Tarjinder Singh

11.2k total citations · 1 hit paper
16 papers, 629 citations indexed

About

Tarjinder Singh is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Tarjinder Singh has authored 16 papers receiving a total of 629 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Tarjinder Singh's work include Genetic Associations and Epidemiology (5 papers), Genomics and Rare Diseases (4 papers) and Epigenetics and DNA Methylation (2 papers). Tarjinder Singh is often cited by papers focused on Genetic Associations and Epidemiology (5 papers), Genomics and Rare Diseases (4 papers) and Epigenetics and DNA Methylation (2 papers). Tarjinder Singh collaborates with scholars based in United States, United Kingdom and Tanzania. Tarjinder Singh's co-authors include Ben Z. Stanger, Tao Gao, Changhong Li, Helena Edlund, Nicolai M. Doliba, Brian D. McKenna, James Nguyen, Maximilian Reichert, Tingting Zhang and Roland Stein and has published in prestigious journals such as Science, Nature Communications and Gastroenterology.

In The Last Decade

Tarjinder Singh

15 papers receiving 624 citations

Hit Papers

Pdx1 Maintains β Cell Identity and Function by Repressing... 2014 2026 2018 2022 2014 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tarjinder Singh United States 8 322 269 256 130 100 16 629
Alena Yermalovich United States 7 255 0.8× 172 0.6× 342 1.3× 71 0.5× 205 2.0× 12 658
Hiroki Hirai Japan 15 149 0.5× 149 0.6× 328 1.3× 102 0.8× 57 0.6× 43 663
Heather M. Stringham United States 13 121 0.4× 346 1.3× 447 1.7× 102 0.8× 125 1.3× 19 833
M O Ott France 7 251 0.8× 280 1.0× 573 2.2× 80 0.6× 71 0.7× 7 766
Jason M. Spaeth United States 12 242 0.8× 226 0.8× 330 1.3× 117 0.9× 44 0.4× 17 668
Stephanie C. Colvin United States 12 299 0.9× 286 1.1× 288 1.1× 197 1.5× 143 1.4× 17 685
Dominika Nąckiewicz Canada 9 164 0.5× 102 0.4× 214 0.8× 45 0.3× 30 0.3× 11 773
Eric D. Bankaitis United States 9 402 1.2× 236 0.9× 293 1.1× 136 1.0× 50 0.5× 11 698
Catarina Darnfors Sweden 15 162 0.5× 164 0.6× 213 0.8× 169 1.3× 41 0.4× 18 503
Jonas Ahnfelt‐Rønne Denmark 13 651 2.0× 356 1.3× 426 1.7× 202 1.6× 41 0.4× 18 826

Countries citing papers authored by Tarjinder Singh

Since Specialization
Citations

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

Fields of papers citing papers by Tarjinder Singh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tarjinder Singh

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

All Works

16 of 16 papers shown
1.
Kun, Eucharist, et al.. (2025). The genetic architecture of and evolutionary constraints on the human pelvic form. Science. 388(6743). eadq1521–eadq1521. 3 indexed citations
2.
Boldrini, Maura, Yang Xiao, Tarjinder Singh, et al.. (2024). Omics Approaches to Investigate the Pathogenesis of Suicide. Biological Psychiatry. 96(12). 919–928. 2 indexed citations
3.
Kurki, Mitja, Elisa Rahikkala, Eija Hämäläinen, et al.. (2024). Evidence for the additivity of rare and common variant burden throughout the spectrum of intellectual disability. European Journal of Human Genetics. 32(5). 576–583. 1 indexed citations
4.
Kun, Eucharist, Javier de la Fuente, Prakash Jayakumar, et al.. (2023). The genetic architecture and evolution of the human skeletal form. Science. 381(6655). eadf8009–eadf8009. 23 indexed citations
5.
Koenig, Karl, et al.. (2023). Deep learning based phenotyping of medical images improves power for gene discovery of complex disease. npj Digital Medicine. 6(1). 155–155. 7 indexed citations
6.
Cohen, Bruce M., et al.. (2022). Clinical phenotypes of five patients with psychotic disorders carrying rare schizophrenia-associated loss-of-function variants. Schizophrenia Research. 250. 100–103. 1 indexed citations
7.
Brown, Carolyn Nicole, Sarah G. Cook, Kevin C. Crosby, et al.. (2021). Characterization of six CaMKIIα variants found in patients with schizophrenia. iScience. 24(10). 103184–103184. 10 indexed citations
8.
Singh, Tarjinder, Benjamin M. Neale, & Mark J. Daly. (2019). INITIAL RESULTS FROM THE META-ANALYSIS OF THE WHOLE-EXOMES OF OVER 20,000 SCHIZOPHRENIA CASES AND 45,000 CONTROLS. European Neuropsychopharmacology. 29. S813–S814. 2 indexed citations
9.
Gardner, Eugene J., Elena Prigmore, Giuseppe Gallone, et al.. (2019). Contribution of retrotransposition to developmental disorders. Nature Communications. 10(1). 4630–4630. 39 indexed citations
10.
Singh, Tarjinder, Benjamin M. Neale, & Mark J. Daly. (2019). 54EXOME SEQUENCING OF 23,851 CASES IMPLICATES NOVEL RISK GENES AND PROVIDES INSIGHTS INTO THE GENETIC ARCHITECTURE OF SCHIZOPHRENIA. European Neuropsychopharmacology. 29. S1098–S1098.
11.
Singh, Tarjinder, Adam P. Levine, Philip J Smith, et al.. (2015). Characterization of Expression Quantitative Trait Loci in the Human Colon. Inflammatory Bowel Diseases. 21(2). 251–256. 17 indexed citations
12.
Nkya, Siana, Josephine Mgaya, Tarjinder Singh, et al.. (2015). Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer. BMC Medical Genetics. 16(1). 4–4. 21 indexed citations
13.
Gao, Tao, Brian D. McKenna, Changhong Li, et al.. (2014). Pdx1 Maintains β Cell Identity and Function by Repressing an α Cell Program. Cell Metabolism. 19(2). 259–271. 312 indexed citations breakdown →
14.
Singh, Tarjinder, J. A. Edwards, & Luana S. Maroja. (2014). Development and characterization of 10 microsatellite markers in Sagina nodosa (Caryophyllaceae). Applications in Plant Sciences. 2(1). 1 indexed citations
15.
Nkya, Siana, Tarjinder Singh, Helen Rooks, et al.. (2014). Genome Wide Association Study of Fetal Hemoglobin in Sickle Cell Anemia in Tanzania. PLoS ONE. 9(11). e111464–e111464. 73 indexed citations
16.
Gao, Tao, Dawang Zhou, Chenghua Yang, et al.. (2013). Hippo Signaling Regulates Differentiation and Maintenance in the Exocrine Pancreas. Gastroenterology. 144(7). 1543–1553.e1. 117 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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