Thomas Nalpathamkalam

4.7k total citations
16 papers, 391 citations indexed

About

Thomas Nalpathamkalam is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, Thomas Nalpathamkalam has authored 16 papers receiving a total of 391 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 4 papers in Immunology. Recurrent topics in Thomas Nalpathamkalam's work include Genomics and Rare Diseases (4 papers), Genetic Associations and Epidemiology (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Thomas Nalpathamkalam is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genetic Associations and Epidemiology (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Thomas Nalpathamkalam collaborates with scholars based in Canada, United States and United Kingdom. Thomas Nalpathamkalam's co-authors include Daniele Merico, Jonathan LaMarre, Pingzhao Hu, Stephen W. Scherer, Christian R. Marshall, Giovanna Pellecchia, Brendan J. Frey, Babak Alipanahi, James D. Mills and Heidi I.L. Jacobs and has published in prestigious journals such as Nature Genetics, International Journal of Molecular Sciences and The American Journal of Human Genetics.

In The Last Decade

Thomas Nalpathamkalam

14 papers receiving 388 citations

Peers

Thomas Nalpathamkalam

GENET

PHEOH

Kurt N. Hetrick United States

Chen Dong United States

Reenal Pattni United States

Amal Abu Rayyan Palestinian Territory

Frédéric Torès France

Toshiyuki Maeda Japan

Rini Pauly United States

Courtney Sebold United States

Xun Li China

Wendy Hutchison Australia

Kurt N. Hetrick United States

Thomas Nalpathamkalam

250 ×1.2

280 ×1.8

GENET

76 ×1.0

16 ×0.3

15 ×0.3

PHEOH

Citations per year, relative to Thomas Nalpathamkalam Thomas Nalpathamkalam (= 1×) peers Kurt N. Hetrick

Countries citing papers authored by Thomas Nalpathamkalam

Since Specialization

Citations

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

Fields of papers citing papers by Thomas Nalpathamkalam

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Nalpathamkalam

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Nalpathamkalam. A scholar is included among the top collaborators of Thomas Nalpathamkalam 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 Thomas Nalpathamkalam. Thomas Nalpathamkalam is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

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.

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

Aquino, Marla Mendes de, D. Chen, Worrawat Engchuan, et al.. (2024). Chromosome X-wide common variant association study in autism spectrum disorder. The American Journal of Human Genetics. 112(1). 135–153. 7 indexed citations

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.

Nalpathamkalam, Thomas, et al.. (2023). Estimating the proportion of nonsense variants undergoing the newly described phenomenon of manufactured splice rescue. European Journal of Human Genetics. 32(2). 238–242. 5 indexed citations

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

Kaushik, Azad, et al.. (2021). Bovine neonate is deficient in innate immunity at birth. Molecular Immunology. 133. 101–109. 5 indexed citations

Nalpathamkalam, Thomas, et al.. (2019). Using Next-Generation Sequencing Transcriptomics To Determine Markers of Post-traumatic Symptoms: Preliminary Findings from a Post-deployment Cohort of Soldiers. G3 Genes Genomes Genetics. 9(2). 463–471. 5 indexed citations

Nalpathamkalam, Thomas, et al.. (2016). MicroRNA Expression during Bovine Oocyte Maturation and Fertilization. International Journal of Molecular Sciences. 17(3). 396–396. 82 indexed citations

10.

Merico, Daniele, Mehdi Zarrei, Gregory Costain, et al.. (2015). Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome. G3 Genes Genomes Genetics. 5(11). 2453–2461. 40 indexed citations

11.

Allen, Upton, Pingzhao Hu, Sérgio L. Pereira, et al.. (2015). The genetic diversity of Epstein–Barr virus in the setting of transplantation relative to non‐transplant settings: A feasibility study. Pediatric Transplantation. 20(1). 124–129. 5 indexed citations

12.

Uddin, Mohammed, Kristiina Tammimies, Giovanna Pellecchia, et al.. (2014). Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder. Nature Genetics. 46(7). 742–747. 98 indexed citations

13.

Ngan, Bo, Daniele Merico, Nufar Marcus, et al.. (2014). Mutations in tetratricopeptide repeat domain 7A (TTC7A) are associated with combined immunodeficiency with dendriform lung ossification but no intestinal atresia. 1(1). 10–26. 7 indexed citations

14.

Nalpathamkalam, Thomas, Andriy Derkach, Andrew D. Paterson, & Daniele Merico. (2014). Genetic Analysis Workshop 18 single-nucleotide variant prioritization based on protein impact, sequence conservation, and gene annotation. BMC Proceedings. 8(S1). S11–S11. 6 indexed citations

15.

Mills, James D., Thomas Nalpathamkalam, Heidi I.L. Jacobs, et al.. (2013). RNA-Seq analysis of the parietal cortex in Alzheimer's disease reveals alternatively spliced isoforms related to lipid metabolism. Neuroscience Letters. 536. 90–95. 57 indexed citations

16.

Dorfman, Ruslan, Thomas Nalpathamkalam, Chelsea Taylor, et al.. (2010). Do common in silico tools predict the clinical consequences of amino‐acid substitutions in the CFTR gene?. Clinical Genetics. 77(5). 464–473. 55 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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