Bhooma Thiruvahindrapuram

10.9k total citations
47 papers, 880 citations indexed

About

Bhooma Thiruvahindrapuram is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Bhooma Thiruvahindrapuram has authored 47 papers receiving a total of 880 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 18 papers in Molecular Biology and 8 papers in Cognitive Neuroscience. Recurrent topics in Bhooma Thiruvahindrapuram's work include Genomic variations and chromosomal abnormalities (21 papers), Genomics and Rare Diseases (12 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Bhooma Thiruvahindrapuram is often cited by papers focused on Genomic variations and chromosomal abnormalities (21 papers), Genomics and Rare Diseases (12 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Bhooma Thiruvahindrapuram collaborates with scholars based in Canada, United States and United Kingdom. Bhooma Thiruvahindrapuram's co-authors include Stephen W. Scherer, Christian R. Marshall, Daniele Merico, John Wei, Anath C. Lionel, Zhuozhi Wang, Gregory Costain, Anne S. Bassett, Matthew J. Gazzellone and Mehdi Zarrei and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and Gastroenterology.

In The Last Decade

Bhooma Thiruvahindrapuram

43 papers receiving 865 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bhooma Thiruvahindrapuram Canada 14 500 420 147 123 110 47 880
Milen Velinov United States 19 476 1.0× 413 1.0× 121 0.8× 103 0.8× 68 0.6× 57 1.0k
Jean‐Baptiste Rivière Canada 18 575 1.1× 591 1.4× 101 0.7× 136 1.1× 85 0.8× 36 1.2k
Abdul Noor Canada 20 620 1.2× 823 2.0× 145 1.0× 118 1.0× 47 0.4× 42 1.4k
Deborah Barbouth United States 11 412 0.8× 285 0.7× 183 1.2× 85 0.7× 54 0.5× 32 678
Roger H. Reeves United States 8 576 1.2× 696 1.7× 95 0.6× 95 0.8× 42 0.4× 10 1.4k
Susan Walker Canada 20 572 1.1× 466 1.1× 210 1.4× 153 1.2× 38 0.3× 48 1.1k
Theresa A. Grebe United States 16 458 0.9× 449 1.1× 102 0.7× 92 0.7× 36 0.3× 34 879
Nathalie Van der Aa Belgium 19 388 0.8× 412 1.0× 92 0.6× 38 0.3× 98 0.9× 26 809
Paul C. Lott United States 13 299 0.6× 1.3k 3.1× 67 0.5× 139 1.1× 50 0.5× 23 1.7k
Karola Rehnström Finland 14 432 0.9× 257 0.6× 256 1.7× 48 0.4× 67 0.6× 21 760

Countries citing papers authored by Bhooma Thiruvahindrapuram

Since Specialization
Citations

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

Fields of papers citing papers by Bhooma Thiruvahindrapuram

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bhooma Thiruvahindrapuram

This figure shows the co-authorship network connecting the top 25 collaborators of Bhooma Thiruvahindrapuram. A scholar is included among the top collaborators of Bhooma Thiruvahindrapuram 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 Bhooma Thiruvahindrapuram. Bhooma Thiruvahindrapuram 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.
Khateeb, Jasmin, Yuchong Li, Giovanna Pellecchia, et al.. (2025). Optimized gene transduction in human lung organoids: A high-efficiency method for advanced research applications. Communications Biology. 8(1). 164–164. 2 indexed citations
2.
Merico, Daniele, Nigel Sharfe, Harjit Dadi, et al.. (2025). Pre-T cell receptor-α immunodeficiency detected exclusively using whole genome sequencing. npj Genomic Medicine. 10(1). 2–2. 1 indexed citations
3.
Wang, Zhuozhi, Eric Sanders, Bhooma Thiruvahindrapuram, et al.. (2025). GWAS SVatalog: a visualization tool to aid fine-mapping of GWAS loci with structural variations. Heredity. 135(3). 199–210. 1 indexed citations
4.
Curtis, Meredith, Thomas Nalpathamkalam, Bhooma Thiruvahindrapuram, et al.. (2025). Leveraging cancer mutation data to inform the pathogenicity classification of germline missense variants. PLoS Genetics. 21(1). e1011540–e1011540.
5.
Heung, Tracy, et al.. (2025). Influence of Polygenic Risk on Height and BMI in Adults With a 22q11.2 Microdeletion. Journal of the Endocrine Society. 9(9). bvaf115–bvaf115. 1 indexed citations
6.
Aquino, Marla Mendes de, Xu Chen, Worrawat Engchuan, et al.. (2024). 81. CHARACTERIZING THE GENETIC ARCHITECTURE OF AUTISM FROM A MULTI-ANCESTRY PERSPECTIVE. European Neuropsychopharmacology. 87. 93–94.
7.
Aquino, Marla Mendes de, Worrawat Engchuan, Bhooma Thiruvahindrapuram, et al.. (2023). F57. INVESTIGATION OF THE SEX CHROMOSOMES IN AUTISM SPECTRUM DISORDER. European Neuropsychopharmacology. 75. S251–S252.
8.
Heung, Tracy, Bhooma Thiruvahindrapuram, Worrawat Engchuan, et al.. (2023). Polygenic risk for triglyceride levels in the presence of a high impact rare variant. BMC Medical Genomics. 16(1). 6 indexed citations
9.
Clouthier, Sharon C., André Dufresne, Eveline J. Emmenegger, et al.. (2023). A New Sturgeon Herpesvirus from Juvenile Lake Sturgeon Acipenser fulvescens Displaying Epithelial Skin Lesions. Pathogens. 12(9). 1115–1115.
10.
Scliar, Marília O., Guilherme Debortoli, Bhooma Thiruvahindrapuram, et al.. (2023). Characterization of pharmacogenomic variants in a Brazilian admixed cohort of elderly individuals based on whole-genome sequencing data. Frontiers in Pharmacology. 14. 1178715–1178715. 6 indexed citations
11.
Costa, Claudia Ismania Samogy, Gabriele da Silva Campos, Marília O. Scliar, et al.. (2023). Three generation families: Analysis of de novo variants in autism. European Journal of Human Genetics. 31(9). 1017–1022. 3 indexed citations
12.
Shum, Carole, Bhooma Thiruvahindrapuram, Zhuozhi Wang, et al.. (2023). Combining Off‐flow, a Nextflow‐coded program, and whole genome sequencing reveals unintended genetic variation in CRISPR/Cas-edited iPSCs. Computational and Structural Biotechnology Journal. 23. 638–647. 2 indexed citations
13.
Mojarad, Bahareh A., Worrawat Engchuan, Brett Trost, et al.. (2022). Genome-wide tandem repeat expansions contribute to schizophrenia risk. Molecular Psychiatry. 27(9). 3692–3698. 22 indexed citations
14.
Tsiplova, Kate, Robin Z. Hayeems, Christian R. Marshall, et al.. (2022). Trio genome sequencing for developmental delay and pediatric heart conditions: A comparative microcost analysis. Genetics in Medicine. 24(5). 1027–1036. 9 indexed citations
15.
Reuter, Miriam S., Rajiv Chaturvedi, Rebekah Jobling, et al.. (2021). Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of Fallot. Circulation Genomic and Precision Medicine. 14(4). e003410–e003410. 18 indexed citations
16.
Sargent, Michael, Qin Kuang, John Wei, et al.. (2017). Genome-Wide Analysis Identifies Rare Copy Number Variations Associated with Inflammatory Bowel Disease. Gastroenterology. 152(5). S984–S984. 1 indexed citations
17.
Richard, Anne, Anne Rovelet‐Lecrux, Elsa Delaby, et al.. (2016). The 22q11 PRODH/DGCR6 deletion is frequent in hyperprolinemic subjects but is not a strong risk factor for ASD. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 171(3). 377–382. 1 indexed citations
18.
19.
Marshall, Christian R., Maude E. Phipps, Bhooma Thiruvahindrapuram, et al.. (2014). Novel Population Specific Autosomal Copy Number Variation and Its Functional Analysis amongst Negritos from Peninsular Malaysia. PLoS ONE. 9(6). e100371–e100371. 7 indexed citations
20.
Silversides, Candice K., Anath C. Lionel, Gregory Costain, et al.. (2012). Rare Copy Number Variations in Adults with Tetralogy of Fallot Implicate Novel Risk Gene Pathways. PLoS Genetics. 8(8). e1002843–e1002843. 118 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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