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Dr. Iris I Schrijver, MD

Dr. Iris I Schrijver, MD

Pathologist

23 Years of Experience

Accepting patients

    Overview

    Dr. Iris Schrijver, MD is a Pathologist, who primarily practices in Stanford, CA. She has been practicing for over 23 years and is board certified by the American Board of Medical Genetics and American Board of Pathology. Dr. Schrijver graduated from Utrecht University Faculty of Medicine and completed her residency at Stanford Univ Hosp, Anatomic And Clinical Pathology. Dr. Schrijver is fluent in English and is currently seeing new patients. Dr. Schrijver’s practice accepts Blue Cross Blue Shield (BCBS), Cigna, UnitedHealthcare and other major insurance plans. To book an appointment or to confirm insurance options, please call Dr. Schrijver’s office at (650) 724-2403.

    Medical Specialties and Areas of Expertise

    Pathologist

    Education & Training

    Stanford Univ Hosp, Anatomic And Clinical Pathology (Residency)

    Stanford Hospitals and Clinics (Residency)

    Stanford University School of Medicine, Stanford, CA (2000) (Internship)

    Stanford University School of Medicine CA (2000) (Internship)

    Stanford University Medical Center (Residency)

    Stanford Hospital and Clinics Program (Residency)

    Other Degree - Rijksuniversiteit Te Utrecht- Fac Der Geneeskunde- Utrecht- Netherlands

    Other Degree - Universiteit Utrecht

    Medical Degree - Utrecht University Faculty of Medicine

    Medical Degree - University Of Utrecht

    Medical Degree - University Sakartvelo Faculty of Medicine

    Board Certifications

    American Board of Medical Genetics

    American Board of Pathology since 2002

    Insurances

    Top Insurances

    • Blue Cross Blue Shield (BCBS)

    • Cigna

    • UnitedHealthcare

    View All Insurances

    Locations

    Iris Schrijver

    300 Pasteur Dr

    Stanford University, Pathology Department L235

    Stanford, CA 94305

    (650) 724-2403

    Get Directions

    Recognitions

    Awards

    Sheard Sanford Pathology Resident Award, American Society for Clinical

    Lifetime Achievement Award, College of American Pathologists

    Young Clinical Scientist Award Association of Clinical Scientists, As

    Publications

    Gender differences and performance in science

    SCIENCE, 2005

    Evaluation of a Gene Expression Microarray

    AMERICAN JOURL OF SURGICAL PATHOLOGY, 2011

    A two-antibody mismatch repair protein immunohistochemistry screening approach for colorectal

    MODERN PATHOLOGY, 2011

    Allele-Specific Impairment of GJB2 Expression by GJB6 Deletion del(GJB6-D13S1854)

    PLOS ONE, 2011

    Mutation Distribution in Expanded Screening for Cystic Fibrosis

    CLINICAL CHEMISTRY, 2011

    Diagnostic Yield in the Workup of Congenital Sensorineural Hearing Loss Is Dependent on Patient

    OTOLOGY & NEUROTOLOGY, 2011

    Identification of rare D variants in mitochondrial disorders with improved array-based sequencing

    NUCLEIC ACIDS RESEARCH, 2011

    Hereditary diffuse gastric cancer due to a previously undescribed CDH1 splice site mutation

    HUMAN PATHOLOGY, 2010

    Genotyping with a 198 Mutation Arrayed Primer Extension Array for Hereditary Hearing Loss

    PLOS ONE, 2010

    A 30-month-old Child With Acute Rel Failure Due to Primary Rel Cytotoxic T-cell Lymphoma

    AMERICAN JOURL OF SURGICAL PATHOLOGY, 2010

    Combined Use of PCR-Based TCRG

    JOURL OF MOLECULAR DIAGNOSTICS, 2010

    Rare Sequence Variation in the Genome Flanking a Short T

    JOURL OF MOLECULAR DIAGNOSTICS, 2010

    Comprehensive and Efficient HBB Mutation Alysis for Detection of beta-Hemoglobinopathies in a Pan

    AMERICAN JOURL OF CLINICAL PATHOLOGY, 2010

    Connexin-26-associated deafness: Phenotypic variability and progression of hearing loss

    GENETICS IN MEDICINE, 2010

    Design and Evaluation of a Real-Time PCR Assay for Quantification of JAK2 V617F and Wild

    JOURL OF MOLECULAR DIAGNOSTICS, 2010

    The digenic hypothesis unraveled

    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2009

    Development and Characterization of Reference Materials for MTHFR

    JOURL OF MOLECULAR DIAGNOSTICS, 2009

    The role of the cytoskeleton in the formation of gap junctions by Connexin 30

    EXPERIMENTAL CELL RESEARCH, 2009

    Mitochondrial D alysis by multiplex deturing high-performance liquid chromatography

    GENETICS IN MEDICINE, 2009

    Diagnostic Value of a Primer Extension Microarray for Sensorineural Hearing Loss

    Schrijver, I., Rodriguez-Paris, J., Lodahl, M., Khababa, I., PIQUE, L., 2008

    Design and Validation of a Real-Time PCR Assay for Quantification of JAK2 V617F and Wild

    Merker, J. D., Jones, C. D., Oh, S. T., Khan, S., Schrijver, I., Gotli, 2008

    Genetic Alysis of Presbycusis by Arrayed Primer Extension

    ANLS OF CLINICAL AND LABORATORY SCIENCE, 2008

    Multiplex ligation-dependent probe amplification identification of whole exon

    JOURL OF MOLECULAR DIAGNOSTICS, 2008

    Microsatellite instability

    AMERICAN JOURL OF SURGICAL PATHOLOGY, 2008

    Profound functiol and sigling changes in viable inflammatory neutrophils homing to cystic fibrosis

    PROCEEDINGS OF THE TIOL ACADEMY OF SCIENCES OF THE UNITED STATES OF AM, 2008

    Inherited hearing loss: molecular genetics and diagnostic testing.

    Expert opinion on medical diagnostics, 2008

    Interlaboratory performance of a microarray

    JOURL OF MOLECULAR DIAGNOSTICS, 2008

    Identification of an intronic single nucleotide polymorphism leading to allele dropout during

    GENETICS IN MEDICINE, 2007

    T-cell clolity alysis in biopsy specimens from two different skin sites shows high specificity in

    JOURL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2007

    Testing for materl cell contamition in pretal samples

    JOURL OF MOLECULAR DIAGNOSTICS, 2007

    A multicenter study of the frequency and distribution of GJB2 and GJB6 mutations

    GENETICS IN MEDICINE, 2007

    Comprehensive arrayed primer extension array for the detection of 59 sequence variants

    JOURL OF MOLECULAR DIAGNOSTICS, 2007

    Clinical evaluation of a novel oncologic tissue of origin assay based on gene expression microarray

    Schrijver, I., Rodriguez-Paris, J., Zehnder, J. L., Pollack, J. R., 2007

    Two patients with the V371/235delC genotype

    INTERTIOL JOURL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2006

    Simultaneous multigene mutation detection

    PEDIATRICS, 2006

    Detection of the JAK2 V617F mutation by LightCycler PCR and probe dissociation alysis

    JOURL OF MOLECULAR DIAGNOSTICS, 2006

    Hereditary sensorineural hearing loss: advances in molecular genetics and mutation alysis

    EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 2006

    Advanced mutation detection for hereditary sensorineural hearing loss through a comprehensive

    Schrijver, I., Rodriguez-Paris, J., Gardner, P., 2006

    GJB2 mutations and degree of hearing loss: A multicenter study

    AMERICAN JOURL OF HUMAN GENETICS, 2005

    Genotyping microarray for the detection of more than 200 CFTR mutations

    JOURL OF MOLECULAR DIAGNOSTICS, 2005

    Identification of mislabeled specimen by molecular methods: Case report and review

    INTERTIOL JOURL OF SURGICAL PATHOLOGY, 2005

    Diagnostic testing by CFTR gene mutation alysis in a large group of Hispanics novel mutations

    JOURL OF MOLECULAR DIAGNOSTICS, 2005

    High frequency of premature termition mutations in the factor V gene

    THROMBOSIS AND HAEMOSTASIS, 2005

    Novel Contributions to the Asian CFTR mutation spectrum

    Am J Med Genet., 2005

    Hereditary non-syndromic sensorineural hearing loss - Transforming silence to sound

    JOURL OF MOLECULAR DIAGNOSTICS, 2004

    Rapid combined genotyping assay for four achondroplasia

    GENETIC TESTING, 2004

    Prothrombin gene variants in non-Caucasians with fetal loss and intrauterine growth retardation

    JOURL OF MOLECULAR DIAGNOSTICS, 2003

    Diagnostic single nucleotide polymorphism alysis of factor V Leiden

    AMERICAN JOURL OF CLINICAL PATHOLOGY, 2003

    Labor and cost requirements of two commercial assays for qualitative molecular detection of

    JOURL OF CLINICAL MICROBIOLOGY, 2002

    Premature termition mutations in FBN1

    AMERICAN JOURL OF HUMAN GENETICS, 2002

    Homozygous factor V splice site mutation associated with severe factor V deficiency

    BLOOD, 2002

    Spontaneous spil cerebrospil fluid leaks and minor skeletal features of Marfan syndrome

    JOURL OF NEUROSURGERY, 2002

    Novel factor VC2-domain mutation (R2074H) in two families with factor V deficiency and bleeding

    THROMBOSIS AND HAEMOSTASIS, 2002

    Multi-exon deletions of the FBN1 gene in Marfan syndrome.

    BMC medical genetics, 2001

    Cysteine substitutions in epidermal growth factor-like domains of fibrillin-1

    AMERICAN JOURL OF HUMAN GENETICS, 1999

    The pathogenicity of the Pro1148Ala substitution in the FBN1 gene

    HUMAN GENETICS, 1997

    Retil dystrophy in long-chain 3-hydroxy-acyl-CoA dehydrogese deficiency

    Br J Opthalmol, 1997

    Methods-Based Proficiency Testing in Molecular Genetic Pathology

    JOURL OF MOLECULAR DIAGNOSTICS, 2014

    Current landscape and new paradigms of proficiency testing and exterl quality

    Archives of pathology & laboratory medicine, 2013

    Identification of the CFTR p.Phe508Del founder mutation

    CLINICAL GENETICS, 2013

    Integration of Genomic Medicine into Pathology Residency Training The Stanford Open Curriculum

    JOURL OF MOLECULAR DIAGNOSTICS, 2013

    Feasibility of using microbeads with holographic barcodes to track D specimens

    PeerJ, 2013

    Feasibility of Using Microbeads with Holographic Barcodes to Track D Specimens

    Schrijver, I., Gojenola, L., Merker, J. D., O'Grady, N., Dao, M. H., L, 2012

    Opportunities and Challenges Associated with Clinical Diagnostic Genome Sequencing A Report of the

    JOURL OF MOLECULAR DIAGNOSTICS, 2012

    College of American Pathologists' Laboratory St

    Aziz, N., Lynn, B., Driscoll, D., Gibson, J., Grody, W., Hegde, M., Ho, 2012

    Increased incidence of profound biotinidase deficiency among Hispanic newborns in California

    MOLECULAR GENETICS AND METABOLISM, 2012

    Molecular genetic testing for fraglie X syndrome

    GENETICS IN MEDICINE, 2012

    Alysis of the Altertive Splicing of an FGFR2 Transcript Due to a Novel 5 ' Splice Site Mutation

    CLEFT PALATE-CRANIOFACIAL JOURL, 2012

    Allelic discrimition of cis-trans relationships by digital polymerase chain reaction: GJB2 (p.V27I

    GENETICS IN MEDICINE, 2011

    Ultrasensitive Detection of Drug-Resistant Pandemic 2009

    JOURL OF CLINICAL MICROBIOLOGY, 2011

    Cystic Fibrosis Carrier Screening in Obstetric Clinical Practice: Knowledge, Practices

    GENETIC TESTING AND MOLECULAR BIOMARKERS, 2011

    Mutation Alysis of SLC26A4 for Pendred Syndrome

    JOURL OF MOLECULAR DIAGNOSTICS, 2011

    Frequently Asked Questions

    Is Dr. Iris Schrijver accepting new patients?

    Yes, Dr. Iris Schrijver is accepting new patients at this time.

    Does Dr. Iris Schrijver offer online booking?

    Please contact Dr. Schrijver's office at (650) 724-2403 for information about online booking, telehealth, or to schedule an appointment.

    Does Dr. Iris Schrijver offer telehealth appointments?

    Please contact Dr. Schrijver's office at (650) 724-2403 for information telehealth appointment availability or for scheduling assistance.

    Which language(s) does Dr. Iris Schrijver speak?

    Dr. Iris Schrijver speaks English.

    Which board certifications does Dr. Iris Schrijver have?

    Dr. Iris Schrijver is certified by the American Board of Medical Genetics and American Board of Pathology.

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