Literature DB >> 26082554

History of Our Understanding of the Causes of Congenital Heart Disease.

Bruce D Gelb1.   

Abstract

Entities:  

Keywords:  causation; congenital heart disease; genetics; history

Mesh：

Year:  2015        PMID： 26082554      PMCID： PMC4870049          DOI： 10.1161/CIRCGENETICS.115.001058

Source DB:  PubMed          Journal:  Circ Cardiovasc Genet        ISSN： 1942-3268


× No keyword cloud information.
  42 in total

1.  [Research on the etiology of congenital angiocardiopathy].

Authors:  W FUHRMANN
Journal:  Acta Genet Stat Med       Date:  1961

2.  Maurice Campbell: first editor of Heart.

Authors:  M E Silverman
Journal:  Heart       Date:  2003-12       Impact factor: 5.994

3.  The laws of combination of haemoglobin with carbon monoxide and oxygen.

Authors:  C G Douglas; J S Haldane; J B Haldane
Journal:  J Physiol       Date:  1912-06-12       Impact factor: 5.182

Review 4.  Multifactorial inheritance hypothesis for the etiology of congenital heart diseases. The genetic-environmental interaction.

Authors:  J J Nora
Journal:  Circulation       Date:  1968-09       Impact factor: 29.690

5.  From generational studies to a multilevel genetic-environmental interaction.

Authors:  J J Nora
Journal:  J Am Coll Cardiol       Date:  1994-05       Impact factor: 24.094

6.  The paediatric cardiology Hall of Fame: Maude Elizabeth Abbott.

Authors:  William N Evans; Marie J Béland
Journal:  Cardiol Young       Date:  2010-04       Impact factor: 1.093

7.  A deletion in chromosome 22 can cause DiGeorge syndrome.

Authors:  A de la Chapelle; R Herva; M Koivisto; P Aula
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

8.  World survey of the common cardiac malformations: developmental error or genetic variant?

Authors:  H B Taussig
Journal:  Am J Cardiol       Date:  1982-09       Impact factor: 2.778

9.  Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot.

Authors:  Heather J Cordell; Ana Töpf; Chrysovalanto Mamasoula; Alex V Postma; Jamie Bentham; Diana Zelenika; Simon Heath; Gillian Blue; Catherine Cosgrove; Javier Granados Riveron; Rebecca Darlay; Rachel Soemedi; Ian J Wilson; Kristin L Ayers; Thahira J Rahman; Darroch Hall; Barbara J M Mulder; Aelko H Zwinderman; Klaartje van Engelen; J David Brook; Kerry Setchfield; Frances A Bu'Lock; Chris Thornborough; John O'Sullivan; A Graham Stuart; Jonathan Parsons; Shoumo Bhattacharya; David Winlaw; Seema Mital; Marc Gewillig; Jeroen Breckpot; Koen Devriendt; Antoon F M Moorman; Anita Rauch; G Mark Lathrop; Bernard D Keavney; Judith A Goodship
Journal:  Hum Mol Genet       Date:  2013-01-07       Impact factor: 6.150

10.  Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data.

Authors:  Joseph T Glessner; Alexander G Bick; Kaoru Ito; Jason Homsy; Laura Rodriguez-Murillo; Menachem Fromer; Erica Mazaika; Badri Vardarajan; Michael Italia; Jeremy Leipzig; Steven R DePalma; Ryan Golhar; Stephan J Sanders; Boris Yamrom; Michael Ronemus; Ivan Iossifov; A Jeremy Willsey; Matthew W State; Jonathan R Kaltman; Peter S White; Yufeng Shen; Dorothy Warburton; Martina Brueckner; Christine Seidman; Elizabeth Goldmuntz; Bruce D Gelb; Richard Lifton; Jonathan Seidman; Hakon Hakonarson; Wendy K Chung
Journal:  Circ Res       Date:  2014-09-09       Impact factor: 17.367
View more
  8 in total

1.  Trends in National Institutes of Health-Funded Congenital Heart Disease Research from 2005 to 2015.

Authors:  Kristin M Burns; Victoria L Pemberton; Charlene A Schramm; Gail D Pearson; Jonathan R Kaltman
Journal:  Pediatr Cardiol       Date:  2017-03-27       Impact factor: 1.655

Review 2.  Genetics and Genomics of Congenital Heart Disease.

Authors:  Samir Zaidi; Martina Brueckner
Journal:  Circ Res       Date:  2017-03-17       Impact factor: 17.367

3.  Combining clinical databases with genetic studies to help advance the causation model of congenital heart disease.

Authors:  Christoph P Hornik; R Thomas Collins; Robert D B Jaquiss; Jeffrey P Jacobs; Marshall L Jacobs; Sara K Pasquali; Amelia S Wallace; Kevin D Hill
Journal:  J Thorac Cardiovasc Surg       Date:  2015-11       Impact factor: 5.209

4.  De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects.

Authors:  James R Priest; Kazutoyo Osoegawa; Nebil Mohammed; Vivek Nanda; Ramendra Kundu; Kathleen Schultz; Edward J Lammer; Santhosh Girirajan; Todd Scheetz; Daryl Waggott; Francois Haddad; Sushma Reddy; Daniel Bernstein; Trudy Burns; Jeffrey D Steimle; Xinan H Yang; Ivan P Moskowitz; Matthew Hurles; Richard P Lifton; Debbie Nickerson; Michael Bamshad; Evan E Eichler; Seema Mital; Val Sheffield; Thomas Quertermous; Bruce D Gelb; Michael Portman; Euan A Ashley
Journal:  PLoS Genet       Date:  2016-04-08       Impact factor: 5.917

5.  The Hole and the Whole: Lessons from Manipulation of Nipbl Deficiency.

Authors:  Bruce D Gelb
Journal:  PLoS Biol       Date:  2016-09-08       Impact factor: 8.029

6.  TAMM41 is required for heart valve differentiation via regulation of PINK-PARK2 dependent mitophagy.

Authors:  Rui Meng Yang; Jiong Tao; Ming Zhan; Hao Yuan; Hai Hong Wang; Sai Juan Chen; Zhu Chen; Hugues de Thé; Jun Zhou; Ying Guo; Jun Zhu
Journal:  Cell Death Differ       Date:  2019-03-01       Impact factor: 15.828

7.  Mutation spectrum of congenital heart disease in a consanguineous Turkish population.

Authors:  Weilai Dong; Hande Kaymakcalan; Sheng Chih Jin; Nicholas S Diab; Cansaran Tanıdır; Ali Seyfi Yalim Yalcin; A Gulhan Ercan-Sencicek; Shrikant Mane; Murat Gunel; Richard P Lifton; Kaya Bilguvar; Martina Brueckner
Journal:  Mol Genet Genomic Med       Date:  2022-04-28       Impact factor: 2.473

8.  Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of Fallot.

Authors:  Miriam S Reuter; Rajiv R Chaturvedi; Rebekah K Jobling; Giovanna Pellecchia; Omar Hamdan; Wilson W L Sung; Thomas Nalpathamkalam; Pratyusha Attaluri; Candice K Silversides; Rachel M Wald; Christian R Marshall; Simon G Williams; Bernard D Keavney; Bhooma Thiruvahindrapuram; Stephen W Scherer; Anne S Bassett
Journal:  Circ Genom Precis Med       Date:  2021-07-30
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.