Minjie Luo

Minjie Luo

UNVERIFIED PROFILE

Are you Minjie Luo?   Register this Author

Register author
Minjie Luo

Minjie Luo

Publications by authors named "Minjie Luo"

Are you Minjie Luo?   Register this Author

32Publications

647Reads

23Profile Views

A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing data.

Genome Med 2020 01 30;12(1):14. Epub 2020 Jan 30.

Division of Genomic Diagnostics, Department of Pathology and Laboaratory Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/s13073-020-0712-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6993336PMC
January 2020

Correction: The topoisomerase I- and p53-binding protein topors is differentially expressed in normal and malignant human tissues and may function as a tumor suppressor.

Oncogene 2019 Aug;38(35):6322

Department of Pharmacology, the Cancer Institute of New Jersey, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, New Brunswick, NJ, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/s41388-019-0874-7DOI Listing
August 2019

Sclerosing Epithelioid Fibrosarcoma of the Bone With Rare EWSR1-CREB3L3 Translocation Driving Upregulation of the PI3K/mTOR Signaling Pathway.

Pediatr Dev Pathol 2019 Nov-Dec;22(6):594-598. Epub 2019 Jul 23.

Children's Hospital of Philadelphia, Pathology, Immunology and Laboratory medicine, Philadelphia, Pennsylvania.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/1093526619864230DOI Listing
July 2019

AUDIOME: a tiered exome sequencing-based comprehensive gene panel for the diagnosis of heterogeneous nonsyndromic sensorineural hearing loss.

Genet Med 2018 12 29;20(12):1600-1608. Epub 2018 Mar 29.

Division of Genomic Diagnostics, Department of Pathology and Laboratory Medicine, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/gim.2018.48DOI Listing
December 2018

Heterogeneity of surface CD19 and CD22 expression in B lymphoblastic leukemia.

Am J Hematol 2018 11 9;93(11):E352-E355. Epub 2018 Sep 9.

Department of Pathology and Laboratory Medicine, The Children's Hospital of Philadelphia, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajh.25235DOI Listing
November 2018

Novel FGFR2-INA fusion identified in two low-grade mixed neuronal-glial tumors drives oncogenesis via MAPK and PI3K/mTOR pathway activation.

Acta Neuropathol 2018 07 16;136(1):167-169. Epub 2018 May 16.

Center for Data Driven Discovery in Biomedicine, Children's Hospital of Philadelphia, 3501 Civic Center Boulevard, Philadelphia, PA, 19104, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00401-018-1864-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6015095PMC
July 2018

CMIP haploinsufficiency in two patients with autism spectrum disorder and co-occurring gastrointestinal issues.

Am J Med Genet A 2017 Aug 15;173(8):2101-2107. Epub 2017 May 15.

Division of Genomic Diagnostics, Department of Pathology and Laboratory Medicine, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.38277DOI Listing
August 2017

Phenotypic predictors and final diagnoses in patients referred for RASopathy testing by targeted next-generation sequencing.

Genet Med 2017 06 20;19(6):715-718. Epub 2016 Oct 20.

Division of Genomic Diagnostics and Department of Pathology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/gim.2016.169DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6095193PMC
June 2017

The Genomic Era of Clinical Oncology: Integrated Genomic Analysis for Precision Cancer Care.

Cytogenet Genome Res 2016 22;150(3-4):162-175. Epub 2016 Dec 22.

Division of Genomic Diagnostics, Department of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia and Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000454655DOI Listing
April 2017

Detection of mutually exclusive mosaicism in a girl with genotype-phenotype discrepancies.

Am J Med Genet A 2015 Dec 21;167A(12):3091-5. Epub 2015 Jul 21.

Department of Pathology & Laboratory Medicine, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.37261DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4715567PMC
December 2015

Krüppel-like factor 9 inhibits glioma cell proliferation and tumorigenicity via downregulation of miR-21.

Cancer Lett 2015 Jan 8;356(2 Pt B):547-55. Epub 2014 Oct 8.

Department of Neurosurgery, Institute of Regeneration of Guangdong, Zhujiang Hospital, Southern Medical University, Guangzhou 510282, China. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.canlet.2014.10.007DOI Listing
January 2015

An Ashkenazi Jewish SMN1 haplotype specific to duplication alleles improves pan-ethnic carrier screening for spinal muscular atrophy.

Genet Med 2014 Feb 20;16(2):149-56. Epub 2013 Jun 20.

Department of Genetics and Genomic Sciences, Mount Sinai School of Medicine of New York University, New York, New York, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/gim.2013.84DOI Listing
February 2014

Experience with carrier screening and prenatal diagnosis for 16 Ashkenazi Jewish genetic diseases.

Hum Mutat 2010 Nov;31(11):1240-50

Department of Genetics and Genomic Sciences, Mount Sinai School of Medicine of New York University, New York, NY 10029, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/humu.21327DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970726PMC
November 2010

Mutagenesis in vivo in T cells of p21-deficient mice.

Mutat Res 2009 Nov 8;670(1-2):103-6. Epub 2009 Sep 8.

Department of Genetics, Rutgers University, Piscataway, NJ 08854, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.mrfmmm.2009.09.001DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2767417PMC
November 2009

Genetic structures of copy number variants revealed by genotyping single sperm.

PLoS One 2009 22;4(4):e5236. Epub 2009 Apr 22.

Department of Molecular Genetics, Microbiology, and Immunology/The Cancer Institute of New Jersey, University of Medicine and Dentistry of New Jersey Robert Wood Johnson Medical School, Piscataway, New Jersey, United States of America.

View Article

Download full-text PDF

Source
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0005236PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2668179PMC
June 2009

Lipopolysaccharide (LPS) potentiates hydrogen peroxide toxicity in T98G astrocytoma cells by suppression of anti-oxidative and growth factor gene expression.

BMC Genomics 2008 Dec 16;9:608. Epub 2008 Dec 16.

Department of Molecular Genetics, Microbiology and Immunology/The Cancer Institute of New Jersey, University of Medicine and Dentistry of New Jersey Robert Wood Johnson Medical School, Piscataway, New Jersey 08854, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/1471-2164-9-608DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2631585PMC
December 2008

AccuTyping: new algorithms for automated analysis of data from high-throughput genotyping with oligonucleotide microarrays.

Nucleic Acids Res 2006 18;34(17):e116. Epub 2006 Sep 18.

Department of Molecular Genetics, Microbiology and Immunology, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, SRB 110, 661 Hoes Lane, Piscataway, NJ 08854, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/nar/gkl601DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1635267PMC
November 2006

Strong correlation between meiotic crossovers and haplotype structure in a 2.5-Mb region on the long arm of chromosome 21.

Genome Res 2006 Feb 29;16(2):208-14. Epub 2005 Dec 29.

Department of Molecular Genetics, Microbiology and Immunology, University of Medicine and Dentistry of New Jersey, Robert Wood Johnson Medical School, Piscataway, NJ 08854, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1101/gr.4641706DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1361716PMC
February 2006

A genotyping system capable of simultaneously analyzing >1000 single nucleotide polymorphisms in a haploid genome.

Genome Res 2005 Feb;15(2):276-83

Department of Molecular Genetics, Microbiology and Immunology/The Cancer Institute of New Jersey, Robert Wood Johnson Medical School, New Brunswick, New Jersey 08903, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1101/gr.2885205DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC546529PMC
February 2005

Reg IV, a differentially expressed gene in colorectal adenoma.

Chin Med J (Engl) 2003 Jun;116(6):918-22

Department of Pathology, School of Medicine of Zhejiang University, Hangzhou 310006, China.

View Article

Download full-text PDF

Source
June 2003