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Elizabeth M. Spiteri, Ph.D. - Publications

Affiliations: 
2002 Yeshiva University, New York, NY, United States 
Area:
Genetics
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8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Church AJ, Akkari Y, Deeb K, Kolhe R, Lin F, Spiteri E, Wolff DJ, Shao L. Section E6.7-6.12 of the American College of Medical Genetics and Genomics (ACMG) Technical Laboratory Standards: Cytogenomic studies of acquired chromosomal abnormalities in solid tumors. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 101070. PMID 38376505 DOI: 10.1016/j.gim.2024.101070  0.337
2003 Babcock M, Pavlicek A, Spiteri E, Kashork CD, Ioshikhes I, Shaffer LG, Jurka J, Morrow BE. Shuffling of genes within low-copy repeats on 22q11 (LCR22) by Alu-mediated recombination events during evolution. Genome Research. 13: 2519-32. PMID 14656960 DOI: 10.1101/Gr.1549503  0.633
2003 Allen E, Horvath S, Tong F, Kraft P, Spiteri E, Riggs AD, Marahrens Y. High concentrations of long interspersed nuclear element sequence distinguish monoallelically expressed genes. Proceedings of the National Academy of Sciences of the United States of America. 100: 9940-5. PMID 12909712 DOI: 10.1073/Pnas.1737401100  0.326
2003 Spiteri E, Babcock M, Kashork CD, Wakui K, Gogineni S, Lewis DA, Williams KM, Minoshima S, Sasaki T, Shimizu N, Potocki L, Pulijaal V, Shanske A, Shaffer LG, Morrow BE. Frequent translocations occur between low copy repeats on chromosome 22q11.2 (LCR22s) and telomeric bands of partner chromosomes. Human Molecular Genetics. 12: 1823-37. PMID 12874103 DOI: 10.1093/Hmg/Ddg203  0.639
2001 Edelmann L, Stankiewicz P, Spiteri E, Pandita RK, Shaffer L, Lupski J, Morrow BE. Two functional copies of the DGCR6 gene are present on human chromosome 22q11 due to a duplication of an ancestral locus Genome Research. 11: 208-217. PMID 11157784 DOI: 10.1101/Gr.Gr-1431R  0.683
2000 Edelmann L, Spiteri E, Koren K, Pulijaal V, Bialer MG, Shanske A, Goldberg R, Morrow BE. AT-rich palindromes mediate the constitutional t(11;22) translocation. American Journal of Human Genetics. 68: 1-13. PMID 11095996 DOI: 10.1086/316952  0.784
1999 Edelmann L, Spiteri E, McCain N, Goldberg R, Pandita RK, Duong S, Fox J, Blumenthal D, Lalani SR, Shaffer LG, Morrow BE. A common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocation. American Journal of Human Genetics. 65: 1608-16. PMID 10577914 DOI: 10.1086/302689  0.784
1999 Edelmann L, Pandita RK, Spiteri E, Funke B, Goldberg R, Palanisamy N, Chaganti RSK, Magenis E, Shprintzen RJ, Morrow BE. A common molecular basis for rearrangement disorders on chromosome 22q11 Human Molecular Genetics. 8: 1157-1167. PMID 10369860 DOI: 10.1093/Hmg/8.7.1157  0.758
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