-
2
-
-
0001395571
-
Testing for heterogeneity of recombination fraction values in human genetics
-
Smith CAB. Testing for heterogeneity of recombination fraction values in human genetics. Ann Hum Genet 1963, 27:175-182.
-
(1963)
Ann Hum Genet
, vol.27
, pp. 175-182
-
-
Smith, C.A.B.1
-
3
-
-
0031784624
-
BRCA1 and BRCA2 proteins: roles in health and disease
-
Duncan JA, Reeves JR, Cooke TG. BRCA1 and BRCA2 proteins: roles in health and disease. Mol Pathol 1998, 51(5):237-247.
-
(1998)
Mol Pathol
, vol.51
, Issue.5
, pp. 237-247
-
-
Duncan, J.A.1
Reeves, J.R.2
Cooke, T.G.3
-
4
-
-
0025613812
-
Linkage of early-onset familial breast cancer to chromosome 17q21
-
Hall JM, Lee MK, Newman B, Morrow JE, Anderson LA, Huey B, King MC. Linkage of early-onset familial breast cancer to chromosome 17q21. Science 1990, 250(4988):1684-1689.
-
(1990)
Science
, vol.250
, Issue.4988
, pp. 1684-1689
-
-
Hall, J.M.1
Lee, M.K.2
Newman, B.3
Morrow, J.E.4
Anderson, L.A.5
Huey, B.6
King, M.C.7
-
5
-
-
0028113345
-
A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1
-
Miki Y, Swensen J, Shattuck-Eidens D, Futreal PA, Harshman K, Tavtigian S, Liu Q, Cochran C, Bennett LM, Ding W, Bell R, Rosenthal J, Hussey C, Tran T, McClure M, Frye C, Hattier T, Phelps R, Haugen-Strano A, Katcher H, Yakumo K, Gholami Z, Shaffer D, Stone S, Bayer S, Wray C, Bogden R, Dayananth P, Ward J, Tonin P, et al. A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science 1994, 266(5182):66-71.
-
(1994)
Science
, vol.266
, Issue.5182
, pp. 66-71
-
-
Miki, Y.1
Swensen, J.2
Shattuck-Eidens, D.3
Futreal, P.A.4
Harshman, K.5
Tavtigian, S.6
Liu, Q.7
Cochran, C.8
Bennett, L.M.9
Ding, W.10
Bell, R.11
Rosenthal, J.12
Hussey, C.13
Tran, T.14
McClure, M.15
Frye, C.16
Hattier, T.17
Phelps, R.18
Haugen-Strano, A.19
Katcher, H.20
Yakumo, K.21
Gholami, Z.22
Shaffer, D.23
Stone, S.24
Bayer, S.25
Wray, C.26
Bogden, R.27
Dayananth, P.28
Ward, J.29
Tonin, P.30
more..
-
6
-
-
0028006563
-
Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13
-
Wooster R, Neuhausen SL, Mangion J, Quirk Y, Ford D, Collins N, Nguyen K, Seal S, Tran T, Averill D, Fields P, Marshall G, Narod S, Lenoir GM, Lynch H, Feunteun J, Devilee P, Cornelisse CJ, Menko FH, Daly PA, Ormiston W, McManus R, Pye C, Lewis CM, Cannon-Albright LA, Peto J, Ponder BAJ, Skolnick MH, Easton DF, Goldgar DE, et al. Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13. Science 1994, 265(5181):2088-2090.
-
(1994)
Science
, vol.265
, Issue.5181
, pp. 2088-2090
-
-
Wooster, R.1
Neuhausen, S.L.2
Mangion, J.3
Quirk, Y.4
Ford, D.5
Collins, N.6
Nguyen, K.7
Seal, S.8
Tran, T.9
Averill, D.10
Fields, P.11
Marshall, G.12
Narod, S.13
Lenoir, G.M.14
Lynch, H.15
Feunteun, J.16
Devilee, P.17
Cornelisse, C.J.18
Menko, F.H.19
Daly, P.A.20
Ormiston, W.21
McManus, R.22
Pye, C.23
Lewis, C.M.24
Cannon-Albright, L.A.25
Peto, J.26
Ponder, B.A.J.27
Skolnick, M.H.28
Easton, D.F.29
Goldgar, D.E.30
more..
-
7
-
-
0033058487
-
Molecular Genetics of Maturity-onset Diabetes of the Young
-
Froguel P, Velho G. Molecular Genetics of Maturity-onset Diabetes of the Young. Trends Endocrinol Metab 1999, 10(4):142-146.
-
(1999)
Trends Endocrinol Metab
, vol.10
, Issue.4
, pp. 142-146
-
-
Froguel, P.1
Velho, G.2
-
8
-
-
33947198192
-
Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy
-
De Marco EV, Gambardella A, Annesi F, Labate A, Carrideo S, Forabosco P, Civitelli D, Candiano IC, Tarantino P, Annesi G, Quattrone A. Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy. Epilepsy Res 2007, 74(1):70-73.
-
(2007)
Epilepsy Res
, vol.74
, Issue.1
, pp. 70-73
-
-
De Marco, E.V.1
Gambardella, A.2
Annesi, F.3
Labate, A.4
Carrideo, S.5
Forabosco, P.6
Civitelli, D.7
Candiano, I.C.8
Tarantino, P.9
Annesi, G.10
Quattrone, A.11
-
9
-
-
0029784838
-
Amyloid beta-protein and the genetics of Alzheimer's disease
-
Selkoe DJ. Amyloid beta-protein and the genetics of Alzheimer's disease. J Biol Chem 1996, 271(31):18295-18298.
-
(1996)
J Biol Chem
, vol.271
, Issue.31
, pp. 18295-18298
-
-
Selkoe, D.J.1
-
10
-
-
33846220233
-
Dissecting the heterogeneity of rheumatoid arthritis through linkage analysis of quantitative traits
-
Criswell LA, Chen WV, Jawaheer D, Lum RF, Wener MH, Gu X, Gregersen PK, Amos CI. Dissecting the heterogeneity of rheumatoid arthritis through linkage analysis of quantitative traits. Arthritis Rheum 2007, 56(1):58-68.
-
(2007)
Arthritis Rheum
, vol.56
, Issue.1
, pp. 58-68
-
-
Criswell, L.A.1
Chen, W.V.2
Jawaheer, D.3
Lum, R.F.4
Wener, M.H.5
Gu, X.6
Gregersen, P.K.7
Amos, C.I.8
-
11
-
-
0028108802
-
Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkage
-
Nystrom-Lahti M, Parsons R, Sistonen P, Pylkkanen L, Aaltonen LA, Leach FS, Hamilton SR, Watson P, Bronson E, Fusaro R, Cavalieri J, Lynch J, Lanspa S, Smyrk T, Lynch P, Drouhard T, Kinzler KW, Vogelstein B, Lynch HT, Chapelle A, Peltomäki P. Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkage. Am J Hum Genet 1994, 55(4):659-665.
-
(1994)
Am J Hum Genet
, vol.55
, Issue.4
, pp. 659-665
-
-
Nystrom-Lahti, M.1
Parsons, R.2
Sistonen, P.3
Pylkkanen, L.4
Aaltonen, L.A.5
Leach, F.S.6
Hamilton, S.R.7
Watson, P.8
Bronson, E.9
Fusaro, R.10
Cavalieri, J.11
Lynch, J.12
Lanspa, S.13
Smyrk, T.14
Lynch, P.15
Drouhard, T.16
Kinzler, K.W.17
Vogelstein, B.18
Lynch, H.T.19
Chapelle, A.20
Peltomäki, P.21
more..
-
12
-
-
0031007349
-
Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
-
Kelsell DP, Dunlop J, Stevens HP, Lench NJ, Liang JN, Parry G, Mueller RF, Leigh IM. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness. Nature 1997, 387(6628):80-83.
-
(1997)
Nature
, vol.387
, Issue.6628
, pp. 80-83
-
-
Kelsell, D.P.1
Dunlop, J.2
Stevens, H.P.3
Lench, N.J.4
Liang, J.N.5
Parry, G.6
Mueller, R.F.7
Leigh, I.M.8
-
13
-
-
0032846415
-
Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus
-
Grifa A, Wagner CA, D'Ambrosio L, Melchionda S, Bernardi F, Lopez-Bigas N, Rabionet R, Arbones M, Monica MD, Estivill X, Zelante L, Lang F, Gasparini P. Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus. Nat Genet 1999, 23(1):16-18.
-
(1999)
Nat Genet
, vol.23
, Issue.1
, pp. 16-18
-
-
Grifa, A.1
Wagner, C.A.2
D'Ambrosio, L.3
Melchionda, S.4
Bernardi, F.5
Lopez-Bigas, N.6
Rabionet, R.7
Arbones, M.8
Monica, M.D.9
Estivill, X.10
Zelante, L.11
Lang, F.12
Gasparini, P.13
-
14
-
-
17344371515
-
Nonsyndromic hearing impairment is associated with a mutation in DFNA5
-
Van Laer L, Huizing EH, Verstreken M, van Zuijlen D, Wauters JG, Bossuyt PJ, Van de Heyning P, McGuirt WT, Smith RJ, Willems PJ, Legan PK, Richardson GP, Van Camp G. Nonsyndromic hearing impairment is associated with a mutation in DFNA5. Nat Genet 1998, 20(2):194-197.
-
(1998)
Nat Genet
, vol.20
, Issue.2
, pp. 194-197
-
-
Van Laer, L.1
Huizing, E.H.2
Verstreken, M.3
van Zuijlen, D.4
Wauters, J.G.5
Bossuyt, P.J.6
Van de Heyning, P.7
McGuirt, W.T.8
Smith, R.J.9
Willems, P.J.10
Legan, P.K.11
Richardson, G.P.12
Van Camp, G.13
-
15
-
-
0029088343
-
Molecular genetics of retinitis pigmentosa
-
Spec No
-
Dryja TP, Li T. Molecular genetics of retinitis pigmentosa. Hum Mol Genet 1995, 4:1739-1743. Spec No.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1739-1743
-
-
Dryja, T.P.1
Li, T.2
-
16
-
-
30744451692
-
A new locus (RP31) for autosomal dominant retinitis pigmentosa maps to chromosome 9p
-
Papaioannou M, Chakarova CF, Prescott DC, Waseem N, Theis T, Lopez I, Gill B, Koenekoop RK, Bhattacharya SS. A new locus (RP31) for autosomal dominant retinitis pigmentosa maps to chromosome 9p. Hum Genet 2005, 118(3-4):501-503.
-
(2005)
Hum Genet
, vol.118
, Issue.3-4
, pp. 501-503
-
-
Papaioannou, M.1
Chakarova, C.F.2
Prescott, D.C.3
Waseem, N.4
Theis, T.5
Lopez, I.6
Gill, B.7
Koenekoop, R.K.8
Bhattacharya, S.S.9
-
17
-
-
33749026952
-
A novel locus for X-linked retinitis pigmentosa
-
Tong Z, Yang Z, Meyer JJ, McInnes AW, Xue L, Azimi AM, Baird J, Zhao Y, Pearson E, Wang C, Chen Y, Zhang K. A novel locus for X-linked retinitis pigmentosa. Ann Acad Med Singapore 2006, 35(7):476-478.
-
(2006)
Ann Acad Med Singapore
, vol.35
, Issue.7
, pp. 476-478
-
-
Tong, Z.1
Yang, Z.2
Meyer, J.J.3
McInnes, A.W.4
Xue, L.5
Azimi, A.M.6
Baird, J.7
Zhao, Y.8
Pearson, E.9
Wang, C.10
Chen, Y.11
Zhang, K.12
-
18
-
-
0035089146
-
Comparison of 'model-free' and 'model-based' linkage statistics in the presence of locus heterogeneity: single data set and multiple data set applications
-
Huang J, Vieland VJ. Comparison of 'model-free' and 'model-based' linkage statistics in the presence of locus heterogeneity: single data set and multiple data set applications. Hum Hered 2001, 51(4):217-225.
-
(2001)
Hum Hered
, vol.51
, Issue.4
, pp. 217-225
-
-
Huang, J.1
Vieland, V.J.2
-
19
-
-
0026631412
-
A new test for linkage in the presence of locus heterogeneity
-
MacLean CJ, Ploughman LM, Diehl SR, Kendler KS. A new test for linkage in the presence of locus heterogeneity. Am J Hum Genet 1992, 50(6):1259-1266.
-
(1992)
Am J Hum Genet
, vol.50
, Issue.6
, pp. 1259-1266
-
-
MacLean, C.J.1
Ploughman, L.M.2
Diehl, S.R.3
Kendler, K.S.4
-
20
-
-
24944561852
-
Genetic linkage studies
-
Teare DM, Barrett JH. Genetic linkage studies. The Lancet 2005, 366(9490):1036-1044.
-
(2005)
The Lancet
, vol.366
, Issue.9490
, pp. 1036-1044
-
-
Teare, D.M.1
Barrett, J.H.2
-
21
-
-
0035089255
-
Power to detect linkage based on multiple sets of data in the presence of locus heterogeneity: comparative evaluation of model-based linkage methods for affected sib pair data
-
Vieland VJ, Wang K, Huang J. Power to detect linkage based on multiple sets of data in the presence of locus heterogeneity: comparative evaluation of model-based linkage methods for affected sib pair data. Hum Hered 2001, 51(4):199-208.
-
(2001)
Hum Hered
, vol.51
, Issue.4
, pp. 199-208
-
-
Vieland, V.J.1
Wang, K.2
Huang, J.3
-
22
-
-
33645743056
-
Detecting linkage disequilibrium in the presence of locus heterogeneity
-
Wang D, Huang J. Detecting linkage disequilibrium in the presence of locus heterogeneity. Ann Hum Genet 2006, 70(Pt 3):397-409.
-
(2006)
Ann Hum Genet
, vol.70
, Issue.PART 3
, pp. 397-409
-
-
Wang, D.1
Huang, J.2
-
23
-
-
0033362231
-
Direct power comparisons between simple LOD scores and NPL scores for linkage analysis in complex diseases
-
Abreu PC, Greenberg DA, Hodge SE. Direct power comparisons between simple LOD scores and NPL scores for linkage analysis in complex diseases. Am J Hum Genet 1999, 65(3):847-857.
-
(1999)
Am J Hum Genet
, vol.65
, Issue.3
, pp. 847-857
-
-
Abreu, P.C.1
Greenberg, D.A.2
Hodge, S.E.3
-
24
-
-
0036144845
-
Quantification of type I error probabilities for heterogeneity LOD scores
-
Abreu PC, Hodge SE, Greenberg DA. Quantification of type I error probabilities for heterogeneity LOD scores. Genet Epidemiol 2002, 22(2):156-169.
-
(2002)
Genet Epidemiol
, vol.22
, Issue.2
, pp. 156-169
-
-
Abreu, P.C.1
Hodge, S.E.2
Greenberg, D.A.3
-
25
-
-
0030731662
-
Effect of genetic heterogeneity and assortative mating on linkage analysis: a simulation study
-
Falk CT. Effect of genetic heterogeneity and assortative mating on linkage analysis: a simulation study. Am J Hum Genet 1997, 61(5):1169-1178.
-
(1997)
Am J Hum Genet
, vol.61
, Issue.5
, pp. 1169-1178
-
-
Falk, C.T.1
-
26
-
-
0028000412
-
Bootstrapping in human genetic linkage
-
Chiano MN, Yates JR. Bootstrapping in human genetic linkage. Ann Hum Genet 1994, 58(Pt 2):129-143.
-
(1994)
Ann Hum Genet
, vol.58
, Issue.PART 2
, pp. 129-143
-
-
Chiano, M.N.1
Yates, J.R.2
-
27
-
-
72049090952
-
Transmission disequilibrium test power and sample size in the presence of locus heterogeneity
-
Article
-
Chen C, Yang G, Buyske S, Matise T, Finch SJ, Gordon D. Transmission disequilibrium test power and sample size in the presence of locus heterogeneity. Stat Appl Genet Mol Biol 2009, 8(1):44. Article.
-
(2009)
Stat Appl Genet Mol Biol
, vol.8
, Issue.1
, pp. 44
-
-
Chen, C.1
Yang, G.2
Buyske, S.3
Matise, T.4
Finch, S.J.5
Gordon, D.6
-
28
-
-
77049298733
-
The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type
-
Morton NE. The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type. Am J Hum Genet 1956, 8:80-96.
-
(1956)
Am J Hum Genet
, vol.8
, pp. 80-96
-
-
Morton, N.E.1
-
29
-
-
0023896149
-
A new statistical test for linkage heterogeneity
-
Risch N. A new statistical test for linkage heterogeneity. Am J Hum Genet 1988, 42(2):353-364.
-
(1988)
Am J Hum Genet
, vol.42
, Issue.2
, pp. 353-364
-
-
Risch, N.1
-
30
-
-
0028041363
-
A combined test of linkage heterogeneity
-
Goldstein DR. A combined test of linkage heterogeneity. Am J Hum Genet 1994, 55(4):841-848.
-
(1994)
Am J Hum Genet
, vol.55
, Issue.4
, pp. 841-848
-
-
Goldstein, D.R.1
-
31
-
-
0021070232
-
The search for heterogeneity in insulin-dependent diabetes mellitus (IDDM): Linkage studies, two-locus models, and genetic heterogeneity
-
Hodge SE, Anderson CE, Neiswanger K, Sparkes RS, Rimoin DL. The search for heterogeneity in insulin-dependent diabetes mellitus (IDDM): Linkage studies, two-locus models, and genetic heterogeneity. Am J Hum Genet 1983, 35:1139-1155.
-
(1983)
Am J Hum Genet
, vol.35
, pp. 1139-1155
-
-
Hodge, S.E.1
Anderson, C.E.2
Neiswanger, K.3
Sparkes, R.S.4
Rimoin, D.L.5
-
32
-
-
0021064786
-
Linkage analysis and family classification under heterogeneity
-
Ott J. Linkage analysis and family classification under heterogeneity. Ann Hum Genet 1983, 47:311-320.
-
(1983)
Ann Hum Genet
, vol.47
, pp. 311-320
-
-
Ott, J.1
-
33
-
-
0020031945
-
X-linkage and genetic heterogeneity in bipolar-related major affective illness: reanalysis of linkage data
-
Risch N, Baron M. X-linkage and genetic heterogeneity in bipolar-related major affective illness: reanalysis of linkage data. Ann Hum Genet 1982, 46(Pt 2):153-166.
-
(1982)
Ann Hum Genet
, vol.46
, Issue.PART 2
, pp. 153-166
-
-
Risch, N.1
Baron, M.2
-
34
-
-
0017614218
-
Counting methods (EM algorithm) in human pedigree analysis: linkage and segregation analysis
-
Ott J. Counting methods (EM algorithm) in human pedigree analysis: linkage and segregation analysis. Ann Hum Genet 1977, 40(4):443-454.
-
(1977)
Ann Hum Genet
, vol.40
, Issue.4
, pp. 443-454
-
-
Ott, J.1
-
35
-
-
0027483312
-
Distribution of the admixture test for the detection of linkage under heterogeneity
-
Faraway JJ. Distribution of the admixture test for the detection of linkage under heterogeneity. Genet Epidemiol 1993, 10(1):75-83.
-
(1993)
Genet Epidemiol
, vol.10
, Issue.1
, pp. 75-83
-
-
Faraway, J.J.1
-
36
-
-
0026629701
-
Strategies for characterizing highly polymorphic markers in human gene mapping
-
Ott J. Strategies for characterizing highly polymorphic markers in human gene mapping. Am J Hum Genet 1992, 51(2):283-290.
-
(1992)
Am J Hum Genet
, vol.51
, Issue.2
, pp. 283-290
-
-
Ott, J.1
-
37
-
-
0043048571
-
Sequential tests for the detection of linkage
-
Morton NE. Sequential tests for the detection of linkage. Am J Hum Genet 1955, 7(3):277-318.
-
(1955)
Am J Hum Genet
, vol.7
, Issue.3
, pp. 277-318
-
-
Morton, N.E.1
-
38
-
-
0003408936
-
Analysis of Human Genetic Linkage
-
Baltimore, MD: The John Hopkins University Press, Third
-
Ott J. Analysis of Human Genetic Linkage. 1999, Baltimore, MD: The John Hopkins University Press, Third.
-
(1999)
-
-
Ott, J.1
-
39
-
-
0032775678
-
Heterogeneity for multiple disease loci in linkage analysis
-
Bhat A, Heath SC, Ott J. Heterogeneity for multiple disease loci in linkage analysis. Hum Hered 1999, 49(4):229-231.
-
(1999)
Hum Hered
, vol.49
, Issue.4
, pp. 229-231
-
-
Bhat, A.1
Heath, S.C.2
Ott, J.3
-
40
-
-
34248682935
-
Genome-wide linkage analysis of blood pressure under locus heterogeneity
-
Yang X, Wang K, Huang J, Vieland VJ. Genome-wide linkage analysis of blood pressure under locus heterogeneity. BMC Genet 2003, 4(Suppl 1):S78.
-
(2003)
BMC Genet
, vol.4
, Issue.SUPPL. 1
-
-
Yang, X.1
Wang, K.2
Huang, J.3
Vieland, V.J.4
-
41
-
-
34248667544
-
Mapping loci influencing blood pressure in the Framingham pedigrees using model-free LOD score analysis of a quantitative trait
-
Knight J, North BV, Sham PC, Curtis D. Mapping loci influencing blood pressure in the Framingham pedigrees using model-free LOD score analysis of a quantitative trait. BMC Genet 2003, 4(Suppl 1):S74.
-
(2003)
BMC Genet
, vol.4
, Issue.SUPPL. 1
-
-
Knight, J.1
North, B.V.2
Sham, P.C.3
Curtis, D.4
-
42
-
-
0042674201
-
Linkage analysis of quantitative trait loci in the presence of heterogeneity
-
Ekstrom CT, Dalgaard P. Linkage analysis of quantitative trait loci in the presence of heterogeneity. Hum Hered 2003, 55(1):16-26.
-
(2003)
Hum Hered
, vol.55
, Issue.1
, pp. 16-26
-
-
Ekstrom, C.T.1
Dalgaard, P.2
-
43
-
-
33749613838
-
Quantitative-trait-locus mapping in the presence of locus heterogeneity
-
Wang K, Peng Y. Quantitative-trait-locus mapping in the presence of locus heterogeneity. Ann Hum Genet 2006, 70(Pt 6):882-892.
-
(2006)
Ann Hum Genet
, vol.70
, Issue.PART 6
, pp. 882-892
-
-
Wang, K.1
Peng, Y.2
-
44
-
-
0003985164
-
Latent Structure Analysis
-
Boston: Houghton Mifflin
-
Lazarsfeld PFWHN. Latent Structure Analysis. 1968, Boston: Houghton Mifflin.
-
(1968)
-
-
Lazarsfeld, P.F.W.H.N.1
-
45
-
-
70349673413
-
Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis
-
Holliday EG, McLean DE, Nyholt DR, Mowry BJ. Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis. Arch Gen Psychiatry 2009, 66(10):1058-1067.
-
(2009)
Arch Gen Psychiatry
, vol.66
, Issue.10
, pp. 1058-1067
-
-
Holliday, E.G.1
McLean, D.E.2
Nyholt, D.R.3
Mowry, B.J.4
-
46
-
-
0035158507
-
Familiality and heritability of subtypes of attention deficit hyperactivity disorder in a population sample of adolescent female twins
-
Todd RD, Rasmussen ER, Neuman RJ, Reich W, Hudziak JJ, Bucholz KK, Madden PA, Heath A. Familiality and heritability of subtypes of attention deficit hyperactivity disorder in a population sample of adolescent female twins. Am J Psychiatry 2001, 158(11):1891-1898.
-
(2001)
Am J Psychiatry
, vol.158
, Issue.11
, pp. 1891-1898
-
-
Todd, R.D.1
Rasmussen, E.R.2
Neuman, R.J.3
Reich, W.4
Hudziak, J.J.5
Bucholz, K.K.6
Madden, P.A.7
Heath, A.8
-
47
-
-
79952509661
-
Latent class model with familial dependence to address heterogeneity in complex diseases: adapting the approach to family-based association studies
-
Bureau A, Croteau J, Tayeb A, Merette C, Labbe A. Latent class model with familial dependence to address heterogeneity in complex diseases: adapting the approach to family-based association studies. Genet Epidemiol 2011, 35(3):182-189.
-
(2011)
Genet Epidemiol
, vol.35
, Issue.3
, pp. 182-189
-
-
Bureau, A.1
Croteau, J.2
Tayeb, A.3
Merette, C.4
Labbe, A.5
-
48
-
-
84888282212
-
Improvement of phenotyping in genome wide association studies on schizophrenia: an application of latent class factor analysis
-
Derks EM, Allardyce J, Boks MP, Ophoff RA. Improvement of phenotyping in genome wide association studies on schizophrenia: an application of latent class factor analysis. Schizophrenia Research 2010, 117(2-3):184-185.
-
(2010)
Schizophrenia Research
, vol.117
, Issue.2-3
, pp. 184-185
-
-
Derks, E.M.1
Allardyce, J.2
Boks, M.P.3
Ophoff, R.A.4
-
49
-
-
33646074053
-
Use of phenotypic covariates in association analysis by sequential addition of cases
-
Macgregor S, Craddock N, Holmans PA. Use of phenotypic covariates in association analysis by sequential addition of cases. Eur J Hum Genet 2006, 14(5):529-534.
-
(2006)
Eur J Hum Genet
, vol.14
, Issue.5
, pp. 529-534
-
-
Macgregor, S.1
Craddock, N.2
Holmans, P.A.3
-
50
-
-
77954184904
-
Ordered subset analysis for case-control studies
-
Qin X, Hauser ER, Schmidt S. Ordered subset analysis for case-control studies. Genet Epidemiol 2010, 34(5):407-417.
-
(2010)
Genet Epidemiol
, vol.34
, Issue.5
, pp. 407-417
-
-
Qin, X.1
Hauser, E.R.2
Schmidt, S.3
-
51
-
-
38049086967
-
An ordered subset approach to including covariates in the transmission disequilibrium test
-
Perdry H, Maher BS, Babron MC, McHenry T, Clerget-Darpoux F, Marazita ML. An ordered subset approach to including covariates in the transmission disequilibrium test. BMC Proc 2007, 1(Suppl 1):S77.
-
(2007)
BMC Proc
, vol.1
, Issue.SUPPL. 1
-
-
Perdry, H.1
Maher, B.S.2
Babron, M.C.3
McHenry, T.4
Clerget-Darpoux, F.5
Marazita, M.L.6
-
52
-
-
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(3):506-516.
-
(1993)
Am J Hum Genet
, vol.52
, Issue.3
, pp. 506-516
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
53
-
-
58949092588
-
Ordered-subset analysis (OSA) for family-based association mapping of complex traits
-
Chung RH, Schmidt S, Martin ER, Hauser ER. Ordered-subset analysis (OSA) for family-based association mapping of complex traits. Genet Epidemiol 2008, 32(7):627-637.
-
(2008)
Genet Epidemiol
, vol.32
, Issue.7
, pp. 627-637
-
-
Chung, R.H.1
Schmidt, S.2
Martin, E.R.3
Hauser, E.R.4
-
54
-
-
0242522464
-
Accounting for linkage in family-based tests of association with missing parental genotypes
-
Martin ER, Bass MP, Hauser ER, Kaplan NL. Accounting for linkage in family-based tests of association with missing parental genotypes. Am J Hum Genet 2003, 73(5):1016-1026.
-
(2003)
Am J Hum Genet
, vol.73
, Issue.5
, pp. 1016-1026
-
-
Martin, E.R.1
Bass, M.P.2
Hauser, E.R.3
Kaplan, N.L.4
-
55
-
-
23844440572
-
The posterior probability of linkage allowing for linkage disequilibrium and a new estimate of disequilibrium between a trait and a marker
-
Yang X, Huang J, Logue MW, Vieland VJ. The posterior probability of linkage allowing for linkage disequilibrium and a new estimate of disequilibrium between a trait and a marker. Hum Hered 2005, 59(4):210-219.
-
(2005)
Hum Hered
, vol.59
, Issue.4
, pp. 210-219
-
-
Yang, X.1
Huang, J.2
Logue, M.W.3
Vieland, V.J.4
-
56
-
-
78649526217
-
Association statistics under the PPL framework
-
Huang Y, Vieland VJ. Association statistics under the PPL framework. Genet Epidemiol 2010, 34(8):835-845.
-
(2010)
Genet Epidemiol
, vol.34
, Issue.8
, pp. 835-845
-
-
Huang, Y.1
Vieland, V.J.2
-
57
-
-
37149035176
-
Increased efficiency of case-control association analysis by using allele-sharing and covariate information
-
Schmidt S, Schmidt MA, Qin X, Martin ER, Hauser ER. Increased efficiency of case-control association analysis by using allele-sharing and covariate information. Hum Hered 2008, 65(3):154-165.
-
(2008)
Hum Hered
, vol.65
, Issue.3
, pp. 154-165
-
-
Schmidt, S.1
Schmidt, M.A.2
Qin, X.3
Martin, E.R.4
Hauser, E.R.5
-
58
-
-
70350521744
-
Binomial mixture model-based association tests under genetic heterogeneity
-
Zhou H, Pan W. Binomial mixture model-based association tests under genetic heterogeneity. Ann Hum Genet 2009, 73(Pt 6):614-630.
-
(2009)
Ann Hum Genet
, vol.73
, Issue.PART 6
, pp. 614-630
-
-
Zhou, H.1
Pan, W.2
-
59
-
-
0035528920
-
A train of thoughts on gene mapping
-
Hoh J, Ott J. A train of thoughts on gene mapping. Theor Popul Biol 2001, 60(3):149-153.
-
(2001)
Theor Popul Biol
, vol.60
, Issue.3
, pp. 149-153
-
-
Hoh, J.1
Ott, J.2
-
60
-
-
0042881041
-
Mathematical multi-locus approaches to localizing complex human trait genes
-
Hoh J, Ott J. Mathematical multi-locus approaches to localizing complex human trait genes. Nat Rev Genet 2003, 4(9):701-709.
-
(2003)
Nat Rev Genet
, vol.4
, Issue.9
, pp. 701-709
-
-
Hoh, J.1
Ott, J.2
-
61
-
-
2542500627
-
Genetic dissection of diseases: design and methods
-
Hoh J, Ott J. Genetic dissection of diseases: design and methods. Curr Opin Genet Dev 2004, 14(3):229-232.
-
(2004)
Curr Opin Genet Dev
, vol.14
, Issue.3
, pp. 229-232
-
-
Hoh, J.1
Ott, J.2
-
62
-
-
0035214299
-
Trimming, weighting, and grouping SNPs in human case-control association studies
-
Hoh J, Wille A, Ott J. Trimming, weighting, and grouping SNPs in human case-control association studies. Genome Res 2001, 11(12):2115-2119.
-
(2001)
Genome Res
, vol.11
, Issue.12
, pp. 2115-2119
-
-
Hoh, J.1
Wille, A.2
Ott, J.3
-
63
-
-
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(5):1114-1126.
-
(1993)
Am J Hum Genet
, vol.53
, Issue.5
, pp. 1114-1126
-
-
Schaid, D.J.1
Sommer, S.S.2
-
64
-
-
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(4):1186-1193.
-
(1999)
Am J Hum Genet
, vol.64
, Issue.4
, pp. 1186-1193
-
-
Weinberg, C.R.1
-
65
-
-
0031949066
-
A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting
-
Weinberg CR, Wilcox AJ, Lie RT. A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting. Am J Hum Genet 1998, 62(4):969-978.
-
(1998)
Am J Hum Genet
, vol.62
, Issue.4
, pp. 969-978
-
-
Weinberg, C.R.1
Wilcox, A.J.2
Lie, R.T.3
-
66
-
-
0029886532
-
Parametric and nonparametric linkage analysis: a unified multipoint approach
-
Kruglyak L, Daly MJ, Reeve-Daly MP, Lander ES. Parametric and nonparametric linkage analysis: a unified multipoint approach. Am J Hum Genet 1996, 58(6):1347-1363.
-
(1996)
Am J Hum Genet
, vol.58
, Issue.6
, pp. 1347-1363
-
-
Kruglyak, L.1
Daly, M.J.2
Reeve-Daly, M.P.3
Lander, E.S.4
-
67
-
-
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(6):1323-1337.
-
(1996)
Am J Hum Genet
, vol.58
, Issue.6
, pp. 1323-1337
-
-
Sobel, E.1
Lange, K.2
-
68
-
-
0028790963
-
The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance
-
O'Connell JR, Weeks DE. The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance. Nat Genet 1995, 11(4):402-408.
-
(1995)
Nat Genet
, vol.11
, Issue.4
, pp. 402-408
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
69
-
-
0036338150
-
Merlin--rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis GR, Cherny SS, Cookson WO, Cardon LR. Merlin--rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 2002, 30(1):97-101.
-
(2002)
Nat Genet
, vol.30
, Issue.1
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
70
-
-
0002629270
-
Maximum likelihood from incomplete data via the EM algorithm
-
Dempster A, Laird N, Rubin D. Maximum likelihood from incomplete data via the EM algorithm. J R Stat Soc Ser B 1977, 39:1-38.
-
(1977)
J R Stat Soc Ser B
, vol.39
, pp. 1-38
-
-
Dempster, A.1
Laird, N.2
Rubin, D.3
-
71
-
-
79952578058
-
Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes
-
Sharma S, Gao X, Londono D, Devroy SE, Mauldin KN, Frankel JT, Brandon JM, Zhang D, Li QZ, Dobbs MB, Gurnett CA, Grant SF, Hakonarson H, Dormans JP, Herring JA, Gordon D, Wise CA. Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes. Hum Mol Genet 20(7):1456-1466.
-
Hum Mol Genet
, vol.20
, Issue.7
, pp. 1456-1466
-
-
Sharma, S.1
Gao, X.2
Londono, D.3
Devroy, S.E.4
Mauldin, K.N.5
Frankel, J.T.6
Brandon, J.M.7
Zhang, D.8
Li, Q.Z.9
Dobbs, M.B.10
Gurnett, C.A.11
Grant, S.F.12
Hakonarson, H.13
Dormans, J.P.14
Herring, J.A.15
Gordon, D.16
Wise, C.A.17
-
72
-
-
41549129915
-
Understanding genetic factors in idiopathic scoliosis, a complex disease of childhood
-
Wise CA, Gao X, Shoemaker S, Gordon D, Herring JA. Understanding genetic factors in idiopathic scoliosis, a complex disease of childhood. Current genomics 2008, 9(1):51-59.
-
(2008)
Current genomics
, vol.9
, Issue.1
, pp. 51-59
-
-
Wise, C.A.1
Gao, X.2
Shoemaker, S.3
Gordon, D.4
Herring, J.A.5
-
73
-
-
84863405665
-
Genetic Markers of Chromosome 7 Associated With Scoliosis And Use Thereof. In., vol. WO/2008/033813
-
Switzerland: World Intellectual Property Organization
-
Nelson LM, Kenneth W. Genetic Markers of Chromosome 7 Associated With Scoliosis And Use Thereof. In., vol. WO/2008/033813. 2008, Switzerland: World Intellectual Property Organization.
-
(2008)
-
-
Nelson, L.M.1
Kenneth, W.2
-
74
-
-
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(3):559-575.
-
(2007)
Am J Hum Genet
, vol.81
, Issue.3
, 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
-
75
-
-
0003854151
-
Exploratory Data Analysis
-
Upper Saddle River, NJ: Pearson Education - Addison Wesley
-
Tukey JW. Exploratory Data Analysis. 1977, Upper Saddle River, NJ: Pearson Education - Addison Wesley.
-
(1977)
-
-
Tukey, J.W.1
-
76
-
-
30044437712
-
Computing asymptotic power and sample size for case-control genetic association studies in the presence of phenotype and/or genotype misclassification errors
-
Article
-
Ji F, Yang Y, Haynes C, Finch SJ, Gordon D. Computing asymptotic power and sample size for case-control genetic association studies in the presence of phenotype and/or genotype misclassification errors. Stat Appl Genet Mol Biol 2005, 4:37. Article.
-
(2005)
Stat Appl Genet Mol Biol
, vol.4
, pp. 37
-
-
Ji, F.1
Yang, Y.2
Haynes, C.3
Finch, S.J.4
Gordon, D.5
-
77
-
-
0003408938
-
Handbook of Human Genetic Linkage
-
Baltimore: Johns Hopkins University Press
-
Terwilliger JD, Ott J. Handbook of Human Genetic Linkage. 1994, Baltimore: Johns Hopkins University Press.
-
(1994)
-
-
Terwilliger, J.D.1
Ott, J.2
-
78
-
-
0036128126
-
HLODs, trait models, and ascertainment: implications of admixture for parameter estimation and linkage detection
-
Vieland VJ, Logue M. HLODs, trait models, and ascertainment: implications of admixture for parameter estimation and linkage detection. Hum Hered 2002, 53(1):23-35.
-
(2002)
Hum Hered
, vol.53
, Issue.1
, pp. 23-35
-
-
Vieland, V.J.1
Logue, M.2
-
80
-
-
0000801438
-
SLINK: a general simulation program for linkage analysis
-
Weeks DE, Ott J, Lathrop GM. SLINK: a general simulation program for linkage analysis. Am J Hum Genet 1990, 47:A204.
-
(1990)
Am J Hum Genet
, vol.47
-
-
Weeks, D.E.1
Ott, J.2
Lathrop, G.M.3
-
81
-
-
0032231325
-
Maximum-likelihood expression of the transmission/disequilibrium test and power considerations
-
Abel L, Muller-Myhsok B. Maximum-likelihood expression of the transmission/disequilibrium test and power considerations. Am J Hum Genet 1998, 63(2):664-667.
-
(1998)
Am J Hum Genet
, vol.63
, Issue.2
, pp. 664-667
-
-
Abel, L.1
Muller-Myhsok, B.2
-
82
-
-
0034917944
-
A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data
-
Gordon D, Heath SC, Liu X, Ott J. A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data. Am J Hum Genet 2001, 69(2):371-380.
-
(2001)
Am J Hum Genet
, vol.69
, Issue.2
, pp. 371-380
-
-
Gordon, D.1
Heath, S.C.2
Liu, X.3
Ott, J.4
-
83
-
-
0033073397
-
Power of association and linkage tests when the disease alleles are unobserved
-
Tu IP, Whittemore AS. Power of association and linkage tests when the disease alleles are unobserved. Am J Hum Genet 1999, 64(2):641-649.
-
(1999)
Am J Hum Genet
, vol.64
, Issue.2
, pp. 641-649
-
-
Tu, I.P.1
Whittemore, A.S.2
|