Natalie Blagowidow

763 total citations
10 papers, 253 citations indexed

About

Natalie Blagowidow is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Natalie Blagowidow has authored 10 papers receiving a total of 253 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Natalie Blagowidow's work include Prenatal Screening and Diagnostics (3 papers), Genetic Syndromes and Imprinting (2 papers) and RNA modifications and cancer (2 papers). Natalie Blagowidow is often cited by papers focused on Prenatal Screening and Diagnostics (3 papers), Genetic Syndromes and Imprinting (2 papers) and RNA modifications and cancer (2 papers). Natalie Blagowidow collaborates with scholars based in United States, Netherlands and Italy. Natalie Blagowidow's co-authors include Joe Leigh Simpson, Antonie D. Kline, Marco A. Grados, Ian D. Krantz, Amy Kimball, Howard P. Levy, Carmen P. Pichard, David N. Tuchman, Paul D. Sponseller and David C. Page and has published in prestigious journals such as PLoS ONE, Human Genetics and Genetics in Medicine.

In The Last Decade

Natalie Blagowidow

10 papers receiving 246 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Natalie Blagowidow United States 6 190 157 25 22 19 10 253
Kim Freriks Netherlands 10 145 0.8× 194 1.2× 19 0.8× 27 1.2× 23 1.2× 14 279
Claudine Fear United Kingdom 10 147 0.8× 229 1.5× 36 1.4× 74 3.4× 30 1.6× 16 312
Carol English United Kingdom 9 115 0.6× 139 0.9× 20 0.8× 64 2.9× 42 2.2× 12 263
Olga Žilina Estonia 12 132 0.7× 242 1.5× 54 2.2× 92 4.2× 11 0.6× 23 314
Diane Hu‐Lince United States 7 143 0.8× 144 0.9× 13 0.5× 22 1.0× 9 0.5× 7 253
Mariana Moysés‐Oliveira Brazil 11 130 0.7× 206 1.3× 35 1.4× 53 2.4× 16 0.8× 45 300
Amelia M. Lindgren United States 5 109 0.6× 154 1.0× 57 2.3× 36 1.6× 24 1.3× 10 238
Jackie Goldstein United Kingdom 3 76 0.4× 111 0.7× 18 0.7× 15 0.7× 9 0.5× 4 178
Isidora López‐Pajares Spain 10 113 0.6× 187 1.2× 55 2.2× 60 2.7× 19 1.0× 11 242
Amelia Villa Spain 9 83 0.4× 176 1.1× 50 2.0× 75 3.4× 33 1.7× 12 241

Countries citing papers authored by Natalie Blagowidow

Since Specialization
Citations

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

Fields of papers citing papers by Natalie Blagowidow

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Natalie Blagowidow

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

All Works

10 of 10 papers shown
1.
Goldmuntz, Elizabeth, Anne S. Bassett, Erik Boot, et al.. (2024). Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation. Prenatal Diagnosis. 44(6-7). 804–814. 2 indexed citations
2.
Pezaro, Sally, Serwet Demirdas, Alan J. Hakim, et al.. (2024). Management of childbearing with hypermobile Ehlers-Danlos syndrome and hypermobility spectrum disorders: A scoping review and expert co-creation of evidence-based clinical guidelines. PLoS ONE. 19(5). e0302401–e0302401. 2 indexed citations
3.
Blagowidow, Natalie, Beata Nowakowska, Erica Schindewolf, et al.. (2023). Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes. 14(1). 160–160. 15 indexed citations
4.
Blagowidow, Natalie. (2021). Obstetrics and gynecology in Ehlers‐Danlos syndrome: A brief review and update. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 187(4). 593–598. 4 indexed citations
5.
Oliver, Chris, Maria Francesca Bedeschi, Natalie Blagowidow, et al.. (2010). Cornelia de Lange syndrome: Extending the physical and psychological phenotype. American Journal of Medical Genetics Part A. 152A(5). 1127–1135. 14 indexed citations
6.
Kline, Antonie D., Marco A. Grados, Paul D. Sponseller, et al.. (2007). Natural history of aging in Cornelia de Lange syndrome. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 145C(3). 248–260. 118 indexed citations
7.
Ming, Jeffrey E., Natalie Blagowidow, Joan H.M. Knoll, et al.. (2000). Submicroscopic deletion in cousins with Prader‐Willi syndrome causes a grandmatrilineal inheritance pattern: Effects of imprinting. American Journal of Medical Genetics. 92(1). 19–24. 18 indexed citations
8.
Finucane, Brenda, et al.. (1999). Fragile X mutation screening among unselected pregnant women seen for genetic counseling: Findings of a pilot study. Genetics in Medicine. 1(2). 54–54. 1 indexed citations
9.
Blagowidow, Natalie, David C. Page, Dale S. Huff, & Michael T. Mennuti. (1989). Ullrich‐Turner syndrome in an XY female fetus with deletion of the sex‐determining portion of the Y chromosome. American Journal of Medical Genetics. 34(2). 159–162. 18 indexed citations
10.
Simpson, Joe Leigh, et al.. (1981). XY gonadal dysgenesis: Genetic heterogeneity based upon clinical observations, H-Y antigen status and segregation analysis. Human Genetics. 58(1). 91–7. 61 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 Kim Freriks Breakdown of academic impact, for papers by Claudine Fear Breakdown of academic impact, for papers by Carol English Breakdown of academic impact, for papers by Olga Žilina Breakdown of academic impact, for papers by Diane Hu‐Lince Breakdown of academic impact, for papers by Mariana Moysés‐Oliveira Breakdown of academic impact, for papers by Amelia M. Lindgren Breakdown of academic impact, for papers by Jackie Goldstein Breakdown of academic impact, for papers by Isidora López‐Pajares Breakdown of academic impact, for papers by Amelia Villa
Rankless by CCL
2026