-
1
-
-
34147154100
-
Medical sequencing at the extremes of human body mass
-
and others
-
Ahituv N, Kavaslar N, Schackwitz W, Ustaszewska A, Martin J, Hebert S, Doelle H, Ersoy B, Kryukov G, Schmidt S and others. 2007. Medical sequencing at the extremes of human body mass. Am J Hum Genet 80(4):779-791.
-
(2007)
Am J Hum Genet
, vol.80
, Issue.4
, pp. 779-791
-
-
Ahituv, N.1
Kavaslar, N.2
Schackwitz, W.3
Ustaszewska, A.4
Martin, J.5
Hebert, S.6
Doelle, H.7
Ersoy, B.8
Kryukov, G.9
Schmidt, S.10
-
2
-
-
82455199557
-
Genetic Analysis Workshop 17 mini-exome simulation
-
Almasy L, Dyer TD, Peralta JM, Kent JW, Jr., Charlesworth JC, Curran JE, Blangero J. 2011. Genetic Analysis Workshop 17 mini-exome simulation. BMC Proc 5(Suppl 9):S2.
-
(2011)
BMC Proc
, vol.5
, Issue.SUPPL.9
, pp. S2
-
-
Almasy, L.1
Dyer, T.D.2
Peralta, J.M.3
Kent Jr, J.W.4
Charlesworth, J.C.5
Curran, J.E.6
Blangero, J.7
-
3
-
-
84896495533
-
Genome-wide association study identifies common loci influencing circulating glycated hemoglobin (HbA) levels in non-diabetic subjects: The Long Life Family Study (LLFS)
-
and others
-
An P, Miljkovic I, Thyagarajan B, Kraja AT, Daw EW, Pankow JS, Selvin E, Kao WH, Maruthur NM, Nalls MA and others. 2014. Genome-wide association study identifies common loci influencing circulating glycated hemoglobin (HbA) levels in non-diabetic subjects: The Long Life Family Study (LLFS). Metabolism 63(4):461-468.
-
(2014)
Metabolism
, vol.63
, Issue.4
, pp. 461-468
-
-
An, P.1
Miljkovic, I.2
Thyagarajan, B.3
Kraja, A.T.4
Daw, E.W.5
Pankow, J.S.6
Selvin, E.7
Kao, W.H.8
Maruthur, N.M.9
Nalls, M.A.10
-
4
-
-
65249120231
-
Multiple rare variants in the etiology of autism spectrum disorders
-
Buxbaum JD. 2009. Multiple rare variants in the etiology of autism spectrum disorders. Dialogues Clin Neurosci 11(1):35-43.
-
(2009)
Dialogues Clin Neurosci
, vol.11
, Issue.1
, pp. 35-43
-
-
Buxbaum, J.D.1
-
5
-
-
84872380261
-
Sequence kernel association test for quantitative traits in family samples
-
Chen H, Meigs JB, Dupuis J. 2013. Sequence kernel association test for quantitative traits in family samples. Genet Epidemiol 37(2):196-204.
-
(2013)
Genet Epidemiol
, vol.37
, Issue.2
, pp. 196-204
-
-
Chen, H.1
Meigs, J.B.2
Dupuis, J.3
-
6
-
-
77949494010
-
GWAF: an R package for genome-wide association analyses with family data
-
Chen MH, Yang Q. 2009. GWAF: an R package for genome-wide association analyses with family data. Bioinformatics 26(4):580-581.
-
(2009)
Bioinformatics
, vol.26
, Issue.4
, pp. 580-581
-
-
Chen, M.H.1
Yang, Q.2
-
7
-
-
3843056691
-
Multiple rare alleles contribute to low plasma levels of HDL cholesterol
-
Cohen JC, Kiss RS, Pertsemlidis A, Marcel YL, McPherson R, Hobbs HH. 2004. Multiple rare alleles contribute to low plasma levels of HDL cholesterol. Science 305(5685):869-872.
-
(2004)
Science
, vol.305
, Issue.5685
, pp. 869-872
-
-
Cohen, J.C.1
Kiss, R.S.2
Pertsemlidis, A.3
Marcel, Y.L.4
McPherson, R.5
Hobbs, H.H.6
-
8
-
-
32444441330
-
Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levels
-
Cohen JC, Pertsemlidis A, Fahmi S, Esmail S, Vega GL, Grundy SM, Hobbs HH. 2006. Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levels. Proc Natl Acad Sci U S A 103(6):1810-1815.
-
(2006)
Proc Natl Acad Sci U S A
, vol.103
, Issue.6
, pp. 1810-1815
-
-
Cohen, J.C.1
Pertsemlidis, A.2
Fahmi, S.3
Esmail, S.4
Vega, G.L.5
Grundy, S.M.6
Hobbs, H.H.7
-
9
-
-
80051559210
-
Assessing the contribution family data can make to case-control studies of rare variants
-
Curtis D. 2011. Assessing the contribution family data can make to case-control studies of rare variants. Ann Hum Genet 75(5):630-638.
-
(2011)
Ann Hum Genet
, vol.75
, Issue.5
, pp. 630-638
-
-
Curtis, D.1
-
10
-
-
84872389630
-
Rare variant analysis for family-based design
-
De G, Yip WK, Ionita-Laza I, Laird N. 2013. Rare variant analysis for family-based design. PLoS ONE 8(1):e48495.
-
(2013)
PLoS ONE
, vol.8
, Issue.1
, pp. e48495
-
-
De, G.1
Yip, W.K.2
Ionita-Laza, I.3
Laird, N.4
-
11
-
-
84862260138
-
Two adaptive weighting methods to test for rare variant associations in family-based designs
-
Fang S, Sha Q, Zhang S. 2012. Two adaptive weighting methods to test for rare variant associations in family-based designs. Genet Epidemiol 36(5):499-507.
-
(2012)
Genet Epidemiol
, vol.36
, Issue.5
, pp. 499-507
-
-
Fang, S.1
Sha, Q.2
Zhang, S.3
-
12
-
-
82455194220
-
A novel method to detect rare variants using both family and unrelated case-control data
-
Feng T, Elston RC, Zhu X. 2012. A novel method to detect rare variants using both family and unrelated case-control data. BMC Proc 5(Suppl 9):S80.
-
(2012)
BMC Proc
, vol.5
, pp. S80
-
-
Feng, T.1
Elston, R.C.2
Zhu, X.3
-
13
-
-
84862203211
-
Detecting rare variants for quantitative traits using nuclear families
-
Guo W, Shugart YY. 2012. Detecting rare variants for quantitative traits using nuclear families. Hum Hered 73(3):148-158.
-
(2012)
Hum Hered
, vol.73
, Issue.3
, pp. 148-158
-
-
Guo, W.1
Shugart, Y.Y.2
-
14
-
-
71249159145
-
Sequencing the IL4 locus in African Americans implicates rare noncoding variants in asthma susceptibility
-
e9
-
Haller G, Torgerson DG, Ober C, Thompson EE. 2009. Sequencing the IL4 locus in African Americans implicates rare noncoding variants in asthma susceptibility. J Allergy Clin Immunol 124(6):1204-1209, e9.
-
(2009)
J Allergy Clin Immunol
, vol.124
, Issue.6
, pp. 1204-1209
-
-
Haller, G.1
Torgerson, D.G.2
Ober, C.3
Thompson, E.E.4
-
15
-
-
77951028197
-
A data-adaptive sum test for disease association with multiple common or rare variants
-
Han F, Pan W. 2010. A data-adaptive sum test for disease association with multiple common or rare variants. Hum Hered 70(1):42-54.
-
(2010)
Hum Hered
, vol.70
, Issue.1
, pp. 42-54
-
-
Han, F.1
Pan, W.2
-
16
-
-
0029941114
-
NHLBI Family Heart Study: objectives and design
-
Higgins M, Province M, Heiss G, Eckfeldt J, Ellison RC, Folsom AR, Rao DC, Sprafka JM, Williams R. 1996. NHLBI Family Heart Study: objectives and design. Am J Epidemiol 143(12):1219-1228.
-
(1996)
Am J Epidemiol
, vol.143
, Issue.12
, pp. 1219-1228
-
-
Higgins, M.1
Province, M.2
Heiss, G.3
Eckfeldt, J.4
Ellison, R.C.5
Folsom, A.R.6
Rao, D.C.7
Sprafka, J.M.8
Williams, R.9
-
17
-
-
72449120796
-
Multiple rare variants as a cause of a common phenotype: several different lactase persistence associated alleles in a single ethnic group
-
Ingram CJ, Raga TO, Tarekegn A, Browning SL, Elamin MF, Bekele E, Thomas MG, Weale ME, Bradman N, Swallow DM. 2009. Multiple rare variants as a cause of a common phenotype: several different lactase persistence associated alleles in a single ethnic group. J Mol Evol 69(6):579-588.
-
(2009)
J Mol Evol
, vol.69
, Issue.6
, pp. 579-588
-
-
Ingram, C.J.1
Raga, T.O.2
Tarekegn, A.3
Browning, S.L.4
Elamin, M.F.5
Bekele, E.6
Thomas, M.G.7
Weale, M.E.8
Bradman, N.9
Swallow, D.M.10
-
18
-
-
79952253512
-
A new testing strategy to identify rare variants with either risk or protective effect on disease
-
Ionita-Laza I, Buxbaum JD, Laird NM, Lange C. 2011. A new testing strategy to identify rare variants with either risk or protective effect on disease. PLoS Genet 7(2):e1001289.
-
(2011)
PLoS Genet
, vol.7
, Issue.2
, pp. e1001289
-
-
Ionita-Laza, I.1
Buxbaum, J.D.2
Laird, N.M.3
Lange, C.4
-
19
-
-
84884595534
-
Family-based association tests for sequence data, and comparisons with population-based association tests
-
Ionita-Laza I, Lee S, Makarov V, Buxbaum JD, Lin X. 2013. Family-based association tests for sequence data, and comparisons with population-based association tests. Eur J Hum Genet 21(10):1158-1162.
-
(2013)
Eur J Hum Genet
, vol.21
, Issue.10
, pp. 1158-1162
-
-
Ionita-Laza, I.1
Lee, S.2
Makarov, V.3
Buxbaum, J.D.4
Lin, X.5
-
20
-
-
42649084334
-
Rare independent mutations in renal salt handling genes contribute to blood pressure variation
-
Ji W, Foo JN, O'Roak BJ, Zhao H, Larson MG, Simon DB, Newton-Cheh C, State MW, Levy D, Lifton RP. 2008. Rare independent mutations in renal salt handling genes contribute to blood pressure variation. Nat Genet 40(5):592-599.
-
(2008)
Nat Genet
, vol.40
, Issue.5
, pp. 592-599
-
-
Ji, W.1
Foo, J.N.2
O'Roak, B.J.3
Zhao, H.4
Larson, M.G.5
Simon, D.B.6
Newton-Cheh, C.7
State, M.W.8
Levy, D.9
Lifton, R.P.10
-
21
-
-
77950301214
-
Variance component model to account for sample structure in genome-wide association studies
-
Kang HM, Sul JH, Service SK, Zaitlen NA, Kong SY, Freimer NB, Sabatti C, Eskin E. 2010. Variance component model to account for sample structure in genome-wide association studies. Nat Genet 42(4):348-354.
-
(2010)
Nat Genet
, vol.42
, Issue.4
, pp. 348-354
-
-
Kang, H.M.1
Sul, J.H.2
Service, S.K.3
Zaitlen, N.A.4
Kong, S.Y.5
Freimer, N.B.6
Sabatti, C.7
Eskin, E.8
-
22
-
-
45149105926
-
Efficient control of population structure in model organism association mapping
-
Kang HM, Zaitlen NA, Wade CM, Kirby A, Heckerman D, Daly MJ, Eskin E. 2008. Efficient control of population structure in model organism association mapping. Genetics 178(3):1709-1723.
-
(2008)
Genetics
, vol.178
, Issue.3
, pp. 1709-1723
-
-
Kang, H.M.1
Zaitlen, N.A.2
Wade, C.M.3
Kirby, A.4
Heckerman, D.5
Daly, M.J.6
Eskin, E.7
-
23
-
-
82455175501
-
Population-based and family-based designs to analyze rare variants in complex diseases
-
Kazma R, Bailey JN. 2011. Population-based and family-based designs to analyze rare variants in complex diseases. Genet Epidemiol 35(Suppl 1):S41-S47.
-
(2011)
Genet Epidemiol
, vol.35
, pp. S41-S47
-
-
Kazma, R.1
Bailey, J.N.2
-
24
-
-
71449105010
-
A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression
-
and others
-
Knight HM, Pickard BS, Maclean A, Malloy MP, Soares DC, McRae AF, Condie A, White A, Hawkins W, McGhee K and others. 2009. A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression. Am J Hum Genet 85(6):833-846.
-
(2009)
Am J Hum Genet
, vol.85
, Issue.6
, pp. 833-846
-
-
Knight, H.M.1
Pickard, B.S.2
Maclean, A.3
Malloy, M.P.4
Soares, D.C.5
McRae, A.F.6
Condie, A.7
White, A.8
Hawkins, W.9
McGhee, K.10
-
25
-
-
84864942403
-
Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies
-
Lee S, Emond MJ, Bamshad MJ, Barnes KC, Rieder MJ, Nickerson DA, Christiani DC, Wurfel MM, Lin X. 2012. Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies. Am J Hum Genet 91(2):224-237.
-
(2012)
Am J Hum Genet
, vol.91
, Issue.2
, pp. 224-237
-
-
Lee, S.1
Emond, M.J.2
Bamshad, M.J.3
Barnes, K.C.4
Rieder, M.J.5
Nickerson, D.A.6
Christiani, D.C.7
Wurfel, M.M.8
Lin, X.9
-
26
-
-
50949095168
-
Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data
-
Li B, Leal SM. 2008. Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. Am J Hum Genet 83(3):311-321.
-
(2008)
Am J Hum Genet
, vol.83
, Issue.3
, pp. 311-321
-
-
Li, B.1
Leal, S.M.2
-
27
-
-
80052731371
-
A general framework for detecting disease associations with rare variants in sequencing studies
-
Lin DY, Tang ZZ. 2011. A general framework for detecting disease associations with rare variants in sequencing studies. Am J Hum Genet 89(3):354-367.
-
(2011)
Am J Hum Genet
, vol.89
, Issue.3
, pp. 354-367
-
-
Lin, D.Y.1
Tang, Z.Z.2
-
28
-
-
78449245227
-
A novel adaptive method for the analysis of next-generation sequencing data to detect complex trait associations with rare variants due to gene main effects and interactions
-
Liu DJ, Leal SM. 2010. A novel adaptive method for the analysis of next-generation sequencing data to detect complex trait associations with rare variants due to gene main effects and interactions. PLoS Genet 6(10):e1001156.
-
(2010)
PLoS Genet
, vol.6
, Issue.10
, pp. e1001156
-
-
Liu, D.J.1
Leal, S.M.2
-
29
-
-
61449168010
-
A groupwise association test for rare mutations using a weighted sum statistic
-
Madsen BE, Browning SR. 2009. A groupwise association test for rare mutations using a weighted sum statistic. PLoS Genet 5(2):e1000384.
-
(2009)
PLoS Genet
, vol.5
, Issue.2
, pp. e1000384
-
-
Madsen, B.E.1
Browning, S.R.2
-
30
-
-
33846014328
-
A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: a cohort allelic sums test (CAST)
-
Morgenthaler S, Thilly WG. 2007. A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: a cohort allelic sums test (CAST). Mutat Res 615(1-2):28-56.
-
(2007)
Mutat Res
, vol.615
, Issue.1-2
, pp. 28-56
-
-
Morgenthaler, S.1
Thilly, W.G.2
-
31
-
-
76649136928
-
An evaluation of statistical approaches to rare variant analysis in genetic association studies
-
Morris AP, Zeggini E. 2010. An evaluation of statistical approaches to rare variant analysis in genetic association studies. Genet Epidemiol 34(2):188-193.
-
(2010)
Genet Epidemiol
, vol.34
, Issue.2
, pp. 188-193
-
-
Morris, A.P.1
Zeggini, E.2
-
32
-
-
71249106757
-
Identification of novel putative rheumatoid arthritis susceptibility genes via analysis of rare variants
-
Morris AP, Zeggini E, Lindgren CM. 2009. Identification of novel putative rheumatoid arthritis susceptibility genes via analysis of rare variants. BMC Proc 3(Suppl 7):S131.
-
(2009)
BMC Proc
, vol.3
, pp. S131
-
-
Morris, A.P.1
Zeggini, E.2
Lindgren, C.M.3
-
33
-
-
79953752624
-
Testing for an unusual distribution of rare variants
-
Neale BM, Rivas MA, Voight BF, Altshuler D, Devlin B, Orho-Melander M, Kathiresan S, Purcell SM, Roeder K, Daly MJ. 2011. Testing for an unusual distribution of rare variants. PLoS Genet 7(3):e1001322.
-
(2011)
PLoS Genet
, vol.7
, Issue.3
, pp. e1001322
-
-
Neale, B.M.1
Rivas, M.A.2
Voight, B.F.3
Altshuler, D.4
Devlin, B.5
Orho-Melander, M.6
Kathiresan, S.7
Purcell, S.M.8
Roeder, K.9
Daly, M.J.10
-
34
-
-
65249131713
-
Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes
-
Nejentsev S, Walker N, Riches D, Egholm M, Todd JA. 2009. Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes. Science 324(5925):387-389.
-
(2009)
Science
, vol.324
, Issue.5925
, pp. 387-389
-
-
Nejentsev, S.1
Walker, N.2
Riches, D.3
Egholm, M.4
Todd, J.A.5
-
35
-
-
79958103103
-
Health and function of participants in the Long Life Family Study: A comparison with other cohorts
-
and others
-
Newman AB, Glynn NW, Taylor CA, Sebastiani P, Perls TT, Mayeux R, Christensen K, Zmuda JM, Barral S, Lee JH and others. 2011. Health and function of participants in the Long Life Family Study: A comparison with other cohorts. Aging (Albany NY) 3(1):63-76.
-
(2011)
Aging (Albany NY)
, vol.3
, Issue.1
, pp. 63-76
-
-
Newman, A.B.1
Glynn, N.W.2
Taylor, C.A.3
Sebastiani, P.4
Perls, T.T.5
Mayeux, R.6
Christensen, K.7
Zmuda, J.M.8
Barral, S.9
Lee, J.H.10
-
36
-
-
84876408555
-
Adjusted sequence kernel association test for rare variants controlling for cryptic and family relatedness
-
Oualkacha K, Dastani Z, Li R, Cingolani PE, Spector TD, Hammond CJ, Richards JB, Ciampi A, Greenwood CM. 2013. Adjusted sequence kernel association test for rare variants controlling for cryptic and family relatedness. Genet Epidemiol 37(4):366-376.
-
(2013)
Genet Epidemiol
, vol.37
, Issue.4
, pp. 366-376
-
-
Oualkacha, K.1
Dastani, Z.2
Li, R.3
Cingolani, P.E.4
Spector, T.D.5
Hammond, C.J.6
Richards, J.B.7
Ciampi, A.8
Greenwood, C.M.9
-
37
-
-
79958100783
-
Adaptive tests for association analysis of rare variants
-
Pan W, Shen X. 2011. Adaptive tests for association analysis of rare variants. Genet Epidemiol. 35(5):381-388.
-
(2011)
Genet Epidemiol.
, vol.35
, Issue.5
, pp. 381-388
-
-
Pan, W.1
Shen, X.2
-
38
-
-
77953121877
-
Pooled association tests for rare variants in exon-resequencing studies
-
Price AL, Kryukov GV, de Bakker PI, Purcell SM, Staples J, Wei LJ, Sunyaev SR. 2010. Pooled association tests for rare variants in exon-resequencing studies. Am J Hum Genet 86(6):832-838.
-
(2010)
Am J Hum Genet
, vol.86
, Issue.6
, pp. 832-838
-
-
Price, A.L.1
Kryukov, G.V.2
de Bakker, P.I.3
Purcell, S.M.4
Staples, J.5
Wei, L.J.6
Sunyaev, S.R.7
-
39
-
-
61749090233
-
Rare loss-of-function mutations in ANGPTL family members contribute to plasma triglyceride levels in humans
-
Romeo S, Yin W, Kozlitina J, Pennacchio LA, Boerwinkle E, Hobbs HH, Cohen JC. 2009. Rare loss-of-function mutations in ANGPTL family members contribute to plasma triglyceride levels in humans. J Clin Invest 119(1):70-79.
-
(2009)
J Clin Invest
, vol.119
, Issue.1
, pp. 70-79
-
-
Romeo, S.1
Yin, W.2
Kozlitina, J.3
Pennacchio, L.A.4
Boerwinkle, E.5
Hobbs, H.H.6
Cohen, J.C.7
-
40
-
-
70349565939
-
Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis
-
and others
-
Sabatelli M, Eusebi F, Al-Chalabi A, Conte A, Madia F, Luigetti M, Mancuso I, Limatola C, Trettel F, Sobrero F and others. 2009. Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis. Hum Mol Genet 18(20):3997-4006.
-
(2009)
Hum Mol Genet
, vol.18
, Issue.20
, pp. 3997-4006
-
-
Sabatelli, M.1
Eusebi, F.2
Al-Chalabi, A.3
Conte, A.4
Madia, F.5
Luigetti, M.6
Mancuso, I.7
Limatola, C.8
Trettel, F.9
Sobrero, F.10
-
41
-
-
84876410197
-
A unified mixed-effects model for rare-variant association in sequencing studies
-
Sun J, Zheng Y, Hsu L. 2013. A unified mixed-effects model for rare-variant association in sequencing studies. Genet Epidemiol 37(4):334-344.
-
(2013)
Genet Epidemiol
, vol.37
, Issue.4
, pp. 334-344
-
-
Sun, J.1
Zheng, Y.2
Hsu, L.3
-
42
-
-
80051499915
-
Rare-variant association testing for sequencing data with the sequence kernel association test
-
Wu MC, Lee S, Cai T, Li Y, Boehnke M, Lin X. 2011. Rare-variant association testing for sequencing data with the sequence kernel association test. Am J Hum Genet 89(1):82-93.
-
(2011)
Am J Hum Genet
, vol.89
, Issue.1
, pp. 82-93
-
-
Wu, M.C.1
Lee, S.2
Cai, T.3
Li, Y.4
Boehnke, M.5
Lin, X.6
-
43
-
-
82455211264
-
Identifying causal rare variants of disease through family-based analysis of Genetics Analysis Workshop 17 data set
-
Yip WK, De G, Raby BA, Laird N. 2011. Identifying causal rare variants of disease through family-based analysis of Genetics Analysis Workshop 17 data set. BMC Proc 5 (Suppl 9):S21.
-
(2011)
BMC Proc
, vol.5
, pp. S21
-
-
Yip, W.K.1
De, G.2
Raby, B.A.3
Laird, N.4
-
44
-
-
31744440502
-
A unified mixed-model method for association mapping that accounts for multiple levels of relatedness
-
and others
-
Yu J, Pressoir G, Briggs WH, Vroh Bi I, Yamasaki M, Doebley JF, McMullen MD, Gaut BS, Nielsen DM, Holland JB and others. 2006. A unified mixed-model method for association mapping that accounts for multiple levels of relatedness. Nat Genet 38(2):203-208.
-
(2006)
Nat Genet
, vol.38
, Issue.2
, pp. 203-208
-
-
Yu, J.1
Pressoir, G.2
Briggs, W.H.3
Vroh Bi, I.4
Yamasaki, M.5
Doebley, J.F.6
McMullen, M.D.7
Gaut, B.S.8
Nielsen, D.M.9
Holland, J.B.10
-
45
-
-
82455183195
-
Methods for adjusting population structure and familial relatedness in association test for collective effect of multiple rare variants on quantitative traits
-
Zhang Q, Chung D, Kraja A, Borecki, II, Province MA. 2011a. Methods for adjusting population structure and familial relatedness in association test for collective effect of multiple rare variants on quantitative traits. BMC Proc 5(Suppl 9):S35.
-
(2011)
BMC Proc
, vol.5
, pp. S35
-
-
Zhang, Q.1
Chung, D.2
Kraja, A.3
Borecki, I.I.4
Province, M.A.5
-
46
-
-
80054750776
-
A data-driven method for identifying rare variants with heterogeneous trait effects
-
Zhang Q, Irvin MR, Arnett DK, Province MA, Borecki I. 2011b. A data-driven method for identifying rare variants with heterogeneous trait effects. Genet Epidemiol 35(7):679-685.
-
(2011)
Genet Epidemiol
, vol.35
, Issue.7
, pp. 679-685
-
-
Zhang, Q.1
Irvin, M.R.2
Arnett, D.K.3
Province, M.A.4
Borecki, I.5
-
47
-
-
76649122154
-
Detecting rare variants for complex traits using family and unrelated data
-
Zhu X, Feng T, Li Y, Lu Q, Elston RC. 2009. Detecting rare variants for complex traits using family and unrelated data. Genet Epidemiol 34(2):171-187.
-
(2009)
Genet Epidemiol
, vol.34
, Issue.2
, pp. 171-187
-
-
Zhu, X.1
Feng, T.2
Li, Y.3
Lu, Q.4
Elston, R.C.5
|