J. Hodge

发表

Rare deletions at the neurexin 3 locus in autism spectrum disorder.

D. Pinto, S. Scherer, D. Collier, 2012, American journal of human genetics.

Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes

S. Scherer, J. Rosenfeld, A. V. Vulto-van Silfhout, 2016, Molecular Psychiatry.

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

Ryan L. Collins, Ryan L Collins, Michael E Talkowski, 2015, American journal of human genetics.

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

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

Systematic evaluation of genome sequencing as a first-tier diagnostic test for prenatal and pediatric disorders

Ryan L. Collins, Stephan J Sanders, D. MacArthur, 2020 .

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 working group.

M. Slovak, F. Quintero-Rivera, G. Raca, 2018, Cancer genetics.

Lysophosphatidic acid stimulates PC‐3 prostate cancer cell matrigel invasion through activation of RhoA and NF‐κB activity

J. Hodge, Y. Hwang, P. Lindholm, 2006, Molecular carcinogenesis.

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, myelodysplastic/myeloproliferative and myeloproliferative n

M. Slovak, F. Quintero-Rivera, G. Raca, 2018, Cancer genetics.

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

A. Clayton, F. Taran, E. Stewart, 2014, American journal of obstetrics and gynecology.

Tumorigenesis and Neoplastic Progression Molecular and Cytogenetic Characterization of Plexiform Leiomyomata Provide Further Evidence for Genetic Heterogeneity Underlying Uterine Fibroids

M. Rubin, C. Morton, B. Quade, 2010 .

The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Myeloid and Histiocytic/Dendritic Neoplasms

Y. Natkunam, R. Siebert, D. de Jong, 2022, Leukemia.

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

F. Sim, A. Folpe, R. Jenkins, 2012, Human pathology.

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

S. Shetty, Navid Sadri, J. Hodge, 2019, Cancer genetics.

Systematic evaluation of genome sequencing for the assessment of fetal structural anomalies

Ryan L. Collins, Jack M. Fu, Christopher W. Whelan, 2020, bioRxiv.

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

M. Freeman, B. Knudsen, I. Garraway, 2020, BMC Cancer.

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

J. Jen, J. Jang, D. Babovic‐Vuksanovic, 2012, American journal of medical genetics. Part A.

JAZF1 Rearrangement in a Mesenchymal Tumor of Nonendometrial Stromal Origin: Report of an Unusual Ossifying Sarcoma of the Heart Demonstrating JAZF1/PHF1 Fusion

A. Folpe, J. K. Schoolmeester, J. Maleszewski, 2013, The American journal of surgical pathology.

TFE3 Rearrangements in Adult Renal Cell Carcinoma: Clinical and Pathologic Features With Outcome in a Large Series of Consecutively Treated Patients

J. Cheville, R. Thompson, C. Lohse, 2012, The American journal of surgical pathology.

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

J. Hand, J. Hodge, C. Runke, 2015, Journal of the American Academy of Dermatology.

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.

Tae-Min Kim, Peter J Park, Elizabeth A Stewart, 2012, Human molecular genetics.

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

John Wei, S. Scherer, J. Rosenfeld, 2014, Human molecular genetics.

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

P. Park, C. Morton, B. Quade, 2009, Genes, chromosomes & cancer.

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

J. Rosenfeld, S. Schwartz, L. Shaffer, 2013, European Journal of Human Genetics.

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

S. Scherer, G. Kirov, D. Merico, 2013, Human molecular genetics.

Disruption of MBD5 contributes to a spectrum of psychopathology and neurodevelopmental abnormalities

J. Gusella, C. Morton, M. Talkowski, 2014, Molecular Psychiatry.

A cross-disorder dosage sensitivity map of the human genome

Ryan L. Collins, Jack M. Fu, Joseph T. Glessner, 2021, Cell.

Genetic heterogeneity among uterine leiomyomata: insights into malignant progression.

C. Morton, J. Hodge, Jennelle C. Hodge, 2007, Human molecular genetics.

Uterine leiomyomata and decreased height: a common HMGA2 predisposition allele

C. Panhuysen, C. Morton, E. Stewart, 2009, Human Genetics.

Two Patients with Complex Rearrangements Suggestive of Germline Chromoanagenesis

A. Breman, G. Vance, J. Hodge, 2021, Cytogenetic and Genome Research.

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

J. Gécz, S. Sisodiya, E. Lemyre, 2018, Genetics in Medicine.

Autism Spectrum Disorder

D. Pinto, S. Scherer, P. Bolton, 2018, Sleep in Children with Neurodevelopmental Disabilities.

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

S. Kirmani, J. Hodge, J. Bair, 2012, American journal of medical genetics. Part A.

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

S. Scherer, J. Rosenfeld, L. Shaffer, 2013, Journal of Medical Genetics.

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

J. Cheville, R. Thompson, C. Lohse, 2012, Modern Pathology.

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

André M. Oliveira, J. Hodge, Xiaoke Wang, 2014, Modern Pathology.

17q12 Recurrent Duplication

H. Mefford, J. Hodge, E. Mitchell, 2016 .

High-grade Endometrial Stromal Sarcomas: A Clinicopathologic Study of a Group of Tumors With Heterogenous Morphologic and Genetic Features

D. Bell, G. Keeney, J. K. Schoolmeester, 2014, The American journal of surgical pathology.

Recurrent duplications of 17q12 associated with variable phenotypes

Tomas W. Fitzgerald, N. Carter, A. Alberti, 2015, American journal of medical genetics. Part A.

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

Jun Wang, Yiping Shen, Xiaoli Chen, 2014, BMC Medical Genetics.

Recommendations for Specimen and Therapy Selection in Colorectal Cancer

Navid Farahani, R. Bookstein, S. Alkan, 2021, Oncology and Therapy.

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

P. D. Dal Cin, M. Nucci, G. Keeney, 2015, International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists.

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

J. Hodge, Snehal B Patel, Colin McCormack, 2020, Journal of Clinical Pathology.

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

S. Scherer, J. Rosenfeld, L. Shaffer, 2012, Archives of General Psychiatry.

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

J. Gécz, S. Sisodiya, E. Lemyre, 2018, Genetics in Medicine.

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

A. Kajdacsy-Balla, J. Bub, J. Hodge, 2003, Cancer research.

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

J. Hodge, W. Sukov, P. P. Bedroske, 2016, The Journal of molecular diagnostics : JMD.