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Contribution of Rare and Potentially Functionally Relevant Sequence Variants in Schizophrenia Risk-Locus Xq28,distal.
Claus I, Sivalingam S, Koller AC, Weiß A, Mathey CM, Sindermann L, Klein D, Henschel L, Ludwig KU, Hoffmann P, Heimbach A, Heilmann-Heimbach S, Vedder H, Kammerer-Ciernioch J, Stürmer T, Streit F, Maaser-Hecker A, Nenadić I, Baune BT, Hartmann AM, Konte B, Giegling I, Heilbronner U, Wagner M, Philipsen A, Schmidt B, Rujescu D, Buness A, Schulze TG, Rietschel M, Forstner AJ, Nöthen MM, Degenhardt F. Claus I, et al. Among authors: nothen mm. Am J Med Genet B Neuropsychiatr Genet. 2024 Oct 30:e33011. doi: 10.1002/ajmg.b.33011. Online ahead of print. Am J Med Genet B Neuropsychiatr Genet. 2024. PMID: 39473393
Investigation of the role of TCF4 rare sequence variants in schizophrenia.
Basmanav FB, Forstner AJ, Fier H, Herms S, Meier S, Degenhardt F, Hoffmann P, Barth S, Fricker N, Strohmaier J, Witt SH, Ludwig M, Schmael C, Moebus S, Maier W, Mössner R, Rujescu D, Rietschel M, Lange C, Nöthen MM, Cichon S. Basmanav FB, et al. Among authors: nothen mm. Am J Med Genet B Neuropsychiatr Genet. 2015 Jul;168B(5):354-62. doi: 10.1002/ajmg.b.32318. Epub 2015 May 22. Am J Med Genet B Neuropsychiatr Genet. 2015. PMID: 26010163
Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2.
Degenhardt F, Heinemann B, Strohmaier J, Pfohl MA, Giegling I, Hofmann A, Ludwig KU, Witt SH, Ludwig M, Forstner AJ, Albus M, Schwab SG, Borrmann-Hassenbach M, Lennertz L, Wagner M, Hoffmann P, Rujescu D, Maier W, Cichon S, Rietschel M, Nöthen MM. Degenhardt F, et al. Among authors: nothen mm. Psychiatr Genet. 2016 Dec;26(6):293-296. doi: 10.1097/YPG.0000000000000145. Psychiatr Genet. 2016. PMID: 27668412 Free PMC article.
Investigation of SHANK3 in schizophrenia.
de Sena Cortabitarte A, Degenhardt F, Strohmaier J, Lang M, Weiss B, Roeth R, Giegling I, Heilmann-Heimbach S, Hofmann A, Rujescu D, Fischer C, Rietschel M, Nöthen MM, Rappold GA, Berkel S. de Sena Cortabitarte A, et al. Among authors: nothen mm. Am J Med Genet B Neuropsychiatr Genet. 2017 Jun;174(4):390-398. doi: 10.1002/ajmg.b.32528. Epub 2017 Mar 28. Am J Med Genet B Neuropsychiatr Genet. 2017. PMID: 28371232
Association study between genetic variants at the PIP5K2A gene locus and schizophrenia and bipolar affective disorder.
Jamra RA, Klein K, Villela AW, Becker T, Schulze TG, Schmael C, Deschner M, Klopp N, Illig T, Propping P, Cichon S, Rietschel M, Nöthen MM, Schumacher J. Jamra RA, et al. Among authors: nothen mm. Am J Med Genet B Neuropsychiatr Genet. 2006 Sep 5;141B(6):663-5. doi: 10.1002/ajmg.b.30358. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16823801
Expert and self-assessment of lifetime symptoms and diagnosis of major depressive disorder in large-scale genetic studies in the general population: comparison of a clinical interview and a self-administered checklist.
Martin J, Streit F, Treutlein J, Lang M, Frank J, Forstner AJ, Degenhardt F, Witt SH, Schulze TG, Cichon S, Nöthen MM, Rietschel M, Strohmaier J. Martin J, et al. Among authors: nothen mm. Psychiatr Genet. 2017 Oct;27(5):187-196. doi: 10.1097/YPG.0000000000000182. Psychiatr Genet. 2017. PMID: 28731911 Free PMC article.
Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy.
Foo JC, Streit F, Frank J, Witt SH, Treutlein J; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium; Baune BT, Moebus S, Jöckel KH, Forstner AJ, Nöthen MM, Rietschel M, Sartorius A, Kranaster L. Foo JC, et al. Among authors: nothen mm. Am J Med Genet B Neuropsychiatr Genet. 2019 Jan;180(1):35-45. doi: 10.1002/ajmg.b.32700. Epub 2018 Dec 2. Am J Med Genet B Neuropsychiatr Genet. 2019. PMID: 30507021 Free PMC article.
"The Heidelberg Five" personality dimensions: Genome-wide associations, polygenic risk for neuroticism, and psychopathology 20 years after assessment.
Heilbronner U, Papiol S, Budde M, Andlauer TFM, Strohmaier J, Streit F, Frank J, Degenhardt F, Heilmann-Heimbach S, Witt SH, Forstner AJ, Loerbroks A, Amelang M, Stürmer T, Müller-Myhsok B, Nöthen MM, Rietschel M, Schulze TG. Heilbronner U, et al. Among authors: nothen mm. Am J Med Genet B Neuropsychiatr Genet. 2021 Mar;186(2):77-89. doi: 10.1002/ajmg.b.32837. Epub 2021 Feb 15. Am J Med Genet B Neuropsychiatr Genet. 2021. PMID: 33590662
1,010 results