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Janine Lamb
Janine Lamb
Reader in Complex Human Genetics/Genomics, University of Manchester
Geverifieerd e-mailadres voor manchester.ac.uk
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Functional impact of global rare copy number variation in autism spectrum disorders
D Pinto, AT Pagnamenta, L Klei, R Anney, D Merico, R Regan, J Conroy, ...
Nature 466 (7304), 368-372, 2010
23062010
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Nature genetics 39 (3), 319-328, 2007
16452007
A genome-wide linkage and association scan reveals novel loci for autism
LA Weiss, DE Arking, ...
Nature 461 (7265), 802-808, 2009
7762009
A genome-wide scan for common alleles affecting risk for autism
R Anney, L Klei, D Pinto, R Regan, J Conroy, TR Magalhaes, C Correia, ...
Human molecular genetics 19 (20), 4072-4082, 2010
7152010
A full genome screen for autism with evidence for linkage to a region on chromosome 7q
International Molecular Genetic Study of Autism Consortium
Human Molecular Genetics 7 (3), 571-578, 1998
5011998
Individual common variants exert weak effects on the risk for autism spectrum disorders
R Anney, L Klei, D Pinto, J Almeida, E Bacchelli, G Baird, N Bolshakova, ...
Human molecular genetics 21 (21), 4781-4792, 2012
4422012
224th ENMC International Workshop:: Clinico-sero-pathological classification of immune-mediated necrotizing myopathies Zandvoort, The Netherlands, 14–16 October 2016
Y Allenbach, AL Mammen, O Benveniste, W Stenzel, A Amato, A Aussey, ...
Neuromuscular disorders 28 (1), 87-99, 2018
4202018
A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia
SE Fisher, AJ Marlow, J Lamb, E Maestrini, DF Williams, AJ Richardson, ...
The American journal of human genetics 64 (1), 146-156, 1999
4191999
A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p
International Molecular Genetic Study of Autism Consortium
The American Journal of Human Genetics 69 (3), 570-581, 2001
4082001
FOXP2 is not a major susceptibility gene for autism or specific language impairment
DF Newbury, E Bonora, JA Lamb, SE Fisher, CSL Lai, G Baird, L Jannoun, ...
The American Journal of Human Genetics 70 (5), 1318-1327, 2002
3692002
A whole-genome scan and fine-mapping linkage study of auditory-visual synesthesia reveals evidence of linkage to chromosomes 2q24, 5q33, 6p12, and 12p12
JE Asher, JA Lamb, D Brocklebank, JB Cazier, E Maestrini, L Addis, ...
The American Journal of Human Genetics 84 (2), 279-285, 2009
2992009
A whole-genome scan and fine-mapping linkage study of auditory-visual synesthesia reveals evidence of linkage to chromosomes 2q24, 5q33, 6p12, and 12p12
JE Asher, JA Lamb, D Brocklebank, JB Cazier, E Maestrini, L Addis, ...
The American Journal of Human Genetics 84 (2), 279-285, 2009
2992009
The EuroMyositis registry: an international collaborative tool to facilitate myositis research
JB Lilleker, J Vencovsky, G Wang, LR Wedderburn, LP Diederichsen, ...
Annals of the rheumatic diseases 77 (1), 30-39, 2018
2382018
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
JP Casey, T Magalhaes, JM Conroy, R Regan, N Shah, R Anney, ...
Human genetics 131, 565-579, 2012
2282012
Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT
G Barnby, A Abbott, N Sykes, A Morris, DE Weeks, R Mott, J Lamb, ...
The American Journal of Human Genetics 76 (6), 950-966, 2005
2152005
Autism: recent molecular genetic advances
JA Lamb, J Moore, A Bailey, AP Monaco
Human Molecular Genetics 9 (6), 861-868, 2000
2142000
239th ENMC international workshop: classification of dermatomyositis, Amsterdam, the Netherlands, 14–16 December 2018
AL Mammen, Y Allenbach, W Stenzel, O Benveniste, J De Bleecker, ...
Neuromuscular Disorders 30 (1), 70-92, 2020
1962020
Risk for myasthenia gravis maps to a 151Pro→Ala change in TNIP1 and to human leukocyte antigen‐B*08
PK Gregersen, R Kosoy, AT Lee, J Lamb, J Sussman, D McKee, ...
Annals of neurology 72 (6), 927-935, 2012
1862012
High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L–DOCK4 gene region in autism susceptibility
E Maestrini, AT Pagnamenta, JA Lamb, E Bacchelli, NH Sykes, I Sousa, ...
Molecular psychiatry 15 (9), 954-968, 2010
1632010
Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic …
S Rothwell, RG Cooper, IE Lundberg, FW Miller, PK Gregersen, J Bowes, ...
Annals of the rheumatic diseases 75 (8), 1558-1566, 2016
1622016
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Artikelen 1–20