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PLoS Genetics, ISSN 1553-7390, 07/2009, Volume 5, Issue 7, pp. e1000540 - e1000540
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2018, Volume 13, Issue 1, pp. e0191319 - e0191319
The Pediatric Cardiac Genomics Consortium (PCGC) designed the Congenital Heart Disease Genetic Network Study to provide phenotype and genotype data for a large... 
UNITED-STATES | METROPOLITAN ATLANTA | DE-NOVO MUTATIONS | MULTIDISCIPLINARY SCIENCES | SEX | BIRTH-DEFECTS | PREVALENCE | OUTCOMES | INFANT | MATERNAL SMOKING | CHILDREN | Congenital heart disease | Research | Children | Health aspects | Index Medicus
Journal Article
by Gelb, Bruce and Brueckner, Martina and Chung, Wendy and Goldmuntz, Elizabeth and Kaltman, Jonathan and Kaski, Juan Pablo and Kim, Richard and Kline, Jennie and Mercer-Rosa, Laura and Porter, George and Roberts, Amy and Rosenberg, Ellen and Seiden, Howard and Seidman, Christine and Sleeper, Lynn and Tennstedt, Sharon and Schramm, Charlene and Burns, Kristin and Pearson, Gail and Breitbart, Roger and Colan, Steven and Geva, Judith and Monafo, Angela and Stryker, Janice and McDonough, Barbara and Seidman, Jonathan and Edman, Sharon and Garbarini, Jennifer and Hakonarson, Hakon and Mitchell, Laura and Tusi, Jessica and White, Peter and Woyciechowski, Stacy and Warburton, Dorothy and Awad, Danielle and Celia, Katrina and Etwaru, Davina and Sond, Jaswinder Kaur and Korsin, Rosalind and Lanz, Alyssa and Marquez, Emma and Williams, Ismee and Wilpers, Abigail and Yee, Roslyn and Guevara, Denise and Julian, Ariel and Neal, Meghan Mac and Mintz, Cassie and Peter, Inga and Sachidanandam, Ravi and Romano-Adesman, Angela and Gruber, Dorota and Stellato, Nancy and Lifton, Richard and Cross, Nancy and Deanfield, John and Giardini, Alessandro and Flack, Karen and Taillie, Eileen and Tran, Nhu and Dandreo, Kimberly and Gallagher, Dianne and Lu, Minmin and Berlin, Dorit and Beiswanger, Christine and Italia, Mike and Brooks, Maria and Olive, Michelle and Botkin, Jeffrey and Dupuis, Josee and Garg, Vidu and Watson, Mike and Bristow, James and Evans, Todd and Kendziorski, Christina and Mardis, Elaine and Murray, Jeffrey and Saltz, Joel and Wong, Hector and Pediatric Cardiac Genomics Consort and Pediatric Cardiac Genomics Consortium and Core Laboratories for PCGC and Biorepository, Coriell Institutes and Clinical Sites and Data Hub, Children’s Hospital Philadelphia and Data Coordinating Center and Genotyping Array, Children’s Hospital Philadelphia and External Advisory Committee and Candidate Gene Evaluation and RNASeq, Harvard Medical School and Confirmation, Columbia University and Observational Study Monitoring Board and National Heart, Lung, and Blood Institute and Whole Genome Sequencing Harvard Medical School and Brigham & Women’s Hospital and Whole Exome Sequencing, Yale University and Writing Committee
Circulation Research, ISSN 0009-7330, 02/2013, Volume 112, Issue 4, pp. 698 - 706
Congenital heart defects (CHD) are the leading cause of infant mortality among birth defects, and later morbidities and premature mortality remain problematic.... 
Congenital cardiac defects | Congenital heart disease | Genomic study | Human genetics | Genome-wide analysis | human genetics | DEFECTS | CARDIAC & CARDIOVASCULAR SYSTEMS | HYPOPLASTIC LEFT-HEART | NKX2-5 MUTATIONS | genomic study | LEFT-RIGHT ASYMMETRY | NATIONAL HEART | congenital cardiac defects | COPY-NUMBER VARIATION | WORKING GROUP | MALFORMATIONS | genome-wide analysis | congenital heart disease | BICUSPID AORTIC-VALVE | PERIPHERAL VASCULAR DISEASE | HEMATOLOGY | ASSOCIATION | Biological Specimen Banks - organization & administration | Prospective Studies | Follow-Up Studies | Outcome Assessment (Health Care) | United States | Genomics | Humans | Child, Preschool | Infant | Data Collection | National Heart, Lung, and Blood Institute (U.S.) - organization & administration | Patient Selection | Schools, Medical - organization & administration | Young Adult | Heart Defects, Congenital - genetics | DNA Mutational Analysis | Adult | Registries - ethics | Child | Infant, Newborn | Databases, Factual | Genetic Association Studies | Genotype | Clinical Trials as Topic | Gene Dosage | Interdisciplinary Communication | Translational Medical Research - organization & administration | Phenotype | Confidentiality | Adolescent | Heart Defects, Congenital - epidemiology | Hospitals, Pediatric - organization & administration | Index Medicus
Journal Article
Journal Article
by Ehret, Georg B and Munroe, Patricia B and Rice, Kenneth M and Bochud, Murielle and Johnson, Anew D and Chasman, Daniel I and Smith, Albert V and Tobin, Martin D and Verwoert, Germaine C and Hwang, Shih-Jen and Pihur, Vasyl and Vollenweider, Peter and O'Reilly, Paul F and Amin, Najaf and Bragg-Gresham, Jennifer L and Teumer, Alexander and Glazer, Nicole L and Launer, Lenore and Zhao, Jing Hua and Aulchenko, Yurii and Heath, Simon and Sõber, Siim and Parsa, Afshin and Luan, Jian'an and Arora, Pankaj and Dehghan, Abbas and Zhang, Feng and Lucas, Gavin and Hicks, Anew A and Jackson, Anne U and Peden, John F and Tanaka, Toshiko and Wild, Sarah H and Rudan, Igor and Igl, Wilmar and Milaneschi, Yuri and Parker, Alex N and Fava, Cristiano and Chambers, John C and Fox, Ervin R and Kumari, Meena and Go, Min Jin and van der Harst, Pim and Kao, Wen Hong Linda and Sjögren, Marketa and Vinay, D. G and Alexander, Myriam and Tabara, Yasuharu and Shaw-Hawkins, Sue and Whincup, Peter H and Liu, Yongmei and Shi, Gang and Kuusisto, Johanna and Tayo, Bamidele and Seielstad, Mark and Sim, Xueling and Nguyen, Khanh-Dung Hoang and Lehtimäki, Terho and Matullo, Giuseppe and Wu, Ying and Gaunt, Tom R and Onland-Moret, N. Charlotte and Cooper, Matthew N and Platou, Carl G. P and Org, Elin and Hardy, Rebecca and Dahgam, Santosh and Palmen, Jutta and Vitart, Veronique and Braund, Peter S and Kuznetsova, Tatiana and Uiterwaal, Cuno S. P. M and Adeyemo, Adebowale and Palmas, Walter and Campbell, Harry and Ludwig, Barbara and Tomaszewski, Maciej and Tzoulaki, Ioanna and Palmer, Nicholette D and Aspelund, Thor and Garcia, Melissa and Chang, Yen-Pei C and O'Connell, Jeffrey R and Steinle, Nanette I and Grobbee, Diederick E and Arking, Dan E and Kardia, Sharon L and Morrison, Alanna C and Hernandez, Dena and Najjar, Samer and McArdle, Wendy L and Hadley, David and Brown, Morris J and Connell, John M and Hingorani, Aroon D and Day, Ian N. M and Lawlor, Debbie A and Beilby, John P and Lawrence, Robert W and Clarke, Robert and ... and CHARGE-HF Consortium and EchoGen Consortium and KidneyGen Consortium and CARDIoGRAM Consortium and Int Consortium Blood Pressure Geno and CKDGen Consortium and The International Consortium for Blood Pressure Genome-Wide Association Studies and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för immunologi, genetik och patologi and Uppsala universitet
Nature, ISSN 0028-0836, 2011, Volume 478, Issue 7367, pp. 103 - 109
Journal Article