Associate Professor of Pathology, Brigham and Women's Hospital

Pathology

Bradley Quade practices Pathology. He attended Washington University School of Medicine in St. Louis. Bradley Quade is a published doctor. He published 43 publications, including: 'Involvement of Chromosome 8 in Mllerian Adenosarcoma.' He is registered with Medicare.

Publications

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• Myxoid Leiomyosarcoma of the Uterus: A Clinicopathologic Analysis of 30 Cases and Review of the Literature With Reappraisal of Its Distinction From Other Uterine Myxoi...
• GATA3 expression in gestational trophoblastic tissues and tumours.
• Epithelioid trophoblastic tumor: A single institution case series at the New England Trophoblastic Disease Center.
• Inflammatory Myofibroblastic Tumor of the Uterus: Clinical and Pathologic Review of 10 Cases Including a Subset With Aggressive Clinical Course.
• Targeted Genomic Analysis of Müllerian Adenosarcoma.
• Perivascular epithelioid cell neoplasm (PEComa) of the gynecologic tract: clinicopathologic and immunohistochemical characterization of 16 cases.
• The Value of Re-exploration in Patients with Inadvertently Morcellated Uterine Sarcoma.
• Targeted development of specific biomarkers of endometrial stromal cell differentiation using bioinformatics: the IFITM1 model.
• p-21-Activated Kinase-1, -4 and -6 and Estrogen Receptor Expression Pattern in Normal Placenta and Gestational Trophoblastic Diseases.
• Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries.
• Gap Junction Assembly: Roles for the Formation Plaque and Regulation by the C-Terminus of Connexin43.
• The cell adhesion gene PVRL3 is associated with congenital ocular defects.
• Disseminated peritoneal leiomyomatosis after laparoscopic supracervical hysterectomy with characteristic molecular cytogenetic findings of uterine leiomyoma.
• Identifying the molecular signature of the interstitial deletion 7q subgroup of uterine leiomyomata using a paired analysis.
• Molecular and cytogenetic characterization of plexiform leiomyomata provide further evidence for genetic heterogeneity underlying uterine fibroids.
• Disruption of chromodomain helicase DNA binding protein 2 (CHD2) causes scoliosis.
• Intraplacental choriocarcinoma arising in a second trimester placenta with partial hydatidiform mole.
• Characterization of apparently balanced chromosomal rearrangements from the developmental genome anatomy project.
• Disruption of neurexin 1 associated with autism spectrum disorder.
• Extensive molecular genetic analysis of the 3p14.3 region in patients with Zimmermann-Laband syndrome.
• A spatially and temporally restricted mouse model of soft tissue sarcoma.
• NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects.
• Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux.
• Disruption of diacylglycerol kinase delta (DGKD) associated with seizures in humans and mice.
• Candidate loci for Zimmermann-Laband syndrome at 3p14.3.
• Uterine leiomyomata with deletions of Ip represent a distinct cytogenetic subgroup associated with unusual histologic features.
• Constitutional rearrangement of the architectural factor HMGA2: a novel human phenotype including overgrowth and lipomas.
• Role of K-ras and Pten in the development of mouse models of endometriosis and endometrioid ovarian cancer.
• Uterine leiomyomata with t(10;17) disrupt the histone acetyltransferase MORF.
• Molecular pathogenesis of uterine smooth muscle tumors from transcriptional profiling.
• Focused ultrasound treatment of uterine fibroid tumors: safety and feasibility of a noninvasive thermoablative technique.
• Cervical cancer screening: from the Papanicolaou smear to the vaccine era.
• Human chromosome 7: DNA sequence and biology.
• Fusion transcripts involving HMGA2 are not a common molecular mechanism in uterine leiomyomata with rearrangements in 12q15.
• Biomarkers in diagnostic obstetric and gynecologic pathology: a review.
• MR imaging-guided focused ultrasound surgery of uterine leiomyomas: a feasibility study.
• Intravenous leiomyomatosis is characterized by a der(14)t(12;14)(q15;q24).
• The role of CD10 staining in distinguishing invasive endometrial adenocarcinoma from adenocarcinoma involving adenomyosis.
• p63 Coordinates anogenital modeling and epithelial cell differentiation in the developing female urogenital tract.
• Granulocyte macrophage colony-stimulating factor in adenomyosis and autologous endometrium.
• Intravenous leiomyomatosis: molecular and cytogenetic analysis of a case.
• Involvement of Chromosome 8 in Müllerian Adenosarcoma.

Schools

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• Washington Center School of Medicine

• Brigham and Women39s Hospital

Doctors Specialties

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• Anatomic Pathology
• Pathology

Accepted Insurances

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Education

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• Brigham and Women's Hospital
• Washington University School of Medicine in St. Louis

Hospital

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• Brigham and Women's Hospital

Helpful Reviews

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Medicare Facts

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National Provider Identifier [NPI]	1063429264
Last Name Of The Provider	QUADE
First Name Of The Provider	BRADLEY
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