-
1
-
-
26444496137
-
Adjusting for treatment effects in studies of quantitative traits: Antihypertensive therapy and systolic blood pressure
-
DOI 10.1002/sim.2165
-
Tobin MD, Sheehan NA, Scurrah KJ, Burton PR: Adjusting for treatment effects in studies of quantitative traits: antihypertensive therapy and systolic blood pressure. Stat Med 2005; 24: 2911-2935. (Pubitemid 41419179)
-
(2005)
Statistics in Medicine
, vol.24
, Issue.19
, pp. 2911-2935
-
-
Tobin, M.D.1
Sheehan, N.A.2
Scurrah, K.J.3
Burton, P.R.4
-
2
-
-
37249022272
-
Mapping quantitative trait loci from a single-tail sample of the phenotype distribution including survival data
-
DOI 10.1534/genetics.107.081299
-
Sillanpaa MJ, Hoti F: Mapping quantitative trait loci from a single-tail sample of the phenotype distribution including survival data. Genetics 2007; 177: 2361-2377. (Pubitemid 350277011)
-
(2007)
Genetics
, vol.177
, Issue.4
, pp. 2361-2377
-
-
Sillanpaa, M.J.1
Hoti, F.2
-
3
-
-
33747850181
-
Quantitative trait linkage analysis using Gaussian copulas
-
DOI 10.1534/genetics.105.054650
-
Li M, Boehnke M, Abecasis GR, Song PX: Quantitative trait linkage analysis using Gaussian copulas. Genetics 2006; 173: 2317-2327. (Pubitemid 44285705)
-
(2006)
Genetics
, vol.173
, Issue.4
, pp. 2317-2327
-
-
Li, M.1
Boehnke, M.2
Abecasis, G.R.3
Song, P.X.-K.4
-
4
-
-
33750293950
-
Semiparametric variance-component models for linkage and association analyses of censored trait data
-
DOI 10.1002/gepi.20168
-
Diao G, Lin DY: Semiparametric variancecomponent models for linkage and association analyses of censored trait data. Genet Epidemiol 2006; 30: 570-581. (Pubitemid 44630927)
-
(2006)
Genetic Epidemiology
, vol.30
, Issue.7
, pp. 570-581
-
-
Diao, G.1
Lin, D.Y.2
-
5
-
-
33746429609
-
A simple linear regression method for quantitative trait loci linkage analysis with censored observations
-
DOI 10.1534/genetics.106.055921
-
Anderson CA, McRae AF, Visscher PM: A simple linear regression method for quantitative trait loci linkage analysis with censored observations. Genetics 2006; 173: 1735-1745. (Pubitemid 44127672)
-
(2006)
Genetics
, vol.173
, Issue.3
, pp. 1735-1745
-
-
Anderson, C.A.1
McRae, A.F.2
Visscher, P.M.3
-
6
-
-
27744450835
-
Semiparametric methods for mapping quantitative trait loci with censored data
-
Diao G, Lin DY: Semiparametric methods for mapping quantitative trait loci with censored data. Biometrics 2005; 61: 789-798.
-
(2005)
Biometrics
, vol.61
, pp. 789-798
-
-
Diao, G.1
Lin, D.Y.2
-
7
-
-
0037369964
-
A tobit variance-component method for linkage analysis of censored trait data
-
DOI 10.1086/367924
-
Epstein MP, Lin X, Boehnke M: A tobit variance-component method for linkage analysis of censored trait data. Am J Hum Genet 2003; 72: 611-620. (Pubitemid 36255960)
-
(2003)
American Journal of Human Genetics
, vol.72
, Issue.3
, pp. 611-620
-
-
Epstein, M.P.1
Lin, X.2
Boehnke, M.3
-
8
-
-
0032728337
-
Genomewide linkage analysis using genetic variance components of alcohol dependency-associated censored and continuous traits
-
Palmer LJ, Tiller KJ, Burton PR: Genomewide linkage analysis using genetic variance components of alcohol dependency-associated censored and continuous traits. Genet Epidemiol 1999; 17(suppl 1):S283-S288.
-
(1999)
Genet Epidemiol
, vol.17
, Issue.SUPPL. 1
-
-
Palmer, L.J.1
Tiller, K.J.2
Burton, P.R.3
-
9
-
-
0037317663
-
Antihypertensive treatments obscure familial contributions to blood pressure variation
-
DOI 10.1161/01.HYP.0000044938.94050.E3
-
Cui JS, Hopper JL, Harrap SB: Antihypertensive treatments obscure familial contributions to blood pressure variation. Hypertension 2003; 41: 207-210. (Pubitemid 36204890)
-
(2003)
Hypertension
, vol.41
, Issue.2
, pp. 207-210
-
-
Cui, J.S.1
Hopper, J.L.2
Harrap, S.B.3
-
10
-
-
79551522663
-
Genome-wide linkage screen for systolic blood pressure in the Veterans Administration Genetic Epidemiology Study (VAGES) of Mexican-Americans and confirmation of a major susceptibility locus on chromosome 6q14. 1
-
Puppala S, Coletta DK, Schneider J, Hu SL, Farook VS, Dyer TD, Arya R, Blangero J, Duggirala R, DeFronzo RA, Jenkinson CP: Genome-wide linkage screen for systolic blood pressure in the Veterans Administration Genetic Epidemiology Study (VAGES) of Mexican-Americans and confirmation of a major susceptibility locus on chromosome 6q14. 1. Hum Hered 2011; 71: 1-10.
-
(2011)
Hum Hered
, vol.71
, pp. 1-10
-
-
Puppala, S.1
Coletta, D.K.2
Schneider, J.3
Hu, S.L.4
Farook, V.S.5
Dyer, T.D.6
Arya, R.7
Blangero, J.8
Duggirala, R.9
Defronzo, R.A.10
Jenkinson, C.P.11
-
12
-
-
33748520872
-
Review: A gentle introduction to imputation of missing values
-
DOI 10.1016/j.jclinepi.2006.01.014, PII S0895435606001971
-
Donders AR, van der Heijden GJ, Stijnen T, Moons KG: Review: a gentle introduction to imputation of missing values. J Clin Epidemiol 2006; 59: 1087-1091. (Pubitemid 44374314)
-
(2006)
Journal of Clinical Epidemiology
, vol.59
, Issue.10
, pp. 1087-1091
-
-
Donders, A.R.T.1
Van Der Heijden, G.J.M.G.2
Stijnen, T.3
Moons, K.G.M.4
-
13
-
-
30344452796
-
Two novel quantitative trait linkage analysis statistics based on the posterior probability of linkage: Application to the COGA families
-
Bartlett CW, Vieland VJ: Two novel quantitative trait linkage analysis statistics based on the posterior probability of linkage: application to the COGA families. BMC Genet 2005; 6(suppl 1):S121.
-
(2005)
BMC Genet
, vol.6
, Issue.SUPPL. 1
-
-
Bartlett, C.W.1
Vieland, V.J.2
-
14
-
-
0000386296
-
An analysis of variability in the number of digits in an inbred strain of guinea pigs
-
Wright S: An analysis of variability in the number of digits in an inbred strain of guinea pigs. Genetics 1934; 19: 506-536.
-
(1934)
Genetics
, vol.19
, pp. 506-536
-
-
Wright, S.1
-
15
-
-
84055184748
-
KELVIN: A software package for rigorous measurement of statistical evidence in human genetics
-
Vieland VJ, Huang Y, Seok SC, Burian J, Catalyurek U, O'Connell J, Segre A, Valentine-Cooper W: KELVIN: a software package for rigorous measurement of statistical evidence in human genetics. Hum Hered 2011; 72: 276-288.
-
(2011)
Hum Hered
, vol.72
, pp. 276-288
-
-
Vieland, V.J.1
Huang, Y.2
Seok, S.C.3
Burian, J.4
Catalyurek, U.5
O'Connell, J.6
Segre, A.7
Valentine-Cooper, W.8
-
16
-
-
2342592462
-
Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment
-
DOI 10.1159/000077385
-
Bartlett CW, Flax JF, Logue MW, Smith BJ, Vieland VJ, Tallal P, Brzustowicz LM: Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment. Hum Hered 2004; 57: 10-20. (Pubitemid 38608305)
-
(2004)
Human Heredity
, vol.57
, Issue.1
, pp. 10-20
-
-
Bartlett, C.W.1
Flax, J.F.2
Logue, M.W.3
Smith, B.J.4
Vieland, V.J.5
Tallal, P.6
Brzustowicz, L.M.7
-
17
-
-
79958065866
-
Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism
-
Vieland VJ, Hallmayer J, Huang Y, Pagnamenta AT, Pinto D, Khan H, Monaco AP, Paterson AD, Scherer SW, Sutcliffe JS, Szatmari P: Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism. J Neurodev Disord 2011; 3: 113-123.
-
(2011)
J Neurodev Disord
, vol.3
, pp. 113-123
-
-
Vieland, V.J.1
Hallmayer, J.2
Huang, Y.3
Pagnamenta, A.T.4
Pinto, D.5
Khan, H.6
Monaco, A.P.7
Paterson, A.D.8
Scherer, S.W.9
Sutcliffe, J.S.10
Szatmari, P.11
-
18
-
-
77957761425
-
Increasing genotype-phenotype model determinism: Application to bivariate reading/language traits and epistatic interactions in languageimpaired families
-
Simmons TR, Flax JF, Azaro MA, Hayter JE, Justice LM, Petrill SA, Bassett AS, Tallal P, Brzustowicz LM, Bartlett CW: Increasing genotype-phenotype model determinism: application to bivariate reading/language traits and epistatic interactions in languageimpaired families. Hum Hered 2010; 70: 232-244.
-
(2010)
Hum Hered
, vol.70
, pp. 232-244
-
-
Simmons, T.R.1
Flax, J.F.2
Azaro, M.A.3
Hayter, J.E.4
Justice, L.M.5
Petrill, S.A.6
Bassett, A.S.7
Tallal, P.8
Brzustowicz, L.M.9
Bartlett, C.W.10
-
19
-
-
64949180420
-
Identification of a schizophreniaassociated functional noncoding variant in NOS1AP
-
Wratten NS, Memoli H, Huang Y, Dulencin AM, Matteson PG, Cornacchia MA, Azaro MA, Messenger J, Hayter JE, Bassett AS, Buyske S, Millonig JH, Vieland VJ, Brzustowicz LM: Identification of a schizophreniaassociated functional noncoding variant in NOS1AP. Am J Psychiatry 2009; 166: 434-441.
-
(2009)
Am J Psychiatry
, vol.166
, pp. 434-441
-
-
Wratten, N.S.1
Memoli, H.2
Huang, Y.3
Dulencin, A.M.4
Matteson, P.G.5
Cornacchia, M.A.6
Azaro, M.A.7
Messenger, J.8
Hayter, J.E.9
Bassett, A.S.10
Buyske, S.11
Millonig, J.H.12
Vieland, V.J.13
Brzustowicz, L.M.14
-
20
-
-
0032231376
-
Bayesian linkage analysis, or: How I learned to stop worrying and love the posterior probability of linkage
-
DOI 10.1086/302076
-
Vieland VJ: Bayesian linkage analysis, or: how I learned to stop worrying and love the posterior probability of linkage. Am J Hum Genet 1998; 63: 947-954. (Pubitemid 30418562)
-
(1998)
American Journal of Human Genetics
, vol.63
, Issue.4
, pp. 947-954
-
-
Vieland, V.J.1
-
21
-
-
0036302206
-
A major susceptibility locus for specific language impairment is located on 13q21
-
DOI 10.1086/341095
-
Bartlett CW, Flax JF, Logue MW, Vieland VJ, Bassett AS, Tallal P, Brzustowicz LM: A major susceptibility locus for specific language impairment is located on 13q21. Am J Hum Genet 2002; 71: 45-55. (Pubitemid 34734706)
-
(2002)
American Journal of Human Genetics
, vol.71
, Issue.1
, pp. 45-55
-
-
Bartlett, C.W.1
Flax, J.F.2
Logue, M.W.3
Vieland, V.J.4
Bassett, A.S.5
Tallal, P.6
Brzustowicz, L.M.7
-
22
-
-
0041318935
-
Bayesian analysis of a previously published genome screen for panic disorder reveals new and compelling evidence for linkage to chromosome 7
-
Logue MW, Vieland VJ, Goedken RJ, Crowe RR: Bayesian analysis of a previously published genome screen for panic disorder reveals new and compelling evidence for linkage to chromosome 7. Am J Med Genet B Neuropsychiatr Genet 2003; 121B:95-99. (Pubitemid 37064037)
-
(2003)
American Journal of Medical Genetics - Neuropsychiatric Genetics
, vol.121
, Issue.1
, pp. 95-99
-
-
Logue, M.W.1
Vieland, V.J.2
Goedken, R.J.3
Crowe, R.R.4
-
23
-
-
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
-
DOI 10.1159/000053343
-
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: 199-208. (Pubitemid 32260825)
-
(2001)
Human Heredity
, vol.51
, Issue.4
, pp. 199-208
-
-
Vieland, V.J.1
Wang, K.2
Huang, J.3
-
24
-
-
0034474140
-
The consistency of the posterior probability of linkage
-
DOI 10.1017/S0003480000008332
-
Wang K, Huang J, Vieland VJ: The consistency of the posterior probability of linkage. Ann Hum Genet 2000; 64: 533-553. (Pubitemid 32166506)
-
(2000)
Annals of Human Genetics
, vol.64
, Issue.6
, pp. 533-553
-
-
Wang, K.1
Huang, J.2
Vieland, V.J.3
-
26
-
-
33846446440
-
Accumulating quantitative trait linkage evidence across multiple datasets using the posterior probability of linkage
-
DOI 10.1002/gepi.20193
-
Bartlett CW, Vieland VJ: Accumulating quantitative trait linkage evidence across multiple datasets using the posterior probability of linkage. Genet Epidemiol 2007; 31: 91-102. (Pubitemid 46147659)
-
(2007)
Genetic Epidemiology
, vol.31
, Issue.2
, pp. 91-102
-
-
Bartlett, C.W.1
Vieland, V.J.2
-
27
-
-
0033358545
-
Testing the robustness of the likelihood-ratio test in a variance- component quantitative-trait loci-mapping procedure
-
DOI 10.1086/302487
-
Allison DB, Neale MC, Zannolli R, Schork NJ, Amos CI, Blangero J: Testing the robustness of the likelihood-ratio test in a variancecomponent quantitative-trait loci-mapping procedure. Am J Hum Genet 1999; 65: 531-544. (Pubitemid 30463010)
-
(1999)
American Journal of Human Genetics
, vol.65
, Issue.2
, pp. 531-544
-
-
Allison, D.B.1
Neale, M.C.2
Zannolli, R.3
Schork, N.J.4
Amos, C.I.5
Blangero, J.6
-
28
-
-
0036077215
-
Powerful regression-based quantitative-trait linkage analysis of general pedigrees
-
DOI 10.1086/341560
-
Sham PC, Purcell S, Cherny SS, Abecasis GR: Powerful regression-based quantitative-trait linkage analysis of general pedigrees. Am J Hum Genet 2002; 71: 238-253. (Pubitemid 34800241)
-
(2002)
American Journal of Human Genetics
, vol.71
, Issue.2
, pp. 238-253
-
-
Sham, P.C.1
Purcell, S.2
Cherny, S.S.3
Abecasis, G.R.4
-
29
-
-
44449155771
-
A multilocus model of the genetic architecture of autoimmune thyroid disorder, with clinical implications
-
Vieland VJ, Huang Y, Bartlett C, Davies TF, Tomer Y: A multilocus model of the genetic architecture of autoimmune thyroid disorder, with clinical implications. Am J Hum Genet 2008; 82: 1349-1356.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 1349-1356
-
-
Vieland, V.J.1
Huang, Y.2
Bartlett, C.3
Davies, T.F.4
Tomer, Y.5
-
30
-
-
0031966959
-
Multipoint quantitative-trait linkage analysis in general pedigrees
-
DOI 10.1086/301844
-
Almasy L, Blangero J: Multipoint quantitative-trait linkage analysis in general pedigrees. Am J Hum Genet 1998; 62: 1198-1211. (Pubitemid 28199022)
-
(1998)
American Journal of Human Genetics
, vol.62
, Issue.5
, pp. 1198-1211
-
-
Almasy, L.1
Blangero, J.2
-
31
-
-
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: 97-101.
-
(2002)
Nat Genet
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
32
-
-
0000726013
-
Mapping quantitative trait loci in oligogenic models
-
DOI 10.1093/biostatistics/2.2.147
-
Tang HK, Siegmund D: Mapping quantitative trait loci in oligogenic models. Biostatistics 2001; 2: 147-162. (Pubitemid 33278603)
-
(2001)
Biostatistics Oxford
, vol.2
, Issue.2
, pp. 147-162
-
-
Tang, H.-K.1
Siegmund, D.2
|