Bharti Morar

2.6k total citations
30 papers, 1.4k citations indexed

About

Bharti Morar is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Bharti Morar has authored 30 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 12 papers in Molecular Biology and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Bharti Morar's work include Forensic and Genetic Research (7 papers), Genetic Associations and Epidemiology (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Bharti Morar is often cited by papers focused on Forensic and Genetic Research (7 papers), Genetic Associations and Epidemiology (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Bharti Morar collaborates with scholars based in Australia, United States and Bulgaria. Bharti Morar's co-authors include Luba Kalaydjieva, Assen Jablensky, David Gresham, Peter A. Underhill, David Chandler, Raphaëlle Chaix, Manfred Kayser, Dora Angelicheva, Ivailo Tournev and Cengiz Cinnioğlu and has published in prestigious journals such as PLoS ONE, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Bharti Morar

30 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bharti Morar Australia 17 759 503 229 141 102 30 1.4k
Dora Angelicheva Australia 22 499 0.7× 650 1.3× 483 2.1× 84 0.6× 167 1.6× 40 1.6k
Chiara Magri Italy 17 780 1.0× 435 0.9× 90 0.4× 229 1.6× 14 0.1× 40 1.2k
Olga Derbeneva United States 15 461 0.6× 1.0k 2.1× 58 0.3× 149 1.1× 21 0.2× 21 1.5k
Cristina Santos Spain 22 467 0.6× 649 1.3× 243 1.1× 138 1.0× 9 0.1× 79 1.2k
Juan L. Rodríguez-Flores United States 19 386 0.5× 432 0.9× 126 0.6× 30 0.2× 11 0.1× 29 1.1k
Francesco Calı̀ Italy 19 683 0.9× 467 0.9× 52 0.2× 159 1.1× 8 0.1× 86 1.2k
Ivailo Tournev Bulgaria 14 366 0.5× 294 0.6× 205 0.9× 90 0.6× 59 0.6× 30 829
Chiara Rengo Italy 18 1.1k 1.4× 884 1.8× 50 0.2× 452 3.2× 26 0.3× 22 1.9k
Antonio J. Martínez‐Fuentes Spain 28 354 0.5× 834 1.7× 357 1.6× 27 0.2× 10 0.1× 57 2.3k
Irene Pichler Italy 21 273 0.4× 401 0.8× 145 0.6× 16 0.1× 13 0.1× 45 1.2k

Countries citing papers authored by Bharti Morar

Since Specialization
Citations

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

Fields of papers citing papers by Bharti Morar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bharti Morar

This figure shows the co-authorship network connecting the top 25 collaborators of Bharti Morar. A scholar is included among the top collaborators of Bharti Morar 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 Bharti Morar. Bharti Morar 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.
Lake, Nicole J., Luke E. Formosa, David A. Stroud, et al.. (2019). A patient with homozygous nonsense variants in two Leigh syndrome disease genes: Distinguishing a dual diagnosis from a hypomorphic protein‐truncating variant. Human Mutation. 40(7). 893–898. 7 indexed citations
2.
Hamilton, Eline M., Enrico Bertini, Luba Kalaydjieva, et al.. (2018). UFM1 founder mutation in the Roma population causes severe variant of Hypomyelination with Atrophy of the Basal ganglia and Cerebellum (H-ABC). European Journal of Neurology. 25. 31–32. 1 indexed citations
3.
Melton, Phillip E., Nina S. McCarthy, Bharti Morar, et al.. (2018). Whole genome sequencing of 91 multiplex schizophrenia families reveals increased burden of rare, exonic copy number variation in schizophrenia probands and genetic heterogeneity. Schizophrenia Research. 197. 337–345. 11 indexed citations
4.
Morar, Bharti, Johanna C. Badcock, Michael Phillips, Osvaldo P. Almeida, & Assen Jablensky. (2017). The longevity gene Klotho is differentially associated with cognition in subtypes of schizophrenia. Schizophrenia Research. 193. 348–353. 15 indexed citations
5.
Almeida, Osvaldo P., Bharti Morar, Graeme J. Hankey, et al.. (2017). Longevity Klotho gene polymorphism and the risk of dementia in older men. Maturitas. 101. 1–5. 16 indexed citations
6.
McCarthy, Nina S., et al.. (2016). Integrity of genome-wide genotype data from low passage lymphoblastoid cell lines. Genomics Data. 9. 18–21. 4 indexed citations
7.
McCarthy, Nina S., Phillip E. Melton, Sarah V. Ward, et al.. (2016). Exome array analysis suggests an increased variant burden in families with schizophrenia. Schizophrenia Research. 185. 9–16. 16 indexed citations
8.
Verbrugghe, Phebe, Steven Wiltshire, Kim W. Carter, et al.. (2012). Impact of the Reelin signaling cascade (Ligands–Receptors–Adaptor Complex) on cognition in schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 159B(4). 392–404. 27 indexed citations
9.
Azmanov, Dimitar N., Bharti Morar, Dora Angelicheva, et al.. (2011). Focal epilepsy of probable temporal lobe origin in a Gypsy family showing linkage to a novel locus on 7p21.3. Epilepsy Research. 96(1-2). 101–108. 7 indexed citations
10.
Morar, Bharti, Milan Dragović, Flavie Waters, et al.. (2010). Neuregulin 3 (NRG3) as a susceptibility gene in a schizophrenia subtype with florid delusions and relatively spared cognition. Molecular Psychiatry. 16(8). 860–866. 60 indexed citations
11.
Angelicheva, Dora, Ivailo Tournev, Velina Guergueltcheva, et al.. (2009). Partial epilepsy syndrome in a Gypsy family linked to 5q31.3‐q32. Epilepsia. 50(7). 1679–1688. 15 indexed citations
12.
Almeida, Osvaldo P., Nicola T. Lautenschlager, Bharti Morar, et al.. (2008). KIBRA genetic polymorphism influences episodic memory in later life, but does not increase the risk of mild cognitive impairment. Journal of Cellular and Molecular Medicine. 12(5a). 1672–1676. 75 indexed citations
13.
Kalaydjieva, Luba, Bharti Morar, Raphaëlle Chaix, & Hua Tang. (2005). A newly discovered founder population: the Roma/Gypsies. BioEssays. 27(10). 1084–1094. 75 indexed citations
14.
Chaix, Raphaëlle, Frédéric Austerlitz, Bharti Morar, Luba Kalaydjieva, & Évelyne Heyer. (2004). Vlax Roma history: what do coalescent-based methods tell us?. European Journal of Human Genetics. 12(4). 285–292. 22 indexed citations
15.
Hunter, Michael, Rafaëlle Bernard, Elizabeth Freitas, et al.. (2003). Mutation screening of the N-myc downstream-regulated gene 1 (NDRG1) in patients with Charcot-Marie-Tooth Disease. Human Mutation. 22(2). 129–135. 41 indexed citations
16.
Wise, C., et al.. (2003). A standard protocol for single nucleotide primer extension in the human genome using matrix‐assisted laser desorption/ionization time‐of‐flight mass spectrometry. Rapid Communications in Mass Spectrometry. 17(11). 1195–1202. 21 indexed citations
17.
Pakendorf, Brigitte, Bharti Morar, Larissa A. Tarskaia, et al.. (2002). Y-chromosomal evidence for a strong reduction in male population size of Yakuts. Human Genetics. 110(2). 198–200. 24 indexed citations
18.
Gresham, David, Bharti Morar, Peter A. Underhill, et al.. (2001). Origins and Divergence of the Roma (Gypsies). The American Journal of Human Genetics. 69(6). 1314–1331. 162 indexed citations
19.
Kídd, Kenneth K., Bharti Morar, Carmela M. Castiglione, et al.. (1998). A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus. Human Genetics. 103(2). 211–227. 163 indexed citations
20.
Morar, Bharti & A.B. Lane. (1996). The molecular characterization of Gaucher disease in South Africa. Clinical Genetics. 50(2). 78–84. 12 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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