Linda Jo Jeng

Linda Jo Bone Jeng

UNVERIFIED PROFILE

Are you Linda Jo Bone Jeng?   Register this Author

Register author
Linda Jo Jeng

Linda Jo Bone Jeng

Publications by authors named "Linda Jo Bone Jeng"

10Publications

307Reads

46Profile Views

1PubMed Central Citations

An openly available online tool for implementing the ACMG/AMP standards and guidelines for the interpretation of sequence variants.

Genet Med 2016 11 17;18(11):1165. Epub 2016 Mar 17.

Program for Personalized and Genomic Medicine, Division of Endocrinology, Diabetes and Nutrition, Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/gim.2016.13DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5026899PMC
November 2016

User-centered design of multi-gene sequencing panel reports for clinicians.

J Biomed Inform 2016 10 14;63:1-10. Epub 2016 Jul 14.

Program for Personalized and Genomic Medicine, University of Maryland School of Medicine, Baltimore, MD, United States; Division of Health Sciences Informatics, Johns Hopkins University School of Medicine, United States; Division of General Internal Medicine, Johns Hopkins University School of Medicine, United States. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jbi.2016.07.014DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5106875PMC
October 2016

Haploinsufficiency and triploinsensitivity of the same 6p25.1p24.3 region in a family.

BMC Med Genomics 2015 Jul 15;8:38. Epub 2015 Jul 15.

Department of Laboratory Medicine, University of California San Francisco, San Francisco, CA, 94107, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/s12920-015-0113-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4502905PMC
July 2015

Reporting incidental findings in genomic scale clinical sequencing--a clinical laboratory perspective: a report of the Association for Molecular Pathology.

J Mol Diagn 2015 Mar 12;17(2):107-17. Epub 2015 Feb 12.

Incidental Findings Working Group of the Association for Molecular Pathology (AMP) Clinical Practice Committee and the Whole Genome Analysis Working Group, Bethesda, Maryland; Department of Pathology, University of Utah School of Medicine, Salt Lake City, Utah; Department of Molecular Genetics, ARUP Laboratories, Salt Lake City, Utah.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jmoldx.2014.10.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5707203PMC
March 2015

Low-level mosaicism of trisomy 14: phenotypic and molecular characterization.

Am J Med Genet A 2008 Jun;146A(11):1395-405

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

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.32287DOI Listing
June 2008

The effects of a dominant connexin32 mutant in myelinating Schwann cells.

Mol Cell Neurosci 2006 Jul 21;32(3):283-98. Epub 2006 Jun 21.

Cell and Molecular Biology Graduate Group, The University of Pennsylvania Medical Center, Philadelphia, PA 19104-6077, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.mcn.2006.05.001DOI Listing
July 2006

Transgenic expression of human connexin32 in myelinating Schwann cells prevents demyelination in connexin32-null mice.

J Neurosci 2005 Feb;25(6):1550-9

Department of Neurology and Cell and Molecular Biology Graduate Group, The University of Pennsylvania Medical Center, Philadelphia, Pennsylvania 19104-6077, USA.

View Article

Download full-text PDF

Source
http://www.jneurosci.org/cgi/doi/10.1523/JNEUROSCI.3082-04.2
Publisher Site
http://dx.doi.org/10.1523/JNEUROSCI.3082-04.2005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6725992PMC
February 2005