-
1
-
-
46249104490
-
Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: The SzGene database
-
Allen NC, Bagade S, McQueen MB, Ioanni-dis JP, Kavvoura FK, Khoury MJ, Tanzi RE, Bertram L: Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database. Nat Genet 2008; 40:827-834.
-
(2008)
Nat Genet
, vol.40
, pp. 827-834
-
-
Allen, N.C.1
Bagade, S.2
McQueen, M.B.3
Ioanni-Dis, J.P.4
Kavvoura, F.K.5
Khoury, M.J.6
Tanzi, R.E.7
Bertram, L.8
-
2
-
-
66149185456
-
Genomewide association studies: History, rationale, and prospects for psychiatric disorders
-
Cichon S, Craddock N, Daly M, Faraone SV, Gejman PV, Kelsoe J, Lehner T, Levinson DF, Moran A, Sklar P, Sullivan PF: Genomewide association studies: history, rationale, and prospects for psychiatric disorders. Am J Psychiatry 2009; 166:540-556.
-
(2009)
Am J Psychiatry
, vol.166
, pp. 540-556
-
-
Cichon, S.1
Craddock, N.2
Daly, M.3
Faraone, S.V.4
Gejman, P.V.5
Kelsoe, J.6
Lehner, T.7
Levinson, D.F.8
Moran, A.9
Sklar, P.10
Sullivan, P.F.11
-
3
-
-
60549106509
-
Disruption of the neurexin 1 gene is associated with schizophrenia
-
Rujescu D, Ingason A, Cichon S, et al: Disruption of the neurexin 1 gene is associated with schizophrenia. Hum Mol Genet 2009; 18: 988-996.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 988-996
-
-
Rujescu, D.1
Ingason, A.2
Cichon, S.3
-
4
-
-
33748676111
-
Schizophrenia and oxidative stress: Glutamate cysteine li-gase modifier as a susceptibility gene
-
Tosic M, Ott J, Barral S, Bovet P, Deppen P, Gheorghita F, Matthey ML, Parnas J, Preisig M, Saraga M, Solida A, Timm S, Wang AG, Werge T, Cuénod M, Do KQ: Schizophrenia and oxidative stress: glutamate cysteine li-gase modifier as a susceptibility gene. Am J Hum Genet 20 06; 79: 586-592.
-
(2006)
Am J Hum Genet
, vol.79
, pp. 586-592
-
-
Tosic, M.1
Ott, J.2
Barral, S.3
Bovet, P.4
Deppen, P.5
Gheorghita, F.6
Matthey, M.L.7
Parnas, J.8
Preisig, M.9
Saraga, M.10
Solida, A.11
Timm, S.12
Wang, A.G.13
Werge, T.14
Cuénod, M.15
Do, K.Q.16
-
5
-
-
33845766980
-
Genome-wide scan supports the existence of a susceptibility locus for schizophrenia and bipolar disorder on chromosome 15q26
-
Vazza G, Bertolin C, Scudellaro E, Vettori A, Boaretto F, Rampinelli S, De Sanctis G, Peri-ni G, Peruzzi P, Mostacciuolo ML: Genome-wide scan supports the existence of a susceptibility locus for schizophrenia and bipolar disorder on chromosome 15q26. Mol Psychiatry 2007; 12:87-93.
-
(2007)
Mol Psychiatry
, vol.12
, pp. 87-93
-
-
Vazza, G.1
Bertolin, C.2
Scudellaro, E.3
Vettori, A.4
Boaretto, F.5
Rampinelli, S.6
De Sanctis, G.7
Peri-Ni, G.8
Peruzzi, P.9
Mostacciuolo, M.L.10
-
6
-
-
49949085933
-
Large recurrent microdeletions associated with schizophrenia
-
Stefansson H, Rujescu D, Cichon S, et al: Large recurrent microdeletions associated with schizophrenia. Nature 2008; 455:232-236.
-
(2008)
Nature
, vol.455
, pp. 232-236
-
-
Stefansson, H.1
Rujescu, D.2
Cichon, S.3
-
7
-
-
51649107017
-
Rare chromosomal deletions and duplications increase risk of schizophrenia
-
International Schizophrenia Consortium
-
International Schizophrenia Consortium: Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 2008; 455: 237-241.
-
(2008)
Nature
, vol.455
, pp. 237-241
-
-
-
8
-
-
42349088634
-
Rare structural variants disrupt multiple genes in neu-rodevelopmental pathways in schizophrenia
-
Strom-berg T, Merriman B, Gogtay N, Butler P, Eck-strand K, Noory L, Gochman P, Long R, Chen Z, Davis S, Baker C, Eichler EE, Melt-zer PS, Nelson SF, Singleton AB, Lee MK, Rapoport JL, King MC, Sebat J: Rare structural variants disrupt multiple genes in neu-rodevelopmental pathways in schizophrenia. Science 2008; 320: 539-543.
-
(2008)
Science
, vol.320
, pp. 539-543
-
-
Walsh, T.1
McClellan, J.M.2
McCarthy, S.E.3
Add-Ington, A.M.4
Pierce, S.B.5
Cooper, G.M.6
Nord, A.S.7
Kusenda, M.8
Malhotra, D.9
Bhandari, A.10
Stray, S.M.11
Rippey, C.F.12
Roccanova, P.13
Makarov, V.14
Lakshmi, B.15
Findling, R.L.16
Sikich, L.17
Strom-Berg, T.18
Merriman, B.19
Gogtay, N.20
Butler, P.21
Eck-Strand, K.22
Noory, L.23
Gochman, P.24
Long, R.25
Chen, Z.26
Davis, S.27
Baker, C.28
Eichler, E.E.29
Melt-Zer, P.S.30
Nelson, S.F.31
Singleton, A.B.32
Lee, M.K.33
Rapoport, J.L.34
King, M.C.35
Sebat, J.36
more..
-
10
-
-
33947699333
-
Tag SNPs chosen from HapMap perform well in several population isolates
-
Service S, Sabatti C, Freimer N: Tag SNPs chosen from HapMap perform well in several population isolates. Genet Epidemiol 2007; 31: 189-194.
-
(2007)
Genet Epidemiol
, vol.31
, pp. 189-194
-
-
Service, S.1
Sabatti, C.2
Freimer, N.3
-
11
-
-
0033918564
-
The genetically isolated populations of Finland and Sardinia may not be a panacea for linkage disequilibrium mapping of common disease genes
-
Eaves IA, Merriman TR, Barber RA, Nutland S, Tuomilehto-Wolf E, Tuomilehto J, Cucca F, Todd JA: The genetically isolated populations of Finland and Sardinia may not be a panacea for linkage disequilibrium mapping of common disease genes. Nat Genet 2000; 25:320-323.
-
(2000)
Nat Genet
, vol.25
, pp. 320-323
-
-
Eaves, I.A.1
Merriman, T.R.2
Barber, R.A.3
Nutland, S.4
Tuomilehto-Wolf, E.5
Tuomilehto, J.6
Cucca, F.7
Todd, J.A.8
-
12
-
-
0003675970
-
-
Princeton, N.J., Princeton University Press
-
Cavalli-Sforza LL, Menozzi P, Piazza A: The History and Geography of Human Genes. Princeton, N.J., Princeton University Press, 1994.
-
(1994)
The History and Geography of Human Genes
-
-
Cavalli-Sforza, L.L.1
Menozzi, P.2
Piazza, A.3
-
13
-
-
18444367379
-
Y chromosome binary markers to study the high prevalence of males in Sardinian centenarians and the genetic structure of the Sardinian population
-
Passarino G, Underhill PA, Cavalli-Sforza LL, Semino O, Pes GM, Carru C, Ferrucci L, Bona fè M, Franceschi C, Deia na L, Baggio G, De Benedictis G: Y chromosome binary markers to study the high prevalence of males in Sardinian centenarians and the genetic structure of the Sardinian population. Hum Hered 2001; 52: 136-139.
-
(2001)
Hum Hered
, Issue.52
, pp. 136-139
-
-
Passarino, G.1
Underhill, P.A.2
Cavalli-Sforza, L.L.3
Semino, O.4
Pes, G.M.5
Carru, C.6
Ferrucci, L.7
Fè, B.M.8
Franceschi, C.9
Deia Na, L.10
Baggio, G.11
De Benedictis, G.12
-
14
-
-
0033772711
-
Italy toasts Sardinia with SharDNA
-
Meldolesi A: Italy toasts Sardinia with SharDNA. Nat Biotechnol 2000; 18: 1032.
-
(2000)
Nat Biotechnol
, vol.18
, pp. 1032
-
-
Meldolesi, A.1
-
15
-
-
0032847498
-
Population genomics in Sardinia: A novel approach to hunt for ge-nomic combinations underlying complex traits and diseases
-
Siniscalco M, Robledo R, Bender PK, Carcas-si C, Contu L, Beck JC: Population genomics in Sardinia: a novel approach to hunt for ge-nomic combinations underlying complex traits and diseases. Cytogenet Cell Genet 1999; 86:148-152.
-
(1999)
Cytogenet Cell Genet
, vol.86
, pp. 148-152
-
-
Siniscalco, M.1
Robledo, R.2
Bender, P.K.3
Carcas-Si, C.4
Contu, L.5
Beck, J.C.6
-
16
-
-
0027942323
-
Genome screening by searching for shared segments: Mapping a gene for benign recurrent intrahepatic cholestasis
-
Houwen RH, Baharloo S, Blankenship K, Raeymaekers P, Juyn J, Sandkuijl LA, Fre-imer NB: Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis. Nat Genet 1994; 8:380-386.
-
(1994)
Nat Genet
, vol.8
, pp. 380-386
-
-
Houwen, R.H.1
Baharloo, S.2
Blankenship, K.3
Raeymaekers, P.4
Juyn, J.5
Sandkuijl, L.A.6
Fre-Imer, N.B.7
-
17
-
-
36549003138
-
Two independent alleles at 6q23 associated with risk of rheumatoid arthritis
-
Plenge RM, Cotsapas C, Davies L, Price AL, de Bakker PI, Maller J, Pe'er I, Burtt N P, Blu-menstiel B, DeFelice M, Parkin M, Barry R, Winslow W, Healy C, Graham RR, Neale BM, Izmailova E, Roubenoff R, Parker AN, Glass R, Karlson EW, Maher N, Hafler DA, Lee DM, Seldin MF, Remmers EF, Lee AT, Padyukov L, Alfredsson L, Coblyn J, Wein-blatt ME, Gabriel SB, Purcell S, Klareskog L, Gregersen PK, Shadick NA, Daly MJ, Alt-shuler D: Two independent alleles at 6q23 associated with risk of rheumatoid arthritis. Nat Genet 2007; 39:1477-1482.
-
(2007)
Nat Genet
, vol.39
, pp. 1477-1482
-
-
Plenge, R.M.1
Cotsapas, C.2
Davies, L.3
Price, A.L.4
De Bakker, P.I.5
Maller, J.6
Pe'Er, I.7
Burtt, N.P.8
Blu-Menstiel, B.9
Defelice, M.10
Parkin, M.11
Barry, R.12
Winslow, W.13
Healy, C.14
Graham, R.R.15
Neale, B.M.16
Izmailova, E.17
Roubenoff, R.18
Parker, A.N.19
Glass, R.20
Karlson, E.W.21
Maher, N.22
Hafler, D.A.23
Lee, D.M.24
Seldin, M.F.25
Remmers, E.F.26
Lee, A.T.27
Padyukov, L.28
Alfredsson, L.29
Coblyn, J.30
Wein-Blatt, M.E.31
Gabriel, S.B.32
Purcell, S.33
Klareskog, L.34
Gregersen, P.K.35
Shadick, N.A.36
Daly, M.J.37
Alt-Shuler, D.38
more..
-
18
-
-
0004245694
-
-
ed 9, New York, Dover Publications
-
Abramowitz M, Stegun IA: Handbook of Mathematical Functions, with Formulas, Graphs, and Mathematical Tables, ed 9. New York, Dover Publications, 1972.
-
(1972)
Handbook of Mathematical Functions, with Formulas, Graphs, and Mathematical Tables
-
-
Abramowitz, M.1
Stegun, I.A.2
-
19
-
-
0001677717
-
Controlling the false discovery rate: A practical and powerful approach to multiple testing
-
Benjamini Y, Hochberg Y: Controlling the false discovery rate: a practical and powerful approach to multiple testing. J Roy Stat Soc Ser B 1995; 57: 289-300.
-
(1995)
J Roy Stat Soc ser B
, vol.57
, pp. 289-300
-
-
Benjamini, Y.1
Hochberg, Y.2
-
20
-
-
0035829361
-
Controlling the false discovery rate in behavior genetics research
-
Benjamini Y, Drai D, Elmer G, Kafkafi N, Golani I: Controlling the false discovery rate in behavior genetics research. Behav Brain Res 2001; 125: 279-284.
-
(2001)
Behav Brain Res
, vol.125
, pp. 279-284
-
-
Benjamini, Y.1
Drai, D.2
Elmer, G.3
Kafkafi, N.4
Golani, I.5
-
21
-
-
60849124211
-
Detecting disease-associated genotype patterns
-
Long Q, Zhang Q, Ott J: Detecting disease-associated genotype patterns. BMC Bioin-formatics 2009; 10:S75.
-
(2009)
BMC Bioin-formatics
, vol.10
-
-
Long, Q.1
Zhang, Q.2
Ott, J.3
-
23
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population-based linkage analyses
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ, Sham PC: PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 2007; 81: 559-575.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.5
Bender, D.6
Maller, J.7
Sklar, P.8
De Bakker, P.I.9
Daly, M.J.10
Sham, P.C.11
-
24
-
-
68449090594
-
Common variants conferring risk of schizophrenia
-
Stefansson H, Ophoff RA, Steinberg S, et al: Common variants conferring risk of schizophrenia. Nature 2009; 460:74 4-747.
-
(2009)
Nature
, vol.460
, Issue.74
, pp. 4-747
-
-
Stefansson, H.1
Ophoff, R.A.2
Steinberg, S.3
-
25
-
-
17944377021
-
A novel approach to search for identity by descent in small samples of patients and controls from the same mendelian breeding unit: A pilot study on myopia
-
Heath S, Robledo R, Beggs W, Feola G, Paro-do C, Rinaldi A, Contu L, Dana D, Stambo-lian D, Siniscalco M: A novel approach to search for identity by descent in small samples of patients and controls from the same mendelian breeding unit: a pilot study on myopia. Hum Hered 2001; 52: 18 3-19 0.
-
(2001)
Hum Hered
, vol.52
, pp. 183-190
-
-
Heath, S.1
Robledo, R.2
Beggs, W.3
Feola, G.4
Paro-Do, C.5
Rinaldi, A.6
Contu, L.7
Dana, D.8
Stambo-Lian, D.9
Siniscalco, M.10
-
26
-
-
0021954195
-
Alpha 1-antitrypsin types in schizophrenia
-
Rudduck C, Franzen G, Lindstrom L: Alpha 1-antitrypsin types in schizophrenia. Hum Hered 1985; 35: 193-195.
-
(1985)
Hum Hered
, vol.35
, pp. 193-195
-
-
Rudduck, C.1
Franzen, G.2
Lindstrom, L.3
-
27
-
-
50449100461
-
Identification of loci associated with schizophrenia by genome-wide association and follow-up
-
O'Donovan MC, Craddock N, Norton N, et al: Identification of loci associated with schizophrenia by genome-wide association and follow-up. Nat Genet 2008; 40:1053-1055.
-
(2008)
Nat Genet
, vol.40
, pp. 1053-1055
-
-
O'Donovan, M.C.1
Craddock, N.2
Norton, N.3
|