-
2
-
-
0002469253
-
On learning from multi-instance examples: empirical evaluation of a theoretical approach
-
In:, Nashville, Tennessee, USA, July 8-12, 2012. p -.
-
Auer P. 1997. On learning from multi-instance examples: empirical evaluation of a theoretical approach. In: Proceedings of the Fourteenth International Conference on Machine Learning, Nashville, Tennessee, USA, July 8-12, 2012. p 21-29.
-
(1997)
Proceedings of the Fourteenth International Conference on Machine Learning
, pp. 21-29
-
-
Auer, P.1
-
3
-
-
0030211964
-
Bagging predictors
-
Breiman L. 1996. Bagging predictors. Machine Learn 24:123-140.
-
(1996)
Machine Learn
, vol.24
, pp. 123-140
-
-
Breiman, L.1
-
4
-
-
0035478854
-
Random forest
-
Breiman L. 2001. Random forest. Machine Learn 45:5-32.
-
(2001)
Machine Learn
, vol.45
, pp. 5-32
-
-
Breiman, L.1
-
5
-
-
79953874274
-
Audioprofile-directed successful mutation analysis in a DFNA2/KCNQ4 (p.Leu274His) family
-
de Heer A-MR, Schraders M, Oostrik J, Hoefsloot L, Huygen PLM, Cremers CWRJ. 2011. Audioprofile-directed successful mutation analysis in a DFNA2/KCNQ4 (p.Leu274His) family. Ann Otol Rhinol Laryngol 120:243-248.
-
(2011)
Ann Otol Rhinol Laryngol
, vol.120
, pp. 243-248
-
-
de Heer, A.-M.1
Schraders, M.2
Oostrik, J.3
Hoefsloot, L.4
Huygen, P.L.M.5
Cremers, C.W.R.J.6
-
6
-
-
84872023730
-
Using the phenome and genome to improve genetic diagnosis for deafness
-
Eppsteiner RW, Shearer AE, Hildebrand MS, Taylor KR, Deluca AP, Scherer S, Huygen P, Scheetz TE, Braun TA, Casavant TL, Smith RJH. 2012. Using the phenome and genome to improve genetic diagnosis for deafness. Otolaryngol Head Neck Surg 147:975-977.
-
(2012)
Otolaryngol Head Neck Surg
, vol.147
, pp. 975-977
-
-
Eppsteiner, R.W.1
Shearer, A.E.2
Hildebrand, M.S.3
Taylor, K.R.4
Deluca, A.P.5
Scherer, S.6
Huygen, P.7
Scheetz, T.E.8
Braun, T.A.9
Casavant, T.L.10
Smith, R.J.H.11
-
7
-
-
7244250182
-
Data mining in bioinformatics using Weka
-
Frank E, Hall M, Trigg L, Holmes G, Witten IH. 2004. Data mining in bioinformatics using Weka. Bioinformatics 20:2479-2481.
-
(2004)
Bioinformatics
, vol.20
, pp. 2479-2481
-
-
Frank, E.1
Hall, M.2
Trigg, L.3
Holmes, G.4
Witten, I.H.5
-
8
-
-
76749092270
-
The WEKA data mining software
-
Hall M, Frank E, Holmes G, Pfahringer B, Reutemann P, Witten IH. 2009. The WEKA data mining software. SIGKDD Explor Newslett 11:10-18.
-
(2009)
SIGKDD Explor Newslett
, vol.11
, pp. 10-18
-
-
Hall, M.1
Frank, E.2
Holmes, G.3
Pfahringer, B.4
Reutemann, P.5
Witten, I.H.6
-
9
-
-
73449093546
-
A contemporary review of AudioGene audioprofiling: a machine-based candidate gene prediction tool for autosomal dominant nonsyndromic hearing loss
-
Hildebrand MS, Deluca AP, Taylor KR, Hoskinson DP, Hur IA, Tack D, McMordie SJ, Huygen PLM, Casavant TL, Smith RJH. 2009. A contemporary review of AudioGene audioprofiling: a machine-based candidate gene prediction tool for autosomal dominant nonsyndromic hearing loss. Laryngoscope 119:2211-2215.
-
(2009)
Laryngoscope
, vol.119
, pp. 2211-2215
-
-
Hildebrand, M.S.1
Deluca, A.P.2
Taylor, K.R.3
Hoskinson, D.P.4
Hur, I.A.5
Tack, D.6
McMordie, S.J.7
Huygen, P.L.M.8
Casavant, T.L.9
Smith, R.J.H.10
-
10
-
-
79959708887
-
DFNA8/12 caused by TECTA mutations is the most identified subtype of non-syndromic autosomal dominant hearing loss
-
Hildebrand MS, Morín M, Meyer NC, Mayo F, Modamio-Hoybjor S, Mencía A, Olavarrieta L, Morales-Angulo C, Nishimura CJ, Workman H, Deluca AP, Del Castillo I, et al. 2011. DFNA8/12 caused by TECTA mutations is the most identified subtype of non-syndromic autosomal dominant hearing loss. Hum Mutat 32:825-834.
-
(2011)
Hum Mutat
, vol.32
, pp. 825-834
-
-
Hildebrand, M.S.1
Morín, M.2
Meyer, N.C.3
Mayo, F.4
Modamio-Hoybjor, S.5
Mencía, A.6
Olavarrieta, L.7
Morales-Angulo, C.8
Nishimura, C.J.9
Workman, H.10
Deluca, A.P.11
Del Castillo, I.12
-
11
-
-
57449102040
-
Audioprofile-directed screening identifies novel mutations in KCNQ4 causing hearing loss at the DFNA2 locus
-
Hildebrand MS, Tack D, McMordie SJ, DeLuca A, Hur IA, Nishimura C, Huygen P, Casavant TL, Smith RJH. 2008. Audioprofile-directed screening identifies novel mutations in KCNQ4 causing hearing loss at the DFNA2 locus. Genet Med 10:797-804.
-
(2008)
Genet Med
, vol.10
, pp. 797-804
-
-
Hildebrand, M.S.1
Tack, D.2
McMordie, S.J.3
DeLuca, A.4
Hur, I.A.5
Nishimura, C.6
Huygen, P.7
Casavant, T.L.8
Smith, R.J.H.9
-
12
-
-
59349118706
-
Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics?
-
Hilgert N, Smith RJH, Van Camp G. 2009. Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics? Mutat Res 681:189-196.
-
(2009)
Mutat Res
, vol.681
, pp. 189-196
-
-
Hilgert, N.1
Smith, R.J.H.2
Van Camp, G.3
-
13
-
-
14744287738
-
-
Springfield, IL: Illinois Department of Public Health.
-
Leonard D, Shen T, Howe H, Egler T. 1999. Trends in the prevalence of birth defects in Illinois and Chicago, 1989 to 1997. Springfield, IL: Illinois Department of Public Health.
-
(1999)
Trends in the prevalence of birth defects in Illinois and Chicago, 1989 to 1997
-
-
Leonard, D.1
Shen, T.2
Howe, H.3
Egler, T.4
-
14
-
-
0033636781
-
The societal costs of severe to profound hearing loss in the United States
-
Mohr PE, Feldman JJ, Dunbar JL, McConkey-Robbins A, Niparko JK, Rittenhouse RK, Skinner MW. 2000. The societal costs of severe to profound hearing loss in the United States. Int J Technol Assess Health Care 16:1120-1135.
-
(2000)
Int J Technol Assess Health Care
, vol.16
, pp. 1120-1135
-
-
Mohr, P.E.1
Feldman, J.J.2
Dunbar, J.L.3
McConkey-Robbins, A.4
Niparko, J.K.5
Rittenhouse, R.K.6
Skinner, M.W.7
-
15
-
-
0003120218
-
Sequential minimal optimization: a fast algorithm for training support vector machines
-
Platt JC. 1998. Sequential minimal optimization: a fast algorithm for training support vector machines. Adv Kernel Methods Support Vector Learn 208:1-21.
-
(1998)
Adv Kernel Methods Support Vector Learn
, vol.208
, pp. 1-21
-
-
Platt, J.C.1
-
16
-
-
1842507432
-
Test-retest reliability of pure-tone thresholds from 0.5 to 16 kHz using Sennheiser HDA 200 and Etymotic Research ER-2 earphones
-
Schmuziger N, Probst R, Smurzynski J. 2004. Test-retest reliability of pure-tone thresholds from 0.5 to 16 kHz using Sennheiser HDA 200 and Etymotic Research ER-2 earphones. Ear Hear 25:127-132.
-
(2004)
Ear Hear
, vol.25
, pp. 127-132
-
-
Schmuziger, N.1
Probst, R.2
Smurzynski, J.3
-
17
-
-
78650506429
-
Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing
-
Shearer AE, Deluca AP, Hildebrand MS, Taylor KR, Gurrola J, Scherer S, Scheetz TE, Smith RJH. 2010. Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing. Proc Natl Acad Sci U S A 107:21104-21109.
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, pp. 21104-21109
-
-
Shearer, A.E.1
Deluca, A.P.2
Hildebrand, M.S.3
Taylor, K.R.4
Gurrola, J.5
Scherer, S.6
Scheetz, T.E.7
Smith, R.J.H.8
-
19
-
-
14744282666
-
Sensorineural hearing loss in children
-
Smith RJ, Bale JF Jr, White KR. 2005. Sensorineural hearing loss in children. Lancet 365:879-890.
-
(2005)
Lancet
, vol.365
, pp. 879-890
-
-
Smith, R.J.1
Bale, J.J.2
White, K.R.3
-
20
-
-
28144444402
-
GJB2 mutations and degree of hearing loss: a multicenter study
-
Snoeckx RL, Huygen PLM, Feldmann D, Marlin S, Denoyelle F, Waligora J, Mueller-Malesinska M, Pollak A, Ploski R, Murgia A, Orzan E, Castorina P, et al. 2005. GJB2 mutations and degree of hearing loss: a multicenter study. Am J Hum Genet 77:945-957.
-
(2005)
Am J Hum Genet
, vol.77
, pp. 945-957
-
-
Snoeckx, R.L.1
Huygen, P.L.M.2
Feldmann, D.3
Marlin, S.4
Denoyelle, F.5
Waligora, J.6
Mueller-Malesinska, M.7
Pollak, A.8
Ploski, R.9
Murgia, A.10
Orzan, E.11
Castorina, P.12
-
22
-
-
0035944525
-
Universal newborn hearing screening: summary of evidence
-
Thompson DC, McPhillips H, Davis RL, Lieu TL, Homer CJ, Helfand M. 2001. Universal newborn hearing screening: summary of evidence. JAMA 286:2000-2010.
-
(2001)
JAMA
, vol.286
, pp. 2000-2010
-
-
Thompson, D.C.1
McPhillips, H.2
Davis, R.L.3
Lieu, T.L.4
Homer, C.J.5
Helfand, M.6
-
23
-
-
84875524632
-
-
The Hereditary Hearing Loss Homepage. Available at: Accessed October 2012.
-
Van Camp G, Smith RJH. 2012. The Hereditary Hearing Loss Homepage. Available at: http://hereditaryhearingloss.org/. Accessed October 2012.
-
(2012)
-
-
Van Camp, G.1
Smith, R.J.H.2
-
25
-
-
0037642358
-
The current status of EHDI programs in the United States
-
White KR. 2003. The current status of EHDI programs in the United States. Ment Retard Dev Disabil Res Rev 9:79-88.
-
(2003)
Ment Retard Dev Disabil Res Rev
, vol.9
, pp. 79-88
-
-
White, K.R.1
-
26
-
-
4344656951
-
Early hearing detection and intervention programs: opportunities for genetic services
-
White KR. 2004. Early hearing detection and intervention programs: opportunities for genetic services. Am J Med Genet A 130A:29-36.
-
(2004)
Am J Med Genet A
, vol.130 A
, pp. 29-36
-
-
White, K.R.1
|