christopher geoffrey woods
christopher geoffrey woods
professor of human genetics
Verified email at cam.ac.uk
Title
Cited by
Cited by
Year
An SCN9A channelopathy causes congenital inability to experience pain
JJ Cox, F Reimann, AK Nicholas, G Thornton, E Roberts, K Springell, ...
Nature 444 (7121), 894-898, 2006
14512006
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase
A Ramirez, A Heimbach, J Gründemann, B Stiller, D Hampshire, LP Cid, ...
Nature genetics 38 (10), 1184-1191, 2006
11082006
A splicing mutation affecting expression of ataxia–telangiectasia and Rad3–related protein (ATR) results in Seckel syndrome
M O'Driscoll, VL Ruiz-Perez, CG Woods, PA Jeggo, JA Goodship
Nature genetics 33 (4), 497-501, 2003
8362003
Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome
J Celli, P Duijf, BCJ Hamel, M Bamshad, B Kramer, APT Smits, ...
Cell 99 (2), 143-153, 1999
7601999
Recurrent rearrangements of chromosome 1q21. 1 and variable pediatric phenotypes
HC Mefford, AJ Sharp, C Baker, A Itsara, Z Jiang, K Buysse, S Huang, ...
New England Journal of Medicine 359 (16), 1685-1699, 2008
7262008
Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation
DJ Marsh, V Coulon, KL Lunetta, P Rocca-Serra, PLM Dahia, Z Zheng, ...
Human molecular genetics 7 (3), 507-515, 1998
7091998
Flies without centrioles
R Basto, J Lau, T Vinogradova, A Gardiol, CG Woods, A Khodjakov, ...
Cell 125 (7), 1375-1386, 2006
6852006
ASPM is a major determinant of cerebral cortical size
J Bond, E Roberts, GH Mochida, DJ Hampshire, S Scott, JM Askham, ...
Nature genetics 32 (2), 316-320, 2002
6462002
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
5812006
Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosis
C Toomes, J James, AJ Wood, CL Wu, D McCormick, N Lench, C Hewitt, ...
Nature genetics 23 (4), 421-424, 1999
5611999
A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size
J Bond, E Roberts, K Springell, S Lizarraga, S Scott, J Higgins, ...
Nature genetics 37 (4), 353-355, 2005
5442005
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
4702002
PLA2G6, encoding a phospholipase A 2, is mutated in neurodegenerative disorders with high brain iron
NV Morgan, SK Westaway, JEV Morton, A Gregory, P Gissen, S Sonek, ...
Nature genetics 38 (7), 752-754, 2006
4682006
Autosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findings
CG Woods, J Bond, W Enard
The American Journal of Human Genetics 76 (5), 717-728, 2005
4312005
Primary microcephaly: do all roads lead to Rome?
GK Thornton, CG Woods
Trends in Genetics 25 (11), 501-510, 2009
3862009
A gain-of-function mutation in TRPA1 causes familial episodic pain syndrome
B Kremeyer, F Lopera, JJ Cox, A Momin, F Rugiero, S Marsh, CG Woods, ...
Neuron 66 (5), 671-680, 2010
3592010
Large-scale discovery of novel genetic causes of developmental disorders
TDDD Study, TW Fitzgerald, SS Gerety, WD Jones, M van Kogelenberg, ...
Nature 519 (7542), 223-228, 2015
3522015
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
3512017
Centrosomes and cilia in human disease
M Bettencourt-Dias, F Hildebrandt, D Pellman, G Woods, SA Godinho
Trends in Genetics 27 (8), 307-315, 2011
3202011
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome
V Cantagrel, JL Silhavy, SL Bielas, D Swistun, SE Marsh, JY Bertrand, ...
The American Journal of Human Genetics 83 (2), 170-179, 2008
3152008
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