Deborah E. McFadden

6.1k total citations · 1 hit paper
79 papers, 3.9k citations indexed

About

Deborah E. McFadden is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Genetics. According to data from OpenAlex, Deborah E. McFadden has authored 79 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Pediatrics, Perinatology and Child Health, 29 papers in Molecular Biology and 28 papers in Genetics. Recurrent topics in Deborah E. McFadden's work include Prenatal Screening and Diagnostics (32 papers), Genetic Syndromes and Imprinting (18 papers) and Gestational Trophoblastic Disease Studies (14 papers). Deborah E. McFadden is often cited by papers focused on Prenatal Screening and Diagnostics (32 papers), Genetic Syndromes and Imprinting (18 papers) and Gestational Trophoblastic Disease Studies (14 papers). Deborah E. McFadden collaborates with scholars based in Canada, United States and Germany. Deborah E. McFadden's co-authors include Wendy P. Robinson, Stevan R. Knezevich, Poul H. Sorensen, Tao Wen, Jerian F. Lim, Maria S. Peñaherrera, Peter von Dadelszen, Ryan K. C. Yuen, Sylvie Langlois and Jan M. Friedman and has published in prestigious journals such as Nature Genetics, The Journal of Cell Biology and PLoS ONE.

In The Last Decade

Deborah E. McFadden

78 papers receiving 3.7k 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.

A novel ETV6-NTRK3 gene fusion in congenital fibrosarcoma

1998 594 citations Deborah E. McFadden et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Deborah E. McFadden Canada	33	1.7k	1.4k	1.0k	783	724	79	3.9k
Yuval Yaron Israel	35	2.6k 1.6×	1.2k 0.8×	1.2k 1.2×	243 0.3×	877 1.2×	182	4.8k
Monica Miozzo Italy	40	669 0.4×	1.9k 1.3×	1.2k 1.2×	853 1.1×	277 0.4×	158	5.0k
Leo P. ten Kate Netherlands	34	1.1k 0.7×	602 0.4×	1.1k 1.1×	655 0.8×	437 0.6×	137	3.3k
J. M. Connor United Kingdom	38	1.4k 0.8×	1.5k 1.0×	1.3k 1.3×	1.5k 2.0×	275 0.4×	105	5.8k
J. Lee Nelson United States	36	1.5k 0.9×	593 0.4×	800 0.8×	167 0.2×	703 1.0×	75	4.7k
Gudrun E. Moore United Kingdom	41	1.8k 1.1×	3.0k 2.1×	2.9k 2.8×	197 0.3×	533 0.7×	135	5.4k
Kaoru Suzumori Japan	30	959 0.6×	799 0.6×	547 0.5×	179 0.2×	631 0.9×	140	3.5k
Angela E. Lin United States	48	1.3k 0.8×	3.0k 2.1×	2.7k 2.7×	1.9k 2.4×	868 1.2×	190	8.6k
Linda M. Ernst United States	31	1.3k 0.8×	457 0.3×	490 0.5×	493 0.6×	499 0.7×	146	3.1k
M Bonduelle Belgium	50	4.1k 2.4×	1.5k 1.1×	2.1k 2.1×	339 0.4×	2.3k 3.2×	208	7.5k

Countries citing papers authored by Deborah E. McFadden

Since Specialization

Citations

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

Fields of papers citing papers by Deborah E. McFadden

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Deborah E. McFadden. 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 Deborah E. McFadden. The network helps show where Deborah E. McFadden may publish in the future.

Co-authorship network of co-authors of Deborah E. McFadden

This figure shows the co-authorship network connecting the top 25 collaborators of Deborah E. McFadden. A scholar is included among the top collaborators of Deborah E. McFadden 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 Deborah E. McFadden. Deborah E. McFadden 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

Blair, John D., Sylvie Langlois, Deborah E. McFadden, & Wendy P. Robinson. (2014). Overlapping DNA methylation profile between placentas with trisomy 16 and early-onset preeclampsia. Placenta. 35(3). 216–222. 27 indexed citations

Hanna, Courtney W., Deborah E. McFadden, & Wendy P. Robinson. (2013). DNA Methylation Profiling of Placental Villi from Karyotypically Normal Miscarriage and Recurrent Miscarriage. American Journal Of Pathology. 182(6). 2276–2284. 30 indexed citations

Hogg, Kirsten, John D. Blair, Deborah E. McFadden, Peter von Dadelszen, & Wendy P. Robinson. (2013). Early Onset Pre-Eclampsia Is Associated with Altered DNA Methylation of Cortisol-Signalling and Steroidogenic Genes in the Placenta. PLoS ONE. 8(5). e62969–e62969. 93 indexed citations

Chau, Vann, Deborah E. McFadden, Kenneth J. Poskitt, & Steven P. Miller. (2013). Chorioamnionitis in the Pathogenesis of Brain Injury in Preterm Infants. Clinics in Perinatology. 41(1). 83–103. 54 indexed citations

Yong, Paul J., Deborah E. McFadden, & Wendy P. Robinson. (2012). Protein Kinase Profiling in Miscarriage: Implications for the Pathogenesis of Trisomic Pregnancy. Journal of Obstetrics and Gynaecology Canada. 34(12). 1141–1148. 6 indexed citations

Yuen, Ryan K. C., et al.. (2011). Genome-wide mapping of imprinted differentially methylated regions by DNA methylation profiling of human placentas from triploidies. Epigenetics & Chromatin. 4(1). 10–10. 56 indexed citations

Cotton, Allison M., Lucia L.C. Lam, Joslynn G. Affleck, et al.. (2011). Chromosome-wide DNA methylation analysis predicts human tissue-specific X inactivation. Human Genetics. 130(2). 187–201. 103 indexed citations

Yuen, Ryan K. C., Sarah Neumann, Alexandra Fok, et al.. (2011). Extensive epigenetic reprogramming in human somatic tissues between fetus and adult. Epigenetics & Chromatin. 4(1). 7–7. 49 indexed citations

Chang, Brent A., Qing Huang, Joanne Quan, et al.. (2011). Early inflammation in the absence of overt infection in preterm neonates exposed to intensive care. Cytokine. 56(3). 621–626. 31 indexed citations

10.

Robinson, Wendy P., Maria S. Peñaherrera, Luana Avila, et al.. (2009). Assessing the role of placental trisomy in preeclampsia and intrauterine growth restriction. Prenatal Diagnosis. 30(1). 1–8. 40 indexed citations

11.

Waye, John S., Barry Eng, Murray Potter, et al.. (2007). De novo mutation of the DHCR7 gene in a fetus with severe Smith–Lemli–Opitz (or RSH) syndrome. American Journal of Medical Genetics Part A. 143A(15). 1799–1801. 1 indexed citations

12.

Robinson, Wendy P., et al.. (2006). Origin and outcome of pregnancies affected by androgenetic/biparental chimerism. Human Reproduction. 22(4). 1114–1122. 62 indexed citations

13.

Bruyèrè, Hélène, Marsha Speevak, E.J.T. Winsor, et al.. (2006). Isodicentric Yp: prenatal diagnosis and outcome in 12 cases. Prenatal Diagnosis. 26(4). 324–329. 27 indexed citations

14.

Allen, Margot I. Van, Erin C. Boyle, Paul Thiessen, et al.. (2006). The impact of prenatal diagnosis on neural tube defect (NTD) pregnancy versus birth incidence in British Columbia. Journal of Applied Genetics. 47(2). 151–158. 28 indexed citations

15.

Robinson, Wendy P., Deborah E. McFadden, Irene Barrett, et al.. (2002). Origin of amnion and implications for evaluation of the fetal genotype in cases of mosaicism. Prenatal Diagnosis. 22(12). 1076–1085. 41 indexed citations

16.

Robinson, Wendy P., Deborah E. McFadden, & Mary D. Stephenson. (2001). The Origin of Abnormalities in Recurrent Aneuploidy/Polyploidy. The American Journal of Human Genetics. 69(6). 1245–1254. 69 indexed citations

17.

Hartwell, T., William E. Schlenger, Lisa M. LaVange, et al.. (1997). Methodological Overview of a Multisite HIV Prevention Trial for Populations at Risk for HIV. AIDS. 11. 9 indexed citations

18.

McFadden, Deborah E., et al.. (1993). Parental origin of triploidy in human fetuses: evidence for genomic imprinting. Human Genetics. 92(5). 465–469. 99 indexed citations

19.

Magee, J. F., Saham Ansari, Deborah E. McFadden, & James E. Dimmick. (1992). Teratoid Wilms' tumour: a report of two cases. Histopathology. 20(5). 427–431. 28 indexed citations

20.

McFadden, Deborah E., et al.. (1989). Survey of neural tube defects in spontaneously aborted embryos. American Journal of Medical Genetics. 32(3). 356–358. 20 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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