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International Journal of Molecular Sciences|March 13, 2024
Mowat-Wilson Syndrome: Case Report and Review of ZEB2 Gene Variant Types, Protein Defects and Molecular InteractionsCaroline St Peter, Waheeda A Hossain, Scott Lovell, et al.American Journal of Medical Genetics. Part A|January 20, 2007
Whole genome microarray analysis of gene expression in Prader-Willi syndromeDouglas C Bittel, Nataliya Kibiryeva, Susan M Sell, et al.International Journal of Molecular Sciences|January 10, 2015
Whole exome sequencing in females with autism implicates novel and candidate genesMerlin G Butler, Syed K Rafi, Waheeda Hossain, et al.British Journal of Haematology|October 27, 2007
Monoclonal B-cell lymphocytosis in blood donorsJane M Rachel, Marjorie L Zucker, Christopher M Fox, et al.Lipids in Health and Disease|March 18, 2011
Metabolic syndrome in South Asian immigrants: more than low HDL requiring aggressive managementSunita Dodani, Rebecca Henkhaus, Jo Wick, et al.Frontiers in Genetics|February 4, 2020
Sex-Dimorphic Interactions of MAOA Genotype and Child Maltreatment Predispose College Students to Polysubstance UsePaula J Fite, Shaquanna Brown, Waheeda A Hossain, et al.Journal of Signal Processing Systems|February 7, 2017
A Comparison of Fuzzy Clustering Approaches for Quantification of Microarray Gene ExpressionYu-Ping Wang, Maheswar Gunampally, Jie Chen, et al.Surgery for Obesity and Related Diseases : Official Journal of the American Society for Bariatric Surgery|October 4, 2015
Laparoscopic sleeve gastrectomy in children and adolescents with Prader-Willi syndrome: a matched-control studyAayed R Alqahtani, Mohamed O Elahmedi, Awadh R Al Qahtani, et al.Journal of Pediatric Genetics|October 24, 2014
20q13.2-q13.33 deletion syndrome: A case reportMerlin G Butler, Kelly M Usrey, Jennifer L Roberts, et al.Drug and Alcohol Dependence|September 3, 2013
Double-blind, randomized placebo-controlled clinical trial of benfotiamine for severe alcohol dependenceAnn M Manzardo, Jianghua He, Albert Poje, et al.Pageof 25