Christine Schmäl

2.8k total citations
10 papers, 523 citations indexed

About

Christine Schmäl is a scholar working on Genetics, Psychiatry and Mental health and Cellular and Molecular Neuroscience. According to data from OpenAlex, Christine Schmäl has authored 10 papers receiving a total of 523 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 5 papers in Psychiatry and Mental health and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Christine Schmäl's work include Bipolar Disorder and Treatment (3 papers), Genetic Associations and Epidemiology (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Christine Schmäl is often cited by papers focused on Bipolar Disorder and Treatment (3 papers), Genetic Associations and Epidemiology (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Christine Schmäl collaborates with scholars based in Germany, Belgium and United States. Christine Schmäl's co-authors include Markus M. Nöthen, Marcella Rietschel, Sven Cichon, Thomas G. Schulze, Johannes Schumacher, Per Hoffmann, Gerd Schulte‐Körne, Rami Abou Jamra, Astrid Zobel and Johannes Schumacher and has published in prestigious journals such as American Journal of Psychiatry, Biological Psychiatry and Journal of Affective Disorders.

In The Last Decade

Christine Schmäl

10 papers receiving 508 citations

Peers

Christine Schmäl

CMN

GENET

PMH

DEP

S C Bakker Netherlands

K. Wigg Canada

Tiffany D. Rogers United States

Mary A. Walker United Kingdom

Melvin Lyon United States

Linda Paul United States

Dominique Bondoux France

Tomasz A. Jarczok Germany

Elizabeth K. Lucas United States

Natallia V. Riddick United States

S C Bakker Netherlands

Christine Schmäl

126 ×0.6

CMN

295 ×1.6

152 ×1.2

GENET

340 ×2.7

PMH

32 ×0.4

DEP

Citations per year, relative to Christine Schmäl Christine Schmäl (= 1×) peers S C Bakker

Countries citing papers authored by Christine Schmäl

Since Specialization

Citations

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

Fields of papers citing papers by Christine Schmäl

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christine Schmäl

This figure shows the co-authorship network connecting the top 25 collaborators of Christine Schmäl. A scholar is included among the top collaborators of Christine Schmäl 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 Christine Schmäl. Christine Schmäl 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

Tawamie, Hasan, Eva Wohlleber, Steffen Uebe, et al.. (2015). Recurrent null mutation in SPG20 leads to Troyer syndrome. Molecular and Cellular Probes. 29(5). 315–318. 11 indexed citations

Schmäl, Christine, Katja Becker, Ruth Berg, et al.. (2014). Pediatric Psychopharmacological Research in the Post EU Regulation 1901/2006 Era. Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie. 42(6). 441–449. 3 indexed citations

Haenisch, Britta, Stefan Herms, Manuel Mattheisen, et al.. (2012). Genome-wide association data provide further support for an association between 5-HTTLPR and major depressive disorder. Journal of Affective Disorders. 146(3). 438–440. 18 indexed citations

Miró, Xavier, Sandra Meier, Josef Frank, et al.. (2012). Studies in Humans and Mice Implicate Neurocan in the Etiology of Mania. American Journal of Psychiatry. 169(9). 982–990. 50 indexed citations

Strohmaier, Jana, Stefan Wüst, Rudolf Uher, et al.. (2011). Sexual dysfunction during treatment with serotonergic and noradrenergic antidepressants: Clinical description and the role of the5-HTTLPR. The World Journal of Biological Psychiatry. 12(7). 528–538. 27 indexed citations

Nieratschker, Vanessa, Josef Frank, Thomas W. Mühleisen, et al.. (2010). The catechol-O-methyl transferase (COMT) gene and its potential association with schizophrenia: Findings from a large German case-control and family-based sample. Schizophrenia Research. 122(1-3). 24–30. 20 indexed citations

Tost, Heike, Matthias Ruf, Christine Schmäl, et al.. (2009). Prefrontal-temporal gray matter deficits in bipolar disorder patients with persecutory delusions. Journal of Affective Disorders. 120(1-3). 54–61. 44 indexed citations

Schumacher, Johannes, Per Hoffmann, Christine Schmäl, Gerd Schulte‐Körne, & Markus M. Nöthen. (2007). Genetics of dyslexia: the evolving landscape. Journal of Medical Genetics. 44(5). 289–297. 97 indexed citations

Jamra, Rami Abou, Tim Becker, Norman Klopp, et al.. (2006). No evidence for an association between variants at the γ-amino-n-butyric acid type A receptor β2 locus and schizophrenia. Psychiatric Genetics. 17(1). 43–45. 6 indexed citations

10.

Schumacher, Johannes, Rami Abou Jamra, Tim Becker, et al.. (2005). Evidence for a Relationship Between Genetic Variants at the Brain-Derived Neurotrophic Factor (BDNF) Locus and Major Depression. Biological Psychiatry. 58(4). 307–314. 247 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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