71 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
2019 Demaerel W, Mostovoy Y, Yilmaz F, Vervoort L, Pastor S, Hestand MS, Swillen A, Vergaelen E, Geiger EA, Coughlin CR, Chow SK, McDonald-McGinn D, Morrow B, Kwok PY, Xiao M, ... ... Shaikh TH, et al. The 22q11 low copy repeats are characterized by unprecedented size and structural variability. Genome Research. 29: 1389-1401. PMID 31481461 DOI: 10.1101/gr.248682.119  0.72
2015 Van Laarhoven PM, Neitzel LR, Quintana AM, Geiger EA, Zackai EH, Clouthier DE, Artinger KB, Ming JE, Shaikh TH. Kabuki syndrome genes KMT2D and KDM6A: functional analyses demonstrate critical roles in craniofacial, heart and brain development. Human Molecular Genetics. 24: 4443-53. PMID 25972376 DOI: 10.1093/hmg/ddv180  0.4
2015 Mlynarski EE, Sheridan MB, Xie M, Guo T, Racedo SE, McDonald-McGinn DM, Gai X, Chow EW, Vorstman J, Swillen A, Devriendt K, Breckpot J, Digilio MC, Marino B, Dallapiccola B, ... ... Shaikh TH, et al. 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. PMID 25892112 DOI: 10.1016/j.ajhg.2015.03.007  1
2015 Coughlin CR, Scharer GH, Friederich MW, Yu HC, Geiger EA, Creadon-Swindell G, Collins AE, Vanlander AV, Coster RV, Powell CA, Swanson MA, Minczuk M, Van Hove JL, Shaikh TH. Mutations in the mitochondrial cysteinyl-tRNA synthase gene, CARS2, lead to a severe epileptic encephalopathy and complex movement disorder. Journal of Medical Genetics. 52: 532-40. PMID 25787132 DOI: 10.1136/jmedgenet-2015-103049  1
2014 Quintana AM, Geiger EA, Achilly N, Rosenblatt DS, Maclean KN, Stabler SP, Artinger KB, Appel B, Shaikh TH. Hcfc1b, a zebrafish ortholog of HCFC1, regulates craniofacial development by modulating mmachc expression. Developmental Biology. 396: 94-106. PMID 25281006 DOI: 10.1016/j.ydbio.2014.09.026  1
2014 Yu HC, Geiger EA, Medne L, Zackai EH, Shaikh TH. An individual with blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) and additional features expands the phenotype associated with mutations in KAT6B American Journal of Medical Genetics, Part A. 164: 950-957. PMID 24458743 DOI: 10.1002/ajmg.a.36379  1
2014 Baker PR, Friederich MW, Swanson MA, Shaikh T, Bhattacharya K, Scharer GH, Aicher J, Creadon-Swindell G, Geiger E, MacLean KN, Lee WT, Deshpande C, Freckmann ML, Shih LY, Wasserstein M, et al. Variant non ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5. Brain : a Journal of Neurology. 137: 366-79. PMID 24334290 DOI: 10.1093/brain/awt328  1
2013 Izumi K, Housam R, Kapadia C, Stallings VA, Medne L, Shaikh TH, Kublaoui BM, Zackai EH, Grimberg A. Endocrine phenotype of 6q16.1-q21 deletion involving SIM1 and Prader-Willi syndrome-like features American Journal of Medical Genetics, Part A. 161: 3137-3143. PMID 24038875 DOI: 10.1002/ajmg.a.36149  1
2013 Yu HC, Sloan JL, Scharer G, Brebner A, Quintana AM, Achilly NP, Manoli I, Coughlin CR, Geiger EA, Schneck U, Watkins D, Suormala T, Van Hove JL, Fowler B, Baumgartner MR, ... ... Shaikh TH, et al. An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1. American Journal of Human Genetics. 93: 506-14. PMID 24011988 DOI: 10.1016/j.ajhg.2013.07.022  1
2013 Delio M, Pope K, Wang T, Samanich J, Haldeman-Englert CR, Kaplan P, Shaikh TH, Cai J, Marion RW, Morrow BE, Babcock M. 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. PMID 23401415 DOI: 10.1002/ajmg.a.35784  1
2012 Gai X, Xie HM, Perin JC, Takahashi N, Murphy K, Wenocur AS, D'arcy M, O'Hara RJ, Goldmuntz E, Grice DE, Shaikh TH, Hakonarson H, Buxbaum JD, Elia J, White PS. Rare structural variation of synapse and neurotransmission genes in autism. Molecular Psychiatry. 17: 402-11. PMID 21358714 DOI: 10.1038/mp.2011.10  1
2012 Coughlin CR, Scharer GH, Shaikh TH. Clinical impact of copy number variation analysis using high-resolution microarray technologies: advantages, limitations and concerns Genome Medicine. 4. DOI: 10.1186/gm381  1
2011 Goldmuntz E, Paluru P, Glessner J, Hakonarson H, Biegel JA, White PS, Gai X, Shaikh TH. Microdeletions and microduplications in patients with congenital heart disease and multiple congenital anomalies. Congenital Heart Disease. 6: 592-602. PMID 22010865 DOI: 10.1111/j.1747-0803.2011.00582.x  1
2011 Hannibal MC, Buckingham KJ, Ng SB, Ming JE, Beck AE, McMillin MJ, Gildersleeve HI, Bigham AW, Tabor HK, Mefford HC, Cook J, Yoshiura K, Matsumoto T, Matsumoto N, Miyake N, ... ... Shaikh TH, et al. Spectrum of MLL2 (ALR) mutations in 110 cases of Kabuki syndrome. American Journal of Medical Genetics. Part A. 155: 1511-6. PMID 21671394 DOI: 10.1002/ajmg.a.34074  1
2011 Dougherty MJ, Wilmoth DM, Tooke LS, Shaikh TH, Gai X, Hakonarson H, Biegel JA. Implementation of high resolution single nucleotide polymorphism array analysis as a clinical test for patients with hematologic malignancies. Cancer Genetics. 204: 26-38. PMID 21356189 DOI: 10.1016/j.cancergencyto.2010.10.007  1
2011 Foley AR, Hu Y, Zou Y, Yang M, Medne L, Leach M, Conlin LK, Spinner N, Shaikh TH, Falk M, Neumeyer AM, Bliss L, Tseng BS, Winder TL, Bönnemann CG. Large genomic deletions: a novel cause of Ullrich congenital muscular dystrophy. Annals of Neurology. 69: 206-11. PMID 21280092 DOI: 10.1002/ana.22283  1
2011 Shaikh TH, Haldeman-Englert C, Geiger EA, Ponting CP, Webber C. Genes and biological processes commonly disrupted in rare and heterogeneous developmental delay syndromes. Human Molecular Genetics. 20: 880-93. PMID 21147756 DOI: 10.1093/hmg/ddq527  1
2010 Gajecka M, Saitta SC, Gentles AJ, Campbell L, Ciprero K, Geiger E, Catherwood A, Rosenfeld JA, Shaikh T, Shaffer LG. Recurrent interstitial 1p36 deletions: Evidence for germline mosaicism and complex rearrangement breakpoints. American Journal of Medical Genetics. Part A. 152: 3074-83. PMID 21108392 DOI: 10.1002/ajmg.a.33733  1
2010 Sheridan MB, Kato T, Haldeman-Englert C, Jalali GR, Milunsky JM, Zou Y, Klaes R, Gimelli G, Gimelli S, Gemmill RM, Drabkin HA, Hacker AM, Brown J, Tomkins D, Shaikh TH, et al. 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. PMID 20673865 DOI: 10.1016/j.ajhg.2010.07.002  1
2010 Girirajan S, Rosenfeld JA, Cooper GM, Antonacci F, Siswara P, Itsara A, Vives L, Walsh T, McCarthy SE, Baker C, Mefford HC, Kidd JM, Browning SR, Browning BL, Dickel DE, ... ... Shaikh TH, et al. A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay. Nature Genetics. 42: 203-9. PMID 20154674 DOI: 10.1038/ng.534  1
2010 Gai X, Perin JC, Murphy K, O'Hara R, D'arcy M, Wenocur A, Xie HM, Rappaport EF, Shaikh TH, White PS. CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics. Bmc Bioinformatics. 11: 74. PMID 20132550 DOI: 10.1186/1471-2105-11-74  1
2010 Haldeman-Englert CR, Chapman KA, Kruger H, Geiger EA, McDonald-McGinn DM, Rappaport E, Zackai EH, Spinner NB, Shaikh TH. A de novo 8.8-Mb deletion of 21q21.1-q21.3 in an autistic male with a complex rearrangement involving chromosomes 6, 10, and 21. American Journal of Medical Genetics. Part A. 152: 196-202. PMID 20034085 DOI: 10.1002/ajmg.a.33176  1
2010 Elia J, Gai X, Xie HM, Perin JC, Geiger E, Glessner JT, D'arcy M, deBerardinis R, Frackelton E, Kim C, Lantieri F, Muganga BM, Wang L, Takeda T, Rappaport EF, ... ... Shaikh TH, et al. Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes. Molecular Psychiatry. 15: 637-46. PMID 19546859 DOI: 10.1038/mp.2009.57  1
2010 Elia J, Gai X, Xie HM, Perin JC, Geiger E, Glessner JT, D'Arcy M, Deberardinis R, Frackelton E, Kim C, Lantieri F, Muganga BM, Wang L, Takeda T, Rappaport EF, ... ... Shaikh TH, et al. Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes (Molecular Psychiatry (2010) 15 (637-646) DOI: 10.1038/mp.2009.57) Molecular Psychiatry. 15: 1122. DOI: 10.1038/mp.2010.75  1
2009 McCarthy SE, Makarov V, Kirov G, Addington AM, McClellan J, Yoon S, Perkins DO, Dickel DE, Kusenda M, Krastoshevsky O, Krause V, Kumar RA, Grozeva D, Malhotra D, Walsh T, ... ... Shaikh TH, et al. Microduplications of 16p11.2 are associated with schizophrenia. Nature Genetics. 41: 1223-7. PMID 19855392 DOI: 10.1038/ng.474  1
2009 Haldeman-Englert CR, Naeem T, Geiger EA, Warnock A, Feret H, Ciano M, Davidson SL, Deardorff MA, Zackai EH, Shaikh TH. A 781-kb deletion of 13q12.3 in a patient with Peters plus syndrome. American Journal of Medical Genetics. Part A. 149: 1842-5. PMID 19610101 DOI: 10.1002/ajmg.a.32980  1
2009 Shaikh TH, Gai X, Perin JC, Glessner JT, Xie H, Murphy K, O'Hara R, Casalunovo T, Conlin LK, D'Arcy M, Frackelton EC, Geiger EA, Haldeman-Englert C, Imielinski M, Kim CE, et al. High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications. Genome Research. 19: 1682-90. PMID 19592680 DOI: 10.1101/gr.083501.108  1
2009 Diskin SJ, Hou C, Glessner JT, Attiyeh EF, Laudenslager M, Bosse K, Cole K, Mossé YP, Wood A, Lynch JE, Pecor K, Diamond M, Winter C, Wang K, Kim C, ... ... Shaikh TH, et al. Copy number variation at 1q21.1 associated with neuroblastoma. Nature. 459: 987-91. PMID 19536264 DOI: 10.1038/nature08035  1
2009 Stankiewicz P, Sen P, Bhatt SS, Storer M, Xia Z, Bejjani BA, Ou Z, Wiszniewska J, Driscoll DJ, Maisenbacher MK, Bolivar J, Bauer M, Zackai EH, McDonald-McGinn D, Nowaczyk MM, ... ... Shaikh TH, et al. Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations. American Journal of Human Genetics. 84: 780-91. PMID 19500772 DOI: 10.1016/j.ajhg.2009.05.005  1
2009 Jackson EM, Sievert AJ, Gai X, Hakonarson H, Judkins AR, Tooke L, Perin JC, Xie H, Shaikh TH, Biegel JA. Genomic analysis using high-density single nucleotide polymorphism-based oligonucleotide arrays and multiplex ligation-dependent probe amplification provides a comprehensive analysis of INI1/SMARCB1 in malignant rhabdoid tumors. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 15: 1923-30. PMID 19276269 DOI: 10.1158/1078-0432.CCR-08-2091  1
2009 Coppinger J, McDonald-McGinn D, Zackai E, Shane K, Atkin JF, Asamoah A, Leland R, Weaver DD, Lansky-Shafer S, Schmidt K, Feldman H, Cohen W, Phalin J, Powell B, Ballif BC, ... ... Shaikh TH, et al. Identification of familial and de novo microduplications of 22q11.21-q11.23 distal to the 22q11.21 microdeletion syndrome region. Human Molecular Genetics. 18: 1377-83. PMID 19193630 DOI: 10.1093/hmg/ddp042  1
2009 Haldeman-Englert CR, Gai X, Perin JC, Ciano M, Halbach SS, Geiger EA, McDonald-McGinn DM, Hakonarson H, Zackai EH, Shaikh TH. A 3.1-Mb microdeletion of 3p21.31 associated with cortical blindness, cleft lip, CNS abnormalities, and developmental delay. European Journal of Medical Genetics. 52: 265-8. PMID 19100872 DOI: 10.1016/j.ejmg.2008.11.005  1
2009 Kamath BM, Thiel BD, Gai X, Conlin LK, Munoz PS, Glessner J, Clark D, Warthen DM, Shaikh TH, Mihci E, Piccoli DA, Grant SF, Hakonarson H, Krantz ID, Spinner NB. SNP array mapping of chromosome 20p deletions: genotypes, phenotypes, and copy number variation. Human Mutation. 30: 371-8. PMID 19058200 DOI: 10.1002/humu.20863  1
2009 Sievert AJ, Jackson EM, Gai X, Hakonarson H, Judkins AR, Resnick AC, Sutton LN, Storm PB, Shaikh TH, Biegel JA. Duplication of 7q34 in pediatric low-grade astrocytomas detected by high-density single-nucleotide polymorphism-based genotype arrays results in a novel BRAF fusion gene. Brain Pathology (Zurich, Switzerland). 19: 449-58. PMID 19016743 DOI: 10.1111/j.1750-3639.2008.00225.x  1
2009 Inagaki H, Ohye T, Kogo H, Kato T, Bolor H, Taniguchi M, Shaikh TH, Emanuel BS, Kurahashi H. Chromosomal instability mediated by non-B DNA: Cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans Genome Research. 19: 191-198. PMID 18997000 DOI: 10.1101/gr.079244.108  1
2009 Sievert AJ, Jackson EM, Gai X, Hakonarson H, Judkins AR, Resnick AC, Sutton LN, Storm PB, Shaikh TH, Biegel JA. Duplication of 7q34 in pediatric low-grade astrocytomas detected by high-density single-nucleotide polymorphism-based genotype arrays results in a novel BRAF fusion gene (Brain Pathol (2008) 19 (449-458)) Brain Pathology. 19: 550. DOI: 10.1111/j.1750-3639.2009.00298.x  1
2009 Stankiewicz P, Sen P, Bhatt SS, Storer M, Xia Z, Bejjani BA, Ou Z, Wiszniewska J, Driscoll DJ, Maisenbacher MK, Bolivar J, Bauer M, Zackai EH, McDonald-McGinn D, Nowaczyk MMJ, ... ... Shaikh TH, et al. Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations (DOI:10.1016/j.ajhg.2009.05.005) American Journal of Human Genetics. 85: 537. DOI: 10.1016/j.ajhg.2009.08.013  1
2008 Keating BJ, Tischfield S, Murray SS, Bhangale T, Price TS, Glessner JT, Galver L, Barrett JC, Grant SF, Farlow DN, Chandrupatla HR, Hansen M, Ajmal S, Papanicolaou GJ, Guo Y, ... ... Shaikh T, et al. Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies. Plos One. 3: e3583. PMID 18974833 DOI: 10.1371/journal.pone.0003583  1
2008 Jalali GR, Vorstman JAS, Errami A, Vijzelaar R, Biegel J, Shaikh T, Emanuel BS. Detailed analysis of 22q11.2 with a high density MLPA probe set Human Mutation. 29: 433-440. PMID 18033723 DOI: 10.1002/humu.20640  1
2007 Shaikh TH. Oligonucleotide arrays for high-resolution analysis of copy number alteration in mental retardation/multiple congenital anomalies. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 9: 617-25. PMID 17873650 DOI: 10.1097/GIM.0b013e318148bb81  1
2007 Shaffer LG, Theisen A, Bejjani BA, Ballif BC, Aylsworth AS, Lim C, McDonald M, Ellison JW, Kostiner D, Saitta S, Shaikh T. The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 9: 607-16. PMID 17873649 DOI: 10.1097/GIM.0b013e3181484b49  1
2007 Ballif BC, Hornor SA, Jenkins E, Madan-Khetarpal S, Surti U, Jackson KE, Asamoah A, Brock PL, Gowans GC, Conway RL, Graham JM, Medne L, Zackai EH, Shaikh TH, Geoghegan J, et al. Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2. Nature Genetics. 39: 1071-3. PMID 17704777 DOI: 10.1038/ng2107  1
2007 Jackson EM, Shaikh TH, Zhang F, Wainwright LM, Storm PB, Hakonarson H, Zackai EH, Biegel JA. Atypical teratoid/rhabdoid tumor in a patient with Beckwith-Wiedemann syndrome. American Journal of Medical Genetics. Part A. 143: 1767-70. PMID 17603804 DOI: 10.1002/ajmg.a.31843  1
2007 Jackson EM, Shaikh TH, Gururangan S, Jones MC, Malkin D, Nikkel SM, Zuppan CW, Wainwright LM, Zhang F, Biegel JA. High-density single nucleotide polymorphism array analysis in patients with germline deletions of 22q11.2 and malignant rhabdoid tumor. Human Genetics. 122: 117-27. PMID 17541642 DOI: 10.1007/s00439-007-0386-3  1
2007 Shaikh TH, O'Connor RJ, Pierpont ME, McGrath J, Hacker AM, Nimmakayalu M, Geiger E, Emanuel BS, Saitta SC. Low copy repeats mediate distal chromosome 22q11.2 deletions: Sequence analysis predicts breakpoint mechanisms Genome Research. 17: 482-491. PMID 17351135 DOI: 10.1101/gr.5986507  1
2006 Ming JE, Geiger E, James AC, Ciprero KL, Nimmakayalu M, Zhang Y, Huang A, Vaddi M, Rappaport E, Zackai EH, Shaikh TH. Rapid detection of submicroscopic chromosomal rearrangements in children with multiple congenital anomalies using high density oligonucleotide arrays. Human Mutation. 27: 467-73. PMID 16619270 DOI: 10.1002/humu.20322  1
2005 Inagaki H, Ohye T, Kogo H, Yamada K, Kowa H, Shaikh TH, Emanuel BS, Kurahashi H. Palindromic AT-rich repeat in the NF1 gene is hypervariable in humans and evolutionarily conserved in primates Human Mutation. 26: 332-342. PMID 16116616 DOI: 10.1002/humu.20228  1
2005 Morrissette JJ, Medne L, Bentley T, Owens NL, Geiger E, Pipan M, Zackai EH, Shaikh T, Spinner NB. A patient with mosaic partial trisomy 18 resulting from dicentric chromosome breakage. American Journal of Medical Genetics. Part A. 137: 208-12. PMID 16082706 DOI: 10.1002/ajmg.a.30845  1
2004 Gotter AL, Shaikh TH, Budarf ML, Rhodes CH, Emanuel BS. A palindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2. Human Molecular Genetics. 13: 103-15. PMID 14613967 DOI: 10.1093/hmg/ddh004  1
2003 Nimmakayalu MA, Gotter AL, Shaikh TH, Emanuel BS. A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22) Human Molecular Genetics. 12: 2817-2825. PMID 12952865 DOI: 10.1093/hmg/ddg301  1
2003 Kurahashi H, Shaikh T, Takata M, Toda T, Emanuel BS. The constitutional t(17;22): Another translocation mediated by palindromic AT-rich repeats American Journal of Human Genetics. 72: 733-738. PMID 12557125 DOI: 10.1086/368062  1
2002 Langford PR, Sheehan BJ, Shaikh T, Kroll JS. Active copper- and zinc-containing superoxide dismutase in the cryptic genospecies of Haemophilus causing urogenital and neonatal infections discriminates them from Haemophilus influenzae sensu stricto. Journal of Clinical Microbiology. 40: 268-70. PMID 11773129 DOI: 10.1128/JCM.40.1.268-270.2002  1
2001 Emanuel BS, Shaikh TH. Segmental duplications: an 'expanding' role in genomic instability and disease. Nature Reviews. Genetics. 2: 791-800. PMID 11584295 DOI: 10.1038/35093500  1
2001 Shaikh TH, Kurahashi H, Emanuel BS. Evolutionarily conserved low copy repeats (LCRs) in 22q11 mediate deletions, duplications, translocations, and genomic instability: an update and literature review. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 3: 6-13. PMID 11339380  1
2000 Alemán C, Roy-Engel AM, Shaikh TH, Deininger PL. Cis-acting influences on Alu RNA levels. Nucleic Acids Research. 28: 4755-61. PMID 11095687  1
2000 Kurahashi H, Shaikh TH, Emanuel BS. Alu-mediated PCR artifacts and the constitutional t(11;22) breakpoint. Human Molecular Genetics. 9: 2727-32. PMID 11063731  1
2000 Kurahashi H, Shaikh TH, Zackai EH, Celle L, Driscoll DA, Budarf ML, Emanuel BS. Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22). American Journal of Human Genetics. 67: 763-8. PMID 10903930 DOI: 10.1086/303054  1
2000 Kurahashi H, Shaikh TH, Hu P, Roe BA, Emanuel BS, Budarf ML. Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22). Human Molecular Genetics. 9: 1665-70. PMID 10861293 DOI: 10.1093/hmg/9.11.1665  1
2000 Shaikh TH, Kurahashi H, Saitta SC, O'Hare AM, Hu P, Roe BA, Driscoll DA, McDonald-McGinn DM, Zackai EH, Budarf ML, Emanuel BS. Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis. Human Molecular Genetics. 9: 489-501. PMID 10699172 DOI: 10.1093/hmg/9.4.489  1
1999 Shaikh TH, Budarf ML, Celle L, Zackai EH, Emanuel BS. Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) families. American Journal of Human Genetics. 65: 1595-607. PMID 10577913 DOI: 10.1086/302666  1
1999 Saitta SC, McGrath JM, Mensch H, Shaikh TH, Zackai EH, Emanuel BS. A 22q11.2 deletion that excludes UFD1L and CDC45L in a patient with conotruncal and craniofacial defects. American Journal of Human Genetics. 65: 562-6. PMID 10417299 DOI: 10.1086/302514  1
1999 Shaikh TH, Gottlieb S, Sellinger B, Chen F, Roe BA, Oakey RJ, Emanuel BS, Budarf ML. Characterization of CDC45L: a gene in the 22q11.2 deletion region expressed during murine and human development. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 10: 322-6. PMID 10051334 DOI: 10.1007/s003359900996  1
1997 Bouyge-Moreau I, Rondeau G, Avet-Loiseau H, André MT, Bézieau S, Chérel M, Saleün S, Cadoret E, Shaikh T, De Angelis MM, Arcot S, Batzer M, Moisan JP, Devilder MC. Construction of a 780-kb PAC, BAC, and cosmid contig encompassing the minimal critical deletion involved in B cell chronic lymphocytic leukemia at 13q14.3 Genomics. 46: 183-190. PMID 9417905 DOI: 10.1006/geno.1997.5008  1
1997 Shaikh TH, Roy AM, Kim J, Batzer MA, Deininger PL. cDNAs derived from primary and small cytoplasmic Alu (scAlu) transcripts. Journal of Molecular Biology. 271: 222-34. PMID 9268654 DOI: 10.1006/jmbi.1997.1161  1
1996 Shaikh TH, Deininger PL. The role and amplification of the HS Alu subfamily founder gene. Journal of Molecular Evolution. 42: 15-21. PMID 8576958 DOI: 10.1007/BF00163206  1
1995 Batzer MA, Rubin CM, Hellmann-Blumberg U, Alegria-Hartman M, Leeflang EP, Stern JD, Bazan HA, Shaikh TH, Deininger PL, Schmid CW. Dispersion and insertion polymorphism in two small subfamilies of recently amplified human Alu repeats. Journal of Molecular Biology. 247: 418-27. PMID 7714898 DOI: 10.1006/jmbi.1994.0150  1
1995 Arcot SS, Shaikh TH, Kim J, Bennett L, Alegria-Hartman M, Nelson DO, Deininger PL, Batzer MA. Sequence diversity and chromosomal distribution of "young" Alu repeats. Gene. 163: 273-8. PMID 7590280 DOI: 10.1016/0378-1119(95)00317-Y  1
1994 Batzer MA, Stoneking M, Alegria-Hartman M, Bazan H, Kass DH, Shaikh TH, Novick GE, Ioannou PA, Scheer WD, Herrera RJ, Deininger PL. African origin of human-specific polymorphic Alu insertions Proceedings of the National Academy of Sciences of the United States of America. 91: 12288-12292. PMID 7991620 DOI: 10.1073/pnas.91.25.12288  1
1992 Batzer MA, Bazan HA, Kim J, Morrow SL, Shaikh TH, Arcot SS, Deininger PL. Large-scale subcloning of bacteriophage lambda ZAP clones. Biotechniques. 12: 370-1. PMID 1533305  1
1991 Batzer MA, Kilroy GE, Richard PE, Shaikh TH, Desselle TD, Hoppens CL, Deininger PL. Structure and variability of recently inserted alu family members Nucleic Acids Research. 19: 698. DOI: 10.1093/nar/19.3.698-b  1
1990 Batzer MA, Kilroy GE, Richard PE, Shaikh TH, Desselle TD, Hoppens CL, Deininger PL. Structure and variability of recently inserted Alu family members. Nucleic Acids Research. 18: 6793-8. PMID 2175877  1
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