Abdul Noor - Concepedia

Author

Abdul Noor

Also Known As

A Noor, A. Noor, A. R. Noor, A.R. NOOR, A.R. Noor, Abdul Noor, Abdul R Noor, Abdul Rahman Noor, Aimen Noor, Chantal Morel

Publications

Citations

H-Index

Concepts

All Affiliations

University of Toronto Hospital for Sick Children Centre for Addiction and Mental Health SickKids Foundation Mount Sinai Hospital

About

Abdul Noor is an author at University of Toronto specializing in medicine, genetics, and autism.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	16	3.9K
2	Social Sciences	3	3	307
3	Education	2	2	32
4	Allied Health Professions	2	2	32
5	Nursing	1	1	16

Abdul Noor

Publications

7.6K

Citations

H-Index

Page 1

	Year	Citations
Functional impact of global rare copy number variation in autism spectrum disorders Dalila Pinto, Alistair T. Pagnamenta, Lambertus Klei, Nature Autism Spectrum DisordersSyndromic AutismGeneticsPsychiatric GeneticsAutism	2010	2K
Structural Variation of Chromosomes in Autism Spectrum Disorder Christian R. Marshall, Abdul Noor, John B. Vincent, The American Journal of Human Genetics ChromatinStructural VariationSyndromic AutismGeneticsMolecular Biology	2008	1.8K
Mapping the NPHP-JBTS-MKS Protein Network Reveals Ciliopathy Disease Genes and Pathways Liyun Sang, Julie J. Miller, Kevin C. Corbit, Cell Molecular NeuroscienceDisease MechanismGliomaMolecular BiologyComplex Disease	2011	617
A genome-wide scan for common alleles affecting risk for autism Richard Anney, Lambertus Klei, Dalila Pinto, Human Molecular Genetics	2010	585
Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability Muzammil Ahmad Khan, Muhammad Rafiq, Abdul Noor, The American Journal of Human Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsFragile X Spectrum	2012	228
Peptidyl argininedeiminase 2 CpG island in multiple sclerosis white matter is hypomethylated Fabrizio G. Mastronardi, Abdul Noor, D. D. Wood, Journal of Neuroscience Research	2007	202
Disruption at the <i>PTCHD1</i> Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability Abdul Noor, Annabel Whibley, Christian R. Marshall, Science Translational Medicine GeneticsMolecular GeneticsDisease Gene IdentificationSocial SciencesAutism Spectrum Disorder	2010	194
Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families Ricardo Harripaul, Nasim Vasli, Muhammad Rafiq, Molecular Psychiatry Mendelian DisorderNovel Candidate GenesGenetic DisorderGeneticsConsanguineous Families	2017	177
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes A. C. Lionel, Kristiina Tammimies, Andrea K. Vaags, Human Molecular Genetics Astn2/trim32 LocusBrain DevelopmentAutism Spectrum DisordersGeneticsMolecular Biology	2013	172
An X-Linked Myopathy with Postural Muscle Atrophy and Generalized Hypertrophy, Termed XMPMA, Is Caused by Mutations in FHL1 Christian Windpassinger, Benedikt Schoser, Volker Straub, The American Journal of Human Genetics Mitochondrial MyopathyMechanobiologyMuscle PathologyKinesiologyMendelian Disorder	2008	156

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