Show items per page
Elements: 51
Page 1 on 3
 TitleAuthors / EditorsDate
add to browser selection
Isolation and initial characterization of the mouse Dnmt3l gene Aapola, Ulla; Lyle, Robert; Krohn, K.; Antonarakis, Stylianos; Peterson, P. 2001
add to browser selection
Association of the connexin36 gene with juvenile myoclonic epilepsy Mas, Christophe; Taske, N.; Deutsch, Samuel; Guipponi, Michel; ... Meda, Paolo 2004
add to browser selection
Conserved noncoding sequences are selectively constrained and not mutation cold spots Drake, J. A.; Bird, Christine; Nemesh, James; Thomas, D. J.; ... Hirschhorn, J. N. 2006
add to browser selection
CNVs and genetic medicine (excitement and consequences of a rediscovery) Beckmann, J. S.; Sharp, A. J.; Antonarakis, Stylianos 2008
add to browser selection
Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations Schwabe, Georg C.; Hoffmann, Katrin; Loges, Niki Tomas; Birker, Daniel; ... Bartoloni, Lucia 2008
add to browser selection
PPARG by dietary fat interaction influences bone mass in mice and humans Ackert-Bicknell, Cheryl L.; Demissie, Serkalem; Marín de Evsikova, Caralina; Hsu, Yi-Hsiang; ... Rosen, Clifford J. 2008
add to browser selection
Glutathione S-transferase genotype increases risk of progression from bronchial hyperresponsiveness to asthma in adults Imboden, Medea; Rochat, Thierry; Brutsche, M.; Schindler, Christian; ... Probst-Hensch, Nicole M. 2008
add to browser selection
Common genetic variation and the control of HIV-1 in humans Fellay, Jacques; Ge, Dongliang 2009
add to browser selection
Tissue biomarker development in a multicentre trial context: a feasibility study on the PETACC3 stage II and III colon cancer adjuvant treatment trial Bosman, Fred T.; Yan, Pu; Tejpar, Sabine; Fiocca, Roberto; ... Roth, Arnaud 2009
add to browser selection
Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms Ibáñez, Pablo; Lesage, Suzanne; Janin, Sabine; Lohmann, Ebba; ... Brice, Alexis 2009
add to browser selection
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry Benjamin, Emelia J.; Ehret, Georg Benedikt 2009
add to browser selection
Genome-wide pharmacogenetics of antidepressant response in the GENDEP project Uher, Rudolf; Perroud, Nader Ali; Ng, Mandy Y. M.; Hauser, Joanna; ... McGuffin, Peter 2010
add to browser selection
A map of human genome variation from population-scale sequencing 1000 Genomes Project Consortium 2010
add to browser selection
Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes Strawbridge, Rona J 2011
add to browser selection
Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals Arking, Dan E; Junttila, M. Juhani; Goyette, Philippe; Huertas-Vazquez, Adriana; ... Newton-Cheh, Christopher 2011
add to browser selection
SNPs and other features as they predispose to complex disease: genome-wide predictive analysis of a quantitative phenotype for hypertension Won, Joong-Ho; Ehret, Georg Benedikt; Chakravarti, Aravinda; Olshen, Richard A 2011
add to browser selection
Epidemiology and virulence insights from MRSA and MSSA genome analysis Lazarevic, Vladimir; Beaume, Marie-Emilie; Corvaglia, Anna; Hernandez, David; ... Francois, Patrice 2011
add to browser selection
IL28B polymorphisms predict reduction of HCV RNA from the first day of therapy in chronic hepatitis C. Bochud, Pierre-Yves; Bibert, Stéphanie; Negro, Francesco; Haagmans, B; ... Lagging, M 2011
add to browser selection
Replication of association between a SCN1A splice variant and febrile seizures Le Gal, François; Trachsler-Salzmann, Annick; Crespel, Arielle; Malafosse, Alain 2011
add to browser selection
Network-guided analysis of genes with altered somatic copy number and gene expression reveals pathways commonly perturbed in metastatic melanoma Valsesia, Armand; Rimoldi, Donata; Martinet, Danielle; Ibberson, Mark; ... Stevenson, Brian J 2011
<< previous | 1 | 2 | 3 |