Jehannine Austin

6.0k total citations · 1 hit paper
168 papers, 3.8k citations indexed

About

Jehannine Austin is a scholar working on Genetics, Clinical Psychology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jehannine Austin has authored 168 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 86 papers in Genetics, 39 papers in Clinical Psychology and 35 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jehannine Austin's work include BRCA gene mutations in cancer (68 papers), Autism Spectrum Disorder Research (32 papers) and Family Support in Illness (20 papers). Jehannine Austin is often cited by papers focused on BRCA gene mutations in cancer (68 papers), Autism Spectrum Disorder Research (32 papers) and Family Support in Illness (20 papers). Jehannine Austin collaborates with scholars based in Canada, United States and United Kingdom. Jehannine Austin's co-authors include William G. Honer, Michael O’Donovan, Bastiaan Hoogendoorn, Peter J. Oefner, Alicia Semaka, Emily Morris, Tim F. Oberlander, Angela Inglis, Catriona Hippman and Angela M. Devlin and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Jehannine Austin

151 papers receiving 3.8k 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.

From Basic Science to Clinical Application of Polygenic Risk Scores

2020 197 citations Jehannine Austin et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jehannine Austin Canada	31	1.8k	820	735	677	533	168	3.8k
Brion S. Maher United States	36	1.5k 0.8×	1.1k 1.4×	462 0.6×	722 1.1×	551 1.0×	140	4.8k
Jouke‐Jan Hottenga Netherlands	39	2.0k 1.1×	891 1.1×	438 0.6×	790 1.2×	456 0.9×	153	5.2k
Edwin J. C. G. van den Oord United States	34	873 0.5×	1.2k 1.5×	428 0.6×	1.1k 1.7×	339 0.6×	90	4.0k
Oliver S. P. Davis United Kingdom	30	1.0k 0.6×	448 0.5×	332 0.5×	702 1.0×	431 0.8×	71	3.1k
Paul F. O’Reilly United Kingdom	30	2.7k 1.5×	1.1k 1.3×	433 0.6×	554 0.8×	400 0.8×	66	5.0k
Chloe C. Y. Wong United Kingdom	30	1.0k 0.6×	2.0k 2.5×	605 0.8×	522 0.8×	511 1.0×	49	3.6k
Benjamin Williams United States	44	972 0.6×	1.1k 1.3×	903 1.2×	1.8k 2.6×	889 1.7×	73	7.2k
Divya Mehta Australia	26	681 0.4×	1.6k 1.9×	802 1.1×	958 1.4×	193 0.4×	72	4.5k
Joanne M. Meyer United States	45	1.7k 1.0×	1.1k 1.4×	450 0.6×	1.9k 2.9×	479 0.9×	95	6.6k
Laramie E. Duncan United States	23	2.8k 1.6×	1.4k 1.7×	325 0.4×	885 1.3×	400 0.8×	42	5.2k

Countries citing papers authored by Jehannine Austin

Since Specialization

Citations

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

Fields of papers citing papers by Jehannine Austin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jehannine Austin

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

All Works

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20 of 20 papers shown

Dick, Danielle M. & Jehannine Austin. (2026). Providing Personalized Genetic Feedback for Psychiatric and Substance Use Disorders: An Urgent Need for Research.. PubMed. 201(1). 3–8.

Austin, Jehannine, et al.. (2025). Using mixed methods for genetic counseling research. Journal of Genetic Counseling. 34(3). e70031–e70031.

Edwards, Louisa, et al.. (2025). Characterizing models for delivery of pharmacogenomic testing: a scoping review. Pharmacogenomics. 26(13-14). 513–527.

Elliott, Alison M., Jehannine Austin, Bartha Maria Knoppers, et al.. (2025). The impact of genetic counselor involvement in genetic and genomic test order review: A scoping review. Genetics in Medicine. 27(3). 101354–101354. 2 indexed citations

Dick, Danielle M., et al.. (2025). Development of the Comprehensive Addiction Risk Evaluation System: Initial Participant Response to an Online Personalized Feedback Program Integrating Genomic, Behavioral, and Environmental Risk Information. PubMed. 11(1). 113–130.

Austin, Jehannine, et al.. (2025). Assessing the prevalence of unmet need for genetic counseling in Canada and exploring associations with sociodemographic factors. European Journal of Human Genetics. 33(5). 633–641. 2 indexed citations

Lynd, Larry D., et al.. (2025). Exploring individuals’ experiences with self-reported unmet need for genetic testing. European Journal of Human Genetics. 33(5). 649–657. 1 indexed citations

Driver, Morgan N., Sally I‐Chun Kuo, Jehannine Austin, & Danielle M. Dick. (2023). Integrating Theory with Education about Genetic Risk for Alcohol Use Disorder: The Effects of a Brief Online Educational Tool on Elements of the Health Belief Model. PubMed. 9(1-4). 89–99. 1 indexed citations

Cressman, Sonya, Louisa Edwards, Sandra Peterson, et al.. (2023). Costs of major depression covered / not covered in British Columbia, Canada. BMC Health Services Research. 23(1). 1446–1446.

10.

Soda, Takahiro, Amanda R. Merner, Brent J. Small, et al.. (2023). Child and adolescent psychiatrists’ use, attitudes, and understanding of genetic testing and pharmacogenetics in clinical practice. Psychiatry Research. 325. 115246–115246. 10 indexed citations

11.

Morris, Emily, Angela Inglis, & Jehannine Austin. (2022). Psychiatric genetic counseling for people with copy number variants associated with psychiatric conditions. Clinical Genetics. 102(5). 369–378. 4 indexed citations

12.

Folkersen, Lasse, et al.. (2022). A qualitative study exploring the consumer experience of receiving self-initiated polygenic risk scores from a third-party website. European Journal of Human Genetics. 31(4). 424–429. 4 indexed citations

13.

Grant, Peter J., et al.. (2021). Out‐of‐pocket and private pay in clinical genetic testing: A scoping review. Clinical Genetics. 100(5). 504–521. 28 indexed citations

14.

Folkersen, Lasse, et al.. (2021). Why do people seek out polygenic risk scores for complex disorders, and how do they understand and react to results?. European Journal of Human Genetics. 30(1). 81–87. 33 indexed citations

15.

Morris, Emily, Catriona Hippman, Arianne Albert, et al.. (2020). A prospective study to explore the relationship between MTHFR C677T genotype, physiological folate levels, and postpartum psychopathology in at-risk women. PLoS ONE. 15(12). e0243936–e0243936. 6 indexed citations

16.

Gobinath, Aarthi R., et al.. (2019). Folic acid, but not folate, regulates different stages of neurogenesis in the ventral hippocampus of adult female rats. Journal of Neuroendocrinology. 31(10). e12787–e12787. 5 indexed citations

17.

Carrion, Prescilla, et al.. (2014). Parents' experiences of receiving their child's genetic diagnosis: A qualitative study to inform clinical genetics practice. American Journal of Medical Genetics Part A. 164(6). 1496–1502. 56 indexed citations

18.

Buxton, Jane A., et al.. (2013). A Pilot Study of the effect of exposure to Stand-up Comedy Performed by People With Mental Illness on Medical Students' Stigmatization of Affected Individuals. 5(1). 3 indexed citations

19.

Hippman, Catriona, et al.. (2009). Genetic counseling for schizophrenia: A review of referrals to a provincial medical genetics program from 1968 to 2007. American Journal of Medical Genetics Part A. 152A(1). 147–152. 17 indexed citations

20.

Austin, Jehannine, Paul R. Buckland, A.G. Cardno, et al.. (2000). The high affinity neurotensin receptor gene (NTSR1): comparative sequencing and association studies in schizophrenia. Molecular Psychiatry. 5(5). 552–557. 22 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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