Publications by authors named "Gregor Andelfinger"

77Publications

Genetic factors in anthracycline-induced cardiotoxicity in patients treated for pediatric cancer.

Expert Opin Drug Metab Toxicol 2020 Sep 24:1-19. Epub 2020 Sep 24.

Immune Diseases and Cancer, Sainte-Justine University Health Center (SJUHC) , Montreal, Quebec, Canada.

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http://dx.doi.org/10.1080/17425255.2020.1807937DOI Listing
September 2020

Maximal cardiopulmonary exercise testing in childhood acute lymphoblastic leukemia survivors exposed to chemotherapy.

Support Care Cancer 2020 Jun 17. Epub 2020 Jun 17.

Laboratory of Pathophysiology of EXercise (LPEX), School of Kinesiology and Physical Activity Sciences, Faculty of Medicine, University of Montreal, CEPSUM, 2100, boulevard Édouard Montpetit, Montréal, QC, H3C 3J7, Canada.

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http://dx.doi.org/10.1007/s00520-020-05582-yDOI Listing
June 2020

The effect of cardiorespiratory fitness and physical activity levels on cognitive functions in survivors of childhood acute lymphoblastic leukemia.

Pediatr Hematol Oncol 2020 Oct 8;37(7):582-598. Epub 2020 Jun 8.

Laboratory of Pathophysiology of EXercise (LPEX), School of Kinesiology and Physical Activity Sciences, Faculty of Medicine, University of Montreal, Montreal, Canada.

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http://dx.doi.org/10.1080/08880018.2020.1767737DOI Listing
October 2020

Predictors of Bicuspid Aortic Valve-Associated Aortopathy in Childhood: A Report From the MIBAVA Consortium.

Circ Cardiovasc Imaging 2020 03 17;13(3):e009717. Epub 2020 Mar 17.

Division of Cardiology, Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Canada (M.G., R.R., C.M., S.M., Ch.-P.S.F., C.M., L.M.).

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http://dx.doi.org/10.1161/CIRCIMAGING.119.009717DOI Listing
March 2020

Developing and validating equations to predict [Formula: see text]O peak from the 6MWT in Childhood ALL Survivors.

Disabil Rehabil 2020 Feb 11:1-8. Epub 2020 Feb 11.

Laboratory of Pathophysiology of EXercise (LPEX), School of Kinesiology and Physical Activity Sciences, Faculty of Medicine, University of Montreal, Montreal, Canada.

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http://dx.doi.org/10.1080/09638288.2020.1725159DOI Listing
February 2020

Physical Activity and Sedentary Behaviors in Childhood Acute Lymphoblastic Leukemia Survivors.

J Pediatr Hematol Oncol 2020 01;42(1):53-60

Laboratory of Pathophysiology of EXercise (LPEX), School of Kinesiology and Physical Activity Sciences, Faculty of Medicine.

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http://dx.doi.org/10.1097/MPH.0000000000001594DOI Listing
January 2020

The expanding phenotypes of cohesinopathies: one ring to rule them all!

Cell Cycle 2019 11 13;18(21):2828-2848. Epub 2019 Sep 13.

Cardiovascular Genetics, Department of Pediatrics, CHU Sainte-Justine , Montréal , QC , Canada.

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https://www.tandfonline.com/doi/full/10.1080/15384101.2019.1
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http://dx.doi.org/10.1080/15384101.2019.1658476DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6791706PMC
November 2019

Childhood Acute Lymphoblastic Leukemia Survivors Have a Substantially Lower Cardiorespiratory Fitness Level Than Healthy Canadians Despite a Clinically Equivalent Level of Physical Activity.

J Adolesc Young Adult Oncol 2019 12 9;8(6):674-683. Epub 2019 Jul 9.

Laboratory of Pathophysiology of EXercise (LPEX), School of Kinesiology and Physical Activity Sciences, Faculty of Medicine, University of Montreal, Montreal, Canada.

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http://dx.doi.org/10.1089/jayao.2019.0024DOI Listing
December 2019

Identification of genetic association between cardiorespiratory fitness and the trainability genes in childhood acute lymphoblastic leukemia survivors.

BMC Cancer 2019 May 14;19(1):443. Epub 2019 May 14.

Laboratoire de Physiopathologie de l'EXercice (LPEX), École de Kinésiologie et des Sciences de l'Activité physique, Faculté de Médecine, Université de Montréal, CEPSUM, 2100, boulevard Édouard Montpetit, Montréal, QC, H3C 3J7, Canada.

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http://dx.doi.org/10.1186/s12885-019-5651-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6515640PMC
May 2019

Doxorubicin treatments induce significant changes on the cardiac autonomic nervous system in childhood acute lymphoblastic leukemia long-term survivors.

Clin Res Cardiol 2019 Sep 18;108(9):1000-1008. Epub 2019 Feb 18.

Laboratoire de Physiopathologie de l'EXercice (LPEX), Département de Kinésiologie, Université de Montréal, CEPSUM, 2100, boulevard Édouard Montpetit, H3C 3J7, Montreal, QC, Canada.

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http://link.springer.com/10.1007/s00392-019-01427-9
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http://dx.doi.org/10.1007/s00392-019-01427-9DOI Listing
September 2019

Molecular Signature of CAID Syndrome: Noncanonical Roles of SGO1 in Regulation of TGF-β Signaling and Epigenomics.

Cell Mol Gastroenterol Hepatol 2019 24;7(2):411-431. Epub 2018 Oct 24.

Cardiovascular Genetics, Department of Pediatrics, Centre Hospitalier Universitaire Sainte Justine Research Center, Université de Montréal, Montréal, Québec, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.jcmgh.2018.10.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6369230PMC
May 2019

Role of Epigenetics in Cardiac Development and Congenital Diseases.

Physiol Rev 2018 10;98(4):2453-2475

Université Aix-Marseille, INSERM UMR- 1251, Marseille , France ; Cardiovascular Genetics, Department of Pediatrics, CHU Sainte-Justine, Montreal, Quebec , Canada ; Université de Montréal, Montreal, Quebec , Canada ; and Laboratoire International Associé INSERM, Marseille France-CHU Ste Justine, Quebec, Canada.

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https://www.physiology.org/doi/10.1152/physrev.00048.2017
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http://dx.doi.org/10.1152/physrev.00048.2017DOI Listing
October 2018

The Power of Rare: An Opportunity to Repurpose an Old Drug for Mitochondrial Cardiomyopathy.

Can J Cardiol 2018 08 27;34(8):950-952. Epub 2018 Apr 27.

Cardiovascular Genetics, CHU Sainte Justine Research Center, Department of Pediatrics, Université de Montréal, Montréal, Québec, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.cjca.2018.04.025DOI Listing
August 2018

Congenital Heart Disease and Neurodevelopment: Clinical Manifestations, Genetics, Mechanisms, and Implications.

Can J Cardiol 2017 12 6;33(12):1543-1555. Epub 2017 Oct 6.

Department of Psychiatry, Seaver Autism Center at Icahn School of Medicine at Mount Sinai, New York, New York, USA. Electronic address:

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http://dx.doi.org/10.1016/j.cjca.2017.09.020DOI Listing
December 2017

Dataset of expression in cardiac, gastrointestinal, hepatic and neuronal tissue in mouse.

Data Brief 2017 Aug 1;13:731-737. Epub 2017 Jul 1.

Cardiovascular Genetics, Department of Pediatrics, CHU Sainte-Justine, Canada.

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http://dx.doi.org/10.1016/j.dib.2017.06.046DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5512188PMC
August 2017

Tissue specific requirements for WNT11 in developing outflow tract and dorsal mesenchymal protrusion.

Dev Biol 2017 09 30;429(1):249-259. Epub 2017 Jun 30.

Skaggs School of Pharmacy and Pharmaceutical Sciences, UCSD, La Jolla, USA; Department of Medicine, UCSD, La Jolla, USA; Department of Pharmacology, UCSD, La Jolla, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ydbio.2017.06.021DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5580348PMC
September 2017

Characterization of Sgo1 expression in developing and adult mouse.

Gene Expr Patterns 2017 11 29;25-26:36-45. Epub 2017 Apr 29.

Cardiovascular Genetics, Department of Pediatrics, CHU Sainte-Justine, Montreal, QC, Canada; Université de Montréal, Montreal, QC, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.gep.2017.04.004DOI Listing
November 2017

Epistatic interaction between the lipase-encoding genes Pnpla2 and Lipe causes liposarcoma in mice.

PLoS Genet 2017 May 1;13(5):e1006716. Epub 2017 May 1.

Division of Medical Genetics, Department of Pediatrics, CHU Sainte-Justine, Université de Montréal, Montréal, Québec, Canada.

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http://dx.doi.org/10.1371/journal.pgen.1006716DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432192PMC
May 2017

KLF13 is a genetic modifier of the Holt-Oram syndrome gene TBX5.

Hum Mol Genet 2017 03;26(5):942-954

Molecular Genetics and Cardiac Regeneration Laboratory, Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, K1N 6N5, Canada.

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http://dx.doi.org/10.1093/hmg/ddx009DOI Listing
March 2017

Genetic testing in congenital heart disease: A clinical approach.

World J Cardiol 2016 Feb;8(2):180-91

Marie A Chaix, Paul Khairy, Montreal Heart Institute Adult Congenital Center, Université de Montréal, Montreal, Quebec H1T 1C8, Canada.

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http://dx.doi.org/10.4330/wjc.v8.i2.180DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766268PMC
February 2016

A Decade of Discovery in the Genetic Understanding of Thoracic Aortic Disease.

Can J Cardiol 2016 Jan 26;32(1):13-25. Epub 2015 Oct 26.

Howard Hughes Medical Institute and Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA; Division of Pediatric Cardiology, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA; Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

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http://dx.doi.org/10.1016/j.cjca.2015.10.017DOI Listing
January 2016

Aortic Dilatation Associated With a De Novo Mutation in the SOX18 Gene: Expanding the Clinical Spectrum of Hypotrichosis-Lymphedema-Telangiectasia Syndrome.

Can J Cardiol 2016 Jan 13;32(1):135.e1-7. Epub 2015 Apr 13.

Cardiovascular Genetics, Department of Pediatrics, CHU Sainte-Justine, Université de Montréal, Montréal, Québec, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.cjca.2015.04.004DOI Listing
January 2016

Cardiology: Race for healthy hearts.

Nature 2015 Apr 1;520(7546):160-1. Epub 2015 Apr 1.

Department of Pediatrics, CHU Sainte Justine Research Center, Université de Montréal, Montreal H3T 1C5, Canada.

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http://dx.doi.org/10.1038/nature14379DOI Listing
April 2015

Next-generation sequencing in congenital heart disease: do new brooms sweep clean?

J Am Coll Cardiol 2014 Dec;64(23):2507-9

Department of Pediatrics, Section of Cardiovascular Genetics, Centre Hospitalier Universitaire Sainte Justine, Université de Montréal, Montréal, Quebec, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.jacc.2014.09.049DOI Listing
December 2014

Adult congenital heart disease: a growing epidemic.

Can J Cardiol 2014 Dec 28;30(12 Suppl):S410-9. Epub 2014 Sep 28.

Montreal Heart Institute Adult Congenital Center, Université de Montréal, Montreal, Quebec, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.cjca.2014.07.749DOI Listing
December 2014

Functional zebrafish studies based on human genotyping point to netrin-1 as a link between aberrant cardiovascular development and thyroid dysgenesis.

Endocrinology 2015 Jan;156(1):377-88

Institute of Interdisciplinary Research in Molecular Human Biology (R.O., I.V., A.T., S.C.), Université Libre de Bruxelles, 1070 Brussels, Belgium; Research Center of Centre Hospitalier Universitaire Sainte-Justine (M.-P.H., I.V., R.A.-K., M.S., G.A., J.D.), Department of Pediatrics, Université de Montréal, Montréal, Québec, Canada H3T 1C5; and Department of Medical Genetics (V.D.), Centre Hospitalier Universitaire de Sherbrooke, Sherbrooke, Canada J1H 1P8.

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https://academic.oup.com/endo/article-lookup/doi/10.1210/en.
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http://dx.doi.org/10.1210/en.2014-1628DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4272402PMC
January 2015

Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythm.

Nat Genet 2014 Nov 5;46(11):1245-9. Epub 2014 Oct 5.

1] Cardiovascular Genetics, Department of Pediatrics, Centre Hospitalier Universitaire Sainte-Justine Research Centre, Université de Montréal, Montreal, Quebec, Canada. [2] Department of Pediatrics, Université de Montréal, Montreal, Quebec, Canada. [3] Department of Biochemistry, Université de Montréal, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1038/ng.3113DOI Listing
November 2014

Subcellular localization of coagulation factor II receptor-like 1 in neurons governs angiogenesis.

Nat Med 2014 Oct 14;20(10):1165-73. Epub 2014 Sep 14.

1] Department of Pediatrics, Centre Hospitalier Universitaire (CHU) Sainte-Justine Research Center, Université de Montréal, Montréal, Québec, Canada. [2] Department of Ophthalmology, Hôpital Maisonneuve-Rosemont Research Center, Université de Montreal, Montreal, Québec, Canada. [3] Department of Pharmacology, Université de Montréal, Montréal, Québec, Canada. [4] Department of Pharmacology and Therapeutics, McGill University, Montréal, Québec, Canada.

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http://dx.doi.org/10.1038/nm.3669DOI Listing
October 2014

Canadian Cardiovascular Society position statement on the management of thoracic aortic disease.

Can J Cardiol 2014 Jun 28;30(6):577-89. Epub 2014 Feb 28.

Division of Cardiology, Western University, London, Ontario, Canada.

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http://dx.doi.org/10.1016/j.cjca.2014.02.018DOI Listing
June 2014

Exome sequencing identifies a novel variant in ACTC1 associated with familial atrial septal defect.

Can J Cardiol 2014 Feb 6;30(2):181-7. Epub 2013 Dec 6.

Department of Cardiac Sciences, University of Calgary and Libin Cardiovascular Institute of Alberta, Calgary, Alberta, Canada; Department of Medical Genetics, University of Calgary, Calgary, Alberta, Canada. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S0828282X130171
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http://dx.doi.org/10.1016/j.cjca.2013.12.003DOI Listing
February 2014

Personalizing the management of heart failure in congenital heart disease: challenges and opportunities.

Pharmacogenomics 2014 Feb;15(2):123-7

Faculty of Pharmacy, Université de Montréal, Montreal, Canada and Montreal Heart Institute, 5000 Belanger Street, Montreal, Quebec H1T 1C8, Canada.

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http://dx.doi.org/10.2217/pgs.13.215DOI Listing
February 2014

[Clinical characteristics and genetic analysis of three pediatric patients with idiopathic restrictive cardiomyopathy].

Zhonghua Xin Xue Guan Bing Za Zhi 2013 Apr;41(4):304-9

Department of Cardiology, Nanjing Children's Hospital, Nanjing Medical University, Nanjing 210008, China.

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April 2013

Genetics of heart failure in congenital heart disease.

Can J Cardiol 2013 Jul 22;29(7):803-10. Epub 2013 May 22.

Service of Cardiology, Centre de Recherche CHU Sainte Justine, Université de Montréal, Montréal, Québec, Canada.

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http://dx.doi.org/10.1016/j.cjca.2013.03.011DOI Listing
July 2013

Prenatal diagnosis of long QT syndrome with the superior vena cava-aorta Doppler approach.

Am J Obstet Gynecol 2012 Oct 7;207(4):e3-7. Epub 2012 Jul 7.

Fetal Cardiology Unit, Department of Pediatrics, Sainte-Justine University Hospital Center, University of Montreal, Montreal, Quebec, Canada.

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https://linkinghub.elsevier.com/retrieve/pii/S00029378120071
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http://dx.doi.org/10.1016/j.ajog.2012.06.058DOI Listing
October 2012

Risk of congenital heart defects is influenced by genetic variation in folate metabolism.

Cardiol Young 2013 Feb 5;23(1):89-98. Epub 2012 Apr 5.

Department of Pediatrics and Human Genetics, McGill University-Montreal Children's Hospital Research Institute, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1017/S1047951112000431DOI Listing
February 2013

Age-dependent recombination rates in human pedigrees.

PLoS Genet 2011 Sep 1;7(9):e1002251. Epub 2011 Sep 1.

Department of Biochemistry, Faculty of Medicine, University of Montreal, Montreal, Canada.

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http://dx.doi.org/10.1371/journal.pgen.1002251DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3164683PMC
September 2011

Loss of Gata5 in mice leads to bicuspid aortic valve.

J Clin Invest 2011 Jul;121(7):2876-87

Program in Molecular Biology, University of Montreal, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1172/JCI44555DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3223824PMC
July 2011

Familial ventricular aneurysms and septal defects map to chromosome 10p15.

Eur Heart J 2011 Mar 18;32(5):568-73. Epub 2010 Dec 18.

Cardiovascular Genetics, Department of Pediatrics, Research Center, Centre Hospitalier Universitaire Sainte Justine, University of Montréal, Montréal, QC, Canada.

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https://academic.oup.com/eurheartj/article-lookup/doi/10.109
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http://dx.doi.org/10.1093/eurheartj/ehq447DOI Listing
March 2011

An endocardial pathway involving Tbx5, Gata4, and Nos3 required for atrial septum formation.

Proc Natl Acad Sci U S A 2010 Nov 25;107(45):19356-61. Epub 2010 Oct 25.

Research Unit in Cardiac Growth and Differentiation and Molecular Biology Program, Université de Montréal, Montréal, QC, Canada H3C 3J7.

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http://www.pnas.org/cgi/doi/10.1073/pnas.0914888107
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http://dx.doi.org/10.1073/pnas.0914888107DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2984205PMC
November 2010

Ventricular septal defect and restrictive cardiomyopathy in a paediatric TNNI3 mutation carrier.

Cardiol Young 2010 Oct 23;20(5):574-6. Epub 2010 Jun 23.

Department of Pediatrics, Sainte Justine Hospital, University of Montréal, Quebec, Canada.

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http://dx.doi.org/10.1017/S1047951110000715DOI Listing
October 2010

Partitioning of copy-number genotypes in pedigrees.

BMC Bioinformatics 2010 May 3;11:226. Epub 2010 May 3.

Montreal Heart Institute Research Center, Montréal, Canada.

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http://dx.doi.org/10.1186/1471-2105-11-226DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2874807PMC
May 2010

Severe left ventricular dysfunction in infants with ventricular preexcitation.

Heart Rhythm 2008 Sep 3;5(9):1320-2. Epub 2008 Aug 3.

Electrophysiology Service, Montreal Heart Institute, University of Montreal, Montreal, Canada.

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http://dx.doi.org/10.1016/j.hrthm.2008.05.022DOI Listing
September 2008

The MTHFD1 p.Arg653Gln variant alters enzyme function and increases risk for congenital heart defects.

Hum Mutat 2009 Feb;30(2):212-20

Department of Pediatrics, McGill University)Montreal Children's Hospital, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1002/humu.20830DOI Listing
February 2009

Genetic interaction between members of the Vangl family causes neural tube defects in mice.

Proc Natl Acad Sci U S A 2008 Mar 22;105(9):3449-54. Epub 2008 Feb 22.

Department of Biochemistry, McGill University, Montreal, QC, Canada H3G 1Y6.

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http://dx.doi.org/10.1073/pnas.0712126105DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2265143PMC
March 2008

Catch me if you can: tracking down the genetic origins of congenital heart disease.

Eur Heart J 2007 Nov 25;28(22):2701-2. Epub 2007 Oct 25.

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http://dx.doi.org/10.1093/eurheartj/ehm479DOI Listing
November 2007

[The aortic valve did not reveal all its secrets].

Med Sci (Paris) 2007 Jan;23(1):93-4

Génétique cardiovasculaire, Hôpital Sainte-Justine, 3175 Côte Sainte-Catherine, Montréal (Québec), H3T 1C5 Canada.

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http://dx.doi.org/10.1051/medsci/200723193DOI Listing
January 2007

Evidence in favor of linkage to human chromosomal regions 18q, 5q and 13q for bicuspid aortic valve and associated cardiovascular malformations.

Hum Genet 2007 Apr 4;121(2):275-84. Epub 2007 Jan 4.

Center for Epidemiology and Biostatistics, University of Cincinnati, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.

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http://link.springer.com/10.1007/s00439-006-0316-9
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http://dx.doi.org/10.1007/s00439-006-0316-9DOI Listing
April 2007

The Kruppel-like transcription factor KLF13 is a novel regulator of heart development.

EMBO J 2006 Nov 19;25(21):5201-13. Epub 2006 Oct 19.

Institut de recherches cliniques de Montréal, Montréal, Quebec, Canada.

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http://dx.doi.org/10.1038/sj.emboj.7601379DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1630408PMC
November 2006

Germ layers to organs: using Xenopus to study "later" development.

Semin Cell Dev Biol 2006 Feb 6;17(1):133-45. Epub 2005 Dec 6.

Department of Developmental and Cell Biology and the Developmental Biology Center, University of California, Irvine, CA 92697, USA, and Division of Pediatric Cardiology, Ste Justine Hospital, Montréal, QC, Canada.

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http://dx.doi.org/10.1016/j.semcdb.2005.11.002DOI Listing
February 2006

Polymorphic ventricular tachycardia and KCNJ2 mutations.

Heart Rhythm 2004 Jul;1(2):235-41

Division of Cardiology, Children's Hospital Medical Center, University of Cincinnati, Cincinnati, Ohio, USA.

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http://dx.doi.org/10.1016/j.hrthm.2004.02.017DOI Listing
July 2004

Genetic analyses in two extended families with deletion 22q11 syndrome: importance of extracardiac manifestations.

J Pediatr 2005 Mar;146(3):382-7

Division of Cardiology, Cincinnati Children's Hospital Medical Center, Ohio 45229-3039, USA.

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http://dx.doi.org/10.1016/j.jpeds.2004.10.038DOI Listing
March 2005

Bicuspid aortic valve is heritable.

J Am Coll Cardiol 2004 Jul;44(1):138-43

Department of Pediatrics, Division of Cardiology, Cincinnati Children's Hospital, Ohio 45229, USA.

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http://dx.doi.org/10.1016/j.jacc.2004.03.050DOI Listing
July 2004

KCNJ2 mutation results in Andersen syndrome with sex-specific cardiac and skeletal muscle phenotypes.

Am J Hum Genet 2002 Sep 29;71(3):663-8. Epub 2002 Jul 29.

Department of Pediatrics, Children's Hospital Medical Center, University of Cincinnati, Cincinnati, OH, 45229, USA.

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http://dx.doi.org/10.1086/342360DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC379203PMC
September 2002