Megan Priston

1.1k total citations
12 papers, 825 citations indexed

About

Megan Priston is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Obstetrics and Gynecology. According to data from OpenAlex, Megan Priston has authored 12 papers receiving a total of 825 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 5 papers in Pediatrics, Perinatology and Child Health and 4 papers in Obstetrics and Gynecology. Recurrent topics in Megan Priston's work include Prenatal Screening and Diagnostics (5 papers), Pregnancy and preeclampsia studies (4 papers) and Connexins and lens biology (4 papers). Megan Priston is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Pregnancy and preeclampsia studies (4 papers) and Connexins and lens biology (4 papers). Megan Priston collaborates with scholars based in Canada, Switzerland and Netherlands. Megan Priston's co-authors include Gail Billingsley, Elise Héon, Daniel F. Schorderet, Alex V. Levin, Andrea L. Vincent, Yvonne M. Buys, Graham E. Trope, Donna Williams-Lyn, Nicolette H. Lubsen and Élise Héon and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and American Journal of Obstetrics and Gynecology.

In The Last Decade

Megan Priston

11 papers receiving 803 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Megan Priston Canada	9	592	385	299	147	70	12	825
J.L. Dufier France	12	208 0.4×	184 0.5×	60 0.2×	61 0.4×	54 0.8×	36	502
Monzer Jabak Saudi Arabia	11	263 0.4×	380 1.0×	110 0.4×	178 1.2×	36 0.5×	13	607
S. Amer Riazuddin United States	13	262 0.4×	321 0.8×	55 0.2×	507 3.4×	22 0.3×	18	707
Monica A. De La Paz United States	14	299 0.5×	429 1.1×	40 0.1×	233 1.6×	21 0.3×	19	606
Lisa R. Grillone United States	15	399 0.7×	527 1.4×	32 0.1×	280 1.9×	25 0.4×	24	1.0k
Yu-Guang He United States	15	396 0.7×	434 1.1×	29 0.1×	238 1.6×	25 0.4×	21	804
Chongfei Jin China	13	239 0.4×	159 0.4×	99 0.3×	32 0.2×	20 0.3×	22	361
Kristin J Al-Ghoul United States	10	436 0.7×	77 0.2×	34 0.1×	53 0.4×	64 0.9×	15	525
K Kigasawa Japan	13	390 0.7×	124 0.3×	54 0.2×	78 0.5×	12 0.2×	21	513
Thomas J. Wubben United States	15	279 0.5×	298 0.8×	40 0.1×	165 1.1×	11 0.2×	46	516

Countries citing papers authored by Megan Priston

Since Specialization

Citations

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

Fields of papers citing papers by Megan Priston

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Megan Priston

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

All Works

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12 of 12 papers shown

Huang, Tianhua, et al.. (2025). Modified multiple marker aneuploidy screening as a primary screening test for preeclampsia: A validation study. Pregnancy Hypertension. 41. 101239–101239.

Huang, Tianhua, et al.. (2023). Prenatal screening for preeclampsia: the roles of placental growth factor and pregnancy–associated plasma protein A in the first trimester and placental growth factor and soluble fms-like tyrosine kinase 1–placental growth factor ratio in the early second trimester. AJOG Global Reports. 3(2). 100193–100193. 3 indexed citations

Huang, Tianhua, H. Melanie Bedford, Megan Priston, et al.. (2022). Modified multiple marker aneuploidy screening as a primary screening test for preeclampsia. BMC Pregnancy and Childbirth. 22(1). 190–190. 8 indexed citations

Huang, Tianhua, Megan Priston, Clare Gibbons, et al.. (2021). Early pregnancy screening for preeclampsia and preterm birth using maternal characteristics and biomarkers. American Journal of Obstetrics and Gynecology. 226(1). S638–S638. 1 indexed citations

Huang, Tianhua, et al.. (2020). Prenatal screening for trisomy 21: a comparative performance and cost analysis of different screening strategies. BMC Pregnancy and Childbirth. 20(1). 713–713. 16 indexed citations

Vincent, Andrea L., Gail Billingsley, Megan Priston, et al.. (2006). Further support of the role of CYP1B1 in patients with Peters anomaly.. PubMed. 12. 506–10. 49 indexed citations

Willoughby, Colin E., Ayad Shafiq, Gail Billingsley, et al.. (2005). CRYBB1 mutation associated with congenital cataract and microcornea.. PubMed. 11. 587–93. 50 indexed citations

Vincent, Andrea L., Gail Billingsley, Yvonne M. Buys, et al.. (2002). Digenic Inheritance of Early-Onset Glaucoma: CYP1B1, a Potential Modifier Gene. The American Journal of Human Genetics. 70(2). 448–460. 244 indexed citations

Héon, Elise, Andrew D. Paterson, Michael Fraser, et al.. (2001). A Progressive Autosomal Recessive Cataract Locus Maps to Chromosome 9q13-q22. The American Journal of Human Genetics. 68(3). 772–777. 45 indexed citations

10.

Priston, Megan. (2001). Functional analyses of two newly identified PITX2 mutants reveal a novel molecular mechanism for Axenfeld-Rieger syndrome. Human Molecular Genetics. 10(16). 1631–1638. 89 indexed citations

11.

Munier, Francis L., Michael J. McFadden, Megan Priston, et al.. (2000). Genetic heterogeneity of the Coppock-like cataract: a mutation in CRYBB2 on chromosome 22q11.2.. PubMed. 41(1). 159–65. 115 indexed citations

12.

Héon, Élise, et al.. (1999). The γ-Crystallins and Human Cataracts: A Puzzle Made Clearer. The American Journal of Human Genetics. 65(5). 1261–1267. 205 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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