Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy (vol 3, 33, 2018)

Mark A. Corbett; Clare L. van Eyk; Dani L. Webber; Stephen J. Bent; Morgan Newman; Kelly Harper; Jesia G. Berry; Dimitar N. Azmanov; Karen J. Woodward; Alison E. Gardner; Jennie Slee; Luis A. Perez-Jurado; Alastair H. MacLennan; Jozef Gecz

doi:10.1038/s41525-019-0086-7

Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy (vol 3, 33, 2018)

Mark A. Corbett, Clare L. van Eyk, Dani L. Webber, Stephen J. Bent, Morgan Newman, Kelly Harper, Jesia G. Berry, Dimitar N. Azmanov, Karen J. Woodward, Alison E. Gardner, Jennie Slee, Luis A. Perez-Jurado, Alastair H. MacLennan, Jozef Gecz

School of Biomedical Sciences

Research output: Contribution to journal › Letter

Original language	English
Article number	11
Number of pages	1
Journal	npj Genomic Medicine
Volume	4
DOIs	https://doi.org/10.1038/s41525-019-0086-7
Publication status	Published - 31 May 2019

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10.1038/s41525-019-0086-7Licence: CC BY

Cite this

Corbett, M. A., van Eyk, C. L., Webber, D. L., Bent, S. J., Newman, M., Harper, K., Berry, J. G., Azmanov, D. N., Woodward, K. J., Gardner, A. E., Slee, J., Perez-Jurado, L. A., MacLennan, A. H., & Gecz, J. (2019). Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy (vol 3, 33, 2018). npj Genomic Medicine, 4, [11]. https://doi.org/10.1038/s41525-019-0086-7

Corbett, Mark A. ; van Eyk, Clare L. ; Webber, Dani L. ; Bent, Stephen J. ; Newman, Morgan ; Harper, Kelly ; Berry, Jesia G. ; Azmanov, Dimitar N. ; Woodward, Karen J. ; Gardner, Alison E. ; Slee, Jennie ; Perez-Jurado, Luis A. ; MacLennan, Alastair H. ; Gecz, Jozef. / Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy (vol 3, 33, 2018). In: npj Genomic Medicine. 2019 ; Vol. 4.

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title = "Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy (vol 3, 33, 2018)",

author = "Corbett, {Mark A.} and {van Eyk}, {Clare L.} and Webber, {Dani L.} and Bent, {Stephen J.} and Morgan Newman and Kelly Harper and Berry, {Jesia G.} and Azmanov, {Dimitar N.} and Woodward, {Karen J.} and Gardner, {Alison E.} and Jennie Slee and Perez-Jurado, {Luis A.} and MacLennan, {Alastair H.} and Jozef Gecz",

year = "2019",

month = may,

day = "31",

doi = "10.1038/s41525-019-0086-7",

language = "English",

volume = "4",

journal = "Genome Medicine",

issn = "1756-994X",

publisher = "BioMed Central",

}

Corbett, MA, van Eyk, CL, Webber, DL, Bent, SJ, Newman, M, Harper, K, Berry, JG, Azmanov, DN, Woodward, KJ, Gardner, AE, Slee, J, Perez-Jurado, LA, MacLennan, AH & Gecz, J 2019, 'Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy (vol 3, 33, 2018)', npj Genomic Medicine, vol. 4, 11. https://doi.org/10.1038/s41525-019-0086-7

Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy (vol 3, 33, 2018). / Corbett, Mark A.; van Eyk, Clare L.; Webber, Dani L.; Bent, Stephen J.; Newman, Morgan; Harper, Kelly; Berry, Jesia G.; Azmanov, Dimitar N.; Woodward, Karen J.; Gardner, Alison E.; Slee, Jennie; Perez-Jurado, Luis A.; MacLennan, Alastair H.; Gecz, Jozef.

In: npj Genomic Medicine, Vol. 4, 11, 31.05.2019.

Research output: Contribution to journal › Letter

TY - JOUR

T1 - Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy (vol 3, 33, 2018)

AU - Corbett, Mark A.

AU - van Eyk, Clare L.

AU - Webber, Dani L.

AU - Bent, Stephen J.

AU - Newman, Morgan

AU - Harper, Kelly

AU - Berry, Jesia G.

AU - Azmanov, Dimitar N.

AU - Woodward, Karen J.

AU - Gardner, Alison E.

AU - Slee, Jennie

AU - Perez-Jurado, Luis A.

AU - MacLennan, Alastair H.

AU - Gecz, Jozef

PY - 2019/5/31

Y1 - 2019/5/31

U2 - 10.1038/s41525-019-0086-7

DO - 10.1038/s41525-019-0086-7

M3 - Letter

C2 - 31231543

VL - 4

JO - Genome Medicine

JF - Genome Medicine

SN - 1756-994X

M1 - 11

ER -