Wendy P. Robinson

14.7k total citations · 1 hit paper
211 papers, 9.5k citations indexed

About

Wendy P. Robinson is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Wendy P. Robinson has authored 211 papers receiving a total of 9.5k indexed citations (citations by other indexed papers that have themselves been cited), including 123 papers in Pediatrics, Perinatology and Child Health, 101 papers in Genetics and 99 papers in Molecular Biology. Recurrent topics in Wendy P. Robinson's work include Prenatal Screening and Diagnostics (107 papers), Genetic Syndromes and Imprinting (69 papers) and Epigenetics and DNA Methylation (66 papers). Wendy P. Robinson is often cited by papers focused on Prenatal Screening and Diagnostics (107 papers), Genetic Syndromes and Imprinting (69 papers) and Epigenetics and DNA Methylation (66 papers). Wendy P. Robinson collaborates with scholars based in Canada, United States and Switzerland. Wendy P. Robinson's co-authors include Maria S. Peñaherrera, Deborah E. McFadden, Albert Schinzel, E. Magda Price, Ryan K. C. Yuen, Peter von Dadelszen, Sylvie Langlois, Karla L. Bretherick, Carolyn J. Brown and Fosco Bernasconi and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Wendy P. Robinson

206 papers receiving 9.2k 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.

Single-cell assessment of primary and stem cell-derived human trophoblast organoids as placenta-modeling platforms

2024 36 citations Maria S. Peñaherrera, Wendy P. Robinson et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Wendy P. Robinson Canada	56	4.9k	4.7k	4.5k	1.6k	785	211	9.5k
Miguel Constância United Kingdom	44	2.6k 0.5×	4.2k 0.9×	3.3k 0.7×	2.4k 1.5×	565 0.7×	78	7.3k
Rosanna Weksberg Canada	55	5.5k 1.1×	3.1k 0.7×	7.2k 1.6×	407 0.3×	482 0.6×	235	11.2k
Anne C. Ferguson‐Smith United Kingdom	73	9.0k 1.8×	6.7k 1.4×	13.7k 3.0×	2.1k 1.4×	1.1k 1.4×	214	19.1k
Kenichiro Hata Japan	42	3.3k 0.7×	1.9k 0.4×	6.8k 1.5×	248 0.2×	916 1.2×	228	8.8k
Jill Clayton‐Smith United Kingdom	51	5.3k 1.1×	4.1k 0.9×	3.7k 0.8×	253 0.2×	2.0k 2.5×	201	9.7k
Eric Haan Australia	48	2.3k 0.5×	2.3k 0.5×	2.4k 0.5×	534 0.3×	519 0.7×	185	7.3k
Vardhman K. Rakyan United Kingdom	36	2.3k 0.5×	1.4k 0.3×	5.0k 1.1×	430 0.3×	266 0.3×	60	6.4k
Cynthia J. Curry United States	54	2.5k 0.5×	1.6k 0.3×	4.4k 1.0×	333 0.2×	536 0.7×	126	9.8k
Reinald Fundele Germany	32	2.7k 0.5×	1.7k 0.4×	4.6k 1.0×	518 0.3×	731 0.9×	80	5.9k
Hongcang Gu United States	36	2.6k 0.5×	1.5k 0.3×	10.5k 2.3×	272 0.2×	525 0.7×	73	12.5k

Countries citing papers authored by Wendy P. Robinson

Since Specialization

Citations

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

Fields of papers citing papers by Wendy P. Robinson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wendy P. Robinson. 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 Wendy P. Robinson. The network helps show where Wendy P. Robinson may publish in the future.

Co-authorship network of co-authors of Wendy P. Robinson

This figure shows the co-authorship network connecting the top 25 collaborators of Wendy P. Robinson. A scholar is included among the top collaborators of Wendy P. Robinson 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 Wendy P. Robinson. Wendy P. Robinson 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

Jones, Meaghan J., Chaini Konwar, Hamid Reza Razzaghian, et al.. (2025). DNA methylation differences between cord and adult white blood cells reflect postnatal immune cell maturation. Communications Biology. 8(1). 237–237. 1 indexed citations

Peñaherrera, Maria S., Victor Yuan, Victor D. Martínez, et al.. (2025). Profiling the cell-specific small non-coding RNA transcriptome of the human placenta. Scientific Reports. 15(1). 14666–14666.

Yuan, Victor, et al.. (2021). Cell-specific characterization of the placental methylome. BMC Genomics. 22(1). 73 indexed citations

Barros‐Filho, Mateus Camargo, Brenda C. Minatel, Erin A. Marshall, et al.. (2021). Reactivation of Multiple Fetal miRNAs in Lung Adenocarcinoma. Cancers. 13(11). 2686–2686. 3 indexed citations

Peñaherrera, Maria S., Christèle du Souich, Lijia Huang, et al.. (2019). Renpenning syndrome in a female. American Journal of Medical Genetics Part A. 182(3). 498–503. 5 indexed citations

Konwar, Chaini, Giulia Gobbo, Victor Yuan, & Wendy P. Robinson. (2019). Considerations when processing and interpreting genomics data of the placenta. Placenta. 84. 57–62. 20 indexed citations

Matthews, Allison, Maja Tarailo‐Graovac, E. Magda Price, et al.. (2017). A de novo mosaic mutation in SPAST with two novel alternative alleles and chromosomal copy number variant in a boy with spastic paraplegia and autism spectrum disorder. European Journal of Medical Genetics. 60(10). 548–552. 11 indexed citations

Barha, Cindy K., Katrina G. Salvante, Courtney W. Hanna, et al.. (2017). Child mortality, hypothalamic-pituitary-adrenal axis activity and cellular aging in mothers. PLoS ONE. 12(5). e0177869–e0177869. 8 indexed citations

Robinson, Wendy P. & E. Magda Price. (2015). The Human Placental Methylome. Cold Spring Harbor Perspectives in Medicine. 5(5). a023044–a023044. 71 indexed citations

10.

Tarailo‐Graovac, Maja, Graham Sinclair, Sylvia Stöckler‐Ipsiroglu, et al.. (2015). The genotypic and phenotypic spectrum of PIGA deficiency. Orphanet Journal of Rare Diseases. 10(1). 23–23. 58 indexed citations

11.

Qiao, Ying, Kajari Mondal, Valentina Trapani, et al.. (2013). Variant ATRX Syndrome with Dysfunction ofATRXandMAGT1Genes. Human Mutation. 35(1). 58–62. 8 indexed citations

12.

Hanna, Courtney W., Michael S. Bloom, Wendy P. Robinson, et al.. (2012). DNA methylation changes in whole blood is associated with exposure to the environmental contaminants, mercury, lead, cadmium and bisphenol A, in women undergoing ovarian stimulation for IVF. Human Reproduction. 27(5). 1401–1410. 123 indexed citations

13.

Hanna, Courtney W., et al.. (2009). Telomere Length and Reproductive Aging. Obstetrical & Gynecological Survey. 64(10). 663–664. 1 indexed citations

14.

Bretherick, Karla L., et al.. (2009). Fertility and aging: do reproductive-aged Canadian women know what they need to know?. Fertility and Sterility. 93(7). 2162–2168. 149 indexed citations

15.

Wieczorek, Dagmar, et al.. (2003). Prenatally detected trisomy 4 and 6 mosaicism—cytogenetic results and clinical phenotype. Prenatal Diagnosis. 23(2). 128–133. 23 indexed citations

16.

Zhao, Hongyu, Jinming Li, & Wendy P. Robinson. (2000). Multipoint Genetic Mapping with Uniparental Disomy Data. The American Journal of Human Genetics. 67(4). 851–861. 6 indexed citations

17.

Robinson, Wendy P., Irene Barrett, L.E. Bernard, et al.. (1997). Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction.. PubMed. 60(4). 917–27. 164 indexed citations

18.

Robinson, Wendy P., Sylvie Langlois, Simone Schuffenhauer, et al.. (1996). CYTOGENETIC AND AGE-DEPENDENT RISK FACTORS ASSOCIATED WITH UNIPARENTAL DISOMY 15. Prenatal Diagnosis. 16(9). 837–844. 50 indexed citations

19.

Schinzel, Albert, Wendy P. Robinson, Franz Binkert, & A Fanconi. (1994). An interstitial deletion of proximal 8q (q11???q13) in a girl with Silver-russell syndrome-like features. Clinical Dysmorphology. 3(1). 63???69–63???69. 35 indexed citations

20.

Klitz, William, Mary K. Kuhner, Wendy P. Robinson, Michael S. Esposito, & Glenys Thomson. (1989). Clues to IDDM pathogenesis from genetic and serological traits in multiply affected families. Genetic Epidemiology. 6(1). 117–122. 3 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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