-
4
-
-
0142209375
-
Genomic priorities and public health
-
PMID: 14576422
-
Merikangas KR, Risch N. (2003) Genomic priorities and public health. Science 302: 599-601. PMID: 14576422
-
(2003)
Science
, vol.302
, pp. 599-601
-
-
Merikangas, K.R.1
Risch, N.2
-
5
-
-
34247481814
-
Strong association of de novo copy number mutations with autism
-
PMID: 17363630
-
Sebat J, Lakshmi B, Malhotra D., Troge J, Lese-Martin C, Walsh T, et al (2007) Strong association of de novo copy number mutations with autism. Science 316: 445-449. PMID: 17363630
-
(2007)
Science
, vol.316
, pp. 445-449
-
-
Sebat, J.1
Lakshmi, B.2
Malhotra, D.3
Troge, J.4
Lese-Martin, C.5
Walsh, T.6
-
6
-
-
67651233780
-
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes
-
PMID: 19557195
-
Bucan M, Abrahams BS, Wang K, Glessner J.T., Herman EI, Sonnenblick LI, et al. (2009) Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. PLoS Genet 5: e1000536. doi: 10.1371/journal.pgen.1000536 PMID: 19557195
-
(2009)
PLoS Genet
, vol.5
-
-
Bucan, M.1
Abrahams, B.S.2
Wang, K.3
Glessner, J.T.4
Herman, E.I.5
Sonnenblick, L.I.6
-
7
-
-
84555208173
-
SnapShot: Genetics of autism
-
e411 PMID: 22017998
-
Aldinger KA, Plummer JT, Qiu S, Levitt P. (2011) SnapShot: genetics of autism. Neuron 72: 418-418 e411. doi: 10.1016/j.neuron.2011.10.007 PMID: 22017998
-
(2011)
Neuron
, vol.72
, pp. 418-418
-
-
Aldinger, K.A.1
Plummer, J.T.2
Qiu, S.3
Levitt, P.4
-
8
-
-
77957735529
-
A genome-wide scan for common alleles affecting risk for autism
-
PMID: 20663923
-
Anney R, Klei L, Pinto D., Regan R, Conroy J, Magalhaes TR, et al. (2010) A genome-wide scan for common alleles affecting risk for autism. Hum Mol Genet 19: 4072-4082. doi: 10.1093/hmg/ddq307 PMID: 20663923
-
(2010)
Hum Mol Genet
, vol.19
, pp. 4072-4082
-
-
Anney, R.1
Klei, L.2
Pinto, D.3
Regan, R.4
Conroy, J.5
Magalhaes, T.R.6
-
9
-
-
65449184161
-
A genome-wide association study of autism reveals a common novel risk locus at 5p14.1
-
PMID: 19456320
-
Ma D, Salyakina D, Jaworski J.M., Konidari I., Whitehead PL, Andersen AN, et al. (2009) A genome-wide association study of autism reveals a common novel risk locus at 5p14.1. Ann Hum Genet 73:263-273. doi: 10.1111/j.1469-1809.2009.00523.x PMID: 19456320
-
(2009)
Ann Hum Genet
, vol.73
, pp. 263-273
-
-
Ma, D.1
Salyakina, D.2
Jaworski, J.M.3
Konidari, I.4
Whitehead, P.L.5
Andersen, A.N.6
-
10
-
-
79955698929
-
Variants in several genomic regions associated with asperger disorder
-
PMID: 21182207
-
Salyakina D, Ma DQ, Jaworski J.M., Konidari I., Whitehead PL, Henson R, et al. (2010) Variants in several genomic regions associated with asperger disorder. Autism Res 3: 303-310. doi: 10.1002/aur.158 PMID: 21182207
-
(2010)
Autism Res
, vol.3
, pp. 303-310
-
-
Salyakina, D.1
Ma, D.Q.2
Jaworski, J.M.3
Konidari, I.4
Whitehead, P.L.5
Henson, R.6
-
11
-
-
67349112868
-
Common genetic variants on 5p14.1 associate with autism spectrum disorders
-
PMID: 19404256
-
Wang K, Zhang H, Ma D., Bucan M, Glessner JT, Abrahams B.S., et al. (2009) Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature 459: 528-533. doi: 10.1038/nature07999 PMID: 19404256
-
(2009)
Nature
, vol.459
, pp. 528-533
-
-
Wang, K.1
Zhang, H.2
Ma, D.3
Bucan, M.4
Glessner, J.T.5
Abrahams, B.S.6
-
12
-
-
70449629672
-
Autism genetics: Emerging data from genome-wide copy-number and single nucleotide polymorphism scans
-
PMID: 19895225
-
Weiss LA (2009) Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans. Expert Rev Mol Diagn 9: 795-803. doi: 10.1586/erm.09.59 PMID: 19895225
-
(2009)
Expert Rev Mol Diagn
, vol.9
, pp. 795-803
-
-
Weiss, L.A.1
-
13
-
-
84859513087
-
Anoncoding RNA anti-sense to moesin at 5p14.1 in autism
-
Kerin T, Ramanathan A, Rivas K., Grepo N, Coetzee GA, Campbell DB (2012) Anoncoding RNA anti-sense to moesin at 5p14.1 in autism. Sci Transl Med 4:128ra140.
-
(2012)
Sci Transl Med
, vol.4
-
-
Kerin, T.1
Ramanathan, A.2
Rivas, K.3
Grepo, N.4
Coetzee, G.A.5
Campbell, D.B.6
-
14
-
-
80051564758
-
No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder
-
PMID: 21656903
-
Curran S, Bolton P, Rozsnyai K., Chiocchetti A, Klauck SM, Duketis E, et al. (2011) No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder. Am J Med Genet B Neuropsychiatr Genet 156B: 633-639. doi: 10.1002/ajmg.b.31201 PMID: 21656903
-
(2011)
Am J Med Genet B Neuropsychiatr Genet
, vol.156 B
, pp. 633-639
-
-
Curran, S.1
Bolton, P.2
Rozsnyai, K.3
Chiocchetti, A.4
Klauck, S.M.5
Duketis, E.6
-
15
-
-
84867829870
-
Individual common variants exert weak effects on the risk for autism spectrum disorderspi
-
PMID: 22843504
-
Anney R, Klei L, Pinto D., Almeida J, Bacchelli E, Baird G, et al. (2012) Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Hum Mol Genet 21: 4781-4792. doi: 10.1093/hmg/dds301 PMID: 22843504
-
(2012)
Hum Mol Genet
, vol.21
, pp. 4781-4792
-
-
Anney, R.1
Klei, L.2
Pinto, D.3
Almeida, J.4
Bacchelli, E.5
Baird, G.6
-
16
-
-
79955512308
-
Genome-wide association scan of Korean autism spectrum disorders with language delay: A preliminary study
-
PMID: 21519539
-
Cho SC, Yoo HJ, Park M, Cho I.H., Kim BN, Kim JW, et al. (2011) Genome-wide association scan of korean autism spectrum disorders with language delay: a preliminary study. Psychiatry Investig 8: 61-66. doi: 10.4306/pi.2011.8.1.61 PMID: 21519539
-
(2011)
Psychiatry Investig
, vol.8
, pp. 61-66
-
-
Cho, S.C.1
Yoo, H.J.2
Park, M.3
Cho, I.H.4
Kim, B.N.5
Kim, J.W.6
-
17
-
-
84871298155
-
Common genetic variants, acting additively, are a major source of risk for autism
-
PMID: 23067556
-
Klei L, Sanders SJ, Murtha MT, Hus V, Lowe JK, Willsey AJ, et al. (2012) Common genetic variants, acting additively, are a major source of risk for autism. Mol Autism 3: 9. doi: 10.1186/2040-2392-3-9 PMID: 23067556
-
(2012)
Mol Autism
, vol.3
, pp. 9
-
-
Klei, L.1
Sanders, S.J.2
Murtha, M.T.3
Hus, V.4
Lowe, J.K.5
Willsey, A.J.6
-
18
-
-
33646250184
-
Optimal two-stage genotyping designs for genomewide association scans
-
PMID: 16607626
-
Wang H, Thomas DC, Pe'er I, Stram DO (2006) Optimal two-stage genotyping designs for genomewide association scans. Genet Epidemiol 30: 356-368. PMID: 16607626
-
(2006)
Genet Epidemiol
, vol.30
, pp. 356-368
-
-
Wang, H.1
Thomas, D.C.2
Pe'Er, I.3
Stram, D.O.4
-
21
-
-
0027997172
-
Autism diagnostic interview-revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders
-
Lord C, Rutter M, Le Couteur A (1994) Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders. Journal of Autism & Developmental Disorders 24: 659-685.
-
(1994)
Journal of Autism & Developmental Disorders
, vol.24
, pp. 659-685
-
-
Lord, C.1
Rutter, M.2
Le Couteur, A.3
-
22
-
-
84655169686
-
Association of HLA-DRB1 alleles and neuropsychological function in autism
-
PMID: 21716163
-
Chien YL, Wu YY, Chen C.H., Gau SS, Huang YS, Chien WH, et al (2012) Association of HLA-DRB1 alleles and neuropsychological function in autism. Psychiatr Genet 22: 46-49. doi: 10.1097/YPG.0b013e32834915ae PMID: 21716163
-
(2012)
Psychiatr Genet
, vol.22
, pp. 46-49
-
-
Chien, Y.L.1
Wu, Y.Y.2
Chen, C.H.3
Gau, S.S.4
Huang, Y.S.5
Chien, W.H.6
-
23
-
-
80855130938
-
Sleep problems among Taiwanese children with autism, their siblings and typically developing children
-
Chou MC, Chou WJ, Chiang H.L., Wu YY, Lee JC, Wong CC, et al. (2012) Sleep problems among Taiwanese children with autism, their siblings and typically developing children. Res Autism Spectr Disord 6: 665-672.
-
(2012)
Res Autism Spectr Disord
, vol.6
, pp. 665-672
-
-
Chou, M.C.1
Chou, W.J.2
Chiang, H.L.3
Wu, Y.Y.4
Lee, J.C.5
Wong, C.C.6
-
24
-
-
84864930479
-
Identification of two inherited copy number variants in a male with autism supports two-hit and compound heterozygosity models of autism
-
Gau SS, Liao HM, Hong C.C., Chien WH, Chen C.H. (2012) Identification of two inherited copy number variants in a male with autism supports two-hit and compound heterozygosity models of Autism. Am J Med Genet B Neuropsychiatr Genet.
-
(2012)
Am J Med Genet B Neuropsychiatr Genet
-
-
Gau, S.S.1
Liao, H.M.2
Hong, C.C.3
Chien, W.H.4
Chen, C.H.5
-
25
-
-
84860503081
-
The WNT2 gene polymorphism associated with speech delay inherent to autism
-
PMID: 22522212
-
Lin PI, Chien YL, Wu Y.Y., Chen CH, Gau SS, Huang YS, et al (2012) The WNT2 gene polymorphism associated with speech delay inherent to autism. Res Dev Disabil 33:1533-1540. doi: 10.1016/j.ridd.2012.03.004 PMID: 22522212
-
(2012)
Res Dev Disabil
, vol.33
, pp. 1533-1540
-
-
Lin, P.I.1
Chien, Y.L.2
Wu, Y.Y.3
Chen, C.H.4
Gau, S.S.5
Huang, Y.S.6
-
26
-
-
84946920219
-
Altered structure-function relations of language processing in adolescents with high-functioning autism: A combined diffusion and functional MRI study
-
Lo YC, Chou TL, Fan L.Y., Gau SS, Tseng W.Y. (2012) Altered structure-function relations of language processing in adolescents with high-functioning autism: A combined diffusion and functional MRI study. Hum Brain Mapp 192:60-66.
-
(2012)
Hum Brain Mapp
, vol.192
, pp. 60-66
-
-
Lo, Y.C.1
Chou, T.L.2
Fan, L.Y.3
Gau, S.S.4
Tseng, W.Y.5
-
27
-
-
84863837045
-
Differentiation of highfunctioning autism and asperger's disorder based on neuromotor behaviour
-
PMID: 21660499
-
Nayate A, Tonge BJ, Bradshaw JL, McGinley JL, Iansek R, Rinehart NJ. (2012) Differentiation of highfunctioning autism and Asperger's disorder based on neuromotor behaviour. J Autism Dev Disord 42: 707-717. doi: 10.1007/s10803-011-1299-5 PMID: 21660499
-
(2012)
J Autism Dev Disord
, vol.42
, pp. 707-717
-
-
Nayate, A.1
Tonge, B.J.2
Bradshaw, J.L.3
McGinley, J.L.4
Iansek, R.5
Rinehart, N.J.6
-
28
-
-
84885695560
-
Chromosomal Abnormalities in patients with autism spectrum disorders from Taiwan
-
710.1002/ajmg.b.32153 PMID: 24132905
-
Liao HM, Gau SS, Tsai W.C., Fang JS, Su YC, Chou MC, et al (2013) Chromosomal abnormalities in patients with autism spectrum disorders from Taiwan. Am J Med Genet B Neuropsychiatr Genet 162B: 734-741. 710.1002/ajmg.b.32153 doi: 10.1002/ajmg.b.32153 PMID: 24132905
-
(2013)
Am J Med Genet B Neuropsychiatr Genet
, vol.162 B
, pp. 734-741
-
-
Liao, H.M.1
Gau, S.S.2
Tsai, W.C.3
Fang, J.S.4
Su, Y.C.5
Chou, M.C.6
-
29
-
-
33646753192
-
Han Chinese cell and genome bank in Taiwan: Purpose, design and ethical considerations
-
PMID: 16534213
-
Pan WH, Fann CS, Wu J.Y., Hung YT, Ho MS, Tai TH, et al (2006) Han Chinese cell and genome bank in Taiwan: purpose, design and ethical considerations. Hum Hered 61: 27-30. PMID: 16534213
-
(2006)
Hum Hered
, vol.61
, pp. 27-30
-
-
Pan, W.H.1
Fann, C.S.2
Wu, J.Y.3
Hung, Y.T.4
Ho, M.S.5
Tai, T.H.6
-
30
-
-
79551576736
-
Sex difference in the rates and co-occurring conditions of psychiatric symptoms in incoming college students in Taiwan
-
PMID: 21295227
-
Chien YL, Gau SS, Gadow K.D. (2011) Sex difference in the rates and co-occurring conditions of psychiatric symptoms in incoming college students in Taiwan. Compr Psychiatry 52:195-207. doi: 10.1016/j.comppsych.2010.03.009 PMID: 21295227
-
(2011)
Compr Psychiatry
, vol.52
, pp. 195-207
-
-
Chien, Y.L.1
Gau, S.S.2
Gadow, K.D.3
-
31
-
-
84866149264
-
Psychometric properties of the Chinese version of the autism spectrum quotient (AQ)
-
210.1016/j. ridd.2012.1008.1005. Epub 2012 Sep 1015 PMID: 22985783
-
Lau WY, Gau SS, Chiu Y.N., Wu YY, Chou WJ, Liu SK, et al (2013) Psychometric properties of the Chinese version of the autism spectrum quotient (AQ). Res Dev Disabil 34: 294-305. 210.1016/j. ridd.2012.1008.1005. Epub 2012 Sep 1015. doi: 10.1016/j.ridd.2012.08.005 PMID: 22985783
-
(2013)
Res Dev Disabil
, vol.34
, pp. 294-305
-
-
Lau, W.Y.1
Gau, S.S.2
Chiu, Y.N.3
Wu, Y.Y.4
Chou, W.J.5
Liu, S.K.6
-
32
-
-
34548292504
-
PLINK: Atool set for whole-genome association and population-based linkage analyses
-
PMID: 17701901
-
Purcell S, Neale B, Todd-Brown K, Thomas L., Ferreira MA, Bender D, et al. (2007) PLINK: atool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81: 559-575. PMID: 17701901
-
(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
-
33
-
-
33747616787
-
-
Package'haplostats'. 1.6.3 ed. pp. A suite of R routines for the analysis of indirectly measured haplotypes. The statistical methods assume that all subjects are unrelated and that haplotypes are ambiguous (due to unknown linkage phase of the genetic markers). The main functions are: haplo.em, haplo.glm, haplo.score, haplo.power,andseqhap
-
Sinnwell JP, Schaid D.J. (2013) Statistical Analysis of Haplotypes with Traits and Covariates when Linkage Phase is Ambiguous. Package'haplostats'. 1.6.3 ed. pp. A suite of R routines for the analysis of indirectly measured haplotypes. The statistical methods assume that all subjects are unrelated and that haplotypes are ambiguous (due to unknown linkage phase of the genetic markers). The main functions are: haplo.em, haplo.glm, haplo.score, haplo.power,andseqhap.
-
(2013)
Statistical Analysis of Haplotypes with Traits and Covariates when Linkage Phase Is Ambiguous
-
-
Sinnwell, J.P.1
Schaid, D.J.2
-
34
-
-
77955064853
-
A versatile gene-based test for genome-wide association studies
-
PMID: 20598278
-
Liu JZ, McRae AF, Nyholt DR, Medland SE, Wray NR, Brown KM, et al. (2010) A versatile gene-based test for genome-wide association studies. Am J Hum Genet 87:139-145. doi: 10.1016/j.ajhg.2010.06.009 PMID: 20598278
-
(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
-
35
-
-
2442690630
-
A novel protein tyrosine kinase NOK that shares homology with platelet-derived growth factor/fibroblast growth factor receptors induces tumorigenesis and metastasis in nude mice
-
PMID: 15150103
-
Liu L, Yu XZ, Li T.S., Song LX, Chen PL, Suo TL, et al (2004) A novel protein tyrosine kinase NOK that shares homology with platelet-derived growth factor/fibroblast growth factor receptors induces tumorigenesis and metastasis in nude mice. Cancer Res 64: 3491-3499. PMID: 15150103
-
(2004)
Cancer Res
, vol.64
, pp. 3491-3499
-
-
Liu, L.1
Yu, X.Z.2
Li, T.S.3
Song, L.X.4
Chen, P.L.5
Suo, T.L.6
-
36
-
-
84864087818
-
Genes associated with autism spectrum disorder
-
PMID: 22688012
-
Li X, Zou H, Brown W.T. (2012) Genes associated with autism spectrum disorder. Brain Res Bull 88: 543-552. doi: 10.1016/j.brainresbull.2012.05.017 PMID: 22688012
-
(2012)
Brain Res Bull
, vol.88
, pp. 543-552
-
-
Li, X.1
Zou, H.2
Brown, W.T.3
-
37
-
-
84946489060
-
The phenotypic manifestations of rare genic CNVs in autism spectrum disorder
-
Merikangas AK, Segurado R, Heron EA, Anney RJ, Paterson AD, Cook EH, et al. (2014) The phenotypic manifestations of rare genic CNVs in autism spectrum disorder. Molecular Psychiatry.
-
(2014)
Molecular Psychiatry
-
-
Merikangas, A.K.1
Segurado, R.2
Heron, E.A.3
Anney, R.J.4
Paterson, A.D.5
Cook, E.H.6
-
38
-
-
84897084865
-
Family-based association study of ZNF533, DOCK4 and IMMP2L gene polymorphisms linked to autism in a northeastern Chinese han population
-
Liang S, Wang XL, Zou M.Y., Wang H., Zhou X, Sun CH, et al. (2014) Family-based association study of ZNF533, DOCK4 and IMMP2L gene polymorphisms linked to autism in a northeastern Chinese Han population. Journal of Zhejiang University SCIENCE (Biomed & Biotechnol).
-
(2014)
Journal of Zhejiang University SCIENCE (Biomed & Biotechnol)
-
-
Liang, S.1
Wang, X.L.2
Zou, M.Y.3
Wang, H.4
Zhou, X.5
Sun, C.H.6
-
39
-
-
0016224019
-
Non-sensory involvement of the olfactory bulbs in the mediation of social behaviors
-
PMID: 4606847
-
Edwards DA (1974) Non-sensory involvement of the olfactory bulbs in the mediation of social behaviors. Behav Biol 11: 287-302. PMID: 4606847
-
(1974)
Behav Biol
, vol.11
, pp. 287-302
-
-
Edwards, D.A.1
-
40
-
-
79959629860
-
Identification of genetic loci underlying the phenotypic constructs of autism spectrum disorders
-
e613 PMID: 21703496
-
Liu XQ, Georgiades S, Duku E., Thompson A, Devlin B, Cook E.H., et al. (2011) Identification of genetic loci underlying the phenotypic constructs of autism spectrum disorders. J Am Acad Child Adolesc Psychiatry 50: 687-696 e613. doi: 10.1016/j.jaac.2011.05.002 PMID: 21703496
-
(2011)
J Am Acad Child Adolesc Psychiatry
, vol.50
, pp. 687-696
-
-
Liu, X.Q.1
Georgiades, S.2
Duku, E.3
Thompson, A.4
Devlin, B.5
Cook, E.H.6
-
41
-
-
84884186027
-
Common variation contributes to the genetic architecture of social communication traits
-
PMID: 24047820
-
St Pourcain B., Whitehouse AJ, Ang W.Q., Warrington NM, Glessner JT, Wang K, et al (2013) Common variation contributes to the genetic architecture of social communication traits. Mol Autism 4: 34. doi: 10.1186/2040-2392-4-34 PMID: 24047820
-
(2013)
Mol Autism
, vol.4
, pp. 34
-
-
St. Pourcain, B.1
Whitehouse, A.J.2
Ang, W.Q.3
Warrington, N.M.4
Glessner, J.T.5
Wang, K.6
-
42
-
-
77949773588
-
An intrinsic vasopressin system in the olfactory bulb is involved in social recognition
-
PMID: 20182426
-
Tobin VA, Hashimoto H, Wacker D.W., Takayanagi Y., Langnaese K, Caquineau C, et al. (2010) An intrinsic vasopressin system in the olfactory bulb is involved in social recognition. Nature 464:413-417. doi: 10.1038/nature08826 PMID: 20182426
-
(2010)
Nature
, vol.464
, pp. 413-417
-
-
Tobin, V.A.1
Hashimoto, H.2
Wacker, D.W.3
Takayanagi, Y.4
Langnaese, K.5
Caquineau, C.6
-
43
-
-
84857651673
-
Sex-specific changes in gene expression and behavior induced by chronic toxoplasma infection in mice
-
PMID: 22240252
-
Xiao J, Kannan G, Jones-Brando L, Brannock C, Krasnova IN, Cadet JL, et al. (2012) Sex-specific changes in gene expression and behavior induced by chronic Toxoplasma infection in mice. Neuroscience 206: 39-48. doi: 10.1016/j.neuroscience.2011.12.051 PMID: 22240252
-
(2012)
Neuroscience
, vol.206
, pp. 39-48
-
-
Xiao, J.1
Kannan, G.2
Jones-Brando, L.3
Brannock, C.4
Krasnova, I.N.5
Cadet, J.L.6
-
44
-
-
84857138766
-
Disrupted cortical connectivity theory as an explanatory model for autism spectrum disorders
-
PMID: 22018722
-
Kana RK, Libero LE, Moore M.S. (2011) Disrupted cortical connectivity theory as an explanatory model for autism spectrum disorders. Phys Life Rev 8: 410-437. doi: 10.1016/j.plrev.2011.10.001 PMID: 22018722
-
(2011)
Phys Life Rev
, vol.8
, pp. 410-437
-
-
Kana, R.K.1
Libero, L.E.2
Moore, M.S.3
-
45
-
-
10944263470
-
The small-subunit processome is a ribosome assembly intermediate
-
PMID: 15590835
-
Bernstein KA, Gallagher JE, Mitchell B.M., Granneman S., Baserga SJ (2004) The small-subunit processome is a ribosome assembly intermediate. Eukaryot Cell 3:1619-1626. PMID: 15590835
-
(2004)
Eukaryot Cell
, vol.3
, pp. 1619-1626
-
-
Bernstein, K.A.1
Gallagher, J.E.2
Mitchell, B.M.3
Granneman, S.4
Baserga, S.J.5
-
46
-
-
0037163031
-
Identification of glis1, a novel gli-related, kruppel-like zinc finger protein containing transactivation and repressor functions
-
PMID: 12042312
-
Kim YS, Lewandoski M, Perantoni A.O., Kurebayashi S., Nakanishi G, Jetten AM. (2002) Identification of Glis1, a novel Gli-related, Kruppel-like zinc finger protein containing transactivation and repressor functions. J BiolChem 277: 30901-30913. PMID: 12042312
-
(2002)
J BiolChem
, vol.277
, pp. 30901-30913
-
-
Kim, Y.S.1
Lewandoski, M.2
Perantoni, A.O.3
Kurebayashi, S.4
Nakanishi, G.5
Jetten, A.M.6
-
47
-
-
84878031443
-
Admixture mapping of coronary artery calcified plaque in African Americans with type 2 diabetes mellitus
-
PMID: 23233742
-
Divers J, Palmer ND, Lu L, Register T.C., Carr JJ, Hicks PJ, et al. (2013) Admixture mapping of coronary artery calcified plaque in African Americans with type 2 diabetes mellitus. Circ Cardiovasc Genet 6: 97-105. doi: 10.1161/CIRCGENETICS.112.964114 PMID: 23233742
-
(2013)
Circ Cardiovasc Genet
, vol.6
, pp. 97-105
-
-
Divers, J.1
Palmer, N.D.2
Lu, L.3
Register, T.C.4
Carr, J.J.5
Hicks, P.J.6
-
48
-
-
84863111623
-
GLIS1 rs797906: An increased riskfactor for late-onset Parkinson's disease in the han Chinese population
-
PMID: 22759478
-
Song W, Chen YP, Huang R, Chen K, Pan PL, Li J, et al. (2012) GLIS1 rs797906: an increased riskfactor for late-onset Parkinson's disease in the Han Chinese population. Eur Neurol 68: 89-92. doi: 10.1159/000337955 PMID: 22759478
-
(2012)
Eur Neurol
, vol.68
, pp. 89-92
-
-
Song, W.1
Chen, Y.P.2
Huang, R.3
Chen, K.4
Pan, P.L.5
Li, J.6
-
49
-
-
33747858143
-
An examination of movement kinematics in young people with high-functioning autism and asperger's disorder: Further evidence for a motor planning deficit
-
PMID: 16865551
-
Rinehart NJ, Bellgrove MA, Tonge BJ, Brereton AV, Howells-Rankin D, Bradshaw JL. (2006) An examination of movement kinematics in young people with high-functioning autism and Asperger's disorder: further evidence for a motor planning deficit. J Autism Dev Disord 36: 757-767. PMID: 16865551
-
(2006)
J Autism Dev Disord
, vol.36
, pp. 757-767
-
-
Rinehart, N.J.1
Bellgrove, M.A.2
Tonge, B.J.3
Brereton, A.V.4
Howells-Rankin, D.5
Bradshaw, J.L.6
-
50
-
-
33747814808
-
Gait function in high-functioning autism and asperger's disorder: Evidence for basal-ganglia and cerebellar involvement?
-
PMID: 16554961
-
Rinehart NJ, Tonge BJ, Bradshaw J.L., Iansek R., Enticott PG, McGinley J. (2006) Gait function in high-functioning autism and Asperger's disorder: evidence for basal-ganglia and cerebellar involvement? Eur Child Adolesc Psychiatry 15:256-264. PMID: 16554961
-
(2006)
Eur Child Adolesc Psychiatry
, vol.15
, pp. 256-264
-
-
Rinehart, N.J.1
Tonge, B.J.2
Bradshaw, J.L.3
Iansek, R.4
Enticott, P.G.5
McGinley, J.6
-
51
-
-
33748915812
-
Gait function in newly diagnosed children with autism: Cerebellar and basal ganglia related motor disorder
-
PMID: 16978461
-
Rinehart NJ, Tonge BJ, Iansek R, McGinley J., Brereton AV, Enticott PG, et al. (2006) Gait function in newly diagnosed children with autism: Cerebellar and basal ganglia related motor disorder. Dev Med Child Neurol 48: 819-824. PMID: 16978461
-
(2006)
Dev Med Child Neurol
, vol.48
, pp. 819-824
-
-
Rinehart, N.J.1
Tonge, B.J.2
Iansek, R.3
McGinley, J.4
Brereton, A.V.5
Enticott, P.G.6
-
52
-
-
3543047320
-
A giant novel gene undergoing extensive alternative splicing is severed by a cornelia de lange-associated translocation breakpoint at 3q26.3
-
PMID: 15168106
-
Tonkin ET, Smith M, Eichhorn P., Jones S, Imamwerdi B, Lindsay S., et al. (2004) A giant novel gene undergoing extensive alternative splicing is severed by a Cornelia de Lange-associated translocation breakpoint at 3q26.3. Hum Genet 115:139-148. PMID: 15168106
-
(2004)
Hum Genet
, vol.115
, pp. 139-148
-
-
Tonkin, E.T.1
Smith, M.2
Eichhorn, P.3
Jones, S.4
Imamwerdi, B.5
Lindsay, S.6
-
53
-
-
59249099537
-
A genome-wide association study identifies novel and functionally related susceptibility loci for kawasaki disease
-
PMID: 19132087
-
Burgner D, Davila S, Breunis W.B., Ng SB, Li Y, Bonnard C, et al (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 PMID: 19132087
-
(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
|