X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (45) 45
female (36) 36
index medicus (31) 31
genetics & heredity (28) 28
male (27) 27
adult (24) 24
life sciences (18) 18
mutation (17) 17
child, preschool (16) 16
infant (16) 16
child (14) 14
pregnancy (13) 13
adolescent (12) 12
infant, newborn (11) 11
genetic aspects (10) 10
phenotype (10) 10
research (10) 10
analysis (9) 9
obstetrics & gynecology (9) 9
prenatal diagnosis (9) 9
biochemistry & molecular biology (8) 8
chromosome deletion (7) 7
epidemiology (7) 7
gene (7) 7
genetics (7) 7
in situ hybridization, fluorescence (7) 7
mutations (7) 7
pedigree (7) 7
young adult (7) 7
abnormalities, multiple - genetics (6) 6
children (6) 6
health aspects (6) 6
human health and pathology (6) 6
middle aged (6) 6
pregnant women (6) 6
risk factors (6) 6
santé publique et épidémiologie (6) 6
aged (5) 5
article (5) 5
base sequence (5) 5
comparative genomic hybridization (5) 5
diagnosis (5) 5
france (5) 5
france - epidemiology (5) 5
infectious diseases (5) 5
karyotyping (5) 5
obesity (5) 5
syndrome (5) 5
[sdv.spee]life sciences [q-bio]/santé publique et épidémiologie (4) 4
amniocentesis (4) 4
animals (4) 4
clinical neurology (4) 4
cohort studies (4) 4
expression (4) 4
family (4) 4
fetus (4) 4
genotype (4) 4
intellectual disability (4) 4
medical genetics (4) 4
mice (4) 4
neurons and cognition (4) 4
polymerase chain reaction (4) 4
prenatal-diagnosis (4) 4
retrospective studies (4) 4
sleep (4) 4
toxoplasmosis (4) 4
[ sdv.spee ] life sciences [q-bio]/santé publique et épidémiologie (3) 3
[sdv.neu]life sciences [q-bio]/neurons and cognition [q-bio.nc] (3) 3
[sdv]life sciences [q-bio] (3) 3
abnormalities (3) 3
abnormalities, multiple - diagnosis (3) 3
abnormalities, multiple - diagnostic imaging (3) 3
child development (3) 3
chromosomes (3) 3
chromosomes, human, x (3) 3
ciliopathy (3) 3
clinical genetics (3) 3
codon, nonsense (3) 3
consanguinity (3) 3
cytogenetics (3) 3
deletion (3) 3
duration (3) 3
epilepsy (3) 3
gene duplication (3) 3
gene mutations (3) 3
genes (3) 3
genetic association studies (3) 3
genetic counseling (3) 3
genetic disorders (3) 3
genetic linkage (3) 3
growth (3) 3
growth disorders - genetics (3) 3
guidelines (3) 3
haploinsufficiency (3) 3
heterozygote (3) 3
individuals (3) 3
intellectual disability - genetics (3) 3
interstitial deletion (3) 3
medical education (3) 3
mesh : humans (3) 3
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The Journal of Infectious Diseases, ISSN 0022-1899, 4/2009, Volume 199, Issue 8, pp. 1155 - 1167
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 11/2014, Volume 51, Issue 11, pp. 724 - 736
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
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 02/2009, Volume 106, Issue 6, pp. 1820 - 1825
Journal Article
Genetics in Medicine, ISSN 1098-3600, 07/2018, Volume 20, Issue 7, pp. 745 - 753
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 06/2016, Volume 24, Issue 6, pp. 844 - 851
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 2012, Volume 158A, Issue 7, pp. 1633 - 1640
Journal Article