X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
motion pictures (14) 14
genetics & heredity (10) 10
dvd (9) 9
humans (9) 9
heart defects, congenital - genetics (8) 8
index medicus (8) 8
congenital heart disease (7) 7
article (5) 5
female (5) 5
genetic aspects (5) 5
male (5) 5
television programs (5) 5
defects (4) 4
genetics (4) 4
genotype (4) 4
motion picture directors & producers (4) 4
polymorphism, single nucleotide (4) 4
570 life sciences; biology (3) 3
610 medicine & health (3) 3
chromosome deletion (3) 3
cohort studies (3) 3
congenital diseases (3) 3
disease (3) 3
gene (3) 3
genetic predisposition to disease (3) 3
genetic variation (3) 3
health aspects (3) 3
institute of medical genetics (3) 3
life sciences & biomedicine (3) 3
mutation (3) 3
phenotype (3) 3
risk factors (3) 3
science & technology (3) 3
tetralogy of fallot - genetics (3) 3
actors (2) 2
alleles (2) 2
animals (2) 2
articles (2) 2
biochemistry & molecular biology (2) 2
biomedical research (2) 2
cardiovascular disease (2) 2
cardiovascular diseases (2) 2
case-control studies (2) 2
causes of (2) 2
chromosome duplication (2) 2
chromosomes, human, pair 1 (2) 2
coaches & managers (2) 2
connexins - genetics (2) 2
databases, genetic (2) 2
exome (2) 2
folate (2) 2
folic acid - blood (2) 2
gene duplication (2) 2
genes (2) 2
genetic association (2) 2
genetic loci (2) 2
genome-wide association study (2) 2
genomes (2) 2
heart (2) 2
heart defects, congenital - pathology (2) 2
hidden-markov model (2) 2
identification and classification (2) 2
medical research (2) 2
mendelian randomization (2) 2
methylenetetrahydrofolate reductase - genetics (2) 2
mice (2) 2
mortality (2) 2
mthfr (2) 2
musical recordings (2) 2
mutations (2) 2
odds ratio (2) 2
recurrence (2) 2
research (2) 2
risk (2) 2
secondary schools (2) 2
snp genotyping data (2) 2
06 biological sciences (1) 1
11 medical and health sciences (1) 1
abnormalities, multiple - genetics (1) 1
abridged index medicus (1) 1
adjunct (1) 1
association (1) 1
atrial-fibrillation (1) 1
atrioventricular septal-defects (1) 1
autism (1) 1
autoantigens (1) 1
autoantigens - genetics (1) 1
binding sites (1) 1
birth defects (1) 1
books (1) 1
cardiac conditioning (1) 1
cardioprotection (1) 1
cardiovascular and metabolic diseases (1) 1
cdc2 protein kinase (1) 1
cdc2 protein kinase - chemistry (1) 1
cdc2 protein kinase - genetics (1) 1
cell line (1) 1
child (1) 1
chromosomes (1) 1
chromosomes, human, pair 12 - genetics (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
by Sifrim, Alejandro and Hitz, Marc-Phillip and Wilsdon, Anna and Breckpot, Jeroen and Turki, Saeed H. Al and Thienpont, Bernard and McRae, Jeremy and Fitzgerald, Tomas W and Singh, Tarjinder and Swaminathan, Ganesh Jawahar and Prigmore, Elena and Rajan, Diana and Abdul-Khaliq, Hashim and Banka, Siddharth and Bauer, Ulrike M.M and Bentham, Jamie and Berger, Felix and Bhattacharya, Shoumo and Bu'Lock, Frances and Canham, Natalie and Colgiu, Irina-Gabriela and Cosgrove, Catherine and Cox, Helen and Daehnert, Ingo and Daly, Allan and Danesh, John and Fryer, Alan and Gewillig, Marc and Hobson, Emma and Hoff, Kirstin and Homfray, Tessa and Kahlert, Anne-Karin and Ketley, Ami and Kramer, Hans-Heiner and Lachlan, Katherine and Lampe, Anne Katrin and Louw, Jacoba J and Manickara, Ashok Kumar and Manase, Dorin and McCarthy, Karen P and Metcalfe, Kay and Moore, Carmel and Newbury-Ecob, Ruth and Omer, Seham Osman and Ouwehand, Willem H and Park, Soo-Mi and Parker, Michael J and Pickardt, Thomas and Pollard, Martin O and Robert, Leema and Roberts, David J and Sambrook, Jennifer and Setchfield, Kerry and Stiller, Brigitte and Thornborough, Chris and Toka, Okan and Watkins, Hugh and Williams, Denise and Wright, Michael and Mital, Seema and Daubeney, Piers E.F and Keavney, Bernard and Goodship, Judith and Abu-Sulaiman, Riyadh Mahdi and Klaassen, Sabine and Wright, Caroline F and Firth, Helen V and Barrett, Jeffrey C and Devriendt, Koenraad and Fitzpatrick, David R and Brook, J David and Hurles, Matthew E and INTERVAL Study and Deciphering Dev Disorders Study and UK10K Consortium and the INTERVAL Study and the Deciphering Developmental Disorders Study and the UK10K Consortium
Nature Genetics, ISSN 1061-4036, 09/2016, Volume 48, Issue 9, pp. 1060 - 1065
Congenital heart defects (CHDs) have a neonatal incidence of 0.8-1% (refs. 1,2). Despite abundant examples of monogenic CHD in humans and mice, CHD has a low... 
DE-NOVO MUTATIONS | GENOTYPE | DISEASE | GENETICS & HEREDITY | FRAMEWORK | RECURRENCE | DISCOVERY | Genetic variation | Exome sequencing | Development and progression | Congenital heart disease | Genetic aspects | Identification and classification | Health aspects | Methods | Heart | Medical research | Biomedical research | Congenital diseases | Funding | Genes | Genomics | Genomes | RNA polymerase | Kinases | Defects | Autism | Mutation
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 04/2014, Volume 94, Issue 4, pp. 574 - 585
Journal Article
Nature genetics, ISSN 1061-4036, 2013, Volume 45, Issue 7, pp. 822 - 824
Journal Article
Journal Article
Human molecular genetics, ISSN 0964-6906, 2013, Volume 22, Issue 7, pp. 1473 - 1481
Journal Article
by Sifrim, Alejandro and Hitz, Marc-Phillip and Wilsdon, Anna and Breckpot, Jeroen and Turki, Saeed H Al and Thienpont, Bernard and McRae, Jeremy and Fitzgerald, Tomas W and Singh, Tarjinder and Swaminathan, Ganesh Jawahar and Prigmore, Elena and Rajan, Diana and Abdul-Khaliq, Hashim and Banka, Siddharth and Bauer, Ulrike M M and Bentham, Jamie and Berger, Felix and Bhattacharya, Shoumo and Bu'Lock, Frances and Canham, Natalie and Colgiu, Irina-Gabriela and Cosgrove, Catherine and Cox, Helen and Daehnert, Ingo and Daly, Allan and Danesh, John and Fryer, Alan and Gewillig, Marc and Hobson, Emma and Hoff, Kirstin and Homfray, Tessa and Kahlert, Anne-Karin and Ketley, Ami and Kramer, Hans-Heiner and Lachlan, Katherine and Lampe, Anne Katrin and Louw, Jacoba J and Manickara, Ashok Kumar and Manase, Dorin and McCarthy, Karen P and Metcalfe, Kay and Moore, Carmel and Newbury-Ecob, Ruth and Omer, Seham Osman and Ouwehand, Willem H and Park, Soo-Mi and Parker, Michael J and Pickardt, Thomas and Pollard, Martin O and Robert, Leema and Roberts, David J and Sambrook, Jennifer and Setchfield, Kerry and Stiller, Brigitte and Thornborough, Chris and Toka, Okan and Watkins, Hugh and Williams, Denise and Wright, Michael and Mital, Seema and Daubeney, Piers E F and Keavney, Bernard and Goodship, Judith and Abu-Sulaiman, Riyadh Mahdi and Klaassen, Sabine and Wright, Caroline F and Firth, Helen V and Barrett, Jeffrey C and Devriendt, Koenraad and FitzPatrick, David R and Brook, J David and Hurles, Matthew E and INTERVAL Study and Deciphering Developmental Disorders Study and UK10K Consortium
Nature genetics, ISSN 1061-4036, 09/2016, Volume 48, Issue 9, p. 1060
Journal Article