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Molecular and Human Genetics - Vandenveyver Lab

Houston, Texas

A BCM research lab.
Van den Veyver Lab
not shown on screen

Former Lab Members

Prisana Panichkul, M.D.
Current position: Faculty, Dept. of Obstetrics & Gynecology, Phramongkutklao Hospital, Bangkok, Thailand

Van den Veyver IB, Panichkul PP, Antalffy BA, Sun Y, Hunter JV, Armstrong DD. Presence of filamin in the astrocytic inclusions of Aicardi syndrome. Pediatr Neurol. 2004 Jan;30(1):7-15. Review. PubMed PMID: 14738943

Panichkul PC , Al-Hussaini TK, Sierra R, Kashork CD, Popek EJ, Stockton DW, Van den Veyver IB. Recurrent biparental hydatidiform mole: additional evidence for a 1.1-Mb locus in 19q13.4 and candidate gene analysis. J Soc Gynecol Investig. 2005 Jul;12(5):376-83. PubMed PMID: 15979551


Ruth Amir, M.D.
Current position: Research Scientist, Zinman College, Wingate Institute, Nathanya, Israel

Amir RE, Fang P, Yu Z, Glaze DG, Percy AK, Zoghbi HY, Roa BB, Van den Veyver IB. Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome. J Med Genet. 2005 Feb;42(2):e15. PubMed PMID: 15689438; PubMed Central PMCID: PMC1735975

Amir RE, Sutton VR, Van den Veyver IB. Newborn screening and prenatal diagnosis for Rett syndrome: implications for therapy. J Child Neurol. 2005 Sep;20(9):779-83. Review. PubMed PMID: 16225835


Ivan Delgado, Ph.D.
Current position: President & CEO, Mouse Genotype, Carlsbad, CA

Delgado IJ, Kim DS, Thatcher KN, LaSalle JM, Van den Veyver IB. Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients. BMC Med Genet. 2006 Jul 21;7:61. PubMed PMID: 16859563; PubMed Central PMCID: PMC1569822


Dong Sun Kim, Ph.D.
Current position: Assistant Professor, Dept. of Anatomy, Kyungpook National University School of Medicine, Taegu, South Korea

Delgado IJ, Kim DS, Thatcher KN, LaSalle JM, Van den Veyver IB. Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients. BMC Med Genet. 2006 Jul 21;7:61. PubMed PMID: 16859563; PubMed Central PMCID: PMC1569822


Ching Yuk Kou

Wang X, Reid Sutton V, Omar Peraza-Llanes J, Yu Z, Rosetta R, Kou YC, Eble TN, Patel A, Thaller C, Fang P, Van den Veyver IB. Mutations in X-linked PORCN, a putative regulator of Wnt signaling, cause focal dermal hypoplasia. Nat Genet. 2007 Jul;39(7):836-8. Epub 2007 Jun 3. PubMed PMID: 17546030

Kou YC, Shao L, Peng HH, Rosetta R, del Gaudio D, Wagner AF, Al-Hussaini TK, Van den Veyver IB. A recurrent intragenic genomic duplication, other novel mutations in NLRP7 and imprinting defects in recurrent biparental hydatidiform moles. Mol Hum Reprod. 2008 Jan;14(1):33-40. Epub 2007 Nov 26. PubMed PMID: 18039680


Hector Mendez-Figueroa, M.D.
Current position: Fellow, Division of Maternal-Fetal Medicine, Women & Infants Hospital, The Warren Alpert Medical School of Brown University, Providence, RI

Mendez-Figueroa H, Lamance K, Sutton VR, Aagaard-Tillery K, Van den Veyver I. Management of ornithine transcarbamylase deficiency in pregnancy. Am J Perinatol. 2010 Nov;27(10):775-84. Epub 2010 May 10. Review. PubMed PMID: 20458665


Monica Louet, Ph.D.
Current position: Instructor, Dept. of Urology, Baylor College of Medicine, Houston, TX


Gary Fruhman, M.D.
Current position: Assistant Professor, Dept. of Obstetrics & Gynecology, Baylor College of Medicine, Houston, TX


Amarillis Sanchez-Valle, M.D.
Current position: Assistant Professor & Director of the Metabolic Clinic, Dept. of Pediatrics, University of South Florida Health, Tampa, FL


Hsiu-Huei Peng, M.D.
Current position: Staff physician, Chang Gung Memorial Hospital, Taiwan

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