|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
|Structural variation of chromosomes in autism spectrum disorder|
CR Marshall, A Noor, JB Vincent, AC Lionel, L Feuk, J Skaug, M Shago, ...
The American Journal of Human Genetics 82 (2), 477-488, 2008
|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
|Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways|
L Sang, JJ Miller, KC Corbit, RH Giles, MJ Brauer, EA Otto, LM Baye, ...
Cell 145 (4), 513-528, 2011
|Peptidyl argininedeiminase 2 CpG island in multiple sclerosis white matter is hypomethylated|
FG Mastronardi, A Noor, DD Wood, T Paton, MA Moscarello
Journal of neuroscience research 85 (9), 2006-2016, 2007
|Disruption at the PTCHD1 Locus on Xp22. 11 in Autism spectrum disorder and intellectual disability|
A Noor, A Whibley, CR Marshall, PJ Gianakopoulos, A Piton, AR Carson, ...
Science translational medicine 2 (49), 49ra68-49ra68, 2010
|An X-linked myopathy with postural muscle atrophy and generalized hypertrophy, termed XMPMA, is caused by mutations in FHL1|
C Windpassinger, B Schoser, V Straub, S Hochmeister, A Noor, ...
The American Journal of Human Genetics 82 (1), 88-99, 2008
|Mutation in NSUN2, which encodes an RNA methyltransferase, causes autosomal-recessive intellectual disability|
MA Khan, MA Rafiq, A Noor, S Hussain, JV Flores, V Rupp, AK Vincent, ...
The American Journal of Human Genetics 90 (5), 856-863, 2012
|Identification of mutations in TRAPPC9, which encodes the NIK-and IKK-β-binding protein, in nonsyndromic autosomal-recessive mental retardation|
A Mir, L Kaufman, A Noor, MM Motazacker, T Jamil, M Azam, K Kahrizi, ...
The American Journal of Human Genetics 85 (6), 909-915, 2009
|Determinants of employee retention in telecom sector of Pakistan|
M Shoaib, A Noor, SR Tirmizi, S Bashir
Proceedings of the 2nd CBRC, Lahore, Pakistan 14, 1-18, 2009
|Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1|
W Xu, S Cohen-Woods, Q Chen, A Noor, J Knight, G Hosang, SV Parikh, ...
BMC medical genetics 15 (1), 2, 2014
|Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes|
AC Lionel, K Tammimies, AK Vaags, JA Rosenfeld, JW Ahn, D Merico, ...
Human molecular genetics 23 (10), 2752-2768, 2014
|CC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosa|
A Noor, C Windpassinger, M Patel, B Stachowiak, A Mikhailov, M Azam, ...
The American Journal of Human Genetics 82 (4), 1011-1018, 2008
|Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families|
R Harripaul, N Vasli, A Mikhailov, MA Rafiq, K Mittal, C Windpassinger, ...
Molecular psychiatry 23 (4), 973-984, 2018
|Mutations in the alpha 1, 2-mannosidase gene, MAN1B1, cause autosomal-recessive intellectual disability|
MA Rafiq, AW Kuss, L Puettmann, A Noor, A Ramiah, G Ali, H Hu, ...
The American Journal of Human Genetics 89 (1), 176-182, 2011
|Examining organizational citizenship behavior as the outcome of organizational commitment: a study of universities teachers of Pakistan|
Proceedings 2nd CBRC, Lahore, Pakistan, 2009
|Oligodontia is caused by mutation in LTBP3, the gene encoding latent TGF-β binding protein 3|
A Noor, C Windpassinger, I Vitcu, M Orlic, MA Rafiq, M Khalid, MN Malik, ...
The American Journal of Human Genetics 84 (4), 519-523, 2009
|Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families|
G Egger, KM Roetzer, A Noor, AC Lionel, H Mahmood, T Schwarzbraun, ...
neurogenetics 15 (2), 117-127, 2014
|Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes|
A Noor, AC Lionel, S Cohen‐Woods, N Moghimi, J Rucker, A Fennell, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 165 …, 2014
|Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome|
E Petek, T Schwarzbraun, A Noor, M Patel, K Nakabayashi, S Choufani, ...
Molecular Genetics and Genomics 277 (1), 71-81, 2007