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
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
CNVs and genetic medicine (excitement and consequences of a rediscovery) Beckmann, J. S.; Sharp, A. J.; Antonarakis, Stylianos 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
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
Common genetic variation and the control of HIV-1 in humans Fellay, Jacques; Ge, Dongliang 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
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
add to browser selection
A two-stage meta-analysis identifies several new loci for Parkinson's disease French Parkinson's Disease Genetics Study Group 2011
add to browser selection
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies Nalls, Michael A; Plagnol, Vincent; Hernandez, Dena G; Sharma, Manu; ... Wood, Nicholas W 2011
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
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study Ross, Owen A 2011
add to browser selection
Rapid detection of genetic variants in hypertrophic cardiomyopathy by custom DNA resequencing array in clinical practice Fokstuen, Siv; Munoz, Analia; Melacini, Paola; Iliceto, Sabino; ... Blouin, Jean-Louis 2011
<< previous | 1 | 2 | 3 |