Renee Stokowski

4.0k total citations
21 papers, 1.6k citations indexed

About

Renee Stokowski is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Renee Stokowski has authored 21 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pediatrics, Perinatology and Child Health, 9 papers in Genetics and 8 papers in Molecular Biology. Recurrent topics in Renee Stokowski's work include Prenatal Screening and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic Associations and Epidemiology (3 papers). Renee Stokowski is often cited by papers focused on Prenatal Screening and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic Associations and Epidemiology (3 papers). Renee Stokowski collaborates with scholars based in United States, Belgium and United Kingdom. Renee Stokowski's co-authors include David A. Hinds, Dennis G. Ballinger, David Kershenobich, Chao Tian, David R. Cox, Robert V. Farese, L. M. Flynn, Stephen G. Young, Martin R. Green and Andrew B. Sparks and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Blood.

In The Last Decade

Renee Stokowski

21 papers receiving 1.5k citations

Peers

Renee Stokowski
Mohammed Al Balwi Saudi Arabia
G Grimber France
Masaaki Masuhara Japan
Duan Ma China
Frank Rutsch Germany
Ruchira Sood United States
Andrew G. Demaine United Kingdom
N. Saha Singapore
Ruth H. Paulssen Norway
George Xinarianos United Kingdom
Mohammed Al Balwi Saudi Arabia
Renee Stokowski
Citations per year, relative to Renee Stokowski Renee Stokowski (= 1×) peers Mohammed Al Balwi

Countries citing papers authored by Renee Stokowski

Since Specialization
Citations

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

Fields of papers citing papers by Renee Stokowski

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Renee Stokowski

This figure shows the co-authorship network connecting the top 25 collaborators of Renee Stokowski. A scholar is included among the top collaborators of Renee Stokowski 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 Renee Stokowski. Renee Stokowski 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.
2.
Stokowski, Renee, et al.. (2020). Hemolysis and Fetal Fraction in Cell-Free DNA Blood Collection Tubes for Noninvasive Prenatal Testing. Molecular Diagnosis & Therapy. 24(2). 185–190. 6 indexed citations
3.
Bevilacqua, Elisa, Jacques Jani, Renee Stokowski, et al.. (2019). P01.04: Cell‐free DNA analysis in twin pregnancies after reduction because of fetal aneuploidy. Ultrasound in Obstetrics and Gynecology. 54(S1). 156–156. 1 indexed citations
4.
Stokowski, Renee, et al.. (2018). Accuracy and reproducibility of fetal‐fraction measurement using relative quantitation at polymorphic loci with microarray. Ultrasound in Obstetrics and Gynecology. 51(6). 813–817. 15 indexed citations
5.
Wang, Eric W., Patrick E. Bogard, Elisa Bevilacqua, et al.. (2017). Prenatal Screening for 22q11.2 Deletion Using a Targeted Microarray-Based Cell-Free DNA Test. Fetal Diagnosis and Therapy. 44(4). 299–304. 21 indexed citations
6.
Lowell, Jennifer L., Michael F. Antolin, Gary L. Andersen, et al.. (2015). Single-Nucleotide Polymorphisms Reveal Spatial Diversity Among Clones of Yersinia pestis During Plague Outbreaks in Colorado and the Western United States. Vector-Borne and Zoonotic Diseases. 15(5). 291–302. 24 indexed citations
7.
8.
Sparks, Andrew B., Eric T. Wang, Craig A. Struble, et al.. (2012). Selective analysis of cell‐free DNA in maternal blood for evaluation of fetal trisomy. Prenatal Diagnosis. 32(1). 3–9. 208 indexed citations
9.
Hidestrand, Mats, Renee Stokowski, Ken Song, et al.. (2012). Influence of Temperature during Transportation on Cell-Free DNA Analysis. Fetal Diagnosis and Therapy. 31(2). 122–128. 57 indexed citations
10.
Huang, Ying, Dennis G. Ballinger, Renee Stokowski, et al.. (2012). Exploring the interaction between SNP genotype and postmenopausal hormone therapy effects on stroke risk. Genome Medicine. 4(7). 57–57. 7 indexed citations
11.
Wessel, Jennifer, Sarah M. McDonald, David A. Hinds, et al.. (2010). Resequencing of Nicotinic Acetylcholine Receptor Genes and Association of Common and Rare Variants with the Fagerström Test for Nicotine Dependence. Neuropsychopharmacology. 35(12). 2392–2402. 48 indexed citations
12.
Stokowski, Renee, et al.. (2010). Assessment of Clinical Validity of a Breast Cancer Risk Model Combining Genetic and Clinical Information. JNCI Journal of the National Cancer Institute. 102(21). 1618–1627. 118 indexed citations
13.
Tian, Chao, Renee Stokowski, David Kershenobich, Dennis G. Ballinger, & David A. Hinds. (2009). Variant in PNPLA3 is associated with alcoholic liver disease. Nature Genetics. 42(1). 21–23. 329 indexed citations
14.
Bohnert, Regina, Georg Zeller, Richard M. Clark, et al.. (2008). Revealing sequence variation patterns in rice with machine learning methods. BMC Bioinformatics. 9(S10). 5 indexed citations
15.
Stokowski, Renee, P.V. Krishna Pant, Tony Dadd, et al.. (2007). A Genomewide Association Study of Skin Pigmentation in a South Asian Population. The American Journal of Human Genetics. 81(6). 1119–1132. 216 indexed citations
16.
Kukita, Yoji, Renee Stokowski, David A. Hinds, et al.. (2005). Genome-wide definitive haplotypes determined using a collection of complete hydatidiform moles. Genome Research. 15(11). 1511–1518. 14 indexed citations
17.
Hinds, David A., Renee Stokowski, Nila Patil, et al.. (2004). Matching Strategies for Genetic Association Studies in Structured Populations. The American Journal of Human Genetics. 74(2). 317–325. 76 indexed citations
18.
Frazer, Kelly A., Renee Stokowski, Xiyin Chen, et al.. (2001). Evolutionarily Conserved Sequences on Human Chromosome 21. Genome Research. 11(10). 1651–1659. 75 indexed citations
19.
Stokowski, Renee & David R. Cox. (2000). Functional Analysis of the Neurofibromatosis Type 2 Protein by Means of Disease-Causing Point Mutations. The American Journal of Human Genetics. 66(3). 873–891. 45 indexed citations
20.
Farese, Robert V., et al.. (1995). Knockout of the mouse apolipoprotein B gene results in embryonic lethality in homozygotes and protection against diet-induced hypercholesterolemia in heterozygotes.. Proceedings of the National Academy of Sciences. 92(5). 1774–1778. 220 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 Mohammed Al Balwi Breakdown of academic impact, for papers by G Grimber Breakdown of academic impact, for papers by Masaaki Masuhara Breakdown of academic impact, for papers by Duan Ma Breakdown of academic impact, for papers by Frank Rutsch Breakdown of academic impact, for papers by Ruchira Sood Breakdown of academic impact, for papers by Andrew G. Demaine Breakdown of academic impact, for papers by N. Saha Breakdown of academic impact, for papers by Ruth H. Paulssen Breakdown of academic impact, for papers by George Xinarianos
Rankless by CCL
2026