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Genetics - Graduate Program

Houston, Texas

Department of Molecular and Human Genetics
Department of Molecular and Human Genetics - Graduate Program
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Student Publications

Jaclyn Bravo

  • Ramocki MB, Bartnik M, Szafranski P, Kołodziejska KE, Xia Z, Bravo J, Miller GS, Rodriguez DL, Williams CA, Bader PI, Szczepanik E, Mazurczak T, Antczak-Marach D, Coldwell JG, Akman CI, McAlmon K, Cohen MP, McGrath J, Roeder E, Mueller J, Kang SH, Bacino CA, Patel A, Bocian E, Shaw CA, Cheung SW, Mazurczak T, Stankiewicz P (2010). Recurrent distal 7q11.23 deletion including HIP1 and YWHAG identified in patients with intellectual disabilities, epilepsy, and neurobehavioral problems. Am. J. Hum. Genet. 87(6): 857-65. PubMed PMID: 21109226

Christie Buchovecky

  • Buchovecky CM, Turley SD, Brown HM, Kyle SM, McDonald JG, Liu B, Pieper AA, Huang W, Katz DM, Russell DW, Shendure J, Justice MJ (2013). A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome. Nat. Genet. 45(9): 1013-20. PubMed PMID: 23892605

Ian Campbell

  • Boone PM, Soens ZT, Campbell IM, Stankiewicz P, Cheung SW, Patel A, Beaudet AL, Plon SE, Shaw CA, McGuire AL, Lupski JR (2012). Incidental copy-number variants identified by routine genome testing in a clinical population. Genet. Med. Aug 9. doi: 10.1038/gim.2012.95. PubMed PMID: 22878507
  • Campbell IM*, Yatsenko SA*, Hixson P, Reimschisel T, Thomas M, Wilson W, Dayal U, Wheless JW, Crunk C, Curry C, Parkinson N, Fishman L, Riviello JJ, Nowaczyk MJM, Zeesman S, Rosenfeld JA, Bejjani BA, Shaffer LG, Cheung SW, Lupski JR, Stankiewicz P, Scaglia F (2012). Novel 9q34.11 contiguous gene deletions encompassing four genes: STXBP1, SPTAN1, ENG, and TOR1A each conveying distinct haploinsufficiency clinical traits. Genet. Med. [Epub ahead of print] *Authors contributed equally. PubMed PMID: 22722545
  • Campbell IM, Kolodziejska KE, Quach M, Wolf VL, Cheung SW, Lalani SR, Ramocki MB, Stankiewicz P (2011). TGFBR2 deletion in a 20 month-old female with developmental delay and microcephaly. Am. J. Med. Genet. A. 155(6): 1442-7. PubMed PMID: 21567932

Hsing-I Ho

  • Hirose S, Benabentos R, Ho HI, Kuspa A, Shaulsky G (2011). Self-Recognition in Social Amoebae Is Mediated by Allelic Pairs of Tiger Genes. Science 33(6041): 467-70. PubMed PMID: 21700835

Ruchi Masand

  • Ricks CB, Masand R, Fang P, Roney EK, Cheung SW, Scott DA (2010). Delineation of a 1.65 Mb critical region for hemihyperplasia and digital anomalies on Xq25. Am. J. Med. Genet. A. 152A(2): 453-8. PubMed PMID: 20101693

Alison Mayle

  • Rossi L, Lin KK, Boles NC, Yang L, King KY, Jeong M, Mayle A, Goodell MA (2012). Less Is More: Unveiling the Functional Core of Hematopoietic Stem Cells through Knockout Mice. Cell Stem Cell 11(3): 302-17. PubMed PMID: 22958929

Amanda Rosewell

  • Prill JM, Espenlaub S, Samen U, Engler T, Schmidt E, Vetrini F, Rosewell A, Grove N, Palmer D, Ng P, Kochanek S, Kreppel F (2011). Modifications of adenovirus hexon allow for either hepatocyte detargeting or targeting with potential evasion from kupffer cells. Mol. Ther. 19(1): 83-92. PubMed PMID: 20959811

Zachry Soens

  • Boone PM, Soens ZT, Campbell IM, Stankiewicz P, Cheung SW, Patel A, Beaudet AL, Plon SE, Shaw CA, McGuire AL, Lupski JR (2012). Incidental copy-number variants identified by routine genome testing in a clinical population. Genet. Med. Aug 9. doi: 10.1038/gim.2012.95. PubMed PMID: 22878507

Xia Wang

  • Wang X, Wang H, Sun V, Tuan HF, Keser V, Wang KQ, Ren H, Lopez I, Zaneveld JE, Siddiqui S, Bowles S, Khan A, Salvo JS, Jacobson SG, Iannaccone A, Wang F, Birch D, Heckenlively JR, Fishman GA, Traboulsi EI, Li YM, Wheaton D, Koenekoop RK, Chen R (2013). Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencing. J. Med. Genet. [Epub ahead of print] PubMed PMID: 23847139
  • Koenekoop RK, Wang H, Majewski J, Wang X, Lopez I, Ren H, Chen Y, Li Y, Fishman GA, Genead M, Schwartzentruber J, Solanki N, Traboulsi EI, Cheng J, Logan CV, McKibbin M, Hayward BE, Parry DA, Johnson CA, Nageeb M; Finding of Rare Disease Genes (FORGE) Canada Consortium, Poulter JA, Mohamed MD, Jafri H, Rashid Y, Taylor GR, Keser V, Mardon G, Xu H, Inglehearn CF, Fu Q, Toomes C, Chen R (2012). Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration. Nat. Genet. 44(9): 1035-9. PubMed PMID: 22842230
  • Wang X, Wang H, Cao M, Li Z, Chen X, Patenia C, Gore A, Abboud EB, Al-Rajhi AA, Lewis RA, Lupski JR, Mardon G, Zhang K, Muzny D, Gibbs RA, Chen R (2011). Whole-exome sequencing identifies ALMS1, IQCB1, CNGA3, and MYO7A mutations in patients with Leber congenital amaurosis. Hum. Mutat. 32(12): 1450-9. PubMed PMID: 21901789
  • Daines B, Wang H, Wang L, Li Y, Han Y, Emmert D, Gelbart W, Wang X, Li W, Gibbs R, Chen R (2011). The Drosophila melanogaster transcriptome by paired-end RNA sequencing. Genome Res. 21(2): 315-24. PubMed PMID: 21177959

Liubin Yang

  • Rossi L, Lin KK, Boles NC, Yang L, King KY, Jeong M, Mayle A, Goodell MA (2012). Less Is More: Unveiling the Functional Core of Hematopoietic Stem Cells through Knockout Mice. Cell. Stem. Cell 11(3): 302-17. PubMed PMID: 22958929

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