TarachandraNarumanchiMD

PubMed

• 13 citations
  221 newborn-screened neonates with medium-chain acyl-coenzyme A dehydrogenase deficiency: Findings from the Inborn Errors of Metabolism Collaborative.
  Kristi Bentler, Shaohui Zhai, Sara A. Elsbecker, Georgianne L. Arnold, Barbara K. Burton
  Molecular Genetics and Metabolism. 2016-09-01
• 58 citations
  Genome-Wide Oligonucleotide Array Comparative Genomic Hybridization for Etiological Diagnosis of Mental Retardation: A Multicenter Experience of 1499 Clinical Cases
  Bixia Xiang, Hongbo Zhu, Yiping Shen, David T. Miller, Kangmo Lu
  The Journal of Molecular Diagnostics. 2010-03-01
• 7 citations
  Expanding the spectrum of CEP55‐associated disease to viable phenotypes
  Elizabeth S. Barrie, Eline Overwater, Mieke M. van Haelst, M. Mahdi Motazacker, Kristen V. Truxal
  American Journal of Medical Genetics. Part A. 2020-02-25

Journal Articles

• 221 newborn-screened neonates with medium-chain acyl-coenzyme A dehydrogenase deficiency: Findings from the Inborn Errors of Metabolism Collaborative  
  Bentler, K., Zhai, S., Elsbecker, S. A., Arnold, G. L., Burton, B. K., Vockley, J., . . . Justice, K., Molecular Genetics and Metabolism, 1/1/2016
• A Newborn with Bilateral Nephromegaly  
  Martinez, T., E. Chong, T. Singleton, T. Narumanchi, and I. Yosypiv, Journal of Investigative Medicine, 1/1/2013
• Idiopathic proximal urea cycle disorder presenting as severe pulmonary hypertension in a neonate--a case report  
  Singh, D., O. Akingbola, M. Dutta, and T. Narumanchi, The Journal of the Louisiana State Medical Society: official organ of the Louisiana State Medical Society, 1/1/2012
• Genome-wide oligonucleotide array comparative genomic hybridization for etiological diagnosis of mental retardation: A multicenter experience of 1499 clinical cases  
  Xiang, B., Zhu, H., Shen, Y., Miller, D. T., Lu, K., Hu, X., Andersson, H.C., Narumanchi, T., Wang, Y., Martinez, J.E., Wu, B., Li, P., Li, M., Chen, T, Fan, Y, The Journal of Molecular Diagnostics, 1/1/2010
• Holt-oram Syndrome: A Novel Mutation in the Tbx5 Gene with Findings of Multiple Ventricular Septal Defects  
  Yang, S., S. Mistry, Y. Li, T. Narumanchi, G. Pridjian, T. Yeh, V. Guerra, and M. R. Recto, Journal of Investigative Medicine, 1/1/2010
• The effect of gestational age, transfusions, and dietary supplementation with medium chain triglyceride on MS/MS profiles of presumptive positive patients for medium c...  
  Narumanchi, T. M., C. T. Dvorak, A. Cunningham, K. Weiss-Becker, M. Jenkins, J. Smith, D. Werling-Baye, C. Meyers, J. Thoene, and H. C. Andersson, Journal of Investigative Medicine, 1/1/2008
• Genetic/metabolic health care delivery during and after hurricanes Katrina and Rita  
  Andersson, H. C., Narumanchi, T. C., Cunningham, A., Bowdish, B., and Thoene, J, Molecular Genetics and Metabolism, 1/1/2006
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Abstracts/Posters

• The effect of gestational age, transfusions, and dietary supplementation with medium chain triglyceride on ms/ms profiles of presumptive positive patients for medium c...
  T. Narumanchi, C. Dvorak , A. Cunningham, K. Weissbecker, M. Jenkins, J. Smith, D. Werling-Baye, C. Myers, J. Thoene, H. Andersson, 2008 Southern Regional Meeting, Southern Society for Clinical Investigation, New Orleans, LA, 1/1/2008
• Glutaric Acidemia - Variability in Expression and Importance of a Comprehensive Workup for Macrocephaly
  T Narumanchi, P Pergami, H Samuelson, 2015 annual meeting of The American College of Medical Genetics, Salt Lake City, Utah, 1/24/2015
• The clinical spectrum of pancreatitis in organic acidemias
  HC Andersson, IS Fortgang, MS Petrescu, TC Narumanchi, A Cunningham, 2011 annual meeting of The Society for Inherited Metabolic Disorders, Asilomar Conference Center, Pacific Grove, California, 1/27/2011
• Case report of a newborn male with a proximal urea cycle disorder and severe pulmonary arterial hypertension
  Meenakshi Dutta, Amy Cunningham, Chris Dvorak, Jessica Hoffman, Jennifer Smith, Hans C. Andersson1, Song-Gui Yang, Dinesh Singh, TaraChandra Murty Narumanchi, 2010 annual meeting of The American College of Medical Genetics, Albuquerque, New Mexico, 1/24/2010
• Holt-Oram: a novel TBX5 mutation with swiss-cheese ventricular septal defects
  Sima Mistry, Yi Qun Li, Kathleen S. Hruska, Vitor C Guerra, Michael R Recto, Gabriella Pridjian, Song-Gui Yang, TaraChandra Murty Narumanchi, 2010 annual meeting of The American College of Medical Genetics, Albuquerque, New Mexico, 1/24/2010
• Patient with a Novel Homozygous VLCAD Mutation
  Chris T Dvorak, Jessica Hoffman, Amy Cunningham, Hans Andersson, TaraChandra Narumanchi, 2010 annual meeting of The American College of Medical Genetics, Albuquerque, New Mexico, 1/24/2010
• Delineating Williams-Beuren Syndrome Chromosomal Region Using High-density Targeted Array CGH
  X. Hu, D. Mercer, T. Narumanchi, H. Andersson, M. Li, 59th annual meeting of The American Society of Human Genetics, Honolulu, Hawaii, 1/21/2009
• Genome-wide oligonucleotide Array CGH for etiological diagnosis of mental retardation and autism spectrum disorders: a multi-center experience on 1,551 clinical cases
  Y. Fan, B. Xiang, B. Wu, P. Li, M. Li, T. Chen, H. Zhu, Y. Shen, K. Lu, M. Mahoney, M. Seashore, A. Bale, J. McGrath, H. Andersson, T. Narumanchi, X. Hu, Y. Wang, J. M..., Annual meeting of The American Society of Human Genetics, Philadelphia, Pennsylvania, 1/15/2008
• Williams syndrome "PLUS": a 4MB deletion identified in a patient with Williams syndrome, congenital anomalies and severe developmental delay
  T. Narumanchi, X. Hu, C. Dvorak, D. Mercer, H. Andersson, M. Li, Annual meeting of The American Society of Human Genetics, San Diego, California, 1/25/2007
• Use of High Density Oligo Array CGH to Characterize Chromosomal Aberrations Associated with Unexplained Clinical Presentations
  M. M. Li, X. Hu, T. Narumanchi, C. Dvorak, D. Mercer, G. Pridjian, H. Andersson, Annual meeting of The American Society of Human Genetics, San Diego, California, 1/25/2007
• The effect of gestational age, transfusions, and dietary supplementation with medium chain triglyceride on ms/ms profiles of presumptive positive patients for medium c...
  C. Dvorak, T. Narumanchi, A. Cunningham, K. Weissbecker, M. Jenkins, J. Smith, D. Werling-Baye, C. Myers, J. Thoene, H. Andersson, Annual meeting of The American Society of Human Genetics, San Diego, California, 1/24/2007
• Long term implications of genetic diagnosis and genetic counseling for families with chromosomal abnormalities
  TC Narumanchi, D. Wesley, J. Thoene, M. Li, Annual meeting of The American Society of Human Genetics, New Orleans, LA, 1/11/2006
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Lectures

• The Inborn Errors of Metabolism Information System (IBEM-IS): Diagnostic Confirmation, Molecular Testing and Clinical Status in Individuals Identified with Short-Chai... 
  1/1/2016
• A Rare Case Presenting as Congenital Microcephaly and Seizures 
  WVU - 1/10/2016
• Please don’t call it the PKU card 
  WVU - 1/29/2013
• OTC Odyssey 
  WVU - 1/15/2012
• Cancer Genetics 
  1/13/2009
• Emergent management of patients with IEMs 
• Intersex 
  Hayward Genetics Center - 1/5./2007
• Ambiguous Genitalia 
  Tulane Ob/Gyn - 1/28/2007
• Triskelion 
  Hayward Genetics Center - 1/6./2007
• Fetus in fetu vs. polymelia (a child with three legs) 
  1/30/2006
• 2006 update on a pilot project to study the effect of gestational age, transfusion with Packed Red Blood Cells (PRBCs), and Medium Chain Triglyceride (MCT) oil on Newb... 
  1/28/2006
• The Case of the Disappearing Birthmark 
  Hayward Genetics Center - 1/3./2006
• The effect of gestational age, transfusion with Packed Red Blood Cells (PRBCs), and Medium Chain Triglyceride (MCT) oil on Newborn screen MS/MS dicarboxylic acid profi... 
  1/29/2005
• Fetus in Fetu 
  Hayward Genetics Center - 1/9./2004
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