Deborah A. Nertney

15.0k total citations
10 papers, 522 citations indexed

About

Deborah A. Nertney is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Deborah A. Nertney has authored 10 papers receiving a total of 522 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Molecular Biology and 3 papers in Physiology. Recurrent topics in Deborah A. Nertney's work include Genetic Associations and Epidemiology (7 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Deborah A. Nertney is often cited by papers focused on Genetic Associations and Epidemiology (7 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Deborah A. Nertney collaborates with scholars based in Australia, United States and India. Deborah A. Nertney's co-authors include Bryan Mowry, David Meunier, Christos Pantelis, Edward T. Bullmore, Karen Shaw, Alex Fornito, Danielle S. Bassett, Andrew Zalesky, Murat Yücel and Ian Ellison-Wright and has published in prestigious journals such as Journal of Neuroscience, American Journal of Psychiatry and Molecular Psychiatry.

In The Last Decade

Deborah A. Nertney

10 papers receiving 510 citations

Peers

Deborah A. Nertney

CN

GENET

MB

RNMI

PMH

Margherita Comazzi Italy

Kamran Razi United States

Brad Zoltick United States

Apostolos Papazacharias Italy

Steven Sust United States

Joanne Doherty United Kingdom

D.G. Cunningham-Owens United Kingdom

Siobhan Schwaiger Ireland

Yanbo Yuan China

Pasquale Di Carlo Italy

Margherita Comazzi Italy

Deborah A. Nertney

211 ×0.8

CN

215 ×1.1

GENET

147 ×1.0

MB

77 ×0.7

RNMI

183 ×2.0

PMH

Citations per year, relative to Deborah A. Nertney Deborah A. Nertney (= 1×) peers Margherita Comazzi

Countries citing papers authored by Deborah A. Nertney

Since Specialization

Citations

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

Fields of papers citing papers by Deborah A. Nertney

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Deborah A. Nertney

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

All Works

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10 of 10 papers shown

1.

Fornito, Alex, Andrew Zalesky, Danielle S. Bassett, et al.. (2011). Genetic Influences on Cost-Efficient Organization of Human Cortical Functional Networks. Journal of Neuroscience. 31(9). 3261–3270. 230 indexed citations

2.

Nyholt, Dale R., T. N. Srinivasan, Sujit John, et al.. (2008). Strong Evidence for a Novel Schizophrenia Risk Locus on Chromosome 1p31.1 in Homogeneous Pedigrees From Tamil Nadu, India. American Journal of Psychiatry. 166(2). 206–215. 17 indexed citations

3.

Holliday, Elizabeth, Herlina Y. Handoko, Michael R. James, et al.. (2006). Association Study of the Dystrobrevin-Binding Gene With Schizophrenia in Australian and Indian Samples. Twin Research and Human Genetics. 9(4). 531–539. 15 indexed citations

4.

Handoko, Herlina Y., Michael R. James, Sujit John, et al.. (2006). Association Study of the Dystrobrevin-Binding Gene With Schizophrenia in Australian and Indian Samples. Twin Research and Human Genetics. 9(4). 531–539. 13 indexed citations

5.

Handoko, Herlina Y., Dale R. Nyholt, Nicholas K. Hayward, et al.. (2004). Separate and interacting effects within the catechol-O-methyltransferase (COMT) are associated with schizophrenia. Molecular Psychiatry. 10(6). 589–597. 72 indexed citations

6.

Handoko, Herlina Y., Derek J. Nancarrow, Nicholas K. Hayward, et al.. (2003). Tumor necrosis factor haplotype analysis amongst schizophrenia probands from four distinct populations in the Asia‐Pacific region. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 121B(1). 1–6. 28 indexed citations

7.

Mowry, Bryan, Kelly R. Ewen, Derek J. Nancarrow, et al.. (2000). Second stage of a genome scan of schizophrenia: Study of five positive regions in an expanded sample. American Journal of Medical Genetics. 96(6). 864–869. 63 indexed citations

8.

Mowry, Bryan, Kelly R. Ewen, Derek J. Nancarrow, et al.. (2000). Second stage of a genome scan of schizophrenia: Study of five positive regions in an expanded sample. American Journal of Medical Genetics. 96(6). 864–869. 2 indexed citations

9.

Martínez, María, Lynn R. Goldin, Jing Zhang, et al.. (1999). Follow-up study on a susceptibility locus for schizophrenia on chromosome 6q. American Journal of Medical Genetics. 88(4). 337–343. 79 indexed citations

10.

Martínez, María, Lynn R. Goldin, Jing Zhang, et al.. (1999). Follow‐up study on a susceptibility locus for schizophrenia on chromosome 6q. American Journal of Medical Genetics. 88(4). 337–343. 3 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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