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Alcoholism, Clinical and Experimental Research|January 25, 2003
NPY Leu7Pro and alcohol dependence in Finnish and Swedish populationsGuanshan Zhu, Lotta Pollak, Salim Mottagui-Tabar, et al.
Human Genetics|July 16, 2005
Complex HTR2C linkage disequilibrium and promoter associations with body mass index and serum leptinShane McCarthy, Salim Mottagui-Tabar, Yumi Mizuno, et al.
Addiction Biology|November 5, 2025
Dysregulation of Central-Medial Amygdala Histone Modifiers in Preclinical Models of Ethanol ExposureKara A Lamb, Alexander V Margetts, Claude-Henry Volmar, et al.
BMC Medical Genetics|March 23, 2019
An immunocompetent patient with a nonsense mutation in NHEJ1 geneHossein Esmaeilzadeh, Mohammad Reza Bordbar, Zahra Hojaji, et al.
Frontiers in Molecular Neuroscience|October 21, 2015
Associating schizophrenia, long non-coding RNAs and neurostructural dynamicsVeronica Merelo, Dante Durand, Adam R Lescallette, et al.
Biochemical and Biophysical Research Communications|June 18, 2003
Effective small interfering RNAs and phosphorothioate antisense DNAs have different preferences for target sites in the luciferase mRNAsYunhe Xu, Hong-Yan Zhang, Dorit Thormeyer, et al.
Diabetes|January 30, 2004
Single nucleotide polymorphisms in the proximal promoter region of the adiponectin (APM1) gene are associated with type 2 diabetes in Swedish caucasiansHarvest F Gu, Adili Abulaiti, Claes-Göran Ostenson, et al.
Cancers|September 9, 2022
Functional Drug Screening of Small Molecule Inhibitors of Epigenetic Modifiers in Refractory AML PatientsJessica L Dennison, Hassan Al-Ali, Claude-Henry Volmar, et al.
Cell Journal|November 27, 2021
Pre-Implantation Genetic Testing for Monogenic Disorders (PGT-M) in A Family with A Novel Mutation in DPAGT1 GeneZahra Tabatabaei, K Hadijeh Karbalaie, Parham Habibzadeh, et al.
BMC Medical Genetics|July 11, 2019
A novel frame-shift deletion in FANCF gene causing autosomal recessive Fanconi anemia: a case reportSoheila Zareifar, Hassan Dastsooz, Mahdi Shahriari, et al.
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