-
2
-
-
37849001811
-
Screening for idiopathic scoliosis in adolescents. An information statement
-
Richards, B.S. and Vitale, M.G. (2008) Screening for idiopathic scoliosis in adolescents. An information statement. J. Bone Joint Surg. Am., 90, 195-198.
-
(2008)
J. Bone Joint Surg. Am.
, vol.90
, pp. 195-198
-
-
Richards, B.S.1
Vitale, M.G.2
-
3
-
-
77954627002
-
Brace wear control of curve progression in adolescent idiopathic scoliosis
-
Katz, D.E., Herring, J.A., Browne, R.H., Kelly, D.M. and Birch, J.G. (2010) Brace wear control of curve progression in adolescent idiopathic scoliosis. J. Bone Joint Surg. Am., 92, 1343-1352.
-
(2010)
J. Bone Joint Surg. Am.
, vol.92
, pp. 1343-1352
-
-
Katz, D.E.1
Herring, J.A.2
Browne, R.H.3
Kelly, D.M.4
Birch, J.G.5
-
4
-
-
41549129915
-
Understanding genetic factors in idiopathic scoliosis, a complex disease of childhood
-
Wise, C.A., Gao, X., Shoemaker, S., Gordon, D. and Herring, J.A. (2008) Understanding genetic factors in idiopathic scoliosis, a complex disease of childhood. Curr. Genomics, 9, 51-59.
-
(2008)
Curr. Genomics
, vol.9
, pp. 51-59
-
-
Wise, C.A.1
Gao, X.2
Shoemaker, S.3
Gordon, D.4
Herring, J.A.5
-
5
-
-
84878192368
-
-
Kusumi, K. and Dunwoodie, S.L. (eds), Springer
-
Wise, C.A. and Sharma, S. (2009) Kusumi, K. and Dunwoodie, S.L. (eds), The Genetics and Development of Scoliosis. Springer, pp. 167-190.
-
(2009)
The Genetics and Development of Scoliosis
, pp. 167-190
-
-
Wise, C.A.1
Sharma, S.2
-
6
-
-
0033583078
-
Synteny-defined candidate genes for congenital and idiopathic scoliosis
-
Giampietro, P.F., Raggio, C.L. and Blank, R.D. (1999) Synteny-defined candidate genes for congenital and idiopathic scoliosis. Am. J. Med. Genet., 83, 164-177.
-
(1999)
Am. J. Med. Genet.
, vol.83
, pp. 164-177
-
-
Giampietro, P.F.1
Raggio, C.L.2
Blank, R.D.3
-
7
-
-
33644781662
-
A novel murine gene, Sickle tail, linked to the Danforth's short tail locus, is required for normal development of the intervertebral disc
-
Semba, K., Araki, K., Li, Z., Matsumoto, K., Suzuki, M., Nakagata, N., Takagi, K., Takeya, M., Yoshinobu, K., Araki, M. et al. (2006) A novel murine gene, Sickle tail, linked to the Danforth's short tail locus, is required for normal development of the intervertebral disc. Genetics, 172, 445-456.
-
(2006)
Genetics
, vol.172
, pp. 445-456
-
-
Semba, K.1
Araki, K.2
Li, Z.3
Matsumoto, K.4
Suzuki, M.5
Nakagata, N.6
Takagi, K.7
Takeya, M.8
Yoshinobu, K.9
Araki, M.10
-
8
-
-
43049133741
-
Disruption of chromodomain helicase DNA binding protein 2 (CHD2) causes scoliosis
-
Kulkarni, S., Nagarajan, P., Wall, J., Donovan, D.J., Donell, R.L., Ligon, A.H., Venkatachalam, S. and Quade, B.J. (2008) Disruption of chromodomain helicase DNA binding protein 2 (CHD2) causes scoliosis. Am. J. Med. Genet. A, 146A, 1117-1127.
-
(2008)
Am. J. Med. Genet. A
, vol.146 A
, pp. 1117-1127
-
-
Kulkarni, S.1
Nagarajan, P.2
Wall, J.3
Donovan, D.J.4
Donell, R.L.5
Ligon, A.H.6
Venkatachalam, S.7
Quade, B.J.8
-
9
-
-
39149144464
-
Zebrafish mutations affecting cilia motility share similar cystic phenotypes and suggest a mechanism of cyst formation that differs from pkd2 morphants
-
Sullivan-Brown, J., Schottenfeld, J., Okabe, N., Hostetter, C.L., Serluca, F.C., Thiberge, S.Y. and Burdine, R.D. (2008) Zebrafish mutations affecting cilia motility share similar cystic phenotypes and suggest a mechanism of cyst formation that differs from pkd2 morphants. Dev. Biol., 314, 261-275.
-
(2008)
Dev. Biol.
, vol.314
, pp. 261-275
-
-
Sullivan-Brown, J.1
Schottenfeld, J.2
Okabe, N.3
Hostetter, C.L.4
Serluca, F.C.5
Thiberge, S.Y.6
Burdine, R.D.7
-
10
-
-
0015723305
-
Genetic aspects of idiopathic scoliosis
-
Wynne-Davies, R. (1973) Genetic aspects of idiopathic scoliosis. Dev. Med. Child Neurol., 15, 809-811.
-
(1973)
Dev. Med. Child Neurol.
, vol.15
, pp. 809-811
-
-
Wynne-Davies, R.1
-
11
-
-
18844369625
-
Identification of candidate regions for familial idiopathic scoliosis
-
Miller, N.H., Justice, C.M., Marosy, B., Doheny, K.F., Pugh, E., Zhang, J., Dietz, H.C. 3rd and Wilson, A.F. (2005) Identification of candidate regions for familial idiopathic scoliosis. Spine, 30, 1181-1187.
-
(2005)
Spine
, vol.30
, pp. 1181-1187
-
-
Miller, N.H.1
Justice, C.M.2
Marosy, B.3
Doheny, K.F.4
Pugh, E.5
Zhang, J.6
Dietz H.C. 3rd7
Wilson, A.F.8
-
12
-
-
39149127931
-
Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtel
-
Ocaka, L., Zhao, C., Reed, J.A., Ebenezer, N.D., Brice, G., Morley, T., Mehta, M., O'Dowd, J., Weber, J.L., Hardcastle, A.J. et al. (2008) Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtel. J. Med. Genet., 45, 87-92.
-
(2008)
J. Med. Genet.
, vol.45
, pp. 87-92
-
-
Ocaka, L.1
Zhao, C.2
Reed, J.A.3
Ebenezer, N.D.4
Brice, G.5
Morley, T.6
Mehta, M.7
O'Dowd, J.8
Weber, J.L.9
Hardcastle, A.J.10
-
13
-
-
14344257057
-
Scoliosis in CHARGE: a prospective survey and two case reports
-
Doyle, C. and Blake, K. (2005) Scoliosis in CHARGE: a prospective survey and two case reports. Am. J. Med. Genet. A, 133A, 340-343.
-
(2005)
Am. J. Med. Genet. A
, vol.133 A
, pp. 340-343
-
-
Doyle, C.1
Blake, K.2
-
14
-
-
34247584973
-
CHD7 gene polymorphisms are associated with susceptibility to idiopathic scoliosis
-
Gao, X., Gordon, D., Zhang, D., Browne, R., Helms, C., Gillum, J., Weber, S., Devroy, S., Swaney, S., Dobbs, M. et al. (2007) CHD7 gene polymorphisms are associated with susceptibility to idiopathic scoliosis. Am. J. Hum. Genet., 80, 957-965.
-
(2007)
Am. J. Hum. Genet.
, vol.80
, pp. 957-965
-
-
Gao, X.1
Gordon, D.2
Zhang, D.3
Browne, R.4
Helms, C.5
Gillum, J.6
Weber, S.7
Devroy, S.8
Swaney, S.9
Dobbs, M.10
-
15
-
-
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., Bender, D., Maller, J., Sklar, P., de Bakker, P.I., Daly, M.J. et al. (2007) PLINK: a tool set for whole-genome association and population-based linkage analyses. Am. J. Hum. Genet., 81, 559-575.
-
(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.5
Bender, D.6
Maller, J.7
Sklar, P.8
de Bakker, P.I.9
Daly, M.J.10
-
16
-
-
0028385263
-
The transmission/disequilibrium test detects cosegregation and linkage
-
(author reply 560-553)
-
Spielman, R.S., McGinnis, R.E. and Ewens, W.J. (1994) The transmission/disequilibrium test detects cosegregation and linkage. Am. J. Hum. Genet., 54, 559-560 (author reply 560-553).
-
(1994)
Am. J. Hum. Genet.
, vol.54
, pp. 559-560
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
17
-
-
72049090952
-
Transmission disequilibrium test power and sample size in the presence of locus heterogeneity
-
Article
-
Chen, C., Yang, G., Buyske, S., Matise, T., Finch, S.J. and Gordon, D. (2009) Transmission disequilibrium test power and sample size in the presence of locus heterogeneity. Stat. Appl. Genet. Mol. Biol., 8, Article 44.
-
(2009)
Stat. Appl. Genet. Mol. Biol.
, vol.8
, pp. 44
-
-
Chen, C.1
Yang, G.2
Buyske, S.3
Matise, T.4
Finch, S.J.5
Gordon, D.6
-
18
-
-
0029739225
-
Structural features of a close homologue of L1 (CHL1) in the mouse: a new member of the L1 family of neural recognition molecules
-
Holm, J., Hillenbrand, R., Steuber, V., Bartsch, U., Moos, M., Lubbert, H., Montag, D. and Schachner, M. (1996) Structural features of a close homologue of L1 (CHL1) in the mouse: a new member of the L1 family of neural recognition molecules. Eur. J. Neurosci., 8, 1613-1629.
-
(1996)
Eur. J. Neurosci.
, vol.8
, pp. 1613-1629
-
-
Holm, J.1
Hillenbrand, R.2
Steuber, V.3
Bartsch, U.4
Moos, M.5
Lubbert, H.6
Montag, D.7
Schachner, M.8
-
19
-
-
37249007666
-
Close homolog of L1 and neuropilin 1 mediate guidance of thalamocortical axons at the ventral telencephalon
-
Wright, A.G., Demyanenko, G.P., Powell, A., Schachner, M., Enriquez-Barreto, L., Tran, T.S., Polleux, F. and Maness, P.F. (2007) Close homolog of L1 and neuropilin 1 mediate guidance of thalamocortical axons at the ventral telencephalon. J. Neurosci., 27, 13667-13679.
-
(2007)
J. Neurosci.
, vol.27
, pp. 13667-13679
-
-
Wright, A.G.1
Demyanenko, G.P.2
Powell, A.3
Schachner, M.4
Enriquez-Barreto, L.5
Tran, T.S.6
Polleux, F.7
Maness, P.F.8
-
20
-
-
2642584008
-
Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis
-
Jen, J.C., Chan, W.M., Bosley, T.M., Wan, J., Carr, J.R., Rub, U., Shattuck, D., Salamon, G., Kudo, L.C., Ou, J. et al. (2004) Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis. Science, 304, 1509-1513.
-
(2004)
Science
, vol.304
, pp. 1509-1513
-
-
Jen, J.C.1
Chan, W.M.2
Bosley, T.M.3
Wan, J.4
Carr, J.R.5
Rub, U.6
Shattuck, D.7
Salamon, G.8
Kudo, L.C.9
Ou, J.10
-
21
-
-
33747043538
-
Diffusion tensor MRI shows abnormal brainstem crossing fibers associated with ROBO3 mutations
-
Sicotte, N.L., Salamon, G., Shattuck, D.W., Hageman, N., Rub, U., Salamon, N., Drain, A.E., Demer, J.L., Engle, E.C., Alger, J.R. et al. (2006) Diffusion tensor MRI shows abnormal brainstem crossing fibers associated with ROBO3 mutations. Neurology, 67, 519-521.
-
(2006)
Neurology
, vol.67
, pp. 519-521
-
-
Sicotte, N.L.1
Salamon, G.2
Shattuck, D.W.3
Hageman, N.4
Rub, U.5
Salamon, N.6
Drain, A.E.7
Demer, J.L.8
Engle, E.C.9
Alger, J.R.10
-
22
-
-
65949107547
-
Common genetic variation and human traits
-
Goldstein, D.B. (2009) Common genetic variation and human traits. N. Engl. J. Med., 360, 1696-1698.
-
(2009)
N. Engl. J. Med.
, vol.360
, pp. 1696-1698
-
-
Goldstein, D.B.1
-
23
-
-
0036264547
-
An association between a missense polymorphism in the close homologue of L1 (CHL1, CALL) gene and schizophrenia
-
Sakurai, K., Migita, O., Toru, M. and Arinami, T. (2002) An association between a missense polymorphism in the close homologue of L1 (CHL1, CALL) gene and schizophrenia. Mol. Psychiatry, 7, 412-415.
-
(2002)
Mol. Psychiatry
, vol.7
, pp. 412-415
-
-
Sakurai, K.1
Migita, O.2
Toru, M.3
Arinami, T.4
-
24
-
-
19944428476
-
Case-control association study of the close homologue of L1 (CHL1) gene and schizophrenia in the Chinese population
-
Chen, Q.Y., Chen, Q., Feng, G.Y., Lindpaintner, K., Chen, Y., Sun, X., Chen, Z., Gao, Z., Tang, J. and He, L. (2005) Case-control association study of the close homologue of L1 (CHL1) gene and schizophrenia in the Chinese population. Schizophr. Res., 73, 269-274.
-
(2005)
Schizophr. Res.
, vol.73
, pp. 269-274
-
-
Chen, Q.Y.1
Chen, Q.2
Feng, G.Y.3
Lindpaintner, K.4
Chen, Y.5
Sun, X.6
Chen, Z.7
Gao, Z.8
Tang, J.9
He, L.10
-
25
-
-
59749096364
-
Dscam guides embryonic axons by Netrin-dependent and -independent functions
-
Andrews, G.L., Tanglao, S., Farmer, W.T., Morin, S., Brotman, S., Berberoglu, M.A., Price, H., Fernandez, G.C., Mastick, G.S., Charron, F. et al. (2008) Dscam guides embryonic axons by Netrin-dependent and -independent functions. Development, 135, 3839-3848.
-
(2008)
Development
, vol.135
, pp. 3839-3848
-
-
Andrews, G.L.1
Tanglao, S.2
Farmer, W.T.3
Morin, S.4
Brotman, S.5
Berberoglu, M.A.6
Price, H.7
Fernandez, G.C.8
Mastick, G.S.9
Charron, F.10
-
26
-
-
62449286259
-
DSCAM functions as a netrin receptor in commissural axon pathfinding
-
Liu, G., Li, W., Wang, L., Kar, A., Guan, K.L., Rao, Y. and Wu, J.Y. (2009) DSCAM functions as a netrin receptor in commissural axon pathfinding. Proc. Natl Acad. Sci. USA, 106, 2951-2956.
-
(2009)
Proc. Natl Acad. Sci. USA
, vol.106
, pp. 2951-2956
-
-
Liu, G.1
Li, W.2
Wang, L.3
Kar, A.4
Guan, K.L.5
Rao, Y.6
Wu, J.Y.7
-
27
-
-
79952580320
-
-
Patent WO/2008/033813
-
Nelson, L.M. and Kenneth, W. (2008) Patent WO/2008/033813.
-
(2008)
-
-
Nelson, L.M.1
Kenneth, W.2
-
28
-
-
53949096095
-
L1 and NCAM adhesion molecules as signaling coreceptors in neuronal migration and process outgrowth
-
Schmid, R.S. and Maness, P.F. (2008) L1 and NCAM adhesion molecules as signaling coreceptors in neuronal migration and process outgrowth. Curr. Opin. Neurobiol., 18, 245-250.
-
(2008)
Curr. Opin. Neurobiol.
, vol.18
, pp. 245-250
-
-
Schmid, R.S.1
Maness, P.F.2
-
29
-
-
77951576522
-
Drosophila neurexin IV interacts with Roundabout and is required for repulsive midline axon guidance
-
Banerjee, S., Blauth, K., Peters, K., Rogers, S.L., Fanning, A.S. and Bhat, M.A. (2010) Drosophila neurexin IV interacts with Roundabout and is required for repulsive midline axon guidance. J. Neurosci., 30, 5653-5667.
-
(2010)
J. Neurosci.
, vol.30
, pp. 5653-5667
-
-
Banerjee, S.1
Blauth, K.2
Peters, K.3
Rogers, S.L.4
Fanning, A.S.5
Bhat, M.A.6
-
30
-
-
57849169034
-
Transcription. Gene expression-where to start?
-
Buratowski, S. (2008) Transcription. Gene expression-where to start? Science, 322, 1804-1805.
-
(2008)
Science
, vol.322
, pp. 1804-1805
-
-
Buratowski, S.1
-
31
-
-
33845882730
-
Neural recognition molecules of the immunoglobulin superfamily: signaling transducers of axon guidance and neuronal migration
-
Maness, P.F. and Schachner, M. (2007) Neural recognition molecules of the immunoglobulin superfamily: signaling transducers of axon guidance and neuronal migration. Nat. Neurosci., 10, 19-26.
-
(2007)
Nat. Neurosci.
, vol.10
, pp. 19-26
-
-
Maness, P.F.1
Schachner, M.2
-
32
-
-
13544268491
-
The zebrafish down syndrome cell adhesion molecule is involved in cell movement during embryogenesis
-
Yimlamai, D., Konnikova, L., Moss, L.G. and Jay, D.G. (2005) The zebrafish down syndrome cell adhesion molecule is involved in cell movement during embryogenesis. Dev. Biol., 279, 44-57.
-
(2005)
Dev. Biol.
, vol.279
, pp. 44-57
-
-
Yimlamai, D.1
Konnikova, L.2
Moss, L.G.3
Jay, D.G.4
-
33
-
-
0028149815
-
Adolescent idiopathic scoliosis
-
Lonstein, J.E. (1994) Adolescent idiopathic scoliosis. Lancet, 344, 1407-1412.
-
(1994)
Lancet
, vol.344
, pp. 1407-1412
-
-
Lonstein, J.E.1
-
34
-
-
0031866760
-
Asymmetric otolith vestibulo-ocular responses in children with idiopathic scoliosis
-
Wiener-Vacher, S.R. and Mazda, K. (1998) Asymmetric otolith vestibulo-ocular responses in children with idiopathic scoliosis. J. Pediatr., 132, 1028-1032.
-
(1998)
J. Pediatr.
, vol.132
, pp. 1028-1032
-
-
Wiener-Vacher, S.R.1
Mazda, K.2
-
35
-
-
0032981256
-
Oculomotor, postural, and perceptual asymmetries associated with a common cause. Craniofacial asymmetries and asymmetries in vestibular organ anatomy
-
Rousie, D., Hache, J.C., Pellerin, P., Deroubaix, J.P., Van Tichelen, P. and Berthoz, A. (1999) Oculomotor, postural, and perceptual asymmetries associated with a common cause. Craniofacial asymmetries and asymmetries in vestibular organ anatomy. Ann. NY Acad. Sci., 871, 439-446.
-
(1999)
Ann. NY Acad. Sci.
, vol.871
, pp. 439-446
-
-
Rousie, D.1
Hache, J.C.2
Pellerin, P.3
Deroubaix, J.P.4
Van Tichelen, P.5
Berthoz, A.6
-
36
-
-
33745232376
-
Balance control in adolescents with idiopathic scoliosis and disturbed somatosensory function
-
Guo, X., Chau, W.W., Hui-Chan, C.W., Cheung, C.S., Tsang, W.W. and Cheng, J.C. (2006) Balance control in adolescents with idiopathic scoliosis and disturbed somatosensory function. Spine, 31, E437-E440.
-
(2006)
Spine
, vol.31
-
-
Guo, X.1
Chau, W.W.2
Hui-Chan, C.W.3
Cheung, C.S.4
Tsang, W.W.5
Cheng, J.C.6
-
37
-
-
33846055318
-
Locomotor skills and balance strategies in adolescents idiopathic scoliosis
-
Mallau, S., Bollini, G., Jouve, J.L. and Assaiante, C. (2007) Locomotor skills and balance strategies in adolescents idiopathic scoliosis. Spine, 32, E14-E22.
-
(2007)
Spine
, vol.32
-
-
Mallau, S.1
Bollini, G.2
Jouve, J.L.3
Assaiante, C.4
-
38
-
-
3042595928
-
The New York Cancer Project: rationale, organization, design, and baseline characteristics
-
Mitchell, M.K., Gregersen, P.K., Johnson, S., Parsons, R. and Vlahov, D. (2004) The New York Cancer Project: rationale, organization, design, and baseline characteristics. J. Urban Health, 81, 301-310.
-
(2004)
J. Urban Health
, vol.81
, pp. 301-310
-
-
Mitchell, M.K.1
Gregersen, P.K.2
Johnson, S.3
Parsons, R.4
Vlahov, D.5
-
39
-
-
35348983887
-
A second generation human haplotype map of over 3.1 million SNPs
-
Frazer, K.A., Ballinger, D.G., Cox, D.R., Hinds, D.A., Stuve, L.L., Gibbs, R.A., Belmont, J.W., Boudreau, A., Hardenbol, P., Leal, S.M. et al. (2007) A second generation human haplotype map of over 3.1 million SNPs. Nature, 449, 851-861.
-
(2007)
Nature
, vol.449
, pp. 851-861
-
-
Frazer, K.A.1
Ballinger, D.G.2
Cox, D.R.3
Hinds, D.A.4
Stuve, L.L.5
Gibbs, R.A.6
Belmont, J.W.7
Boudreau, A.8
Hardenbol, P.9
Leal, S.M.10
-
40
-
-
0034917944
-
A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data
-
Gordon, D., Heath, S.C., Liu, X. and Ott, J. (2001) A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data. Am. J. Hum. Genet., 69, 371-380.
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 371-380
-
-
Gordon, D.1
Heath, S.C.2
Liu, X.3
Ott, J.4
-
41
-
-
27544482357
-
PAWE-3D: visualizing power for association with error in case-control genetic studies of complex traits
-
Gordon, D., Haynes, C., Blumenfeld, J. and Finch, S.J. (2005) PAWE-3D: visualizing power for association with error in case-control genetic studies of complex traits. Bioinformatics, 21, 3935-3937.
-
(2005)
Bioinformatics
, vol.21
, pp. 3935-3937
-
-
Gordon, D.1
Haynes, C.2
Blumenfeld, J.3
Finch, S.J.4
-
42
-
-
37549064336
-
Mach 1.0: rapid haplotype reconstruction and missing genotype inference
-
Li, Y. and Abecasis, G. (2006) Mach 1.0: rapid haplotype reconstruction and missing genotype inference. Am. J. Hum. Genet., S79, 2290.
-
(2006)
Am. J. Hum. Genet.
, vol.S79
, pp. 2290
-
-
Li, Y.1
Abecasis, G.2
-
43
-
-
38949093617
-
Application of ancestry informative markers to association studies in European Americans
-
Seldin, M.F. and Price, A.L. (2008) Application of ancestry informative markers to association studies in European Americans. PLoS Genet., 4, e5.
-
(2008)
PLoS Genet.
, vol.4
-
-
Seldin, M.F.1
Price, A.L.2
-
44
-
-
42049106461
-
Catmap: case-control and TDT meta-analysis package
-
Nicodemus, K.K. (2008) Catmap: case-control and TDT meta-analysis package. BMC Bioinformatics, 9, 130.
-
(2008)
BMC Bioinformatics
, vol.9
, pp. 130
-
-
Nicodemus, K.K.1
-
46
-
-
13444269543
-
Haploview: analysis and visualization of LD and haplotype maps
-
Barrett, J.C., Fry, B., Maller, J. and Daly, M.J. (2005) Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics, 21, 263-265.
-
(2005)
Bioinformatics
, vol.21
, pp. 263-265
-
-
Barrett, J.C.1
Fry, B.2
Maller, J.3
Daly, M.J.4
-
48
-
-
0031019267
-
Magnitude of type I error when single-locus linkage analysis is maximized over models: a simulation study
-
Hodge, S.E., Abreu, P.C. and Greenberg, D.A. (1997) Magnitude of type I error when single-locus linkage analysis is maximized over models: a simulation study. Am. J. Hum. Genet., 60, 217-227.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 217-227
-
-
Hodge, S.E.1
Abreu, P.C.2
Greenberg, D.A.3
-
49
-
-
41649083448
-
WGAViewer: software for genomic annotation of whole genome association studies
-
Ge, D., Zhang, K., Need, A.C., Martin, O., Fellay, J., Urban, T.J., Telenti, A. and Goldstein, D.B. (2008) WGAViewer: software for genomic annotation of whole genome association studies. Genome Res., 18, 640-643.
-
(2008)
Genome Res.
, vol.18
, pp. 640-643
-
-
Ge, D.1
Zhang, K.2
Need, A.C.3
Martin, O.4
Fellay, J.5
Urban, T.J.6
Telenti, A.7
Goldstein, D.B.8
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