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List of works by Jennelle C. Hodge

A cytogenetic analysis of 2 cases of phosphaturic mesenchymal tumor of mixed connective tissue type

scientific article published on 11 April 2012

A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay

scientific article published on 24 September 2018

ALK alterations in adult renal cell carcinoma: frequency, clinicopathologic features and outcome in a large series of consecutively treated patients ⬇️

scientific article published on June 29, 2012

Analysis of MDM2 Amplification in 43 Endometrial Stromal Tumors: A Potential Diagnostic Pitfall

scientific article published in November 2015

Array CGH on unstimulated blood does not detect all cases of Pallister–Killian syndrome: A skin biopsy should remain the diagnostic gold standard ⬇️

scientific article published on 07 February 2012

Assessing copy number aberrations and copy neutral loss of heterozygosity across the genome as best practice: An evidence based review of clinical utility from the cancer genomics consortium (CGC) working group for myelodysplastic syndrome, myelodysp

scientific article published on 10 October 2018

Assessing copy number abnormalities and copy-neutral loss-of-heterozygosity across the genome as best practice in diagnostic evaluation of acute myeloid leukemia: An evidence-based review from the cancer genomics consortium (CGC) myeloid neoplasms wo

scientific article published on 06 October 2018

Chromosomal instability in untreated primary prostate cancer as an indicator of metastatic potential

scientific article published on 07 May 2020

Correction: A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay

scientific article published on 01 September 2019

Deletions in 16q24.2 are associated with autism spectrum disorder, intellectual disability and congenital renal malformation

scientific article published on 18 January 2013

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes

scientific article published on 30 December 2013

Distinct ALK-rearranged and VCL-negative papillary renal cell carcinoma variant in two adults without sickle cell trait.

scientific article published in April 2013

Expression profiling of uterine leiomyomata cytogenetic subgroups reveals distinct signatures in matched myometrium: transcriptional profilingof the t(12;14) and evidence in support of predisposing genetic heterogeneity

scientific article published on 17 February 2012

Genetic heterogeneity among uterine leiomyomata: insights into malignant progression

scientific article

High-grade endometrial stromal sarcomas: a clinicopathologic study of a group of tumors with heterogenous morphologic and genetic features

scientific article published on 01 September 2014

Highly penetrant alterations of a critical region including BDNF in human psychopathology and obesity

scientific article published on December 2012

Identifying the molecular signature of the interstitial deletion 7q subgroup of uterine leiomyomata using a paired analysis

scientific article published on October 2009

In‐frame multi‐exon deletion of SMC1A in a severely affected female with Cornelia de Lange Syndrome ⬇️

scientific article published on November 21, 2011

JAZF1 rearrangement in a mesenchymal tumor of nonendometrial stromal origin: report of an unusual ossifying sarcoma of the heart demonstrating JAZF1/PHF1 fusion

scientific article published in June 2013

Lysophosphatidic acid stimulates PC-3 prostate cancer cell Matrigel invasion through activation of RhoA and NF-kappaB activity

scientific article published on July 2006

Molecular Cytogenetic Analysis of JAZF1, PHF1, and YWHAE in Endometrial Stromal Tumors: Discovery of Genetic Complexity by Fluorescence in Situ Hybridization

scientific article

Molecular and cytogenetic characterization of plexiform leiomyomata provide further evidence for genetic heterogeneity underlying uterine fibroids

scientific article published on 10 April 2008

Molecular and pathologic characterization of AML with double Inv(3)(q21q26.2)

scientific article published on 16 November 2018

Molecular cytogenetic analysis for TFE3 rearrangement in Xp11.2 renal cell carcinoma and alveolar soft part sarcoma: validation and clinical experience with 75 cases ⬇️

scientific article published on July 5, 2013

Non-fusion mutations in endometrial stromal sarcomas: what is the potential impact on tumourigenesis through cell cycle dysregulation?

scientific article published on 08 May 2020

Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural Variation

scientific article published on 18 June 2015

Rare deletions at the neurexin 3 locus in autism spectrum disorder

scientific article

Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures

scientific article published on 7 February 2013

Reciprocal deletion and duplication at 2q23.1 indicates a role for MBD5 in autism spectrum disorder.

scientific article published on May 2013

Recurrent 8q13.2-13.3 microdeletions associated with branchio-oto-renal syndrome are mediated by human endogenous retroviral (HERV) sequence blocks

scientific article

Recurrent duplications of 17q12 associated with variable phenotypes.

scientific article published on 30 September 2015

Requirement of RhoA activity for increased nuclear factor kappaB activity and PC-3 human prostate cancer cell invasion

scientific article published on 01 March 2003

Response to Cobben et al. “Array CGH on unstimulated blood does not detect all cases of Pallister‐Killian Syndrome: Buccal smear analysis should remain the diagnostic procedure of first choice” ⬇️

scientific article published on April 23, 2013

TFE3 rearrangements in adult renal cell carcinoma: clinical and pathologic features with outcome in a large series of consecutively treated patients

scientific article published on 01 May 2012

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

scientific article

The phenotype spectrum of X-linked ichthyosis identified by chromosomal microarray

scientific article published on 7 February 2015

Uterine cellular leiomyomata with chromosome 1p deletions represent a distinct entity

scientific article

Uterine leiomyomata and decreased height: a common HMGA2 predisposition allele

scientific article

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