skip to main content
Language:
Search Limited to: Search Limited to: Resource type Show Results with: Show Results with: Index

Results 1 - 50 of 186  for Everything (Includes Articles)

Results 1 2 3 4 next page
Show only
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Material Type:
Article
Add to e-Shelf

5-HT2A receptor and bipolar affective disorder: association studies in affected patients

Arranz, M J ; Erdmann, J ; Kirov, G ; Rietschel, M ; Sodhi, M ; Albus, M ; Ball, D ; Maier, W ; Davies, N ; Franzek, E ; Abusaad, I ; Weigelt, B ; Murray, R ; Shimron-Abarbanell, D ; Kerwin, R ; Propping, P ; Sham, P ; Nöthen, M M ; Collier, D A

Neuroscience letters, 14 March 1997, Vol.224(2), pp.95-8 [Peer Reviewed Journal]

Full text available

View all versions
2
Material Type:
Article
Add to e-Shelf

5-HT2A receptor gene polymorphisms, anorexia nervosa, and obesity

Hinney, A ; Ziegler, A ; Nöthen, M M ; Remschmidt, H ; Hebebrand, J

Lancet (London, England), 01 November 1997, Vol.350(9087), pp.1324-5 [Peer Reviewed Journal]

Full text available

View all versions
3
Material Type:
Article
Add to e-Shelf

5HT 2a receptor T102C polymorphism and schizophrenia

Jönsson, E ; Nöthen, M M ; Bunzel, R ; Propping, P ; Sedvall, G

Lancet (London, England), 29 June 1996, Vol.347(9018), pp.1831 [Peer Reviewed Journal]

Full text available

View all versions
4
Material Type:
Article
Add to e-Shelf

A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults

Ludwig, K U ; Sämann, P ; Alexander, M ; Becker, J ; Bruder, J ; Moll, K ; Spieler, D ; Czisch, M ; Warnke, A ; Docherty, S J ; Davis, O S P ; Plomin, R ; Nöthen, M M ; Landerl, K ; Müller-Myhsok, B ; Hoffmann, P ; Schumacher, J ; Schulte-Körne, G ; Czamara, D

Translational psychiatry, 19 February 2013, Vol.3, pp.e229 [Peer Reviewed Journal]

Full text available

View all versions
5
Material Type:
Article
Add to e-Shelf

A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family

Cichon, S ; Kruse, R ; Hillmer, A M ; Kukuk, G ; Anker, M ; Altland, K ; Knapp, M ; Propping, P ; Nöthen, M M

The British journal of dermatology, October 2000, Vol.143(4), pp.811-4 [Peer Reviewed Journal]

Full text available

View all versions
6
Material Type:
Article
Add to e-Shelf

A family-based and case-control association study of trace amine receptor genes on chromosome 6q23 in bipolar affective disorder

Abou Jamra, R ; Sircar, I ; Becker, T ; Freudenberg-Hua, Y ; Ohlraun, S ; Freudenberg, J ; Brockschmidt, F ; Schulze, T G ; Gross, M ; Spira, F ; Deschner, M ; Schmäl, C ; Maier, W ; Propping, P ; Rietschel, M ; Cichon, S ; Nöthen, M M ; Schumacher, J

Molecular psychiatry, July 2005, Vol.10(7), pp.618-20 [Peer Reviewed Journal]

Full text available

View all versions
7
Material Type:
Article
Add to e-Shelf

A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3

Betz, R C ; Lee, Y A ; Bygum, A ; Brandrup, F ; Bernal, A I ; Toribio, J ; Alvarez, J I ; Kukuk, G M ; Ibsen, H H ; Rasmussen, H B ; Wienker, T F ; Reis, A ; Propping, P ; Kruse, R ; Cichon, S ; Nöthen, M M

American journal of human genetics, June 2000, Vol.66(6), pp.1979-83 [Peer Reviewed Journal]

Full text available

View all versions
8
Material Type:
Article
Add to e-Shelf

A gene for universal congenital alopecia maps to chromosome 8p21-22

Nöthen, M M ; Cichon, S ; Vogt, I R ; Hemmer, S ; Kruse, R ; Knapp, M ; Höller, T ; Faiyaz Ul Haque, M ; Haque, S ; Propping, P ; Ahmad, M ; Rietschel, M

American journal of human genetics, February 1998, Vol.62(2), pp.386-90 [Peer Reviewed Journal]

Full text available

View all versions
9
Material Type:
Article
Add to e-Shelf

A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1

Vijayakrishnan, J ; Kumar, R ; Henrion, M Y R ; Moorman, A V ; Rachakonda, P S ; Hosen, I ; Da Silva Filho, M I ; Holroyd, A ; Dobbins, S E ; Koehler, R ; Thomsen, H ; Irving, J A ; Allan, J M ; Lightfoot, T ; Roman, E ; Kinsey, S E ; Sheridan, E ; Thompson, P D ; Hoffmann, P ; Nöthen, M M ; Heilmann-Heimbach, S ; Jöckel, K H ; Greaves, M ; Harrison, C J ; Bartram, C R ; Schrappe, M ; Stanulla, M ; Hemminki, K ; Houlston, R S

Leukemia, March 2017, Vol.31(3), pp.573-579 [Peer Reviewed Journal]

Full text available

View all versions
10
Material Type:
Article
Add to e-Shelf

A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder

Baum, A E ; Akula, N ; Cabanero, M ; Cardona, I ; Corona, W ; Klemens, B ; Schulze, T G ; Cichon, S ; Rietschel, M ; Nöthen, M M ; Georgi, A ; Schumacher, J ; Schwarz, M ; Abou Jamra, R ; Höfels, S ; Propping, P ; Satagopan, J ; Detera-Wadleigh, S D ; Hardy, J ; Mcmahon, F J

Molecular psychiatry, February 2008, Vol.13(2), pp.197-207 [Peer Reviewed Journal]

Full text available

View all versions
11
Material Type:
Article
Add to e-Shelf

A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp

Dávalos, N O ; García-Vargas, A ; Pforr, J ; Dávalos, I P ; Picos-Cárdenas, V J ; García-Cruz, D ; Kruse, R ; Figuera, L E ; Nöthen, M M ; Betz, R C

The British journal of dermatology, December 2005, Vol.153(6), pp.1216-9 [Peer Reviewed Journal]

Full text available

View all versions
12
Material Type:
Article
Add to e-Shelf

A novel Alzheimer disease locus located near the gene encoding tau protein

Jun, G ; Ibrahim-Verbaas, C A ; Vronskaya, M ; Lambert, J-C ; Chung, J ; Naj, A C ; Kunkle, B W ; Wang, L-S ; Bis, J C ; Bellenguez, C ; Harold, D ; Lunetta, K L ; Destefano, A L ; Grenier-Boley, B ; Sims, R ; Beecham, G W ; Smith, A V ; Chouraki, V ; Hamilton-Nelson, K L ; Ikram, M A ; Fievet, N ; Denning, N ; Martin, E R ; Schmidt, H ; Kamatani, Y ; Dunstan, M L ; Valladares, O ; Laza, A R ; Zelenika, D ; Ramirez, A ; Foroud, T M ; Choi, S-H ; Boland, A ; Becker, T ; Kukull, W A ; Van Der Lee, S J ; Pasquier, F ; Cruchaga, C ; Beekly, D ; Fitzpatrick, A L ; Hanon, O ; Gill, M ; Barber, R ; Gudnason, V ; Campion, D ; Love, S ; Bennett, D A ; Amin, N ; Berr, C ; Tsolaki, Magda ; Buxbaum, J D ; Lopez, O L ; Deramecourt, V ; Fox, N C ; Cantwell, L B ; Tárraga, L ; Dufouil, C ; Hardy, J ; Crane, P K ; Eiriksdottir, G ; Hannequin, D ; Clarke, R ; Evans, D ; Mosley, T H ; Letenneur, L ; Brayne, C ; Maier, W ; De Jager, P ; Emilsson, V ; Dartigues, J-F ; Hampel, H ; Kamboh, M I ; De Bruijn, R F A G ; Tzourio, C ; Pastor, P ; Larson, E B ; Rotter, J I ; O'Donovan, M C ; Montine, T J ; Nalls, M A ; Mead, S ; Reiman, E M ; Jonsson, P V ; Holmes, C ; St George-Hyslop, P H ; Boada, M ; Passmore, P ; Wendland, J R ; Schmidt, R ; Morgan, K ; Winslow, A R ; Powell, J F ; Carasquillo, M ; Younkin, S G ; Jakobsdóttir, J ; Kauwe, J S K ; Wilhelmsen, K C ; Rujescu, D ; Nöthen, M M ; Hofman, A ; Jones, L ; Haines, J L ; Psaty, B M ; Van Broeckhoven, C ; Holmans, P ; Launer, L J ; Mayeux, R ; Lathrop, M ; Goate, A M ; Escott-Price, V ; Seshadri, S ; Pericak-Vance, M A ; Amouyel, P ; Williams, J ; Van Duijn, C M ; Schellenberg, G D ; Farrer, L A

Molecular psychiatry, January 2016, Vol.21(1), pp.108-17 [Peer Reviewed Journal]

Full text available

View all versions
13
Material Type:
Article
Add to e-Shelf

A novel KRT86 mutation in a Turkish family with monilethrix, and identification of maternal mosaicism

Redler, S ; Pasternack, S M ; Wolf, S ; Stienen, D ; Wenzel, J ; Nöthen, M M ; Betz, R C

Clinical and experimental dermatology, October 2015, Vol.40(7), pp.781-5 [Peer Reviewed Journal]

Full text available

View all versions
14
Material Type:
Article
Add to e-Shelf

A novel splice site associated polymorphism in the tuberous sclerosis 2 (TSC2) gene may predispose to the development of sporadic gangliogliomas

Platten, M ; Meyer-Puttlitz, B ; Blümcke, I ; Waha, A ; Wolf, H K ; Nöthen, M M ; Louis, D N ; Sampson, J R ; Von Deimling, A

Journal of neuropathology and experimental neurology, July 1997, Vol.56(7), pp.806-10 [Peer Reviewed Journal]

Full text available

View all versions
15
Material Type:
Article
Add to e-Shelf

A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25--q26

Cichon, S ; Schmidt-Wolf, G ; Schumacher, J ; Müller, D J ; Hürter, M ; Schulze, T G ; Albus, M ; Borrmann-Hassenbach, M ; Franzek, E ; Lanczik, M ; Fritze, J ; Kreiner, R ; Weigelt, B ; Minges, J ; Lichtermann, D ; Lerer, B ; Kanyas, K ; Strauch, K ; Windemuth, C ; Baur, M P ; Wienker, T F ; Maier, W ; Rietschel, M ; Propping, P ; Nöthen, M M

Molecular psychiatry, May 2001, Vol.6(3), pp.342-9 [Peer Reviewed Journal]

Full text available

View all versions
16
Material Type:
Article
Add to e-Shelf

A serine to glycine substitution at position 9 in the extracellular N-terminal part of the dopamine D3 receptor protein: no role in the genetic predisposition to bipolar affective disorder

Rietschel, M ; Nöthen, M M ; Lannfelt, L ; Sokoloff, P ; Schwartz, J C ; Lanczik, M ; Fritze, J ; Cichon, S ; Fimmers, R ; Körner, J

Psychiatry research, March 1993, Vol.46(3), pp.253-9 [Peer Reviewed Journal]

Full text available

View all versions
17
Material Type:
Article
Add to e-Shelf

Adenosine A1 receptor and bipolar affective disorder: systematic screening of the gene and association studies

Deckert, J ; Nöthen, M M ; Albus, M ; Franzek, E ; Rietschel, M ; Ren, H ; Stiles, G L ; Knapp, M ; Weigelt, B ; Maier, W ; Beckmann, H ; Propping, P

American journal of medical genetics, 07 February 1998, Vol.81(1), pp.18-23 [Peer Reviewed Journal]

Full text available

18
Material Type:
Article
Add to e-Shelf

Affective symptomatology in schizophrenia: a risk factor for tardive dyskinesia?

Schulze, T G ; Müller, D J ; Krauss, H ; Marwinski, K ; Maroldt, A O ; Novo Y Fernández, A ; Fimmers, R ; Held, T ; Maier, W ; Nöthen, M M ; Rietschel, M

European psychiatry : the journal of the Association of European Psychiatrists, February 2001, Vol.16(1), pp.71-4 [Peer Reviewed Journal]

Full text available

View all versions
19
Material Type:
Article
Add to e-Shelf

Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility

Li, M ; Luo, X-J ; Rietschel, M ; Lewis, C M ; Mattheisen, M ; Müller-Myhsok, B ; Jamain, S ; Leboyer, M ; Landén, M ; Thompson, P M ; Cichon, S ; Nöthen, M M ; Schulze, T G ; Sullivan, P F ; Bergen, S E ; Donohoe, G ; Morris, D W ; Hargreaves, A ; Gill, M ; Corvin, A ; Hultman, C ; Toga, A W ; Shi, L ; Lin, Q ; Shi, H ; Gan, L ; Meyer-Lindenberg, A ; Czamara, D ; Henry, C ; Etain, B ; Bis, J C ; Ikram, M A ; Fornage, M ; Debette, S ; Launer, L J ; Seshadri, S ; Erk, S ; Walter, H ; Heinz, A ; Bellivier, F ; Stein, J L ; Medland, S E ; Arias Vasquez, A ; Hibar, D P ; Franke, B ; Martin, N G ; Wright, M J ; Su, B

Molecular psychiatry, April 2014, Vol.19(4), pp.452-61 [Peer Reviewed Journal]

Full text available

View all versions
20
Material Type:
Article
Add to e-Shelf

Allelic variants of dopamine receptor D4 (DRD4) and serotonin receptor 5HT2c (HTR2c) and temperament factors: replication tests

Kühn, K U ; Meyer, K ; Nöthen, M M ; Gänsicke, M ; Papassotiropoulos, A ; Maier, W

American journal of medical genetics, 16 April 1999, Vol.88(2), pp.168-72

Full text available

21
Material Type:
Article
Add to e-Shelf

Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2

O'Donovan, M C ; Norton, N ; Williams, H ; Peirce, T ; Moskvina, V ; Nikolov, I ; Hamshere, M ; Carroll, L ; Georgieva, L ; Dwyer, S ; Holmans, P ; Marchini, J L ; Spencer, C C A ; Howie, B ; Leung, H-T ; Giegling, I ; Hartmann, A M ; Möller, H-J ; Morris, D W ; Shi, Y ; Feng, G ; Hoffmann, P ; Propping, P ; Vasilescu, C ; Maier, W ; Rietschel, M ; Zammit, S ; Schumacher, J ; Quinn, E M ; Schulze, T G ; Iwata, N ; Ikeda, M ; Darvasi, A ; Shifman, S ; He, L ; Duan, J ; Sanders, A R ; Levinson, D F ; Adolfsson, R ; Osby, U ; Terenius, L ; Jönsson, E G ; Cichon, S ; Nöthen, M M ; Gill, M ; Corvin, A P ; Rujescu, D ; Gejman, P V ; Kirov, G ; Craddock, N ; Williams, N M ; Owen, M J

Molecular psychiatry, January 2009, Vol.14(1), pp.30-6 [Peer Reviewed Journal]

Full text available

View all versions
22
Material Type:
Article
Add to e-Shelf

Apolipoprotein E epsilon 4 and clinical phenotype in schizophrenia

Rietschel, M ; Krauss, H ; Müller, D J ; Nöthen, M M ; Macciardi, F

Lancet (London, England), 1997, Vol.350(9094), pp.1857-8 [Peer Reviewed Journal]

Full text available

View all versions
23
Material Type:
Article
Add to e-Shelf

Assessing the effect of obesity-related traits on multiple myeloma using a Mendelian randomisation approach

Went, M ; Sud, A ; Law, P J ; Johnson, D C ; Weinhold, N ; Försti, A ; Van Duin, M ; Mitchell, J S ; Chen, B ; Kuiper, R ; Stephens, O W ; Bertsch, U ; Campo, C ; Einsele, H ; Gregory, W M ; Henrion, M ; Hillengass, J ; Hoffmann, P ; Jackson, G H ; Lenive, O ; Nickel, J ; Nöthen, M M ; Da Silva Filho, M I ; Thomsen, H ; Walker, B A ; Broyl, A ; Davies, F E ; Langer, C ; Hansson, M ; Kaiser, M ; Sonneveld, P ; Goldschmidt, H ; Hemminki, K ; Nilsson, B ; Morgan, G J ; Houlston, R S

Blood cancer journal, 16 June 2017, Vol.7(6), pp.e573 [Peer Reviewed Journal]

Full text available

View all versions
24
Material Type:
Article
Add to e-Shelf

Association analysis of the monoamine oxidase A gene in bipolar affective disorder by using family-based internal controls

Nöthen, M M ; Eggermann, K ; Albus, M ; Borrmann, M ; Rietschel, M ; Körner, J ; Maier, W ; Minges, J ; Lichtermann, D ; Franzek, E

American journal of human genetics, October 1995, Vol.57(4), pp.975-8 [Peer Reviewed Journal]

Full text available

View all versions
25
Material Type:
Article
Add to e-Shelf

Association between a functional polymorphism in the monoamine oxidase A gene promoter and major depressive disorder

Schulze, T G ; Müller, D J ; Krauss, H ; Scherk, H ; Ohlraun, S ; Syagailo, Y V ; Windemuth, C ; Neidt, H ; Grässle, M ; Papassotiropoulos, A ; Heun, R ; Nöthen, M M ; Maier, W ; Lesch, K P ; Rietschel, M

American journal of medical genetics, 04 December 2000, Vol.96(6), pp.801-3 [Peer Reviewed Journal]

Full text available

26
Material Type:
Article
Add to e-Shelf

Association between a promoter polymorphism in the dopamine D2 receptor gene and schizophrenia

Jönsson, E G ; Nöthen, M M ; Neidt, H ; Forslund, K ; Rylander, G ; Mattila-Evenden, M ; Asberg, M ; Propping, P ; Sedvall, G C

Schizophrenia research, 09 November 1999, Vol.40(1), pp.31-6 [Peer Reviewed Journal]

Full text available

View all versions
27
Material Type:
Article
Add to e-Shelf

Association between schizophrenia and T102C polymorphism of the 5-hydroxytryptamine type 2a-receptor gene. European Multicentre Association Study of Schizophrenia (EMASS) Group

Williams, J ; Spurlock, G ; Mcguffin, P ; Mallet, J ; Nöthen, M M ; Gill, M ; Aschauer, H ; Nylander, P O ; Macciardi, F ; Owen, M J

Lancet (London, England), 11 May 1996, Vol.347(9011), pp.1294-6 [Peer Reviewed Journal]

Full text available

View all versions
28
Material Type:
Article
Add to e-Shelf

Association between the insulin-induced gene 2 (INSIG2) and weight gain in a German sample of antipsychotic-treated schizophrenic patients: perturbation of SREBP-controlled lipogenesis in drug-related metabolic adverse effects?

Le Hellard, S ; Theisen, F M ; Haberhausen, M ; Raeder, M B ; Fernø, J ; Gebhardt, S ; Hinney, A ; Remschmidt, H ; Krieg, J C ; Mehler-Wex, C ; Nöthen, M M ; Hebebrand, J ; Steen, V M

Molecular psychiatry, March 2009, Vol.14(3), pp.308-17 [Peer Reviewed Journal]

Full text available

View all versions
29
Material Type:
Article
Add to e-Shelf

Association of the DTNBP1 genotype with cognition and personality traits in healthy subjects

Kircher, T ; Markov, V ; Krug, A ; Eggermann, T ; Zerres, K ; Nöthen, M M ; Skowronek, M H ; Rietschel, M

Psychological medicine, October 2009, Vol.39(10), pp.1657-65 [Peer Reviewed Journal]

Full text available

View all versions
30
Material Type:
Article
Add to e-Shelf

Association study of the low-activity allele of catechol-O-methyltransferase and alcoholism using a family-based approach

Wang, T ; Franke, P ; Neidt, H ; Cichon, S ; Knapp, M ; Lichtermann, D ; Maier, W ; Propping, P ; Nöthen, M M

Molecular psychiatry, January 2001, Vol.6(1), pp.109-11 [Peer Reviewed Journal]

Full text available

View all versions
31
Material Type:
Article
Add to e-Shelf

Association study of the tryptophan hydroxylase gene and bipolar affective disorder using family-based internal controls

Rietschel, M ; Schorr, A ; Albus, M ; Franzek, E ; Kreiner, R ; Held, T ; Knapp, M ; Müller, D J ; Schulze, T G ; Propping, P ; Maier, W ; Nöthen, M M

American journal of medical genetics, 12 June 2000, Vol.96(3), pp.310-1

Full text available

32
Material Type:
Article
Add to e-Shelf

Association versus linkage studies in psychosis genetics.

Nöthen, M M ; Propping, P ; Fimmers, R

Journal of Medical Genetics, Aug 1993, Vol.30(8), p.634 [Peer Reviewed Journal]

Full text available

View all versions
33
Material Type:
Article
Add to e-Shelf

Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome Sequencing

Hoebel, A K ; Drichel, D ; Van De Vorst, M ; Böhmer, A C ; Sivalingam, S ; Ishorst, N ; Klamt, J ; Gölz, L ; Alblas, M ; Maaser, A ; Keppler, K ; Zink, A M ; Dixon, M J ; Dixon, J ; Hemprich, A ; Kruse, T ; Graf, I ; Dunsche, A ; Schmidt, G ; Daratsianos, N ; Nowak, S ; Aldhorae, K A ; Nöthen, M M ; Knapp, M ; Thiele, H ; Gilissen, C ; Reutter, H ; Hoischen, A ; Mangold, E ; Ludwig, K U

Journal of dental research, October 2017, Vol.96(11), pp.1314-1321 [Peer Reviewed Journal]

Full text available

View all versions
34
Material Type:
Article
Add to e-Shelf

Caspase recruitment domain 15 gene haplotypes in sarcoidosis

Pabst, S ; Golebiewski, M ; Herms, S ; Karpushova, A ; Díaz-Lacava, A ; Walier, M ; Zimmer, S ; Cichon, S ; Wienker, T F ; Nöthen, M M ; Nickenig, G ; Meyer, R ; Skowasch, D ; Grohé, C

Tissue antigens, April 2011, Vol.77(4), pp.333-7 [Peer Reviewed Journal]

Full text available

View all versions
35
Material Type:
Article
Add to e-Shelf

Caught in the trio trap? Potential selection bias inherent to association studies using parent-offspring trios

Schulze, T G ; Müller, D J ; Krauss, H ; Gross, M ; Bauer, I ; Fangerau-Lefèvre, H ; Illes, F ; Ohlraun, S ; Fimmers, R ; Cichon, S ; Held, T ; Propping, P ; Nöthen, M M ; Maier, W ; Rietschel, M

American journal of medical genetics, 08 May 2001, Vol.105(4), pp.351-3 [Peer Reviewed Journal]

Full text available

View all versions
36
Material Type:
Article
Add to e-Shelf

Common variant at 16p11.2 conferring risk of psychosis

Steinberg, S ; De Jong, S ; Mattheisen, M ; Costas, J ; Demontis, D ; Jamain, S ; Pietiläinen, O P H ; Lin, K ; Papiol, S ; Huttenlocher, J ; Sigurdsson, E ; Vassos, E ; Giegling, I ; Breuer, R ; Fraser, G ; Walker, N ; Melle, I ; Djurovic, S ; Agartz, I ; Tuulio-Henriksson, A ; Suvisaari, J ; Lönnqvist, J ; Paunio, T ; Olsen, L ; Hansen, T ; Ingason, A ; Pirinen, M ; Strengman, E ; Hougaard, D M ; Orntoft, T ; Didriksen, M ; Hollegaard, M V ; Nordentoft, M ; Abramova, L ; Kaleda, V ; Arrojo, M ; Sanjuán, J ; Arango, C ; Etain, B ; Bellivier, F ; Méary, A ; Schürhoff, F ; Szoke, A ; Ribolsi, M ; Magni, V ; Siracusano, A ; Sperling, S ; Rossner, M ; Christiansen, C ; Kiemeney, L A ; Franke, B ; Van Den Berg, L H ; Veldink, J ; Curran, S ; Bolton, P ; Poot, M ; Staal, W ; Rehnstrom, K ; Kilpinen, H ; Freitag, C M ; Meyer, J ; Magnusson, P ; Saemundsen, E ; Martsenkovsky, I ; Bikshaieva, I ; Martsenkovska, I ; Vashchenko, O ; Raleva, M ; Paketchieva, K ; Stefanovski, B ; Durmishi, N ; Pejovic Milovancevic, M ; Lecic Tosevski, D ; Silagadze, T ; Naneishvili, N ; Mikeladze, N ; Surguladze, S ; Vincent, J B ; Farmer, A ; Mitchell, P B ; Wright, A ; Schofield, P R ; Fullerton, J M ; Montgomery, G W ; Martin, N G ; Rubino, I A ; Van Winkel, R ; Kenis, G ; De Hert, M ; Réthelyi, J M ; Bitter, I ; Terenius, L ; Jönsson, E G ; Bakker, S ; Van Os, J ; Jablensky, A ; Leboyer, M ; Bramon, E ; Powell, J ; Murray, R ; Corvin, A ; Gill, M ; Morris, D ; O'Neill, F A ; Kendler, K ; Riley, B ; Craddock, N ; Owen, M J ; O'Donovan, M C ; Thorsteinsdottir, U ; Kong, A ; Ehrenreich, H ; Carracedo, A ; Golimbet, V ; Andreassen, O A ; Børglum, A D ; Mors, O ; Mortensen, P B ; Werge, T ; Ophoff, R A ; Nöthen, M M ; Rietschel, M ; Cichon, S ; Ruggeri, M ; Tosato, S ; Palotie, A ; St Clair, D ; Rujescu, D ; Collier, D A ; Stefansson, H ; Stefansson, K

Molecular psychiatry, January 2014, Vol.19(1), pp.108-14 [Peer Reviewed Journal]

Full text available

View all versions
37
Material Type:
Article
Add to e-Shelf

Common variation in NCAN, a risk factor for bipolar disorder and schizophrenia, influences local cortical folding in schizophrenia

Schultz, C C ; Mühleisen, T W ; Nenadic, I ; Koch, K ; Wagner, G ; Schachtzabel, C ; Siedek, F ; Nöthen, M M ; Rietschel, M ; Deufel, T ; Kiehntopf, M ; Cichon, S ; Reichenbach, J R ; Sauer, H ; Schlösser, R G M

Psychological medicine, March 2014, Vol.44(4), pp.811-20 [Peer Reviewed Journal]

Full text available

View all versions