Quinn Stein

1.6k total citations
31 papers, 214 citations indexed

About

Quinn Stein is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Quinn Stein has authored 31 papers receiving a total of 214 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 9 papers in Molecular Biology and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Quinn Stein's work include BRCA gene mutations in cancer (11 papers), Metabolism and Genetic Disorders (5 papers) and Prenatal Screening and Diagnostics (5 papers). Quinn Stein is often cited by papers focused on BRCA gene mutations in cancer (11 papers), Metabolism and Genetic Disorders (5 papers) and Prenatal Screening and Diagnostics (5 papers). Quinn Stein collaborates with scholars based in United States, Qatar and Denmark. Quinn Stein's co-authors include Jason Flanagan, Susan E. Puumala, Erin Thorpe, MaryAnn Campion, Jennifer Hoskovec, Elizabeth A. Sellars, Henrik Toft Simonsen, Mariam Al‐Mureikhi, Paul A. Thompson and Allan M. Lund and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of the American Society of Nephrology and Fertility and Sterility.

In The Last Decade

Quinn Stein

30 papers receiving 210 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Quinn Stein United States 9 133 72 50 27 23 31 214
Grace E. VanNoy United States 8 155 1.2× 72 1.0× 47 0.9× 24 0.9× 22 1.0× 15 232
Shawn Fayer United States 7 166 1.2× 95 1.3× 47 0.9× 37 1.4× 30 1.3× 13 241
Helen Dolling United Kingdom 2 130 1.0× 52 0.7× 32 0.6× 26 1.0× 8 0.3× 3 159
ACMG Board of Directors 6 208 1.6× 60 0.8× 46 0.9× 5 0.2× 80 3.5× 10 299
Stacy J. Hines‐Dowell United States 7 109 0.8× 39 0.5× 57 1.1× 3 0.1× 22 1.0× 10 156
Susan Rojahn United States 8 137 1.0× 79 1.1× 18 0.4× 5 0.2× 20 0.9× 13 263
Vigdís Stefánsdóttir Iceland 9 210 1.6× 42 0.6× 55 1.1× 5 0.2× 69 3.0× 18 282
Brian M. Faux United States 7 41 0.3× 153 2.1× 14 0.3× 18 0.7× 28 1.2× 13 265
Chloe Mighton Canada 10 252 1.9× 64 0.9× 36 0.7× 6 0.2× 49 2.1× 30 318
David Fasel United States 7 111 0.8× 124 1.7× 62 1.2× 3 0.1× 19 0.8× 8 228

Countries citing papers authored by Quinn Stein

Since Specialization
Citations

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

Fields of papers citing papers by Quinn Stein

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Quinn Stein

This figure shows the co-authorship network connecting the top 25 collaborators of Quinn Stein. A scholar is included among the top collaborators of Quinn Stein 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 Quinn Stein. Quinn Stein 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.
Stein, Quinn, et al.. (2025). Role of Comprehensive Renal Genetic Testing in Diagnosing a RMND‐1 Mitochondrial Disease in Two Adult Cases Exhibiting Variable Disease Phenotypes. Clinical Case Reports. 13(4). e70421–e70421. 1 indexed citations
2.
Stein, Quinn, et al.. (2025). P687: A master in mimicry: Expanding the renal phenotype of COL4A1-related disorders. Genetics in Medicine Open. 3. 103056–103056.
3.
Hager, Megan M., et al.. (2024). Patient Satisfaction and Outcomes following a Session with a Genetic Counselor for Kidney Diseases. Journal of the American Society of Nephrology. 35(10S). 1 indexed citations
4.
Stein, Quinn, et al.. (2024). Townes-Brocks Syndrome Revealed by Kidney Gene Panel Testing. Kidney International Reports. 9(6). 1810–1816. 3 indexed citations
5.
Stein, Quinn, et al.. (2023). Genetic Counseling in Kidney Disease: A Perspective. Kidney Medicine. 5(7). 100668–100668. 10 indexed citations
6.
Stein, Quinn, et al.. (2023). Isolated benign persistent proteinuria with novel association of CUBN (cubilin) variants. SHILAP Revista de lepidopterología. 11(6). e7502–e7502. 2 indexed citations
7.
Stein, Quinn, et al.. (2022). The State of Newborn Screening in South Dakota.. PubMed. 75(11). 509–512. 1 indexed citations
8.
Stein, Quinn, Megan Landsverk, Daria Salyakina, et al.. (2021). Perspectives of Pediatric Providers Regarding Clinical Use of Pharmacogenetics.. PubMed. 74(7). 294–301. 4 indexed citations
9.
Stein, Quinn, et al.. (2021). Genesurance counseling: Current training practices of genetic counseling graduate programs in the United States. Journal of Genetic Counseling. 30(6). 1757–1766. 1 indexed citations
10.
Puumala, Susan E., et al.. (2020). Geographical analysis of the distribution of certified genetic counselors in the United States. Journal of Genetic Counseling. 30(2). 448–456. 15 indexed citations
11.
Stein, Quinn, et al.. (2018). Genetic Counseling in Pediatrics. Pediatrics in Review. 39(7). 323–331. 4 indexed citations
12.
Puumala, Susan E., et al.. (2017). Genesurance Counseling: Genetic Counselors’ Roles and Responsibilities in Regards to Genetic Insurance and Financial Topics. Journal of Genetic Counseling. 27(4). 800–813. 14 indexed citations
13.
Stein, Quinn, Cate Walsh Vockley, Mathew J. Edick, et al.. (2017). An Exploration of Genetic Test Utilization, Genetic Counseling, and Consanguinity within the Inborn Errors of Metabolism Collaborative (IBEMC). Journal of Genetic Counseling. 26(6). 1238–1243. 4 indexed citations
14.
Zárate, Yuri A., Hazel Perry, Tawfeg Ben‐Omran, et al.. (2015). Further supporting evidence for the SATB2‐associated syndrome found through whole exome sequencing. American Journal of Medical Genetics Part A. 167(5). 1026–1032. 37 indexed citations
15.
Flanagan, Jason, et al.. (2012). Solving the Puzzle: Case Examples of Array Comparative Genomic Hybridization as a Tool to End the Diagnostic Odyssey. Current problems in pediatric and adolescent health care. 42(3). 74–78. 8 indexed citations
16.
Stein, Quinn, et al.. (2011). The influential role of genes in obesity.. PubMed. Spec No. 12–5, 17. 2 indexed citations
17.
Stein, Quinn, et al.. (2008). Blepharophimosis-ptosis-epicanthus inversus syndrome and hypergonadotropic hypogonadism. Fertility and Sterility. 90(5). 2016.e11–2016.e12. 5 indexed citations
18.
Stein, Quinn, et al.. (2008). Clinical course of a 20-month-old child diagnosed prenatally with mosaic ring chromosome 18 and monosomy 18.. PubMed. 61(9). 327–9, 331. 7 indexed citations
19.
Stein, Quinn, et al.. (2007). Screening for mutations in the cystic fibrosis transmembrane regulator gene in an infertility clinic. Fertility and Sterility. 88(6). 1687–1688. 3 indexed citations
20.
Pedersen, Christina B., Claus Bischoff, Ernst Christensen, et al.. (2006). Variations in IBD (ACAD8) in Children with Elevated C4-Carnitine Detected by Tandem Mass Spectrometry Newborn Screening. Pediatric Research. 60(3). 315–320. 26 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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