Jennelle C Hodge

发表

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.

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.

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.

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.

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

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

Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype

K. Wain, Jennelle C Hodge, N. Hoppman-Chaney, 2013, Clinical 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.

Autism Spectrum Disorder

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

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.

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.

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, Jennelle C Hodge, 2014, Modern Pathology.