Kim L McBride

Kim L McBride

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Kim L McBride

Publications by authors named "Kim L McBride"

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Reclassification of Variants of Uncertain Significance in Children with Inherited Arrhythmia Syndromes is Predicted by Clinical Factors.

Pediatr Cardiol 2019 Dec 18;40(8):1679-1687. Epub 2019 Sep 18.

Department of Pediatrics, The Ohio State University College of Medicine, Columbus, OH, USA.

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http://dx.doi.org/10.1007/s00246-019-02203-2DOI Listing
December 2019

A pediatric perspective on genomics and prevention in the twenty-first century.

Pediatr Res 2019 Oct 2. Epub 2019 Oct 2.

Division of Genetic and Genomic Medicine, Nationwide Children's Hospital, Columbus, OH, USA.

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http://dx.doi.org/10.1038/s41390-019-0597-zDOI Listing
October 2019

Phenylalanine and tyrosine measurements across gestation by tandem mass spectrometer on dried blood spot cards from normal pregnant women.

Genet Med 2019 08 10;21(8):1821-1826. Epub 2019 Jan 10.

Division of Genetic and Genomic Medicine, Nationwide Children's Hospital, Columbus, OH, 43205, USA.

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http://dx.doi.org/10.1038/s41436-018-0407-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6620164PMC
August 2019

De novo loss-of-function variants in () associate with a subset of Wolf-Hirschhorn syndrome.

Cold Spring Harb Mol Case Stud 2019 Aug 1;5(4). Epub 2019 Aug 1.

The Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, Ohio 43215, USA.

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http://dx.doi.org/10.1101/mcs.a004044DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6672030PMC
August 2019

Evaluation of biomarkers for Sanfilippo syndrome.

Mol Genet Metab 2019 Sep - Oct;128(1-2):68-74. Epub 2019 May 9.

Genetics and Molecular Pathology, SA Pathology at Women's and Children's Hospital, 72 King William Road, North Adelaide 5006, Australia; School of Medicine, University of Adelaide, Adelaide 5005, Australia. Electronic address:

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http://dx.doi.org/10.1016/j.ymgme.2019.05.005DOI Listing
May 2019

Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).

Genet Med 2018 09 14;20(9):899-909. Epub 2018 Jun 14.

Departments of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, USA.

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http://dx.doi.org/10.1038/s41436-018-0039-zDOI Listing
September 2018

Natural history of echocardiographic abnormalities in mucopolysaccharidosis III.

Mol Genet Metab 2018 06 27;124(2):131-134. Epub 2018 Apr 27.

Center for Gene Therapy, Nationwide Children's Hospital, Columbus, OH, United States; Departments of Pediatrics, Nationwide Children's Hospital, Columbus, OH, United States; Departments of Neurology, The Ohio State University, Columbus, OH, United States.

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http://dx.doi.org/10.1016/j.ymgme.2018.04.010DOI Listing
June 2018

Genetic Evaluation of Cardiomyopathy-A Heart Failure Society of America Practice Guideline.

J Card Fail 2018 May 19;24(5):281-302. Epub 2018 Mar 19.

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana; Department of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana.

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https://linkinghub.elsevier.com/retrieve/pii/S10719164183010
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http://dx.doi.org/10.1016/j.cardfail.2018.03.004DOI Listing
May 2018

Familial co-occurrence of congenital heart defects follows distinct patterns.

Eur Heart J 2018 03;39(12):1015-1022

Wilhelm Johannsen Centre for Functional Genome Research, Department of Cellular and Molecular Medicine, University of Copenhagen, Blegdamsvej 3, DK-2200 Copenhagen, Denmark.

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http://dx.doi.org/10.1093/eurheartj/ehx314DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018923PMC
March 2018

Abnormal Longitudinal Growth of the Aorta in Children with Familial Bicuspid Aortic Valve.

Pediatr Cardiol 2017 Dec 25;38(8):1709-1715. Epub 2017 Sep 25.

Center for Cardiovascular Research, Research Institute at Nationwide Children's Hospital, Columbus, OH, 43205, USA.

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http://dx.doi.org/10.1007/s00246-017-1740-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5798863PMC
December 2017

A cohort study of multiple families with FBN1 p.R650C variant, ectopia lentis, and low but not absent risk for aortopathy.

Am J Med Genet A 2017 Nov 21;173(11):2995-3002. Epub 2017 Sep 21.

The Heart Center, Nationwide Children's Hospital, Columbus, Ohio.

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http://doi.wiley.com/10.1002/ajmg.a.38489
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http://dx.doi.org/10.1002/ajmg.a.38489DOI Listing
November 2017

Modifying Mendel Redux: Unbiased Approaches Can Find Modifiers.

Circ Cardiovasc Genet 2017 10;10(5)

From the Center for Cardiovascular Research (K.L.M.) and Department of Pediatrics, College of Medicine (K.L.M.), Nationwide Children's Hospital, Ohio State University, Columbus; and Departments of Pediatrics and Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis (S.M.W.).

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http://dx.doi.org/10.1161/CIRCGENETICS.117.001891DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5659730PMC
October 2017

General anesthesia with a native airway for patients with mucopolysaccharidosis type III.

Paediatr Anaesth 2017 Apr 8;27(4):370-376. Epub 2017 Feb 8.

Department of Anesthesiology & Pain Medicine, Nationwide Children's Hospital, Columbus, OH, USA.

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http://dx.doi.org/10.1111/pan.13108DOI Listing
April 2017

Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease.

Circ Cardiovasc Genet 2016 Aug 14;9(4):320-9. Epub 2016 Jul 14.

From the Center for Cardiovascular Research, The Research Institute (S.L., M.B., S.F.-B., G.Z., K.B., K.L.M., V.G.), The Heart Center (S.L., M.B., J.L.B., S.F.-B., K.L.M., V.G.), and Biomedical Genomics Core and the Center for Microbial Pathogenesis, The Research Institute (D.C., P.W.), Nationwide Children's Hospital, Columbus, OH; and Department of Molecular Genetics (S.L., V.G.) and Department of Pediatrics (J.L.B., S.F.-B., K.L.M., P.W., V.G.), The Ohio State University, Columbus.

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http://dx.doi.org/10.1161/CIRCGENETICS.115.001324DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412122PMC
August 2016

Lifetime prevalence of sexual intercourse and contraception use at last sex among adolescents and young adults with congenital heart disease.

J Adolesc Health 2015 Apr;56(4):396-401

Center for Cardiovascular and Pulmonary Research, The Research Institute, Nationwide Children's Hospital, Columbus, Ohio; Department of Pediatrics, College of Medicine, The Ohio State University, Columbus, Ohio. Electronic address:

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http://dx.doi.org/10.1016/j.jadohealth.2014.12.013DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4821850PMC
April 2015

Rationale for the Cytogenomics of Cardiovascular Malformations Consortium: A Phenotype Intensive Registry Based Approach.

J Cardiovasc Dev Dis 2015 Apr 29;2(2):76-92. Epub 2015 Apr 29.

Departments of Pediatrics and Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN 46202, USA.

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http://dx.doi.org/10.3390/jcdd2020076DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753096PMC
April 2015

Genetic knowledge and attitudes of parents of children with congenital heart defects.

Am J Med Genet A 2014 Dec 24;164A(12):3069-75. Epub 2014 Sep 24.

Center for Cardiovascular and Pulmonary Research, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio; Department of Pediatrics, College of Medicine, The Ohio State University, Columbus, Ohio.

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http://dx.doi.org/10.1002/ajmg.a.36763DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236279PMC
December 2014

Rare GATA5 sequence variants identified in individuals with bicuspid aortic valve.

Pediatr Res 2014 Aug 5;76(2):211-6. Epub 2014 May 5.

1] Department of Pediatrics, The Ohio State University, Columbus, Ohio [2] Center for Cardiovascular and Pulmonary Research, Nationwide Children's Hospital, Columbus, Ohio [3] The Heart Center, Nationwide Children's Hospital, Columbus, Ohio [4] Department of Molecular Genetics, The Ohio State University, Columbus, Ohio.

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http://dx.doi.org/10.1038/pr.2014.67DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5717758PMC
August 2014

An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.

Authors:
Catherine A Brownstein Alan H Beggs Nils Homer Barry Merriman Timothy W Yu Katherine C Flannery Elizabeth T DeChene Meghan C Towne Sarah K Savage Emily N Price Ingrid A Holm Lovelace J Luquette Elaine Lyon Joseph Majzoub Peter Neupert David McCallie Peter Szolovits Huntington F Willard Nancy J Mendelsohn Renee Temme Richard S Finkel Sabrina W Yum Livija Medne Shamil R Sunyaev Ivan Adzhubey Christopher A Cassa Paul I W de Bakker Hatice Duzkale Piotr Dworzyński William Fairbrother Laurent Francioli Birgit H Funke Monica A Giovanni Robert E Handsaker Kasper Lage Matthew S Lebo Monkol Lek Ignaty Leshchiner Daniel G MacArthur Heather M McLaughlin Michael F Murray Tune H Pers Paz P Polak Soumya Raychaudhuri Heidi L Rehm Rachel Soemedi Nathan O Stitziel Sara Vestecka Jochen Supper Claudia Gugenmus Bernward Klocke Alexander Hahn Max Schubach Mortiz Menzel Saskia Biskup Peter Freisinger Mario Deng Martin Braun Sven Perner Richard J H Smith Janeen L Andorf Jian Huang Kelli Ryckman Val C Sheffield Edwin M Stone Thomas Bair E Ann Black-Ziegelbein Terry A Braun Benjamin Darbro Adam P DeLuca Diana L Kolbe Todd E Scheetz Aiden E Shearer Rama Sompallae Kai Wang Alexander G Bassuk Erik Edens Katherine Mathews Steven A Moore Oleg A Shchelochkov Pamela Trapane Aaron Bossler Colleen A Campbell Jonathan W Heusel Anne Kwitek Tara Maga Karin Panzer Thomas Wassink Douglas Van Daele Hela Azaiez Kevin Booth Nic Meyer Michael M Segal Marc S Williams Gerard Tromp Peter White Donald Corsmeier Sara Fitzgerald-Butt Gail Herman Devon Lamb-Thrush Kim L McBride David Newsom Christopher R Pierson Alexander T Rakowsky Aleš Maver Luca Lovrečić Anja Palandačić Borut Peterlin Ali Torkamani Anna Wedell Mikael Huss Andrey Alexeyenko Jessica M Lindvall Måns Magnusson Daniel Nilsson Henrik Stranneheim Fulya Taylan Christian Gilissen Alexander Hoischen Bregje van Bon Helger Yntema Marcel Nelen Weidong Zhang Jason Sager Lu Zhang Kathryn Blair Deniz Kural Michael Cariaso Greg G Lennon Asif Javed Saloni Agrawal Pauline C Ng Komal S Sandhu Shuba Krishna Vamsi Veeramachaneni Ofer Isakov Eran Halperin Eitan Friedman Noam Shomron Gustavo Glusman Jared C Roach Juan Caballero Hannah C Cox Denise Mauldin Seth A Ament Lee Rowen Daniel R Richards F Anthony San Lucas Manuel L Gonzalez-Garay C Thomas Caskey Yu Bai Ying Huang Fang Fang Yan Zhang Zhengyuan Wang Jorge Barrera Juan M Garcia-Lobo Domingo González-Lamuño Javier Llorca Maria C Rodriguez Ignacio Varela Martin G Reese Francisco M De La Vega Edward Kiruluta Michele Cargill Reece K Hart Jon M Sorenson Gholson J Lyon David A Stevenson Bruce E Bray Barry M Moore Karen Eilbeck Mark Yandell Hongyu Zhao Lin Hou Xiaowei Chen Xiting Yan Mengjie Chen Cong Li Can Yang Murat Gunel Peining Li Yong Kong Austin C Alexander Zayed I Albertyn Kym M Boycott Dennis E Bulman Paul M K Gordon A Micheil Innes Bartha M Knoppers Jacek Majewski Christian R Marshall Jillian S Parboosingh Sarah L Sawyer Mark E Samuels Jeremy Schwartzentruber Isaac S Kohane David M Margulies

Genome Biol 2014 Mar 25;15(3):R53. Epub 2014 Mar 25.

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http://dx.doi.org/10.1186/gb-2014-15-3-r53DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4073084PMC
March 2014

Understanding of informed consent by parents of children enrolled in a genetic biobank.

Genet Med 2014 Feb 27;16(2):141-8. Epub 2013 Jun 27.

1] Center for Cardiovascular and Pulmonary Research, Nationwide Children's Hospital, Columbus, Ohio, USA [2] Department of Pediatrics, College of Medicine, The Ohio State University, Columbus, Ohio, USA.

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http://www.nature.com/articles/gim201386
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http://dx.doi.org/10.1038/gim.2013.86DOI Listing
February 2014

Neurodevelopmental disorders among individuals with duplication of 4p13 to 4p12 containing a GABAA receptor subunit gene cluster.

Eur J Hum Genet 2014 Jan 22;22(1):105-9. Epub 2013 May 22.

1] Division of Molecular and Human Genetics, The Research Institute, Nationwide Children's Hospital, Columbus, OH, USA [2] Department of Pediatrics, The Ohio State University, Columbus, OH, USA [3] Center for Cardiovascular and Pulmonary Research, The Research Institute, Nationwide Children's Hospital, Columbus, OH, USA.

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http://dx.doi.org/10.1038/ejhg.2013.99DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3865421PMC
January 2014

Successful Medical Therapy for Hypophosphatemic Rickets due to Mitochondrial Complex I Deficiency Induced de Toni-Debré-Fanconi Syndrome.

Case Rep Pediatr 2013 10;2013:354314. Epub 2013 Dec 10.

Center for Cardiovascular and Pulmonary Research, Department of Pediatrics, Nationwide Children's Hospital, The Ohio State University College of Medicine, Columbus, OH 43205, USA.

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http://dx.doi.org/10.1155/2013/354314DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3872385PMC
January 2014

Genetic abnormalities in FOXP1 are associated with congenital heart defects.

Hum Mutat 2013 Sep 11;34(9):1226-30. Epub 2013 Jul 11.

Center for Cardiovascular and Pulmonary Research and The Heart Center, Nationwide Children's Hospital, Columbus, Ohio, USA.

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http://dx.doi.org/10.1002/humu.22366DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5717756PMC
September 2013

Severe hypertrophic cardiomyopathy in Noonan syndrome-consider sequencing genes encoding sarcomeric proteins.

Authors:
Kim L McBride

Am J Med Genet A 2013 Jan 13;161A(1):230-1. Epub 2012 Dec 13.

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http://dx.doi.org/10.1002/ajmg.a.35669DOI Listing
January 2013

Cardiac teratogenicity in mouse maternal phenylketonuria: defining phenotype parameters and genetic background influences.

Mol Genet Metab 2012 Dec 8;107(4):650-8. Epub 2012 Aug 8.

Center for Molecular and Human Genetics, Nationwide Children's Hospital, USA.

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http://linkinghub.elsevier.com/retrieve/pii/S109671921200301
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http://dx.doi.org/10.1016/j.ymgme.2012.08.001DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504168PMC
December 2012

Pediatric sub-specialist controversies in the treatment of congenital heart disease in trisomy 13 or 18.

J Genet Couns 2011 Oct 18;20(5):495-509. Epub 2011 May 18.

Nationwide Children's Hospital and Research Institute, Columbus, OH, USA.

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http://dx.doi.org/10.1007/s10897-011-9373-xDOI Listing
October 2011

Heredity of bicuspid aortic valve: is family screening indicated?

Heart 2011 Aug 1;97(15):1193-5. Epub 2011 Apr 1.

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http://dx.doi.org/10.1136/hrt.2011.222489DOI Listing
August 2011

Rebuttal to the invited comment of Opitz and Carey.

Authors:
Kim L McBride

Am J Med Genet A 2011 Aug 7;155A(8):2037-8. Epub 2011 Jul 7.

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http://dx.doi.org/10.1002/ajmg.a.34112DOI Listing
August 2011

Association of common variants in ERBB4 with congenital left ventricular outflow tract obstruction defects.

Birth Defects Res A Clin Mol Teratol 2011 Mar 2;91(3):162-8. Epub 2011 Feb 2.

Center for Molecular and Human Genetics, Nationwide Children's Hospital, Department of Pediatrics, Ohio State University, Columbus, Ohio 43205, USA.

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http://dx.doi.org/10.1002/bdra.20764DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3736588PMC
March 2011

Novel X-linked glomerulopathy is associated with a COL4A5 missense mutation in a non-collagenous interruption.

Kidney Int 2011 Jan 29;79(1):120-7. Epub 2010 Sep 29.

Department of Pediatrics, College of Medicine and Public Health, The Ohio State University, Columbus, Ohio 43205, USA.

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http://dx.doi.org/10.1038/ki.2010.354DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3248803PMC
January 2011

NOTCH1 missense alleles associated with left ventricular outflow tract defects exhibit impaired receptor processing and defective EMT.

Biochim Biophys Acta 2011 Jan 14;1812(1):121-9. Epub 2010 Oct 14.

Department of Molecular Genetics, Ohio State University, Columbus, OH, USA.

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http://dx.doi.org/10.1016/j.bbadis.2010.10.002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180902PMC
January 2011

Impact of Mendelian inheritance in cardiovascular disease.

Ann N Y Acad Sci 2010 Dec 19;1214:122-37. Epub 2010 Oct 19.

Departments of Pediatrics, The Ohio State University College of Medicine, Columbus, Ohio, USA.

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http://doi.wiley.com/10.1111/j.1749-6632.2010.05791.x
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http://dx.doi.org/10.1111/j.1749-6632.2010.05791.xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3489013PMC
December 2010

Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephaly.

Autism Res 2010 Jun;3(3):137-41

Center for Molecular and Human Genetics, Research Institute at Nationwide Children's Hospital, Columbus, Ohio 43205, USA.

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http://dx.doi.org/10.1002/aur.132DOI Listing
June 2010

Parental knowledge and attitudes toward hypertrophic cardiomyopathy genetic testing.

Pediatr Cardiol 2010 Feb 1;31(2):195-202. Epub 2009 Dec 1.

Center for Molecular and Human Genetics, The Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.

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http://link.springer.com/10.1007/s00246-009-9583-2
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http://dx.doi.org/10.1007/s00246-009-9583-2DOI Listing
February 2010

Significant contributions of the extraembryonic membranes and maternal genotype to the placental pathology in heterozygous Nsdhl deficient female embryos.

Hum Mol Genet 2010 Jan 30;19(2):364-73. Epub 2009 Oct 30.

Department of Pediatrics, The Research Institute at Nationwide Children's Hospital, The Ohio State University, Columbus, OH 43205, USA.

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http://dx.doi.org/10.1093/hmg/ddp502DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2796896PMC
January 2010

Acute dilated cardiomyopathy in a patient with deficiency of long-chain 3-hydroxyacyl-CoA dehydrogenase.

Pediatr Cardiol 2009 May 16;30(4):523-6. Epub 2008 Dec 16.

Department of Pediatrics, Nationwide Children's Hospital Heart Center, Columbus, OH 43205-2696, USA.

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http://dx.doi.org/10.1007/s00246-008-9351-8DOI Listing
May 2009

The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly.

Genet Med 2009 Feb;11(2):111-7

Center for Molecular and Human Genetics, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio 43205, USA.

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http://dx.doi.org/10.1097/GIM.0b013e31818fd762DOI Listing
February 2009

NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling.

Hum Mol Genet 2008 Sep 30;17(18):2886-93. Epub 2008 Jun 30.

Center for Molecular and Human Genetics, The Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.

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http://dx.doi.org/10.1093/hmg/ddn187DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2722892PMC
September 2008

Genetic testing in autism: how much is enough?

Genet Med 2007 May;9(5):268-74

Center for Molecular and Human Genetics, Columbus Children's Research Institute, Columbus, Ohio 43205, USA.

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http://dx.doi.org/10.1097/gim.0b013e31804d683bDOI Listing
May 2007

Heritability of plasma amino acid levels in different nutritional states.

Mol Genet Metab 2007 Feb 26;90(2):217-20. Epub 2006 Sep 26.

Center for Molecular and Human Genetics, Columbus Children's Research Institute, Department of Pediatrics, The Ohio State University, Columbus, OH 43205, USA.

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http://dx.doi.org/10.1016/j.ymgme.2006.08.010DOI Listing
February 2007

Renal anomalies in family members of infants with bilateral renal agenesis/adysplasia.

Pediatr Nephrol 2007 Jan 15;22(1):52-6. Epub 2006 Sep 15.

Division of Nephrology, Department of Pediatrics, Columbus Children's Hospital, The Ohio State University College of Medicine, 700 Children's Drive, Columbus, OH 43205, USA.

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http://dx.doi.org/10.1007/s00467-006-0295-zDOI Listing
January 2007

Idursulfase: enzyme replacement therapy for mucopolysaccharidosis Type II (Hunter syndrome).

Authors:
Kim L McBride

Expert Rev Endocrinol Metab 2007 Jan;2(1):19-26

a Investigator, Columbus Children's Research Institute, and Assistant Professor, Department of Pediatrics, College of Medicine, The Ohio State University, 700 Children's Drive, Columbus, OH 43205, USA.

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http://dx.doi.org/10.1586/17446651.2.1.19DOI Listing
January 2007

Genome-wide linkage scan for spontaneous DZ twinning.

Eur J Hum Genet 2006 Jan;14(1):117-22

Department of Human Genetics, University Hospital Gasthuisberg, Katholieke Universiteit Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1038/sj.ejhg.5201522DOI Listing
January 2006

Cardiovascular genetics clinics.

Am J Med Genet A 2005 Jun;135(2):229

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http://dx.doi.org/10.1002/ajmg.a.30657DOI Listing
June 2005

A family-based association study of congenital left-sided heart malformations and 5,10 methylenetetrahydrofolate reductase.

Birth Defects Res A Clin Mol Teratol 2004 Oct;70(10):825-30

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA.

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http://doi.wiley.com/10.1002/bdra.20049
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http://dx.doi.org/10.1002/bdra.20049DOI Listing
October 2004

Case 27-2002: late-onset infantile neuronal ceroid lipofuscinosis.

Authors:
Kim L McBride

N Engl J Med 2003 May;348(21):2159

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http://dx.doi.org/10.1056/NEJM200305223482124DOI Listing
May 2003

Aortoesophageal fistula in a 13-yr-old girl: complication after nasogastric tube placement in the setting of right-sided aortic arch.

Pediatr Crit Care Med 2002 Oct;3(4):378-80

Department of Pediatrics and Pathology, Mayo Clinic and Mayo Foundation, Rochester, MN 55905, USA.

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http://dx.doi.org/10.1097/00130478-200210000-00011DOI Listing
October 2002