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	Title	Authors / Editors	Date
unige:136251	A Maternally Deposited Endosperm Cuticle Contributes to the Physiological Defects of transparent testa Seeds	Loubery, Sylvain Philippe; De Giorgi, Julien; Utz-Pugin, Anne; Demonsais, Lara; Lopez Molina, Luis	2018
unige:86827	Sequential transcriptional waves direct the differentiation of newborn neurons in the mouse neocortex	Telley, Ludovic; Govindan, Subashika; Prados, Julien; Stevant, Isabelle; ... Jabaudon, Denis	2016
unige:89750	Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration	van der Zee, Julie	2014
unige:74864	Identification of genes preventing transgenerational transmission of stress-induced epigenetic states	Iwasaki, Mayumi; Paszkowski, Jerzy	2014
unige:32604	DNA binding of the cell cycle transcriptional regulator GcrA depends on N6-adenosine methylation in Caulobacter crescentus and other Alphaproteobacteria	Fioravanti, Antonella; Fumeaux, Coralie; Mohapatra, Saswat S; Bompard, Coralie; ... Biondi, Emanuele G	2013
unige:90324	Phenotypes in Swiss patients with familial ALS carrying TARDBP mutations	Czell, D; Andersen, P M; Morita, M; Neuwirth, C; ... Weber, M	2013
unige:42923	Transcription factor occupancy can mediate active turnover of DNA methylation at regulatory regions	Feldmann, Angelika; Ivanek, Robert; Murr, Rabih; Gaidatzis, Dimos; ... Schübeler, Dirk	2013
unige:32198	Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis	Paternoster, Lavinia; Standl, Marie	2012
unige:32871	Screening of the THAP1 gene in patients with early-onset dystonia: myoclonic jerks are part of the dystonia 6 phenotype	Clot, Fabienne; Grabli, David; Burbaud, Pierre; Aya, Magali; ... Brice, Alexis	2011
unige:138403	Perturbations in ataxia telangiectasia mutant signaling pathways after drug-induced acute liver failure and their reversal during rescue of animals by cell therapy	Bandi, Sriram; Joseph, Brigid; Berishvili Berney, Ekaterine; Singhania, Rohit; ... Gupta, Sanjeev	2011
unige:25875	PAX5 mutations occur frequently in adult B-cell progenitor acute lymphoblastic leukemia and PAX5 haploinsufficiency is associated with BCR-ABL1 and TCF3-PBX1 fusion genes: a GRAALL study	Familiades, J; Bousquet, M; Lafage-Pochitaloff, M; Béné, M-C; ... Delabesse, E	2009
unige:4600	Transcriptome analysis of the responses of Staphylococcus aureus to antimicrobial peptides and characterization of the roles of vraDE and vraSR in antimicrobial resistance	Pietiäinen, Milla; Francois, Patrice; Hyyryläinen, Hanne-Leena; Tangomo, Manuela; ... Kontinen, Vesa P.	2009
unige:2185	A pure population of ectodermal cells derived from human embryonic stem cells	Aberdam, Edith; Barak, Efrat; Rouleau, Matthieu; de LaForest, Stephanie; ... Aberdam, Daniel	2008
unige:866	Detection of ATM gene deletion/duplication by multiplex ligation-dependant probe amplification in childhood lymphoid malignancies: a report from the Children's Oncology Group	Gumy Pause, Fabienne; Ozsahin, Ayse Hulya; Khoshbeen-Boudal, Mary; Betts, David R.; ... Sappino, Pascal	2008
unige:1712	International Lung Cancer Consortium: pooled analysis of sequence variants in DNA repair and cell cycle pathways	International Lung Cancer Consortium	2008
unige:9171	A whole-genome association study of major determinants for host control of HIV-1	Fellay, Jacques; Shianna, K. V.; Ge, Dongliang; Colombo, Sara; ... Goldstein, D. B.	2007
unige:43624	PR-Set7-dependent lysine methylation ensures genome replication and stability through S phase	Tardat, Mathieu; Murr, Rabih; Herceg, Zdenko; Sardet, Claude; Julien, Eric	2007
unige:148713	Evolutionary appearance of mononucleotide repeats in the coding sequences of four genes in primates	Giacobino, Ariane; Chaillet, John Richard	2007
unige:73117	ATM alterations in childhood non-Hodgkin lymphoma	Gumy Pause, Fabienne; Wacker, Pierre; Maillet, Philippe; Betts, David R; Sappino, Pascal	2006
unige:73118	ATM promoter analysis in childhood lymphoid malignancies: a brief communication	Gumy Pause, Fabienne; Wacker, Pierre; Maillet, Philippe; Betts, David R; Sappino, Pascal	2006

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