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, Vicente M. Cabrera 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

Peers

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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Role of diagnostic intracytoplasmic sperm injection (ICSI) in the management of genetically determined zona pellucida-free oocytes during in vitro fertilization: a case report 2020 ·Zygote ·(unknown), (unknown), Sandro C. Esteves, Mohamed Fawzy, (unknown), Ali Hellani, (unknown), (unknown)	11
2	Chromosome 6 microdeletion in a patient with syndromic congenital cranial dysinnervation disorder 2016 ·Neurosciences ·Khaled K. Abu‐Amero, Altaf A. Kondkar, Ali Hellani, Thomas M. Bosley, Arif O. Khan	1
3	Morphokinetic analysis of cleavage stage embryos and its relationship to aneuploidy in a retrospective time-lapse imaging study 2014 ·Journal of Assisted Reproduction and Genetics ·(unknown), Michael Fakih, (unknown), A Bayram, Ali Hellani, Perumal Vanamail, (unknown), Erdal Budak	74
4	Ophthalmologic Observations in a Patient with Partial Mosaic Trisomy 8 2013 ·Ophthalmic Genetics ·Khaled K. Abu‐Amero, Altaf A. Kondkar, Mustafa A. Salih, Muneera Al-Husain, (unknown), (unknown), Darren T. Oystreck, Ali Hellani, Amal Y. Kentab, Thomas M. Bosley	2
5	Horizontal gaze palsy and progressive scoliosis due to a deleterious mutation inROBO3 2011 ·Ophthalmic Genetics ·Khaled K. Abu‐Amero, Seema Kapoor, Ali Hellani, (unknown), Thomas M. Bosley	12
6	Isolated foveal hypoplasia: report of a new case and detailed genetic investigation 2011 ·International Ophthalmology ·(unknown), Ali Hellani, Khaled K. Abu‐Amero	11
7	Horizontal gaze palsy and progressive scoliosis withoutROBO3mutations 2011 ·Ophthalmic Genetics ·Khaled K. Abu‐Amero, Flavio Faletra, Paolo Gasparini, Fulvio Parentin, Stefano Pensiero, Ibrahim A. Alorainy, Ali Hellani, (unknown), Thomas M. Bosley	10
8	Ophthalmologic abnormalities in a de novo terminal 6q deletion 2010 ·Ophthalmic Genetics ·Khaled K. Abu‐Amero, Ali Hellani, Mustafa A. Salih, (unknown), (unknown), (unknown), Ibrahim A. Alorainy, Thomas M. Bosley	14
9	A t(5;16)(p15.32;q23.3) generating 16q23.3 → qter duplication and 5p15.32 → pter deletion in two siblings with mental retardation, dysmorphic features, and speech delay 2010 ·American Journal of Medical Genetics Part A ·Ali Hellani, Sarar Mohamed, (unknown), Thomas M. Bosley, Khaled K. Abu‐Amero	7
10	G6PD Mediterranean S188F Codon Mutation Is Common Among Saudi Sickle Cell Patients and Increases the Risk of Stroke 2009 ·Genetic Testing and Molecular Biomarkers ·Ali Hellani, (unknown), Khaled K. Abu‐Amero	13
11	Saudi Arabian Y-Chromosome diversity and its relationship with nearby regions 2009 ·BMC Genetics ·Khaled K. Abu‐Amero, Ali Hellani, Ana González, José M Larruga, Vicente M. Cabrera, Peter A. Underhill	72
12	Pregnancy after preimplantation genetic diagnosis for brachydactyly type B 2009 ·Reproductive BioMedicine Online ·Ali Hellani, Khaled K. Abu‐Amero, (unknown), Hadeel Alsharif, (unknown), (unknown)	4
13	Molecular Spectrum of α-Thalassemia Mutations in Microcytic Hypochromic Anemia Patients from Saudi Arabia 2009 ·Genetic Testing and Molecular Biomarkers ·Ali Hellani, (unknown), (unknown), (unknown), (unknown), Khaled K. Abu‐Amero	26
14	A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report 2009 ·Journal of Medical Case Reports ·Khaled K. Abu‐Amero, Hesham Aldhalaan, Saeed Bohlega, Ali Hellani, Robert W. Taylor	6
15	Absence of mtDNA mutations in leukocytes of CADASIL patients 2008 ·BMC Research Notes ·Khaled K. Abu‐Amero, Ali Hellani, Saeed Bohlega	1
16	Successful pregnancies after application of array-comparative genomic hybridization in PGS-aneuploidy screening 2008 ·Reproductive BioMedicine Online ·Ali Hellani, Khaled K. Abu‐Amero, (unknown), (unknown)	98
17	Five new consanguineous families with horizontal gaze palsy and progressive scoliosis and novel ROBO3 mutations 2008 ·Journal of the Neurological Sciences ·Khaled K. Abu‐Amero, (unknown), (unknown), Ali Hellani, Thomas M. Bosley	33
18	Y chromosome microdeletions: are they implicated in teratozoospermia? 2005 ·Human Reproduction ·Ali Hellani, Saad S. M. Hassan, (unknown), Serdar Coşkun	7
19	Preimplantation genetic diagnosis for Niemann‐Pick disease type B 2004 ·Prenatal Diagnosis ·Ali Hellani, Edward H. Schuchman, Ali Al‐Odaib, (unknown), Kamal Jaroudi, Pinar T. Ozand, Serdar Coşkun	6
20	Pregnancy after preimplantation genetic diagnosis for Sanjad–Sakati syndrome 2004 ·Prenatal Diagnosis ·Ali Hellani, (unknown), Kamal Jaroudi, Pinar T. Ozand, Serdar Coşkun	10

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.

Explore authors with similar magnitude of impact