Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

938 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Effects of polygenic risk for major mental disorders and cross-disorder on cortical complexity.
Schmitt S, Meller T, Stein F, Brosch K, Ringwald K, Pfarr JK, Bordin C, Peusch N, Steinsträter O, Grotegerd D, Dohm K, Meinert S, Förster K, Redlich R, Opel N, Hahn T, Jansen A, Forstner AJ, Streit F, Witt SH, Rietschel M, Müller-Myhsok B, Nöthen MM, Dannlowski U, Krug A, Kircher T, Nenadić I. Schmitt S, et al. Among authors: rietschel m. Psychol Med. 2021 Apr 8;52(16):1-12. doi: 10.1017/S0033291721001082. Online ahead of print. Psychol Med. 2021. PMID: 33827729 Free PMC article.
[Genetic counseling in psychiatric diseases].
Körner J, Rietschel M, Nöthen MM, Propping P. Körner J, et al. Among authors: rietschel m. Nervenarzt. 1996 Jan;67(1):3-14. Nervenarzt. 1996. PMID: 8676986 Review. German.
Systematic screening for mutations in the human serotonin 1F receptor gene in patients with bipolar affective disorder and schizophrenia.
Shimron-Abarbanell D, Harms H, Erdmann J, Albus M, Maier W, Rietschel M, Körner J, Weigelt B, Franzek E, Sander T, Knapp M, Propping P, Nöthen MM. Shimron-Abarbanell D, et al. Among authors: rietschel m. Am J Med Genet. 1996 Apr 9;67(2):225-8. doi: 10.1002/(SICI)1096-8628(19960409)67:2<225::AID-AJMG16>3.0.CO;2-L. Am J Med Genet. 1996. PMID: 8723053
938 results