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
21462013
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
7072014
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
6712006
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
5652006
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
5432001
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
4682002
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
3872017
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
3332012
Prevalence and architecture of de novo mutations in developmental disorders
DDD Study, JF McRae, S Clayton, TW Fitzgerald, J Kaplanis, E Prigmore, ...
Nature 542 (7642), 433-438, 2017
3222017
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
3122007
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, 2008
3092008
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, 2008
3092008
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
2262011
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
2222004
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, 2011
2012011
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
1902006
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
1872006
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
1772011
Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pter
AP Jackson, DP McHale, DA Campbell, H Jafri, Y Rashid, J Mannan, ...
The American Journal of Human Genetics 63 (2), 541-546, 1998
1751998
Mechanisms and pathways of growth failure in primordial dwarfism
A Klingseisen, AP Jackson
Genes & development 25 (19), 2011
1712011
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Articles 1–20