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Methylation in Predicting Progression of Untreated High-grade Cervical Intraepithelial Neoplasia

Clinical infectious diseases, 2020-06, Vol.70 (12), p.2582-2590

2020

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Characterization of MED12, HMGA2, and FH alterations reveals molecular variability in uterine smooth muscle tumors

Molecular cancer, 2017-06, Vol.16 (1), p.101-101, Article 101

2017

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Exome Sequencing of Uterine Leiomyosarcomas Identifies Frequent Mutations in TP53, ATRX, and MED12

PLoS genetics, 2016-02, Vol.12 (2), p.e1005850-e1005850

2016

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Activation of vestibule-associated lymphoid tissue in localized provoked vulvodynia

American journal of obstetrics and gynecology, 2015-04, Vol.212 (4), p.476.e1-476.e8

2015

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Exome sequencing identifies FANCM as a susceptibility gene for triple-negative breast cancer

Proceedings of the National Academy of Sciences - PNAS, 2014-10, Vol.111 (42), p.15172-15177

2014

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Clinical factors as prognostic variables among molecular subgroups of endometrial cancer

PloS one, 2020-11, Vol.15 (11), p.e0242733-e0242733

2020

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Distinct expression levels and patterns of stem cell marker, aldehyde dehydrogenase isoform 1 (ALDH1), in human epithelial cancers

PloS one, 2010-04, Vol.5 (4), p.e10277-e10277

2010

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Glucocorticoids induce differentiation and chemoresistance in ovarian cancer by promoting ROR1-mediated stemness

Cell death & disease, 2020-09, Vol.11 (9), p.790-790, Article 790

2020

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The FOXL2 C134W mutation is characteristic of adult granulosa cell tumors of the ovary

Modern pathology, 2010-11, Vol.23 (11), p.1477-1485

2010

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Double-Negative Feedback Loop between Reprogramming Factor LIN28 and microRNA let-7 Regulates Aldehyde Dehydrogenase 1-Positive Cancer Stem Cells

Cancer research (Chicago, Ill.), 2010-11, Vol.70 (22), p.9463-9472

2010

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Identification of six new susceptibility loci for invasive epithelial ovarian cancer

Nature genetics, 2015-02, Vol.47 (2), p.164-171

2015

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GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer

Nature genetics, 2013-04, Vol.45 (4), p.362-370

2013

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Characteristics and outcome of recurrence in molecularly defined adult-type ovarian granulosa cell tumors

Gynecologic oncology, 2016-12, Vol.143 (3), p.571-577

2016

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Comparison of 2SC, AKR1B10, and FH Antibodies as Potential Biomarkers for FH-deficient Uterine Leiomyomas

The American journal of surgical pathology, 2022-04, Vol.46 (4), p.537

2022

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Clinicopathological significance of deficient DNA mismatch repair and MLH1 promoter methylation in endometrioid endometrial carcinoma

Modern pathology, 2020-07, Vol.33 (7), p.1443-1452

2020

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3′RNA and whole‐genome sequencing of archival uterine leiomyomas reveal a tumor subtype with chromosomal rearrangements affecting either HMGA2, HMGA1, or PLAG1

Genes chromosomes & cancer, 2023-01, Vol.62 (1), p.27-38

2023

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Inherited mutations affecting the SRCAP complex are central in moderate-penetrance predisposition to uterine leiomyomas

American journal of human genetics, 2023-03, Vol.110 (3), p.460-474

2023

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Molecular Subtypes of Breast Cancers Detected in Mammography Screening and Outside of Screening

Clinical cancer research, 2008-07, Vol.14 (13), p.4103-4110

2008

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Multiple clinical characteristics separate MED12-mutation-positive and -negative uterine leiomyomas

Scientific reports, 2017-04, Vol.7 (1), p.1015-7, Article 1015

2017

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RAD51C is a susceptibility gene for ovarian cancer

Human molecular genetics, 2011-08, Vol.20 (16), p.3278-3288

2011

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Molecular subclass of uterine fibroids predicts tumor shrinkage in response to ulipristal acetate

Human molecular genetics, 2023-03, Vol.32 (7), p.1063-1071

2023

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MED12 exon 2 mutations in histopathological uterine leiomyoma variants

European journal of human genetics : EJHG, 2013-11, Vol.21 (11), p.1300-1303

2013

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STRN-ALK rearranged pediatric malignant peritoneal mesothelioma – Functional testing of 527 cancer drugs in patient-derived cancer cells

Translational oncology, 2021-04, Vol.14 (4), p.101027-101027, Article 101027

2021

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Altered glycosylation of glycodelin in endometrial carcinoma

Laboratory investigation, 2020-07, Vol.100 (7), p.1014-1025

2020

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A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk

Cancer research (Chicago, Ill.), 2018-09, Vol.78 (18), p.5419-5430

2018

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Methylation in Predicting Progression of Untreated High-grade Cervical Intraepithelial Neoplasia

Characterization of MED12, HMGA2, and FH alterations reveals molecular variability in uterine smooth muscle tumors

Exome Sequencing of Uterine Leiomyosarcomas Identifies Frequent Mutations in TP53, ATRX, and MED12

Activation of vestibule-associated lymphoid tissue in localized provoked vulvodynia

Exome sequencing identifies FANCM as a susceptibility gene for triple-negative breast cancer

Clinical factors as prognostic variables among molecular subgroups of endometrial cancer

Distinct expression levels and patterns of stem cell marker, aldehyde dehydrogenase isoform 1 (ALDH1), in human epithelial cancers

Glucocorticoids induce differentiation and chemoresistance in ovarian cancer by promoting ROR1-mediated stemness

The FOXL2 C134W mutation is characteristic of adult granulosa cell tumors of the ovary

Double-Negative Feedback Loop between Reprogramming Factor LIN28 and microRNA let-7 Regulates Aldehyde Dehydrogenase 1-Positive Cancer Stem Cells

Identification of six new susceptibility loci for invasive epithelial ovarian cancer

GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer

Characteristics and outcome of recurrence in molecularly defined adult-type ovarian granulosa cell tumors

Comparison of 2SC, AKR1B10, and FH Antibodies as Potential Biomarkers for FH-deficient Uterine Leiomyomas

Clinicopathological significance of deficient DNA mismatch repair and MLH1 promoter methylation in endometrioid endometrial carcinoma

3′RNA and whole‐genome sequencing of archival uterine leiomyomas reveal a tumor subtype with chromosomal rearrangements affecting either HMGA2, HMGA1, or PLAG1

Inherited mutations affecting the SRCAP complex are central in moderate-penetrance predisposition to uterine leiomyomas

Molecular Subtypes of Breast Cancers Detected in Mammography Screening and Outside of Screening

Multiple clinical characteristics separate MED12-mutation-positive and -negative uterine leiomyomas

RAD51C is a susceptibility gene for ovarian cancer

Molecular subclass of uterine fibroids predicts tumor shrinkage in response to ulipristal acetate

MED12 exon 2 mutations in histopathological uterine leiomyoma variants

STRN-ALK rearranged pediatric malignant peritoneal mesothelioma – Functional testing of 527 cancer drugs in patient-derived cancer cells

Altered glycosylation of glycodelin in endometrial carcinoma

A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk

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