L. Scutt

435 total citations
7 papers, 336 citations indexed

About

L. Scutt is a scholar working on Molecular Biology, Genetics and Speech and Hearing. According to data from OpenAlex, L. Scutt has authored 7 papers receiving a total of 336 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Speech and Hearing. Recurrent topics in L. Scutt's work include Congenital heart defects research (5 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetic Associations and Epidemiology (2 papers). L. Scutt is often cited by papers focused on Congenital heart defects research (5 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetic Associations and Epidemiology (2 papers). L. Scutt collaborates with scholars based in Canada. L. Scutt's co-authors include Anne S. Bassett, Rosanna Weksberg, Eva W.C. Chow, Kathy Hodgkinson, Robert B. Zipursky, David J. Mikulis, Janice Husted, Eva W. C. Chow, William G. Honer and Philip AbdelMalik and has published in prestigious journals such as Biological Psychiatry, Schizophrenia Research and American Journal of Medical Genetics.

In The Last Decade

L. Scutt

7 papers receiving 327 citations

Peers

L. Scutt
Malgorzata Lamacz United States
Jayne Henry United Kingdom
Merav Burg Israel
Christine Hinard Switzerland
Daneen Whinna United States
Jananne Khuri United States
Malgorzata Lamacz United States
L. Scutt
Citations per year, relative to L. Scutt L. Scutt (= 1×) peers Malgorzata Lamacz

Countries citing papers authored by L. Scutt

Since Specialization
Citations

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

Fields of papers citing papers by L. Scutt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of L. Scutt

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

All Works

7 of 7 papers shown
1.
Chow, Eva W.C., et al.. (2001). Low platelet count in a 22q11 deletion syndrome subtype of schizophrenia. Schizophrenia Research. 50(3). 177–180. 12 indexed citations
2.
Scutt, L., et al.. (2001). Patterns of dysmorphic features in schizophrenia. American Journal of Medical Genetics. 105(8). 713–723. 19 indexed citations
3.
Chow, Eva W.C., David J. Mikulis, Robert B. Zipursky, et al.. (1999). Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia. Biological Psychiatry. 46(10). 1436–1442. 98 indexed citations
4.
Husted, Janice, L. Scutt, & Anne S. Bassett. (1998). Paternal transmission and anticipation in schizophrenia. American Journal of Medical Genetics. 81(2). 156–162. 2 indexed citations
5.
Husted, Janice, L. Scutt, & Anne S. Bassett. (1998). Paternal transmission and anticipation in schizophrenia. American Journal of Medical Genetics. 81(2). 156–162. 23 indexed citations
6.
Bassett, Anne S., et al.. (1998). 22q11 deletion syndrome in adults with schizophrenia. American Journal of Medical Genetics. 81(4). 328–337. 9 indexed citations
7.
Bassett, Anne S., et al.. (1998). 22q11 deletion syndrome in adults with schizophrenia. American Journal of Medical Genetics. 81(4). 328–337. 173 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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