Nöthen MM - Search Results

1

Predictive power of the ADHD GWAS 2019 polygenic risk scores in independent samples of bipolar patients with childhood ADHD.

Grigoroiu-Serbanescu M, Giaroli G, Thygesen JH, Shenyan O, Bigdeli TB, Bass NJ, Diaconu CC, Neagu AI, Forstner AJ, Degenhardt F, Herms S, Nöthen MM, McQuillin A. Grigoroiu-Serbanescu M, et al. Among authors: nothen mm. J Affect Disord. 2020 Mar 15;265:651-659. doi: 10.1016/j.jad.2019.11.109. Epub 2019 Nov 23. J Affect Disord. 2020. PMID: 31791676

2

Clinical evidence for genomic imprinting in bipolar I disorder.

Grigoroiu-Serbanescu M, Nothen M, Propping P, Poustka F, Magureanu S, Vasilescu R, Marinescu E, Ardelean V. Grigoroiu-Serbanescu M, et al. Acta Psychiatr Scand. 1995 Nov;92(5):365-70. doi: 10.1111/j.1600-0447.1995.tb09598.x. Acta Psychiatr Scand. 1995. PMID: 8619341

3

Patterns of parental transmission and familial aggregation models in bipolar affective disorder.

Grigoroiu-Serbanescu M, Martinez M, Nöthen MM, Propping P, Milea S, Mihailescu R, Marinescu E. Grigoroiu-Serbanescu M, et al. Among authors: nothen mm. Am J Med Genet. 1998 Sep 7;81(5):397-404. Am J Med Genet. 1998. PMID: 9754625

4

Different familial transmission patterns in bipolar I disorder with onset before and after age 25.

Grigoroiu-Serbanescu M, Martinez M, Nöthen MM, Grinberg M, Sima D, Propping P, Marinescu E, Hrestic M. Grigoroiu-Serbanescu M, et al. Among authors: nothen mm. Am J Med Genet. 2001 Dec 8;105(8):765-73. doi: 10.1002/ajmg.10047. Am J Med Genet. 2001. PMID: 11803528

5

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder.

Segurado R, Detera-Wadleigh SD, Levinson DF, Lewis CM, Gill M, Nurnberger JI Jr, Craddock N, DePaulo JR, Baron M, Gershon ES, Ekholm J, Cichon S, Turecki G, Claes S, Kelsoe JR, Schofield PR, Badenhop RF, Morissette J, Coon H, Blackwood D, McInnes LA, Foroud T, Edenberg HJ, Reich T, Rice JP, Goate A, McInnis MG, McMahon FJ, Badner JA, Goldin LR, Bennett P, Willour VL, Zandi PP, Liu J, Gilliam C, Juo SH, Berrettini WH, Yoshikawa T, Peltonen L, Lönnqvist J, Nöthen MM, Schumacher J, Windemuth C, Rietschel M, Propping P, Maier W, Alda M, Grof P, Rouleau GA, Del-Favero J, Van Broeckhoven C, Mendlewicz J, Adolfsson R, Spence MA, Luebbert H, Adams LJ, Donald JA, Mitchell PB, Barden N, Shink E, Byerley W, Muir W, Visscher PM, Macgregor S, Gurling H, Kalsi G, McQuillin A, Escamilla MA, Reus VI, Leon P, Freimer NB, Ewald H, Kruse TA, Mors O, Radhakrishna U, Blouin JL, Antonarakis SE, Akarsu N. Segurado R, et al. Among authors: nothen mm. Am J Hum Genet. 2003 Jul;73(1):49-62. doi: 10.1086/376547. Epub 2003 Jun 11. Am J Hum Genet. 2003. PMID: 12802785 Free PMC article.

6

Systematic screening for mutations in the human N-methyl-D-aspartate receptor 1 gene in schizophrenic patients from the German population.

Paus S, Rietschel M, Schulze TG, Ohlraun S, Diaconu CC, Van Den Bogaert A, Maier W, Propping P, Cichon S, Nöthen MM. Paus S, et al. Among authors: nothen mm. Psychiatr Genet. 2004 Dec;14(4):233-4. doi: 10.1097/00041444-200412000-00013. Psychiatr Genet. 2004. PMID: 15564900

7

Family history influences age of onset in bipolar I disorder in females but not in males.

Grigoroiu-Serbanescu M, Nöthen MM, Ohlraun S, Propping P, Maier W, Wickramaratne P, Georgescu MJ, Prelipceanu D, Grimberg M, Sima D, Rietschel M. Grigoroiu-Serbanescu M, et al. Among authors: nothen mm. Am J Med Genet B Neuropsychiatr Genet. 2005 Feb 5;133B(1):6-11. doi: 10.1002/ajmg.b.30133. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15635595

8

Investigation of the tryptophan hydroxylase 2 gene in bipolar I disorder in the Romanian population.

Grigoroiu-Serbanescu M, Diaconu CC, Herms S, Bleotu C, Vollmer J, Mühleisen TW, Prelipceanu D, Priebe L, Mihailescu R, Georgescu MJ, Sima D, Grimberg M, Nöthen MM, Cichon S. Grigoroiu-Serbanescu M, et al. Among authors: nothen mm. Psychiatr Genet. 2008 Oct;18(5):240-7. doi: 10.1097/YPG.0b013e3283053045. Psychiatr Genet. 2008. PMID: 18797398

9

Variation in P2RX7 candidate gene (rs2230912) is not associated with bipolar I disorder and unipolar major depression in four European samples.

Grigoroiu-Serbanescu M, Herms S, Mühleisen TW, Georgi A, Diaconu CC, Strohmaier J, Czerski P, Hauser J, Leszczynska-Rodziewicz A, Jamra RA, Babadjanova G, Tiganov A, Krasnov V, Kapiletti S, Neagu AI, Vollmer J, Breuer R, Rietschel M, Nöthen MM, Cichon S, Propping P, Nöthen MM, Cichon S. Grigoroiu-Serbanescu M, et al. Among authors: nothen mm. Am J Med Genet B Neuropsychiatr Genet. 2009 Oct 5;150B(7):1017-21. doi: 10.1002/ajmg.b.30952. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 19330776

10

Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia.

Ludwig KU, Roeske D, Herms S, Schumacher J, Warnke A, Plume E, Neuhoff N, Bruder J, Remschmidt H, Schulte-Körne G, Müller-Myhsok B, Nöthen MM, Hoffmann P. Ludwig KU, et al. Among authors: nothen mm. Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):503-511. doi: 10.1002/ajmg.b.31007. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19591125

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