Emily Hardisty

834 total citations
17 papers, 301 citations indexed

About

Emily Hardisty is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Cancer Research. According to data from OpenAlex, Emily Hardisty has authored 17 papers receiving a total of 301 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Pediatrics, Perinatology and Child Health, 6 papers in Genetics and 4 papers in Cancer Research. Recurrent topics in Emily Hardisty's work include Prenatal Screening and Diagnostics (14 papers), Fetal and Pediatric Neurological Disorders (4 papers) and Cancer Genomics and Diagnostics (4 papers). Emily Hardisty is often cited by papers focused on Prenatal Screening and Diagnostics (14 papers), Fetal and Pediatric Neurological Disorders (4 papers) and Cancer Genomics and Diagnostics (4 papers). Emily Hardisty collaborates with scholars based in United States, Netherlands and United Kingdom. Emily Hardisty's co-authors include Neeta L. Vora, Kelly L. Gilmore, Sarah K. Dotters‐Katz, Matthew R. Grace, Anne Drapkin Lyerly, Ann Katherine M. Foreman, Jeffrey A. Kuller, Alicia Brandt, Natasha T. Strande and Jonathan S. Berg and has published in prestigious journals such as American Journal of Obstetrics and Gynecology, Obstetrics and Gynecology and Genetics in Medicine.

In The Last Decade

Emily Hardisty

16 papers receiving 291 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Emily Hardisty United States	8	239	147	80	33	29	17	301
Rhiannon Mellis United Kingdom	11	349 1.5×	250 1.7×	107 1.3×	32 1.0×	53 1.8×	17	456
Fatao Li China	10	185 0.8×	157 1.1×	120 1.5×	34 1.0×	40 1.4×	20	326
Yongyi Ma China	10	95 0.4×	102 0.7×	112 1.4×	24 0.7×	39 1.3×	20	263
Gillian Mellars United Kingdom	6	137 0.6×	57 0.4×	79 1.0×	47 1.4×	28 1.0×	8	310
Theresa Boomer United States	10	214 0.9×	110 0.7×	107 1.3×	65 2.0×	16 0.6×	15	330
Achilleas Achilleos Cyprus	10	119 0.5×	56 0.4×	62 0.8×	29 0.9×	37 1.3×	16	197
Molka Kammoun Tunisia	9	144 0.6×	128 0.9×	86 1.1×	16 0.5×	64 2.2×	18	368
Fucheng Li China	9	77 0.3×	52 0.4×	69 0.9×	30 0.9×	31 1.1×	35	216
Varaprasad Kolla Switzerland	7	144 0.6×	34 0.2×	84 1.1×	27 0.8×	12 0.4×	12	279

Countries citing papers authored by Emily Hardisty

Since Specialization

Citations

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

Fields of papers citing papers by Emily Hardisty

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emily Hardisty

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

All Works

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17 of 17 papers shown

Hardisty, Emily, et al.. (2024). Disparities in access to reproductive genetic services associated with geographic location of residence and maternal race and ethnicity. Genetics in Medicine. 26(11). 101221–101221. 1 indexed citations

Boynton, Marcella H., et al.. (2024). Unequal Uptake: Insurance‐Related Disparities in Prenatal Genetic Counseling and Screening at a Quaternary Medical Center. Prenatal Diagnosis. 45(7). 878–885. 1 indexed citations

Hardisty, Emily, et al.. (2024). Novel Missense Variant in the SMARCD1 Gene as the Cause of Coffin–Siris Syndrome 11 in a Fetus With Ambiguous Genitalia and Multiple Dysmorphic Features. Prenatal Diagnosis. 44(12). 1522–1525.

Johnson, Erin, et al.. (2023). Understanding the experiences and perspectives of prenatal screening among a diverse cohort. Prenatal Diagnosis. 43(5). 605–612. 3 indexed citations

Vora, Neeta L., Kelly L. Gilmore, Alicia Brandt, et al.. (2020). An approach to integrating exome sequencing for fetal structural anomalies into clinical practice. Genetics in Medicine. 22(5). 954–961. 51 indexed citations

Hardisty, Emily, Matthew R. Grace, Sarah K. Dotters‐Katz, Jeffrey A. Kuller, & Neeta L. Vora. (2020). Cell-Free DNA Screening: Complexities and Challenges of Clinical Implementation. UNC Libraries. 2 indexed citations

Vora, Neeta L., Kelly L. Gilmore, Alicia Brandt, et al.. (2020). An Approach to Integrating Exome Sequencing for Fetal Structural Anomalies Into Clinical Practice. Obstetrical & Gynecological Survey. 75(10). 585–587. 1 indexed citations

Hardisty, Emily, et al.. (2018). Maternal Malignancy Evaluation After Discordant Cell-Free DNA Results. Obstetrics and Gynecology. 131(3). 464–468. 27 indexed citations

Harris, Sarah, Kelly L. Gilmore, Emily Hardisty, Anne Drapkin Lyerly, & Neeta L. Vora. (2018). Ethical and counseling challenges in prenatal exome sequencing. Prenatal Diagnosis. 38(12). 897–903. 22 indexed citations

10.

Vora, Neeta L., Bradford C. Powell, Alicia Brandt, et al.. (2017). Prenatal exome sequencing in anomalous fetuses: new opportunities and challenges. Genetics in Medicine. 19(11). 1207–1216. 105 indexed citations

11.

Dotters‐Katz, Sarah K., et al.. (2017). Trisomy 13‐confined placental mosaicism: is there an increased risk of gestational hypertensive disorders?. Prenatal Diagnosis. 37(9). 938–939. 9 indexed citations

12.

Grace, Matthew R., Emily Hardisty, Sarah K. Dotters‐Katz, Neeta L. Vora, & Jeffrey A. Kuller. (2016). Cell-Free DNA Screening. Obstetrical & Gynecological Survey. 71(8). 477–487. 45 indexed citations

13.

Osborne, Christine, et al.. (2016). Development, Implementation, and Assessment of a Genetics Curriculum Across Institutions. American Journal of Perinatology Reports. 6(4). e372–e377. 4 indexed citations

14.

Grace, Matthew R., et al.. (2015). Cell free DNA testing–interpretation of results using an online calculator. American Journal of Obstetrics and Gynecology. 213(1). 30.e1–30.e4. 13 indexed citations

15.

Hardisty, Emily, et al.. (2015). Attitudes and Knowledge of Maternal‐Fetal Medicine Fellows Regarding Noninvasive Prenatal Testing. Journal of Genetic Counseling. 25(1). 73–78. 14 indexed citations

16.

Vora, Neeta L., et al.. (2014). More chorionic villi obtained at a single center compared to previously published reports. The Journal of Maternal-Fetal & Neonatal Medicine. 28(1). 46–48. 2 indexed citations

17.

Beamon, Carmen, Emily Hardisty, Sarah Harris, & Neeta L. Vora. (2012). 571: Promises and pitfalls of a new technology: a single center experience with noninvasive prenatal testing (NIPT). American Journal of Obstetrics and Gynecology. 208(1). S244–S245. 1 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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