Brett Casey

4.0k total citations
33 papers, 2.7k citations indexed

About

Brett Casey is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Brett Casey has authored 33 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 10 papers in Genetics and 7 papers in Surgery. Recurrent topics in Brett Casey's work include Congenital heart defects research (17 papers), Congenital Heart Disease Studies (6 papers) and Developmental Biology and Gene Regulation (6 papers). Brett Casey is often cited by papers focused on Congenital heart defects research (17 papers), Congenital Heart Disease Studies (6 papers) and Developmental Biology and Gene Regulation (6 papers). Brett Casey collaborates with scholars based in United States, Canada and Italy. Brett Casey's co-authors include Kenjiro Kosaki, John W. Belmont, Jeffrey A. Towbin, Marinella Gebbia, Maria Teresa Bassi, Stephanie M. Ware, Mark Lewin, Peter N. Bowers, Susan Fernbach and G Sándor and has published in prestigious journals such as Circulation, Nature Genetics and Journal of Neuroscience.

In The Last Decade

Brett Casey

33 papers receiving 2.6k citations

Peers

Brett Casey

EPIDE

SURGE

GENET

PRM

Judith Goodship United Kingdom

Paul Grossfeld United States

Alessandro De Luca Italy

Thomy de Ravel Belgium

Ruth Newbury‐Ecob United Kingdom

Kwame Anyane‐Yeboa United States

Kérsti K. Linask United States

Karen L. Waldo United States

Margherita Silengo Italy

J. Murdoch United Kingdom

Judith Goodship United Kingdom

Brett Casey

2.1k ×1.2

792 ×1.0

EPIDE

448 ×0.7

SURGE

1.2k ×1.9

GENET

592 ×1.0

PRM

Citations per year, relative to Brett Casey Brett Casey (= 1×) peers Judith Goodship

Countries citing papers authored by Brett Casey

Since Specialization

Citations

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

Fields of papers citing papers by Brett Casey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Brett Casey

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

D’Alessandro, Lisa C.A., Brett Casey, & Victoria Mok Siu. (2011). Situs Inversus Totalis and a NovelZIC3Mutation in a Family with X-linked Heterotaxy. Congenital Heart Disease. 8(2). E36–E40. 26 indexed citations

Mercimek‐Mahmutoglu, Saadet, Tracy Tucker, & Brett Casey. (2011). Phenotypic heterogeneity in two siblings with 3-methylglutaconic aciduria type I caused by a novel intragenic deletion. Molecular Genetics and Metabolism. 104(3). 410–413. 7 indexed citations

Mercimek‐Mahmutoglu, Saadet, Mary Connolly, Kenneth J. Poskitt, et al.. (2010). Treatment of intractable epilepsy in a female with SLC6A8 deficiency. Molecular Genetics and Metabolism. 101(4). 409–412. 52 indexed citations

Arbour, Laura, Saman Rezazadeh, Jodene Eldstrom, et al.. (2008). A KCNQ1 V205M missense mutation causes a high rate of long QT syndrome in a First Nations community of northern British Columbia: a community-based approach to understanding the impact. Genetics in Medicine. 10(7). 545–550. 26 indexed citations

Kalman, Lisa V., Monique Johnson, Jeanne C. Beck, et al.. (2007). Development of genomic reference materials for Huntington disease genetic testing. Genetics in Medicine. 9(10). 719–723. 16 indexed citations

Alvarez, Christine M., et al.. (2007). Evaluation of the Anatomic Burden of Patients with Hereditary Multiple Exostoses. Clinical Orthopaedics and Related Research. 462. 73–79. 36 indexed citations

Potts, James E., et al.. (2007). A Population-Based Study of Cardiac Malformations and Outcomes Associated With Dextrocardia. The American Journal of Cardiology. 100(2). 305–309. 136 indexed citations

Ware, Stephanie M., Lirong Zhu, Susan Fernbach, et al.. (2004). Identification and Functional Analysis of ZIC3 Mutations in Heterotaxy and Related Congenital Heart Defects. The American Journal of Human Genetics. 74(1). 93–105. 200 indexed citations

Yoshihashi, Hiroshi, et al.. (2001). Mutation analysis of left‐right axis determining genes in NOD and ICR, strains susceptible to maternal diabetes. Teratology. 63(3). 119–126. 15 indexed citations

10.

Bamford, Richard N., Erich Roessler, Rebecca D. Burdine, et al.. (2000). Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects. Nature Genetics. 26(3). 365–369. 250 indexed citations

11.

Casey, Brett. (2000). Left–right axis malformations in man and mouse. Current Opinion in Genetics & Development. 10(3). 257–261. 50 indexed citations

12.

Towbin, Jeffrey A., Brett Casey, & John W. Belmont. (1999). The Molecular Basis of Vascular Disorders. The American Journal of Human Genetics. 64(3). 678–684. 41 indexed citations

13.

Kosaki, Kenjiro, Rika Kosaki, Maria Teresa Bassi, et al.. (1999). Characterization and Mutation Analysis of Human LEFTY A and LEFTY B, Homologues of Murine Genes Implicated in Left-Right Axis Development. The American Journal of Human Genetics. 64(3). 712–721. 150 indexed citations

14.

Casey, Brett. (1998). Two rights make a wrong: human left-right malformations. Human Molecular Genetics. 7(10). 1565–1571. 90 indexed citations

15.

Kosaki, Kenjiro & Brett Casey. (1998). Genetics of human left–right axis malformations. Seminars in Cell and Developmental Biology. 9(1). 89–99. 90 indexed citations

16.

Ferrero, Giovanni Battista, Marinella Gebbia, Giuseppe Pilia, et al.. (1997). A Submicroscopic Deletion in Xq26 Associated with Familial Situs Ambiguus. The American Journal of Human Genetics. 61(2). 395–401. 58 indexed citations

17.

Gebbia, Marinella, Giovanni Battista Ferrero, Giuseppe Pilia, et al.. (1997). X-linked situs abnormalities result from mutations in ZIC3. Nature Genetics. 17(3). 305–308. 297 indexed citations

18.

Casey, Brett, et al.. (1996). Autosomal dominant transmission of familial laterality defects. American Journal of Medical Genetics. 61(4). 325–328. 34 indexed citations

19.

Casey, Brett, Marcella Devoto, Kenneth L. Jones, & Andrea Ballabio. (1993). Mapping a gene for familial situs abnormalities to human chromosome Xq24-q27.1. Nature Genetics. 5(4). 403–407. 92 indexed citations

20.

O’Neal, Wanda K., Paul Hasty, Paul B. McCray, et al.. (1993). A severe phenotype in mice with a duplication of exon 3 in the cystic fibrosis locus. Human Molecular Genetics. 2(10). 1561–1569. 104 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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