J E Loth

1.0k total citations
10 papers, 764 citations indexed

About

J E Loth is a scholar working on Genetics, Psychiatry and Mental health and Molecular Biology. According to data from OpenAlex, J E Loth has authored 10 papers receiving a total of 764 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 3 papers in Psychiatry and Mental health and 2 papers in Molecular Biology. Recurrent topics in J E Loth's work include Genetic Associations and Epidemiology (8 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). J E Loth is often cited by papers focused on Genetic Associations and Epidemiology (8 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). J E Loth collaborates with scholars based in United States, Israel and Taiwan. J E Loth's co-authors include Bernard Lerer, T. Conrad Gilliam, Kyra Kanyas, Jean Endicott, Jane Endicott, Miron Baron, Adina Grunn, Lawrence Sharpe, Jürg Ott and Rong Cheng and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Molecular Psychiatry.

In The Last Decade

J E Loth

10 papers receiving 749 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J E Loth United States 8 488 266 229 65 62 10 764
N. Craddock United Kingdom 8 207 0.4× 170 0.6× 255 1.1× 109 1.7× 100 1.6× 15 605
Nick Craddock United Kingdom 5 402 0.8× 304 1.1× 259 1.1× 84 1.3× 114 1.8× 5 800
Liam Carroll United Kingdom 9 221 0.5× 185 0.7× 113 0.5× 97 1.5× 163 2.6× 14 483
Alison Fordyce United Kingdom 5 380 0.8× 447 1.7× 77 0.3× 128 2.0× 90 1.5× 6 742
Hany Goubran‐Botros France 10 139 0.3× 181 0.7× 109 0.5× 49 0.8× 167 2.7× 13 545
E. Claffey Ireland 10 129 0.3× 141 0.5× 142 0.6× 83 1.3× 25 0.4× 11 323
Sibylle G. Schwab Germany 11 336 0.7× 259 1.0× 121 0.5× 122 1.9× 170 2.7× 14 609
Siobhan Schwaiger Ireland 12 240 0.5× 284 1.1× 146 0.6× 151 2.3× 109 1.8× 12 658
Carole Harris‐Kerr United States 7 437 0.9× 867 3.3× 118 0.5× 271 4.2× 139 2.2× 10 1.4k
Stacy Steinberg Iceland 12 378 0.8× 241 0.9× 109 0.5× 73 1.1× 109 1.8× 14 785

Countries citing papers authored by J E Loth

Since Specialization
Citations

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

Fields of papers citing papers by J E Loth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J E Loth. 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 J E Loth. The network helps show where J E Loth may publish in the future.

Co-authorship network of co-authors of J E Loth

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

All Works

10 of 10 papers shown
1.
Cheng, Rong, Suh‐Hang Hank Juo, Jianjun Liu, et al.. (2010). Fine mapping of candidate regions for bipolar disorder provides strong evidence for susceptibility loci on chromosomes 7q. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(2). 168–176. 4 indexed citations
3.
Cheng, Rong, J E Loth, J. Nee, et al.. (2004). Linkage analysis of psychosis in bipolar pedigrees suggests novel putative loci for bipolar disorder and shared susceptibility with schizophrenia. Molecular Psychiatry. 9(12). 1091–1099. 135 indexed citations
4.
Juo, Suh‐Hang Hank, Andrew T. DeWan, Adina Grunn, et al.. (2003). Evidence for a putative bipolar disorder locus on 2p13–16 and other potential loci on 4q31, 7q34, 8q13, 9q31, 10q21–24, 13q32, 14q21 and 17q11–12. Molecular Psychiatry. 8(3). 333–342. 95 indexed citations
5.
Liu, Jianjun, Joseph D. Terwilliger, Adina Grunn, et al.. (2001). A follow-up linkage study supports evidence for a bipolar affective disorder locus on chromosome 21q22. American Journal of Medical Genetics. 105(2). 189–194. 37 indexed citations
6.
Aita, Vincent M., James A. Knowles, Joseph D. Terwilliger, et al.. (1999). A Comprehensive Linkage Analysis of Chromosome 21q22 Supports Prior Evidence for a Putative Bipolar Affective Disorder Locus. The American Journal of Human Genetics. 64(1). 210–217. 87 indexed citations
7.
Knowles, James A., Peter A. Rao, J E Loth, et al.. (1998). No Evidence for Significant Linkage between Bipolar Affective Disorder and Chromosome 18 Pericentromeric Markers in a Large Series of Multiplex Extended Pedigrees. The American Journal of Human Genetics. 62(4). 916–924. 26 indexed citations
8.
Straub, Richard E., Thomas Lehner, Ying Luo, et al.. (1994). A possible vulnerability locus for bipolar affective disorder on chromosome 21q22.3. Nature Genetics. 8(3). 291–296. 230 indexed citations
9.
Baron, Miron, Jane Endicott, Bernard Lerer, et al.. (1994). A pedigree series for mapping disease genes in bipolar affective disorder. Psychiatric Genetics. 4(1). 43–56. 26 indexed citations
10.
Loth, J E, et al.. (1983). Computer modeling of blood acid-base disorders for diagnostics, therapy and education.. PubMed. 1 Suppl 1. 411–3. 1 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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