IgnatiaBVan Den VeyverMD

PubMed

• 3 citations
  Implication of chromosomal microarray analysis prior to in-utero repair of fetal open neural tube defect.
  R Zemet, E Krispin, R M Johnson, N R Kumar, L E Westerfield
  Ultrasound in Obstetrics & Gynecology. 2023-06-01
• 4 citations
  International Society for Prenatal Diagnosis 2022 debate 3-Fetal genome sequencing should be offered to all pregnant patients.
  Ignatia B Van den Veyver, Yuval Yaron, Zandra C Deans
  Prenatal Diagnosis. 2023-04-01
• Compound heterozygosity of a de novo submicroscopic deletion and an inherited frameshift pathogenic variant in thegene in a fetus with bilaterally enlarged and echogen...
  Takuya Sakyu, Samantha R Stover, Yue Wang, Patricia Ward, Manisha Gandhi
  Clinical Case Reports. 2023-02-01

Journal Articles

• A genome-wide screen for copy number alterations in an adolescent pilot cohort with mullerian anomalies  
  70. Murry JB, Santos XM, Wang X, Wan YW, Van den Veyver IB, Dietrich JE, Fertility and sterility, 2/2/2015
• Counseling challenges with variants of uncertain significance and incidental findings in prenatal genetic screening and diagnosis  
  Westerfield L, Darilek S, Van den Veyver IB, J. Clin. Med, 1/1/2014
• Non-random X chromosome inactivation in Aicardi syndrome  
  Eble TN, Sutton VR, Sangi-Haghpeykar H, Wang X, Jin W, Lewis RA, Fang P, Van den Veyver IB, Human genetics, 1/1/2009
• Mutations in exon 1 of MECP2are a rare cause of Rett Syndrome  
  Amir RE, Fang P, Yu Z, Glaze D, Percy A, Zoghbi H, Roa B, Van den Veyver IB, J Med Genet, 1/1/2005
• A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by Notch in Xenopus embryos  
  Stancheva I, Collins AL, Van den Veyver IB, Zoghbi H, Meehan RR, Molec Cell, 1/1/2003
• Cerebrovascular vasospasm in eclampsia: Transcranial Doppler ultrasound findings  
  Van den Veyver I, Belfort M, Rowe T, Moise K, J Mat Fetal Med, 1/1/1994
• Ultrasound guided blood sampling of the rabbit fetus  
  Moise K, Hesketh D, Belfort M, Saade G, Van den Veyver I, Hudson K, Rodkey S, Laboratory Animal Science, 1/1/1992
• Clinical aspects in the surgical treatment of varicocele in subfertile men II The role of the epididymal factor  
  Gerris J, Van Neuten J, Van Camp C, Gentens P, Van de Vijver I, Van Camp K., The role of the epididymal factor, Eur J ObstetGynecol Reprod Biol, 1/1/1988
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Books/Book Chapters

• Obstetric Imaging (A Volume in the Expert Radiology Series) 
  Chapter: Deletion (DiGeorge, Shprintzen, Velocardiofacial) Syndrome 
  Page 693 - 697Zacharias NM and Van den Veyver IBEditors: Joshua Copel, MD.2012
• Obstetric Imaging (A Volume in the Expert Radiology Series) 
  Chapter: 4p- Deletion Syndrome (Wolf-Hirschhorn Syndrome) 
  Page 698 - 701Zacharias NM and Van den Veyver IBEditors: Joshua Copel, MD.2012
• Obstetric Imaging (A Volume in the Expert Radiology Series) 
  Chapter: 5p- Syndrome (Cri du Chat) 
  Page 702 - 706Zacharias NM and Van den Veyver IBEditors: Joshua Copel, MD.2012
• Annual Reviews of Genomics and Human Genetics 
  Chapter: Noninvasive prenatal screening by next generation sequencing 
  Page 327 - 347Gregg AR, Van den Veyver IB, Gross SJ, Mandankumar R, Rink BD, Norton MEEditors: Aravinda Chakravarti and Eric Green.Annual Reviews Publishing, Palo Alto, CA2012
• Textbook of Pediatric Dermatology 
  Chapter: Focal Dermal Hypoplasia 
  Sanchez-Valle A, Sutton VR and Van den Veyver IBBlackwell Publishing, Oxford, UK2011
• The Placenta: from Development to Disease 
  Chapter: Imprinting in the Human Placenta 
  Page 87 - 95Wen S, Van den Veyver IBEditors: Helen Kay, D. Michael Nelson, Yuping Wang.Blackwell Publishing, Oxford, UK2011
• The NORD Guide to Rare Disorders 
  Chapter: Rett syndrome 
  Van den Veyver IB, Glaze DGLippincott, Williams & Wilkins, Philadelphia, PA2003
• Former Sciara JJ, Gynecology and Obstetrics. Vol. 5: Reproductive Endocrinology, Infertility, and Genetics. Section: Principles of Human Genetics 
  Chapter: Mendelian inheritance and its exceptions 
  Van den Veyver I, Peng HGlob. libr. women's med2001
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Abstracts/Posters

• In obstetrics, is surprise ever a good thing?
  Salmanian B, Antony K, Fox K, Ballas J, Hosseinzadeh P, Wagner R, Moaddab A, Van den Veyver IB, Dildy G, Lee W, Aagaard K, Ramin S, Belfort M, Shamshirsaz A, SMFM: The Pregnancy Meeting, San Diego, CA, 1/2/2015
• Nervous System: The role of prenatal exposures in modulation of neurodevelopment using the SHANK3e4-9/+ mutant mouse model
  Bravo J, Fang H, Engler D, Balasa A, Van den Veyver IB, Environmental Stressors in disease and implications for human health by the Endocrine Society, Boston, MA, 1/26/2014
• Positive NIPT resulting from structurally abnormal chromosomes highlights importance of invasive confirmatory testing
  Smith JL, Cvjetkovic N, Fosler L, Van den Veyver IB, Peacock S, Breman A, Patel A, ACMG Annual Clinical Genetics Meeting, Nashville, TN, 1/25/2014
• Not a simple false positive: genetic counseling challenges in cases of discrepant NIPT and invasive testing results
  Coles K, Cvjetkovic N, Lemoine J, Van den Veyver IB, ACMG Annual Clinical Genetics Meeting, Nashville, TN, 1/25/2014
• CLOVES Syndrome: The First Prenatal Molecular Diagnosis
  Murphy L, Emrick L, Shamshirsaz A, Ruano R, Cassady C, Liu L, Chang , Sutton RV, Li, Van den Veyver IB, ACMG Annual Clinical Genetics Meeting, Nashville, TN, 1/25/2014
• Role of NLRP7 in imprinting and anomalous reproductive outcomes
  Mahadevan S, Wan Y-W, Liu Z, Van den Veyver IB, Mammalian Reproduction, Gordon Research Conference, New London, NH, 1/10/2014
• HIV and pregnancy, a review
  Van den Veyver I, Lindeque G, Ob Gyn Forum, South Africa, 1/1/2014
• Exploring the role of NLRP7 in reprogramming of CpG methylation in the oocyte and early embryo
  Mahadevan S, Van den Veyver IB, American Society of Human Genetics Annual Meeting, Epigenetics, Boston, MA, 1/22/2013
• Comparison of three single-cell whole genome amplification (WGA) methods for detection of genomic aberrations by array CGH: A step towards noninvasive prenatal diagnos...
  Breman A, Bi W, Shaw CA, Van den Veyver I, Shaw CJ, Stubbs A, Withers M, Fruhman G, Patel A, Lupski J.R, Beaudet A, American Society of Human Genetics Annual Meeting, Prenatal and Reproductive Genetics, Boston, MA, 1/22/2013
• Chronic maternal protein deprivation affects body composition and energy expenditure of adult male offspring
  Balasa A, Fiorotto M, Van den Veyver IB, SGI 60th Annual Scientific Meeting “Plasticity: Molecules to Motherhood and Beyond”, Orlando, FL, 1/20/2013
• Transcriptome analysis of the hypothalamus of 21-day and 1-year old male mice exposed to chronic maternal protein deprivation during early development
  Balasa A, Dove C, Anders A, Allen G, Van den Veyver IB, SGI 60th Annual Scientific Meeting “Plasticity: Molecules to Motherhood and Beyond”, Orlando, FL, 1/20/2013
• Chronic maternal protein deprivation causes anxiety-like traits in adult male offspring mice
  Balasa A, Van den Veyver IB, SGI 60th Annual Scientific Meeting “Plasticity: Molecules to Motherhood and Beyond”, Orlando, FL, 1/20/2013
• Exposure to chronic unpredictable mild stress (CUMS) during early development causes autistic like traits in genetically predisposed Shank3 mutant male mice
  Balasa A, Stinnett G, Bravo J, Mahadevan S, Pautler R, Van den Veyver IB, SGI 60th Annual Scientific Meeting “Plasticity: Molecules to Motherhood and Beyond”, Orlando, FL, 1/20/2013
• Prenatal Presentations of 4q Interstitial Deletions
  Murphy L, Breman A, Brown C, Cheung S, Maliszewski K, Stankiewicz P, Tam Tam K, Van den Veyver IB, ACMG Annual Clinical Genetics Meeting, Phoenix, AZ, 1/19/2013
• The PDPK1 gene variants do not seem to be associated with Premature Ovarian Failure
  Liu Q, Van den Veyver I, Gibbons WE, and Kovanci E., Conjoint Meeting of the International Federation of Fertility Societies and the American Society for Reproductive Medicine, Boston, MA, 1/12/2013
• Transcriptome analysis of the hypothalamus of 1-year-old male mice exposed during early development to chronic maternal protein deprivation
  Balasa A, Dove CL, Van den Veyver IB, 59th Annual Society for Gynecologic Investigation, San Diego, CA, 1/21/2012
• Evaluating NLRP7 mutations in hydatidiform moles
  Mahadevan S, Wen S, Balasa A, Van den Veyver IB, 59th Annual Society for Gynecologic Investigation, San Diego, CA, 1/21/2012
• Sequencing analysis of NLRP7 and NLRP2: Can their mutations cause infertility or are they specific only for gestational trophoblastic disease?
  Aghajanova L, Mahadevan S, Altmae S, Stavreus-Evers A, Van den Veyver I, 59th Annual Society for Gynecologic Investigation, San Diego, CA, 1/21/2012
• Rapid Prenatal Diagnosis of Cytogenic Abnormalities by Array CGH Analysis
  Cheung SW, Shaw CA, Kang S-HL, Simovich MJ, Pursley AN, Darilek S, Ward PA, Chinault AC, Patel A, Lupski JR, Beaudet AL, Eng CM, Van den Veyver IB, Society for Maternal-Fetal Medicine 28st Annual meeting – The Pregnancy Meeting, Am J Ob Gyn, Dallas, TX, 1/7/2012
• Metagenomic-based approach to a comprehensive characterization of the vaginal microbiome signature in pregnancy
  Aagaard K, Versalovic J, Petrosino J, Mistretta T, Riehle K, Coarfa C, Raza S, Dowlin D, Rosenbaum S, Van den Veyver I, Milosavljevic A, Society for Maternal-Fetal Medicine 31st Annual meeting – The Pregnancy Meeting, Am J Obstet Gynecol, San Francisco, CA, 1/7/2012
• Evaluation of fetal demise by array comparative genomic hybridization of formalin-fixed paraffin-embedded tissue: a pilot study
  Evaluation of fetal demise by array comparative genomic hybridization of formalin-fixed paraffin-embedded tissue: a pilot study, Society for Maternal-Fetal Medicine 31st Annual meeting – The Pregnancy Meeting, San Francisco, CA, 1/7/2012
• Prenatal array comparative genomic hybridization: When it is indicated and what sample is best? Our experiences in over 1000 Prenatal Cases
  Cheung SW, Breman A, Pursley A, Hixson P, Bi W, Ward P, Shaw C, Lupski J, Van den Veyver I, Beaudet A, Patel A, Society for Maternal-Fetal Medicine 32nd Annual meeting – The Pregnancy Meeting, Am J Obstet Gynecol, Dallas, TX, 1/6/2012
• Genome-wide profiling of human uniparental tissues to search for novel imprinted genes
  Wen S, Wan W, Balasa A, Mahadevan S, Liu Z, Van den Veyver IB, American Society of Human Genetics Annual Meeting, San Francisco, CA, 1/6/2012
• Analysis of Aicardi syndrome genome using array CGH and EXOME sequencing
  Liu W, Bainbridge M, Balasa A, Wang X, Murdock D, Gibbs R, Van den Veyver IB, American Society of Human Genetics Annual Meeting, San Francisco, CA, 1/6/2012
• Counseling for variants of uncertain clinical significance (VOUS) in prenatal chromosomal microarray analysis (pCMA)
  Breman A. Pursley A, Ward P, Patel A, Bi W, Lupski J, Van den Veyver IB, Beaudet A, 16th International conference for prenatal diagnosis, Miami, FL, 1/3/2012
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Lectures

• Implementation of Prenatal Diagnostic Exome Sequencing: Scenarios and Challenges 
  Salt Lake, UT - 1/24/2015
• NIPT: Technology and biology 
  San Diego, CA - 1/23/2015
• Roles of NLRP7, NLRP2 and KHDC3L in imprinting and reproductive outcome 
  Galveston, TX - 1/15/2015
• Whole genome and whole exome sequencing 
  San Diego, CA - 1/3/2015
• Current Advances in Prenatal Genetic Diagnosis and Counseling 
  The Houstonian Hotel, Houston, TX - 1/24/2014
• Ethical issues in future PND fetal exome and genome sequencing 
  Brisbane, Australia - 1/20/2014
• CNS abnormalities and genetic syndromes 
  Brisbane, Australia - 1/20/2014
• Counseling issues in prenatal microarrays 
  Brisbane, Australia - 1/20/2014
• Counseling challenges for prenatal chromosomal microarray analysis; what to do with CNV’s and VOUS’s 
  New Orleans, LA - 1/17/2014
• Microarray technology: a foundation 
  San Francisco, CA, 2013; Phoenix, AZ, 2013 - 1/19/2013
• Arrays, NIPT and Expanded Carrier Screening: Advances and Controversies in Prenatal Genetics 
  Phoenix, AZ - 1/19/2013
• Prenatal Genetic Diagnosis – New Techniques and Who Should Be Tested? 
  Houston, TX - 1/18/2013
• NIPT technologies 
  San Francisco, CA - 1/13/2013
• Current State of Aicardi Syndrome Research: Challenges and Questions 
  Houston, TX - 1/11/2013
• Use of arrays in IUFD and miscarriage 
  Lisbon, Portugal - 1/2/2013
• From array to exome or whole genome sequencing in prenatal diagnosis? 
  Lisbon, Portugal - 1/2/2013
• Preconception Counseling 
  Houston, TX - 1/28/2012
• Prenatal Genetics 
  Houston, TX - 1/26/2012
• Research on Aicardi syndrome, update 
  Multiple locations, 2006, 2008, 2010, 2012 - 1/20/2012
• Prenatal exposures and autism risk in genetically predisposed individuals 
  Houston, TX - 1/13/2012
• A mouse model for Goltz syndrome 
  Houston, TX - 1/9/2012
• Update on prenatal genetic diagnostic technologies 
  Houston, TX - 1/5/2012
• Prenatal genetic diagnosis and screening today and in the future 
  Houston, TX - 1/4/2012
• Array in prenatal diagnosis 
  Miami, FL - 1/3/2012
• Update on prenatal diagnostic use of microarrays 
  San Francisco, CA - 1/9/2011
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Other

• Focal dermal hypoplasia 
  Sutton VR, Van den Veyver IB, GeneReviews™ [Internet]
  Seattle, WA - 1/15/2008
• Aicardi Syndrome 
  Sutton VR, Van den Veyver IB, GeneReviews™ [Internet]
  http://www.ncbi.nlm.nih.gov/books/NBK1381/
  Seattle, WA - 1/30/2006