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Human Mutation|August 31, 2002
Data mining of public SNP databases for the selection of intragenic SNPsJan Aerts, Yves Wetzels, Nadine Cohen, et al.
Molecular Medicine (Cambridge, Mass.)|November 19, 2002
Lack of plasma membrane targeting of a G172D mutant thiamine transporter derived from Rogers syndrome familyDana Baron, Yehuda G Assaraf, Nadine Cohen, et al.
Genetic Testing|June 25, 2003
Mutation analysis in congenital Long QT Syndrome--a case with missense mutations in KCNQ1 and SCN5AAimée Paulussen, Gert Matthijs, Marc Gewillig, et al.
Pharmacogenomics|December 24, 2008
Developing the evidence base for applying pharmacogenomics: proceeds from DIA Workshop IV--Breakout Session 1Martin Armstrong, Christina Bromley, Nadine Cohen, et al.
The Journal of Biological Chemistry|October 2, 2002
A novel mutation (T65P) in the PAS domain of the human potassium channel HERG results in the long QT syndrome by trafficking deficiencyAimée Paulussen, Adam Raes, Gert Matthijs, et al.
Annals of Neurology|September 5, 2002
A novel mutation in the deoxyguanosine kinase gene causing depletion of mitochondrial DNAJan-Willem Taanman, Ihab Kateeb, Ania C Muntau, et al.
Kidney International|December 11, 2002
A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromesIsrael Zelikovic, Raymonde Szargel, Ali Hawash, et al.
The Pediatric Infectious Disease Journal|December 14, 2016
Bilateral Dacryoadenitis: Don't Forget Tuberculosis!Marta Ruman-Colombier, Pierre-Alex Crisinel, Nadine Cohen-Dumani, et al.
Scientific Reports|October 30, 2013
GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locusPatrick Sleiman, Dai Wang, Joseph Glessner, et al.
Pharmacogenomics|October 24, 2014
SULT4A1 haplotype: conflicting results on its role as a biomarker of antipsychotic responseDai Wang, Qingqin Li, Reyna Favis, et al.
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