Z. Ordulu

发表

Structural Chromosomal Rearrangements Require Nucleotide-Level Resolution: Lessons from Next-Generation Sequencing in Prenatal Diagnosis.

Ryan L. Collins, D. Warburton, J. Gusella, 2016, American journal of human genetics.

Intravenous Leiomyomatosis: An Unusual Intermediate between Benign and Malignant Uterine Smooth Muscle Tumors

P. Park, P. D. Dal Cin, C. Morton, 2016, Modern Pathology.

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

Edwin Cuppen, Claire Redin, Ryan L. Collins, 2016, Nature Genetics.

Implication of LRRC4C and DPP6 in neurodevelopmental disorders

Ryan L. Collins, S. Scherer, J. Rosenfeld, 2017, American journal of medical genetics. Part A.

Approach to Helicobacter pylori infection in geriatric population.

Z. Ordulu, S. Cizginer, A. Kadayifci, 2014, World journal of gastrointestinal pharmacology and therapeutics.

Clinical, pathologic, cytogenetic, and molecular profiling in self-identified black women with uterine leiomyomata.

C. Morton, B. Quade, Z. Ordulu, 2018, Cancer genetics.

Uterine PEComas: Correlation Between Melanocytic Marker Expression and TSC Alterations/TFE3 Fusions

Lauren L. Ritterhouse, C. Antonescu, E. Oliva, 2021, Modern Pathology.

Morphologic and Molecular Heterogeneity of Cervical Neuroendocrine Neoplasia

M. Mino‐Kenudson, E. Oliva, K. K. van de Vijver, 2022, The American journal of surgical pathology.

Molecular Detection of Oncogenic Gene Rearrangements.

Z. Ordulu, Valentina Nardi, Zehra Ordulu, 2022, Clinics in laboratory medicine.

The selective expression of ret finger protein in endometrial cancer: can RFP be a marker of serous carcinomas?

Z. Ordulu, G. Tezel, A. Usubütün, 2012, Turk patoloji dergisi.

Describing sequencing results of structural chromosome rearrangements with a suggested next-generation cytogenetic nomenclature.

Michael E Talkowski, Cynthia C Morton, J. Gusella, 2014, American journal of human genetics.

Haploinsufficiency of KDM6A is associated with severe psychomotor retardation, global growth restriction, seizures and cleft palate

J. Rosenfeld, L. Shaffer, J. Vermeesch, 2013, Human Genetics.

Update on Ovarian Sex Cord-Stromal Tumors.

Z. Ordulu, Zehra Ordulu, 2022, Surgical pathology clinics.

Hyperprogression of a mismatch repair-deficient colon cancer in a humanized mouse model following administration of immune checkpoint inhibitor pembrolizumab

W. El-Deiry, Shengliang Zhang, Lanlan Zhou, 2021, Oncotarget.

Phenotypic interpretation of complex chromosomal rearrangements informed by nucleotide-level resolution and structural organization of chromatin

C. Morton, M. Talkowski, D. Harris, 2018, European Journal of Human Genetics.

Computational Prediction of Position Effects of Apparently Balanced Human Chromosomal Rearrangements.

Fowzan S Alkuraya, Michael E Talkowski, Karen W Gripp, 2017, American journal of human genetics.

Pediatric liver transplant following near catastrophic head bleed: Lessons learned

A. Cuenca, H. Yeh, Z. Ordulu, 2020, Pediatric transplantation.

Disseminated peritoneal leiomyomatosis after laparoscopic supracervical hysterectomy with characteristic molecular cytogenetic findings of uterine leiomyoma

P. Cin, C. Morton, B. Quade, 2010, Genes, chromosomes & cancer.

Clinical diagnosis by whole-genome sequencing of a prenatal sample.

Michael E Talkowski, Naveed Hussain, Lisa G Shaffer, 2012, The New England journal of medicine.

Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole‐genome sequencing

V. Jobanputra, C. Morton, M. Talkowski, 2015, Prenatal diagnosis.

Molecular and Clinicopathologic Characterization of Intravenous Leiomyomatosis

E. Oliva, Z. Ordulu, P. Hui, 2020, Modern Pathology.

Fibroids: Genotype and Phenotype

Z. Ordulu, Zehra Ordulu, 2016, Clinical obstetrics and gynecology.

Sertoli-Leydig Cell Tumors of the Ovary With Follicular Differentiation Often Resembling Juvenile Granulosa Cell Tumor

Z. Ordulu, R. Young, Zehra Ordulu, 2020, The American journal of surgical pathology.

Embryonal rhabdomyosarcoma of the uterine corpus: a clinicopathological and molecular analysis of 21 cases highlighting a frequent association with DICER1 mutations

Lauren L. Ritterhouse, W. Foulkes, E. Oliva, 2021, Modern Pathology.

Reproducibility of scoring criteria for HER2 immunohistochemistry in endometrial serous carcinoma: a multi-institutional interobserver agreement study

E. Oliva, X. Matías-Guiu, Serena Wong, 2021, Modern Pathology.

Locally recurrent secretory carcinoma of the breast.

Barbara L. Smith, A. Bardia, A. Taghian, 2021, The oncologist.

Locally Recurrent Secretory Carcinoma of the Breast with NTRK3 Gene Fusion

Jochen, A. Bardia, A. Taghian, 2021 .

Haploinsufficiency of KDM6A is associated with severe psychomotor retardation, global growth restriction, seizures and cleft palate

J. Rosenfeld, L. Shaffer, J. Vermeesch, 2013, Human Genetics.

Systematic identification of anticancer drug targets reveals a nucleus-to-mitochondria ROS-sensing pathway

E. Oliva, S. Beausoleil, N. Bardeesy, 2023, Cell.