Andrew P. Jackson
Andrew P. Jackson
Verified email at igmm.ed.ac.uk - Homepage
Title
Cited by
Cited by
Year
Cerebral organoids model human brain development and microcephaly
MA Lancaster, M Renner, CA Martin, D Wenzel, LS Bicknell, ME Hurles, ...
Nature 501 (7467), 373-379, 2013
27642013
The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data
S Köhler, SC Doelken, CJ Mungall, S Bauer, HV Firth, I Bailleul-Forestier, ...
Nucleic acids research 42 (D1), D966-D974, 2014
7632014
Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 cause Aicardi-Goutieres syndrome at the AGS1 locus
YJ Crow, BE Hayward, R Parmar, P Robins, A Leitch, M Ali, DN Black, ...
Nature genetics 38 (8), 917-920, 2006
7332006
cGAS surveillance of micronuclei links genome instability to innate immunity
KJ Mackenzie, P Carroll, CA Martin, O Murina, A Fluteau, DJ Simpson, ...
Nature 548 (7668), 461-465, 2017
6342017
Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutieres syndrome and mimic congenital viral brain infection
YJ Crow, A Leitch, BE Hayward, A Garner, R Parmar, E Griffith, M Ali, ...
Nature genetics 38 (8), 910-916, 2006
6152006
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease
ARJ Curtis, C Fey, CM Morris, LA Bindoff, PG Ince, PF Chinnery, ...
Nature genetics 28 (4), 350-354, 2001
5622001
Identification of microcephalin, a protein implicated in determining the size of the human brain
AP Jackson, H Eastwood, SM Bell, J Adu, C Toomes, IM Carr, E Roberts, ...
The American Journal of Human Genetics 71 (1), 136-142, 2002
4752002
Prevalence and architecture of de novo mutations in developmental disorders
TDDD Study
Nature 542 (7642), 433, 2017
4332017
Enzymatic removal of ribonucleotides from DNA is essential for mammalian genome integrity and development
MAM Reijns, B Rabe, RE Rigby, P Mill, KR Astell, LA Lettice, S Boyle, ...
Cell 149 (5), 1008-1022, 2012
3922012
Clinical and molecular phenotype of Aicardi-Goutieres syndrome
G Rice, T Patrick, R Parmar, CF Taylor, A Aeby, J Aicardi, R Artuch, ...
The American Journal of Human Genetics 81 (4), 713-725, 2007
3482007
Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling
E Griffith, S Walker, CA Martin, P Vagnarelli, T Stiff, B Vernay, N Al Sanna, ...
Nature genetics 40 (2), 232-236, 2008
3272008
Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling
E Griffith, S Walker, CA Martin, P Vagnarelli, T Stiff, B Vernay, N Al Sanna, ...
Nature genetics 40 (2), 232-236, 2008
3272008
CEP152 is a genome maintenance protein disrupted in Seckel syndrome
E Kalay, G Yigit, Y Aslan, KE Brown, E Pohl, LS Bicknell, H Kayserili, Y Li, ...
Nature genetics 43 (1), 23-26, 2011
2382011
Mutations in microcephalin cause aberrant regulation of chromosome condensation
M Trimborn, SM Bell, C Felix, Y Rashid, H Jafri, PD Griffiths, LM Neumann, ...
The American Journal of Human Genetics 75 (2), 261-266, 2004
2312004
Mutations in the pre-replication complex cause Meier-Gorlin syndrome
LS Bicknell, EMHF Bongers, A Leitch, S Brown, J Schoots, ME Harley, ...
Nature genetics 43 (4), 356-359, 2011
2242011
Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome
LS Bicknell, S Walker, A Klingseisen, T Stiff, A Leitch, C Kerzendorfer, ...
Nature genetics 43 (4), 350-355, 2011
2012011
Mechanisms and pathways of growth failure in primordial dwarfism
A Klingseisen, AP Jackson
Genes & development 25 (19), 2011
1992011
BRIT1/MCPH1 links chromatin remodelling to DNA damage response
G Peng, EK Yim, H Dai, AP Jackson, I Van Der Burgt, MR Pan, R Hu, K Li, ...
Nature cell biology 11 (7), 865-872, 2009
1922009
What primary microcephaly can tell us about brain growth
J Cox, AP Jackson, J Bond, CG Woods
Trends in molecular medicine 12 (8), 358-366, 2006
1922006
Regulation of mitotic entry by microcephalin and its overlap with ATR signalling
GK Alderton, L Galbiati, E Griffith, KH Surinya, H Neitzel, AP Jackson, ...
Nature cell biology 8 (7), 725-733, 2006
1912006
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