Anjali K. Henders

33.4k total citations · 1 hit paper
83 papers, 6.5k citations indexed

About

Anjali K. Henders is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Anjali K. Henders has authored 83 papers receiving a total of 6.5k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Genetics, 28 papers in Molecular Biology and 13 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Anjali K. Henders's work include Genetic Associations and Epidemiology (27 papers), Genetic Mapping and Diversity in Plants and Animals (11 papers) and Epigenetics and DNA Methylation (11 papers). Anjali K. Henders is often cited by papers focused on Genetic Associations and Epidemiology (27 papers), Genetic Mapping and Diversity in Plants and Animals (11 papers) and Epigenetics and DNA Methylation (11 papers). Anjali K. Henders collaborates with scholars based in Australia, United States and United Kingdom. Anjali K. Henders's co-authors include Nicholas G. Martin, Grant W. Montgomery, Andrew C. Heath, Peter M. Visscher, Pamela A. F. Madden, Dale R. Nyholt, Scott D. Gordon, Beben Benyamin, Brian P. McEvoy and Jian Yang and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and PLoS ONE.

In The Last Decade

Anjali K. Henders

79 papers receiving 6.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Common SNPs explain a large proportion of the heritability for human height

2010 2.8k citations Beben Benyamin, Brian P. McEvoy et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anjali K. Henders Australia	35	3.3k	1.8k	498	411	364	83	6.5k
Shashaank Vattikuti United States	10	4.3k 1.3×	1.9k 1.0×	657 1.3×	297 0.7×	358 1.0×	11	7.1k
Christopher Chang United States	12	4.4k 1.3×	1.9k 1.0×	664 1.3×	268 0.7×	339 0.9×	26	7.3k
Scott D. Gordon Australia	31	3.0k 0.9×	1.2k 0.6×	502 1.0×	216 0.5×	196 0.5×	83	6.2k
Daníel F. Guðbjartsson Iceland	41	3.9k 1.2×	3.2k 1.7×	705 1.4×	592 1.4×	359 1.0×	81	8.1k
Yurii S. Aulchenko Netherlands	42	2.9k 0.9×	2.0k 1.1×	424 0.9×	208 0.5×	526 1.4×	156	6.6k
Beben Benyamin Australia	23	3.2k 1.0×	1.0k 0.6×	514 1.0×	321 0.8×	106 0.3×	55	5.7k
Andres Metspalu Estonia	46	2.6k 0.8×	3.6k 1.9×	233 0.5×	378 0.9×	476 1.3×	211	7.4k
Alicia R. Martin United States	28	3.3k 1.0×	1.4k 0.8×	199 0.4×	301 0.7×	171 0.5×	57	5.3k
Roberto Giorda Italy	41	2.0k 0.6×	2.0k 1.1×	622 1.2×	765 1.9×	668 1.8×	157	5.1k
Maja Bućan United States	40	2.8k 0.9×	4.1k 2.2×	546 1.1×	275 0.7×	315 0.9×	102	7.3k

Countries citing papers authored by Anjali K. Henders

Since Specialization

Citations

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

Fields of papers citing papers by Anjali K. Henders

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anjali K. Henders. 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 Anjali K. Henders. The network helps show where Anjali K. Henders may publish in the future.

Co-authorship network of co-authors of Anjali K. Henders

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Rodrigues, Miriam, Chitra Vinnakota, Christina M. Buchanan, et al.. (2025). The genetics of motor neuron disease in New Zealand. Journal of the Neurological Sciences. 474. 123472–123472.

Mehta, Divya, Karen Grewen, Brenda Pearson, et al.. (2021). Genome-wide gene expression changes in postpartum depression point towards an altered immune landscape. Translational Psychiatry. 11(1). 155–155. 22 indexed citations

Crouse, Jacob J., Joanne S. Carpenter, Frank Iorfino, et al.. (2021). Schizophrenia polygenic risk scores in youth mental health: preliminary associations with diagnosis, clinical stage and functioning. BJPsych Open. 7(2). e58–e58. 6 indexed citations

Lavoie, Suzie, Kelly Allott, G. Paul Amminger, et al.. (2019). Harmonised collection of data in youth mental health: Towards large datasets. Australian & New Zealand Journal of Psychiatry. 54(1). 46–56. 8 indexed citations

Steyn, Frederik J., Zara A. Ioannides, Ruben P. A. van Eijk, et al.. (2018). Hypermetabolism in ALS is associated with greater functional decline and shorter survival. Journal of Neurology Neurosurgery & Psychiatry. 89(10). 1016–1023. 169 indexed citations

Mills, Natalie, Robert Maier, John B. Whitfield, et al.. (2017). Investigating the relationship between iron and depression. Journal of Psychiatric Research. 94. 148–155. 10 indexed citations

Kassam, Irfahan, Luke R. Lloyd‐Jones, Alexander Holloway, et al.. (2016). Evidence for mitochondrial genetic control of autosomal gene expression. Human Molecular Genetics. 25(24). ddw347–ddw347. 6 indexed citations

Zhou, Yuan, Gu Zhu, Jac Charlesworth, et al.. (2016). Genetic loci for Epstein-Barr virus nuclear antigen-1 are associated with risk of multiple sclerosis. Multiple Sclerosis Journal. 22(13). 1655–1664. 32 indexed citations

Sapkota, Yadav, John Attia, Scott D. Gordon, et al.. (2015). Genetic burden associated with varying degrees of disease severity in endometriosis. QUT ePrints (Queensland University of Technology).

10.

Sapkota, Yadav, Siew‐Kee Low, John Attia, et al.. (2015). Association between endometriosis and the interleukin 1A (IL1A) locus. QUT ePrints (Queensland University of Technology). 3 indexed citations

11.

Benyamin, Beben, Sonia Shah, Anjali K. Henders, et al.. (2015). Sharing a Placenta is Associated With a Greater Similarity in DNA Methylation in Monochorionic Versus Dichorionic Twin Pars in Blood at Age 14. Twin Research and Human Genetics. 18(6). 680–685. 4 indexed citations

12.

Dennis, Emily L., Neda Jahanshad, Omid Kohannim, et al.. (2014). Serum cholesterol and variant in cholesterol-related gene CETP predict white matter microstructure. Neurobiology of Aging. 35(11). 2504–2513. 23 indexed citations

13.

Sapkota, Yadav, Siew‐Kee Low, John Attia, et al.. (2014). Association between endometriosis and the interleukin 1A (IL1A) locus. Human Reproduction. 30(1). 239–248. 55 indexed citations

14.

Luong, Hien, Jodie N. Painter, Konstantin Shakhbazov, et al.. (2013). Fine mapping of variants associated with endometriosis in the WNT4 region on chromosome 1p36. QUT ePrints (Queensland University of Technology). 17 indexed citations

15.

Powell, Joseph E., Anjali K. Henders, Allan F. McRae, et al.. (2012). The Brisbane Systems Genetics Study: Genetical Genomics Meets Complex Trait Genetics. PLoS ONE. 7(4). e35430–e35430. 66 indexed citations

16.

Ebejer, Jane L., Sarah E. Medland, J. H. J. van der Werf, et al.. (2012). Attention Deficit Hyperactivity Disorder in Australian Adults: Prevalence, Persistence, Conduct Problems and Disadvantage. PLoS ONE. 7(10). e47404–e47404. 85 indexed citations

17.

Nyholt, Dale R., Stuart MacGregor, Anjali K. Henders, et al.. (2010). A simple and fast two-locus quality control test to detect false positives due to batch effects in genome-wide association studies. QUT ePrints (Queensland University of Technology).

18.

Lee, Sang, Dale R. Nyholt, Stuart MacGregor, et al.. (2010). A simple and fast two‐locus quality control test to detect false positives due to batch effects in genome‐wide association studies. Genetic Epidemiology. 34(8). 854–862. 19 indexed citations

19.

Verweij, Karin J. H., Brendan P. Zietsch, Sarah E. Medland, et al.. (2010). A genome-wide association study of Cloninger's temperament scales: Implications for the evolutionary genetics of personality. Biological Psychology. 85(2). 306–317. 71 indexed citations

20.

Benyamin, Beben, Manuel A. R. Ferreira, Gonneke Willemsen, et al.. (2009). Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. Nature Genetics. 41(11). 1173–1175. 188 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.

Explore authors with similar magnitude of impact