Gail Shields

1.8k total citations
18 papers, 1.2k citations indexed

About

Gail Shields is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Gail Shields has authored 18 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 6 papers in Molecular Biology and 5 papers in Psychiatry and Mental health. Recurrent topics in Gail Shields's work include Genetic Associations and Epidemiology (10 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genomics and Rare Diseases (4 papers). Gail Shields is often cited by papers focused on Genetic Associations and Epidemiology (10 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genomics and Rare Diseases (4 papers). Gail Shields collaborates with scholars based in United States, United Kingdom and Italy. Gail Shields's co-authors include Lynn E. DeLisi, Anne L. Hoff, John Stewart, Antonio Vita, Azad K. Anand, Joseph E. Schwartz, Fritz A. Henn, Timothy J. Crow, Angela Smith and J. Loftus and has published in prestigious journals such as American Journal of Psychiatry, Biological Psychiatry and The British Journal of Psychiatry.

In The Last Decade

Gail Shields

18 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gail Shields United States 13 532 479 425 282 183 18 1.2k
Adrianne M. Reveley United Kingdom 15 541 1.0× 390 0.8× 239 0.6× 179 0.6× 87 0.5× 22 1.1k
John R. Kelsoe United States 17 483 0.9× 353 0.7× 300 0.7× 271 1.0× 130 0.7× 27 1.1k
Nadia Davies United Kingdom 7 381 0.7× 316 0.7× 185 0.4× 148 0.5× 60 0.3× 8 805
L. E. DeLisi United States 14 240 0.5× 245 0.5× 256 0.6× 157 0.6× 181 1.0× 29 737
R.S. Kahn Netherlands 14 504 0.9× 142 0.3× 452 1.1× 106 0.4× 296 1.6× 28 930
Benjamin Baig United Kingdom 9 275 0.5× 184 0.4× 304 0.7× 170 0.6× 174 1.0× 21 799
S. J. M. C. Palmen Netherlands 13 273 0.5× 536 1.1× 861 2.0× 244 0.9× 87 0.5× 18 1.3k
Valeria Latorre Italy 19 475 0.9× 229 0.5× 897 2.1× 364 1.3× 174 1.0× 28 1.8k
Liana Romaniuk United Kingdom 22 524 1.0× 159 0.3× 673 1.6× 141 0.5× 171 0.9× 55 1.3k
Daqiang Sun United States 10 604 1.1× 133 0.3× 657 1.5× 254 0.9× 382 2.1× 15 1.3k

Countries citing papers authored by Gail Shields

Since Specialization
Citations

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

Fields of papers citing papers by Gail Shields

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gail Shields

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

All Works

18 of 18 papers shown
1.
Hoff, Anne L., et al.. (2005). Ten year longitudinal study of neuropsychological functioning subsequent to a first episode of schizophrenia. Schizophrenia Research. 78(1). 27–34. 206 indexed citations
2.
DeLisi, Lynn E., et al.. (2002). Hand preference and hand skill in families with schizophrenia. Laterality Asymmetries of Body Brain and Cognition. 7(4). 321–332. 34 indexed citations
3.
DeLisi, Lynn E., Sarah H. Shaw, Timothy J. Crow, et al.. (2002). A Genome-Wide Scan for Linkage to Chromosomal Regions in 382 Sibling Pairs With Schizophrenia or Schizoaffective Disorder. American Journal of Psychiatry. 159(5). 803–812. 187 indexed citations
4.
DeLisi, Lynn E., Sarah H. Shaw, Timothy J. Crow, et al.. (2001). A genome-wide scan in 301 families with sibling-pairs diagnosed with schizophrenia of schizoaffective disorder suggests linkage to chromosomes 2pcen and 10p14. Institutional Research Information System (Università degli Studi di Brescia). 105(7). 1 indexed citations
5.
DeLisi, Lynn E., Kamran Razi, John Stewart, et al.. (2000). No evidence for a parent-of-origin effect detected in the pattern of inheritance of schizophrenia. Biological Psychiatry. 48(7). 706–709. 30 indexed citations
6.
DeLisi, Lynn E., Sarah H. Shaw, Timothy J. Crow, et al.. (2000). Lack of evidence for linkage to chromosomes 13 and 8 for schizophrenia and schizoaffective disorder. American Journal of Medical Genetics. 96(2). 235–239. 15 indexed citations
7.
Shaw, Sarah H., Mary T. Kelly, Angela Smith, et al.. (1998). A genome-wide search for schizophrenia susceptibility genes. American Journal of Medical Genetics. 81(5). 364–376. 208 indexed citations
8.
Garner, Chad, Mary T. Kelly, Lon R. Cardon, et al.. (1996). Linkage analyses of schizophrenia to chromosome 6p24-p22: An attempt to replicate. American Journal of Medical Genetics. 67(6). 595–610. 26 indexed citations
9.
Garner, Chad, Mary T. Kelly, Lon R. Cardon, et al.. (1996). Linkage analyses of schizophrenia to chromosome 6p24‐p22: An attempt to replicate. American Journal of Medical Genetics. 67(6). 595–610. 1 indexed citations
10.
Bass, Nicholas, et al.. (1995). Affective illness and schizophrenia in families with multiple schizophrenic members: independent illnesses or variant gene(s)?. European Neuropsychopharmacology. 5. 31–36. 13 indexed citations
11.
DeLisi, Lynn E., R. Lofthouse, Thomas Lehner, et al.. (1995). Failure to find a chromosome 18 pericentric linkage in families with schizophrenia. American Journal of Medical Genetics. 60(6). 532–534. 14 indexed citations
12.
DeLisi, Lynn E., Marcella Devoto, Mark Poulter, et al.. (1994). Search for linkage to schizophrenia on the X and Y chromosomes. American Journal of Medical Genetics. 54(2). 113–121. 53 indexed citations
13.
Polymeropoulos, Mihael H., Hilary Coon, William Byerley, et al.. (1994). Search for a schizophrenia susceptibility locus on human chromosome 22. American Journal of Medical Genetics. 54(2). 93–99. 63 indexed citations
14.
Crow, Timothy J., Lynn E. DeLisi, Mark Poulter, et al.. (1994). An Examination of Linkage of Schizophrenia and Schizoaffective Disorder to the Pseudoautosomal Region (Xp22.3). The British Journal of Psychiatry. 164(2). 159–164. 42 indexed citations
15.
Coon, Hilary, Mark Hoff, John Holik, et al.. (1993). C to T nucleotide substitution in codon 713 of amyloid precursor protein gene not found in 86 unrelated schizophrenics from multiplex families. American Journal of Medical Genetics. 48(1). 36–39. 8 indexed citations
16.
Shields, Gail, et al.. (1993). DSM‐III‐R personality disorders in parents of schizophrenic patients. American Journal of Medical Genetics. 48(1). 60–62. 9 indexed citations
17.
DeLisi, Lynn E., Anne L. Hoff, Joseph E. Schwartz, et al.. (1991). Brain morphology in first-episode schizophrenic-like psychotic patients: A quantitative magnetic resonance imaging study. Biological Psychiatry. 29(2). 159–175. 316 indexed citations
18.
Shields, Gail, et al.. (1990). A family with Alport syndrome and psychosis. Schizophrenia Research. 3(4). 235–239. 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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