Kari Casas

998 total citations
19 papers, 545 citations indexed

About

Kari Casas is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Kari Casas has authored 19 papers receiving a total of 545 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 8 papers in Clinical Biochemistry and 7 papers in Genetics. Recurrent topics in Kari Casas's work include Metabolism and Genetic Disorders (8 papers), Mitochondrial Function and Pathology (6 papers) and Genomics and Rare Diseases (5 papers). Kari Casas is often cited by papers focused on Metabolism and Genetic Disorders (8 papers), Mitochondrial Function and Pathology (6 papers) and Genomics and Rare Diseases (5 papers). Kari Casas collaborates with scholars based in United States, Israel and Netherlands. Kari Casas's co-authors include Nathan Fischel‐Ghodsian, Yelena Bykhovskaya, Rena E. Falk, Emebet Mengesha, Aida Inbal, John J. Mulvihill, Tarja Mononen, Henry J. Lin, Susan J. Hassed and Shibo Li and has published in prestigious journals such as PEDIATRICS, The American Journal of Human Genetics and Nutrients.

In The Last Decade

Kari Casas

19 papers receiving 534 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kari Casas United States	10	424	152	142	44	38	19	545
Sophie Monnot France	13	403 1.0×	191 1.3×	206 1.5×	45 1.0×	28 0.7×	27	585
Mathilde Nizon France	13	239 0.6×	70 0.5×	153 1.1×	22 0.5×	14 0.4×	26	387
Eyby Leon United States	9	263 0.6×	60 0.4×	104 0.7×	22 0.5×	18 0.5×	29	379
Margarita Sáenz United States	6	304 0.7×	38 0.3×	177 1.2×	9 0.2×	30 0.8×	12	413
Mary Willis United States	10	200 0.5×	72 0.5×	197 1.4×	22 0.5×	10 0.3×	17	361
Sonia Nizard France	10	131 0.3×	27 0.2×	227 1.6×	36 0.8×	36 0.9×	12	357
Rebecca I. Torene United States	10	165 0.4×	17 0.1×	206 1.5×	44 1.0×	36 0.9×	20	506
Manuela Morleo Italy	15	398 0.9×	30 0.2×	361 2.5×	12 0.3×	24 0.6×	22	597
Angela L. Duker United States	10	284 0.7×	13 0.1×	267 1.9×	58 1.3×	72 1.9×	25	471
Maria Rosaria Piemontese Italy	12	248 0.6×	12 0.1×	141 1.0×	17 0.4×	17 0.4×	23	393

Countries citing papers authored by Kari Casas

Since Specialization

Citations

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

Fields of papers citing papers by Kari Casas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kari Casas

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

All Works

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19 of 19 papers shown

Casas, Kari, et al.. (2025). Assessing Teledentistry versus In-Person Examinations to Detect Dental Caries: A Systematic Review and Meta-analysis. JDR Clinical & Translational Research. 11(1). 4–15. 1 indexed citations

Turgeon, Coleman, Kari Casas, Ryan Flanagan, et al.. (2024). Pre-analytic decrease of phenylalanine in plasma of patients with phenylketonuria treated with pegvaliase. Molecular Genetics and Metabolism Reports. 40. 101110–101110. 1 indexed citations

Larson, Austin, Lisa Salz, Regan Veith, et al.. (2024). Multi-center implementation of rapid whole genome sequencing provides additional evidence of its utility in the pediatric inpatient setting. Frontiers in Pediatrics. 12. 1349519–1349519. 4 indexed citations

Casas, Kari, et al.. (2021). Reduction in Newborn Screening False Positive Results Following a New Collection Protocol: a Quality Improvement Project. The Journal of Pediatric Pharmacology and Therapeutics. 26(7). 723–727. 4 indexed citations

Verdonschot, Job A.J., Emma Robinson, Kiely N. James, et al.. (2019). Mutations in PDLIM5 are rare in dilated cardiomyopathy but are emerging as potential disease modifiers. Molecular Genetics & Genomic Medicine. 8(2). e1049–e1049. 12 indexed citations

Vliet, Danique van, Annemiek M. J. van Wegberg, Kirsten Ahring, et al.. (2019). Untreated PKU Patients without Intellectual Disability: What Do They Teach Us?. Nutrients. 11(11). 2572–2572. 20 indexed citations

Smith, J.L., et al.. (2018). Reduction in Newborn Screening False Positive Results in the Nicu: A Quality Improvement Project. PEDIATRICS. 141(1_MeetingAbstract). 554–554. 1 indexed citations

Casas, Kari. (2018). Adoptees’ Pursuit of Genomic Testing to Fill Gaps in Family Health History and Reduce Healthcare Disparity. Narrative Inquiry in Bioethics. 8(2). 131–135. 14 indexed citations

Smith, J.L., et al.. (2018). Reduction in Newborn Screening False Positive Results in the Nicu: A Quality Improvement Project. 554–554. 1 indexed citations

10.

Sanmann, Jennifer N., et al.. (2016). The first patient with tandem duplication of 6q14q16: Molecular and phenotypic characterization. American Journal of Medical Genetics Part A. 170(9). 2416–2420. 1 indexed citations

11.

Chan, Sherine S.L., Robert K. Naviaux, Alice Basinger, Kari Casas, & William C. Copeland. (2009). De novo mutation in POLG leads to haplotype insufficiency and Alpers syndrome. Mitochondrion. 9(5). 340–345. 8 indexed citations

12.

Purandare, Smita M., Roberto Mendoza‐Londono, Svetlana A. Yatsenko, et al.. (2008). De novo three‐way chromosome translocation 46,XY,t(4;6;21)(p16;p21.1;q21) in a male with cleidocranial dysplasia. American Journal of Medical Genetics Part A. 146A(4). 453–458. 10 indexed citations

13.

Falk, Rena E. & Kari Casas. (2007). Chromosome 2q37 deletion: Clinical and molecular aspects. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 145C(4). 357–371. 77 indexed citations

14.

Zeharia, Avraham, Nathan Fischel‐Ghodsian, Kari Casas, et al.. (2005). Mitochondrial Myopathy, Sideroblastic Anemia, and Lactic Acidosis: An Autosomal Recessive Syndrome in Persian Jews Caused by a Mutation in the PUS1 Gene. Journal of Child Neurology. 20(5). 449–452. 54 indexed citations

15.

Bykhovskaya, Yelena, Kari Casas, Emebet Mengesha, Aida Inbal, & Nathan Fischel‐Ghodsian. (2004). Missense Mutation in Pseudouridine Synthase 1 (PUS1) Causes Mitochondrial Myopathy and Sideroblastic Anemia (MLASA). The American Journal of Human Genetics. 74(6). 1303–1308. 223 indexed citations

16.

Casas, Kari, Tarja Mononen, Susan J. Hassed, et al.. (2004). Chromosome 2q terminal deletion: Report of 6 new patients and review of phenotype‐breakpoint correlations in 66 individuals. American Journal of Medical Genetics Part A. 130A(4). 331–339. 70 indexed citations

17.

Casas, Kari, Yelena Bykhovskaya, Emebet Mengesha, et al.. (2004). Gene responsible for mitochondrial myopathy and sideroblastic anemia (MSA) maps to chromosome 12q24.33. American Journal of Medical Genetics Part A. 127A(1). 44–49. 11 indexed citations

18.

Casas, Kari & Nathan Fischel‐Ghodsian. (2003). Mitochondrial myopathy and sideroblastic anemia. American Journal of Medical Genetics Part A. 125A(2). 201–204. 24 indexed citations

19.

Dierssen, Mara, Eulàlia Martı́, Vassiliki Fotaki, et al.. (2001). Functional genomics of Down syndrome: a multidisciplinary approach. PubMed. 131–148. 9 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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