-
1
-
-
0742305866
-
Network biology: understanding the cells functional organization
-
Barabasi, A. L., and Oltvai, Z. N. (2004). Network biology: understanding the cells functional organization. Nat. Rev. Genet. 5, 101-113.
-
(2004)
Nat. Rev. Genet.
, vol.5
, pp. 101-113
-
-
Barabasi, A.L.1
Oltvai, Z.N.2
-
2
-
-
33750466904
-
Small-world brain networks
-
Bassett, D. S., and Bullmore, E. (2006). Small-world brain networks. Neuro-scientist 12, 512-523.
-
(2006)
Neuro-scientist
, vol.12
, pp. 512-523
-
-
Bassett, D.S.1
Bullmore, E.2
-
3
-
-
66449133984
-
HLA and infectious diseases
-
Blackwell, J. M., Jamieson, S. E., and Burgner, D. (2009). HLA and infectious diseases. Clin. Microbiol. Rev. 22, 370-385.
-
(2009)
Clin. Microbiol. Rev.
, vol.22
, pp. 370-385
-
-
Blackwell, J.M.1
Jamieson, S.E.2
Burgner, D.3
-
4
-
-
83055172813
-
Test-retest reliability of resting-state connectivity network characteristics using fMRI and graph theoretical measures
-
Braun, U., Plichta, M. M., Esslinger, C., Sauer, C., Haddad, L., Grimm, O., Mier, D., Mohnke, S., Heinz, A., Erk, S., Walter, H., Seiferth, N., Kirsch, P., and Meyer-Lindenberg, A. (2011). Test-retest reliability of resting-state connectivity network characteristics using fMRI and graph theoretical measures. Neuroimage 59, 1404-1412.
-
(2011)
Neuroimage
, vol.59
, pp. 1404-1412
-
-
Braun, U.1
Plichta, M.M.2
Esslinger, C.3
Sauer, C.4
Haddad, L.5
Grimm, O.6
Mier, D.7
Mohnke, S.8
Heinz, A.9
Erk, S.10
Walter, H.11
Seiferth, N.12
Kirsch, P.13
Meyer-Lindenberg, A.14
-
5
-
-
59249099537
-
International Kawasaki Disease Genetics Consortium A genome-wide association study identifies novel and functionally related susceptibility loci for kawasaki disease
-
doi:10.1371/journal.pgen.1000319
-
Burgner, D., Davila, S., Breunis, W. B., Ng, S. B., Li, Y., Bonnard, C., Ling, L., Wright, V. J., Thala-muthu, A., Odam, M., Shimizu, C., Burns, J. C., Levin, M., Kuijpers, T. W., Hibberd, M. L., and International Kawasaki Disease Genetics Consortium. (2009). A genome-wide association study identifies novel and functionally related susceptibility loci for kawasaki disease. PLoS Genet. 5, e1000319. doi:10.1371/journal.pgen.1000319
-
(2009)
PLoS Genet
, vol.5
-
-
Burgner, D.1
Davila, S.2
Breunis, W.B.3
Ng, S.B.4
Li, Y.5
Bonnard, C.6
Ling, L.7
Wright, V.J.8
Thala-muthu, A.9
Odam, M.10
Shimizu, C.11
Burns, J.C.12
Levin, M.13
Kuijpers, T.W.14
Hibberd, M.L.15
-
6
-
-
79960637074
-
International Multiple Sclerosis Genetics Consortium A knowledge-driven interaction analysis reveals potential neurodegenerative mechanism of multiple sclerosis susceptibility
-
Bush, W S., McCauley, J. L., DeJager, P. L., Dudek, S. M., Hafler, D. A., Gibson, R. A., Matthews, P. M., Kap-pos, L., Naegelin, Y., Polman, C. H., Hauser, S. L., Oksenberg, J., Haines, J. L., Ritchie, M. D., and International Multiple Sclerosis Genetics Consortium. (2011). A knowledge-driven interaction analysis reveals potential neurodegenerative mechanism of multiple sclerosis susceptibility. Genes Immun. 12, 335-340.
-
(2011)
Genes Immun
, vol.12
, pp. 335-340
-
-
Bush, W.S.1
McCauley, J.L.2
DeJager, P.L.3
Dudek, S.M.4
Hafler, D.A.5
Gibson, R.A.6
Matthews, P.M.7
Kap-pos, L.8
Naegelin, Y.9
Polman, C.H.10
Hauser, S.L.11
Oksenberg, J.12
Haines, J.L.13
Ritchie, M.D.14
-
7
-
-
77957734984
-
Donor selection for natural killer cell receptor genes leads to superior survival after unrelated transplantation for acute myelogenous leukemia
-
Cooley, S., Weisdorf, D. J., Guethlein, L. A., Klein, J. P., Wang, T., Le, C. T., Marsh, S. G., Geraghty D., Spell-man, S., Haagenson, M. D., Ladner, M., Trachtenberg, E., Parham, P., and Miller, J. S. (2010). Donor selection for natural killer cell receptor genes leads to superior survival after unrelated transplantation for acute myelogenous leukemia. Blood 116, 2411-2419.
-
(2010)
Blood
, vol.116
, pp. 2411-2419
-
-
Cooley, S.1
Weisdorf, D.J.2
Guethlein, L.A.3
Klein, J.P.4
Wang, T.5
Le, C.T.6
Marsh, S.G.7
Geraghty, D.8
Spell-man, S.9
Haagenson, M.D.10
Ladner, M.11
Trachtenberg, E.12
Parham, P.13
Miller, J.S.14
-
8
-
-
67349166946
-
Detecting gene-gene interactions that underlie human diseases
-
Cordell, H. J. (2009). Detecting gene-gene interactions that underlie human diseases. Nat. Rev. Genet. 10, 392-404.
-
(2009)
Nat. Rev. Genet.
, vol.10
, pp. 392-404
-
-
Cordell, H.J.1
-
9
-
-
78649701338
-
Surfing a genetic association interaction network to identify modulators of antibody response to smallpox vaccine
-
Davis, N. A., Crowe, J. E. Jr., Pajewski, N. M., and McKinney, B. A. (2010). Surfing a genetic association interaction network to identify modulators of antibody response to smallpox vaccine. Genes Immun. 11, 630-636.
-
(2010)
Genes Immun
, vol.11
, pp. 630-636
-
-
Davis, N.A.1
Crowe Jr, J.E.2
Pajewski, N.M.3
McKinney, B.A.4
-
10
-
-
84857780876
-
Evidence for network evolution in an Arabidop-sis interactome map
-
Dreze, M., Carvunis, A. R., Charloteaux, B., Galli, M., Pevzner, S. J., Tasan, M., Ahn, Y.-Y., Balumuri, P., Barabasi, A.-L., Bautista, V., Braun, P., Byrd-song, D., Chen, H., Chesnut, J. D., Cusick, M. E., Dangl, J. L., de los Reyes, C., Dricot, A., Duarte, M., Ecker, J. R., Fan, C., Gai, L., Gebreab, E, Ghoshal, G., Gilles, P., Gutierrez, B. J., Hao, T., Hill, D. E., Kim, C. J., Kim, R. C., Lurin, C., Mac Williams, A., Matrubutham, U., Milenkovic, T., Mirchandani, J., Monachello, D., Moore Jonathan, D., Mukhtar, M. S., Olivares, E., Patnaik, S., Poulin, M. M., Przulj, N., Quan, R., Rabello, S., Ramaswamy G., Reichert, P., Riet-man, E. A., Rolland, T., Romero, V., Roth, F. P., Santhanam, B., Schmitz, R. J., Shinn, P., Spooner, W., Stein, J., Swamilingiah, G. M., Tam, S., Van-denhaute, J., Vidal, M., Waaijers, S., Ware, D., Weiner, E. M., Wu, S., and Yazaki, J. (2011) Evidence for network evolution in an Arabidop-sis interactome map. Science 333, 601-607.
-
(2011)
Science
, vol.333
, pp. 601-607
-
-
Dreze, M.1
Carvunis, A.R.2
Charloteaux, B.3
Galli, M.4
Pevzner, S.J.5
Tasan, M.6
Ahn, Y.Y.7
Balumuri, P.8
Barabasi, A.L.9
Bautista, V.10
Braun, P.11
Byrd-song, D.12
Chen, H.13
Chesnut, J.D.14
Cusick, M.E.15
Dangl, J.L.16
de los Reyes, C.17
Dricot, A.18
Duarte, M.19
Ecker, J.R.20
Fan, C.21
Gai, L.22
Gebreab, E.23
Ghoshal, G.24
Gilles, P.25
Gutierrez, B.J.26
Hao, T.27
Hill, D.E.28
Kim, C.J.29
Kim, R.C.30
Lurin, C.31
Mac Williams, A.32
Matrubutham, U.33
Milenkovic, T.34
Mirchandani, J.35
Monachello, D.36
Moore Jonathan, D.37
Mukhtar, M.S.38
Olivares, E.39
Patnaik, S.40
Poulin, M.M.41
Przulj, N.42
Quan, R.43
Rabello, S.44
Ramaswamy, G.45
Reichert, P.46
Riet-man, E.A.47
Rolland, T.48
Romero, V.49
Roth, F.P.50
Santhanam, B.51
Schmitz, R.J.52
Shinn, P.53
Spooner, W.54
Stein, J.55
Swamilingiah, G.M.56
Tam, S.57
Van-denhaute, J.58
Vidal, M.59
Waaijers, S.60
Ware, D.61
Weiner, E.M.62
Wu, S.63
Yazaki, J.64
more..
-
11
-
-
77952557918
-
Missing heritability and strategies for finding the underlying causes of complex disease
-
Eichler, E. E., Flint, J., Gibson, G., Kong, A., Leal, S. M., Moore, J. H., and Nadeau, J. H. (2010). Missing heritability and strategies for finding the underlying causes of complex disease. Nat. Rev. Genet. 11, 446-450.
-
(2010)
Nat. Rev. Genet.
, vol.11
, pp. 446-450
-
-
Eichler, E.E.1
Flint, J.2
Gibson, G.3
Kong, A.4
Leal, S.M.5
Moore, J.H.6
Nadeau, J.H.7
-
12
-
-
80054755102
-
Entropy-based information gain approaches to detect and to characterize gene-gene and gene-environment interactions/correlations of complex diseases
-
Fan, R., Zhong, M., Wang, S., Zhang, Y., Andrew, A., Karagas, M., Chen, H., Amos, C. I., Xiong, M., and Moore, J. H. (2011). Entropy-based information gain approaches to detect and to characterize gene-gene and gene-environment interactions/correlations of complex diseases. Genet. Epidemiol. 35, 706-721.
-
(2011)
Genet. Epidemiol.
, vol.35
, pp. 706-721
-
-
Fan, R.1
Zhong, M.2
Wang, S.3
Zhang, Y.4
Andrew, A.5
Karagas, M.6
Chen, H.7
Amos, C.I.8
Xiong, M.9
Moore, J.H.10
-
13
-
-
77955646179
-
Association of trypanolytic ApoL1 variants with kidney disease in African Americans
-
Genovese, G., Friedman, D. J., Ross, M. D., Lecordier, L., Uzureau, P., Freed-man, B. I., Bowden, D. W., Lange-feld, C. D., Oleksyk, T. K., Uscinski Knob, A. L., Bernhardy, A. J., Hicks, P. J., Nelson, G. W., Vanhollebeke, B., Winkler, C. A., Kopp, J. B., Pays, E., and Pollak, M. R. (2010). Association of trypanolytic ApoL1 variants with kidney disease in African Americans. Science 329, 841-845.
-
(2010)
Science
, vol.329
, pp. 841-845
-
-
Genovese, G.1
Friedman, D.J.2
Ross, M.D.3
Lecordier, L.4
Uzureau, P.5
Freed-man, B.I.6
Bowden, D.W.7
Lange-feld, C.D.8
Oleksyk, T.K.9
Uscinski Knob, A.L.10
Bernhardy, A.J.11
Hicks, P.J.12
Nelson, G.W.13
Vanhollebeke, B.14
Winkler, C.A.15
Kopp, J.B.16
Pays, E.17
Pollak, M.R.18
-
14
-
-
40149087235
-
Data and theory point to mainly additive genetic variance for complex traits
-
doi:10.1371/journal.pgen.1000008
-
Hill, W. G., Goddard, M. E., and Visscher, P. M. (2008). Data and theory point to mainly additive genetic variance for complex traits. PLoS Genet. 4, e1000008. doi:10.1371/journal.pgen.1000008
-
(2008)
PLoS Genet
, vol.4
-
-
Hill, W.G.1
Goddard, M.E.2
Visscher, P.M.3
-
15
-
-
79959918492
-
Evolving hard problems: generating human genetics datasets with a complex etiology
-
Himmelstein, D. S., Greene, C. S., and Moore, J. H. (2011). Evolving hard problems: generating human genetics datasets with a complex etiology. BioDataMin. 4, 21.
-
(2011)
BioDataMin
, vol.4
, pp. 21
-
-
Himmelstein, D.S.1
Greene, C.S.2
Moore, J.H.3
-
17
-
-
84887989803
-
A new measure of rank correlation. Biometrika 30, 81-89. Kraft, P., Zeggini, E., and Ioannidis, J. P. (2009). Replication in genome-wide association studies
-
Kendall, M. (1938). A new measure of rank correlation. Biometrika 30, 81-89. Kraft, P., Zeggini, E., and Ioannidis, J. P. (2009). Replication in genome-wide association studies. Stat. Sci. 24, 561-573.
-
(1938)
Stat. Sci.
, vol.24
, pp. 561-573
-
-
Kendall, M.1
-
18
-
-
56549090945
-
The Yin and Yang of HLA and KIR in human disease
-
Kulkarni, S., Martin, M. P., and Carring-ton, M. (2008). The Yin and Yang of HLA and KIR in human disease. Semin. Immunol. 20, 343-352.
-
(2008)
Semin. Immunol
, vol.20
, pp. 343-352
-
-
Kulkarni, S.1
Martin, M.P.2
Carring-ton, M.3
-
20
-
-
79952489475
-
Estimating missing heritability for disease from genome-wide association studies
-
Lee, S. H., Wray, N. R., Goddard, M. E., and Visscher, P. M. (2011a). Estimating missing heritability for disease from genome-wide association studies. Am. J. Hum. Genet. 88, 294-305.
-
(2011)
Am. J. Hum. Genet.
, vol.88
, pp. 294-305
-
-
Lee, S.H.1
Wray, N.R.2
Goddard, M.E.3
Visscher, P.M.4
-
21
-
-
79959898376
-
Prioritizing candidate disease genes by network-based boosting of genome-wide association data
-
Lee, I., Blom, U. M., Wang, P. I., Shim, J. E., and Marcotte, E. M. (2011b). Prioritizing candidate disease genes by network-based boosting of genome-wide association data. Genome Res. 21, 1109-1121.
-
(2011)
Genome Res
, vol.21
, pp. 1109-1121
-
-
Lee, I.1
Blom, U.M.2
Wang, P.I.3
Shim, J.E.4
Marcotte, E.M.5
-
22
-
-
77952570889
-
International Warfarin Pharmacogenet-ics Consortium Warfarin pharmacogenetics: a single VKORC1 polymorphism is predictive of dose across 3 racial groups
-
Limdi, N. A., Wadelius, M., Cavallari, L., Eriksson, N., Crawford, D. C., Lee, M. T., Chen, C. H., Motsinger-Reif, A., Sagreiya, H., Liu, N., Wu, A. H., Gage, B. F., Jorgensen, A., Pirmo-hamed, M., Shin, J. G., Suarez-Kurtz, G., Kimmel, S. E., Johnson, J. A., Klein, T. E., Wagner, M. J., and International Warfarin Pharmacogenet-ics Consortium. (2010). Warfarin pharmacogenetics: a single VKORC1 polymorphism is predictive of dose across 3 racial groups. Blood 115, 3827-3834.
-
(2010)
Blood
, vol.115
, pp. 3827-3834
-
-
Limdi, N.A.1
Wadelius, M.2
Cavallari, L.3
Eriksson, N.4
Crawford, D.C.5
Lee, M.T.6
Chen, C.H.7
Motsinger-Reif, A.8
Sagreiya, H.9
Liu, N.10
Wu, A.H.11
Gage, B.F.12
Jorgensen, A.13
Pirmo-hamed, M.14
Shin, J.G.15
Suarez-Kurtz, G.16
Kimmel, S.E.17
Johnson, J.A.18
Klein, T.E.19
Wagner, M.J.20
more..
-
23
-
-
77955064853
-
A versatile gene-based test for genome-wide association studies
-
Amfs Investigators
-
Liu, J. Z., McRae, A. F., Nyholt, D. R., Medland, S. E., Wray, N. R., Brown, K. M., AMFS Investigators, Hayward, N. K., Montgomery, G. W., Visscher, P. M., Martin, N. G., and Macgregor, S. (2010). A versatile gene-based test for genome-wide association studies. Am. J. Hum. Genet. 87, 139-145.
-
(2010)
Am. J. Hum. Genet.
, vol.87
, pp. 139-145
-
-
Liu, J.Z.1
McRae, A.F.2
Nyholt, D.R.3
Medland, S.E.4
Wray, N.R.5
Brown, K.M.6
Hayward, N.K.7
Montgomery, G.W.8
Visscher, P.M.9
Martin, N.G.10
Macgregor, S.11
-
24
-
-
63449100294
-
Capturing the spectrum of interaction effects in genetic association studies by simulated evaporative cooling network analysis
-
doi:10.1371/journal.pgen.1000432
-
McKinney, B. A., Crowe, J. E., Guo, J., and Tian, D. (2009). Capturing the spectrum of interaction effects in genetic association studies by simulated evaporative cooling network analysis. PLoS Genet. 5, e1000432. doi:10.1371/journal.pgen.1000432
-
(2009)
PLoS Genet
, vol.5
-
-
McKinney, B.A.1
Crowe, J.E.2
Guo, J.3
Tian, D.4
-
25
-
-
77953151341
-
Pathway analysis of breast cancer genome-wide association study highlights three pathways and one canonical signaling cascade
-
Menashe, I., Maeder, D., Garcia-Closas, M., Figueroa, J. D., Bhattacharjee, S., Rotunno, M., Kraft, P., Hunter, D. J., Chanock, S. J., Rosenberg, P. S., and Chatterjee, N. (2010). Pathway analysis of breast cancer genome-wide association study highlights three pathways and one canonical signaling cascade. Cancer Res. 70, 4453-4459.
-
(2010)
Cancer Res
, vol.70
, pp. 4453-4459
-
-
Menashe, I.1
Maeder, D.2
Garcia-Closas, M.3
Figueroa, J.D.4
Bhattacharjee, S.5
Rotunno, M.6
Kraft, P.7
Hunter, D.J.8
Chanock, S.J.9
Rosenberg, P.S.10
Chatterjee, N.11
-
26
-
-
33745599582
-
A flexible computational framework for detecting, characterizing, and interpreting statistical patterns of epistasis in genetic studies of human disease susceptibility
-
Moore, J. H., Gilbert, J. C., Tsai, C. T., Chiang, F. T., Holden, T., Barney, N., and White, B. C. (2006). A flexible computational framework for detecting, characterizing, and interpreting statistical patterns of epistasis in genetic studies of human disease susceptibility. J. Theor. Biol. 241, 252-261.
-
(2006)
J. Theor. Biol.
, vol.241
, pp. 252-261
-
-
Moore, J.H.1
Gilbert, J.C.2
Tsai, C.T.3
Chiang, F.T.4
Holden, T.5
Barney, N.6
White, B.C.7
-
27
-
-
79959768170
-
An examination of single nucleotide polymorphism selection prioritiza-tion strategies for tests of gene-gene interaction
-
Moskvina, V., Craddock, N., Muller-Myhsok, B., Kam-Thong, T., Green, E., Holmans, P., Owen, M. J., and ODonovan, M. C. (2011). An examination of single nucleotide polymorphism selection prioritiza-tion strategies for tests of gene-gene interaction. Biol. Psychiatry 70, 198-203.
-
(2011)
Biol. Psychiatry
, vol.70
, pp. 198-203
-
-
Moskvina, V.1
Craddock, N.2
Muller-Myhsok, B.3
Kam-Thong, T.4
Green, E.5
Holmans, P.6
Owen, M.J.7
O'Donovan, M.C.8
-
28
-
-
0003780986
-
The PageRank Citation Ranking: Bringing Order to the Web. Technical Report
-
Page, L., Brin, S., Motwani, R., and Winograd, T. (1999). The PageRank Citation Ranking: Bringing Order to the Web. Technical Report, Stanford InfoLab, 1-17.
-
(1999)
Stanford InfoLab
, pp. 1-17
-
-
Page, L.1
Brin, S.2
Motwani, R.3
Winograd, T.4
-
29
-
-
82255162545
-
A rare penetrant mutation in CFH confers high risk of age-related mac-ular degeneration
-
Raychaudhuri, S., Iartchouk, O., Chin, K., Tan, P. L., Tai, A. K., Ripke, S., Gowrisankar, S., Vemuri, S., Montgomery, K., Yu, Y., Reynolds, R., Zack, D. J., Campochiaro, B., Cam-pochiaro, P., Katsanis, N., Daly, M. J., and Seddon, J. M. (2011). A rare penetrant mutation in CFH confers high risk of age-related mac-ular degeneration. Nat. Genet. 43, 1232-1236.
-
(2011)
Nat. Genet.
, vol.43
, pp. 1232-1236
-
-
Raychaudhuri, S.1
Iartchouk, O.2
Chin, K.3
Tan, P.L.4
Tai, A.K.5
Ripke, S.6
Gowrisankar, S.7
Vemuri, S.8
Montgomery, K.9
Yu, Y.10
Reynolds, R.11
Zack, D.J.12
Campochiaro, B.13
Cam-pochiaro, P.14
Katsanis, N.15
Daly, M.J.16
Seddon, J.M.17
-
30
-
-
0034973569
-
Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer
-
Ritchie, M. D., Hahn, L. W., Roodi, N., Bailey, L. R., Dupont, W D., Parl, F. F., and Moore, J. H. (2001). Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer. Am. J. Hum. Genet. 69, 138-147.
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 138-147
-
-
Ritchie, M.D.1
Hahn, L.W.2
Roodi, N.3
Bailey, L.R.4
Dupont, W.D.5
Parl, F.F.6
Moore, J.H.7
-
31
-
-
80054975975
-
Deep sequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease
-
National Institute of Diabetes Digestive Kidney Diseases Inflammatory Bowel Disease Genetics Consortium (Niddk Ibdgc) United Kingdom Inflammatory Bowel Disease Genetics Consortium International Inflammatory Bowel Disease Genetics Consortium
-
Rivas, M. A., Beaudoin, M., Gardet, A., Stevens, C., Sharma, Y., Zhang, C. K., Boucher, G., Ripke, S., Elling-haus, D., Burtt, N., Fennell, T., Kirby, A., Latiano, A., Goyette, P., Green, T., Halfvarson, J., Haritu-nians, T., Korn, J. M., Kuruvilla, E, Lagace, C., Neale, B., Lo, K. S., Schumm, P., Törkvist, L., National Institute of Diabetes and Digestive Kidney Diseases Inflammatory Bowel Disease Genetics Consortium (NIDDK IBDGC), United Kingdom Inflammatory Bowel Disease Genetics Consortium, International Inflammatory Bowel Disease Genetics Consortium, Dubinsky, M. C., Brant, S. R., Silverberg, M. S., Duerr, R. H., Altshuler, D., Gabriel, S., Lettre, G., Franke, A., DAmato, M., McGovern, D. P., Cho, J. H., Rioux, J. D., Xavier, R. J., and Daly, M. J. (2011) Deep sequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease. Nat Genet. 43, 1066-1073.
-
(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
Boucher, G.7
Ripke, S.8
Elling-Haus, D.9
Burtt, N.10
Fennell, T.11
Kirby, A.12
Latiano, A.13
Goyette, P.14
Green, T.15
Halfvarson, J.16
Haritu-nians, T.17
Korn, J.M.18
Kuruvilla, E.19
Lagace, C.20
Neale, B.21
Lo, K.S.22
Schumm, P.23
Törkvist, L.24
Dubinsky, M.C.25
Brant, S.R.26
Silverberg, M.S.27
Duerr, R.H.28
Altshuler, D.29
Gabriel, S.30
Lettre, G.31
Franke, A.32
DAmato, M.33
McGovern, D.P.34
Cho, J.H.35
Rioux, J.D.36
Xavier, R.J.37
Daly, M.J.38
more..
-
32
-
-
77951133654
-
Genome-wide association studies in diverse populations
-
Rosenberg, N. A., Huang, L., Jewett, E. M., Szpiech, Z. A., Jankovic, I., and Boehnke, M. (2010). Genome-wide association studies in diverse populations. Nat. Rev. Genet. 11, 356-366.
-
(2010)
Nat. Rev. Genet.
, vol.11
, pp. 356-366
-
-
Rosenberg, N.A.1
Huang, L.2
Jewett, E.M.3
Szpiech, Z.A.4
Jankovic, I.5
Boehnke, M.6
-
33
-
-
0037387365
-
Does accounting for gene-environment (GxE) interaction increase the power to detect the effect of a gene in amul-tifactorial disease? Genet
-
Selinger-Leneman, H., Genin, E., Nor-ris, J. M., and Khlat, M. (2003). Does accounting for gene-environment (GxE) interaction increase the power to detect the effect of a gene in amul-tifactorial disease? Genet. Epidemiol. 24, 200-207.
-
(2003)
Epidemiol
, vol.24
, pp. 200-207
-
-
Selinger-Leneman, H.1
Genin, E.2
Nor-ris, J.M.3
Khlat, M.4
-
34
-
-
68449096727
-
Common variants on chromosome 6p22 1 are associated with schizophrenia
-
Shi, J., Levinson, D. F., Duan, J., Sanders, A. R., Zheng, Y., Peer, I., Dudbridge, E, Holmans, P. A., Whittemore, A. S., Mowry, B. J., Olincy, A., Amin, E, Cloninger, C. R., Silverman, J. M., Buccola, N. G., Byerley, W. F., Black, D. W., Crowe, R. R., Oksen-berg, J. R., Mirel, D. B., Kendler, K. S., Freedman, R., and Gejman, P. V. (2009). Common variants on chromosome 6p22.1 are associated with schizophrenia. Nature 460, 753-757.
-
(2009)
Nature
, vol.460
, pp. 753-757
-
-
Shi, J.1
Levinson, D.F.2
Duan, J.3
Sanders, A.R.4
Zheng, Y.5
Peer, I.6
Dudbridge, E.7
Holmans, P.A.8
Whittemore, A.S.9
Mowry, B.J.10
Olincy, A.11
Amin, E.12
Cloninger, C.R.13
Silverman, J.M.14
Buccola, N.G.15
Byerley, W.F.16
Black, D.W.17
Crowe, R.R.18
Oksen-berg, J.R.19
Mirel, D.B.20
Kendler, K.S.21
Freedman, R.22
Gejman, P.V.23
more..
-
35
-
-
75649149885
-
Methodological challenges of genome-wide association analysis in Africa
-
Teo, Y Y, Small, K. S., and Kwiatkowski, D. P. (2010). Methodological challenges of genome-wide association analysis in Africa. Nat. Rev. Genet. 11, 149-160.
-
(2010)
Nat. Rev. Genet.
, vol.11
, pp. 149-160
-
-
Teo, Y.Y.1
Small, K.S.2
Kwiatkowski, D.P.3
-
36
-
-
53649098737
-
Pathway analysis of seven common diseases assessed by genome-wide association
-
Torkamani, A., Topol, E. J., and Schork, N. J. (2008). Pathway analysis of seven common diseases assessed by genome-wide association. Genomics 92, 265-272.
-
(2008)
Genomics
, vol.92
, pp. 265-272
-
-
Torkamani, A.1
Topol, E.J.2
Schork, N.J.3
-
37
-
-
82255192188
-
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
-
Spanish Consortium on the Genetics of Coeliac Disease (Cegec) Prevent C.D. Study Group Wellcome Trust Case Control Consortium (Wtccc)
-
Trynka, G., Hunt, K. A., Bockett, N. A., Romanos, J., Mistry, V., Szperl, A., Bakker, S. F., Bardella, M. T., Bhaw-Rosun, L., Castillejo, G., de la Concha, E. G., de Almeida, R. C., Dias, K. R., van Diemen, C. C., Dubois, P. C., Duerr, R. H., Edkins, S., Franke, L., Fransen, K., Gutierrez, J., Heap, G. A., Hrdlickova, B., Hunt, S., Izurieta, L. P., Izzo, V., Joosten, L. A., Lang-ford, C., Mazzilli, M. C., Mein, C. A., Midah, V., Mitrovic, M., Mora, B., Morelli, M., Nutland, S., Núñez, C., Onengut-Gumuscu, S., Pearce, K., Platteel, M., Polanco, I., Potter, S., Ribes-Koninckx, C., Ricaño-Ponce, I., Rich, S. S., Rybak, A., Santiago, J. L., Senapati, S., Sood, A., Sza-jewska, H., Troncone, R., Varadé, J., Wallace, C., Wolters, V. M., Zher-nakova, A., Spanish Consortium on the Genetics of Coeliac Disease (CEGEC), Prevent CD Study Group, Wellcome Trust Case Control Consortium (WTCCC), Thelma, B. K., Cukrowska, B., Urcelay, E., Bilbao, J. R., Mearin, M. L., Barisani, D., Barrett, J. C., Plagnol, V., Deloukas, P., Wijmenga, C., and van Heel, D. A. (2011) Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease. Nat. Genet. 43, 1193-1201.
-
(2011)
Nat. Genet.
, vol.43
, pp. 1193-1201
-
-
Trynka, G.1
Hunt, K.A.2
Bockett, N.A.3
Romanos, J.4
Mistry, V.5
Szperl, A.6
Bakker, S.F.7
Bardella, M.T.8
Bhaw-Rosun, L.9
Castillejo, G.10
de la Concha, E.G.11
de Almeida, R.C.12
Dias, K.R.13
Van Diemen, C.C.14
Dubois, P.C.15
Duerr, R.H.16
Edkins, S.17
Franke, L.18
Fransen, K.19
Gutierrez, J.20
Heap, G.A.21
Hrdlickova, B.22
Hunt, S.23
Izurieta, L.P.24
Izzo, V.25
Joosten, L.A.26
Lang-ford, C.27
Mazzilli, M.C.28
Mein, C.A.29
Midah, V.30
Mitrovic, M.31
Mora, B.32
Morelli, M.33
Nutland, S.34
Núñez, C.35
Onengut-Gumuscu, S.36
Pearce, K.37
Platteel, M.38
Polanco, I.39
Potter, S.40
Ribes-Koninckx, C.41
Ricaño-Ponce, I.42
Rich, S.S.43
Rybak, A.44
Santiago, J.L.45
Senapati, S.46
Sood, A.47
Sza-jewska, H.48
Troncone, R.49
Varadé, J.50
Wallace, C.51
Wolters, V.M.52
Zher-nakova, A.53
Thelma, B.K.54
Cukrowska, B.55
Urcelay, E.56
Bilbao, J.R.57
Mearin, M.L.58
Barisani, D.59
Barrett, J.C.60
Plagnol, V.61
Deloukas, P.62
Wijmenga, C.63
van Heel, D.A.64
more..
-
38
-
-
84860151961
-
Evidence-based psychiatric genetics AKA the false dichotomy between common and rare variant hypotheses
-
doi:10.1038/mp.2011.65. [Epub ahead of print]
-
Visscher, P. M., Goddard, M. E., Derks, E. M., and Wray, N. R. (2011). Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses. Mol Psychiatry 14. doi:10.1038/mp.2011.65. [Epub ahead of print].
-
(2011)
Mol Psychiatry
, vol.14
-
-
Visscher, P.M.1
Goddard, M.E.2
Derks, E.M.3
Wray, N.R.4
-
39
-
-
77954140531
-
Common SNPs explain a large proportion of the heritability for human height
-
Yang, J., Benyamin, B., McEvoy, B. P., Gordon, S., Henders, A. K., Nyholt, D. R., Madden, P. A., Heath, A. C., Martin, N. G., Montgomery, G. W., Goddard, M. E., and Visscher, P. M. (2010). Common SNPs explain a large proportion of the heritability for human height. Nat. Genet. 42, 565-569.
-
(2010)
Nat. Genet
, vol.42
, pp. 565-569
-
-
Yang, J.1
Benyamin, B.2
McEvoy, B.P.3
Gordon, S.4
Henders, A.K.5
Nyholt, D.R.6
Madden, P.A.7
Heath, A.C.8
Martin, N.G.9
Montgomery, G.W.10
Goddard, M.E.11
Visscher, P.M.12
|