Pratibha Nair

1.2k total citations
47 papers, 735 citations indexed

About

Pratibha Nair is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Pratibha Nair has authored 47 papers receiving a total of 735 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 19 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Pratibha Nair's work include Genomics and Rare Diseases (10 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Poverty, Education, and Child Welfare (5 papers). Pratibha Nair is often cited by papers focused on Genomics and Rare Diseases (10 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Poverty, Education, and Child Welfare (5 papers). Pratibha Nair collaborates with scholars based in United Arab Emirates, Lebanon and France. Pratibha Nair's co-authors include Mahmoud Taleb Al Ali, Hanan Hamamy, Ghazi Omar Tadmouri, Abdul Rezzak Hamzeh, Mahmoud Taleb Al‐Ali, Najib Al‐Khaja, Stephany El‐Hayek, André Mégarbané, Robert D. Retherford and Griffith Feeney and has published in prestigious journals such as Demography, Human Mutation and Journal of Translational Medicine.

In The Last Decade

Pratibha Nair

43 papers receiving 702 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Pratibha Nair United Arab Emirates 12 248 221 139 117 76 47 735
Akella Radha Rama Devi India 15 147 0.6× 176 0.8× 74 0.5× 188 1.6× 70 0.9× 30 621
Mahmoud Taleb Al Ali United Arab Emirates 5 149 0.6× 71 0.3× 121 0.9× 90 0.8× 73 1.0× 7 455
Nader Al‐Dewik Qatar 16 167 0.7× 251 1.1× 287 2.1× 96 0.8× 277 3.6× 85 933
Mahera Abdulrahman United Arab Emirates 18 94 0.4× 321 1.5× 45 0.3× 39 0.3× 37 0.5× 45 877
Christine Garcia United States 16 67 0.3× 95 0.4× 76 0.5× 35 0.3× 84 1.1× 71 668
Sharon Durfy United States 15 496 2.0× 250 1.1× 32 0.2× 101 0.9× 15 0.2× 40 878
Charles L. Chase United States 15 656 2.6× 1.3k 5.8× 52 0.4× 86 0.7× 43 0.6× 26 2.1k
Suzanne Cole United States 16 53 0.2× 158 0.7× 27 0.2× 18 0.2× 81 1.1× 53 702
Heather Zierhut United States 20 635 2.6× 402 1.8× 33 0.2× 306 2.6× 102 1.3× 74 1.4k
P T Rowley United States 16 237 1.0× 242 1.1× 170 1.2× 195 1.7× 158 2.1× 32 909

Countries citing papers authored by Pratibha Nair

Since Specialization
Citations

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

Fields of papers citing papers by Pratibha Nair

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pratibha Nair

This figure shows the co-authorship network connecting the top 25 collaborators of Pratibha Nair. A scholar is included among the top collaborators of Pratibha Nair 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 Pratibha Nair. Pratibha Nair 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.
Nair, Pratibha, et al.. (2023). Spectrum of genetic disorders and gene variants in the United Arab Emirates national population: insights from the CTGA database. Frontiers in Genetics. 14. 1177204–1177204. 4 indexed citations
2.
Nair, Pratibha, Hicham Mansour, Sandra Sabbagh, et al.. (2019). Further Delineation of the TRAPPC6B Disorder: Report on a New Family and Review. Journal of Pediatric Genetics. 8(4). 252–256. 2 indexed citations
3.
Nair, Pratibha, Stephany El‐Hayek, Samantha Stora, et al.. (2018). COQ8A and MED25 Mutations in a Child with Intellectual Disability, Microcephaly, Seizures, and Spastic Ataxia: Synergistic Effect of Digenic Variants. Molecular Syndromology. 9(6). 319–323. 9 indexed citations
4.
Hamzeh, Abdul Rezzak, et al.. (2018). Identification of a novel homozygous UNC80 variant in a child with infantile hypotonia with psychomotor retardation and characteristic facies-2 (IHPRF2). Metabolic Brain Disease. 33(3). 869–873. 9 indexed citations
5.
6.
Hamzeh, Abdul Rezzak, et al.. (2017). Novel SPG20 mutation in an extended family with Troyer syndrome. Metabolic Brain Disease. 32(6). 2155–2159. 7 indexed citations
7.
Nair, Pratibha, et al.. (2017). Identification of a novel CTCF mutation responsible for syndromic intellectual disability – a case report. BMC Medical Genetics. 18(1). 68–68. 28 indexed citations
8.
Nair, Pratibha, et al.. (2016). Microcephalic primordial dwarfism in an Emirati patient with PNKP mutation. American Journal of Medical Genetics Part A. 170(8). 2127–2132. 7 indexed citations
9.
Hamzeh, Abdul Rezzak, et al.. (2016). A novel missense mutation in ATRX uncovered in a Yemeni family leads to alpha-thalassemia/mental retardation syndrome without alpha-thalassemia. Irish Journal of Medical Science (1971 -). 186(2). 333–337. 5 indexed citations
10.
Nair, Pratibha, et al.. (2016). Meta-analyses of the association of HLA-DRB1 alleles with rheumatoid arthritis among Arabs. International Journal of Rheumatic Diseases. 20(7). 832–838. 5 indexed citations
11.
Nair, Pratibha, et al.. (2016). Novel ECHS1 mutation in an Emirati neonate with severe metabolic acidosis. Metabolic Brain Disease. 31(5). 1189–1192. 19 indexed citations
12.
Hamzeh, Abdul Rezzak, et al.. (2016). A novel nonsense GPSM2 mutation in a Yemeni family underlying Chudley-McCullough syndrome. European Journal of Medical Genetics. 59(6-7). 337–341. 7 indexed citations
13.
Nair, Pratibha, et al.. (2016). Genetics of multifactorial disorders: proceedings of the 6th Pan Arab Human Genetics Conference. Journal of Translational Medicine. 14(1). 96–96. 1 indexed citations
14.
Nair, Pratibha, et al.. (2016). Identification of a Novel Homozygous <b><i>INSR</i></b> Variant in a Patient with Rabson-Mendenhall Syndrome from the United Arab Emirates. Hormone Research in Paediatrics. 87(1). 64–68. 3 indexed citations
15.
Nair, Pratibha, et al.. (2015). A novel SOX18 mutation uncovered in Jordanian patient with hypotrichosis–lymphedema–telangiectasia syndrome by Whole Exome Sequencing. Molecular and Cellular Probes. 30(1). 18–21. 13 indexed citations
16.
Nair, Pratibha, et al.. (2012). Structural patterns of internal migration flows inBotswana: log-linear modeling approach. African Population Studies. 26(2). 1 indexed citations
17.
Nair, Pratibha, et al.. (2012). Cancers in Arab populations: concise notes. Hamdan Medical Journal. 5(1). 79–79. 1 indexed citations
18.
Nair, Pratibha. (2010). Population aging in Botswana: Trends and implications. Journal of African studies. 2(3). 58–64. 1 indexed citations
19.
Nair, Pratibha. (2010). Understanding Below-replacement Fertility in Kerala, India. Journal of Health Population and Nutrition. 28(4). 405–12. 18 indexed citations
20.
Nair, Pratibha, et al.. (1987). Adolescent pregnancy prevention.. PubMed. 36(11). 959–61. 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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