-
1
-
-
0034961104
-
Amyotrophic lateral sclerosis: Pathogenesis
-
Brown RH Jr, Robberecht W. Amyotrophic lateral sclerosis: Pathogenesis. Semin Neurol. 2001;21:131-9.
-
(2001)
Semin Neurol
, vol.21
, pp. 131-139
-
-
Brown Jr, R.H.1
Robberecht, W.2
-
2
-
-
0035516124
-
From Charcot to Lou Gehrig: Deciphering selective motor neuron death in ALS
-
Cleveland DW, Rothstein JD. From Charcot to Lou Gehrig: Deciphering selective motor neuron death in ALS. Nat Rev Neurosci. 2001;2:806-19.
-
(2001)
Nat Rev Neurosci
, vol.2
, pp. 806-819
-
-
Cleveland, D.W.1
Rothstein, J.D.2
-
3
-
-
0035978743
-
Amyotrophic lateral sclerosis
-
Rowland LP, Shneider NA. Amyotrophic lateral sclerosis. N Engl J Med. 2001;344:1688-700.
-
(2001)
N Engl J Med
, vol.344
, pp. 1688-1700
-
-
Rowland, L.P.1
Shneider, N.A.2
-
4
-
-
0034790894
-
-
Shaw PJ. Genetic inroads in familial ALS. Nat Genet. 2001;29:103-4. Gros-Louis F, Gaspar C, Rouleau GA. Genetics of familial and sporadic amyotrophic lateral sclerosis. Biochim Biophys Acta. 2006;1762:956-72.
-
Shaw PJ. Genetic inroads in familial ALS. Nat Genet. 2001;29:103-4. Gros-Louis F, Gaspar C, Rouleau GA. Genetics of familial and sporadic amyotrophic lateral sclerosis. Biochim Biophys Acta. 2006;1762:956-72.
-
-
-
-
5
-
-
0028918944
-
Identification of new mutations in the Cu/Zn superoxide dismutase gene of patients with familial amyotrophic lateral sclerosis
-
Pramatarova A, Figlewicz DA, Krizus A, Han FY, Ceballos- Picot I, Nicole A, et al. Identification of new mutations in the Cu/Zn superoxide dismutase gene of patients with familial amyotrophic lateral sclerosis. Am J Hum Genet. 1995;56: 592-6.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 592-596
-
-
Pramatarova, A.1
Figlewicz, D.A.2
Krizus, A.3
Han, F.Y.4
Ceballos- Picot, I.5
Nicole, A.6
-
6
-
-
33750474894
-
SOD1 gene mutations in Italian patients with sporadic amyotrophic lateral sclerosis (SALS)
-
Corrado L, D'Alfonso S, Bergamaschi L, Testa L, Leone M, Nasuelli N, et al. SOD1 gene mutations in Italian patients with sporadic amyotrophic lateral sclerosis (SALS). Neuromuscul Disord. 2006;16:800-4.
-
(2006)
Neuromuscul Disord
, vol.16
, pp. 800-804
-
-
Corrado, L.1
D'Alfonso, S.2
Bergamaschi, L.3
Testa, L.4
Leone, M.5
Nasuelli, N.6
-
7
-
-
0030780350
-
Copper/zinc superoxide dismutase 1 and sporadic amyotrophic lateral sclerosis: Analysis of 155 cases and identification of a novel insertion mutation
-
Jackson M, Al-Chalabi A, Enayat ZE, Chioza B, Leigh PN, Morrison KE. Copper/zinc superoxide dismutase 1 and sporadic amyotrophic lateral sclerosis: Analysis of 155 cases and identification of a novel insertion mutation. Ann Neurol. 1997;42:803-7.
-
(1997)
Ann Neurol
, vol.42
, pp. 803-807
-
-
Jackson, M.1
Al-Chalabi, A.2
Enayat, Z.E.3
Chioza, B.4
Leigh, P.N.5
Morrison, K.E.6
-
8
-
-
0028273306
-
Identification of a novel SOD1 mutation in an apparently sporadic amyotrophic lateral sclerosis patient and the detection of Ile113Thr in three others
-
Jones CT, Swingler RJ, Brock DJ. Identification of a novel SOD1 mutation in an apparently sporadic amyotrophic lateral sclerosis patient and the detection of Ile113Thr in three others. Hum Mol Genet. 1994;3:649-50.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 649-650
-
-
Jones, C.T.1
Swingler, R.J.2
Brock, D.J.3
-
9
-
-
33847622526
-
Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: First stage analysis and public release of data
-
Schymick JC, Scholz SW, Fung HC, Britton A, Arepalli S, Gibbs JR, et al. Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: First stage analysis and public release of data. Lancet Neurol. 2007;6: 322-8.
-
(2007)
Lancet Neurol
, vol.6
, pp. 322-328
-
-
Schymick, J.C.1
Scholz, S.W.2
Fung, H.C.3
Britton, A.4
Arepalli, S.5
Gibbs, J.R.6
-
10
-
-
34548083742
-
Whole-genome analysis of sporadic amyotrophic lateral sclerosis
-
Dunckley T, Huentelman MJ, Craig DW, Pearson JV, Szelinger S, Joshipura K, et al. Whole-genome analysis of sporadic amyotrophic lateral sclerosis. N Engl J Med. 2007;357:775-88.
-
(2007)
N Engl J Med
, vol.357
, pp. 775-788
-
-
Dunckley, T.1
Huentelman, M.J.2
Craig, D.W.3
Pearson, J.V.4
Szelinger, S.5
Joshipura, K.6
-
11
-
-
34548646702
-
ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: A genome-wide association study
-
van Es MA, van Vught PW, Blauw HM, Franke L, Saris CG, Andersen PM, et al. ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: A genome-wide association study. Lancet Neurol. 2007;6:869-77.
-
(2007)
Lancet Neurol
, vol.6
, pp. 869-877
-
-
van Es, M.A.1
van Vught, P.W.2
Blauw, H.M.3
Franke, L.4
Saris, C.G.5
Andersen, P.M.6
-
12
-
-
39749119374
-
A genome-wide association study of sporadic ALS in a homogenous Irish population
-
Cronin S, Berger S, Ding J, Schymick JC, Washecka N, Hernandez DG, et al. A genome-wide association study of sporadic ALS in a homogenous Irish population. Hum Mol Genet. 2008;17:768-74.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 768-774
-
-
Cronin, S.1
Berger, S.2
Ding, J.3
Schymick, J.C.4
Washecka, N.5
Hernandez, D.G.6
-
13
-
-
37549062995
-
Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis
-
van Es MA, van Vught PW, Blauw HM, Franke L, Saris CG, van den Bosch L, et al. Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis. Nat Genet. 2008;40:29-31.
-
(2008)
Nat Genet
, vol.40
, pp. 29-31
-
-
van Es, M.A.1
van Vught, P.W.2
Blauw, H.M.3
Franke, L.4
Saris, C.G.5
van den Bosch, L.6
-
14
-
-
0028001606
-
Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosis
-
Figlewicz DA, Krizus A, Martinoli MG,Meininger V, Dib M, Rouleau GA, et al. Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosis. Hum Mol Genet. 1994;3:1757-61.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1757-1761
-
-
Figlewicz, D.A.1
Krizus, A.2
Martinoli, M.G.3
Meininger, V.4
Dib, M.5
Rouleau, G.A.6
-
15
-
-
5044244266
-
Analysis of heavy neurofilament subunit gene polymorphism in Russian patients with sporadic motor neuron disease (MND)
-
Skvortsova V, Shadrina M, Slominsky P, Levitsky G, Kondratieva E, Zherebtsova A, et al. Analysis of heavy neurofilament subunit gene polymorphism in Russian patients with sporadic motor neuron disease (MND). Eur J Hum Genet. 2004;12:241-4.
-
(2004)
Eur J Hum Genet
, vol.12
, pp. 241-244
-
-
Skvortsova, V.1
Shadrina, M.2
Slominsky, P.3
Levitsky, G.4
Kondratieva, E.5
Zherebtsova, A.6
-
16
-
-
0041903805
-
VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motor neurons against ischaemic death
-
Lambrechts D, Storkebaum E, Morimoto M, Del-Favero J, Desmet F, Marklund SL, et al. VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motor neurons against ischaemic death. Nat Genet. 2003;34:383-94.
-
(2003)
Nat Genet
, vol.34
, pp. 383-394
-
-
Lambrechts, D.1
Storkebaum, E.2
Morimoto, M.3
Del-Favero, J.4
Desmet, F.5
Marklund, S.L.6
-
17
-
-
0036156999
-
Abnormal SMN1 gene copy number is a susceptibility factor for amyotrophic lateral sclerosis
-
Corcia P, Mayeux-Portas V, Khoris J, de Toffol B, Autret A, Muh JP, et al. Abnormal SMN1 gene copy number is a susceptibility factor for amyotrophic lateral sclerosis. Ann Neurol. 2002;51:243-6.
-
(2002)
Ann Neurol
, vol.51
, pp. 243-246
-
-
Corcia, P.1
Mayeux-Portas, V.2
Khoris, J.3
de Toffol, B.4
Autret, A.5
Muh, J.P.6
-
18
-
-
0035957312
-
Homozygous deletion of the survival motor neuron 2 gene is a prognostic factor in sporadic ALS
-
Veldink JH, van den Berg LH, Cobben JM, Stulp RP, de Jong JM, Vogels OJ, et al. Homozygous deletion of the survival motor neuron 2 gene is a prognostic factor in sporadic ALS. Neurology. 2001;56:749-52.
-
(2001)
Neurology
, vol.56
, pp. 749-752
-
-
Veldink, J.H.1
van den Berg, L.H.2
Cobben, J.M.3
Stulp, R.P.4
de Jong, J.M.5
Vogels, O.J.6
-
19
-
-
0030927075
-
Glutamate, excitotoxicity and amyotrophic lateral sclerosis
-
Shaw PJ, Ince PG. Glutamate, excitotoxicity and amyotrophic lateral sclerosis. J Neurol. 1997;244(Suppl 2):S3-14.
-
(1997)
J Neurol
, vol.244
, Issue.SUPPL. 2
-
-
Shaw, P.J.1
Ince, P.G.2
-
20
-
-
33645422711
-
ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis
-
Greenway MJ, Andersen PM, Russ C, Ennis S, Cashman S, Donaghy C, et al. ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis. Nat Genet. 2006;38:411-3.
-
(2006)
Nat Genet
, vol.38
, pp. 411-413
-
-
Greenway, M.J.1
Andersen, P.M.2
Russ, C.3
Ennis, S.4
Cashman, S.5
Donaghy, C.6
-
21
-
-
4143084861
-
Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS
-
Munch C, Sedlmeier R, Meyer T, Homberg V, Sperfeld AD, Kurt A, et al. Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS. Neurology. 2004;63:724-6.
-
(2004)
Neurology
, vol.63
, pp. 724-726
-
-
Munch, C.1
Sedlmeier, R.2
Meyer, T.3
Homberg, V.4
Sperfeld, A.D.5
Kurt, A.6
-
22
-
-
8844233445
-
Complex genetics of amyotrophic lateral sclerosis
-
Kunst CB. Complex genetics of amyotrophic lateral sclerosis. Am J Hum Genet. 2004;75:933-47.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 933-947
-
-
Kunst, C.B.1
-
24
-
-
33751120678
-
Amyotrophic lateral sclerosis as a complex genetic disease
-
Simpson CL, Al-Chalabi A. Amyotrophic lateral sclerosis as a complex genetic disease. Biochim Biophys Acta. 2006;1762: 973-85.
-
(2006)
Biochim Biophys Acta
, vol.1762
, pp. 973-985
-
-
Simpson, C.L.1
Al-Chalabi, A.2
-
25
-
-
0029030610
-
Selective loss of glial glutamate transporter GLT-1 in amyotrophic lateral sclerosis
-
Rothstein JD, van Kammen M, Levey AI, Martin LJ, Kuncl RW. Selective loss of glial glutamate transporter GLT-1 in amyotrophic lateral sclerosis. Ann Neurol. 1995;38:73-84.
-
(1995)
Ann Neurol
, vol.38
, pp. 73-84
-
-
Rothstein, J.D.1
van Kammen, M.2
Levey, A.I.3
Martin, L.J.4
Kuncl, R.W.5
-
26
-
-
0037461293
-
High rate of constitutional chromosomal rearrangements in apparently sporadic ALS
-
Meyer T, Alber B, Roemer K, Martin T, Kalscheuer VM, Gottert E, et al. High rate of constitutional chromosomal rearrangements in apparently sporadic ALS. Neurology. 2003;60:1348-50.
-
(2003)
Neurology
, vol.60
, pp. 1348-1350
-
-
Meyer, T.1
Alber, B.2
Roemer, K.3
Martin, T.4
Kalscheuer, V.M.5
Gottert, E.6
-
27
-
-
40849141981
-
Copy-number variation in sporadic amyotrophic lateral sclerosis: A genome-wide screen
-
Blauw HM, Veldink JH, van Es MA, van Vught PW, Saris CG, van der Zwaag B, et al. Copy-number variation in sporadic amyotrophic lateral sclerosis: A genome-wide screen. Lancet Neurol. 2008;7:319-26.
-
(2008)
Lancet Neurol
, vol.7
, pp. 319-326
-
-
Blauw, H.M.1
Veldink, J.H.2
van Es, M.A.3
van Vught, P.W.4
Saris, C.G.5
van der Zwaag, B.6
-
28
-
-
39749119374
-
Analysis of genome-wide copy number variation in Irish and Dutch ALS populations
-
Cronin S, Blauw HM, Veldink JH, van Es MA, Ophoff RA, Bradley DG, et al. Analysis of genome-wide copy number variation in Irish and Dutch ALS populations. Hum Mol Genet. 2008;17:768-74.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 768-774
-
-
Cronin, S.1
Blauw, H.M.2
Veldink, J.H.3
van Es, M.A.4
Ophoff, R.A.5
Bradley, D.G.6
-
29
-
-
17344371740
-
High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays
-
Pinkel D, Segraves R, Sudar D, Clark S, Poole I, Kowbel D, et al. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Nat Genet. 1998;20:207-11.
-
(1998)
Nat Genet
, vol.20
, pp. 207-211
-
-
Pinkel, D.1
Segraves, R.2
Sudar, D.3
Clark, S.4
Poole, I.5
Kowbel, D.6
-
30
-
-
0030701970
-
Matrix-based comparative genomic hybridization: Biochips to screen for genomic imbalances
-
Solinas-Toldo S, Lampel S, Stilgenbauer S, Nickolenko J, Benner A, Dohner H, et al. Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances. Genes Chromosomes Cancer. 1997;20:399-407.
-
(1997)
Genes Chromosomes Cancer
, vol.20
, pp. 399-407
-
-
Solinas-Toldo, S.1
Lampel, S.2
Stilgenbauer, S.3
Nickolenko, J.4
Benner, A.5
Dohner, H.6
-
31
-
-
33751503669
-
Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation
-
Erdogan F, Chen W, Kirchhoff M, Kalscheuer VM, Hultschig C, Muller I, et al. Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation. Cytogenet Genome Res. 2006;115:247-53.
-
(2006)
Cytogenet Genome Res
, vol.115
, pp. 247-253
-
-
Erdogan, F.1
Chen, W.2
Kirchhoff, M.3
Kalscheuer, V.M.4
Hultschig, C.5
Muller, I.6
-
32
-
-
10744233914
-
A tiling resolution DNA microarray with complete coverage of the human genome
-
Ishkanian AS, Malloff CA, Watson SK, de Leeuw RJ, Chi B, Coe BP, et al. A tiling resolution DNA microarray with complete coverage of the human genome. Nat Genet. 2004;36:299-303.
-
(2004)
Nat Genet
, vol.36
, pp. 299-303
-
-
Ishkanian, A.S.1
Malloff, C.A.2
Watson, S.K.3
de Leeuw, R.J.4
Chi, B.5
Coe, B.P.6
-
33
-
-
3142698256
-
A set of BAC clones spanning the human genome
-
Krzywinski M, Bosdet I, Smailus D, Chiu R, Mathewson C, Wye N, et al. A set of BAC clones spanning the human genome. Nucleic Acids Res. 2004;32:3651-60.
-
(2004)
Nucleic Acids Res
, vol.32
, pp. 3651-3660
-
-
Krzywinski, M.1
Bosdet, I.2
Smailus, D.3
Chiu, R.4
Mathewson, C.5
Wye, N.6
-
34
-
-
0035080952
-
A bacterial artificial chromosome library for sequencing the complete human genome
-
Osoegawa K, Mammoser AG, Wu C, Frengen E, Zeng C, Catanese JJ, et al. A bacterial artificial chromosome library for sequencing the complete human genome. Genome Res. 2001;11:483-96.
-
(2001)
Genome Res
, vol.11
, pp. 483-496
-
-
Osoegawa, K.1
Mammoser, A.G.2
Wu, C.3
Frengen, E.4
Zeng, C.5
Catanese, J.J.6
-
35
-
-
0037376804
-
DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones
-
Fiegler H, Carr P, Douglas EJ, Burford DC, Hunt S, Scott CE, et al. DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones. Genes Chromosomes Cancer. 2003;36: 361-74.
-
(2003)
Genes Chromosomes Cancer
, vol.36
, pp. 361-374
-
-
Fiegler, H.1
Carr, P.2
Douglas, E.J.3
Burford, D.C.4
Hunt, S.5
Scott, C.E.6
-
36
-
-
13444304325
-
NCBI GEO: Mining millions of expression profiles - database and tools
-
Barrett T, Suzek TO, Troup DB, Wilhite SE, Ngau WC, Ledoux P, et al. NCBI GEO: Mining millions of expression profiles - database and tools. Nucleic Acids Res. 2005;33:D562-6.
-
(2005)
Nucleic Acids Res
, vol.33
-
-
Barrett, T.1
Suzek, T.O.2
Troup, D.B.3
Wilhite, S.E.4
Ngau, W.C.5
Ledoux, P.6
-
37
-
-
0036081355
-
Gene Expression Omnibus: NCBI gene expression and hybridization array data repository
-
Edgar R, Domrachev M, Lash AE. Gene Expression Omnibus: NCBI gene expression and hybridization array data repository. Nucleic Acids Res. 2002;30:207-10.
-
(2002)
Nucleic Acids Res
, vol.30
, pp. 207-210
-
-
Edgar, R.1
Domrachev, M.2
Lash, A.E.3
-
38
-
-
22844435668
-
CGHPRO: A comprehensive data analysis tool for array CGH
-
Chen W, Erdogan F, Ropers HH, Lenzner S, Ullmann R. CGHPRO: A comprehensive data analysis tool for array CGH. BMC Bioinformatics. 2005;6:85.
-
(2005)
BMC Bioinformatics
, vol.6
, pp. 85
-
-
Chen, W.1
Erdogan, F.2
Ropers, H.H.3
Lenzner, S.4
Ullmann, R.5
-
39
-
-
1542378930
-
Glutamate receptors: RNA editing and death of motor neurons
-
Kawahara Y, Ito K, Sun H, Aizawa H, Kanazawa I, Kwak S. Glutamate receptors: RNA editing and death of motor neurons. Nature Feb; 427. 2004;26(6977):801.
-
(2004)
Nature Feb; 427
, vol.26
, Issue.6977
, pp. 801
-
-
Kawahara, Y.1
Ito, K.2
Sun, H.3
Aizawa, H.4
Kanazawa, I.5
Kwak, S.6
-
40
-
-
33751503099
-
Molecular karyotyping of patients with MCA/MR: The blurred boundary between normal and pathogenic variation
-
de Ravel TJ, Balikova I, Thienpont B, Hannes F, Maas N, Fryns JP, et al. Molecular karyotyping of patients with MCA/MR: The blurred boundary between normal and pathogenic variation. Cytogenet Genome Res. 2006;115:225-30.
-
(2006)
Cytogenet Genome Res
, vol.115
, pp. 225-230
-
-
de Ravel, T.J.1
Balikova, I.2
Thienpont, B.3
Hannes, F.4
Maas, N.5
Fryns, J.P.6
-
41
-
-
33846562388
-
Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia- absent radius syndrome
-
Klopocki E, Schulze H, Strauss G, Ott CE, Hall J, Trotier F, et al. Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia- absent radius syndrome. Am J Hum Genet. 2007;80:232-40.
-
(2007)
Am J Hum Genet
, vol.80
, pp. 232-240
-
-
Klopocki, E.1
Schulze, H.2
Strauss, G.3
Ott, C.E.4
Hall, J.5
Trotier, F.6
-
43
-
-
4444291843
-
Detection of large-scale variation in the human genome
-
Iafrate AJ, Feuk L, Rivera MN, Listewnik ML, Donahoe PK, Qi Y, et al. Detection of large-scale variation in the human genome. Nat Genet. 2004;36:949-51.
-
(2004)
Nat Genet
, vol.36
, pp. 949-951
-
-
Iafrate, A.J.1
Feuk, L.2
Rivera, M.N.3
Listewnik, M.L.4
Donahoe, P.K.5
Qi, Y.6
-
44
-
-
29444457877
-
Common deletion polymorphisms in the human genome
-
McCarroll SA, Hadnott TN, Perry GH, Sabeti PC, Zody MC, Barrett JC, et al. Common deletion polymorphisms in the human genome. Nat Genet. 2006;38:86-92.
-
(2006)
Nat Genet
, vol.38
, pp. 86-92
-
-
McCarroll, S.A.1
Hadnott, T.N.2
Perry, G.H.3
Sabeti, P.C.4
Zody, M.C.5
Barrett, J.C.6
-
45
-
-
33751329250
-
Global variation in copy number in the human genome
-
Redon R, Ishikawa S, Fitch KR, Feuk L, Perry GH, Andrews TD, et al. Global variation in copy number in the human genome. Nature; 444. 2006;23:444-54.
-
(2006)
Nature
, vol.444
, Issue.23
, pp. 444-454
-
-
Redon, R.1
Ishikawa, S.2
Fitch, K.R.3
Feuk, L.4
Perry, G.H.5
Andrews, T.D.6
-
46
-
-
3242808027
-
Large-scale copy number polymorphism in the human genome
-
Sebat J, Lakshmi B, Troge J, Alexander J, Young J, Lundin P, et al. Large-scale copy number polymorphism in the human genome. Science. 2004;305:525-8.
-
(2004)
Science
, vol.305
, pp. 525-528
-
-
Sebat, J.1
Lakshmi, B.2
Troge, J.3
Alexander, J.4
Young, J.5
Lundin, P.6
-
47
-
-
22844451617
-
Fine-scale structural variation of the human genome
-
Tuzun E, Sharp AJ, Bailey JA, Kaul R, Morrison VA, Pertz LM, et al. Fine-scale structural variation of the human genome. Nat Genet. 2005;37:727-32.
-
(2005)
Nat Genet
, vol.37
, pp. 727-732
-
-
Tuzun, E.1
Sharp, A.J.2
Bailey, J.A.3
Kaul, R.4
Morrison, V.A.5
Pertz, L.M.6
-
48
-
-
32844460938
-
Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans
-
Aitman TJ, Dong R, Vyse TJ, Norsworthy PJ, Johnson MD, Smith J, et al. Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans. Nature. 2006;439:851-5.
-
(2006)
Nature
, vol.439
, pp. 851-855
-
-
Aitman, T.J.1
Dong, R.2
Vyse, T.J.3
Norsworthy, P.J.4
Johnson, M.D.5
Smith, J.6
-
49
-
-
33846006596
-
A comprehensive analysis of common copy-number variations in the human genome
-
Wong KK, de Leeuw RJ, Dosanjh NS, Kimm LR, Cheng Z, Horsman DE, et al. A comprehensive analysis of common copy-number variations in the human genome. Am J Hum Genet. 2007;80:91-104.
-
(2007)
Am J Hum Genet
, vol.80
, pp. 91-104
-
-
Wong, K.K.1
de Leeuw, R.J.2
Dosanjh, N.S.3
Kimm, L.R.4
Cheng, Z.5
Horsman, D.E.6
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