Literature DB >> 29025762

Modifying Mendel Redux: Unbiased Approaches Can Find Modifiers.

Kim L McBride1, Stephanie M Ware2.   

Abstract

Entities:  

Keywords:  Editorials; genome-wide association study; genomics; heart defects, congenital; tetralogy of Fallot

Mesh：

Substances：

Year:  2017        PMID： 29025762      PMCID： PMC5659730          DOI： 10.1161/CIRCGENETICS.117.001891

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


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  19 in total

1.  Modifying Mendel: approaches for identification of susceptibility alleles for human cardiovascular malformations.

Authors:  Kim L McBride; Stephanie M Ware
Journal:  Circ Cardiovasc Genet       Date:  2012-06

2.  Genetic modifiers predisposing to congenital heart disease in the sensitized Down syndrome population.

Authors:  Huiqing Li; Sheila Cherry; Donna Klinedinst; Valerie DeLeon; Jennifer Redig; Benjamin Reshey; Michael T Chin; Stephanie L Sherman; Cheryl L Maslen; Roger H Reeves
Journal:  Circ Cardiovasc Genet       Date:  2012-04-20

3.  De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot.

Authors:  Steven C Greenway; Alexandre C Pereira; Jennifer C Lin; Steven R DePalma; Samuel J Israel; Sonia M Mesquita; Emel Ergul; Jessie H Conta; Joshua M Korn; Steven A McCarroll; Joshua M Gorham; Stacey Gabriel; David M Altshuler; Maria de Lourdes Quintanilla-Dieck; Maria Alexandra Artunduaga; Roland D Eavey; Robert M Plenge; Nancy A Shadick; Michael E Weinblatt; Philip L De Jager; David A Hafler; Roger E Breitbart; Jonathan G Seidman; Christine E Seidman
Journal:  Nat Genet       Date:  2009-07-13       Impact factor: 38.330

4.  Prevalence of congenital heart disease.

Authors:  Julien I E Hoffman; Samuel Kaplan; Richard R Liberthson
Journal:  Am Heart J       Date:  2004-03       Impact factor: 4.749

5.  Association between maternal chronic conditions and congenital heart defects: a population-based cohort study.

Authors:  Shiliang Liu; K S Joseph; Sarka Lisonkova; Jocelyn Rouleau; Michiel Van den Hof; Reg Sauve; Michael S Kramer
Journal:  Circulation       Date:  2013-06-28       Impact factor: 29.690

6.  A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20.

Authors:  Neil A Hanchard; Shanker Swaminathan; Kristine Bucasas; Dieter Furthner; Susan Fernbach; Mahshid S Azamian; Xueqing Wang; Mark Lewin; Jeffrey A Towbin; Lisa C A D'Alessandro; Shaine A Morris; William Dreyer; Susan Denfield; Nancy A Ayres; Wayne J Franklin; Henri Justino; M Regina Lantin-Hermoso; Elena C Ocampo; Alexia B Santos; Dhaval Parekh; Douglas Moodie; Aamir Jeewa; Emily Lawrence; Hugh D Allen; Daniel J Penny; Charles D Fraser; James R Lupski; Mojisola Popoola; Lalita Wadhwa; J David Brook; Frances A Bu'Lock; Shoumo Bhattacharya; Seema R Lalani; Gloria A Zender; Sara M Fitzgerald-Butt; Jessica Bowman; Don Corsmeier; Peter White; Kelsey Lecerf; Gladys Zapata; Patricia Hernandez; Judith A Goodship; Vidu Garg; Bernard D Keavney; Suzanne M Leal; Heather J Cordell; John W Belmont; Kim L McBride
Journal:  Hum Mol Genet       Date:  2016-03-09       Impact factor: 6.150

7.  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

8.  Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.

Authors:  Alejandro Sifrim; Marc-Phillip Hitz; Anna Wilsdon; Jeroen Breckpot; Saeed H Al Turki; Bernard Thienpont; Jeremy McRae; Tomas W Fitzgerald; Tarjinder Singh; Ganesh Jawahar Swaminathan; Elena Prigmore; Diana Rajan; Hashim Abdul-Khaliq; Siddharth Banka; Ulrike M M Bauer; Jamie Bentham; Felix Berger; Shoumo Bhattacharya; Frances Bu'Lock; Natalie Canham; Irina-Gabriela Colgiu; Catherine Cosgrove; Helen Cox; Ingo Daehnert; Allan Daly; John Danesh; Alan Fryer; Marc Gewillig; Emma Hobson; Kirstin Hoff; Tessa Homfray; Anne-Karin Kahlert; Ami Ketley; Hans-Heiner Kramer; Katherine Lachlan; Anne Katrin Lampe; Jacoba J Louw; Ashok Kumar Manickara; Dorin Manase; Karen P McCarthy; Kay Metcalfe; Carmel Moore; Ruth Newbury-Ecob; Seham Osman Omer; Willem H Ouwehand; Soo-Mi Park; Michael J Parker; Thomas Pickardt; Martin O Pollard; Leema Robert; David J Roberts; Jennifer Sambrook; Kerry Setchfield; Brigitte Stiller; Chris Thornborough; Okan Toka; Hugh Watkins; Denise Williams; Michael Wright; Seema Mital; Piers E F Daubeney; Bernard Keavney; Judith Goodship; Riyadh Mahdi Abu-Sulaiman; Sabine Klaassen; Caroline F Wright; Helen V Firth; Jeffrey C Barrett; Koenraad Devriendt; David R FitzPatrick; J David Brook; Matthew E Hurles
Journal:  Nat Genet       Date:  2016-08-01       Impact factor: 38.330

9.  Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3.

Authors:  Tingwei Guo; Gabriela M Repetto; Donna M McDonald McGinn; Jonathan H Chung; Hiroko Nomaru; Christopher L Campbell; Anna Blonska; Anne S Bassett; Eva W C Chow; Elisabeth E Mlynarski; Ann Swillen; Joris Vermeesch; Koen Devriendt; Doron Gothelf; Miri Carmel; Elena Michaelovsky; Maude Schneider; Stephan Eliez; Stylianos E Antonarakis; Karlene Coleman; Aoy Tomita-Mitchell; Michael E Mitchell; M Cristina Digilio; Bruno Dallapiccola; Bruno Marino; Nicole Philip; Tiffany Busa; Leila Kushan-Wells; Carrie E Bearden; Małgorzata Piotrowicz; Wanda Hawuła; Amy E Roberts; Flora Tassone; Tony J Simon; Esther D A van Duin; Thérèse A van Amelsvoort; Wendy R Kates; Elaine Zackai; H Richard Johnston; David J Cutler; A J Agopian; Elizabeth Goldmuntz; Laura E Mitchell; Tao Wang; Beverly S Emanuel; Bernice E Morrow
Journal:  Circ Cardiovasc Genet       Date:  2017-10

10.  De novo mutations in histone-modifying genes in congenital heart disease.

Authors:  Samir Zaidi; Murim Choi; Hiroko Wakimoto; Lijiang Ma; Jianming Jiang; John D Overton; Angela Romano-Adesman; Robert D Bjornson; Roger E Breitbart; Kerry K Brown; Nicholas J Carriero; Yee Him Cheung; John Deanfield; Steve DePalma; Khalid A Fakhro; Joseph Glessner; Hakon Hakonarson; Michael J Italia; Jonathan R Kaltman; Juan Kaski; Richard Kim; Jennie K Kline; Teresa Lee; Jeremy Leipzig; Alexander Lopez; Shrikant M Mane; Laura E Mitchell; Jane W Newburger; Michael Parfenov; Itsik Pe'er; George Porter; Amy E Roberts; Ravi Sachidanandam; Stephan J Sanders; Howard S Seiden; Mathew W State; Sailakshmi Subramanian; Irina R Tikhonova; Wei Wang; Dorothy Warburton; Peter S White; Ismee A Williams; Hongyu Zhao; Jonathan G Seidman; Martina Brueckner; Wendy K Chung; Bruce D Gelb; Elizabeth Goldmuntz; Christine E Seidman; Richard P Lifton
Journal:  Nature       Date:  2013-05-12       Impact factor: 49.962
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