147–154. 4 indexed citations
10.
Hellani, Ali, et al.. (2009). G6PD Mediterranean S188F Codon Mutation Is Common Among Saudi Sickle Cell Patients and Increases the Risk of Stroke. Genetic Testing and Molecular Biomarkers. 13(4). 449–452. 13 indexed citations
11.
Hellani, Ali, et al.. (2009). Molecular Spectrum of α-Thalassemia Mutations in Microcytic Hypochromic Anemia Patients from Saudi Arabia. Genetic Testing and Molecular Biomarkers. 13(2). 219–221. 26 indexed citations
12.
Abu‐Amero, Khaled K., Ali Hellani, Ana González, et al.. (2009). Saudi Arabian Y-Chromosome diversity and its relationship with nearby regions. BMC Genetics. 10(1). 59–59. 72 indexed citations
13.
Hellani, Ali, et al.. (2008). Successful pregnancies after application of array-comparative genomic hybridization in PGS-aneuploidy screening. Reproductive BioMedicine Online. 17(6). 841–847. 98 indexed citations
14.
Abu‐Amero, Khaled K., et al.. (2008). Five new consanguineous families with horizontal gaze palsy and progressive scoliosis and novel ROBO3 mutations. Journal of the Neurological Sciences. 276(1-2). 22–26. 33 indexed citations
15.
Abu‐Amero, Khaled K., Ali Hellani, & Saeed Bohlega. (2008). Absence of mtDNA mutations in leukocytes of CADASIL patients. BMC Research Notes. 1(1). 16–16. 1 indexed citations
16.
Hellani, Ali, et al.. (2006). Y chromosome microdeletions in infertile men with idiopathic oligo- or azoospermia. PubMed. 3(1). 1–1. 47 indexed citations
17.
Hellani, Ali, et al.. (2005). Clinical application of multiple displacement amplification in preimplantation genetic diagnosis. Reproductive BioMedicine Online. 10(3). 376–380. 64 indexed citations
18.
Hellani, Ali, et al.. (2005). Y chromosome microdeletions: are they implicated in teratozoospermia?. Human Reproduction. 20(12). 3505–3509. 7 indexed citations
19.
Hellani, Ali, Edward H. Schuchman, Ali Al‐Odaib, et al.. (2004). Preimplantation genetic diagnosis for Niemann‐Pick disease type B. Prenatal Diagnosis. 24(12). 943–948. 6 indexed citations
20.
Coşkun, Serdar, et al.. (2003). Nucleolar precursor body distribution in pronuclei is correlated to chromosomal abnormalities in embryos. Reproductive BioMedicine Online. 7(1). 86–90. 22 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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