-
1
-
-
0023875083
-
A controlled family study of chronic psychoses. Schizophrenia and schizoaffective disorder
-
Gershon ES, DeLisi LE, Hamovit J, Nurnberger Jr, JI, Maxwell ME, Schreiber J et al. A controlled family study of chronic psychoses. Schizophrenia and schizoaffective disorder. Arch Gen Psychiatry. 1988; 45: 328-336.
-
(1988)
Arch Gen Psychiatry
, vol.45
, pp. 328-336
-
-
Gershon, E.S.1
DeLisi, L.E.2
Hamovit, J.3
Nurnberger J.I., Jr.4
Maxwell, M.E.5
Schreiber, J.6
-
2
-
-
0027272195
-
The Roscommon family study: I. Methods, diagnosis of probands, and risk of schizophrenia in relatives
-
Kendler KS, McGuire M, Gruenberg AM, O'Hare A, Spellman M, Walsh D. The Roscommon family study: I. Methods, diagnosis of probands, and risk of schizophrenia in relatives. Arch Gen Psychiatry 1993; 50: 527-540.
-
(1993)
Arch Gen Psychiatry
, vol.50
, pp. 527-540
-
-
Kendler, K.S.1
McGuire, M.2
Gruenberg, A.M.3
O'Hare, A.4
Spellman, M.5
Walsh, D.6
-
3
-
-
0013935897
-
Schizophrenia in twins: 16 years' consecutive admissions to a psychiatric clinic
-
Gottesman II, Shields J. Schizophrenia in twins: 16 years' consecutive admissions to a psychiatric clinic. Br J Psychiatry 1966; 112: 809-818.
-
(1966)
Br J Psychiatry
, vol.112
, pp. 809-818
-
-
Gottesman, I.I.1
Shields, J.2
-
4
-
-
0020512809
-
Overview: A current perspective on twin studies of schizophrenia
-
Kendler KS. Overview: a current perspective on twin studies of schizophrenia. Am J Psychiatry 1983; 140: 1413-1425.
-
(1983)
Am J Psychiatry
, vol.140
, pp. 1413-1425
-
-
Kendler, K.S.1
-
5
-
-
0023255401
-
Twin concordance for DSM-III schizophrenia. Scrutinizing the validity of the definition
-
Farmer AE, McGuffin P, Gottesman II. Twin concordance for DSM-III schizophrenia. Scrutinizing the validity of the definition. Arch Gen Psychiatry 1987; 44: 634-640.
-
(1987)
Arch Gen Psychiatry
, vol.44
, pp. 634-640
-
-
Farmer, A.E.1
McGuffin, P.2
Gottesman, I.I.3
-
6
-
-
0023514436
-
The significance of genetic factors in the etiology of schizophrenia: Results from the national study of adoptees in Denmark
-
Kety SS. The significance of genetic factors in the etiology of schizophrenia: results from the national study of adoptees in Denmark. J Psychiatr Res 1987; 21: 423-429.
-
(1987)
J Psychiatr Res
, vol.21
, pp. 423-429
-
-
Kety, S.S.1
-
7
-
-
0028288450
-
The Finnish adoptive family study of schizophrenia. Implications for family research
-
Tienari P, Wynne LC, Moring J, Lahti I, Naarala M, Sorri A et al. The Finnish adoptive family study of schizophrenia. Implications for family research. Br J Psychiatry 1994; 17(Suppl): 20-26.
-
(1994)
Br J Psychiatry
, vol.17
, Issue.SUPPL.
, pp. 20-26
-
-
Tienari, P.1
Wynne, L.C.2
Moring, J.3
Lahti, I.4
Naarala, M.5
Sorri, A.6
-
8
-
-
0026084805
-
The genetic epidemiology of schizophrenia and the design of linkage studies
-
McGue M, Gottesman I. The genetic epidemiology of schizophrenia and the design of linkage studies. Eur Arch Psychiatry Clin Neurosci 1991; 240: 174-181.
-
(1991)
Eur Arch Psychiatry Clin Neurosci
, vol.240
, pp. 174-181
-
-
McGue, M.1
Gottesman, I.2
-
9
-
-
0028147374
-
Genomic scan for genes predisposing to schizophrenia
-
Coon H, Jensen S, Holik J, Hoff M, Myles-Worsley M, Reimherr F et al. Genomic scan for genes predisposing to schizophrenia. Am J Med Genet 1994; 54: 59-71.
-
(1994)
Am J Med Genet
, vol.54
, pp. 59-71
-
-
Coon, H.1
Jensen, S.2
Holik, J.3
Hoff, M.4
Myles-Worsley, M.5
Reimherr, F.6
-
10
-
-
0028871785
-
An international two-stage genome-wide search for schizophrenia susceptibility genes
-
Moises HW, Yang L, Kristbjarnarson H, Wiese C, Byerley W, Macciardi F et al. An international two-stage genome-wide search for schizophrenia susceptibility genes. Nat Genet 1995; 11: 321-324.
-
(1995)
Nat Genet
, vol.11
, pp. 321-324
-
-
Moises, H.W.1
Yang, L.2
Kristbjarnarson, H.3
Wiese, C.4
Byerley, W.5
Macciardi, F.6
-
11
-
-
0029071768
-
Schizophrenia: A genome scan targets chromosomes 3p and 8p as potential sites of susceptibility genes
-
Pulver AE, Lasseter VK, Kasch L, Wolyniec P, Nestadt G, Blouin JL et al. Schizophrenia: a genome scan targets chromosomes 3p and 8p as potential sites of susceptibility genes. Am J Med Genet Neuropsychiatr Genet 1995; 60: 252-260.
-
(1995)
Am J Med Genet Neuropsychiatr Genet
, vol.60
, pp. 252-260
-
-
Pulver, A.E.1
Lasseter, V.K.2
Kasch, L.3
Wolyniec, P.4
Nestadt, G.5
Blouin, J.L.6
-
12
-
-
17344364477
-
Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21
-
Blouin JL, Dombroski BA, Nath SK, Lasseter VK, Wolyniec PS, Nestadt G et al. Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21. Nat Genet 1998; 20: 70-73.
-
(1998)
Nat Genet
, vol.20
, pp. 70-73
-
-
Blouin, J.L.1
Dombroski, B.A.2
Nath, S.K.3
Lasseter, V.K.4
Wolyniec, P.S.5
Nestadt, G.6
-
13
-
-
17444448778
-
Genome scan of European-American schizophrenia pedigrees: Results of the NIMH genetics initiative and millennium consortium
-
Faraone SV, Matise T, Svrakic D, Pepple J, Malaspina D, Suarez B et al. Genome scan of European-American schizophrenia pedigrees: results of the NIMH genetics initiative and millennium consortium. Am J Med Genet Neuropsychiatr Genet 1998; 81: 290-295.
-
(1998)
Am J Med Genet Neuropsychiatr Genet
, vol.81
, pp. 290-295
-
-
Faraone, S.V.1
Matise, T.2
Svrakic, D.3
Pepple, J.4
Malaspina, D.5
Suarez, B.6
-
14
-
-
0000858694
-
Genome-wide scan and schizophrenia in African Americans
-
Garver DL, Barnes R, Holcombe J, Filbey F, Wilson R, Bowcock A. Genome-wide scan and schizophrenia in African Americans. Am J Med Genet Neuropsychiatr Genet 1998; 81: 454-455.
-
(1998)
Am J Med Genet Neuropsychiatr Genet
, vol.81
, pp. 454-455
-
-
Garver, D.L.1
Barnes, R.2
Holcombe, J.3
Filbey, F.4
Wilson, R.5
Bowcock, A.6
-
15
-
-
0032503891
-
NIMH genetics initiative millennium schizophrenia consortium: Linkage analysis of African-American pedigrees
-
Kaufmann CA, Suarez B, Malaspina D, Pepple J, Svrakic D, Markel PD et al. NIMH genetics initiative millennium schizophrenia consortium: linkage analysis of African-American pedigrees. Am J Med Genet Neuropsychiatr Genet 1998; 81: 282-289.
-
(1998)
Am J Med Genet Neuropsychiatr Genet
, vol.81
, pp. 282-289
-
-
Kaufmann, C.A.1
Suarez, B.2
Malaspina, D.3
Pepple, J.4
Svrakic, D.5
Markel, P.D.6
-
16
-
-
17944393918
-
Genome scan of schizophrenia
-
Levinson DF, Mahtani MM, Nancarrow DJ, Brown DM, Kruglyak L, Kirby A et al. Genome scan of schizophrenia. Am J Psychiatry 1998; 155: 741-750.
-
(1998)
Am J Psychiatry
, vol.155
, pp. 741-750
-
-
Levinson, D.F.1
Mahtani, M.M.2
Nancarrow, D.J.3
Brown, D.M.4
Kruglyak, L.5
Kirby, A.6
-
17
-
-
0031713339
-
A genome-wide search for schizophrenia susceptibility genes
-
Shaw SH, Kelly M, Smith AB, Shields G, Hopkins PJ, Loftus J et al. A genome-wide search for schizophrenia susceptibility genes. Am J Med Genet Neuropsychiat Genet 1998; 81: 364-376.
-
(1998)
Am J Med Genet Neuropsychiat Genet
, vol.81
, pp. 364-376
-
-
Shaw, S.H.1
Kelly, M.2
Smith, A.B.3
Shields, G.4
Hopkins, P.J.5
Loftus, J.6
-
18
-
-
0033364825
-
A genome-wide screen for schizophrenia genes in an isolated Finnish subpopulation suggesting multiple susceptibility loci
-
Hovatta I, Varilo T, Suvisaari J, Terwilliger JD, Olikainen V, Arajärvi R et al. A genome-wide screen for schizophrenia genes in an isolated Finnish subpopulation suggesting multiple susceptibility loci. Am J Hum Genet 1999; 65: 1114-1124.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 1114-1124
-
-
Hovatta, I.1
Varilo, T.2
Suvisaari, J.3
Terwilliger, J.D.4
Olikainen, V.5
Arajärvi, R.6
-
19
-
-
0032858459
-
A two-stage genome scan for schizophrenia susceptibility genes in 196 affected sibling pairs
-
Williams NM, Rees MI, Holmans P, Norton N, Cardno AG, Jones LA et al. A two-stage genome scan for schizophrenia susceptibility genes in 196 affected sibling pairs. Hum Mol Genet 1999; 8: 1729-1739.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 1729-1739
-
-
Williams, N.M.1
Rees, M.I.2
Holmans, P.3
Norton, N.4
Cardno, A.G.5
Jones, L.A.6
-
20
-
-
0032880798
-
Autosome search for schizophrenia susceptibility genes in multiply affected families
-
Rees MI, Fenton I, Williams NM, Holmans P, Norton N, Cardno A et al. Autosome search for schizophrenia susceptibility genes in multiply affected families. Mol Psychiatry 1999; 4: 353-359.
-
(1999)
Mol Psychiatry
, vol.4
, pp. 353-359
-
-
Rees, M.I.1
Fenton, I.2
Williams, N.M.3
Holmans, P.4
Norton, N.5
Cardno, A.6
-
21
-
-
0034724924
-
Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22
-
Brzustowicz LM, Hodgkinson KA, Chow EWC, Honer WG, Bassett AS. Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22. Science 2000; 288: 678-682.
-
(2000)
Science
, vol.288
, pp. 678-682
-
-
Brzustowicz, L.M.1
Hodgkinson, K.A.2
Chow, E.W.C.3
Honer, W.G.4
Bassett, A.S.5
-
22
-
-
18144434579
-
Genome-wide scan for schizophrenia in the Finnish population: Evidence for a locus on chromosome 7q22
-
Ekelund J, Lichtermann D, Hovatta I, Ellonen P, Suvisaari J, Terwilliger JD et al. Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22. Hum Mol Genet 2000; 9: 1049-1057.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1049-1057
-
-
Ekelund, J.1
Lichtermann, D.2
Hovatta, I.3
Ellonen, P.4
Suvisaari, J.5
Terwilliger, J.D.6
-
23
-
-
0033647377
-
A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: Support for loci on chromosome 10p and 6
-
Schwab SG, Hallmayer J, Albus M, Lerer B, Eckstein GN, Borrmann M et al. A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: support for loci on chromosome 10p and 6. Mol Psychiatry 2000; 5: 638-649.
-
(2000)
Mol Psychiatry
, vol.5
, pp. 638-649
-
-
Schwab, S.G.1
Hallmayer, J.2
Albus, M.3
Lerer, B.4
Eckstein, G.N.5
Borrmann, M.6
-
24
-
-
0035089756
-
Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23
-
Gurling HM, Kalsi G, Brynjolfson J, Sigmundsson T, Sherrington R, Mankoo BS, et al. Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23. Am J Hum Genet 2001; 68: 661-673.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 661-673
-
-
Gurling, H.M.1
Kalsi, G.2
Brynjolfson, J.3
Sigmundsson, T.4
Sherrington, R.5
Mankoo, B.S.6
-
26
-
-
0025019555
-
Linkage strategies for genetically complex traits. I. Multilocus models
-
Risch N. Linkage strategies for genetically complex traits. I. Multilocus models. Am J Hum Genet 1990; 46: 222-228.
-
(1990)
Am J Hum Genet
, vol.46
, pp. 222-228
-
-
Risch, N.1
-
27
-
-
0030799204
-
-
Riley BP, Tahir E, Rajagopalan S, Mogudi-Carter M, Faure S, Weissenbach J et al. Psychiatr Genet 1997; 7: 57-74.
-
(1997)
Psychiatr Genet
, vol.7
, pp. 57-74
-
-
Riley, B.P.1
Tahir, E.2
Rajagopalan, S.3
Mogudi-Carter, M.4
Faure, S.5
Weissenbach, J.6
-
28
-
-
0029983060
-
Irish study on high-density schizophrenia families: Field methods and power to detect linkage
-
Kendler KS, O'Neill FA, Burke J, Murphy B, Duke F, Straub RE et al. Irish study on high-density schizophrenia families: field methods and power to detect linkage. Am J Med Genet 1996; 67: 179-190.
-
(1996)
Am J Med Genet
, vol.67
, pp. 179-190
-
-
Kendler, K.S.1
O'Neill, F.A.2
Burke, J.3
Murphy, B.4
Duke, F.5
Straub, R.E.6
-
29
-
-
0028820161
-
A potential vulnerability locus for schizophrenia on chromosome 6p24-22: Evidence for genetic heterogeneity
-
Straub RE, MacLean CJ, O'Neill FA, Burke J, Murphy B, Duke F et al. A potential vulnerability locus for schizophrenia on chromosome 6p24-22: evidence for genetic heterogeneity. Nat Genet 1995; 11: 287-293.
-
(1995)
Nat Genet
, vol.11
, pp. 287-293
-
-
Straub, R.E.1
MacLean, C.J.2
O'Neill, F.A.3
Burke, J.4
Murphy, B.5
Duke, F.6
-
30
-
-
0030576156
-
Linkage results in schizophrenia
-
Baron M. Linkage results in schizophrenia. Am J Med Genet 1996; 67: 121-123.
-
(1996)
Am J Med Genet
, vol.67
, pp. 121-123
-
-
Baron, M.1
-
31
-
-
0030576155
-
Reflections on the evidence for a vulnerability locus for schizophrenia on chromosome 6p24-22
-
Kendler KS, Straub RE, MacLean CJ, Walsh D. Reflections on the evidence for a vulnerability locus for schizophrenia on chromosome 6p24-22. Am J Med Genet 1996; 67: 124-126.
-
(1996)
Am J Med Genet
, vol.67
, pp. 124-126
-
-
Kendler, K.S.1
Straub, R.E.2
MacLean, C.J.3
Walsh, D.4
-
32
-
-
0028862998
-
Evaluation of a susceptibility gene for schizophrenia on chromosome 6p by multipoint affected sib-pair linkage analysis
-
Schwab SG, Albus M, Hallmayer J, Honig S, Borrmann M, Lichtermann D et al. Evaluation of a susceptibility gene for schizophrenia on chromosome 6p by multipoint affected sib-pair linkage analysis. Nat Genet 1995; 11: 325-327.
-
(1995)
Nat Genet
, vol.11
, pp. 325-327
-
-
Schwab, S.G.1
Albus, M.2
Hallmayer, J.3
Honig, S.4
Borrmann, M.5
Lichtermann, D.6
-
33
-
-
0030913474
-
6p24-22 region and major psychoses in the Eastern Quebec population. Le Groupe IREP
-
Maziade M, Bissonnette L, Rouillard E, Martinez M, Turgeon M, Charron L et al. 6p24-22 region and major psychoses in the Eastern Quebec population. Le Groupe IREP. Am J Med Genet 1997; 74: 311-318.
-
(1997)
Am J Med Genet
, vol.74
, pp. 311-318
-
-
Maziade, M.1
Bissonnette, L.2
Rouillard, E.3
Martinez, M.4
Turgeon, M.5
Charron, L.6
-
34
-
-
0033588260
-
Linkage analysis of a large Swedish kindred provides further support for a susceptibility locus for schizophrenia on chromosome 6p23
-
Lindholm E, Ekholm B, Balciuniene J, Johansson G, Castensson A, Koisti M et al. Linkage analysis of a large Swedish kindred provides further support for a susceptibility locus for schizophrenia on chromosome 6p23. Am J Med Genet 1999; 88: 369-377.
-
(1999)
Am J Med Genet
, vol.88
, pp. 369-377
-
-
Lindholm, E.1
Ekholm, B.2
Balciuniene, J.3
Johansson, G.4
Castensson, A.5
Koisti, M.6
-
35
-
-
17744410092
-
Schizophrenia susceptibility and chromosome 6p24-22
-
Mowry BJ, Nancarrow DJ, Lennon DP, Sandkuijl LA, Crowe RR, Silverman JM et al. Schizophrenia susceptibility and chromosome 6p24-22. Nat Genet 1995; 11: 233-234.
-
(1995)
Nat Genet
, vol.11
, pp. 233-234
-
-
Mowry, B.J.1
Nancarrow, D.J.2
Lennon, D.P.3
Sandkuijl, L.A.4
Crowe, R.R.5
Silverman, J.M.6
-
36
-
-
0029411507
-
Schizophrenia susceptibility and chromosome 6p24-22
-
Gurling H, Kalsi G, Chen AHS, Green M, Butler R, Read T et al. Schizophrenia susceptibility and chromosome 6p24-22. Nat Genet 1995; 11: 234-235.
-
(1995)
Nat Genet
, vol.11
, pp. 234-235
-
-
Gurling, H.1
Kalsi, G.2
Chen, A.H.S.3
Green, M.4
Butler, R.5
Read, T.6
-
37
-
-
0029782566
-
No evidence for linkage of chromosome 6p markers to schizophrenia in Southern African Bantu-speaking families
-
Riley BP, Rajagopalan S, Mogudi-Carter M, Jenkins T, Williamson R. No evidence for linkage of chromosome 6p markers to schizophrenia in Southern African Bantu-speaking families. Psychiatr Genet 1996; 6: 41-49.
-
(1996)
Psychiatr Genet
, vol.6
, pp. 41-49
-
-
Riley, B.P.1
Rajagopalan, S.2
Mogudi-Carter, M.3
Jenkins, T.4
Williamson, R.5
-
38
-
-
17544398904
-
Schizophrenia susceptibility and chromosome 6p24-22
-
Antonarakis SE, Blouin J-L, Pulver AE, Wolniec P, Lasseter VK, Nestadt G et al. Schizophrenia susceptibility and chromosome 6p24-22. Nat Genet 1995; 11: 235-236.
-
(1995)
Nat Genet
, vol.11
, pp. 235-236
-
-
Antonarakis, S.E.1
Blouin, J.-L.2
Pulver, A.E.3
Wolniec, P.4
Lasseter, V.K.5
Nestadt, G.6
-
39
-
-
0030913476
-
Linkage study of chromosome 6p in sib-pairs with schizophrenia
-
Daniels JK, Spurlock G, Williams NM, Cardno AG, Jones LA, Murphy KC et al. Linkage study of chromosome 6p in sib-pairs with schizophrenia. Am J Med Genet 1997; 74: 319-323.
-
(1997)
Am J Med Genet
, vol.74
, pp. 319-323
-
-
Daniels, J.K.1
Spurlock, G.2
Williams, N.M.3
Cardno, A.G.4
Jones, L.A.5
Murphy, K.C.6
-
40
-
-
0029845435
-
Additional support for schizophrenia linkage on chromosomes 6 and 8: A multicenter study
-
Levinson DF, Wildenauer DB, Schwab SG, Albus M, Hallmayer J, Lerer B et al. Additional support for schizophrenia linkage on chromosomes 6 and 8: a multicenter study. Am J Med Genet Neuropsychiatr Genet 1996; 67: 580-594.
-
(1996)
Am J Med Genet Neuropsychiatr Genet
, vol.67
, pp. 580-594
-
-
Levinson, D.F.1
Wildenauer, D.B.2
Schwab, S.G.3
Albus, M.4
Hallmayer, J.5
Lerer, B.6
-
41
-
-
0030936084
-
Schizophrenia and chromosome 6p
-
Turecki G, Rouleau GA, Joober R, Mari J, Morgan K. Schizophrenia and chromosome 6p. Am J Med Genet Neuropsychiatr Genet 1997; 74: 195-198.
-
(1997)
Am J Med Genet Neuropsychiatr Genet
, vol.74
, pp. 195-198
-
-
Turecki, G.1
Rouleau, G.A.2
Joober, R.3
Mari, J.4
Morgan, K.5
-
42
-
-
0037838619
-
-
submitted
-
Lewis CM, Levinson DF, Wise LH, DeLisi LE, Straub RE, Hovatta I et al. Meta-analysis of schizophrenia genome scans demonstrates significant linkage findings. 2002; submitted.
-
(2002)
Meta-analysis of Schizophrenia Genome Scans Demonstrates Significant Linkage Findings
-
-
Lewis, C.M.1
Levinson, D.F.2
Wise, L.H.3
DeLisi, L.E.4
Straub, R.E.5
Hovatta, I.6
-
43
-
-
0036258079
-
Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia
-
Badner JA, Gershon ES. Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia. Mol Psychiatry 2002; 7: 405-411.
-
(2002)
Mol Psychiatry
, vol.7
, pp. 405-411
-
-
Badner, J.A.1
Gershon, E.S.2
-
44
-
-
18444364206
-
Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of mouse dysbindin is associated with schizophrenia
-
Straub RE, Jiang Y, MacLean C, Ma Y, Webb BT, Myakishev MV et al. Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of mouse dysbindin is associated with schizophrenia. Am J Hum Genet 2002; 71: 337-348.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 337-348
-
-
Straub, R.E.1
Jiang, Y.2
MacLean, C.3
Ma, Y.4
Webb, B.T.5
Myakishev, M.V.6
-
45
-
-
0037838626
-
-
submitted
-
Jiang Y, Straub RE, Sullivan PF, Harris-Kerr C, Webb BT, Wormley B et al. Genomic structure and identification of a human DTNBP1 gene from a putative schizophrenia susceptibility locus on 6p22.3. 2002; submitted.
-
(2002)
Genomic Structure and Identification of a Human DTNBP1 Gene from a Putative Schizophrenia Susceptibility Locus on 6p22.3
-
-
Jiang, Y.1
Straub, R.E.2
Sullivan, P.F.3
Harris-Kerr, C.4
Webb, B.T.5
Wormley, B.6
-
46
-
-
0035968170
-
Dysbindin, a novel coiled-coil-containing protein that interacts with the dystrobrevins in muscle and brain
-
Benson MA, Newey SE, Martin-Rendon E, Hawkes R, Blake DJ. Dysbindin, a novel coiled-coil-containing protein that interacts with the dystrobrevins in muscle and brain. J Biol Chem 2001; 276: 24232-24241.
-
(2001)
J Biol Chem
, vol.276
, pp. 24232-24241
-
-
Benson, M.A.1
Newey, S.E.2
Martin-Rendon, E.3
Hawkes, R.4
Blake, D.J.5
-
47
-
-
0037336629
-
FP-TDI SNP scoring by manual and statistical procedures: A study of error rates and types
-
Van den Oord EJCG, Jiang Y, Riley BP, Kendler KS, Chen X. FP-TDI SNP scoring by manual and statistical procedures: A study of error rates and types. BioTechniques 34: 610-624.
-
BioTechniques
, vol.34
, pp. 610-624
-
-
Van Den Oord, E.J.C.G.1
Jiang, Y.2
Riley, B.P.3
Kendler, K.S.4
Chen, X.5
-
48
-
-
0034791035
-
High-resolution haplotype structure in the human genome
-
Daly MJ, Rioux JD, Schaffner SF, Hudson TJ, Lander ES. High-resolution haplotype structure in the human genome. Nat Genet 2001; 29: 229-232.
-
(2001)
Nat Genet
, vol.29
, pp. 229-232
-
-
Daly, M.J.1
Rioux, J.D.2
Schaffner, S.F.3
Hudson, T.J.4
Lander, E.S.5
-
49
-
-
18444369013
-
The structure of haplotype blocks in the human genome
-
Gabriel SB, Schaffner SF, Nguyen H, Moore JM, Roy J, Blumenstiel B et al. The structure of haplotype blocks in the human genome. Science 2002.
-
(2002)
Science
-
-
Gabriel, S.B.1
Schaffner, S.F.2
Nguyen, H.3
Moore, J.M.4
Roy, J.5
Blumenstiel, B.6
-
50
-
-
0035941029
-
Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21
-
Patil N, Berno AJ, Hinds DA, Barrett WA, Doshi JM, Hacker CR et al. Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21. Science 2001; 294: 1719-1723.
-
(2001)
Science
, vol.294
, pp. 1719-1723
-
-
Patil, N.1
Berno, A.J.2
Hinds, D.A.3
Barrett, W.A.4
Doshi, J.M.5
Hacker, C.R.6
-
51
-
-
0026769858
-
The structured clinical interview for DSM-III-R (SCID). I. History, rationale, and description
-
Spitzer RL, Williams JB, Gibbon M, First MB. The structured clinical interview for DSM-III-R (SCID). I. History, rationale, and description. Arch Gen Psychiatry 1992; 49: 624-629.
-
(1992)
Arch Gen Psychiatry
, vol.49
, pp. 624-629
-
-
Spitzer, R.L.1
Williams, J.B.2
Gibbon, M.3
First, M.B.4
-
52
-
-
0024784245
-
The structured interview for schizotypy (SIS): A preliminary report
-
Kendler KS, Lieberman JA, Walsh D. The structured interview for schizotypy (SIS): a preliminary report. Schizophr Bull 1989; 15: 559-571.
-
(1989)
Schizophr Bull
, vol.15
, pp. 559-571
-
-
Kendler, K.S.1
Lieberman, J.A.2
Walsh, D.3
-
54
-
-
84973587732
-
A coefficient of agreement for nominal scales
-
Cohen J. A coefficient of agreement for nominal scales. Educ Psychol Meas 1960; 20: 37-46.
-
(1960)
Educ Psychol Meas
, vol.20
, pp. 37-46
-
-
Cohen, J.1
-
55
-
-
0033058730
-
Fluorescence polarization in homogeneous nucleic acid analysis
-
Chen X, Levine L, Kwok PY. Fluorescence polarization in homogeneous nucleic acid analysis. Genome Res 1999; 9: 492-498.
-
(1999)
Genome Res
, vol.9
, pp. 492-498
-
-
Chen, X.1
Levine, L.2
Kwok, P.Y.3
-
56
-
-
0026548894
-
An approach to the localization of the susceptibility genes for generalized myasthenia gravis by mapping recombinant ancestral haplotypes
-
Degli-Espost M, Andreas A, Christiansen F, Schalke B, Albert E. An approach to the localization of the susceptibility genes for generalized myasthenia gravis by mapping recombinant ancestral haplotypes. Immunogenetics 1992; 35: 355-364.
-
(1992)
Immunogenetics
, vol.35
, pp. 355-364
-
-
Degli-Espost, M.1
Andreas, A.2
Christiansen, F.3
Schalke, B.4
Albert, E.5
-
57
-
-
0029945706
-
Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics
-
Sobel E, Lange K. Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics. Am J Hum Genet 1996; 58: 1323-1337.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1323-1337
-
-
Sobel, E.1
Lange, K.2
-
58
-
-
0032948850
-
Loss of information due to ambiguous haplotyping of SNPs
-
Hodge SE, Boehnke M, Spence MA. Loss of information due to ambiguous haplotyping of SNPs. Nat Genet 1999; 21: 360-361.
-
(1999)
Nat Genet
, vol.21
, pp. 360-361
-
-
Hodge, S.E.1
Boehnke, M.2
Spence, M.A.3
-
61
-
-
0000960565
-
The contiguity ratio and statistical mapping
-
Geary RC. The contiguity ratio and statistical mapping. The incorporated statistician. 1954; 5: 115-145.
-
(1954)
The Incorporated Statistician
, vol.5
, pp. 115-145
-
-
Geary, R.C.1
-
63
-
-
0033237335
-
A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission
-
Clayton D. A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission. Am J Hum Genet 1999; 65: 1170-1177.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 1170-1177
-
-
Clayton, D.1
-
64
-
-
0033358595
-
Transmission/disequilibrium tests for extended marker haplotypes
-
Clayton D, Jones H. Transmission/disequilibrium tests for extended marker haplotypes. Am J Hum Genet 1999; 65: 1161-1169.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 1161-1169
-
-
Clayton, D.1
Jones, H.2
-
65
-
-
0033910787
-
A test for linkage and association in general pedigrees: The pedigree disequilibrium test
-
Martin ER, Monks SA, Warren LL, Kaplan NL. A test for linkage and association in general pedigrees: the pedigree disequilibrium test. Am J Hum Genet 2000; 67: 146-154.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 146-154
-
-
Martin, E.R.1
Monks, S.A.2
Warren, L.L.3
Kaplan, N.L.4
-
66
-
-
0035076031
-
Correcting for a potential bias in the pedigree disequilibrium test
-
Martin ER, Bass MP, Kaplan NL. Correcting for a potential bias in the pedigree disequilibrium test. Am J Hum Genet 2001; 68: 1065-1067.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 1065-1067
-
-
Martin, E.R.1
Bass, M.P.2
Kaplan, N.L.3
-
67
-
-
0000575788
-
Genetics of HLA disease associations: The use of the haplotype relative risk (HRR) and the "haplo=delta" (DH) estimates in juvenile diabetes from three racial groups
-
Rubinstein P, Walker M, Carpenter C, Carrier C, Krassner J, Falk C et al. Genetics of HLA disease associations: the use of the haplotype relative risk (HRR) and the "haplo=delta" (DH) estimates in juvenile diabetes from three racial groups. Hum Immunol 1981; 3: 384.
-
(1981)
Hum Immunol
, vol.3
, pp. 384
-
-
Rubinstein, P.1
Walker, M.2
Carpenter, C.3
Carrier, C.4
Krassner, J.5
Falk, C.6
-
68
-
-
0027377799
-
Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
-
Spielman RS, McGinnis RE, Ewens WJ. Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am J Hum Genet 1993; 52: 506-516.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 506-516
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
70
-
-
0033362166
-
Allowing for missing parents in genetic studies of case-parent triads
-
Weinberg CR. Allowing for missing parents in genetic studies of case-parent triads. Am J Hum Genet 1999; 64: 1186-1193.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 1186-1193
-
-
Weinberg, C.R.1
-
71
-
-
0032470875
-
A discordant-sibship test for disequilibrium and linkage: No need for parental data
-
Horvath S, Laird NM. A discordant-sibship test for disequilibrium and linkage: no need for parental data. Am J Hum Genet 1998; 63: 1886-1897.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1886-1897
-
-
Horvath, S.1
Laird, N.M.2
-
72
-
-
0023796209
-
On measures of gametic disequilibrium
-
Lewontin RC. On measures of gametic disequilibrium. Genetics 1988; 120: 849-852.
-
(1988)
Genetics
, vol.120
, pp. 849-852
-
-
Lewontin, R.C.1
-
73
-
-
0034789532
-
Haplotype tagging for the identification of common disease genes
-
Johnson GC, Esposito L, Barratt BJ, Smith AN, Heward J, Di Genova G et al. Haplotype tagging for the identification of common disease genes. Nat Genet 2001; 29: 233-237.
-
(2001)
Nat Genet
, vol.29
, pp. 233-237
-
-
Johnson, G.C.1
Esposito, L.2
Barratt, B.J.3
Smith, A.N.4
Heward, J.5
Di Genova, G.6
-
74
-
-
0036208832
-
Patterns of linkage disequilibrium in the human genome
-
Ardlie KG, Kruglyak L, Seielstad M. Patterns of linkage disequilibrium in the human genome. Nat Rev Genet 2002; 3: 299-309.
-
(2002)
Nat Rev Genet
, vol.3
, pp. 299-309
-
-
Ardlie, K.G.1
Kruglyak, L.2
Seielstad, M.3
-
76
-
-
0034892915
-
Lower-than-expected linkage disequilibrium between tightly linked markers in humans suggests a role for gene conversion
-
Ardlie K, Liu-Cordero SN, Eberle MA, Daly M, Barrett J, Winchester E et al. Lower-than-expected linkage disequilibrium between tightly linked markers in humans suggests a role for gene conversion. Am J Hum Genet 2001; 69: 582-589.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 582-589
-
-
Ardlie, K.1
Liu-Cordero, S.N.2
Eberle, M.A.3
Daly, M.4
Barrett, J.5
Winchester, E.6
-
77
-
-
0034835229
-
Gene conversion and different population histories may explain the contrast between polymorphism and linkage disequilibrium levels
-
Frisse L, Hudson RR, Bartoszewicz A, Wall JD, Donfack J, Di Rienzo A. Gene conversion and different population histories may explain the contrast between polymorphism and linkage disequilibrium levels. Am J Hum Genet 2001; 69: 831-843.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 831-843
-
-
Frisse, L.1
Hudson, R.R.2
Bartoszewicz, A.3
Wall, J.D.4
Donfack, J.5
Di Rienzo, A.6
-
78
-
-
0033957844
-
ALFRED: An allele frequency database for diverse populations and DNA polymorphisms
-
Cheung KH, Osier MV, Kidd JR, Pakstis AJ, Miller PL, Kidd KK. ALFRED: an allele frequency database for diverse populations and DNA polymorphisms. Nucleic Acids Res 2000; 28: 361-363.
-
(2000)
Nucleic Acids Res
, vol.28
, pp. 361-363
-
-
Cheung, K.H.1
Osier, M.V.2
Kidd, J.R.3
Pakstis, A.J.4
Miller, P.L.5
Kidd, K.K.6
-
80
-
-
0027367005
-
Genotype relative risks: Methods for design and analysis of candidate-gene association studies
-
Schaid DJ, Sommer SS. Genotype relative risks: methods for design and analysis of candidate-gene association studies. Am J Hum Genet 1993; 53: 1114-1126.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 1114-1126
-
-
Schaid, D.J.1
Sommer, S.S.2
-
81
-
-
0033925716
-
Testing for linkage disequilibrium, maternal effects, and imprinting with (in)complete case-parent triads, by use of the computer program LEM
-
Van den Oord EJCG, Vermunt JK. Testing for linkage disequilibrium, maternal effects, and imprinting with (in)complete case-parent triads, by use of the computer program LEM. Am J Hum Genet 2000; 66: 335-338.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 335-338
-
-
Van Den Oord, E.J.C.G.1
Vermunt, J.K.2
|