Nöthen MM - Search Results

1

Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors.

Mullins N, Kang J, Campos AI, Coleman JRI, Edwards AC, Galfalvy H, Levey DF, Lori A, Shabalin A, Starnawska A, Su MH, Watson HJ, Adams M, Awasthi S, Gandal M, Hafferty JD, Hishimoto A, Kim M, Okazaki S, Otsuka I, Ripke S, Ware EB, Bergen AW, Berrettini WH, Bohus M, Brandt H, Chang X, Chen WJ, Chen HC, Crawford S, Crow S, DiBlasi E, Duriez P, Fernández-Aranda F, Fichter MM, Gallinger S, Glatt SJ, Gorwood P, Guo Y, Hakonarson H, Halmi KA, Hwu HG, Jain S, Jamain S, Jiménez-Murcia S, Johnson C, Kaplan AS, Kaye WH, Keel PK, Kennedy JL, Klump KL, Li D, Liao SC, Lieb K, Lilenfeld L, Liu CM, Magistretti PJ, Marshall CR, Mitchell JE, Monson ET, Myers RM, Pinto D, Powers A, Ramoz N, Roepke S, Rozanov V, Scherer SW, Schmahl C, Sokolowski M, Strober M, Thornton LM, Treasure J, Tsuang MT, Witt SH, Woodside DB, Yilmaz Z, Zillich L, Adolfsson R, Agartz I, Air TM, Alda M, Alfredsson L, Andreassen OA, Anjorin A, Appadurai V, Soler Artigas M, Van der Auwera S, Azevedo MH, Bass N, Bau CHD, Baune BT, Bellivier F, Berger K, Biernacka JM, Bigdeli TB, Binder EB, Boehnke M, Boks MP, Bosch R, Braff DL, Bryant R, Budde M, Byrne EM, Cahn W, Casas M, Castelao E, Cervilla JA, Chaumette B, Cichon S, Corvin A, … See abstract for full author list ➔ Mullins N, et al. Among authors: nothen mm. Biol Psychiatry. 2022 Feb 1;91(3):313-327. doi: 10.1016/j.biopsych.2021.05.029. Epub 2021 Sep 9. Biol Psychiatry. 2022. PMID: 34861974 Free PMC article.

2

An association study of debrisoquine hydroxylase (CYP2D6) polymorphisms in schizophrenia.

Dawson E, Powell JF, Nöthen MM, Crocq MA, Lanczik M, Körner J, Rietschel M, van Os J, Wright P, Gill M. Dawson E, et al. Among authors: nothen mm. Psychiatr Genet. 1994 Winter;4(4):215-8. doi: 10.1097/00041444-199400440-00005. Psychiatr Genet. 1994. PMID: 7712118

3

Association and haplotype analysis at the tyrosine hydroxylase locus in a combined German-British sample of manic depressive patients and controls.

Körner J, Rietschel M, Hunt N, Castle D, Gill M, Nöthen MM, Craddock N, Daniels J, Owen M, Fimmers R, et al. Körner J, et al. Among authors: nothen mm. Psychiatr Genet. 1994 Fall;4(3):167-75. doi: 10.1097/00041444-199400430-00007. Psychiatr Genet. 1994. PMID: 7719703

4

Association analysis of the dopamine D2 receptor gene in Tourette's syndrome using the haplotype relative risk method.

Nöthen MM, Hebebrand J, Knapp M, Hebebrand K, Camps A, von Gontard A, Wettke-Schäfer R, Lisch S, Cichon S, Poustka F, et al. Nöthen MM, et al. Am J Med Genet. 1994 Sep 15;54(3):249-52. doi: 10.1002/ajmg.1320540311. Am J Med Genet. 1994. PMID: 7810582

5

[Genetic association in psychiatric diseases. Concepts and findings].

Propping P, Nöthen MM, Körner J, Rietschel M, Maier W. Propping P, et al. Among authors: nothen mm. Nervenarzt. 1994 Nov;65(11):725-40. Nervenarzt. 1994. PMID: 7816149 Review. German. No abstract available.

6

Human dopamine D4 receptor gene: frequent occurrence of a null allele and observation of homozygosity.

Nöthen MM, Cichon S, Hemmer S, Hebebrand J, Remschmidt H, Lehmkuhl G, Poustka F, Schmidt M, Catalano M, Fimmers R, et al. Nöthen MM, et al. Hum Mol Genet. 1994 Dec;3(12):2207-12. doi: 10.1093/hmg/3.12.2207. Hum Mol Genet. 1994. PMID: 7881421

7

Single-strand conformation analysis (SSCA) of the dopamine D1 receptor gene (DRD1) reveals no significant mutation in patients with schizophrenia and manic depression.

Cichon S, Nöthen MM, Rietschel M, Körner J, Propping P. Cichon S, et al. Among authors: nothen mm. Biol Psychiatry. 1994 Dec 15;36(12):850-3. doi: 10.1016/0006-3223(94)90597-5. Biol Psychiatry. 1994. PMID: 7893850 Clinical Trial. No abstract available.

8

[Pemphigus chronicus benignus familiaris (Hailey-Hailey disease) and bipolar affective disease in 3 members of a family].

Wilk M, Rietschel M, Körner J, Möller HJ, Nöthen MM, Bauer R, Kreysel HW. Wilk M, et al. Among authors: nothen mm. Hautarzt. 1994 May;45(5):313-7. doi: 10.1007/s001050050075. Hautarzt. 1994. PMID: 8050901 German.

9

Polymorphism of human complement component C6: an amino acid substitution (Glu/Ala) within the second thrombospondin repeat differentiates between the two common allotypes C6 A and C6 B.

Dewald G, Nöthen MM, Cichon S. Dewald G, et al. Among authors: nothen mm. Biochem Biophys Res Commun. 1993 Jul 15;194(1):458-64. doi: 10.1006/bbrc.1993.1841. Biochem Biophys Res Commun. 1993. PMID: 8101442

10

Detection of four polymorphic sites in the human dopamine D1 receptor gene (DRD1).

Cichon S, Nöthen MM, Erdmann J, Propping P. Cichon S, et al. Among authors: nothen mm. Hum Mol Genet. 1994 Jan;3(1):209. doi: 10.1093/hmg/3.1.209. Hum Mol Genet. 1994. PMID: 8162032 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,053 results

Search Page

Filters