-
1
-
-
13444268381
-
Cancer as a complex phenotype: Pattern of cancer distribution within and beyond the nuclear family
-
AMUNDADOTTIR, L. T., S. THORVALDSSON, D. F. GUDBJARTSSON, P. SULEM, K. KRISTJANSSON et al., 2004 Cancer as a complex phenotype: pattern of cancer distribution within and beyond the nuclear family. PLoS Med. 1: 229-236.
-
(2004)
PLoS Med
, vol.1
, pp. 229-236
-
-
AMUNDADOTTIR, L.T.1
THORVALDSSON, S.2
GUDBJARTSSON, D.F.3
SULEM, P.4
KRISTJANSSON, K.5
-
2
-
-
7544236904
-
Effects of genetic drift on variance components under a general model of epistasis
-
BARTON, N. H., and M. TURELLI, 2004 Effects of genetic drift on variance components under a general model of epistasis. Evolution 58: 2111-2132.
-
(2004)
Evolution
, vol.58
, pp. 2111-2132
-
-
BARTON, N.H.1
TURELLI, M.2
-
3
-
-
0019732410
-
Measuring the strength of associations between HLA antigens and diseases
-
BENGTSSON, B. O., and G. THOMSON, 1981 Measuring the strength of associations between HLA antigens and diseases. Tissue Antigens 18: 356-363.
-
(1981)
Tissue Antigens
, vol.18
, pp. 356-363
-
-
BENGTSSON, B.O.1
THOMSON, G.2
-
4
-
-
0001344844
-
The latent roots of certain Markov chains arising in genetics: A new approach, 1. Haploid models
-
CANNINGS, C., 1974 The latent roots of certain Markov chains arising in genetics: a new approach, 1. Haploid models. Adv. Appl. Probab. 6: 260-290.
-
(1974)
Adv. Appl. Probab
, vol.6
, pp. 260-290
-
-
CANNINGS, C.1
-
5
-
-
0037883402
-
Multifactorial models for familial diseases in man
-
CURNOW, R. N., and C. SMITH, 1975 Multifactorial models for familial diseases in man. J. R. Stat. Soc. Ser. A Stat. Soc. 138: 131-169.
-
(1975)
J. R. Stat. Soc. Ser. A Stat. Soc
, vol.138
, pp. 131-169
-
-
CURNOW, R.N.1
SMITH, C.2
-
6
-
-
84940811817
-
The simulation of Mendelism
-
EDWARDS, J. H., 1960 The simulation of Mendelism. Acta Genet. Stat. Med. 10: 63-70.
-
(1960)
Acta Genet. Stat. Med
, vol.10
, pp. 63-70
-
-
EDWARDS, J.H.1
-
8
-
-
0026500144
-
Familial recurrence-pattern analysis of cleft lip with or without cleft palate
-
FARRALL, M., and S. HOLDER, 1992 Familial recurrence-pattern analysis of cleft lip with or without cleft palate. Am. J. Hum. Genet. 50: 270-277.
-
(1992)
Am. J. Hum. Genet
, vol.50
, pp. 270-277
-
-
FARRALL, M.1
HOLDER, S.2
-
9
-
-
0015091972
-
Frequency in relatives for an all-or-none trait
-
JAMES, J. W., 1971 Frequency in relatives for an all-or-none trait. Ann. Hum. Genet. 35: 47-49.
-
(1971)
Ann. Hum. Genet
, vol.35
, pp. 47-49
-
-
JAMES, J.W.1
-
10
-
-
18244383791
-
Familial recurrence rates and genetic models of multiple sclerosis
-
LINDSEY, J. W., 2005 Familial recurrence rates and genetic models of multiple sclerosis. Am. J. Med. Genet. A 135A: 53-58.
-
(2005)
Am. J. Med. Genet. A
, vol.135 A
, pp. 53-58
-
-
LINDSEY, J.W.1
-
11
-
-
31344443340
-
-
LIU, W., and B. WEIR, 2005 Genotypic probabilities for pairs of inbred relatives. Philos. Trans. R. Soc. B Biol. Sci. 360: 1379-1385.
-
LIU, W., and B. WEIR, 2005 Genotypic probabilities for pairs of inbred relatives. Philos. Trans. R. Soc. B Biol. Sci. 360: 1379-1385.
-
-
-
-
13
-
-
33748309136
-
Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration
-
MALLER, J., S. GEORGE, S. PURCELL, J. FAGERNESS, D. ALTSHULER et al., 2006 Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration. Nat. Genet. 38: 1055-1059.
-
(2006)
Nat. Genet
, vol.38
, pp. 1055-1059
-
-
MALLER, J.1
GEORGE, S.2
PURCELL, S.3
FAGERNESS, J.4
ALTSHULER, D.5
-
14
-
-
84984364838
-
Discontinuity and quasi-continuity: Alternative hypotheses of multifactorial inheritance
-
MORTON, N. E., S. YEE, R. C. ELSTON and R. LEW, 1970 Discontinuity and quasi-continuity: alternative hypotheses of multifactorial inheritance. Clin. Genet. 1: 81-94.
-
(1970)
Clin. Genet
, vol.1
, pp. 81-94
-
-
MORTON, N.E.1
YEE, S.2
ELSTON, R.C.3
LEW, R.4
-
15
-
-
28444460187
-
Multiple sclerosis genetics: Leaving no stone unturned
-
OKSENBERG, J. R., and L. F. BARCELLOS, 2005 Multiple sclerosis genetics: leaving no stone unturned. Genes Immun. 6: 375-387.
-
(2005)
Genes Immun
, vol.6
, pp. 375-387
-
-
OKSENBERG, J.R.1
BARCELLOS, L.F.2
-
16
-
-
34047236641
-
Simulations provide support for the common disease-common variant hypothesis
-
PENG, B., and M. KIMMEL, 2007 Simulations provide support for the common disease-common variant hypothesis. Genetics 175: 763-776.
-
(2007)
Genetics
, vol.175
, pp. 763-776
-
-
PENG, B.1
KIMMEL, M.2
-
18
-
-
0034969437
-
Are rare variants responsible for susceptibility to complex diseases?
-
PRITCHARD, J. K., 2001 Are rare variants responsible for susceptibility to complex diseases? Am. J. Hum. Genet. 69: 124-137.
-
(2001)
Am. J. Hum. Genet
, vol.69
, pp. 124-137
-
-
PRITCHARD, J.K.1
-
19
-
-
0036799545
-
The allelic architecture of human disease genes: Common disease - common variant. . . or not?
-
PRITCHARD, J. K., and N. J. COX, 2002 The allelic architecture of human disease genes: common disease - common variant. . . or not? Hum. Mol. Genet. 11: 2417-2423.
-
(2002)
Hum. Mol. Genet
, vol.11
, pp. 2417-2423
-
-
PRITCHARD, J.K.1
COX, N.J.2
-
20
-
-
0035451780
-
On the allelic spectrum of human disease
-
REICH, D. E., and E. S. LANDER, 2001 On the allelic spectrum of human disease. Trends Genet. 17: 502-510.
-
(2001)
Trends Genet
, vol.17
, pp. 502-510
-
-
REICH, D.E.1
LANDER, E.S.2
-
21
-
-
0025019555
-
Linkage strategies for genetically complex traits: I. Multilocus models
-
RISCH, N., 1990 Linkage strategies for genetically complex traits: I. Multilocus models. Am. J. Hum. Genet. 46: 222-228.
-
(1990)
Am. J. Hum. Genet
, vol.46
, pp. 222-228
-
-
RISCH, N.1
-
22
-
-
0035006126
-
The risk for congenital heart defects in offspring of individuals with congenital heart defects
-
ROMANO-ZELEKHA, O., R. HIRSH, L. BLIEDEN, M. S. GREEN and T. SHOHAT, 2001 The risk for congenital heart defects in offspring of individuals with congenital heart defects. Clin. Genet. 59: 325-329.
-
(2001)
Clin. Genet
, vol.59
, pp. 325-329
-
-
ROMANO-ZELEKHA, O.1
HIRSH, R.2
BLIEDEN, L.3
GREEN, M.S.4
SHOHAT, T.5
-
23
-
-
0036908801
-
Multiplex relative risk and estimation of the number of loci underlying an inherited disease
-
SCHLIEKELMAN, P., and M. SLATKIN, 2002 Multiplex relative risk and estimation of the number of loci underlying an inherited disease. Am. J. Hum. Genet. 71: 1369-1385.
-
(2002)
Am. J. Hum. Genet
, vol.71
, pp. 1369-1385
-
-
SCHLIEKELMAN, P.1
SLATKIN, M.2
-
24
-
-
34249885875
-
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants
-
SCOTT, L. J., K. L. MOHLKE, L. L. BONNYCASTLE, C. J. WILLER, Y. LI et al., 2007 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. Science 316: 1341-1345.
-
(2007)
Science
, vol.316
, pp. 1341-1345
-
-
SCOTT, L.J.1
MOHLKE, K.L.2
BONNYCASTLE, L.L.3
WILLER, C.J.4
LI, Y.5
-
25
-
-
33847176604
-
A genome-wide association study identifies novel risk loci for type 2 diabetes
-
SLADEK, R., G. ROCHELEAU, J. RUNG, C. DINA, L. SHEN et al., 2007 A genome-wide association study identifies novel risk loci for type 2 diabetes. Nature 445: 881-885.
-
(2007)
Nature
, vol.445
, pp. 881-885
-
-
SLADEK, R.1
ROCHELEAU, G.2
RUNG, J.3
DINA, C.4
SHEN, L.5
-
26
-
-
0015183543
-
Discriminating between different modes of inheritance in genetic disease
-
SMITH, C., 1971 Discriminating between different modes of inheritance in genetic disease. Clin. Genet. 2: 303-314.
-
(1971)
Clin. Genet
, vol.2
, pp. 303-314
-
-
SMITH, C.1
-
27
-
-
0242354132
-
Family, twin, and adoption studies of bipolar disorder
-
SMOLLER, J. W., and C. T. FINN, 2003 Family, twin, and adoption studies of bipolar disorder. Am. J. Med. Genet. C Semin. Med. Genet. 123C: 48-58.
-
(2003)
Am. J. Med. Genet. C Semin. Med. Genet
, vol.123 C
, pp. 48-58
-
-
SMOLLER, J.W.1
FINN, C.T.2
-
28
-
-
0344305525
-
Schizophrenia as a complex trait - evidence from a meta-analysis of twin studies
-
SULLIVAN, P. F., K. S. KENDLER and M. C. NEALE, 2003 Schizophrenia as a complex trait - evidence from a meta-analysis of twin studies. Arch. Gen. Psych. 60: 1187-1192.
-
(2003)
Arch. Gen. Psych
, vol.60
, pp. 1187-1192
-
-
SULLIVAN, P.F.1
KENDLER, K.S.2
NEALE, M.C.3
-
29
-
-
33847327313
-
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
-
SZATMARI, P., A. D. PATERSON, L. ZWAIGENBAUM, W. ROBERTS, J. BRIAN et al., 2007 Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat. Genet. 39: 319-328.
-
(2007)
Nat. Genet
, vol.39
, pp. 319-328
-
-
SZATMARI, P.1
PATERSON, A.D.2
ZWAIGENBAUM, L.3
ROBERTS, W.4
BRIAN, J.5
-
30
-
-
34249895023
-
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes
-
ZEGGINI, E., M. N. WEEDON, C. M. LINDGREN, T. M. FRAYLING, K. S. ELLIOTT et al., 2007 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. Science 316: 1336-1341.
-
(2007)
Science
, vol.316
, pp. 1336-1341
-
-
ZEGGINI, E.1
WEEDON, M.N.2
LINDGREN, C.M.3
FRAYLING, T.M.4
ELLIOTT, K.S.5
|