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International Journal of Cancer|April 21, 2015
Integrated pathway and epistasis analysis reveals interactive effect of genetic variants at TERF1 and AFAP1L2 loci on melanoma riskMyriam Brossard, Shenying Fang, Amaury Vaysse, et al.
Thorax|October 5, 2018
Interactive effect between ATPase-related genes and early-life tobacco smoke exposure on bronchial hyper-responsiveness detected in asthma-ascertained familiesMarie-Hélène Dizier, Patricia Margaritte-Jeannin, Lucile Pain, et al.
European Journal of Human Genetics : EJHG|March 14, 2003
Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1Saber Masmoudi, Abdelaziz Tlili, Marja Majava, et al.
Mechanisms of Ageing and Development|July 12, 2011
A genome-wide association study confirms APOE as the major gene influencing survival in long-lived individualsAlmut Nebel, Rabea Kleindorp, Amke Caliebe, et al.
The European Respiratory Journal|January 23, 2016
Interaction between the DNAH9 gene and early smoke exposure in bronchial hyperresponsivenessMarie-Hélène Dizier, Rachel Nadif, Patricia Margaritte-Jeannin, et al.
Oncotarget|June 5, 2018
Aberration hubs in protein interaction networks highlight actionable targets in cancerMehran Karimzadeh, Pouria Jandaghi, Andreas I Papadakis, et al.
The Journal of Infectious Diseases|December 8, 2017
Genetic Susceptibility to Postdiarrheal Hemolytic-Uremic Syndrome After Shiga Toxin-Producing Escherichia coli Infection: A Centers for Disease Control and Prevention FoodNet StudyAsha R Kallianpur, Yuki Bradford, Rajal K Mody, et al.
The Journal of Allergy and Clinical Immunology|July 17, 2012
Patients with cystic fibrosis have inducible IL-17+IL-22+ memory cells in lung draining lymph nodesYvonne R Chan, Kong Chen, Steven R Duncan, et al.
Nature Genetics|June 29, 2006
Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathySedigheh Delmaghani, Francisco J del Castillo, Vincent Michel, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 25, 2002
Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22Ingrid Zwaenepoel, Mirna Mustapha, Michel Leibovici, et al.
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