Jie Hu

发表

Genome-wide allelotype study of primary glioblastoma multiforme.

H. Ng, Jie Hu, Cheng-chuan Jiang, 2003, Chinese medical journal.

Reproductive outcomes in individuals with chromosomal reciprocal translocations

U. Surti, A. Rajkovic, D. Saller, 2021, Genetics in Medicine.

Genomic Characterization of a Metastatic Alveolar Rhabdomyosarcoma Case Using FISH Studies and CGH+SNP Microarray Revealing FOXO1-PAX7 Rearrangement with MYCN and MDM2 Amplification and RB1 Region Loss

U. Surti, S. Ranganathan, S. Yatsenko, 2017, Cytogenetic and Genome Research.

Loss of DNA copy number of 10q is associated with aggressive behavior of leiomyosarcomas: a comparative genomic hybridization study.

U. Surti, U. Rao, Jie Hu, 2005, Cancer genetics and cytogenetics.

Co‐existence of 9p deletion and Silver‐Russell syndromes in a patient with maternally inherited cryptic complex chromosome rearrangement involving chromosomes 4, 9, and 11

U. Surti, Marianne Mcguire, Jie Hu, 2013, American journal of medical genetics. Part A.

A genome-wide allelotype study of primary and corresponding recurrent glioblastoma multiforme in one patient.

H. Ng, Jie Hu, Cheng-chuan Jiang, 2004, Chinese medical journal.

Genomic imbalances in ovarian borderline serous and mucinous tumors.

U. Surti, Jie Hu, Mirka W. Jones, 2002, Cancer genetics and cytogenetics.

Chromosome 14q may harbor multiple tumor suppressor genes in primary glioblastoma multiforme.

H. Ng, Jie Hu, Cheng-chuan Jiang, 2002, Chinese medical journal.

Maternal GRB10 microdeletion is a novel cause of cystic placenta: Spectrum of genomic changes in the etiology of enlarged cystic placenta.

U. Surti, D. Bellissimo, W. Parks, 2017, Placenta.

The Genomic Landscape of PAX5, IKZF1, and CDKN2A/B Alterations in B-Cell Precursor Acute Lymphoblastic Leukemia

U. Surti, Z. Ou, S. Gollin, 2017, Cytogenetic and Genome Research.

Molecular and clinical characterization of a recurrent cryptic unbalanced t(4q;18q) resulting in an 18q deletion and 4q duplication

U. Surti, S. Gunn, J. Vockley, 2008, American journal of medical genetics. Part A.

Molecular and Clinical Characterization of a Recurrent Cryptic Unbalanced t ( 4 q ; 18 q ) Resulting in an 18 q Deletion and 4 q Duplication

U. Surti, S. Gunn, J. Vockley, 2008 .

Genomic alterations in uterine leiomyosarcomas: Potential markers for clinical diagnosis and prognosis

U. Surti, Jie Hu, Mirka W. Jones, 2001, Genes, chromosomes & cancer.

Chromosome 2q12.3-q13 copy number variants in patients with neurodevelopmental disorders: genotype-phenotype correlation and new hotspots

Z. Ou, M. Aarabi, S. Yatsenko, 2022, Psychiatric genetics.

Deletion mapping of 6q21-26 and frequency of 1p36 deletion in childhood endodermal sinus tumors by microsatellite analysis

M. Fritsch, E. Perlman, Jie Hu, 2001, Oncogene.

Comparative genomic hybridization of esophageal and gastroesophageal adenocarcinomas shows consensus areas of DNA gain and loss

C. Moskaluk, E. Perlman, Jie Hu, 1998, Genes, chromosomes & cancer.

Application of multicolor banding for identification of complex chromosome 18 rearrangements.

U. Surti, Jie Hu, M. Sathanoori, 2006, The Journal of molecular diagnostics : JMD.

Genomic alterations in distal bile duct carcinoma by comparative genomic hybridization and karyotype analysis

R. Hruban, S. Kern, C. Yeo, 1999, Genes, chromosomes & cancer.

Three Supernumerary Marker Chromosomes in a Patient with Developmental Delay, Mental Retardation, and Dysmorphic Features

U. Surti, A. S. Serrano Russi, Jie Hu, 2011, Genetics research international.

Concurrent Hypermethylation of Multiple Genes Is Associated with Grade of Oligodendroglial Tumors

K. To, W. Poon, H. Ng, 2001, Journal of neuropathology and experimental neurology.

Copy number alterations involving 59 ACMG‐recommended secondary findings genes

U. Surti, D. Bellissimo, A. Rajkovic, 2020, Clinical genetics.

A novel maternally inherited 8q24.3 and a rare paternally inherited 14q23.3 CNVs in a family with neurodevelopmental disorders

U. Surti, A. Goldstein, Jie Hu, 2015, American journal of medical genetics. Part A.

Deletion of conserved non‐coding sequences downstream from NKX2‐1: A novel disease‐causing mechanism for benign hereditary chorea

U. Surti, A. Rajkovic, J. Locker, 2021, Molecular genetics & genomic medicine.

Prenatal detection of del(10)(q11.2) mosaicism in chorionic villus specimens likely caused by a common chromosomal fragile site FRA10G is associated with a normal phenotype

U. Surti, W. A. Hogge, S. Yatsenko, 2012, Prenatal diagnosis.

Beyond Down syndrome phenotype: Paternally derived isodicentric chromosome 21 with partial monosomy 21q22.3

U. Surti, A. Rajkovic, D. Saller, 2017, American journal of medical genetics. Part A.

Absence of skeletal anomalies in siblings with a maternally inherited 12q13.13‐q13.2 microdeletion partially involving the HOXC gene cluster

U. Surti, Jie Hu, Lina Ghaloul-Gonzalez, 2014, American journal of medical genetics. Part A.

A small homozygous microdeletion of 15q13.3 including the CHRNA7 gene in a girl with a spectrum of severe neurodevelopmental features

U. Surti, Jie Hu, Suneeta Madan‐Khetarpal, 2011, American journal of medical genetics. Part A.

Targeted exome sequencing reveals novel USH2A mutations in Chinese patients with simplex Usher syndrome

Jie Hu, Jian-xin Song, Hai-rong Shu, 2015, BMC Medical Genetics.

Chromosome 12q13.13q13.13 microduplication and microdeletion: a case report and literature review

U. Surti, Z. Ou, Elena Infante, 2017, Molecular Cytogenetics.

Transcriptional inactivation of TP73 expression in oligodendroglial tumors

H. Ng, Jie Hu, J. Pang, 2002, International journal of cancer.

Clinical features and treatment of World Health Organization grade II and III meningiomas in childhood: report of 23 cases.

Jie Hu, Cheng-chuan Jiang, Y. Gong, 2012, Journal of neurosurgery. Pediatrics.

Erratum: Clinical features and treatment of World Health Organization Grade II and III meningiomas in childhood: report of 23 cases.

Jie Hu, Cheng-chuan Jiang, Hong Chen, 2012, Journal of neurosurgery. Pediatrics.

CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders

Urvashi Surti, Jie Hu, U. Surti, 2015, Journal of Neurodevelopmental Disorders.

Intracranial papillary meningioma: a clinicopathologic study of 30 cases at a single institution.

Lin Zhao, Shi-ting Li, Jie Hu, 2013, Neurosurgery.

Four children with postnatally diagnosed mosaic trisomy 12: Clinical features, literature review, and current diagnostic capabilities of genetic testing

U. Surti, Z. Ou, S. Yatsenko, 2020, American Journal of Medical Genetics. Part A.

CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders

U. Surti, S. Yatsenko, Jie Hu, 2015, Journal of Neurodevelopmental Disorders.

A case of myelodysplastic syndrome with acquired monosomy 7 in a child with a constitutional t(1;19) and a mosaicism for trisomy 21.

U. Surti, Jie Hu, Peter H Shaw, 2005, Cancer genetics and cytogenetics.

Chromosome 3 may harbor multiple tumor suppressor genes associated with primary glioblastoma multiforme

Jie Hu, Cheng-chuan Jiang, C. Y. Tong, 2002 .

Tetrasomy 15q25.3 --> qter resulting from an analphoid supernumerary marker chromosome in a patient with multiple anomalies and bilateral Wilms tumors.

U. Surti, S. Gollin, E. McPherson, 2002, American journal of medical genetics.

Maternal GRB10 microdeletion is a novel cause of cystic placenta: Spectrum of genomic changes in the etiology of enlarged cystic placenta.

U. Surti, D. Bellissimo, S. Yatsenko, 2017, Placenta.

A small homozygous microdeletion of 15q13.3 including the CHRNA7 gene in a girl with a spectrum of severe neurodevelopmental features

U. Surti, Jie Hu, Suneeta Madan‐Khetarpal, 2011, American journal of medical genetics. Part A.

Erratum: Clinical features and treatment of World Health Organization Grade II and III meningiomas in childhood: report of 23 cases.

Jie Hu, Cheng-chuan Jiang, Hong Chen, 2012, Journal of neurosurgery. Pediatrics.