Virginia K. Lasseter

4.1k total citations
23 papers, 1.7k citations indexed

About

Virginia K. Lasseter is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Virginia K. Lasseter has authored 23 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 6 papers in Molecular Biology and 5 papers in Psychiatry and Mental health. Recurrent topics in Virginia K. Lasseter's work include Genetic Associations and Epidemiology (17 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Genomic variations and chromosomal abnormalities (8 papers). Virginia K. Lasseter is often cited by papers focused on Genetic Associations and Epidemiology (17 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Genomic variations and chromosomal abnormalities (8 papers). Virginia K. Lasseter collaborates with scholars based in United States, Switzerland and Japan. Virginia K. Lasseter's co-authors include Paula Wolyniec, Gerald Nestadt, John A. McGrath, Ann E. Pulver, M. Daniele Fallin, David Valle, Maria Karayiorgou, Kung‐Yee Liang, Michael A. Morris and Julian Borrow and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The American Journal of Human Genetics and Molecular Psychiatry.

In The Last Decade

Virginia K. Lasseter

23 papers receiving 1.6k citations

Peers

Virginia K. Lasseter

GENET

MB

PMH

CMN

CN

Ivan Nikolov United Kingdom

Déborah Morris-Rosendahl Germany

Hugh Gurling United Kingdom

Gursharan Kalsi United Kingdom

Andrés Ingason Denmark

Elaine Green United Kingdom

Radhakrishna Vakkalanka United States

Detelina Grozeva United Kingdom

Kevin A. McGhee United Kingdom

Patrice L. Whitehead United States

Ivan Nikolov United Kingdom

Virginia K. Lasseter

681 ×0.7

GENET

520 ×0.6

MB

376 ×1.2

PMH

214 ×0.7

CMN

224 ×1.1

CN

Citations per year, relative to Virginia K. Lasseter Virginia K. Lasseter (= 1×) peers Ivan Nikolov

Countries citing papers authored by Virginia K. Lasseter

Since Specialization

Citations

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

Fields of papers citing papers by Virginia K. Lasseter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Virginia K. Lasseter. 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 Virginia K. Lasseter. The network helps show where Virginia K. Lasseter may publish in the future.

Co-authorship network of co-authors of Virginia K. Lasseter

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

All Works

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20 of 20 papers shown

1.

Cubells, Joseph F., Xiangqing Sun, Wenbiao Li, et al.. (2011). Linkage analysis of plasma dopamine β-hydroxylase activity in families of patients with schizophrenia. Human Genetics. 130(5). 635–643. 44 indexed citations

2.

Li, Qing, M. Daniele Fallin, Thomas A. Louis, et al.. (2010). Detection of SNP‐SNP interactions in trios of parents with schizophrenic children. Genetic Epidemiology. 34(5). 396–406. 19 indexed citations

3.

Fallin, M. Daniele, Virginia K. Lasseter, Yaping Liu, et al.. (2010). Linkage and association on 8p21.2-p21.1 in schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(2). 188–197. 25 indexed citations

4.

Chen, Pei-Lung, Dimitrios Avramopoulos, Virginia K. Lasseter, et al.. (2009). Fine Mapping on Chromosome 10q22-q23 Implicates Neuregulin 3 in Schizophrenia. The American Journal of Human Genetics. 84(1). 21–34. 67 indexed citations

5.

McGrath, John A., Dimitrios Avramopoulos, Virginia K. Lasseter, et al.. (2009). Familiality of Novel Factorial Dimensions of Schizophrenia. Archives of General Psychiatry. 66(6). 591–591. 61 indexed citations

6.

Avramopoulos, Dimitrios, Virginia K. Lasseter, M. Daniele Fallin, et al.. (2007). Stage II follow-up on a linkage scan for bipolar disorder in the Ashkenazim provides suggestive evidence for chromosome 12p and the GRIN2B gene. Genetics in Medicine. 9(11). 745–751. 25 indexed citations

7.

Fallin, M. Daniele, Virginia K. Lasseter, Dimitrios Avramopoulos, et al.. (2005). Bipolar I Disorder and Schizophrenia: A 440–Single-Nucleotide Polymorphism Screen of 64 Candidate Genes among Ashkenazi Jewish Case-Parent Trios. The American Journal of Human Genetics. 77(6). 918–936. 315 indexed citations

8.

McGrath, John A., Gerald Nestadt, K.-Y. Liang, et al.. (2004). Five Latent Factors Underlying Schizophrenia: Analysis and Relationship to Illnesses in Relatives. Schizophrenia Bulletin. 30(4). 855–873. 29 indexed citations

9.

Fallin, M. Daniele, Virginia K. Lasseter, Paula Wolyniec, et al.. (2004). Genomewide Linkage Scan for Bipolar-Disorder Susceptibility Loci among Ashkenazi Jewish Families. The American Journal of Human Genetics. 75(2). 204–219. 71 indexed citations

10.

Fallin, M. Daniele, Virginia K. Lasseter, Paula Wolyniec, et al.. (2003). Genomewide Linkage Scan for Schizophrenia Susceptibility Loci among Ashkenazi Jewish Families Shows Evidence of Linkage on Chromosome 10q22. The American Journal of Human Genetics. 73(3). 601–611. 87 indexed citations

11.

Pulver, Ann E., John A. McGrath, Kung‐Yee Liang, et al.. (2003). An indirect test of the new mutation hypothesis associating advanced paternal age with the etiology of schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 124B(1). 6–9. 19 indexed citations

12.

Mullé, Jennifer G., M. Daniele Fallin, Virginia K. Lasseter, et al.. (2002). Dense SNP association study for bipolar I disorder on chromosome 18p11 suggests two loci with excess paternal transmission. Molecular Psychiatry. 12(4). 367–375. 11 indexed citations

13.

Pulver, Ann E., Jennifer G. Mullé, Gerald Nestadt, et al.. (2000). Genetic heterogeneity in schizophrenia: stratification of genome scan data using co-segregating related phenotypes. Molecular Psychiatry. 5(6). 650–653. 72 indexed citations

14.

Antonarakis, Stylianos E., Jean‐Louis Blouin, Virginia K. Lasseter, et al.. (1999). Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21. American Journal of Medical Genetics. 88(4). 348–351. 30 indexed citations

15.

Antonarakis, Stylianos E., Jean‐Louis Blouin, Virginia K. Lasseter, et al.. (1999). Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21. American Journal of Medical Genetics. 88(4). 348–351. 2 indexed citations

16.

Curtis, Logos, Jean-Louis Blouin, Uppala Radhakrishna, et al.. (1999). No evidence for linkage between schizophrenia and markers at chromosome 15q13-14. American Journal of Medical Genetics. 88(2). 109–112. 57 indexed citations

17.

Antonarakis, Stylianos E., Jean‐Louis Blouin, H H Kazazian, et al.. (1996). Linkage and sib-pair analysis reveal a potential schizophrenia susceptibility gene on chromosome 13q32. Psychiatric Genetics. 6(3). 136–136. 16 indexed citations

18.

Pulver, Ann E., Virginia K. Lasseter, Laura Kasch, et al.. (1995). Schizophrenia: A genome scan targets chromosomes 3p and 8p as potential sites of susceptibility genes. American Journal of Medical Genetics. 60(3). 252–260. 202 indexed citations

19.

Lasseter, Virginia K., Ann E. Pulver, & Paula Wolyniec. (1994). Schizophrenia: A genome search targets chromosomes 3 and 8 for exploration. The American Journal of Human Genetics. 55. 1 indexed citations

20.

Karayiorgou, Maria, Laura Kasch, Virginia K. Lasseter, et al.. (1994). Report from the Maryland epidemiology schizophrenia linkage study: No evidence for linkage between schizophrenia and a number of candidate and other genomic regions using a complex dominant model. American Journal of Medical Genetics. 54(4). 345–353. 18 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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