Tamim Shaikh, Ph.D.
Affiliations: | University of Colorado Anschutz Medical Campus, Denver, Aurora, CO |
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"Tamim Shaikh"Parents
Sign in to add mentorPrescott Deininger | grad student | LSU Health Science Center New Orleans (Chemistry Tree) | |
Beverly Emanuel | post-doc | 1995-1999 | Penn |
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Publications
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Yilmaz F, Gurusamy U, Mosley TJ, et al. (2023) High level of complexity and global diversity of the 3q29 locus revealed by optical mapping and long-read sequencing. Genome Medicine. 15: 35 |
Vervoort L, Dierckxsens N, Pereboom Z, et al. (2021) 22q11.2 Low Copy Repeats Expanded in the Human Lineage. Frontiers in Genetics. 12: 706641 |
Mostovoy Y, Yilmaz F, Chow SK, et al. (2021) Genomic regions associated with microdeletion/microduplication syndromes exhibit extreme diversity of structural variation. Genetics. 217 |
Demaerel W, Mostovoy Y, Yilmaz F, et al. (2019) The 22q11 low copy repeats are characterized by unprecedented size and structural variability. Genome Research. 29: 1389-1401 |
Hu T, Kruszka P, Martinez AF, et al. (2018) Cytogenetics and holoprosencephaly: A chromosomal microarray study of 222 individuals with holoprosencephaly. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 178: 175-186 |
Mlynarski EE, Sheridan MB, Xie M, et al. (2015) Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome. American Journal of Human Genetics. 96: 753-64 |
Delio M, Pope K, Wang T, et al. (2013) Spectrum of elastin sequence variants and cardiovascular phenotypes in 49 patients with Williams-Beuren syndrome American Journal of Medical Genetics, Part A. 161: 527-533 |
Stankiewicz P, Kulkarni S, Dharmadhikari AV, et al. (2012) Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats. Human Mutation. 33: 165-79 |
Gajecka M, Saitta SC, Gentles AJ, et al. (2010) Recurrent interstitial 1p36 deletions: Evidence for germline mosaicism and complex rearrangement breakpoints. American Journal of Medical Genetics. Part A. 152: 3074-83 |
Sheridan MB, Kato T, Haldeman-Englert C, et al. (2010) A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: The t(8;22)(q24.13;q11.21) American Journal of Human Genetics. 87: 209-218 |