Krista Charen

910 total citations
19 papers, 588 citations indexed

About

Krista Charen is a scholar working on Genetics, Cognitive Neuroscience and Clinical Psychology. According to data from OpenAlex, Krista Charen has authored 19 papers receiving a total of 588 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 18 papers in Cognitive Neuroscience and 7 papers in Clinical Psychology. Recurrent topics in Krista Charen's work include Genetics and Neurodevelopmental Disorders (19 papers), Autism Spectrum Disorder Research (18 papers) and Family and Disability Support Research (7 papers). Krista Charen is often cited by papers focused on Genetics and Neurodevelopmental Disorders (19 papers), Autism Spectrum Disorder Research (18 papers) and Family and Disability Support Research (7 papers). Krista Charen collaborates with scholars based in United States. Krista Charen's co-authors include Stephanie L. Sherman, Emily G. Allen, Weiya He, Jessica Ezzell Hunter, Celia E. Dominguez, Michael P. Epstein, Lisa Shubeck, Michele Marcus, Kira C. Taylor and Amy K. Sullivan and has published in prestigious journals such as The American Journal of Human Genetics, Human Reproduction and Neuropsychology.

In The Last Decade

Krista Charen

19 papers receiving 578 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Krista Charen United States 11 501 357 175 111 63 19 588
Weiya He United States 8 418 0.8× 258 0.7× 193 1.1× 55 0.5× 56 0.9× 14 506
Amy K. Sullivan United States 7 756 1.5× 463 1.3× 352 2.0× 73 0.7× 90 1.4× 8 894
Michael D. Wittenberger United States 7 537 1.1× 368 1.0× 254 1.5× 49 0.4× 103 1.6× 8 696
Aimee Anido United States 7 397 0.8× 250 0.7× 271 1.5× 48 0.4× 48 0.8× 8 566
D.M. Hougaard Denmark 4 148 0.3× 229 0.6× 103 0.6× 60 0.5× 48 0.8× 6 430
Jasmine Paquin Canada 5 302 0.6× 183 0.5× 156 0.9× 31 0.3× 60 1.0× 7 416
Paramjit Joshi United States 7 196 0.4× 141 0.4× 143 0.8× 89 0.8× 24 0.4× 9 410
Martine Borghgraef Belgium 18 780 1.6× 408 1.1× 381 2.2× 59 0.5× 11 0.2× 54 925
Behrang Mahjani United States 12 126 0.3× 190 0.5× 50 0.3× 109 1.0× 24 0.4× 28 342
Brian Coppin United Kingdom 6 484 1.0× 160 0.4× 314 1.8× 39 0.4× 18 0.3× 7 680

Countries citing papers authored by Krista Charen

Since Specialization
Citations

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

Fields of papers citing papers by Krista Charen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Krista Charen

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

All Works

19 of 19 papers shown
1.
Albizua, Igor, Krista Charen, Lisa Shubeck, et al.. (2022). Descriptive analysis of seizures and comorbidities associated with fragile X syndrome. Molecular Genetics & Genomic Medicine. 10(8). e2001–e2001. 4 indexed citations
2.
Charen, Krista, Lisa Shubeck, Allyn McConkie‐Rosell, et al.. (2021). Men with an FMR1 premutation and their health education needs. Journal of Genetic Counseling. 30(4). 1156–1167. 1 indexed citations
3.
Allen, Emily G., Krista Charen, Heather S. Hipp, et al.. (2021). Refining the risk for fragile X–associated primary ovarian insufficiency (FXPOI) by FMR1 CGG repeat size. Genetics in Medicine. 23(9). 1648–1655. 31 indexed citations
4.
Allen, Emily G., Krista Charen, Heather S. Hipp, et al.. (2021). Predictors of Comorbid Conditions in Women Who Carry an FMR1 Premutation. Frontiers in Psychiatry. 12. 715922–715922. 6 indexed citations
5.
Charen, Krista, et al.. (2020). Health knowledge of women with a fragile X premutation: Improving understanding with targeted educational material. Journal of Genetic Counseling. 29(6). 983–991. 7 indexed citations
6.
Allen, Emily G., Krista Charen, Heather S. Hipp, et al.. (2020). Clustering of comorbid conditions among women who carry an FMR1 premutation. Genetics in Medicine. 22(4). 758–766. 36 indexed citations
7.
Hunter, Jessica Ezzell, et al.. (2019). Feasibility of an app-based mindfulness intervention among women with an FMR1 premutation experiencing maternal stress. Research in Developmental Disabilities. 89. 76–82. 8 indexed citations
8.
Allen, Emily G., Anne Glicksman, Krista Charen, et al.. (2018). FXPOI: Pattern of AGG Interruptions Does not Show an Association With Age at Amenorrhea Among Women With a Premutation. Frontiers in Genetics. 9. 292–292. 7 indexed citations
9.
Charen, Krista, et al.. (2017). Parental Perspectives on Pharmacological Clinical Trials: a Qualitative Study in Down Syndrome and Fragile X Syndrome. Journal of Genetic Counseling. 26(6). 1333–1340. 12 indexed citations
10.
Hipp, Heather S., Krista Charen, Jessica B. Spencer, Emily G. Allen, & Stephanie L. Sherman. (2016). Reproductive and gynecologic care of women with fragile X primary ovarian insufficiency (FXPOI). Menopause The Journal of The North American Menopause Society. 23(9). 993–999. 39 indexed citations
11.
Charen, Krista, et al.. (2015). Improving Health Education for Women Who Carry an FMR1 Premutation. Journal of Genetic Counseling. 25(2). 228–238. 6 indexed citations
12.
Hunter, Jessica Ezzell, Mary Leslie, Debra Hamilton, et al.. (2012). Depression and anxiety symptoms among women who carry the FMR1 premutation: Impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphisms. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 159B(5). 549–559. 32 indexed citations
13.
Allen, Emily G., Jessica Ezzell Hunter, Jorge L. Juncos, et al.. (2011). Neuropsychological findings from older premutation carrier males and their noncarrier siblings from families with fragile X syndrome.. Neuropsychology. 25(3). 404–411. 15 indexed citations
14.
Visootsak, Jeannie, Krista Charen, Julia K. Rohr, Emily G. Allen, & Stephanie L. Sherman. (2011). Diagnosis of Fragile X Syndrome: A Qualitative Study of African American Families. Journal of Genetic Counseling. 21(6). 845–853. 9 indexed citations
15.
Allen, Emily G., Krista Charen, James R. Giles, et al.. (2008). Anti-Mullerian hormone indicates early ovarian decline in fragile X mental retardation (FMR1) premutation carriers: a preliminary study. Human Reproduction. 23(5). 1220–1225. 64 indexed citations
16.
Hunter, Jessica Ezzell, Michael P. Epstein, Stuart W. Tinker, Krista Charen, & Stephanie L. Sherman. (2008). Fragile X‐associated primary ovarian insufficiency: evidence for additional genetic contributions to severity. Genetic Epidemiology. 32(6). 553–559. 28 indexed citations
17.
Hunter, Jessica Ezzell, Emily G. Allen, Ann Abramowitz, et al.. (2008). No Evidence for a Difference in Neuropsychological Profile among Carriers and Noncarriers of the FMR1 Premutation in Adults under the Age of 50. The American Journal of Human Genetics. 83(6). 692–702. 61 indexed citations
18.
Hunter, Jessica Ezzell, Emily G. Allen, Ann Abramowitz, et al.. (2008). Investigation of Phenotypes Associated with Mood and Anxiety Among Male and Female Fragile X Premutation Carriers. Behavior Genetics. 38(5). 493–502. 52 indexed citations
19.
Allen, Emily G., Amy K. Sullivan, Michele Marcus, et al.. (2007). Examination of reproductive aging milestones among women who carry the FMR1premutation. Human Reproduction. 22(8). 2142–2152. 170 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

Breakdown of academic impact, for papers by Weiya He Breakdown of academic impact, for papers by Amy K. Sullivan Breakdown of academic impact, for papers by Michael D. Wittenberger Breakdown of academic impact, for papers by Aimee Anido Breakdown of academic impact, for papers by D.M. Hougaard Breakdown of academic impact, for papers by Jasmine Paquin Breakdown of academic impact, for papers by Paramjit Joshi Breakdown of academic impact, for papers by Martine Borghgraef Breakdown of academic impact, for papers by Behrang Mahjani Breakdown of academic impact, for papers by Brian Coppin
Rankless by CCL
2026