-
1
-
-
0031912090
-
Genetic and familial aspects of narcolepsy
-
Mignot, E Genetic and familial aspects of narcolepsy. Neurology 50, S16-S22 (1998
-
(1998)
Neurology
, vol.50
, pp. S16-S22
-
-
Mignot, E.1
-
2
-
-
0034967934
-
Narcolepsy: Clinical features, new pathophysiologic insights, and future perspectives
-
Overeem, S., Mignot, E., van Dijk, J. G., & Lammers, G. J. Narcolepsy: clinical features, new pathophysiologic insights, and future perspectives. J. Clin. Neurophysiol. 18, 78-105 (2001
-
(2001)
J. Clin. Neurophysiol
, vol.18
, pp. 78-105
-
-
Overeem, S.1
Mignot, E.2
Van Dijk, J.G.3
Lammers, G.J.4
-
3
-
-
0021678613
-
HLA antigens in Japanese patients with narcolepsy all the patients were dr2 positive
-
Juji, T., Satake, M., Honda, Y., & Doi, Y. HLA antigens in Japanese patients with narcolepsy. All the patients were DR2 positive. Tissue Antigens 24, 316-319 (1984
-
(1984)
Tissue Antigens
, vol.24
, pp. 316-319
-
-
Juji, T.1
Satake, M.2
Honda, Y.3
Doi, Y.4
-
4
-
-
0021713242
-
Genetic markers in narcolepsy
-
Langdon, N., Welsh, K I., van Dam, M., Vaughan, R. W., & Parkes, D. Genetic markers in narcolepsy. Lancet 2, 1178-1180 (1984
-
(1984)
Lancet
, vol.2
, pp. 1178-1180
-
-
Langdon, N.1
Welsh, K.I.2
Van Dam, M.3
Vaughan, R.W.4
Parkes, D.5
-
5
-
-
0022338992
-
Human histocompatibility leukocyte antigen (HLA) haplotype frequencies estimated from the data on HLA class i II, and III antigens in 111 Japanese narcoleptics
-
Matsuki, K., Juji, T., Tokunaga, K., Naohara, T., Satake, M., & Honda, Y. Human histocompatibility leukocyte antigen (HLA) haplotype frequencies estimated from the data on HLA class I, II, and III antigens in 111 Japanese narcoleptics. J. Clin. Invest. 76, 2078-2083 (1985
-
(1985)
J. Clin. Invest
, vol.76
, pp. 2078-2083
-
-
Matsuki, K.1
Juji, T.2
Tokunaga, K.3
Naohara, T.4
Satake, M.5
Honda, Y.6
-
6
-
-
0034433373
-
Identification of a telomeric boundary of the HLA region with potential for predisposition to human narcolepsy
-
Miyagawa, T., Hohjoh, H., Honda, Y., Juji, T., & Tokunaga, K Identification of a telomeric boundary of the HLA region with potential for predisposition to human narcolepsy. Immunogenetics 52, 12-18 (2000
-
(2000)
Immunogenetics
, vol.52
, pp. 12-18
-
-
Miyagawa, T.1
Hohjoh, H.2
Honda, Y.3
Juji, T.4
Tokunaga, K.5
-
7
-
-
0035091595
-
Complex HLA-DR and-DQ interactions confer risk of narcolepsy-cataplexy in three ethnic groups
-
Mignot, E., Lin, L., Rogers, W., Honda, Y., Qiu, X., Lin, X., et al. Complex HLA-DR and-DQ interactions confer risk of narcolepsy-cataplexy in three ethnic groups. Am. J. Hum. Genet. 68, 686-699 (2001
-
(2001)
Am. J. Hum. Genet
, vol.68
, pp. 686-699
-
-
Mignot, E.1
Lin, L.2
Rogers, W.3
Honda, Y.4
Qiu, X.5
Lin, X.6
-
8
-
-
55049121064
-
Variant between CPT1B and CHKB associated with susceptibility to narcolepsy
-
Miyagawa, T., Kawashima, M., Nishida, N., Ohashi, J., Kimura, R., Fujimoto, A., et al. Variant between CPT1B and CHKB associated with susceptibility to narcolepsy. Nat. Genet. 40, 1324-1328 (2008
-
(2008)
Nat. Genet
, vol.40
, pp. 1324-1328
-
-
Miyagawa, T.1
Kawashima, M.2
Nishida, N.3
Ohashi, J.4
Kimura, R.5
Fujimoto, A.6
-
9
-
-
66649111903
-
Narcolepsy is strongly associated with the T-cell receptor alpha locus
-
Hallmayer, J., Faraco, J., Lin, L., Hesselson, S., Winkelmann, J., Kawashima, M., et al. Narcolepsy is strongly associated with the T-cell receptor alpha locus. Nat. Genet. 41, 708-711 (2009
-
(2009)
Nat. Genet
, vol.41
, pp. 708-711
-
-
Hallmayer, J.1
Faraco, J.2
Lin, L.3
Hesselson, S.4
Winkelmann, J.5
Kawashima, M.6
-
10
-
-
78651245467
-
Common variants in P2RY11 are associated with narcolepsy
-
Kornum, B. R., Kawashima, M., Faraco, J., Lin, L., Rico, T. J., Hesselson, S., et al. Common variants in P2RY11 are associated with narcolepsy. Nat. Genet. 43, 66-71 (2011
-
(2011)
Nat. Genet
, vol.43
, pp. 66-71
-
-
Kornum, B.R.1
Kawashima, M.2
Faraco, J.3
Lin, L.4
Rico, T.J.5
Hesselson, S.6
-
11
-
-
84874783317
-
ImmunoChip study implicates antigen presentation to T cells in narcolepsy
-
Faraco, J., Lin, L., Kornum, B R., Kenny, E. E., Trynka, G., Einen, M., et al. ImmunoChip study implicates antigen presentation to T cells in narcolepsy. PLoS Genet. 9, e1003270 (2013
-
(2013)
PLoS Genet
, vol.9
, pp. e1003270
-
-
Faraco, J.1
Lin, L.2
Kornum, B.R.3
Kenny, E.E.4
Trynka, G.5
Einen, M.6
-
12
-
-
84887299056
-
Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic
-
Han, F., Faraco, J., Dong, X S., Ollila, H. M., Lin, L., Li, J., et al. Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic. PLoS Genet. 9, e1003880 (2013
-
(2013)
PLoS Genet
, vol.9
, pp. e1003880
-
-
Han, F.1
Faraco, J.2
Dong, X.S.3
Ollila, H.M.4
Lin, L.5
Li, J.6
-
13
-
-
0033588184
-
Narcolepsy in orexin knockout mice: Molecular genetics of sleep regulation
-
Chemelli, R M., Willie, J. T., Sinton, C. M., Elmquist, J. K., Scammell, T., Lee, C., et al. Narcolepsy in orexin knockout mice: molecular genetics of sleep regulation. Cell 98, 437-451 (1999
-
(1999)
Cell
, vol.98
, pp. 437-451
-
-
Chemelli, R.M.1
Willie, J.T.2
Sinton, C.M.3
Elmquist, J.K.4
Scammell, T.5
Lee, C.6
-
14
-
-
0033529520
-
The sleep disorder canine narcolepsy is caused by a mutation in the hypocretin (orexin) receptor 2 gene
-
Lin, L., Faraco, J., Li, R., Kadotani, H., Rogers, W., Lin, X., et al The sleep disorder canine narcolepsy is caused by a mutation in the hypocretin (orexin) receptor 2 gene. Cell 98, 365-376 (1999
-
(1999)
Cell
, vol.98
, pp. 365-376
-
-
Lin, L.1
Faraco, J.2
Li, R.3
Kadotani, H.4
Rogers, W.5
Lin, X.6
-
15
-
-
0036791834
-
The role of cerebrospinal fluid hypocretin measurement in the diagnosis of narcolepsy and other hypersomnias
-
Mignot, E., Lammers, G. J., Ripley, B., Okun, M., Nevsimalova, S., Overeem, S., et al. The role of cerebrospinal fluid hypocretin measurement in the diagnosis of narcolepsy and other hypersomnias. Arch. Neurol. 59, 1553-1562 (2002
-
(2002)
Arch. Neurol
, vol.59
, pp. 1553-1562
-
-
Mignot, E.1
Lammers, G.J.2
Ripley, B.3
Okun, M.4
Nevsimalova, S.5
Overeem, S.6
-
16
-
-
0033971611
-
Hypocretin (orexin deficiency in human narcolepsy
-
Nishino, S., Ripley, B., Overeem, S., Lammers, G. J., & Mignot, E. Hypocretin (orexin) deficiency in human narcolepsy. Lancet 355, 39-40 (2000
-
(2000)
Lancet
, vol.355
, pp. 39-40
-
-
Nishino, S.1
Ripley, B.2
Overeem, S.3
Lammers, G.J.4
Mignot, E.5
-
17
-
-
0035830409
-
A prepro-orexin gene polymorphism is associated with narcolepsy
-
Gencik, M., Dahmen, N., Wieczorek, S., Kasten, M., Bierbrauer, J., Anghelescu, I., et al. A prepro-orexin gene polymorphism is associated with narcolepsy. Neurology 56, 115-117 (2001
-
(2001)
Neurology
, vol.56
, pp. 115-117
-
-
Gencik, M.1
Dahmen, N.2
Wieczorek, S.3
Kasten, M.4
Bierbrauer, J.5
Anghelescu, I.6
-
18
-
-
0035960580
-
Polymorphisms in hypocretin/orexin pathway genes and narcolepsy
-
Olafsdottir, B R., Rye, D. B., Scammell, T. E., Matheson, J. K., Stefansson, K., & Gulcher, J. R. Polymorphisms in hypocretin/orexin pathway genes and narcolepsy. Neurology 57, 1896-1899 (2001
-
(2001)
Neurology
, vol.57
, pp. 1896-1899
-
-
Olafsdottir, B.R.1
Rye, D.B.2
Scammell, T.E.3
Matheson, J.K.4
Stefansson, K.5
Gulcher, J.R.6
-
19
-
-
0033826856
-
A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains
-
Peyron, C., Faraco, J., Rogers, W., Ripley, B., Overeem, S., Charnay, Y., et al. A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains. Nat. Med. 6, 991-997 (2000
-
(2000)
Nat. Med
, vol.6
, pp. 991-997
-
-
Peyron, C.1
Faraco, J.2
Rogers, W.3
Ripley, B.4
Overeem, S.5
Charnay, Y.6
-
20
-
-
0035960658
-
Polymorphisms in the vicinity of the hypocretin/orexin are not associated with human narcolepsy
-
Hungs, M., Lin, L., Okun, M., & Mignot, E Polymorphisms in the vicinity of the hypocretin/orexin are not associated with human narcolepsy. Neurology 57, 1893-1895 (2001
-
(2001)
Neurology
, vol.57
, pp. 1893-1895
-
-
Hungs, M.1
Lin, L.2
Okun, M.3
Mignot, E.4
-
21
-
-
35148900346
-
Idiopathic hypersomnia: A study of 77 cases
-
Anderson, K N., Pilsworth, S., Sharples, L. D., Smith, I. E., & Shneerson, J. M. Idiopathic hypersomnia: a study of 77 cases. Sleep 30, 1274-1281 (2007
-
(2007)
Sleep
, vol.30
, pp. 1274-1281
-
-
Anderson, K.N.1
Pilsworth, S.2
Sharples, L.D.3
Smith, I.E.4
Shneerson, J.M.5
-
22
-
-
65549133714
-
Polymorphism located between CPT1B and CHKB, and HLA-DRB1 1501-DQB1 0602 haplotype confer susceptibility to CNS hypersomnias (essential hypersomnia
-
Miyagawa, T., Honda, M., Kawashima, M., Shimada, M., Tanaka, S., Honda, Y., et al Polymorphism located between CPT1B and CHKB, and HLA-DRB1 1501-DQB1 0602 haplotype confer susceptibility to CNS hypersomnias (essential hypersomnia). PLoS ONE 4, e5394 (2009
-
(2009)
PLoS ONE
, vol.4
, pp. e5394
-
-
Miyagawa, T.1
Honda, M.2
Kawashima, M.3
Shimada, M.4
Tanaka, S.5
Honda, Y.6
-
23
-
-
0022852908
-
HLA-DR2 and Dw2 in narcolepsy and in other disorders of excessive somnolence without cataplexy
-
Honda, Y., Juji, T., Matsuki, K., Naohara, T., Satake, M., Inoko, H., et al HLA-DR2 and Dw2 in narcolepsy and in other disorders of excessive somnolence without cataplexy. Sleep 9, 1-2 (1986
-
(1986)
Sleep
, vol.9
, pp. 1-2
-
-
Honda, Y.1
Juji, T.2
Matsuki, K.3
Naohara, T.4
Satake, M.5
Inoko, H.6
-
24
-
-
0002196714
-
-
eds Inoue, S., & Hayashi, O. Academic Press, New York, NY, USA
-
Honda, Y., Takahashi, Y., Honda, M., Watanabe, Y., Sato, T., Miki, T., et al in Sleep and Sleep Disorders: From Molecule to Behavior. (eds Inoue, S., & Hayashi, O.) 341-358 (Academic Press, New York, NY, USA, 1997
-
(1997)
Sleep and Sleep Disorders: From Molecule to Behavior
, pp. 341-358
-
-
Honda, Y.1
Takahashi, Y.2
Honda, M.3
Watanabe, Y.4
Sato, T.5
Miki, T.6
-
25
-
-
17144399243
-
Difference in the characteristics of subjective and objective sleepiness between narcolepsy and essential hypersomnia
-
Komada, Y., Inoue, Y., Mukai, J., Shirakawa, S., Takahashi, K., & Honda, Y Difference in the characteristics of subjective and objective sleepiness between narcolepsy and essential hypersomnia. Psychiatry Clin Neurosci. 59, 194-199 (2005
-
(2005)
Psychiatry Clin Neurosci
, vol.59
, pp. 194-199
-
-
Komada, Y.1
Inoue, Y.2
Mukai, J.3
Shirakawa, S.4
Takahashi, K.5
Honda, Y.6
-
26
-
-
76149113932
-
Polymorphism located in TCRA locus confers susceptibility to essential hypersomnia with HLA-DRB1 1501-DQB1 0602 haplotype
-
Miyagawa, T., Honda, M., Kawashima, M., Shimada, M., Tanaka, S., Honda, Y., et al. Polymorphism located in TCRA locus confers susceptibility to essential hypersomnia with HLA-DRB1 1501-DQB1 0602 haplotype. J. Hum. Genet. 55, 63-65 (2010
-
(2010)
J. Hum. Genet
, vol.55
, pp. 63-65
-
-
Miyagawa, T.1
Honda, M.2
Kawashima, M.3
Shimada, M.4
Tanaka, S.5
Honda, Y.6
-
27
-
-
55549147191
-
Personal genomes: The case of the missing heritability
-
Maher, B Personal genomes: the case of the missing heritability. Nature 456, 18-21 (2008
-
(2008)
Nature
, vol.456
, pp. 18-21
-
-
Maher, B.1
-
28
-
-
70349956433
-
Finding the missing heritability of complex diseases
-
Manolio, T A., Collins, F. S., Cox, N. J., Goldstein, D. B., Hindorff, L. A., Hunter, D. J., et al. Finding the missing heritability of complex diseases. Nature 461, 747-753 (2009
-
(2009)
Nature
, vol.461
, pp. 747-753
-
-
Manolio, T.A.1
Collins, F.S.2
Cox, N.J.3
Goldstein, D.B.4
Hindorff, L.A.5
Hunter, D.J.6
-
29
-
-
84940597465
-
A polymorphism in CCR1/CCR3 is associated with narcolepsy
-
Toyoda, H., Miyagawa, T., Koike, A., Kanbayashi, T., Imanishi, A., Sagawa, Y., et al. A polymorphism in CCR1/CCR3 is associated with narcolepsy. Brain Behav. Immun. 49, 148-155 (2015
-
(2015)
Brain Behav. Immun
, vol.49
, pp. 148-155
-
-
Toyoda, H.1
Miyagawa, T.2
Koike, A.3
Kanbayashi, T.4
Imanishi, A.5
Sagawa, Y.6
-
30
-
-
84877128327
-
Genome-wide association study of HLA-DQB1 06: 02 negative essential hypersomnia
-
Khor, S S., Miyagawa, T., Toyoda, H., Yamasaki, M., Kawamura, Y., Tanii, H., et al. Genome-wide association study of HLA-DQB1 06: 02 negative essential hypersomnia. PeerJ 1, e66 (2013
-
(2013)
PeerJ
, vol.1
, pp. e66
-
-
Khor, S.S.1
Miyagawa, T.2
Toyoda, H.3
Yamasaki, M.4
Kawamura, Y.5
Tanii, H.6
-
31
-
-
84869795630
-
Meta-Analysis of genome-wide association studies for panic disorder in the Japanese population
-
Otowa, T., Kawamura, Y., Nishida, N., Sugaya, N., Koike, A., Yoshida, E., et al. Meta-Analysis of genome-wide association studies for panic disorder in the Japanese population. Transl. Psychiatry 2, e186 (2012
-
(2012)
Transl Psychiatry
, vol.2
, pp. e186
-
-
Otowa, T.1
Kawamura, Y.2
Nishida, N.3
Sugaya, N.4
Koike, A.5
Yoshida, E.6
-
32
-
-
77950213320
-
Association of the oxytocin receptor (OXTR) gene polymorphisms with autism spectrum disorder (ASD) in the Japanese population
-
Liu, X. X., Kawamura, Y., Shimada, T., Otowa, T., Koishi, S., Sugiyama, T., et al. Association of the oxytocin receptor (OXTR) gene polymorphisms with autism spectrum disorder (ASD) in the Japanese population. J. Hum. Genet. 55, 137-141 (2010
-
(2010)
J. Hum. Genet
, vol.55
, pp. 137-141
-
-
Liu, X.X.1
Kawamura, Y.2
Shimada, T.3
Otowa, T.4
Koishi, S.5
Sugiyama, T.6
-
33
-
-
52649146975
-
Association and interaction analyses of NRG1 and ERBB4 genes with schizophrenia in a Japanese population
-
Shiota, S., Tochigi, M., Shimada, H., Ohashi, J., Kasai, K., Kato, N., et al. Association and interaction analyses of NRG1 and ERBB4 genes with schizophrenia in a Japanese population. J. Hum. Genet. 53, 929-935 (2008
-
(2008)
J. Hum. Genet
, vol.53
, pp. 929-935
-
-
Shiota, S.1
Tochigi, M.2
Shimada, H.3
Ohashi, J.4
Kasai, K.5
Kato, N.6
-
34
-
-
34247364967
-
Association study between the TNXB locus and schizophrenia in a Japanese population
-
Tochigi, M., Zhang, X., Ohashi, J., Hibino, H., Otowa, T., Rogers, M., et al. Association study between the TNXB locus and schizophrenia in a Japanese population. Am. J. Med. Genet. B Neuropsychiatr. Genet. 144B, 305-309 (2007
-
(2007)
Am. J. Med. Genet. B Neuropsychiatr. Genet
, vol.144 B
, pp. 305-309
-
-
Tochigi, M.1
Zhang, X.2
Ohashi, J.3
Hibino, H.4
Otowa, T.5
Rogers, M.6
-
35
-
-
78650570457
-
Meta-Analysis of genome-wide association scans for genetic susceptibility to endometriosis in Japanese population
-
Adachi, S., Tajima, A., Quan, J., Haino, K., Yoshihara, K., Masuzaki, H., et al. Meta-Analysis of genome-wide association scans for genetic susceptibility to endometriosis in Japanese population. J. Hum. Genet. 55, 816-821 (2010
-
(2010)
J. Hum. Genet
, vol.55
, pp. 816-821
-
-
Adachi, S.1
Tajima, A.2
Quan, J.3
Haino, K.4
Yoshihara, K.5
Masuzaki, H.6
-
36
-
-
52949141845
-
Integrated detection and population-genetic analysis of SNPs and copy number variation
-
McCarroll, S. A., Kuruvilla, F. G., Korn, J. M., Cawley, S., Nemesh, J., Wysoker, A., et al. Integrated detection and population-genetic analysis of SNPs and copy number variation. Nat. Genet. 40, 1166-1174 (2008
-
(2008)
Nat. Genet
, vol.40
, pp. 1166-1174
-
-
McCarroll, S.A.1
Kuruvilla, F.G.2
Korn, J.M.3
Cawley, S.4
Nemesh, J.5
Wysoker, A.6
-
37
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population-based linkage analyses
-
Purcell, S., Neale, B., Todd-Brown, K., Thomas, L., Ferreira, M. A. R., Bender, D., et al. PLINK: A tool set for whole-genome association and population-based linkage analyses. Am. J. Hum. Genet. 81, 559-575 (2007
-
(2007)
Am. J. Hum. Genet
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.R.5
Bender, D.6
-
38
-
-
33846006923
-
Population structure and eigenanalysis
-
Patterson, N., Price, A L., & Reich, D. Population structure and eigenanalysis. PLoS Genet. 2, 2074-2093 (2006
-
(2006)
PLoS Genet
, vol.2
, pp. 2074-2093
-
-
Patterson, N.1
Price, A.L.2
Reich, D.3
-
39
-
-
79959503826
-
The international hapmap project
-
International HapMap Consortium
-
International HapMap Consortium The International HapMap Project. Nature 426, 789-796 (2003
-
(2003)
Nature
, vol.426
, pp. 789-796
-
-
-
40
-
-
79959716798
-
PredictABEL: An R package for the assessment of risk prediction models
-
Kundu, S., Aulchenko, Y. S., van Duijn, C. M., & Janssens, A. C. PredictABEL: an R package for the assessment of risk prediction models. Eur. J. Epidemiol. 26, 261-264 (2011
-
(2011)
Eur. J. Epidemiol
, vol.26
, pp. 261-264
-
-
Kundu, S.1
Aulchenko, Y.S.2
Van Duijn, C.M.3
Janssens, A.C.4
-
41
-
-
84992381175
-
The new s language-A programming environment for data-Analysis and graphics
-
Austin, G. The New S Language-A programming environment for data-Analysis and graphics. Econ. J. 100, 650-652 (1990
-
(1990)
Econ J.
, vol.100
, pp. 650-652
-
-
Austin, G.1
-
42
-
-
78650856517
-
GCTA: A tool for genome-wide complex trait analysis
-
Yang, J., Lee, S. H., Goddard, M. E., & Visscher, P. M. GCTA: a tool for genome-wide complex trait analysis. Am. J. Hum. Genet. 88, 76-82 (2011
-
(2011)
Am. J. Hum. Genet
, vol.88
, pp. 76-82
-
-
Yang, J.1
Lee, S.H.2
Goddard, M.E.3
Visscher, P.M.4
-
43
-
-
0025104345
-
Discordant for narcolepsy
-
Pollmacher, T., Schulz, H., Geisler, P., Kiss, E., Albert, E D., Schwarzfischer, F., et al. Discordant for narcolepsy. Sleep 13, 336-343 (1990
-
(1990)
Sleep
, vol.13
, pp. 336-343
-
-
Pollmacher, T.1
Schulz, H.2
Geisler, P.3
Kiss, E.4
Albert, E.D.5
Schwarzfischer, F.6
-
44
-
-
0031265368
-
Influence of dominance relationships on the estimation of dominance variance with sire-dam subclass effects
-
Gengler, N., VanVleck, L. D., MacNeil, M. D., Misztal, I., & Pariacote, F. A. Influence of dominance relationships on the estimation of dominance variance with sire-dam subclass effects. J. Anim. Sci. 75, 2885-2891 (1997
-
(1997)
J. Anim. Sci
, vol.75
, pp. 2885-2891
-
-
Gengler, N.1
VanVleck, L.D.2
MacNeil, M.D.3
Misztal, I.4
Pariacote, F.A.5
-
45
-
-
34247535497
-
Non-Additive genetic effects for fertility traits in canadian holstein cattle (open access publication)
-
Palucci, V., Schaeffer, L. R., Miglior, F., & Osborne, V. Non-Additive genetic effects for fertility traits in Canadian Holstein cattle (Open Access publication). Genet. Sel. Evol. 39, 181-193 (2007
-
(2007)
Genet. Sel. Evol
, vol.39
, pp. 181-193
-
-
Palucci, V.1
Schaeffer, L.R.2
Miglior, F.3
Osborne, V.4
-
46
-
-
77953285391
-
Estimation of the additive and dominance variances in SA Duroc pigs
-
Norris, D., Varona, L., Ngambi, J. W., Visser, D. P., Mbajiorgu, C. A., & Voordewind, S. F. Estimation of the additive and dominance variances in SA Duroc pigs. Livest. Sci. 131, 144-147 (2010
-
(2010)
Livest. Sci
, vol.131
, pp. 144-147
-
-
Norris, D.1
Varona, L.2
Ngambi, J.W.3
Visser, D.P.4
Mbajiorgu, C.A.5
Voordewind, S.F.6
-
47
-
-
84873091770
-
Genome-wide association analysis identifies new susceptibility loci for Behcet's disease and epistasis between HLA-B51 and ERAP1
-
Kirino, Y., Bertsias, G., Ishigatsubo, Y., Mizuki, N., Tugal-Tutkun, I., Seyahi, E., et al. Genome-wide association analysis identifies new susceptibility loci for Behcet's disease and epistasis between HLA-B. 51 and ERAP1. Nat. Genet. 45, 202-207 (2013
-
(2013)
Nat. Genet
, vol.45
, pp. 202-207
-
-
Kirino, Y.1
Bertsias, G.2
Ishigatsubo, Y.3
Mizuki, N.4
Tugal-Tutkun, I.5
Seyahi, E.6
|