Rare structural variation of synapse and neurotransmission genes in autism
Gai, X, Xie, H M, Perin, J C, Takahashi, N, Murphy, K, Wenocur, A S, D'arcy, M, O'Hara, R J, Goldmuntz, E, Grice, D E, Shaikh, T H, Hakonarson, H, Buxbaum, J D, Elia, J, White, P S
Published in Molecular psychiatry (01.04.2012)
Published in Molecular psychiatry (01.04.2012)
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Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome : genomic organization and deletion endpoint analysis
SHAIKH, T. H, KURAHASHI, H, EMANUEL, B. S, SAITTA, S. C, O'HARE, A. M, PING HU, ROE, B. A, DRISCOLL, D. A, MCDONALD-MCGINN, D. M, ZACKAI, E. H, BUDARF, M. L
Published in Human molecular genetics (01.03.2000)
Published in Human molecular genetics (01.03.2000)
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Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes
Elia, J, Gai, X, Xie, H M, Perin, J C, Geiger, E, Glessner, J T, D'arcy, M, deBerardinis, R, Frackelton, E, Kim, C, Lantieri, F, Muganga, B M, Wang, L, Takeda, T, Rappaport, E F, Grant, S F A, Berrettini, W, Devoto, M, Shaikh, T H, Hakonarson, H, White, P S
Published in Molecular psychiatry (01.06.2010)
Published in Molecular psychiatry (01.06.2010)
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Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22)
KURAHASHI, H, SHAIKH, T. H, PING HU, ROE, B. A, EMANUEL, B. S, BUDARF, M. L
Published in Human molecular genetics (01.07.2000)
Published in Human molecular genetics (01.07.2000)
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African Origin of Human-Specific Polymorphic Alu Insertions
Batzer, Mark A., Stoneking, Mark, Alegria-Hartman, Michelle, Bazan, Hernan, Kass, David H., Shaikh, Tamim H., Novick, Gabriel E., Ioannou, Panayiotis A., Scheer, W. Douglas, Herrera, Rene J., Deininger, Prescott L.
Published in Proceedings of the National Academy of Sciences - PNAS (06.12.1994)
Published in Proceedings of the National Academy of Sciences - PNAS (06.12.1994)
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Tightly Clustered 11q23 and 22q11 Breakpoints Permit PCR-Based Detection of the Recurrent Constitutional t(11;22)
Kurahashi, Hiroki, Shaikh, Tamim H., Zackai, Elaine H., Celle, Livija, Driscoll, Deborah A., Budarf, Marcia L., Emanuel, Beverly S.
Published in American journal of human genetics (01.09.2000)
Published in American journal of human genetics (01.09.2000)
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A 22q11.2 Deletion That Excludes UFD1L and CDC45L in a Patient with Conotruncal and Craniofacial Defects
Saitta, Sulagna C., McGrath, James M., Mensch, Holly, Shaikh, Tamim H., Zackai, Elaine H., Emanuel, Beverly S.
Published in American journal of human genetics (01.08.1999)
Published in American journal of human genetics (01.08.1999)
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Structure and variability of recently inserted alu family members
BDATZER, M. A, KILROY, G. E, RICHARD, P. E, SHAIKH, T. H, DESSELLE, T. D, HOPPENS, C. L, DEININGER, P. L
Published in Nucleic acids research (11.12.1990)
Published in Nucleic acids research (11.12.1990)
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Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes
Elia, J, Gai, X, Xie, H M, Perin, J C, Geiger, E, Glessner, J T, D'arcy, M, Deberardinis, R, Frackelton, E, Kim, C, Lantieri, F, Muganga, B M, Wang, L, Takeda, T, Rappaport, E F, Grant, S F A, Berrettini, W, Devoto, M, Shaikh, T H, Hakonarson, H, White, P S
Published in Molecular psychiatry (01.11.2010)
Published in Molecular psychiatry (01.11.2010)
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Large-scale subcloning of bacteriophage lambda ZAP clones
Batzer, M A, Bazan, H A, Kim, J, Morrow, S L, Shaikh, T H, Arcot, S S, Deininger, P L
Published in BioTechniques (01.03.1992)
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Published in BioTechniques (01.03.1992)
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Cis-acting influences on Alu RNA levels
Alemán, C, Roy-Engel, A M, Shaikh, T H, Deininger, P L
Published in Nucleic acids research (01.12.2000)
Published in Nucleic acids research (01.12.2000)
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Alu-mediated PCR artifacts and the constitutional t(11;22) breakpoint
KURAHASHI, Hiroki, SHAIKH, Tamim H, EMANUEL, Beverly S
Published in Human molecular genetics (01.11.2000)
Published in Human molecular genetics (01.11.2000)
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cDNAs derived from primary and small cytoplasmic Alu (scAlu) transcripts
Shaikh, Tamim H, Roy, Astrid M, Kim, Joomyeong, Batzer, Mark A, Deininger, Prescott L
Published in Journal of molecular biology (15.08.1997)
Published in Journal of molecular biology (15.08.1997)
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Dispersion and insertion polymorphism in two small subfamilies of recently amplified human Alu repeats
Batzer, M A, Rubin, C M, Hellmann-Blumberg, U, Alegria-Hartman, M, Leeflang, E P, Stern, J D, Bazan, H A, Shaikh, T H, Deininger, P L, Schmid, C W
Published in Journal of molecular biology (31.03.1995)
Published in Journal of molecular biology (31.03.1995)
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Identification of familial and de novo microduplications of 22q11.21–q11.23 distal to the 22q11.21 microdeletion syndrome region
Coppinger, Justine, McDonald-McGinn, Donna, Zackai, Elaine, Shane, Kate, Atkin, Joan F., Asamoah, Alexander, Leland, Robert, Weaver, David D., Lansky-Shafer, Susan, Schmidt, Karen, Feldman, Heidi, Cohen, William, Phalin, Judy, Powell, Berkley, Ballif, Blake C., Theisen, Aaron, Geiger, Elizabeth, Haldeman-Englert, Chad, Shaikh, Tamim H., Saitta, Sulagna, Bejjani, Bassem A., Shaffer, Lisa G.
Published in Human molecular genetics (15.04.2009)
Published in Human molecular genetics (15.04.2009)
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