Casie A. Genetti

4.8k total citations
37 papers, 689 citations indexed

About

Casie A. Genetti is a scholar working on Genetics, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Casie A. Genetti has authored 37 papers receiving a total of 689 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 16 papers in Molecular Biology and 5 papers in Clinical Biochemistry. Recurrent topics in Casie A. Genetti's work include Genomics and Rare Diseases (16 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Casie A. Genetti is often cited by papers focused on Genomics and Rare Diseases (16 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Casie A. Genetti collaborates with scholars based in United States, Türkiye and Netherlands. Casie A. Genetti's co-authors include Pankaj B. Agrawal, Alan H. Beggs, Timothy W. Yu, Monica H. Wojcik, Talia S. Schwartz, Richard B. Parad, Robert C. Green, Ingrid A. Holm, Amy L. McGuire and Grace E. VanNoy and has published in prestigious journals such as PEDIATRICS, The American Journal of Human Genetics and PLoS Genetics.

In The Last Decade

Casie A. Genetti

34 papers receiving 679 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Casie A. Genetti United States 14 432 274 154 101 68 37 689
Alice Masurel‐Paulet France 15 386 0.9× 344 1.3× 105 0.7× 164 1.6× 20 0.3× 26 800
Hanna Faghfoury Canada 9 355 0.8× 403 1.5× 51 0.3× 85 0.8× 40 0.6× 26 670
Alecia Willis United States 14 195 0.5× 373 1.4× 61 0.4× 132 1.3× 65 1.0× 17 643
Cynthia S. Gubbels United States 14 196 0.5× 160 0.6× 219 1.4× 238 2.4× 32 0.5× 19 606
Chupong Ittiwut Thailand 14 151 0.3× 261 1.0× 45 0.3× 60 0.6× 37 0.5× 53 496
Jingsi Luo China 13 197 0.5× 290 1.1× 156 1.0× 62 0.6× 11 0.2× 65 556
Khalid Al‐Thihli Oman 13 116 0.3× 219 0.8× 58 0.4× 135 1.3× 21 0.3× 50 456
Itsuro Hibi Japan 18 366 0.8× 442 1.6× 193 1.3× 22 0.2× 18 0.3× 92 1.0k
Sarah Macklin United States 9 183 0.4× 176 0.6× 25 0.2× 121 1.2× 43 0.6× 21 423
Florence Roucher‐Boulez France 13 167 0.4× 223 0.8× 50 0.3× 17 0.2× 36 0.5× 36 517

Countries citing papers authored by Casie A. Genetti

Since Specialization
Citations

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

Fields of papers citing papers by Casie A. Genetti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Casie A. Genetti. 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 Casie A. Genetti. The network helps show where Casie A. Genetti may publish in the future.

Co-authorship network of co-authors of Casie A. Genetti

This figure shows the co-authorship network connecting the top 25 collaborators of Casie A. Genetti. A scholar is included among the top collaborators of Casie A. Genetti 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 Casie A. Genetti. Casie A. Genetti 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.
Genetti, Casie A., Tanya Logvinenko, Leslie H. Hayes, et al.. (2025). Retrospective Cohort Analysis of Clinical, Molecular, and Histopathologic Characteristics of 275 Patients With Nemaline Myopathy. Neurology Genetics. 11(4). e200277–e200277.
2.
Luo, Shiyu, Valérie Gailus-Durner, Qifei Li, et al.. (2025). Recessive variants in WSB2 encoding a substrate receptor of E3 ubiquitin ligase underlie a neurodevelopmental syndrome. European Journal of Human Genetics. 34(1). 37–44.
3.
Uveges, Melissa Kurtz, Hadley Stevens Smith, Stacey Pereira, et al.. (2024). Family genetic risk communication and reverse cascade testing in the BabySeq project. Genetics in Medicine. 27(3). 101350–101350.
4.
Inoue, Michio, Divya Jayaraman, Rocío Bengoechea, et al.. (2024). Genotype‒phenotype correlation in recessive DNAJB4 myopathy. Acta Neuropathologica Communications. 12(1). 171–171. 4 indexed citations
5.
6.
Green, Robert C., Nidhi Shah, Casie A. Genetti, et al.. (2023). Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project. The American Journal of Human Genetics. 110(7). 1034–1045. 25 indexed citations
7.
Hojlo, Margaret A., Casie A. Genetti, Richard S. Smith, et al.. (2023). Children with Early-Onset Psychosis Have Increased Burden of Rare GRIN2A Variants. Genes. 14(4). 779–779. 5 indexed citations
8.
Li, Qifei, Klaus Schmitz‐Abe, Casie A. Genetti, et al.. (2023). Reanalysis of clinical exome identifies the second variant in two individuals with recessive disorders. European Journal of Human Genetics. 31(6). 712–715. 4 indexed citations
9.
Pereira, Stacey, Amanda M. Gutierrez, Jill O. Robinson, et al.. (2022). Parents’ decision-making regarding whether to receive adult-onset only genetic findings for their children: Findings from the BabySeq Project. Genetics in Medicine. 25(3). 100002–100002. 13 indexed citations
10.
Li, Jianqiao, Margaret A. Hojlo, Kent Shefchek, et al.. (2021). Underrepresentation of Phenotypic Variability of 16p13.11 Microduplication Syndrome Assessed With an Online Self-Phenotyping Tool (Phenotypr): Cohort Study. Journal of Medical Internet Research. 23(3). e21023–e21023. 3 indexed citations
11.
Li, Qifei, Alicia Casey, Christina Yee, et al.. (2021). A homozygous stop-gain variant in ARHGAP42 is associated with childhood interstitial lung disease, systemic hypertension, and immunological findings. PLoS Genetics. 17(7). e1009639–e1009639. 5 indexed citations
12.
Boone, Philip M., Scott Paterson, Kiana Mohajeri, et al.. (2019). Biallelic mutation of FBXL7 suggests a novel form of Hennekam syndrome. American Journal of Medical Genetics Part A. 182(1). 189–194. 12 indexed citations
13.
Graham, Robert J., Francesco Muntoni, Imelda Hughes, et al.. (2019). Mortality and respiratory support in X-linked myotubular myopathy: a RECENSUS retrospective analysis. Archives of Disease in Childhood. 105(4). 332–338. 25 indexed citations
14.
VanNoy, Grace E., Casie A. Genetti, Amy L. McGuire, et al.. (2019). Challenging the Current Recommendations for Carrier Testing in Children. PEDIATRICS. 143(Supplement_1). S27–S32. 17 indexed citations
15.
Murry, Jaclyn B., Kalotina Machini, Ozge Ceyhan‐Birsoy, et al.. (2018). Reconciling newborn screening and a novel splice variant in BTD associated with partial biotinidase deficiency: a BabySeq Project case report. Molecular Case Studies. 4(4). a002873–a002873. 4 indexed citations
16.
Brownstein, Catherine A., Casie A. Genetti, Kelsey Graber, et al.. (2018). De novo variant of TRRAP in a patient with very early onset psychosis in the context of non-verbal learning disability and obsessive-compulsive disorder: a case report. BMC Medical Genetics. 19(1). 197–197. 8 indexed citations
17.
Deisseroth, Cole A., Johannes Birgmeier, Ethan E. Bodle, et al.. (2018). ClinPhen extracts and prioritizes patient phenotypes directly from medical records to expedite genetic disease diagnosis. Genetics in Medicine. 21(7). 1585–1593. 62 indexed citations
18.
Wojcik, Monica H., et al.. (2018). Genetic disorders and mortality in infancy and early childhood: delayed diagnoses and missed opportunities. Genetics in Medicine. 20(11). 1396–1404. 52 indexed citations
19.
Sacharow, Stephanie, Elizabeth E. Dudenhausen, Carrie L. Lomelino, et al.. (2017). Characterization of a novel variant in siblings with Asparagine Synthetase Deficiency. Molecular Genetics and Metabolism. 123(3). 317–325. 22 indexed citations
20.
Wojcik, Monica H., Klaas J. Wierenga, Lance H. Rodan, et al.. (2017). Beta-Ketothiolase Deficiency Presenting with Metabolic Stroke After a Normal Newborn Screen in Two Individuals. JIMD Reports. 39. 45–54. 7 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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