Exploring genome-wide DNA methylation patterns in Aicardi syndrome

Ignazio S. Piras; Gabrielle Mills; Lorida Llaci; Marcus Naymik; Keri Ramsey; Newell Belnap; Chris D. Balak; Wayne M. Jepsen; Szabolcs Szelinger; Ashley L. Siniard; Candace R. Lewis; Madison LaFleur; Ryan F. Richholt; Matt D. De Both; Kristiina Avela; Sampathkumar Rangasamy; David W. Craig; Vinodh Narayanan; Irma Jarvela; Matthew J. Huentelman; Isabelle Schrauwen

doi:10.2217/epi-2017-0060

Exploring genome-wide DNA methylation patterns in Aicardi syndrome

Ignazio S. Piras, Gabrielle Mills, Lorida Llaci, Marcus Naymik, Keri Ramsey, Newell Belnap, Chris D. Balak, Wayne M. Jepsen, Szabolcs Szelinger, Ashley L. Siniard, Candace R. Lewis, Madison LaFleur, Ryan F. Richholt, Matt D. De Both, Kristiina Avela, Sampathkumar Rangasamy, David W. Craig, Vinodh Narayanan, Irma Jarvela, Matthew J. HuentelmanIsabelle Schrauwen

Research output: Contribution to journal › Article › Scientific › peer-review

Original language	English
Journal	Epigenomics
Volume	9
Issue number	11
Pages (from-to)	1373-1386
Number of pages	14
ISSN	1750-1911
DOIs	https://doi.org/10.2217/epi-2017-0060
Publication status	Published - Nov 2017
MoE publication type	A1 Journal article-refereed

Fields of Science

Aicardi syndrome
DNA methylation
KCNAB3
EPIGENETIC EPIDEMIOLOGY
GENE-EXPRESSION
EPILEPSY
BLOOD
MUTATION
DISORDERS
DELETION
3111 Biomedicine
1184 Genetics, developmental biology, physiology

Access to Document

10.2217/epi-2017-0060

Cite this

Piras, I. S., Mills, G., Llaci, L., Naymik, M., Ramsey, K., Belnap, N., Balak, C. D., Jepsen, W. M., Szelinger, S., Siniard, A. L., Lewis, C. R., LaFleur, M., Richholt, R. F., De Both, M. D., Avela, K., Rangasamy, S., Craig, D. W., Narayanan, V., Jarvela, I., ... Schrauwen, I. (2017). Exploring genome-wide DNA methylation patterns in Aicardi syndrome. Epigenomics, 9(11), 1373-1386. https://doi.org/10.2217/epi-2017-0060

@article{2ad370aa092945959ece739eed1035bd,

title = "Exploring genome-wide DNA methylation patterns in Aicardi syndrome",

keywords = "Aicardi syndrome, DNA methylation, KCNAB3, EPIGENETIC EPIDEMIOLOGY, GENE-EXPRESSION, EPILEPSY, BLOOD, MUTATION, DISORDERS, DELETION, 3111 Biomedicine, 1184 Genetics, developmental biology, physiology",

author = "Piras, {Ignazio S.} and Gabrielle Mills and Lorida Llaci and Marcus Naymik and Keri Ramsey and Newell Belnap and Balak, {Chris D.} and Jepsen, {Wayne M.} and Szabolcs Szelinger and Siniard, {Ashley L.} and Lewis, {Candace R.} and Madison LaFleur and Richholt, {Ryan F.} and {De Both}, {Matt D.} and Kristiina Avela and Sampathkumar Rangasamy and Craig, {David W.} and Vinodh Narayanan and Irma Jarvela and Huentelman, {Matthew J.} and Isabelle Schrauwen",

year = "2017",

month = nov,

doi = "10.2217/epi-2017-0060",

language = "English",

volume = "9",

pages = "1373--1386",

journal = "Epigenomics",

issn = "1750-1911",

publisher = "Taylor and Francis Ltd.",

number = "11",

}

Piras, IS, Mills, G, Llaci, L, Naymik, M, Ramsey, K, Belnap, N, Balak, CD, Jepsen, WM, Szelinger, S, Siniard, AL, Lewis, CR, LaFleur, M, Richholt, RF, De Both, MD, Avela, K, Rangasamy, S, Craig, DW, Narayanan, V, Jarvela, I, Huentelman, MJ & Schrauwen, I 2017, 'Exploring genome-wide DNA methylation patterns in Aicardi syndrome', Epigenomics, vol. 9, no. 11, pp. 1373-1386. https://doi.org/10.2217/epi-2017-0060

TY - JOUR

T1 - Exploring genome-wide DNA methylation patterns in Aicardi syndrome

AU - Piras, Ignazio S.

AU - Mills, Gabrielle

AU - Llaci, Lorida

AU - Naymik, Marcus

AU - Ramsey, Keri

AU - Belnap, Newell

AU - Balak, Chris D.

AU - Jepsen, Wayne M.

AU - Szelinger, Szabolcs

AU - Siniard, Ashley L.

AU - Lewis, Candace R.

AU - LaFleur, Madison

AU - Richholt, Ryan F.

AU - De Both, Matt D.

AU - Avela, Kristiina

AU - Rangasamy, Sampathkumar

AU - Craig, David W.

AU - Narayanan, Vinodh

AU - Jarvela, Irma

AU - Huentelman, Matthew J.

AU - Schrauwen, Isabelle

PY - 2017/11

Y1 - 2017/11

KW - Aicardi syndrome

KW - DNA methylation

KW - KCNAB3

KW - EPIGENETIC EPIDEMIOLOGY

KW - GENE-EXPRESSION

KW - EPILEPSY

KW - BLOOD

KW - MUTATION

KW - DISORDERS

KW - DELETION

KW - 3111 Biomedicine

KW - 1184 Genetics, developmental biology, physiology

U2 - 10.2217/epi-2017-0060

DO - 10.2217/epi-2017-0060

M3 - Article

SN - 1750-1911

VL - 9

SP - 1373

EP - 1386

JO - Epigenomics

JF - Epigenomics

IS - 11

ER -