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American Journal of Human Genetics|May 1, 2012
Mutation in NSUN2, which encodes an RNA methyltransferase, causes autosomal-recessive intellectual disabilityMuzammil Ahmad Khan, Muhammad Arshad Rafiq, Abdul Noor, et al.Nature Medicine|April 18, 1998
Estrogen reduces neuronal generation of Alzheimer beta-amyloid peptidesH Xu, G K Gouras, J P Greenfield, et al.American Journal of Human Genetics|December 17, 2009
Identification of mutations in TRAPPC9, which encodes the NIK- and IKK-beta-binding protein, in nonsyndromic autosomal-recessive mental retardationAsif Mir, Liana Kaufman, Abdul Noor, et al.Journal of Psychiatric Research|April 29, 2015
A genome-wide association study of suicide severity scores in bipolar disorderClement C Zai, Vanessa F Gonçalves, Arun K Tiwari, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 5, 2014
Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genesAbdul Noor, Anath C Lionel, Sarah Cohen-Woods, et al.Ecology|July 19, 2026
Historical vertebrate herbivory drives ontogenetic shifts in plant defense across oceanic islandsXoaquín Moreira, Luis Abdala-Roberts, Cláudia Baider, et al.Cephalalgia : an International Journal of Headache|May 24, 2015
Improving the detection of chronic migraine: Development and validation of Identify Chronic Migraine (ID-CM)Richard B Lipton, Daniel Serrano, Dawn C Buse, et al.American Journal of Medical Genetics|December 20, 2000
Long repeat tracts at SCA8 in major psychosisJ B Vincent, Q P Yuan, M Schalling, et al.Human Molecular Genetics|June 13, 2018
Biallelic missense variants in ZBTB11 can cause intellectual disability in humansZohreh Fattahi, Taimoor I Sheikh, Luciana Musante, et al.The Journal of Allergy and Clinical Immunology|April 4, 2016
DNA methylation within melatonin receptor 1A (MTNR1A) mediates paternally transmitted genetic variant effect on asthma plus rhinitisChloé Sarnowski, Catherine Laprise, Giovanni Malerba, et al.Pageof 56