Kandamurugu Manickam

Kandamurugu Manickam

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Kandamurugu Manickam

Kandamurugu Manickam

Publications by authors named "Kandamurugu Manickam"

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27Publications

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

Pediatr Res 2020 Jan 2;87(2):338-344. 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
January 2020

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

COL4A1 Mutation in a Neonate With Intrauterine Stroke and Anterior Segment Dysgenesis.

Pediatr Neurol 2017 01 24;66:100-103. Epub 2016 Apr 24.

Nationwide Children's Hospital, Columbus, Ohio; Department of Pediatrics, Ohio State University, Columbus, Ohio; Center for Perinatal Research, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio. Electronic address:

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http://dx.doi.org/10.1016/j.pediatrneurol.2016.04.010DOI Listing
January 2017

Reciprocal deletion and duplication at 2q23.1 indicates a role for MBD5 in autism spectrum disorder.

Eur J Hum Genet 2014 Jan 1;22(1):57-63. Epub 2013 May 1.

1] Department of Human and Molecular Genetics, Virginia Commonwealth University School of Medicine, Richmond, VA, USA [2] Department of Pediatrics, Virginia Commonwealth University School of Medicine, Richmond, VA, USA [3] Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.

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http://dx.doi.org/10.1038/ejhg.2013.67DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3865402PMC
January 2014

Suppression of severe achondroplasia with developmental delay and acanthosis nigricans by the p.Thr651Pro mutation.

Am J Med Genet A 2014 Jan 29;164A(1):243-50. Epub 2013 Oct 29.

Section of Human and Molecular Genetics, Nationwide Children's Hospital, Columbus, Ohio.

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http://dx.doi.org/10.1002/ajmg.a.36236DOI Listing
January 2014

The Pharmacogenomics Research Network Translational Pharmacogenetics Program: overcoming challenges of real-world implementation.

Clin Pharmacol Ther 2013 Aug 19;94(2):207-10. Epub 2013 Mar 19.

Program in Personalized and Genomic Medicine and Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland, USA.

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http://dx.doi.org/10.1038/clpt.2013.59DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3720847PMC
August 2013

Direct-to-consumer personal genomic testing: a case study and practical recommendations for “genomic counseling”.

J Genet Couns 2012 Jun;21(3):402-412

Division of Human Genetics, Department of Internal Medicine, The Ohio State University Medical Center, Columbus, OH, USA.

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http://dx.doi.org/10.1007/s10897-012-9489-7DOI Listing
June 2012

Validation of My Family Health Portrait for six common heritable conditions.

Genet Med 2010 Jun;12(6):370-5

National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.

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http://dx.doi.org/10.1097/GIM.0b013e3181e15bd5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3258571PMC
June 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