Articles

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (325) 325
Newspaper Article (309) 309
Publication (51) 51
Book / eBook (27) 27
Book Review (14) 14
Conference Proceeding (5) 5
Magazine Article (4) 4
Book Chapter (3) 3
Trade Publication Article (2) 2
Dissertation (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (179) 179
humans (168) 168
female (99) 99
male (93) 93
genetics & heredity (72) 72
middle aged (62) 62
dk/atira/pure/researchoutput/pubmedpublicationtype/d016428 (59) 59
journal article (59) 59
polymorphism, single nucleotide (56) 56
genetics (53) 53
aged (47) 47
genotype (47) 47
research (46) 46
genome-wide association (45) 45
genome-wide association study (44) 44
article (40) 40
genetic aspects (40) 40
genomes (40) 40
epidemiology (39) 39
analysis (37) 37
dna methylation (37) 37
risk factors (37) 37
adult (36) 36
risk (33) 33
phenotype (31) 31
studies (31) 31
child (30) 30
cohort studies (30) 30
genomics (29) 29
association (28) 28
dk/atira/pure/researchoutput/pubmedpublicationtype/d013485 (28) 28
mendelian randomization (28) 28
research support, non-u.s. gov't (28) 28
cardiovascular disease (27) 27
genes (27) 27
medicine (27) 27
multidisciplinary sciences (27) 27
biochemistry & molecular biology (26) 26
genetic variation (26) 26
health aspects (26) 26
metaanalysis (26) 26
obesity (26) 26
body mass index (25) 25
disease (25) 25
longitudinal studies (25) 25
adolescent (24) 24
loci (24) 24
medical and health sciences (24) 24
medicin och hälsovetenskap (24) 24
polymorphism, single nucleotide - genetics (24) 24
mutation (23) 23
cardiovascular diseases (22) 22
children (22) 22
gene expression (22) 22
alleles (21) 21
biotechnology & applied microbiology (19) 19
genotype & phenotype (19) 19
haplotypes (19) 19
gene frequency (18) 18
genetic predisposition to disease (18) 18
meta-analysis (18) 18
prospective studies (18) 18
public, environmental & occupational health (18) 18
abridged index medicus (17) 17
alspac (17) 17
variants (17) 17
blood-pressure (16) 16
expression (16) 16
genetic research (16) 16
population (16) 16
pregnancy (16) 16
research article (16) 16
software (16) 16
united kingdom (16) 16
bioinformatics (15) 15
common variants (15) 15
diabetes (15) 15
genome, human (15) 15
heart (15) 15
infant, newborn (15) 15
linkage disequilibrium (15) 15
methylation (15) 15
biochemical research methods (14) 14
biology (14) 14
deoxyribonucleic acid--dna (14) 14
dk/atira/pure/researchoutput/pubmedpublicationtype/d052061 (14) 14
genetic association studies (14) 14
genetic loci (14) 14
medical genetics (14) 14
quantitative trait loci (14) 14
research support, n.i.h., extramural (14) 14
usage (14) 14
blood pressure (13) 13
cardiovascular diseases - genetics (13) 13
coronary-heart-disease (13) 13
lipids (13) 13
medical research (13) 13
medicinsk genetik (13) 13
proteins (13) 13
science (13) 13
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (18) 18
UTL at Downsview - May be requested (6) 6
UofT at Mississauga - Stacks (4) 4
Royal Ontario Museum - Stacks (3) 3
Earth Sciences (Noranda) - Stacks (2) 2
St. Michael's College (John M. Kelly) - 2nd Floor (2) 2
UofT at Scarborough - Stacks (2) 2
Victoria University E.J. Pratt - Stacks (2) 2
Collection Dvlpm't (Acquisitions) - Closed Orders (1) 1
Collection Dvlpm't (Acquisitions) - Vendor file (1) 1
Gerstein Science - Stacks (1) 1
Institute for Christian Studies - Stacks (1) 1
Online Resources - Online (1) 1
Royal Ontario Museum - Reference (1) 1
Trinity College (John W Graham) - Oversize (1) 1
Trinity College (John W Graham) - Stacks (1) 1
Trinity College (John W Graham) - Storage (1) 1
UofT at Scarborough - Withdrawn (1) 1
Victoria University CRRS - Library use only (1) 1
Victoria University E.J. Pratt - Reference (1) 1
Victoria University E.J. Pratt - Storage (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data
by Holmes, Michael V and Dale, Caroline E and Zuccolo, Luisa and Silverwood, Richard J and Guo, Yiran and Ye, Zheng and Prieto-Merino, David and Dehghan, Abbas and Trompet, Stella and Wong, Andrew and Cavadino, Alana and Drogan, Dagmar and Padmanabhan, Sandosh and Li, Shanshan and Yesupriya, Ajay and Leusink, Maarten and Sundstrom, Johan and Hubacek, Jaroslav A and Pikhart, Hynek and Swerdlow, Daniel I and Panayiotou, Andrie G and Borinskaya, Svetlana A and Finan, Chris and Shah, Sonia and Kuchenbaecker, Karoline B and Shah, Tina and Engmann, Jorgen and Folkersen, Lasse and Eriksson, Per and Ricceri, Fulvio and Melander, Olle and Sacerdote, Carlotta and Gamble, Dale M and Rayaprolu, Sruti and Ross, Owen A and McLachlan, Stela and Vikhireva, Olga and Sluijs, Ivonne and Scott, Robert A and Adamkova, Vera and Flicker, Leon and Bockxmeer, Frank M van and Power, Christine and Marques-Vidal, Pedro and Meade, Tom and Marmot, Michael G and Ferro, Jose M and Paulos-Pinheiro, Sofia and Humphries, Steve E and Talmud, Philippa J and Leach, Irene Mateo and Verweij, Niek and Linneberg, Allan and Skaaby, Tea and Doevendans, Pieter A and Cramer, Maarten J and Harst, Pim van der and Klungel, Olaf H and Dowling, Nicole F and Dominiczak, Anna F and Kumari, Meena and Nicolaides, Andrew N and Weikert, Cornelia and Boeing, Heiner and Ebrahim, Shah and Gaunt, Tom R and Price, Jackie F and Lannfelt, Lars and Peasey, Anne and Kubinova, Ruzena and Pajak, Andrzej and Malyutina, Sofia and Voevoda, Mikhail I and Tamosiunas, Abdonas and Maitland-van der Zee, Anke H and Norman, Paul E and Hankey, Graeme J and Bergmann, Manuela M and Hofman, Albert and Franco, Oscar H and Cooper, Jackie and Palmen, Jutta and Spiering, Wilko and Jong, Pim A de and Kuh, Diana and Hardy, Rebecca and Uitterlinden, Andre G and Ikram, M Arfan and Ford, Ian and Hyppönen, Elina and Almeida, Osvaldo P and Wareham, Nicholas J and Khaw, Kay-Tee and Hamsten, Anders and Husemoen, Lise Lotte N and Tjønneland, Anne and Tolstrup, Janne S and Rimm, Eric and Beulens, Joline W J and Verschuren, W M Monique and ... and InterAct Consortium and IMPROVE Study Grp and on behalf of The InterAct Consortium and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Kardiologi and Medicinska och farmaceutiska vetenskapsområdet, centrumbildningar mm and Geriatrik and Uppsala universitet and Institutionen för medicinska vetenskaper and Institutionen för folkhälso- och vårdvetenskap and Uppsala kliniska forskningscentrum (UCR)
BMJ : British Medical Journal, ISSN 0959-8138, 7/2014, Volume 349, Issue jul10 6, pp. g4164 - g4164
Objective To use the rs1229984 variant in the alcohol dehydrogenase 1B gene (ADH1B) as an instrument to investigate the causal role of alcohol in... 
RESEARCH | MORTALITY | MEDICINE, GENERAL & INTERNAL | DESIGN | RISK-FACTORS | METAANALYSIS | VARIANTS | HEALTH | CORONARY-HEART-DISEASE | CONSUMPTION | DEHYDROGENASE | DEPENDENCE | Coronary Disease - blood | Humans | Middle Aged | Coronary Disease - etiology | Genotype | Male | Biomarkers - blood | Genetic Markers | Models, Statistical | Alcohol Drinking - adverse effects | Alcohol Drinking - genetics | Stroke - genetics | Stroke - blood | Stroke - etiology | Coronary Disease - genetics | Alcohol Dehydrogenase - genetics | Mendelian Randomization Analysis | Adult | Female | Aged | Polymorphism, Single Nucleotide | Index Medicus | Abridged Index Medicus | Other Medical Sciences | Medical and Health Sciences | Medicin och hälsovetenskap | Annan medicin och hälsovetenskap
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text Gene-centric Meta-analysis in 87,736 Individuals of European Ancestry Identifies Multiple Blood-Pressure-Related Loci
by Tragante, Vinicius and Barnes, Michael R and Ganesh, Santhi K and Lanktree, Matthew B and Guo, Xiuqing and Guo, Wei and Franceschini, Nora and Smith, Erin N and Johnson, Andrew D and Johnson, Julie A and Johnson, Toby and Holmes, Michael V and Padmanabhan, Sandosh and Karczewski, Konrad J and Almoguera, Berta and Barnard, John and Baumert, Jens and Chang, Yen-Pei Christy and Elbers, Clara C and Farrall, Martin and Fischer, Mary E and Gaunt, Tom R and Gho, Johannes M.I.H and Gieger, Christian and Goel, Anuj and Gong, Yan and Isaacs, Aaron and Kleber, Marcus E and Leach, Irene Mateo and McDonough, Caitrin W and Meijs, Matthijs F.L and Melander, Olle and Nelson, Christopher P and Nolte, Ilja M and Pankratz, Nathan and Price, Tom S and Shaffer, Jonathan and Shah, Sonia and Tomaszewski, Maciej and van der Most, Peter J and Van Iperen, Erik P.A and Vonk, Judith M and Witkowska, Kate and Wong, Caroline O.L and Zhang, Li and Beitelshees, Amber L and Berenson, Gerald S and Bhatt, Deepak L and Brown, Morris and Burt, Amber and Cooper-DeHoff, Rhonda M and Connell, John M and Cruickshanks, Karen J and Curtis, Sean P and Davey-Smith, George and Delles, Christian and Gansevoort, Ron T and Haiqing, Shen and Hastie, Claire E and Hofker, Marten H and Hovingh, G. Kees and Kim, Daniel S and Kirkland, Susan A and Klein, Barbara E and Klein, Ronald and Li, Yun R and Maiwald, Steffi and Newton-Cheh, Christopher and O’Brien, Eoin T and Onland-Moret, N. Charlotte and Palmas, Walter and Parsa, Afshin and Penninx, Brenda W and Pettinger, Mary and Vasan, Ramachandran S and Ranchalis, Jane E and M Ridker, Paul and Rose, Lynda M and Sever, Peter and Shimbo, Daichi and Steele, Laura and Stolk, Ronald P and Thorand, Barbara and Trip, Mieke D and van Duijn, Cornelia M and Verschuren, W. Monique and Wijmenga, Cisca and Wyatt, Sharon and Young, J. Hunter and Zwinderman, Aeilko H and Bezzina, Connie R and Boerwinkle, Eric and Casas, Juan P and Caulfield, Mark J and Chakravarti, Aravinda and Chasman, Daniel I and Davidson, Karina W and Doevendans, Pieter A and Dominiczak, Anna F and FitzGerald, Garret A and ... and Kardiovaskulär forskning - hypertoni and Cardiovascular Research - Hypertension and EpiHealth: Epidemiology for Health and Lund University and Lunds universitet and EXODIAB: Excellence in Diabetes Research in Sweden
The American Journal of Human Genetics, ISSN 0002-9297, 03/2014, Volume 94, Issue 3, pp. 349 - 360
Blood pressure (BP) is a heritable risk factor for cardiovascular disease. To investigate genetic associations with systolic BP (SBP), diastolic BP (DBP), mean... 
COMMON VARIANTS | CANDIDATE GENES | DRUG DISCOVERY | GENETICS & HEREDITY | HUMAN PREFRONTAL CORTEX | FACTOR-KAPPA-B | ESSENTIAL-HYPERTENSION | SUSCEPTIBILITY LOCUS | PULSE PRESSURE | CORONARY-ARTERY-DISEASE | GENOME-WIDE ASSOCIATION | Blood Pressure | Genetics, Population | Computational Biology - methods | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Diastole | Europe | Humans | Risk Factors | Genotype | Genetic Loci | Systole | Phenotype | Arterial Pressure | Polymorphism, Single Nucleotide | Quantitative Trait Loci | Quality Control | Quantitative trait loci | Physiological aspects | Genetic research | Blood pressure | Genetic aspects | Research | Identification and classification | Meta-analysis | Molecules | Genes | Cardiovascular disease | Gene loci | Risk factors | Index Medicus | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Prioritizing putative influential genes in cardiovascular disease susceptibility by applying tissue-specific Mendelian randomization
by Taylor, K and Smith, GD and Relton, CL and Gaunt, TR and Richardson, TG
GENOME MEDICINE, ISSN 1756-994X, 01/2019, Volume 11, Issue 1, pp. 6 - 6
BackgroundThe extent to which changes in gene expression can influence cardiovascular disease risk across different tissue types has not yet been... 
CHOLESTEROL | DETERMINANTS | Tissue specificity | Cardiovascular disease | RISK | ALSPAC | LOCI | Mendelian randomization | Gene expression | LIPOPROTEIN-LIPASE | VARIANT | Quantitative trait loci | GENETICS & HEREDITY | DNA methylation | ARIES | COMPLEX TRAITS | EXPRESSION | CORONARY-ARTERY-DISEASE | GENOME-WIDE ASSOCIATION | Genome-wide association studies | Usage | Genetic susceptibility | Genetic variation | Analysis | Genetic aspects | Research | Cardiovascular diseases | Statistical analysis | Liver | Genomes | Cholesterol | Studies | Genetic variance | Body mass index | Gene loci | Gene mapping | Methylation | Bayesian analysis
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text Leveraging brain cortex-derived molecular data to elucidate epigenetic and transcriptomic drivers of complex traits and disease
by Hatcher, Charlie and Relton, Caroline L and Gaunt, Tom R and Richardson, Tom G
Translational Psychiatry, ISSN 2158-3188, 12/2019, Volume 9, Issue 1, pp. 105 - 10
Integrative approaches that harness large-scale molecular datasets can help develop mechanistic insight into findings from genome-wide association studies... 
GWAS | DNA METHYLATION | EQTL | PSYCHIATRY | SCHIZOPHRENIA | LOCI | GENOME-WIDE ASSOCIATION | DNA methylation | Schizophrenia | Epigenetics | Genomes | Gene expression | Deoxyribonucleic acid--DNA
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text Incorporating non-coding annotations into rare variant analysis
by Richardson, Tom G and Campbell, Colin and Timpson, Nicholas J and Gaunt, Tom R
PLoS ONE, ISSN 1932-6203, 04/2016, Volume 11, Issue 4, pp. e0154181 - e0154181
Background The success of collapsing methods which investigate the combined effect of rare variants on complex traits has so far been limited. The manner in... 
PATHOGENICITY | MULTIDISCIPLINARY SCIENCES | DISEASE | FREQUENCY | FRAMEWORK | COMMON | POWER | MODEL | GENOME-WIDE ASSOCIATION | Computational Biology - methods | Genetic Predisposition to Disease - genetics | Gene Frequency | Humans | Genetic Diseases, Inborn - genetics | Genotype | United Kingdom | Molecular Sequence Annotation - methods | Genome, Human - genetics | Genetic Variation | Phenotype | Polymorphism, Single Nucleotide | Genome-Wide Association Study - methods | High-Throughput Nucleotide Sequencing - methods | Genetic Diseases, Inborn - diagnosis | Cohort Studies | Genome-wide association studies | Nucleotide sequencing | Genetic variation | Analysis | Computational biology | DNA sequencing | Haplotypes | Collapsing | Filtration | Laboratories | Genes | Lipids | Principal components analysis | Genomes | Epidemiology | Proteins | Medicine | Studies | Lipoproteins | Annotations | Alzheimers disease | Twins | Bioinformatics | Lipoproteins (high density) | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text DNA Methylation in Newborns and Maternal Smoking in Pregnancy: Genome-wide Consortium Meta-analysis
by Joubert, Bonnie R and Felix, Janine F and Yousefi, Paul and Bakulski, Kelly M and Just, Allan C and Breton, Carrie and Reese, Sarah E and Markunas, Christina A and Richmond, Rebecca C and Xu, Cheng-Jian and Xu, Zongli and Küpers, Leanne K and Oh, Sam S and Hoyo, Cathrine and Gruzieva, Olena and Söderhäll, Cilla and Salas, Lucas A and Baïz, Nour and Zhang, Hongmei and Lepeule, Johanna and Ruiz, Carlos and Ligthart, Symen and Wang, Tianyuan and Taylor, Jack A and Duijts, Liesbeth and Sharp, Gemma C and Jankipersadsing, Soesma A and Nilsen, Roy M and Vaez, Ahmad and Fallin, M. Daniele and Hu, Donglei and Litonjua, Augusto A and Fuemmeler, Bernard F and Huen, Karen and Kere, Juha and Kull, Inger and Munthe-Kaas, Monica Cheng and Gehring, Ulrike and Bustamante, Mariona and Saurel-Coubizolles, Marie José and Quraishi, Bilal M and Ren, Jie and Tost, Jörg and Gonzalez, Juan R and Peters, Marjolein J and Håberg, Siri E and van Meurs, Joyce B and Gaunt, Tom R and Kerkhof, Marjan and Corpeleijn, Eva and Feinberg, Andrew P and Eng, Celeste and Baccarelli, Andrea A and Benjamin Neelon, Sara E and Bradman, Asa and Merid, Simon Kebede and Bergström, Anna and Herceg, Zdenko and Hernandez-Vargas, Hector and Brunekreef, Bert and Pinart, Mariona and Heude, Barbara and Ewart, Susan and Yao, Jin and Lemonnier, Nathanaël and Franco, Oscar H and Wu, Michael C and Hofman, Albert and McArdle, Wendy and Van der Vlies, Pieter and Falahi, Fahimeh and Gillman, Matthew W and Barcellos, Lisa F and Kumar, Ashish and Wickman, Magnus and Guerra, Stefano and Charles, Marie-Aline and Holloway, John and Auffray, Charles and Tiemeier, Henning W and Smith, George Davey and Postma, Dirkje and Hivert, Marie-France and Eskenazi, Brenda and Vrijheid, Martine and Arshad, Hasan and Antó, Josep M and Dehghan, Abbas and Karmaus, Wilfried and Annesi-Maesano, Isabella and Sunyer, Jordi and Ghantous, Akram and Pershagen, Göran and Holland, Nina and Murphy, Susan K and DeMeo, Dawn L and Burchard, Esteban G and Ladd-Acosta, Christine and Snieder, Harold and Nystad, Wenche and ...
The American Journal of Human Genetics, ISSN 0002-9297, 04/2016, Volume 98, Issue 4, pp. 680 - 696
Epigenetic modifications, including DNA methylation, represent a potential mechanism for environmental impacts on human disease. Maternal smoking in pregnancy... 
BREAST-CANCER | IN-UTERO | CIGARETTE-SMOKING | LYMPH-NODE METASTASIS | PRENATAL EXPOSURE | TOBACCO-SMOKING | GENETICS & HEREDITY | LUNG-FUNCTION DECLINE | NEUROPILIN-2 EXPRESSION | AUTISM SPECTRUM DISORDERS | POSTSYNAPTIC DENSITY | Smoking - adverse effects | European Continental Ancestry Group - genetics | Genetic Association Studies | Epigenesis, Genetic | Humans | Child, Preschool | Infant | Chromosome Mapping | Cleft Palate - genetics | Asthma - genetics | Pregnancy | Cleft Lip - genetics | DNA Methylation | Cleft Palate - etiology | Female | Asthma - etiology | Child | Infant, Newborn | Cleft Lip - etiology | Genome-wide association studies | Genetic aspects | Nucleotide sequencing | Methylation | Health aspects | Methods | DNA sequencing | Smoking | Newborn babies | DNA methylation | Genomes | Mothers | Meta-analysis | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height
by Lanktree, Matthew B and Guo, Yiran and Murtaza, Muhammed and Glessner, Joseph T and Bailey, Swneke D and Bailey, Kristian M and Onland-Moret, N. Charlotte and Lettre, Guillaume and Ongen, Halit and Rajagopalan, Ramakrishnan and Johnson, W. Craig and Johnson, Toby and Johnson, Julie A and Shen, Haiqing and Nelson, Christopher P and Klopp, Norman and Baumert, Jens and Padmanabhan, Sandosh and Pankratz, Nathan and Pankow, James S and Shah, Sonia and Taylor, Kira and Barnard, John and Peters, Bas J and M. Maloney, Cliona and Lobmeyer, Maximilian T and Stanton, Alice and Zafarmand, M. Hadi and Romaine, Simon P.R and Mehta, Amar and van Iperen, Erik P.A and Gong, Yan and Price, Tom S and Smith, George Davey and Smith, Erin N and Kim, Cecilia E and Li, Mingyao and Li, Qing and Li, Yun R and Asselbergs, Folkert W and Atwood, Larry D and Bhatt, Deepak and Bauer, Florianne and Behr, Elijah R and Bhangale, Tushar and Boer, Jolanda M.A and Boer, Anthonius de and Boehm, Bernhard O and Bradfield, Jonathan P and Brown, Morris and Braund, Peter S and Burton, Paul R and Carty, Cara and Chandrupatla, Hareesh R and Chen, Wei and Connell, John and Dalgeorgou, Chrysoula and Drenos, Fotios and Elbers, Clara C and Fang, James C and Fox, Caroline S and Frackelton, Edward C and Fuchs, Barry and Furlong, Clement E and Gibson, Quince and Gieger, Christian and Goel, Anuj and Grobbee, Diederik E and Hastie, Claire and Howard, Philip J and Huang, Guan-Hua and Kleber, Marcus E and Klein, Ronald and Klein, Barbara E.K and Kooperberg, Charles and Ky, Bonnie and LaCroix, Andrea and Lanken, Paul and Lathrop, Mark and Marshall, Vanessa and Melander, Olle and Mentch, Frank D and J. Meyer, Nuala and Monda, Keri L and Montpetit, Alexandre and Murugesan, Gurunathan and Nakayama, Karen and Nondahl, Dave and Onipinla, Abiodun and Rafelt, Suzanne and Newhouse, Stephen J and Otieno, F. George and Patel, Sanjey R and Putt, Mary E and Rodriguez, Santiago and Safa, Radwan N and Sawyer, Douglas B and Schreiner, Pamela J and Simpson, Claire and Sivapalaratnam, Suthesh and ... and PROCARDIS and Whitehall II Study and WHII 50K Grp and Hugh Watkins on behalf of PROCARDIS and Meena Kumari on behalf of the Whitehall II Study and the WHII 50K Group
The American Journal of Human Genetics, ISSN 0002-9297, 01/2011, Volume 88, Issue 1, pp. 6 - 18
Height is a classic complex trait with common variants in a growing list of genes known to contribute to the phenotype. Using a genecentric genotyping array... 
POPULATION | BIOLOGICAL PATHWAYS | GENETICS & HEREDITY | LOCI | INTERLEUKIN-11 | MICE | IDENTIFICATION | TRAITS | ADULT HEIGHT | HERITABILITY | GENOME-WIDE ASSOCIATION | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Hispanic Americans - genetics | Gene Frequency | Humans | Asian Continental Ancestry Group - genetics | African Americans - genetics | Interleukin-11 - genetics | Male | Genetic Loci | Cardiovascular System | Body Height - genetics | Genetic Heterogeneity | Smad3 Protein - genetics | Adult | Female | Polymorphism, Single Nucleotide | Stature | Genetic aspects | Research | Single nucleotide polymorphisms | Human population genetics | Intraspecific genetic variation | Genotype & phenotype | Genetics | Ethnicity | Height | Genes | Meta-analysis | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights