W.G. Kearns

3.0k total citations
97 papers, 2.2k citations indexed

About

W.G. Kearns is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, W.G. Kearns has authored 97 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 56 papers in Pediatrics, Perinatology and Child Health, 39 papers in Genetics and 35 papers in Public Health, Environmental and Occupational Health. Recurrent topics in W.G. Kearns's work include Prenatal Screening and Diagnostics (55 papers), Reproductive Biology and Fertility (32 papers) and Assisted Reproductive Technology and Twin Pregnancy (25 papers). W.G. Kearns is often cited by papers focused on Prenatal Screening and Diagnostics (55 papers), Reproductive Biology and Fertility (32 papers) and Assisted Reproductive Technology and Twin Pregnancy (25 papers). W.G. Kearns collaborates with scholars based in United States, United Kingdom and Spain. W.G. Kearns's co-authors include Paul R. Brezina, Terence R. Flotte, P. Pearson, Garry R. Cutting, Mindy S. Christianson, Sandra Afione, Myung‐Geol Pang, Lisa M. Pastore, James H. Segars and J. Stelling and has published in prestigious journals such as Science, Nature Communications and Nature Genetics.

In The Last Decade

W.G. Kearns

97 papers receiving 2.0k citations

Peers

W.G. Kearns
Duan Ma China
Güven Lüleci Türkiye
Tomohiro Fukaya Japan
Mark W. Nachtigal Canada
Schu‐Rern Chern Taiwan
Jung Jae Ko South Korea
Abdelhamid Barakat Morocco
Fanyi Zeng China
Masahiro Tahara Japan
Biserka Mulac‐Jeričević United States
Duan Ma China
W.G. Kearns
Citations per year, relative to W.G. Kearns W.G. Kearns (= 1×) peers Duan Ma

Countries citing papers authored by W.G. Kearns

Since Specialization
Citations

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

Fields of papers citing papers by W.G. Kearns

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by W.G. Kearns. 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 W.G. Kearns. The network helps show where W.G. Kearns may publish in the future.

Co-authorship network of co-authors of W.G. Kearns

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

All Works

20 of 20 papers shown
1.
Kearns, W.G., et al.. (2025). Biomimetic Digital Twins and Multiomics. Journal of Molecular Diagnostics. 27(4). 256–269. 1 indexed citations
2.
Griffin, Darren K., Paul R. Brezina, K.J. Tobler, et al.. (2022). The human embryonic genome is karyotypically complex, with chromosomally abnormal cells preferentially located away from the developing fetus. Human Reproduction. 38(1). 180–188. 22 indexed citations
3.
Kearns, W.G., et al.. (2021). Embryo quality, ploidy, and transfer outcomes in male versus female blastocysts. Journal of Assisted Reproduction and Genetics. 38(9). 2363–2370. 5 indexed citations
4.
5.
6.
Pastore, Lisa M., Mindy S. Christianson, J. Stelling, W.G. Kearns, & James H. Segars. (2017). Reproductive ovarian testing and the alphabet soup of diagnoses: DOR, POI, POF, POR, and FOR. Journal of Assisted Reproduction and Genetics. 35(1). 17–23. 145 indexed citations
7.
Tobler, K.J., Yulian Zhao, Richard Ross, et al.. (2014). The potential use of blastocoel fluid (BF) from expanded blastocysts as a less invasive form of embryo biopsy for preimplantation genetic testing. Fertility and Sterility. 102(3). e183–e184. 2 indexed citations
8.
Tobler, K.J., Yulian Zhao, Robert M. Ross, et al.. (2014). Blastocoel fluid (BF) harbors embryonic DNA that may result from the marginalization of aneuploid cells during embryogenesis. Fertility and Sterility. 102(3). e205–e205. 5 indexed citations
9.
Anchan, Raymond M., et al.. (2013). Ovarian granulosa cells are a viable source of iPSCs with the capacity for epigenetically-biased differentiation into steroidogenic tissue of the ovary. Fertility and Sterility. 100(3). S454–S454. 1 indexed citations
10.
11.
Resetkova, Nina, K.J. Tobler, W.G. Kearns, & Erika F. Werner. (2013). In vitro fertilization (IVF) with 23-chromosome pair preimplantation genetic screening (PGS) is cost effective to achieve a live birth compared to IVF alone for recurrent pregnancy loss (RPL). Fertility and Sterility. 100(3). S99–S100. 1 indexed citations
12.
13.
Tobler, K.J., et al.. (2012). The Incidence of Aneuploidy Significantly Increases After the Age of 40 in Women With a History of Recurrent Pregnancy Loss. Fertility and Sterility. 97(3). S24–S25. 1 indexed citations
14.
Eyaid, Wafaa, Mark V. Clough, Kathleen M. Scott, et al.. (1998). Physical mapping of the nail patella syndrome interval at 9q34: ordering of STSs and ESTs. Human Genetics. 103(4). 525–526. 4 indexed citations
15.
Ponnazhagan, Selvarangan, et al.. (1997). Lack of Site-Specific Integration of the Recombinant Adeno-Associated Virus 2 Genomes in Human Cells. Human Gene Therapy. 8(3). 275–284. 104 indexed citations
16.
17.
Geraghty, Michael T., W.G. Kearns, P. Pearson, & David Valle. (1993). Isolation and Characterization of an Ornithine Aminotransferase-Related Sequence (OATL3) Mapping to 10q26. Genomics. 17(2). 510–513. 3 indexed citations
18.
Lamb, Bruce T., Sangram S. Sisodia, Ann M. Lawler, et al.. (1993). Introduction and expression of the 400 kilobase precursor amyloid protein gene in transgenic mice. Nature Genetics. 5(1). 22–30. 229 indexed citations
19.
Migeon, Barbara R., Matthew J. McGinniss, Stylianos E. Antonarakis, et al.. (1993). Severe Hemophilia A in a Female by Cryptic Translocation: Order and Orientation of Factor VIII within Xq28. Genomics. 16(1). 20–25. 20 indexed citations
20.
Rosenberg, Carla, Gail Stetten, W.G. Kearns, P. Pearson, & John W. Littlefield. (1991). Origin of chromosome rearrangements in two long-lived human keratinocyte lines. In Vitro Cellular & Developmental Biology - Animal. 27(10). 823–825. 4 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 Duan Ma Breakdown of academic impact, for papers by Güven Lüleci Breakdown of academic impact, for papers by Tomohiro Fukaya Breakdown of academic impact, for papers by Mark W. Nachtigal Breakdown of academic impact, for papers by Schu‐Rern Chern Breakdown of academic impact, for papers by Jung Jae Ko Breakdown of academic impact, for papers by Abdelhamid Barakat Breakdown of academic impact, for papers by Fanyi Zeng Breakdown of academic impact, for papers by Masahiro Tahara Breakdown of academic impact, for papers by Biserka Mulac‐Jeričević
Rankless by CCL
2026