X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (12) 12
index medicus (12) 12
mutation (10) 10
female (7) 7
male (7) 7
genomics (6) 6
article (5) 5
genes (5) 5
genetics & heredity (5) 5
life sciences (5) 5
adolescent (4) 4
adult (4) 4
analysis (4) 4
case-control studies (4) 4
child (4) 4
gene expression (4) 4
genetic variation (4) 4
genetics (4) 4
genome, human (4) 4
genome-wide association study (4) 4
genomes (4) 4
genotype (4) 4
polymorphism, single nucleotide (4) 4
schizophrenia (4) 4
studies (4) 4
association (3) 3
dna methylation (3) 3
family (3) 3
gene dosage - genetics (3) 3
genetic aspects (3) 3
human health and pathology (3) 3
mental disorders (3) 3
research (3) 3
[ sdv.mhep.psm ] life sciences [q-bio]/human health and pathology/psychiatrics and mental health (2) 2
abridged index medicus (2) 2
aging (2) 2
animals (2) 2
autism (2) 2
body mass index (2) 2
child, preschool (2) 2
children (2) 2
chromosome deletion (2) 2
chromosome mapping (2) 2
chromosomes (2) 2
chromosomes, human, pair 16 - genetics (2) 2
circular binary segmentation (2) 2
cognition disorders (2) 2
cognitive science (2) 2
cohort studies (2) 2
comparative genomic hybridization (2) 2
copy number (2) 2
copy number variation (2) 2
deletion (2) 2
deoxyribonucleic acid--dna (2) 2
europe (2) 2
gene dosage (2) 2
genetic association studies (2) 2
genetic predisposition to disease - genetics (2) 2
genotype & phenotype (2) 2
heterozygote (2) 2
infant (2) 2
infant, newborn (2) 2
linkage disequilibrium (2) 2
mental disorders - genetics (2) 2
mental-retardation (2) 2
mesh : humans (2) 2
mesh : schizophrenia (2) 2
microdeletion (2) 2
microsatellite (2) 2
missing heritability (2) 2
monkeys & apes (2) 2
multidisciplinary sciences (2) 2
mutation - genetics (2) 2
mutations (2) 2
obesity (2) 2
obesity - genetics (2) 2
psychiatrics and mental health (2) 2
public health (2) 2
quantitative trait loci (2) 2
reproducibility of results (2) 2
schizophrenia - genetics (2) 2
tandem repeat sequences (2) 2
young adult (2) 2
22q11 (1) 1
5' untranslated regions (1) 1
[ scco ] cognitive science (1) 1
[ scco.neur ] cognitive science/neuroscience (1) 1
[ sdv ] life sciences [q-bio] (1) 1
[ sdv.bdd ] life sciences [q-bio]/development biology (1) 1
[ sdv.gen ] life sciences [q-bio]/genetics (1) 1
[scco.neur]cognitive science/neuroscience (1) 1
[sdv.bdd]life sciences [q-bio]/development biology (1) 1
[sdv.gen]life sciences [q-bio]/genetics (1) 1
[sdv.mhep.psm]life sciences [q-bio]/human health and pathology/psychiatrics and mental health (1) 1
[shs.archeo]humanities and social sciences/archaeology and prehistory (1) 1
age of onset (1) 1
aged (1) 1
alleles (1) 1
alzheimer disease (1) 1
alzheimer disease - genetics (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Developmental Neurobiology, ISSN 1932-8451, 02/2014, Volume 74, Issue 2, pp. 113 - 122
Journal Article
by Jacquemont, S and Reymond, A and Zufferey, F and Harewood, L and Walters, R.G and Kutalik, Z and Martinet, D and Shen, Y and Valsesia, A and Beckmann, N.D and Thorleifsson, G and Belfiore, M and Bouquillon, S and Campion, D and Leeuw, N. de and Vries, L.B.A. de and Esko, T and Fernandez, B.A and Fernandez-Aranda, F and Fernandez-Real, J.M and Gratacos, M and Guilmatre, A and Hoyer, J and Jarvelin, M.R and Kooy, R.F and Kurg, A and Caignec, C. Le and Mannik, K and Platt, O.S and Sanlaville, D and Haelst, M.M. van and Villatoro Gomez, S and Walha, F and Wu, B.L and Yu, Y and Aboura, A and Addor, M.C and Alembik, Y and Antonarakis, S.E and Arveiler, B and Barth, M and Bednarek, N and Bena, F and Bergmann, S and Beri, M and Bernardini, L and Blaumeiser, B and Bonneau, D and Bottani, A and Boute, O and Brunner, H.G and Cailley, D and Callier, P and Chiesa, J and Chrast, J and Coin, L and Coutton, C and Cuisset, J.M and Cuvellier, J.C and David, A and Freminville, B. de and Delobel, B and Delrue, M.A and Demeer, B and Descamps, D and Didelot, G and Dieterich, K and Disciglio, V and Doco-Fenzy, M and nat, S and Duban-Bedu, B and Dubourg, C and El-Sayed Moustafa, J.S and Elliott, P and Faas, B.H.W and Faivre, L and Faudet, A and Fellmann, F and Ferrarini, A and Fisher, R and Flori, E and Forer, L and Gaillard, D and Gerard, M and Gieger, C and Gimelli, S and Gimelli, G and Grabe, H.J and Guichet, A and Guillin, O and Hartikainen, A.L and Heron, D and Hippolyte, L and Holder, M and Homuth, G and Isidor, B and Jaillard, S and Jaros, Z and Jimenez-Murcia, S and Helas, G.J and ...
Nature, ISSN 0028-0836, 2011, Volume 478, Issue 7367, pp. 97 - 102
Both obesity and being underweight have been associated with increased mortality. Underweight, defined as a body mass index (BMI) DEPENDENT PROBE AMPLIFICATION | FAILURE-TO-THRIVE | METABOLIC SYNDROME | RELATIVE QUANTIFICATION | SNP GENOTYPING DATA | HIDDEN-MARKOV MODEL | MULTIDISCIPLINARY SCIENCES | BODY-MASS INDEX | TIME QUANTITATIVE PCR | COPY NUMBER VARIATION | CIRCULAR BINARY SEGMENTATION | Humans | Middle Aged | Child, Preschool | RNA, Messenger - analysis | Head - anatomy & histology | Infant | Male | Developmental Disabilities - genetics | Gene Expression Profiling | North America | Obesity - genetics | Case-Control Studies | Young Adult | Mental Disorders - genetics | Aging | Gene Duplication - genetics | Adult | Female | Transcription, Genetic | Energy Metabolism - genetics | Child | Infant, Newborn | Chromosomes, Human, Pair 16 - genetics | Body Mass Index | Gene Dosage - genetics | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Europe | RNA, Messenger - genetics | Mutation - genetics | Body Height - genetics | Thinness - genetics | Phenotype | Comparative Genomic Hybridization | Adolescent | Heterozygote | Aged | Cohort Studies | Sequence Deletion - genetics | Obesity | Chromosome mapping | Usage | Genetic variation | Genetic aspects | Cognition disorders | Research | Risk factors | Schizophrenia | Gender | Behavior | Gene expression | Bias | Life Sciences | Human health and pathology | Genetics | Endocrinology and metabolism | Gene Duplication | Developmental Disabilities | Sequence Deletion | Thinness | genetics | Genetic Predisposition to Disease | Head | Gene Dosage | analysis | Energy Metabolism | Mental Disorders | Chromosomes, Human, Pair 16 | Body Height | Mutation | anatomy & histology | RNA, Messenger
Journal Article
Nucleic Acids Research, ISSN 0305-1048, 05/2016, Volume 44, Issue 8, pp. 3750 - 3762
Despite representing an important source of genetic variation, tandem repeats (TRs) remain poorly studied due to technical difficulties. We hypothesized that... 
NUCLEOTIDE | MICROSATELLITE | LANDSCAPE | BIOCHEMISTRY & MOLECULAR BIOLOGY | COPY NUMBER | MUTATION | ASSOCIATION | Promoter Regions, Genetic | DNA Methylation | Humans | Gene Expression Regulation | Polymorphism, Single Nucleotide | Tandem Repeat Sequences | Genotyping Techniques | Quantitative Trait Loci | Sequence Analysis, DNA | Linkage Disequilibrium | Genomics
Journal Article
by Walters, R.G and Jacquemont, S and Valsesia, A and De Smith, A.J and Martinet, D and Andersson, J and Falchi, M and Chen, F and Andrieux, J and Lobbens, S and Delobel, B and Stutzmann, F and El-Sayed Moustafa, J.S and Chèvre, J.-C and Lecoeur, C and Vatin, V and Bouquillon, S and Buxton, J.L and Boute, O and Holder-Espinasse, M and Cuisset, J.-M and Lemaitre, M.-P and Ambresin, A.-E and Brioschi, A and Gaillard, M and Giusti, V and Fellmann, F and Ferrarini, A and Hadjikhani, N and Campion, D and Guilmatre, A and Goldenberg, A and Calmels, N and Mandel, J.-L and Le Caignec, C and David, A and Isidor, B and Cordier, M.-P and Dupuis-Girod, S and Labalme, A and Sanlaville, D and Béri-Dexheimer, M and Jonveaux, P and Leheup, B and Õunap, K and Bochukova, E.G and Henning, E and Keogh, J and Ellis, R.J and MacDermot, K.D and Van Haelst, M.M and Vincent-Delorme, C and Plessis, G and Touraine, R and Philippe, A and Malan, V and Mathieu-Dramard, M and Chiesa, J and Blaumeiser, B and Kooy, R.F and Caiazzo, R and Pigeyre, M and Balkau, B and Sladek, R and Bergmann, S and Mooser, V and Waterworth, D and Reymond, A and Vollenweider, P and Waeber, G and Kurg, A and Palta, P and Esko, T and Metspalu, A and Nelis, M and Elliott, P and Hartikainen, A.-L and McCarthy, M.I and Peltonen, L and Carlsson, L and Jacobson, P and Sjöström, L and Huang, N and Hurles, M.E and O'Rahilly, S and Farooqi, I.S and Männik, K and Jarvelin, M.-R and Pattou, F and Meyre, D and Walley, A.J and Coin, L.J.M and Blakemore, A.I.F and Froguel, P and Beckmann, J.S and Sahlgrenska akademin and Institute of Medicine, Department of Molecular and Clinical Medicine and Institutionen för medicin, avdelningen för molekylär och klinisk medicin and Göteborgs universitet and Gothenburg University and Sahlgrenska Academy
Nature, ISSN 0028-0836, 02/2010, Volume 463, Issue 7281, pp. 671 - 675
Journal Article