Wen-IWendyChangMD

PubMed

• 525 citations
  Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands
  Sheng Chih Jin, Jason Homsy, Samir Zaidi, Qiongshi Lu, Sarah U. Morton
  Nature Genetics. 2017-10-09
• 93 citations
  ONC201 and imipridones: Anti-cancer compounds with clinical efficacy.
  Varun V. Prabhu, Sara Morrow, Abed Rahman Kawakibi, Lanlan Zhou, Marie D. Ralff
  Neoplasia. 2020-10-23
• 32 citations
  Role of metastasectomy in the management of thyroid carcinoma: the NIH experience.
  Ho Pak, Loukas Gourgiotis, Wendy Chang, Lori C. Guthrie, Monica C. Skarulis
  Journal of Surgical Oncology. 2003-01-01

Journal Articles

• Early neutrophilic expression of vascular endothelial growth factor after traumatic brain injury  
  Chodobski A, Chung I, Kozniewska E, Ivanenko T, Chang W, Harrington JF, Duncan JA, Szmydynger-Chodobska J, Neuroscience, 1/1/2003

Abstracts/Posters

• Identification of Cancer Predisposition Syndromes in the Pediatric Population Shows Low Rates of Referral in At-Risk Patients
  Amodei K, Kessler E, Chang W, University of Pittsburgh School of Medicine Dean’s Summer Research Project Poster Symposium, Pittsburgh, PA, 9/2018
• Exome sequencing and analyses in a familial breast cancer cohort to identify novel cancer predisposition variation
  4. Praveen K, Chang W, Terry MB, Chung JH, Mukherjee S, Staples J, Arunachalam V, Balasubramanian S, Huang Q, Penn J, Reid J, Overton JD, Shen Y, Dewey FE, Gonzaga-Jau..., American Society of Human Genetics Annual Meeting, Vancouver, Canada., 10/2016
• A rapidly progressive malignant rhabdoid tumor (MRT) with a novel somatic mutation in a three-month old infant.
  League-Pascual JC, Chang W, Malafronte PJ, Fagen KE, Khan J, and Hartman KR, American Society of Pediatric Hematology/Oncology Annual Meeting, Minneapolis, MN, 1/1/2016
• Clinical exome and transcriptome sequencing for identification of actionable cancer targets: a pilot study for children and young adults with relapsed or refractory ca...
  Chang W, Brohl AS, Patidar R, Lin J, Shern JF, Wei JS, Song YK, Sindiri, S, Yohe ME, Chen L, Liao H, Gryder B, Zhang S, Merchant MS, Widemann BC, and Khan J, American Association for Cancer Research Annual Meeting, Philadelphia, PA, 1/21/2015
• The genomic landscape of the Ewing Sarcoma family of tumors reveals recurrent STAG2 mutation and novel fusions.
  Chang W, Brohl AS, Solomon DA, Wang J, Song YK, Sindiri, S, Patidar R, Hurd L, Chen L, Shern JF, Liao H, Wen X, Gerard J, Kim JS, Lopez-Guerrero JA, Machado, I, Wai D..., Pediatric Oncology Branch Round Up, Bethesda, MD, 1/19/2014
• MECP2 Exon 1 Mutation in a Male Child with Rett Syndrome.
  Shuhaiber H, Chang W, and Yeboa K, American College of Medical Genetics Clinical Genetics Meeting, Tampa, FL, 1/1/2009
• Histone deacetylase inhibitor LBH589 increases survival motor neuron transcript and protein levels in spinal muscular atrophy patient cells.
  Chang W, Weissman T, and Chung W, Dean's Day for Research, Columbia University College of Physicians and Surgeons, New York, NY, 1/1/2008
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Lectures

• Genomics Guided Precision Therapy for Pediatric Oncology: A Report from the NCI Center for Cancer Research. 
  Bethesda, MD - 1/1/2015
• Workshop in the Challenges We Face with Medical Interpreting, and Other Issues of Health Care Access for Immigrants. 
  Chicago, IL - 1/1/2004
• Health Care Effects on Immigrants with a Need for Medical Interpreting, and the Future -- Remote Simultaneous Medical Interpreting (RSMI). 
  New York, NY - 1/1/2004