-
1
-
-
0003415792
-
-
5th edn Churchill, Livingstone
-
Ronald, H., Edward, J. B., Sanford, J. S., Bruce, F., Leslie, E., Philip, M. et al. Hematology: basic principles and practice 5th edn (Churchill, Livingstone, 2009).
-
(2009)
Hematology: Basic Principles and Practice
-
-
Ronald, H.1
Edward, J.B.2
Sanford, J.S.3
Bruce, F.4
Leslie, E.5
Philip, M.6
-
2
-
-
70350657093
-
Genes determining blood cell traits
-
Andrews, N. C. Genes determining blood cell traits. Nat. Genet. 41, 1161-1162 (2009).
-
(2009)
Nat. Genet.
, vol.41
, pp. 1161-1162
-
-
Andrews, N.C.1
-
3
-
-
0025720068
-
Influence of platelet size on outcome after myocardial infarction
-
Martin, J. F., Bath, P. M. & Burr, M. L. Influence of platelet size on outcome after myocardial infarction. Lancet. 338, 1409-1411 (1991).
-
(1991)
Lancet
, vol.338
, pp. 1409-1411
-
-
Martin, J.F.1
Bath, P.M.2
Burr, M.L.3
-
4
-
-
0021821260
-
Genetic and environmental influences on the size and number of cells in the blood
-
Whitfield, J. B. & Martin, N. G. Genetic and environmental influences on the size and number of cells in the blood. Genet. Epidemiol. 2, 133-144 (1985).
-
(1985)
Genet. Epidemiol.
, vol.2
, pp. 133-144
-
-
Whitfield, J.B.1
Martin, N.G.2
-
5
-
-
0033374163
-
Genetic and environmental causes of variation in basal levels of blood cells
-
Evans, D. M., Frazer, I. H. & Martin, N. G. Genetic and environmental causes of variation in basal levels of blood cells. Twin. Res. 2, 250-257 (1999).
-
(1999)
Twin. Res.
, vol.2
, pp. 250-257
-
-
Evans, D.M.1
Frazer, I.H.2
Martin, N.G.3
-
6
-
-
0034303433
-
Genetic influence on peripheral blood T lymphocyte levels
-
Hall, M. A., Ahmadi, K. R., Norman, P., Snieder, H., MacGregor, A. J., Vaughan, R. W. et al. Genetic influence on peripheral blood T lymphocyte levels. Genes. Immun. 1, 423-427 (2000).
-
(2000)
Genes. Immun.
, vol.1
, pp. 423-427
-
-
Hall, M.A.1
Ahmadi, K.R.2
Norman, P.3
Snieder, H.4
MacGregor, A.J.5
Vaughan, R.W.6
-
7
-
-
0016842252
-
Smoking, oral contraceptives, and obesity. Effects on white blood cell count
-
Fisch, I. R. & Freedman, S. H. Smoking, oral contraceptives, and obesity. Effects on white blood cell count. JAMA. 234, 500-506 (1975).
-
(1975)
JAMA
, vol.234
, pp. 500-506
-
-
Fisch, I.R.1
Freedman, S.H.2
-
8
-
-
0027524618
-
Apparent polycythaemia: Diagnosis, pathogenesis and management
-
Messinezy, M. & Pearson, T. C. Apparent polycythaemia: diagnosis, pathogenesis and management. Eur. J. Haematol. 51, 125-131 (1993).
-
(1993)
Eur. J. Haematol.
, vol.51
, pp. 125-131
-
-
Messinezy, M.1
Pearson, T.C.2
-
9
-
-
77949908008
-
A revised scheme for developmental pathways of hematopoietic cells: The myeloid-based model
-
Kawamoto, H., Wada, H. & Katsura, Y. A revised scheme for developmental pathways of hematopoietic cells: the myeloid-based model. Int. Immunol. 22, 65-70 (2010).
-
(2010)
Int. Immunol.
, vol.22
, pp. 65-70
-
-
Kawamoto, H.1
Wada, H.2
Katsura, Y.3
-
10
-
-
77049273556
-
Correlation of absolute basophil and eosinophil counts in blood from institutionalized human subjects
-
Elveback, L., Gully, R. J., Halberg, F. & Hamerston, O. Correlation of absolute basophil and eosinophil counts in blood from institutionalized human subjects. J. Appl. Physiol. 9, 205-207 (1956).
-
(1956)
J. Appl. Physiol.
, vol.9
, pp. 205-207
-
-
Elveback, L.1
Gully, R.J.2
Halberg, F.3
Hamerston, O.4
-
11
-
-
0021330196
-
Normal values for peripheral blood white cell counts in women of four different ethnic origins
-
Bain, B., Seed, M. & Godsland, I. Normal values for peripheral blood white cell counts in women of four different ethnic origins. J. Clin. Pathol. 37, 188-193 (1984).
-
(1984)
J. Clin. Pathol.
, vol.37
, pp. 188-193
-
-
Bain, B.1
Seed, M.2
Godsland, I.3
-
12
-
-
77952915346
-
2008 Japanese Society for Dialysis Therapy: Guidelines for renal anemia in chronic kidney disease
-
Tsubakihara, Y., Nishi, S., Akiba, T., Hirakata, H., Iseki, K., Kubota, M. et al. 2008 Japanese Society for Dialysis Therapy: guidelines for renal anemia in chronic kidney disease. Ther. Apher. Dial. 14, 240-275 (2010).
-
(2010)
Ther. Apher. Dial.
, vol.14
, pp. 240-275
-
-
Tsubakihara, Y.1
Nishi, S.2
Akiba, T.3
Hirakata, H.4
Iseki, K.5
Kubota, M.6
-
13
-
-
67249117049
-
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
-
Hindorff, L. A., Sethupathy, P., Junkins, H. A., Ramos, E. M., Mehta, J. P., Collins, F. S. et al. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc. Natl. Acad. Sci. U.S.A. 106, 9362-9367 (2009).
-
(2009)
Proc. Natl. Acad. Sci. U.S.A.
, vol.106
, pp. 9362-9367
-
-
Hindorff, L.A.1
Sethupathy, P.2
Junkins, H.A.3
Ramos, E.M.4
Mehta, J.P.5
Collins, F.S.6
-
14
-
-
18744407845
-
Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction
-
Ozaki, K., Ohnishi, Y., Iida, A., Sekine, A., Yamada, R., Tsunoda, T. et al. Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction. Nat. Genet. 32, 650-654 (2002).
-
(2002)
Nat. Genet.
, vol.32
, pp. 650-654
-
-
Ozaki, K.1
Ohnishi, Y.2
Iida, A.3
Sekine, A.4
Yamada, R.5
Tsunoda, T.6
-
15
-
-
23944469845
-
Recent developments in genomewide association scans: A workshop summary and review
-
Thomas, D. C., Haile, R. W. & Duggan, D. Recent developments in genomewide association scans: a workshop summary and review. Am. J. Hum. Genet. 77, 337-345 (2005).
-
(2005)
Am. J. Hum. Genet.
, vol.77
, pp. 337-345
-
-
Thomas, D.C.1
Haile, R.W.2
Duggan, D.3
-
17
-
-
84969213492
-
Genome-wide association study of 14000 cases of seven common diseases and 3000 shared controls
-
The WTCCC. Genome-wide association study of 14000 cases of seven common diseases and 3000 shared controls. Nature 447, 661-678 (2007).
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
The, W.1
-
18
-
-
77957947562
-
Hundreds of variants clustered in genomic loci and biological pathways affect human height
-
Lango Allen, H., Estrada, K., Lettre, G., Berndt, S. I., Weedon, M. N., Rivadeneira, F. et al. Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature. 467, 832-838 (2010).
-
(2010)
Nature
, vol.467
, pp. 832-838
-
-
Lango Allen, H.1
Estrada, K.2
Lettre, G.3
Berndt, S.I.4
Weedon, M.N.5
Rivadeneira, F.6
-
19
-
-
77953507639
-
A genome-wide association study in 19633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci
-
Okada, Y., Kamatani, Y., Takahashi, A., Matsuda, K., Hosono, N., Ohmiya, H. et al. A genome-wide association study in 19633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. Hum. Mol. Genet. 19, 2303-2312 (2010).
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. 2303-2312
-
-
Okada, Y.1
Kamatani, Y.2
Takahashi, A.3
Matsuda, K.4
Hosono, N.5
Ohmiya, H.6
-
20
-
-
34547450531
-
Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults
-
Thein, S. L., Menzel, S., Peng, X., Best, S., Jiang, J., Close, J. et al. Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults. Proc. Natl. Acad. Sci. U. S. A. 104, 11346-11351 (2007).
-
(2007)
Proc. Natl. Acad. Sci. U. S. A.
, vol.104
, pp. 11346-11351
-
-
Thein, S.L.1
Menzel, S.2
Peng, X.3
Best, S.4
Jiang, J.5
Close, J.6
-
21
-
-
38749132020
-
Admixture mapping of white cell count: Genetic locus responsible for lower white blood cell count in the Health ABC and Jackson Heart studies
-
Nalls, M. A., Wilson, J. G., Patterson, N. J., Tandon, A., Zmuda, J. M., Huntsman, S. et al. Admixture mapping of white cell count: genetic locus responsible for lower white blood cell count in the Health ABC and Jackson Heart studies. Am. J. Hum. Genet. 82, 81-87 (2008).
-
(2008)
Am. J. Hum. Genet.
, vol.82
, pp. 81-87
-
-
Nalls, M.A.1
Wilson, J.G.2
Patterson, N.J.3
Tandon, A.4
Zmuda, J.M.5
Huntsman, S.6
-
22
-
-
40349092939
-
Genomewide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia
-
Uda, M., Galanello, R., Sanna, S., Lettre, G., Sankaran, V. G., Chen, W. et al. Genomewide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. Proc. Natl. Acad. Sci. U. S. A. 105, 1620-1625 (2008).
-
(2008)
Proc. Natl. Acad. Sci. U. S. A.
, vol.105
, pp. 1620-1625
-
-
Uda, M.1
Galanello, R.2
Sanna, S.3
Lettre, G.4
Sankaran, V.G.5
Chen, W.6
-
23
-
-
50149117726
-
DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease
-
Lettre, G., Sankaran, V. G., Bezerra, M. A., Araujo, A. S., Uda,M., Sanna, S. et al. DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease. Proc. Natl. Acad. Sci. U. S. A. 105, 11869-11874 (2008).
-
(2008)
Proc. Natl. Acad. Sci. U. S. A.
, vol.105
, pp. 11869-11874
-
-
Lettre, G.1
Sankaran, V.G.2
Bezerra, M.A.3
Araujo, A.S.4
Uda, M.5
Sanna, S.6
-
24
-
-
58049220179
-
A genome-wide association study identifies three loci associated with mean platelet volume
-
Meisinger, C., Prokisch, H., Gieger, C., Soranzo, N., Mehta, D., Rosskopf, D. et al. A genome-wide association study identifies three loci associated with mean platelet volume. Am. J. Hum. Genet. 84, 66-71 (2009).
-
(2009)
Am. J. Hum. Genet.
, vol.84
, pp. 66-71
-
-
Meisinger, C.1
Prokisch, H.2
Gieger, C.3
Soranzo, N.4
Mehta, D.5
Rosskopf, D.6
-
25
-
-
59249102648
-
Reduced neutrophil count in people of African descent is due to a regulatory variant in the Duffy antigen receptor for chemokines gene
-
Reich, D., Nalls, M. A., Kao, W. H., Akylbekova, E. L., Tandon, A., Patterson, N. et al. Reduced neutrophil count in people of African descent is due to a regulatory variant in the Duffy antigen receptor for chemokines gene. PLoS. Genet. 5, e1000360 (2009).
-
(2009)
PLoS. Genet.
, vol.5
-
-
Reich, D.1
Nalls, M.A.2
Kao, W.H.3
Akylbekova, E.L.4
Tandon, A.5
Patterson, N.6
-
26
-
-
61349089164
-
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction
-
Gudbjartsson, D. F., Bjornsdottir, U. S., Halapi, E., Helgadottir, A., Sulem, P., Jonsdottir, G. M. et al. Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. Nat. Genet. 41, 342-347 (2009).
-
(2009)
Nat. Genet.
, vol.41
, pp. 342-347
-
-
Gudbjartsson, D.F.1
Bjornsdottir, U.S.2
Halapi, E.3
Helgadottir, A.4
Sulem, P.5
Jonsdottir, G.M.6
-
27
-
-
65549162781
-
A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function
-
Soranzo, N., Rendon, A., Gieger, C., Jones, C. I., Watkins, N. A., Menzel, S. et al. A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function. Blood. 113, 3831-3837 (2009).
-
(2009)
Blood
, vol.113
, pp. 3831-3837
-
-
Soranzo, N.1
Rendon, A.2
Gieger, C.3
Jones, C.I.4
Watkins, N.A.5
Menzel, S.6
-
28
-
-
70350644759
-
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
-
Soranzo, N., Spector, T. D., Mangino, M., Kuhnel, B., Rendon, A., Teumer, A. et al. A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. Nat. Genet. 41, 1182-1190 (2009).
-
(2009)
Nat. Genet.
, vol.41
, pp. 1182-1190
-
-
Soranzo, N.1
Spector, T.D.2
Mangino, M.3
Kuhnel, B.4
Rendon, A.5
Teumer, A.6
-
29
-
-
70350646902
-
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
-
Ganesh, S. K., Zakai, N. A., van Rooij, F. J., Soranzo, N., Smith, A. V., Nalls, M. A. et al. Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. Nat. Genet. 41, 1191-1198 (2009).
-
(2009)
Nat. Genet.
, vol.41
, pp. 1191-1198
-
-
Ganesh, S.K.1
Zakai, N.A.2
Van Rooij, F.J.3
Soranzo, N.4
Smith, A.V.5
Nalls, M.A.6
-
30
-
-
70350638919
-
Genomewide association study identifies variants in TMPRSS6 associated with hemoglobin levels
-
Chambers, J. C., Zhang, W., Li, Y., Sehmi, J., Wass, M. N., Zabaneh, D. et al. Genomewide association study identifies variants in TMPRSS6 associated with hemoglobin levels. Nat. Genet. 41, 1170-1172 (2009).
-
(2009)
Nat. Genet.
, vol.41
, pp. 1170-1172
-
-
Chambers, J.C.1
Zhang, W.2
Li, Y.3
Sehmi, J.4
Wass, M.N.5
Zabaneh, D.6
-
31
-
-
70350628958
-
Common variants in TMPRSS6 are associated with iron status and erythrocyte volume
-
Benyamin, B., Ferreira, M. A., Willemsen, G., Gordon, S., Middelberg, R. P., McEvoy, B. P. et al. Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. Nat. Genet. 41, 1173-1175 (2009).
-
(2009)
Nat. Genet.
, vol.41
, pp. 1173-1175
-
-
Benyamin, B.1
Ferreira, M.A.2
Willemsen, G.3
Gordon, S.4
Middelberg, R.P.5
McEvoy, B.P.6
-
32
-
-
72149102717
-
Sequence variants in three loci influence monocyte counts and erythrocyte volume
-
Ferreira, M. A., Hottenga, J. J., Warrington, N. M., Medland, S. E., Willemsen, G., Lawrence, R. W. et al. Sequence variants in three loci influence monocyte counts and erythrocyte volume. Am. J. Hum. Genet. 85, 745-749 (2009).
-
(2009)
Am. J. Hum. Genet.
, vol.85
, pp. 745-749
-
-
Ferreira, M.A.1
Hottenga, J.J.2
Warrington, N.M.3
Medland, S.E.4
Willemsen, G.5
Lawrence, R.W.6
-
33
-
-
73149124061
-
Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control
-
Ferreira, M. A., Mangino, M., Brumme, C. J., Zhao, Z. Z., Medland, S. E., Wright, M. J. et al. Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control. Am. J. Hum. Genet. 86, 88-92 (2010).
-
(2010)
Am. J. Hum. Genet.
, vol.86
, pp. 88-92
-
-
Ferreira, M.A.1
Mangino, M.2
Brumme, C.J.3
Zhao, Z.Z.4
Medland, S.E.5
Wright, M.J.6
-
34
-
-
77649184039
-
Genomewide association study of hematological and biochemical traits in a Japanese population
-
Kamatani, Y., Matsuda, K., Okada, Y., Kubo, M., Hosono, N., Daigo, Y. et al. Genomewide association study of hematological and biochemical traits in a Japanese population. Nat. Genet. 42, 210-215 (2010).
-
(2010)
Nat. Genet.
, vol.42
, pp. 210-215
-
-
Kamatani, Y.1
Matsuda, K.2
Okada, Y.3
Kubo, M.4
Hosono, N.5
Daigo, Y.6
-
35
-
-
77952473808
-
Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count
-
Okada, Y., Kamatani, Y., Takahashi, A., Matsuda, K., Hosono, N., Ohmiya, H. et al. Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count. Hum. Mol. Genet. 19, 2079-2085 (2010).
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. 2079-2085
-
-
Okada, Y.1
Kamatani, Y.2
Takahashi, A.3
Matsuda, K.4
Hosono, N.5
Ohmiya, H.6
-
36
-
-
77954926596
-
Natural selection on EPAS1 (HIF2alpha) associated with low hemoglobin concentration in Tibetan highlanders
-
Beall, C. M., Cavalleri, G. L., Deng, L., Elston, R. C., Gao, Y., Knight, J. et al. Natural selection on EPAS1 (HIF2alpha) associated with low hemoglobin concentration in Tibetan highlanders. Proc. Natl. Acad. Sci. U. S. A. 107, 11459-11464 (2010).
-
(2010)
Proc. Natl. Acad. Sci. U. S. A.
, vol.107
, pp. 11459-11464
-
-
Beall, C.M.1
Cavalleri, G.L.2
Deng, L.3
Elston, R.C.4
Gao, Y.5
Knight, J.6
-
37
-
-
77958522275
-
A genome-wide association study of red blood cell traits using the electronic medical record
-
Kullo, I. J., Ding, K., Jouni, H., Smith, C. Y. & Chute, C. G. A genome-wide association study of red blood cell traits using the electronic medical record. PLoS. One. 5, e13011 (2010).
-
(2010)
PLoS. One
, vol.5
-
-
Kullo, I.J.1
Ding, K.2
Jouni, H.3
Smith, C.Y.4
Chute, C.G.5
-
38
-
-
79953756857
-
Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans
-
Lo, K. S., Wilson, J. G., Lange, L. A., Folsom, A. R., Galarneau, G., Ganesh, S. K. et al. Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans. Hum. Genet. 129, 307-317 (2011).
-
(2011)
Hum. Genet.
, vol.129
, pp. 307-317
-
-
Lo, K.S.1
Wilson, J.G.2
Lange, L.A.3
Folsom, A.R.4
Galarneau, G.5
Ganesh, S.K.6
-
39
-
-
79959824142
-
Multiple Loci are associated with white blood cell phenotypes
-
Nalls, M. A., Couper, D. J., Tanaka, T., van Rooij, F. J., Chen, M. H., Smith, A. V. et al. Multiple Loci are associated with white blood cell phenotypes. PLoS. Genet. 7, e1002113 (2011).
-
(2011)
PLoS. Genet.
, vol.7
-
-
Nalls, M.A.1
Couper, D.J.2
Tanaka, T.3
Van Rooij, F.J.4
Chen, M.H.5
Smith, A.V.6
-
40
-
-
79959812503
-
Genome-Wide Association Study of White Blood Cell Count in 16388 African Americans: The Continental Origins and Genetic Epidemiology Network (COGENT)
-
Reiner, A. P., Lettre, G., Nalls, M. A., Ganesh, S. K., Mathias, R., Austin, M. A. et al. Genome-Wide Association Study of White Blood Cell Count in 16388 African Americans: the Continental Origins and Genetic Epidemiology Network (COGENT). PLoS. Genet. 7, e1002108 (2011).
-
(2011)
PLoS. Genet.
, vol.7
-
-
Reiner, A.P.1
Lettre, G.2
Nalls, M.A.3
Ganesh, S.K.4
Mathias, R.5
Austin, M.A.6
-
41
-
-
79959859184
-
Identification of nine novel loci associated with white blood cell subtypes in a Japanese population
-
Okada, Y., Hirota, T., Kamatani, Y., Takahashi, A., Ohmiya, H., Kumasaka, N. et al. Identification of nine novel loci associated with white blood cell subtypes in a Japanese population. PLoS. Genet. 7, e1002067 (2011).
-
(2011)
PLoS. Genet.
, vol.7
-
-
Okada, Y.1
Hirota, T.2
Kamatani, Y.3
Takahashi, A.4
Ohmiya, H.5
Kumasaka, N.6
-
42
-
-
79960845833
-
LPAR1 and ITGA4 regulate peripheral blood monocyte counts
-
Maugeri, N., Powell, J. E., t Hoen, P. A., de Geus, E. J., Willemsen, G., Kattenberg, M. et al. LPAR1 and ITGA4 regulate peripheral blood monocyte counts. Hum. Mutat. 32, 873-876 (2011).
-
(2011)
Hum. Mutat.
, vol.32
, pp. 873-876
-
-
Maugeri, N.1
Powell, J.E.2
T Hoen, P.A.3
De Geus, E.J.4
Willemsen, G.5
Kattenberg, M.6
-
43
-
-
83055161438
-
New gene functions in megakaryopoiesis and platelet formation
-
Gieger, C., Radhakrishnan, A., Cvejic, A., Tang, W., Porcu, E., Pistis, G. et al. New gene functions in megakaryopoiesis and platelet formation. Nature. 480, 201-208 (2011).
-
(2011)
Nature.
, vol.480
, pp. 201-208
-
-
Gieger, C.1
Radhakrishnan, A.2
Cvejic, A.3
Tang, W.4
Porcu, E.5
Pistis, G.6
-
44
-
-
69549124480
-
CD4+CD25-LAG3+ regulatory T cells controlled by the transcription factor Egr-2
-
Okamura, T., Fujio, K., Shibuya, M., Sumitomo, S., Shoda, H., Sakaguchi, S. et al. CD4+CD25-LAG3+ regulatory T cells controlled by the transcription factor Egr-2. Proc. Natl. Acad. Sci. U. S. A. 106, 13974-13979 (2009).
-
(2009)
Proc. Natl. Acad. Sci. U. S. A.
, vol.106
, pp. 13974-13979
-
-
Okamura, T.1
Fujio, K.2
Shibuya, M.3
Sumitomo, S.4
Shoda, H.5
Sakaguchi, S.6
-
45
-
-
0034119167
-
Neutrophils: Molecules, functions and pathophysiological aspects
-
Witko-Sarsat, V., Rieu, P., Descamps-Latscha, B., Lesavre, P. & Halbwachs-Mecarelli, L. Neutrophils: molecules, functions and pathophysiological aspects. Lab. Invest. 80, 617-653 (2000).
-
(2000)
Lab. Invest.
, vol.80
, pp. 617-653
-
-
Witko-Sarsat, V.1
Rieu, P.2
Descamps-Latscha, B.3
Lesavre, P.4
Halbwachs-Mecarelli, L.5
-
46
-
-
67049144615
-
Eosinophilic and neutrophilic inflammation in asthma: Insights from clinical studies
-
Fahy, J. V. Eosinophilic and neutrophilic inflammation in asthma: insights from clinical studies. Proc. Am. Thorac. Soc. 6, 256-259 (2009).
-
(2009)
Proc. Am. Thorac. Soc.
, vol.6
, pp. 256-259
-
-
Fahy, J.V.1
-
47
-
-
77958185103
-
Nomenclature of monocytes and dendritic cells in blood
-
Ziegler-Heitbrock, L., Ancuta, P., Crowe, S., Dalod, M., Grau, V., Hart, D. N. et al. Nomenclature of monocytes and dendritic cells in blood. Blood. 116, e74-e80 (2010).
-
(2010)
Blood
, vol.116
-
-
Ziegler-Heitbrock, L.1
Ancuta, P.2
Crowe, S.3
Dalod, M.4
Grau, V.5
Hart, D.N.6
-
48
-
-
58149218230
-
Basophils: A nonredundant contributor to host immunity
-
Sullivan, B. M. & Locksley, R. M. Basophils: a nonredundant contributor to host immunity. Immunity. 30, 12-20 (2009).
-
(2009)
Immunity.
, vol.30
, pp. 12-20
-
-
Sullivan, B.M.1
Locksley, R.M.2
-
49
-
-
68349130434
-
Haemopoietic processes in allergic disease: Eosinophil/basophil development
-
Gauvreau, G. M., Ellis, A. K. & Denburg, J. A. Haemopoietic processes in allergic disease: eosinophil/basophil development. Clin. Exp. Allergy. 39, 1297-1306 (2009).
-
(2009)
Clin. Exp. Allergy
, vol.39
, pp. 1297-1306
-
-
Gauvreau, G.M.1
Ellis, A.K.2
Denburg, J.A.3
-
50
-
-
67649227119
-
Basophils contribute to T(H)2-IgE responses in vivo via IL-4 production and presentation of peptide-MHC class II complexes to CD4+ T cells
-
Yoshimoto, T., Yasuda, K., Tanaka, H., Nakahira, M., Imai, Y., Fujimori, Y. et al. Basophils contribute to T(H)2-IgE responses in vivo via IL-4 production and presentation of peptide-MHC class II complexes to CD4+ T cells. Nat. Immunol. 10, 706-712 (2009).
-
(2009)
Nat. Immunol.
, vol.10
, pp. 706-712
-
-
Yoshimoto, T.1
Yasuda, K.2
Tanaka, H.3
Nakahira, M.4
Imai, Y.5
Fujimori, Y.6
-
51
-
-
70349756907
-
Genetic control of resistance to human malaria
-
Allison, A. C. Genetic control of resistance to human malaria. Curr. Opin. Immunol. 21, 499-505 (2009).
-
(2009)
Curr. Opin. Immunol.
, vol.21
, pp. 499-505
-
-
Allison, A.C.1
-
52
-
-
0022621191
-
Molecular cloning and expression of cDNA for human granulocyte colony-stimulating factor
-
Nagata, S., Tsuchiya, M., Asano, S., Kaziro, Y., Yamazaki, T., Yamamoto, O. et al. Molecular cloning and expression of cDNA for human granulocyte colony-stimulating factor. Nature. 319, 415-418 (1986).
-
(1986)
Nature
, vol.319
, pp. 415-418
-
-
Nagata, S.1
Tsuchiya, M.2
Asano, S.3
Kaziro, Y.4
Yamazaki, T.5
Yamamoto, O.6
-
53
-
-
33646490285
-
Lineage-specific hematopoietic growth factors
-
Kaushansky, K. Lineage-specific hematopoietic growth factors. N. Engl. J. Med. 354, 2034-2045 (2006).
-
(2006)
N. Engl. J. Med.
, vol.354
, pp. 2034-2045
-
-
Kaushansky, K.1
-
54
-
-
0036696904
-
Alpha4 integrins and the immune response
-
Rose, D. M., Han, J. & Ginsberg, M. H. Alpha4 integrins and the immune response. Immunol. Rev. 186, 118-124 (2002).
-
(2002)
Immunol. Rev.
, vol.186
, pp. 118-124
-
-
Rose, D.M.1
Han, J.2
Ginsberg, M.H.3
-
55
-
-
77956637896
-
Genetics and beyond-the transcriptome of human monocytes and disease susceptibility
-
Zeller, T., Wild, P., Szymczak, S., Rotival, M., Schillert, A., Castagne, R. et al. Genetics and beyond-the transcriptome of human monocytes and disease susceptibility. PLoS. One. 5, e10693 (2010).
-
(2010)
PLoS. One
, vol.5
-
-
Zeller, T.1
Wild, P.2
Szymczak, S.3
Rotival, M.4
Schillert, A.5
Castagne, R.6
-
56
-
-
0037413240
-
Alpha4 integrins as therapeutic targets in autoimmune disease
-
von Andrian, U. H. & Engelhardt, B. Alpha4 integrins as therapeutic targets in autoimmune disease. N. Engl. J. Med. 348, 68-72 (2003).
-
(2003)
N. Engl. J. Med.
, vol.348
, pp. 68-72
-
-
Von Andrian, U.H.1
Engelhardt, B.2
-
57
-
-
63449100039
-
Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: Design of prospective meta-analyses of genome-wide association studies from 5 cohorts
-
Psaty, B. M., O'Donnell, C. J., Gudnason, V., Lunetta, K. L., Folsom, A. R., Rotter, J. I. et al. Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: Design of prospective meta-analyses of genome-wide association studies from 5 cohorts. Circ. Cardiovasc. Genet. 2, 73-80 (2009).
-
(2009)
Circ. Cardiovasc. Genet.
, vol.2
, pp. 73-80
-
-
Psaty, B.M.1
O'Donnell, C.J.2
Gudnason, V.3
Lunetta, K.L.4
Folsom, A.R.5
Rotter, J.I.6
-
59
-
-
52949111858
-
Common variants at CD40 and other loci confer risk of rheumatoid arthritis
-
Raychaudhuri, S., Remmers, E. F., Lee, A. T., Hackett, R., Guiducci, C., Burtt, N. P. et al. Common variants at CD40 and other loci confer risk of rheumatoid arthritis. Nat. Genet. 40, 1216-1223 (2008).
-
(2008)
Nat. Genet.
, vol.40
, pp. 1216-1223
-
-
Raychaudhuri, S.1
Remmers, E.F.2
Lee, A.T.3
Hackett, R.4
Guiducci, C.5
Burtt, N.P.6
-
60
-
-
77952888454
-
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci
-
Stahl, E. A., Raychaudhuri, S., Remmers, E. F., Xie, G., Eyre, S., Thomson, B. P. et al. Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. Nat. Genet. 42, 508-514 (2010).
-
(2010)
Nat. Genet.
, vol.42
, pp. 508-514
-
-
Stahl, E.A.1
Raychaudhuri, S.2
Remmers, E.F.3
Xie, G.4
Eyre, S.5
Thomson, B.P.6
-
61
-
-
73249142153
-
Contribution of a haplotype in the HLA region to anti-cyclic citrullinated peptide antibody positivity in rheumatoid arthritis, independently of HLA-DRB1
-
Okada, Y., Yamada, R., Suzuki, A., Kochi, Y., Shimane, K., Myouzen, K. et al. Contribution of a haplotype in the HLA region to anti-cyclic citrullinated peptide antibody positivity in rheumatoid arthritis, independently of HLA-DRB1. Arthritis. Rheum. 60, 3582-3590 (2009).
-
(2009)
Arthritis. Rheum.
, vol.60
, pp. 3582-3590
-
-
Okada, Y.1
Yamada, R.2
Suzuki, A.3
Kochi, Y.4
Shimane, K.5
Myouzen, K.6
-
62
-
-
77955439698
-
HLADRB1*0901 lowers anti-cyclic citrullinated peptide antibody levels in Japanese patients with rheumatoid arthritis
-
Okada, Y., Suzuki, A., Yamada, R., Kochi, Y., Shimane, K., Myouzen, K. et al. HLADRB1*0901 lowers anti-cyclic citrullinated peptide antibody levels in Japanese patients with rheumatoid arthritis. Ann. Rheum. Dis. 69, 1569-1570 (2010).
-
(2010)
Ann. Rheum. Dis.
, vol.69
, pp. 1569-1570
-
-
Okada, Y.1
Suzuki, A.2
Yamada, R.3
Kochi, Y.4
Shimane, K.5
Myouzen, K.6
-
63
-
-
34547216747
-
Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma
-
Moffatt, M. F., Kabesch, M., Liang, L., Dixon, A. L., Strachan, D., Heath, S. et al. Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma. Nature. 448, 470-473 (2007).
-
(2007)
Nature.
, vol.448
, pp. 470-473
-
-
Moffatt, M.F.1
Kabesch, M.2
Liang, L.3
Dixon, A.L.4
Strachan, D.5
Heath, S.6
-
64
-
-
45549102935
-
The transcription factor Erg is essential for definitive hematopoiesis and the function of adult hematopoietic stem cells
-
Loughran, S. J., Kruse, E. A., Hacking, D. F., de Graaf, C. A., Hyland, C. D., Willson, T. A. et al. The transcription factor Erg is essential for definitive hematopoiesis and the function of adult hematopoietic stem cells. Nat. Immunol. 9, 810-819 (2008).
-
(2008)
Nat. Immunol.
, vol.9
, pp. 810-819
-
-
Loughran, S.J.1
Kruse, E.A.2
Hacking, D.F.3
De Graaf, C.A.4
Hyland, C.D.5
Willson, T.A.6
-
65
-
-
0025069873
-
The prognostic value of cellular and serologic markers in infection with human immunodeficiency virus type 1
-
Fahey, J. L., Taylor, J. M., Detels, R., Hofmann, B., Melmed, R., Nishanian, P. et al. The prognostic value of cellular and serologic markers in infection with human immunodeficiency virus type 1. N. Engl. J. Med. 322, 166-172 (1990).
-
(1990)
N. Engl. J. Med.
, vol.322
, pp. 166-172
-
-
Fahey, J.L.1
Taylor, J.M.2
Detels, R.3
Hofmann, B.4
Melmed, R.5
Nishanian, P.6
-
66
-
-
27644504938
-
A prospective study of anemia status, hemoglobin concentration, and mortality in an elderly cohort: The Cardiovascular Health Study
-
Zakai, N. A., Katz, R., Hirsch, C., Shlipak, M. G., Chaves, P. H., Newman, A. B. et al. A prospective study of anemia status, hemoglobin concentration, and mortality in an elderly cohort: the Cardiovascular Health Study. Arch. Intern. Med. 165, 2214-2220 (2005).
-
(2005)
Arch. Intern. Med.
, vol.165
, pp. 2214-2220
-
-
Zakai, N.A.1
Katz, R.2
Hirsch, C.3
Shlipak, M.G.4
Chaves, P.H.5
Newman, A.B.6
-
67
-
-
0031712378
-
The therapeutic reactivation of fetal haemoglobin
-
Olivieri, N. F. & Weatherall, D. J. The therapeutic reactivation of fetal haemoglobin. Hum. Mol. Genet. 7, 1655-1658 (1998).
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1655-1658
-
-
Olivieri, N.F.1
Weatherall, D.J.2
-
68
-
-
44449177930
-
The serine protease TMPRSS6 is required to sense iron deficiency
-
Du, X., She, E., Gelbart, T., Truksa, J., Lee, P., Xia, Y. et al. The serine protease TMPRSS6 is required to sense iron deficiency. Science. 320, 1088-1092 (2008).
-
(2008)
Science.
, vol.320
, pp. 1088-1092
-
-
Du, X.1
She, E.2
Gelbart, T.3
Truksa, J.4
Lee, P.5
Xia, Y.6
-
69
-
-
58049202750
-
Variants in TF and HFE explain approximately 40% of genetic variation in serumtransferrin levels
-
Benyamin, B., McRae, A. F., Zhu, G., Gordon, S., Henders, A. K., Palotie, A. et al. Variants in TF and HFE explain approximately 40% of genetic variation in serumtransferrin levels. Am. J. Hum. Genet. 84, 60-65 (2009).
-
(2009)
Am. J. Hum. Genet.
, vol.84
, pp. 60-65
-
-
Benyamin, B.1
McRae, A.F.2
Zhu, G.3
Gordon, S.4
Henders, A.K.5
Palotie, A.6
-
70
-
-
74949090955
-
A genome-wide association analysis of serum iron concentrations
-
Tanaka, T., Roy, C. N., Yao, W., Matteini, A., Semba, R. D., Arking, D. et al. A genome-wide association analysis of serum iron concentrations. Blood. 115, 94-96 (2010).
-
(2010)
Blood
, vol.115
, pp. 94-96
-
-
Tanaka, T.1
Roy, C.N.2
Yao, W.3
Matteini, A.4
Semba, R.D.5
Arking, D.6
-
71
-
-
79551586854
-
Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels
-
Oexle, K., Ried, J. S., Hicks, A. A., Tanaka, T., Hayward, C., Bruegel, M. et al. Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels. Hum. Mol. Genet. 20, 1042-1047 (2011).
-
(2011)
Hum. Mol. Genet.
, vol.20
, pp. 1042-1047
-
-
Oexle, K.1
Ried, J.S.2
Hicks, A.A.3
Tanaka, T.4
Hayward, C.5
Bruegel, M.6
-
72
-
-
79952016793
-
Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels
-
Pichler, I., Minelli, C., Sanna, S., Tanaka, T., Schwienbacher, C., Naitza, S. et al. Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. Hum. Mol. Genet. 20, 1232-1240 (2011).
-
(2011)
Hum. Mol. Genet.
, vol.20
, pp. 1232-1240
-
-
Pichler, I.1
Minelli, C.2
Sanna, S.3
Tanaka, T.4
Schwienbacher, C.5
Naitza, S.6
-
73
-
-
84858952847
-
Identification of genetic loci associated with quantitative traits using GWAS in a Japanese population
-
Okada, Y., Kamatani, Y., Takahashi, A., Matsuda, K., Honoso, N., Ohmiya, H. et al. Identification of genetic loci associated with quantitative traits using GWAS in a Japanese population. The 55th meeting of the Japan Society of Human Genetics (2010).
-
The 55th Meeting of the Japan Society of Human Genetics (2010)
-
-
Okada, Y.1
Kamatani, Y.2
Takahashi, A.3
Matsuda, K.4
Honoso, N.5
Ohmiya, H.6
-
74
-
-
0036380553
-
Sequence variation at the human ABO locus
-
Yip, S. P. Sequence variation at the human ABO locus. Ann. Hum. Genet. 66, 1-27 (2002).
-
(2002)
Ann. Hum. Genet.
, vol.66
, pp. 1-27
-
-
Yip, S.P.1
-
75
-
-
37249068975
-
A new method for ABO genotyping to avoid discrepancy between genetic and serological determinations
-
Shintani-Ishida, K., Zhu, B. L., Maeda, H., Uemura, K. & Yoshida, K. A new method for ABO genotyping to avoid discrepancy between genetic and serological determinations. Int. J. Legal. Med. 122, 7-9 (2008).
-
(2008)
Int. J. Legal. Med.
, vol.122
, pp. 7-9
-
-
Shintani-Ishida, K.1
Zhu, B.L.2
Maeda, H.3
Uemura, K.4
Yoshida, K.5
-
76
-
-
44149090296
-
Role of platelet-derived growth factors in physiology and medicine
-
Andrae, J., Gallini, R. & Betsholtz, C. Role of platelet-derived growth factors in physiology and medicine. Genes. Dev. 22, 1276-1312 (2008).
-
(2008)
Genes. Dev.
, vol.22
, pp. 1276-1312
-
-
Andrae, J.1
Gallini, R.2
Betsholtz, C.3
-
77
-
-
61849095255
-
Shear activates platelet-derived latent TGF-beta
-
Miyazono, K. Shear activates platelet-derived latent TGF-beta. Blood. 112, 3533-3534 (2008).
-
(2008)
Blood.
, vol.112
, pp. 3533-3534
-
-
Miyazono, K.1
-
78
-
-
0031975482
-
An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia
-
Wiestner, A., Schlemper, R. J., van der Maas, A. P. & Skoda, R. C. An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia. Nat. Genet. 18, 49-52 (1998).
-
(1998)
Nat. Genet.
, vol.18
, pp. 49-52
-
-
Wiestner, A.1
Schlemper, R.J.2
Van Der Maas, A.P.3
Skoda, R.C.4
-
79
-
-
29644444727
-
Two candidate genes for low platelet count identified in an Asian Indian kindred by genome-wide linkage analysis: Glycoprotein IX and thrombopoietin
-
Garner, C., Best, S., Menzel, S., Rooks, H., Spector, T. D. & Thein, S. L. Two candidate genes for low platelet count identified in an Asian Indian kindred by genome-wide linkage analysis: glycoprotein IX and thrombopoietin. Eur. J. Hum. Genet. 14, 101-108 (2006).
-
(2006)
Eur. J. Hum. Genet.
, vol.14
, pp. 101-108
-
-
Garner, C.1
Best, S.2
Menzel, S.3
Rooks, H.4
Spector, T.D.5
Thein, S.L.6
-
80
-
-
79957604338
-
A genome-wide association study of metabolic traits in human urine
-
Suhre, K., Wallaschofski, H., Raffler, J., Friedrich, N., Haring, R., Michael, K. et al. A genome-wide association study of metabolic traits in human urine. Nat. Genet. 43, 565-569 (2011).
-
(2011)
Nat. Genet.
, vol.43
, pp. 565-569
-
-
Suhre, K.1
Wallaschofski, H.2
Raffler, J.3
Friedrich, N.4
Haring, R.5
Michael, K.6
-
81
-
-
77950217693
-
Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium
-
Smith, N. L., Chen, M. H., Dehghan, A., Strachan, D. P., Basu, S., Soranzo, N. et al. Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium. Circulation. 121, 1382-1392 (2010).
-
(2010)
Circulation.
, vol.121
, pp. 1382-1392
-
-
Smith, N.L.1
Chen, M.H.2
Dehghan, A.3
Strachan, D.P.4
Basu, S.5
Soranzo, N.6
-
82
-
-
78649735165
-
Genome-wide association study identifies novel loci for plasma levels of protein C: The ARIC study
-
Tang, W., Basu, S., Kong, X., Pankow, J. S., Aleksic, N., Tan, A. et al. Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. Blood. 116, 5032-5036 (2010).
-
(2010)
Blood.
, vol.116
, pp. 5032-5036
-
-
Tang, W.1
Basu, S.2
Kong, X.3
Pankow, J.S.4
Aleksic, N.5
Tan, A.6
-
83
-
-
77649222029
-
Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17686 women: The Women's Genome Health Study
-
Danik, J. S., Pare, G., Chasman, D. I., Zee, R. Y., Kwiatkowski, D. J., Parker, A. et al. Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17686 women: the Women's Genome Health Study. Circ. Cardiovasc. Genet. 2, 134-141 (2009).
-
(2009)
Circ. Cardiovasc. Genet.
, vol.2
, pp. 134-141
-
-
Danik, J.S.1
Pare, G.2
Chasman, D.I.3
Zee, R.Y.4
Kwiatkowski, D.J.5
Parker, A.6
-
84
-
-
67849121952
-
Association of novel genetic Loci with circulating fibrinogen levels: A genome-wide association study in 6 population-based cohorts
-
Dehghan, A., Yang, Q., Peters, A., Basu, S., Bis, J. C., Rudnicka, A. R. et al. Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts. Circ. Cardiovasc. Genet. 2, 125-133 (2009).
-
(2009)
Circ. Cardiovasc. Genet.
, vol.2
, pp. 125-133
-
-
Dehghan, A.1
Yang, Q.2
Peters, A.3
Basu, S.4
Bis, J.C.5
Rudnicka, A.R.6
-
85
-
-
77954145555
-
Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists
-
Johnson, A. D., Yanek, L. R., Chen, M. H., Faraday, N., Larson, M. G., Tofler, G. et al. Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. Nat. Genet. 42, 608-613 (2010).
-
(2010)
Nat. Genet.
, vol.42
, pp. 608-613
-
-
Johnson, A.D.1
Yanek, L.R.2
Chen, M.H.3
Faraday, N.4
Larson, M.G.5
Tofler, G.6
-
86
-
-
61349108698
-
SNPs in BRAP associated with risk of myocardial infarction in Asian populations
-
Ozaki, K., Sato, H., Inoue, K., Tsunoda, T., Sakata, Y., Mizuno, H. et al. SNPs in BRAP associated with risk of myocardial infarction in Asian populations. Nat. Genet. 41, 329-333 (2009).
-
(2009)
Nat. Genet.
, vol.41
, pp. 329-333
-
-
Ozaki, K.1
Sato, H.2
Inoue, K.3
Tsunoda, T.4
Sakata, Y.5
Mizuno, H.6
-
87
-
-
79957585975
-
Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians
-
Kato, N., Takeuchi, F., Tabara, Y., Kelly, T. N., Go, M. J., Sim, X. et al. Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. Nat. Genet. 43, 531-538 (2011).
-
(2011)
Nat. Genet.
, vol.43
, pp. 531-538
-
-
Kato, N.1
Takeuchi, F.2
Tabara, Y.3
Kelly, T.N.4
Go, M.J.5
Sim, X.6
-
88
-
-
79951521421
-
Progress and promise of genome-wide association studies for human complex trait genetics
-
Stranger, B. E., Stahl, E. A. & Raj, T. Progress and promise of genome-wide association studies for human complex trait genetics. Genetics. 187, 367-383 (2011).
-
(2011)
Genetics
, vol.187
, pp. 367-383
-
-
Stranger, B.E.1
Stahl, E.A.2
Raj, T.3
-
89
-
-
78650860672
-
Genetic basis of autoantibody positive and negative rheumatoid arthritis risk in a multi-ethnic cohort derived from electronic health records
-
Kurreeman, F., Liao, K., Chibnik, L., Hickey, B., Stahl, E., Gainer, V. et al. Genetic basis of autoantibody positive and negative rheumatoid arthritis risk in a multi-ethnic cohort derived from electronic health records. Am. J. Hum. Genet. 88, 57-69 (2011).
-
(2011)
Am. J. Hum. Genet.
, vol.88
, pp. 57-69
-
-
Kurreeman, F.1
Liao, K.2
Chibnik, L.3
Hickey, B.4
Stahl, E.5
Gainer, V.6
-
90
-
-
77952885768
-
A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility
-
Kochi, Y., Okada, Y., Suzuki, A., Ikari, K., Terao, C., Takahashi, A. et al. A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility. Nat. Genet. 42, 515-519 (2010).
-
(2010)
Nat. Genet.
, vol.42
, pp. 515-519
-
-
Kochi, Y.1
Okada, Y.2
Suzuki, A.3
Ikari, K.4
Terao, C.5
Takahashi, A.6
-
91
-
-
54049083105
-
SLC22A4 polymorphism and rheumatoid arthritis susceptibility: A replication study in a Japanese population and a metaanalysis
-
Okada, Y., Mori, M., Yamada, R., Suzuki, A., Kobayashi, K., Kubo, M. et al. SLC22A4 polymorphism and rheumatoid arthritis susceptibility: a replication study in a Japanese population and a metaanalysis. J. Rheumatol. 35, 1723-1728 (2008).
-
(2008)
J. Rheumatol.
, vol.35
, pp. 1723-1728
-
-
Okada, Y.1
Mori, M.2
Yamada, R.3
Suzuki, A.4
Kobayashi, K.5
Kubo, M.6
-
92
-
-
79955860273
-
Random-effects model aimed at discovering associations in metaanalysis of genome-wide association studies
-
Han, B. & Eskin, E. Random-effects model aimed at discovering associations in metaanalysis of genome-wide association studies. Am. J. Hum. Genet. 88, 586-598 (2011).
-
(2011)
Am. J. Hum. Genet.
, vol.88
, pp. 586-598
-
-
Han, B.1
Eskin, E.2
-
93
-
-
73149103718
-
Prioritizing GWAS results: A review of statistical methods and recommendations for their application
-
Cantor, R. M., Lange, K. & Sinsheimer, J. S. Prioritizing GWAS results: a review of statistical methods and recommendations for their application. Am. J. Hum. Genet. 86, 6-22 (2010).
-
(2010)
Am. J. Hum. Genet.
, vol.86
, pp. 6-22
-
-
Cantor, R.M.1
Lange, K.2
Sinsheimer, J.S.3
-
94
-
-
84857487791
-
A genomewide association study identified AFF1 as a susceptibility locus for systemic lupus eyrthematosus in Japanese
-
doi:10.1371/journal.pgen.1002455.
-
Okada, Y., Shimane, K., Kochi, Y., Tahira, T., Suzuki, A., Higasa, K. et al. A genomewide association study identified AFF1 as a susceptibility locus for systemic lupus eyrthematosus in Japanese. PLoS. Genet doi:10.1371/journal.pgen. 1002455.
-
PLoS. Genet
-
-
Okada, Y.1
Shimane, K.2
Kochi, Y.3
Tahira, T.4
Suzuki, A.5
Higasa, K.6
-
95
-
-
78549251736
-
Analysing biological pathways in genome-wide association studies
-
Wang, K., Li, M. & Hakonarson, H. Analysing biological pathways in genome-wide association studies. Nat. Rev. Genet. 11, 843-854 (2010).
-
(2010)
Nat. Rev. Genet.
, vol.11
, pp. 843-854
-
-
Wang, K.1
Li, M.2
Hakonarson, H.3
-
96
-
-
67651205715
-
Identifying relationships among genomic disease regions: Predicting genes at pathogenic SNP associations and rare deletions
-
Raychaudhuri, S., Plenge, R. M., Rossin, E. J., Ng, A. C., Purcell, S. M., Sklar, P. et al. Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions. PLoS. Genet. 5, e1000534 (2009).
-
(2009)
PLoS. Genet.
, vol.5
-
-
Raychaudhuri, S.1
Plenge, R.M.2
Rossin, E.J.3
Ng, A.C.4
Purcell, S.M.5
Sklar, P.6
-
97
-
-
80052111188
-
HLA-Cw*1202-B*5201-DRB1*1502 haplotype increases risk for ulcerative colitis but reduces risk for Crohn's disease
-
Okada, Y., Yamazaki, K., Umeno, J., Takahashi, A., Kumasaka, N., Ashikawa, K. et al. HLA-Cw*1202-B*5201-DRB1*1502 haplotype increases risk for ulcerative colitis but reduces risk for Crohn's disease. Gastroenterology. 141, 864-871 (2011).
-
(2011)
Gastroenterology.
, vol.141
, pp. 864-871
-
-
Okada, Y.1
Yamazaki, K.2
Umeno, J.3
Takahashi, A.4
Kumasaka, N.5
Ashikawa, K.6
-
98
-
-
79952019307
-
Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus
-
Okada, Y., Takahashi, A., Ohmiya, H., Kumasaka, N., Kamatani, Y., Hosono, N. et al. Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus. Hum. Mol. Genet. 20, 1224-1231 (2011).
-
(2011)
Hum. Mol. Genet.
, vol.20
, pp. 1224-1231
-
-
Okada, Y.1
Takahashi, A.2
Ohmiya, H.3
Kumasaka, N.4
Kamatani, Y.5
Hosono, N.6
-
99
-
-
77950405093
-
Genome-wide association study of CNVs in 16000 cases of eight common diseases and 3000 shared controls
-
The WTCCC. Genome-wide association study of CNVs in 16000 cases of eight common diseases and 3000 shared controls. Nature 464, 713-720 (2010).
-
(2010)
Nature
, vol.464
, pp. 713-720
-
-
The, W.1
-
100
-
-
82455203887
-
PlatinumCNV: A Bayesian Gaussian mixture model for genotyping copy number polymorphisms using SNP array signal intensity data
-
Kumasaka, N., Fujisawa, H., Hosono, N., Okada, Y., Takahashi, A., Nakamura, Y. et al. PlatinumCNV: a Bayesian Gaussian mixture model for genotyping copy number polymorphisms using SNP array signal intensity data. Genet. Epidemiol. 35, 831-844 (2011).
-
(2011)
Genet. Epidemiol.
, vol.35
, pp. 831-844
-
-
Kumasaka, N.1
Fujisawa, H.2
Hosono, N.3
Okada, Y.4
Takahashi, A.5
Nakamura, Y.6
-
101
-
-
79960556965
-
Epigenome-wide association studies for common human diseases
-
Rakyan, V. K., Down, T. A., Balding, D. J. & Beck, S. Epigenome-wide association studies for common human diseases. Nat. Rev. Genet. 12, 529-541 (2011).
-
(2011)
Nat. Rev. Genet.
, vol.12
, pp. 529-541
-
-
Rakyan, V.K.1
Down, T.A.2
Balding, D.J.3
Beck, S.4
-
102
-
-
67349166946
-
Detecting gene-gene interactions that underlie human diseases
-
Cordell, H. J. Detecting gene-gene interactions that underlie human diseases. Nat. Rev. Genet. 10, 392-404 (2009).
-
(2009)
Nat. Rev. Genet.
, vol.10
, pp. 392-404
-
-
Cordell, H.J.1
-
103
-
-
78049321495
-
Whole-genome sequencing and comprehensive variant analysis of a Japanese individual using massively parallel sequencing
-
Fujimoto, A., Nakagawa, H., Hosono, N., Nakano, K., Abe, T., Boroevich, K. A. et al. Whole-genome sequencing and comprehensive variant analysis of a Japanese individual using massively parallel sequencing. Nat. Genet. 42, 931-936 (2010).
-
(2010)
Nat. Genet.
, vol.42
, pp. 931-936
-
-
Fujimoto, A.1
Nakagawa, H.2
Hosono, N.3
Nakano, K.4
Abe, T.5
Boroevich, K.A.6
-
104
-
-
77956838065
-
Advances in understanding cancer genomes through second-generation sequencing
-
Meyerson, M., Gabriel, S. & Getz, G. Advances in understanding cancer genomes through second-generation sequencing. Nat. Rev. Genet. 11, 685-696 (2010).
-
(2010)
Nat. Rev. Genet.
, vol.11
, pp. 685-696
-
-
Meyerson, M.1
Gabriel, S.2
Getz, G.3
-
105
-
-
84975742565
-
Consortium A map of human genome variation from population-scale sequencing
-
1000 Genomes Project
-
1000 Genomes Project, Consortium A map of human genome variation from population-scale sequencing. Nature 467, 1061-1073 (2010).
-
(2010)
Nature
, vol.467
, pp. 1061-1073
-
-
-
106
-
-
79953212557
-
A rare variant in MYH6 is associated with high risk of sick sinus syndrome
-
Holm, H., Gudbjartsson, D. F., Sulem, P., Masson, G., Helgadottir, H. T., Zanon, C. et al. A rare variant in MYH6 is associated with high risk of sick sinus syndrome. Nat. Genet. 43, 316-320 (2011).
-
(2011)
Nat. Genet.
, vol.43
, pp. 316-320
-
-
Holm, H.1
Gudbjartsson, D.F.2
Sulem, P.3
Masson, G.4
Helgadottir, H.T.5
Zanon, C.6
-
107
-
-
80054975975
-
Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease
-
Rivas, M. A., Beaudoin, M., Gardet, A., Stevens, C., Sharma, Y., Zhang, C. K. et al. Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease. Nat. Genet. 43, 1066-1073 (2011).
-
(2011)
Nat. Genet.
, vol.43
, pp. 1066-1073
-
-
Rivas, M.A.1
Beaudoin, M.2
Gardet, A.3
Stevens, C.4
Sharma, Y.5
Zhang, C.K.6
-
108
-
-
79959378465
-
Family-based designs for genome-wide association studies
-
Ott, J., Kamatani, Y. & Lathrop, M. Family-based designs for genome-wide association studies. Nat. Rev. Genet. 12, 465-474 (2011).
-
(2011)
Nat. Rev. Genet.
, vol.12
, pp. 465-474
-
-
Ott, J.1
Kamatani, Y.2
Lathrop, M.3
-
109
-
-
80052398214
-
Human metabolic individuality in biomedical and pharmaceutical research
-
Suhre, K., Shin, S. Y., Petersen, A. K., Mohney, R. P., Meredith, D., Wagele, B. et al. Human metabolic individuality in biomedical and pharmaceutical research. Nature. 477, 54-60 (2011).
-
(2011)
Nature.
, vol.477
, pp. 54-60
-
-
Suhre, K.1
Shin, S.Y.2
Petersen, A.K.3
Mohney, R.P.4
Meredith, D.5
Wagele, B.6
|