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United States Department of Agriculture

Agricultural Research Service

Related Topics

Ignatia Van Den Veyver
Children's Nutrition Research Center
Nutrition Scientist

Phone: (713) 798-4914

1100 BATES ST
HOUSTON, TX, 77030


Publications (Clicking on the reprint icon Reprint Icon will take you to the publication reprint.)
Rapid prenatal diagnosis of cytogenetic abnormalities by array CGH analysis - (Abstract Only)
Cheung, S.W., Shaw, C., Kang, S., Simovich, M., Pursley, A., Darilek, S., Ward, P., Chinault, A.C., Patel, A., Lupski, J., Beaudet, A., Eng, C., Van Den Veyver, I. 2007. Rapid prenatal diagnosis of cytogenetic abnormalities by array CGH analysis [abstract]. American Journal of Obstetrics and Gynecology. 197(6)Supplement:S173.
A recurrent intragenic genomic duplication, other novel mutations in NLRP7 and imprinting defects in recurrent biparental hydatidiform moles - (Peer Reviewed Journal)
Kou, Y.C., Shao, L., Peng, H.H., Rosetta, R., del Gaudio, D., Wagner, A.F., Al-Hussaini, T.K., Van den Veyver, I.B. 2008. A recurrent intragenic genomic duplication, other novel mutations in NLRP7 and imprinting defects in recurrent biparental hydatidiform moles. Molecular Human Reproduction. 14(1):33-40.
Mecp2 deficiency leads to altered Htr2c pre-mRNA editing and HTR2C isoform distribution in mouse hippocampus and cerebellum - (Abstract Only)
Landers, M., Yu, Z., Van Den Veyver, I. 2007. Mecp2 deficiency leads to altered Htr2c pre-mRNA editing and HTR2C isoform distribution in mouse hippocampus and cerebellum [abstract]. In: 57th Annual Meeting of The American Society of Human Genetics, October 23-27, 2007, San Diego, California. p. 159.
Genome-wide array-based comparative genomic hybridization (array-CGH) analysis in Aicardi Syndrome - (Abstract Only)
Wang, X., Sutton, V.R., Eble, T., O'Neill, C., Lewis, R.A., Van Den Veyver, I.B. 2007. Genome-wide array-based comparative genomic hybridization (array-CGH) analysis in Aicardi Syndrome [abstract]. In: 57th Annual Meeting of The American Society of Human Genetics, October 23-27, 2007, San Diego, California. p. 472.
An intragenic genomic duplication resulting in loss of function and other novel mutations in NLRP7 in women with recurrent biparental hydatidiform moles - (Abstract Only)
Kou, Y., Shao, L., Rosetta, R., Del Gaudio, D., Peng, H., Al-Hussaini, T., Van Den Veyver, I.B. 2007. An intragenic genomic duplication resulting in loss of function and other novel mutations in NLRP7 in women with recurrent biparental hydatidiform moles [abstract]. In: 57th Annual Meeting of The American Society of Human Genetics, October 23-27, 2007, San Diego, California. p. 47.
Prenatal detection and characterization of supernumerary marker chromosomes by array-CGH - (Abstract Only)
Simovich, M.J., Kang, S.H.L., Patel, A., Pursley, A., Chinault, A.C., Lupski, J.R., Beaudet, A.L., Van Den Veyver, I.B., Cheung, S.W. 2007. Prenatal detection and characterization of supernumerary marker chromosomes by array-CGH [abstract]. In: 57th Annual Meeting of The American Society of Human Genetics, October 23-27, 2007, San Diego, California. p. 458.
Spectrum of PORCN mutations in Focal Dermal Hypoplasia - (Abstract Only)
Sutton, V.R., Wang, X., Peraza-Llanes, J.O., Yu, Z., Rosetta, R., Kou, Y.C., Eble, T.N., Patel, A., Thaller, C., Fang, P., Fernandes, P.H., Van Den Veyver, I.B. 2007. Spectrum of PORCN mutations in Focal Dermal Hypoplasia [abstract]. In: 57th Annual Meeting of The American Society of Human Genetics, October 23-27, 2007, San Diego, California. p. 90.
Mutations in X-linked PORCN, a putative regulator of Wnt signaling, cause focal dermal hypoplasia - (Peer Reviewed Journal)
Wang, X., Sutton, V.R., Peraza-Llanes, J.O., Yu, Z., Rosetta, R., Kou, Y., Eble, T.N., Patel, A., Thaller, C., Fang, P., Van den Veyver, I.B. 2007. Mutations in X-linked PORCN, a putative regulator of Wnt signaling, cause focal dermal hypoplasia. Nature Genetics. 39(7):836-838.
C57bl/6j Male Offspring Exposed "in Utero" and During Weaning to a Maternal Low Protein Diet Have Reduced Muscle Weight by 12 Months of Age - (Abstract Only)
Fiorotto, M.L., Rosetta, R., Yu, Z., Oliver, W., Van den Veyver, I. 2007. C57BL/6J Male offspring exposed "in utero" and during weaning to a maternal low protein diet have reduced muscle weight by 12 months of age [abstract]. Reproductive Sciences. 14(1)[Suppl]:95A.
Phenotype and management of Aicardi syndrome: new findings from a survey of 69 children - (Peer Reviewed Journal)
Glasmacher, M.A.K., Sutton, V.R., Hopkins, B., Eble, T., Lewis, R.A., Parsons, D.P., Van den Veyver, I.B. 2007. Phenotype and management of Aicardi syndrome: New findings from a survey of 69 children. Journal of Child Neurology. 22(2):176-184.
Evaluation of Mecp2(R308/Y) mutant mice as a model to study fetal programming - (Abstract Only)
Yu, Z., Rosetta, R., Sangi-Haghpeykar, H., Van Den Veyver, I. 2007. Evaluation of Mecp2(R308/Y) mutant mice as a model to study fetal programming [abstract]. Society for Gynecologic Investigation 2007 Annual Scientific Meeting. Abstract No. 950304.
Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization - (Peer Reviewed Journal)
Sahoo, T., Cheung, S.W., Ward, P., Darilek, S., Patel, A., del Gaudio, D., Kang, S.H.L., Lalani, S.R., Li, J., McAdoo, S., Burke, A., Shaw, C.A., Stankiewicz, P., Chinault, A.C., Van den Veyver, I.B., Roa, B.B., Beaudet, A.L., Eng, C.M. 2006. Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization. Genetics in Medicine. 8(11):719-727.
Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients - (Peer Reviewed Journal)
Delgado, I.J., Kim, D.S., Thatcher, K.N., LaSalle, J.M., Van den Veyver, I.B. 2006. Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients. BMC Medical Genetics [serial online]. 7:61.
Array-based comparative genomic hybridization (array CGH) for rapid prenatal diagnosis of cytogenetic abnormalities - (Abstract Only)
Van den Veyver, I.B., Sahoo, T., Shaw, C., Kang, S., Del Gaudio, D., Darilek, S., Patel, A., Ward, P., Li, J., Chinault, C., Roa, B., Lupski, J., Beaudet, A., Cheung, S., Eng, C. 2006. Array-based comparative genomic hybridization (array CGH) for rapid prenatal diagnosis of cytogenetic abnormalities [abstract]. American Society of Human Genetics, 2006 Annual Meeting, October 9-13, 2006, New Orleans, Louisiana. p. 27.
X-inactivation patterns in Aicardi syndrome - (Abstract Only)
Eble, T.N., Fang, P., Jin, W., Sutton, V.R., Lewis, R.A., Van den Veyver, I.B. 2006. X-inactivation patterns in Aicardi syndrome [abstract]. American Society of Human Genetics, 2006 Annual Meeting, October 9-13, 2006, New Orleans, Louisiana. p. 122.
Comparison between BAC and oligo array platforms in detecting submicroscopic genomic rearrangements - (Abstract Only)
Hixson, P., Laritsky, E., Wang, X., Jiang, T., Cheung, S., Van Den Veyver, I., Cai, W. 2006. Comparison between BAC and oligo array platforms in detecting submicroscopic genomic rearrangements [abstract]. American Society of Human Genetics, 2006 Annual Meeting, October 9-13, 2006, New Orleans, Louisiana. p. 239.
A Cpg Island at the Promoter of the Pde8b Gene Is Methylated in Placenta and Hydatidiform Moles, But Not in Control DNA - (Abstract Only)
Van Den Veyver, I.B., Smiraglia, D.J., Panichkul, P.C. 2004. A CpG island at the promoter of the PDE8B gene is methylated in placenta and hydatidiform moles, but not in control DNA [abstract]. Journal of the Society for Gynecologic Investigation. 11(2 Supplement 1):299A.
Genetic Effects of Methylation Diets - (Peer Reviewed Journal)
Van den Veyver, IB. 2002. Genetic effects of methylation diets. Annual Review of Nutrition. 22:255-282.
Last Modified: 10/1/2014
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