Publications by authors named "Iris Schrijver"

95Publications

A panoramic view of the accuracy of molecular genetic testing.

Genet Med 2016 12 18;18(12):1188-1189. Epub 2016 Aug 18.

Department of Pathology, Stanford University School of Medicine, Stanford, California, USA.

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December 2016

Cystic fibrosis newborn screening programs: implications of the CFTR variant spectrum in nonwhite patients.

Genet Med 2017 01 5;19(1):36-44. Epub 2016 May 5.

Department of Pathology, Stanford University Medical Center, Stanford, California, USA.

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January 2017

An exploration of key issues and potential solutions that impact physician wellbeing and professional fulfillment at an academic center.

PeerJ 2016 10;4:e1783. Epub 2016 Mar 10.

Department of Psychiatry & Behavioral Sciences, Stanford University School of Medicine , Stanford, CA , United States.

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March 2016

Next-Generation Molecular Testing of Newborn Dried Blood Spots for Cystic Fibrosis.

J Mol Diagn 2016 Mar 1;18(2):267-82. Epub 2016 Feb 1.

Department of Pathology, Stanford University Medical Center, Stanford, California; Stanford Genome Technology Center, Stanford University, Palo Alto, California. Electronic address:

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March 2016

Pathology in the Medical Profession?: Taking the Pulse of Physician Wellness and Burnout.

Authors:
Iris Schrijver

Arch Pathol Lab Med 2016 Sep 1;140(9):976-82. Epub 2016 Feb 1.

From the Departments of Pathology and Pediatrics, Stanford University School of Medicine, Stanford, California.

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September 2016

The Spectrum of CFTR Variants in Nonwhite Cystic Fibrosis Patients: Implications for Molecular Diagnostic Testing.

J Mol Diagn 2016 Jan;18(1):39-50

Environmental Health Investigations Branch, California Department of Public Health, Richmond, California.

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January 2016

Cystic Fibrosis: A Review of Associated Phenotypes, Use of Molecular Diagnostic Approaches, Genetic Characteristics, Progress, and Dilemmas.

J Mol Diagn 2016 Jan 26;18(1):3-14. Epub 2015 Nov 26.

Department of Pathology, Stanford University Medical Center, Stanford, California; Department of Pediatrics, Stanford University Medical Center, Stanford, California. Electronic address:

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January 2016

Lymph node involvement by mycosis fungoides and Sézary syndrome mimicking angioimmunoblastic T-cell lymphoma.

Hum Pathol 2015 Sep 10;46(9):1382-9. Epub 2015 Jun 10.

Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305. Electronic address:

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September 2015

The Evolving Role of the Laboratory Professional in the Age of Genome Sequencing: A Vision of the Association for Molecular Pathology.

J Mol Diagn 2015 Jul 2;17(4):335-8. Epub 2015 Jun 2.

Association for Molecular Pathology (AMP) Executive Committee, Bethesda, Maryland; AMP Whole Genome Analysis Working Group, Bethesda, Maryland; Department of Pathology, University of Utah School of Medicine, Salt Lake City, Utah.

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July 2015

Assessment of epithelial sodium channel variants in nonwhite cystic fibrosis patients with non-diagnostic CFTR genotypes.

J Cyst Fibros 2016 Jan 18;15(1):52-9. Epub 2015 Apr 18.

Department of Pathology, Stanford University Medical Center, Stanford, CA 94305, USA; Department of Pediatrics, Stanford University Medical Center, Stanford, CA 94305, USA. Electronic address:

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January 2016

Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss.

BMC Genomics 2014 Dec 20;15:1155. Epub 2014 Dec 20.

Department of Genetics, Stanford University School of Medicine, 300 Pasteur Dr,, M-344A, Stanford, CA 94305, USA.

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December 2014

A Balanced Look at the Implications of Genomic (and Other "Omics") Testing for Disease Diagnosis and Clinical Care.

Genes (Basel) 2014 Sep 1;5(3):748-66. Epub 2014 Sep 1.

Department of Pathology, Stanford University, Stanford, CA 94305, USA.

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September 2014

College of American Pathologists' laboratory standards for next-generation sequencing clinical tests.

Arch Pathol Lab Med 2015 Apr 25;139(4):481-93. Epub 2014 Aug 25.

From Molecular Medicine (Dr Aziz), Laboratory Improvement Programs (Dr Zhao and Ms Palicki), and Laboratory Accreditation and Regulatory Affairs (Ms Driscoll), College of American Pathologists, Northfield, Illinois; the Department of Pathology, Brigham & Women's Hospital, Harvard Medical School, Boston, Massachusetts (Dr Bry); the Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts (Dr Funke); the Department of Clinical Sciences, University of Central Florida College of Medicine, Orlando (Dr Gibson); the Divisions of Medical Genetics and Molecular Diagnostics, Department of Pathology & Laboratory Medicine, Pediatrics, and Human Genetics, UCLA School of Medicine, UCLA Institute for Society and Genetics, Molecular Diagnostic Laboratories and Clinical Genomics Center, UCLA Medical Center, Los Angeles, California (Dr Grody); the Department of Human Genetics, Emory University School of Medicine, Decatur, Georgia (Dr Hegde); Robert J. Tomsich Pathology & Laboratory Medicine Institute, Cleveland Clinic, Cleveland, Ohio (Dr Hoeltge); the Department of Pathology, University of Vermont College of Medicine, Burlington (Dr Leonard); the Departments of Pathology (Drs Merker and Schrijver) and Pediatrics (Dr Schrijver), Stanford University School of Medicine, Stanford, California; the Department of Pathology & Immunology, Washington University School of Medicine, St Louis, Missouri (Dr Nagarajan); the Department of Laboratory Medicine & Pathology, Mayo Clinic in Arizona, Phoenix (Dr Robetorye); the Departments of Pathology & Laboratory Medicine and Genetics, University of North Carolina at Chapel Hill, Chapel Hill (Dr Weck); and ARUP Laboratories Institute for Clinical and Experimental Pathology, and Department of Pathology, University of Utah School of Medicine, Salt Lake City (Dr Voelkerding). Dr Aziz is now with Phoenix Children's Hospital, Phoenix, Arizona.

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April 2015

Molecular genetic testing for cystic fibrosis: laboratory performance on the College of American Pathologists external proficiency surveys.

Genet Med 2015 Mar 31;17(3):219-25. Epub 2014 Jul 31.

Department of Pathology and Laboratory Medicine, Women & Infants Hospital, Alpert Medical School, Brown University, Providence, Rhode Island, USA.

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March 2015

Mutation analysis of the SLC26A4, FOXI1 and KCNJ10 genes in individuals with congenital hearing loss.

PeerJ 2014 8;2:e384. Epub 2014 May 8.

Department of Pathology, Stanford University Medical Center , Stanford, CA , USA ; Department of Pediatrics, Stanford University Medical Center , Stanford, CA , USA.

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May 2014

Progress and potential: training in genomic pathology.

Arch Pathol Lab Med 2014 Apr;138(4):498-504

From the Department of Pathology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts (Dr Haspel); the Department of Pathology and Genomic Medicine, The Methodist Hospital, Houston, Texas (Dr Olsen); the Department of Pathology, University of California San Francisco, San Francisco (Dr Berry); the Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia (Dr Hill); the Department of Pathology, Washington University, St Louis, Missouri (Dr Pfeifer); the Departments of Pathology and Pediatrics and the Center for Genomics and Personalized Medicine, Stanford University Medical Center, Stanford, California (Dr Schrijver); and the Department of Pathology and Laboratory Medicine, NorthShore University HealthSystem, Evanston, Illinois (Dr Kaul).

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April 2014