S D Detera-Wadleigh

1.0k total citations
19 papers, 777 citations indexed

About

S D Detera-Wadleigh is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, S D Detera-Wadleigh has authored 19 papers receiving a total of 777 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Molecular Biology and 4 papers in Psychiatry and Mental health. Recurrent topics in S D Detera-Wadleigh's work include Genetics and Neurodevelopmental Disorders (6 papers), Bipolar Disorder and Treatment (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). S D Detera-Wadleigh is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Bipolar Disorder and Treatment (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). S D Detera-Wadleigh collaborates with scholars based in United States, Germany and Australia. S D Detera-Wadleigh's co-authors include Takeo Yoshikawa, Gordon Turner, Constantine A. Stratakis, Ignacio Encı́o, Steven W. J. Lamberts, David M. Hurley, Michael Karl, G P Chrousos, Domenico Accili and Roel H. DeRijk and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Biochemical and Biophysical Research Communications and Neuropsychopharmacology.

In The Last Decade

S D Detera-Wadleigh

19 papers receiving 765 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
S D Detera-Wadleigh United States 12 289 266 250 161 86 19 777
Heike Jung Germany 19 352 1.2× 429 1.6× 298 1.2× 50 0.3× 45 0.5× 57 1.1k
Shinobu Takayasu Japan 16 185 0.6× 348 1.3× 64 0.3× 83 0.5× 28 0.3× 52 864
F. W. SELBY United States 8 141 0.5× 512 1.9× 144 0.6× 54 0.3× 44 0.5× 8 944
F. Tronche France 7 246 0.9× 119 0.4× 101 0.4× 135 0.8× 13 0.2× 8 720
GK Stalla Germany 18 247 0.9× 528 2.0× 64 0.3× 56 0.3× 27 0.3× 36 938
Jürg Girard Switzerland 13 183 0.6× 458 1.7× 145 0.6× 42 0.3× 26 0.3× 18 914
Michael E. Carney United States 13 281 1.0× 60 0.2× 247 1.0× 165 1.0× 20 0.2× 15 977
Kunihiko Hanew Japan 15 224 0.8× 540 2.0× 135 0.5× 216 1.3× 9 0.1× 78 1.0k
Lynn Loriaux United States 15 413 1.4× 529 2.0× 296 1.2× 121 0.8× 10 0.1× 26 1.1k
Joachim Sauer Germany 15 116 0.4× 276 1.0× 75 0.3× 134 0.8× 19 0.2× 25 746

Countries citing papers authored by S D Detera-Wadleigh

Since Specialization
Citations

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

Fields of papers citing papers by S D Detera-Wadleigh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S D Detera-Wadleigh. 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 S D Detera-Wadleigh. The network helps show where S D Detera-Wadleigh may publish in the future.

Co-authorship network of co-authors of S D Detera-Wadleigh

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

All Works

19 of 19 papers shown
1.
Gupta, Ajay, Thomas G. Schulze, Vijayaraj Nagarajan, et al.. (2011). Interaction networks of lithium and valproate molecular targets reveal a striking enrichment of apoptosis functional clusters and neurotrophin signaling. The Pharmacogenomics Journal. 12(4). 328–341. 32 indexed citations
2.
Chen, Yih‐Sharng, Nirmala Akula, S D Detera-Wadleigh, et al.. (2003). Findings in an independent sample support an association between bipolar affective disorder and the G72/G30 locus on chromosome 13q33. Molecular Psychiatry. 9(1). 5–5. 4 indexed citations
3.
Segurado, Ricardo, S D Detera-Wadleigh, Michael Gill, Douglas F. Levinson, & Cathryn M. Lewis. (2002). Meta-analysis of genome scans for bipolar affective disorder.. American Journal of Medical Genetics Part A. 114(7). 701–701. 5 indexed citations
4.
DeRijk, Roel H., Marcel J. M. Schaaf, Gordon Turner, et al.. (2001). A human glucocorticoid receptor gene variant that increases the stability of the glucocorticoid receptor beta-isoform mRNA is associated with rheumatoid arthritis.. PubMed. 28(11). 2383–8. 214 indexed citations
5.
Yoshikawa, Takeo, Muralidhara Padigaru, Jayaprakash D. Karkera, et al.. (2000). Genomic structure and novel variants of myo-inositol monophosphatase 2 (IMPA2). Molecular Psychiatry. 5(2). 165–171. 39 indexed citations
6.
Curtis, David, Vincent M. Aita, Maayan Baron, et al.. (1999). Chromosome 21 workshop. American Journal of Medical Genetics. 88(3). 272–275. 12 indexed citations
7.
Kennedy, James L., Vincenzo S. Basile, Fabìo Macciardi, et al.. (1999). Chromosome 4 workshop summary: Sixth World Congress on Psychiatric Genetics, Bonn, Germany, October 6-10, 1998. American Journal of Medical Genetics. 88(3). 224–228. 16 indexed citations
8.
Rhoads, Allen R., Jayaprakash D. Karkera, & S D Detera-Wadleigh. (1999). Radiation hybrid mapping of genes in the lithium-sensitive Wnt signaling pathway. Molecular Psychiatry. 4(5). 437–442. 9 indexed citations
9.
Yoshikawa, Takeo, et al.. (1998). Multiple Transcriptional Variants and RNA Editing inC18orf1,a Novel Gene with LDLRA and Transmembrane Domains on 18p11.2. Genomics. 47(2). 246–257. 13 indexed citations
10.
McInnis, M. G., Francis J. McMahon, Tatiana Foroud, et al.. (1998). Evidence for a susceptibility locus for bipolar disorder on chromosome 11p11.5. 81(6). 2 indexed citations
11.
Foroud, Tatiana, Daphne Koller, Howard J. Edenberg, et al.. (1998). Genomewide scan of affected relative pairs using the NIMH Genetics Initiative Bipolar affective Disorder pedigrees. 81(6). 5 indexed citations
12.
Yoshikawa, Takeo, Lisa E. Esterling, Joan Overhauser, et al.. (1997). Isolation of chromosome 18-specific brain transcripts as positional candidates for bipolar disorder. American Journal of Medical Genetics. 74(2). 140–149. 14 indexed citations
13.
Altemus, Margaret, et al.. (1997). Discussion. Neuropsychopharmacology. 17(2). 100–109. 70 indexed citations
14.
Yoshikawa, Takeo, et al.. (1997). A novel human myo-inositol monophosphatase gene, IMP.18p, maps to a susceptibility region for bipolar disorder. Molecular Psychiatry. 2(5). 393–397. 44 indexed citations
15.
Esterling, Lisa E., Tara C. Matise, Alan R. Sanders, et al.. (1997). An integrated physical map of 18p11.2: a susceptibility region for bipolar disorder. Molecular Psychiatry. 2(6). 501–504. 10 indexed citations
16.
Stratakis, Constantine A., Nicholas J. Sarlis, Wade H. Berrettini, et al.. (1997). Lack of linkage between the corticotropin-releasing hormone (CRH) gene and bipolar affective disorder. Molecular Psychiatry. 2(6). 483–485. 9 indexed citations
17.
Yoshikawa, Takeo, Zoran Brkanac, Barbara R. DuPont, et al.. (1996). Assignment of the Human Nuclear Hormone Receptor, NUC1 (PPARD), to Chromosome 6p21.1–p21.2. Genomics. 35(3). 637–638. 33 indexed citations
18.
Xing, Guichun, Li Zhang, Takeo Yoshikawa, et al.. (1995). Rat PPARδ Contains a CGG Triplet Repeat and Is Prominently Expressed in the Thalamic Nuclei. Biochemical and Biophysical Research Communications. 217(3). 1015–1025. 69 indexed citations
19.
Karl, Michael, Steven W. J. Lamberts, S D Detera-Wadleigh, et al.. (1993). Familial glucocorticoid resistance caused by a splice site deletion in the human glucocorticoid receptor gene.. The Journal of Clinical Endocrinology & Metabolism. 76(3). 683–689. 177 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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