Bernice Morrow - Publications

Yeshiva University, New York, NY, United States 
Human Development, Genetics, Neuroscience Biology

57 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
2018 Guo T, Diacou A, Hiroko N, McDonald-McGinn DM, Hestand M, Demaerel W, Zhang L, Zhao Y, Ujueta F, Shan J, Montagna C, Zheng D, Crowley TB, Kushan-Wells L, Bearden CE, ... ... Morrow BE, et al. Deletion size analysis of 1,680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2. Human Molecular Genetics. PMID 29361080 DOI: 10.1093/hmg/ddy028  0.32
2016 Guo X, Delio M, Haque N, Castellanos R, Hestand MS, Vermeesch JR, Morrow BE, Zheng D. Variant discovery and breakpoint region prediction for studying the human 22q11.2 deletion using BAC clone and whole genome sequencing analysis. Human Molecular Genetics. PMID 27436579 DOI: 10.1093/hmg/ddw221  0.32
2015 Guo T, Chung JH, Wang T, McDonald-McGinn DM, Kates WR, Hawuła W, Coleman K, Zackai E, Emanuel BS, Morrow BE. Histone Modifier Genes Alter Conotruncal Heart Phenotypes in 22q11.2 Deletion Syndrome. American Journal of Human Genetics. PMID 26608785 DOI: 10.1016/j.ajhg.2015.10.013  0.8
2015 Patel K, Giese AP, Grossheim JM, Hegde RS, Delio M, Samanich J, Riazuddin S, Frolenkov GI, Cai J, Ahmed ZM, Morrow BE. Correction: A Novel C-Terminal CIB2 (Calcium and Integrin Binding Protein 2) Mutation Associated with Non-Syndromic Hearing Loss in a Hispanic Family. Plos One. 10: e0141259. PMID 26473954 DOI: 10.1371/journal.pone.0141259  0.4
2015 Patel K, Giese AP, Grossheim JM, Hegde RS, Delio M, Samanich J, Riazuddin S, Frolenkov GI, Cai J, Ahmed ZM, Morrow BE. A Novel C-Terminal CIB2 (Calcium and Integrin Binding Protein 2) Mutation Associated with Non-Syndromic Hearing Loss in a Hispanic Family. Plos One. 10: e0133082. PMID 26426422 DOI: 10.1371/journal.pone.0133082  0.8
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, ... ... Morrow BE, 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  0.8
2015 Racedo SE, McDonald-McGinn DM, Chung JH, Goldmuntz E, Zackai E, Emanuel BS, Zhou B, Funke B, Morrow BE. Mouse and human CRKL is dosage sensitive for cardiac outflow tract formation. American Journal of Human Genetics. 96: 235-44. PMID 25658046 DOI: 10.1016/j.ajhg.2014.12.025  0.8
2014 Radoeva PD, Coman IL, Salazar CA, Gentile KL, Higgins AM, Middleton FA, Antshel KM, Fremont W, Shprintzen RJ, Morrow BE, Kates WR. Association between autism spectrum disorder in individuals with velocardiofacial (22q11.2 deletion) syndrome and PRODH and COMT genotypes. Psychiatric Genetics. 24: 269-72. PMID 25325218 DOI: 10.1097/YPG.0000000000000062  0.8
2014 Castellanos R, Xie Q, Zheng D, Cvekl A, Morrow BE. Mammalian TBX1 preferentially binds and regulates downstream targets via a tandem T-site repeat. Plos One. 9: e95151. PMID 24797903 DOI: 10.1371/journal.pone.0095151  0.32
2014 Kong P, Racedo SE, Macchiarulo S, Hu Z, Carpenter C, Guo T, Wang T, Zheng D, Morrow BE. Tbx1 is required autonomously for cell survival and fate in the pharyngeal core mesoderm to form the muscles of mastication. Human Molecular Genetics. 23: 4215-31. PMID 24705356 DOI: 10.1093/hmg/ddu140  0.8
2014 Zaveri HP, Beck TF, Hernández-García A, Shelly KE, Montgomery T, van Haeringen A, Anderlid BM, Patel C, Goel H, Houge G, Morrow BE, Cheung SW, Lalani SR, Scott DA. Identification of critical regions and candidate genes for cardiovascular malformations and cardiomyopathy associated with deletions of chromosome 1p36. Plos One. 9: e85600. PMID 24454898 DOI: 10.1371/journal.pone.0085600  0.8
2013 Freyer L, Nowotschin S, Pirity MK, Baldini A, Morrow BE. Conditional and constitutive expression of a Tbx1-GFP fusion protein in mice. Bmc Developmental Biology. 13: 33. PMID 23971992 DOI: 10.1186/1471-213X-13-33  1
2013 Delio M, Guo T, McDonald-McGinn DM, Zackai E, Herman S, Kaminetzky M, Higgins AM, Coleman K, Chow C, Jalbrzikowski M, Jarlbrzkowski M, Bearden CE, Bailey A, Vangkilde A, Olsen L, ... ... Morrow BE, et al. Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes. American Journal of Human Genetics. 92: 439-47. PMID 23453669 DOI: 10.1016/j.ajhg.2013.01.018  0.8
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  0.8
2013 Widdershoven JCC, Bowser M, Sheridan MB, McDonald-McGinn DM, Zackai EH, Solot CB, Kirschner RE, Beemer FA, Morrow BE, Devoto M, Emanuel BS. A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patients International Journal of Pediatric Otorhinolaryngology. 77: 123-127. PMID 23121717 DOI: 10.1016/j.ijporl.2012.10.009  0.8
2012 Samanich J, Montagna C, Morrow BE, Babcock M. Interstitial duplication of 22q13.2 in a girl with short stature, impaired speech and language, and dysmorphism. Journal of Pediatric Genetics. 1: 47-53. PMID 27625801 DOI: 10.3233/PGE-2012-009  0.4
2012 Herman SB, Guo T, McGinn DM, Blonska A, Shanske AL, Bassett AS, Chow EW, Bowser M, Sheridan M, Beemer F, Devriendt K, Swillen A, Breckpot J, Digilio MC, Marino B, ... ... Morrow BE, et al. Overt cleft palate phenotype and TBX1 genotype correlations in velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. American Journal of Medical Genetics. Part A. 158: 2781-7. PMID 23034814 DOI: 10.1002/ajmg.a.35512  0.8
2012 Monks DC, Morrow BE. Identification of putative retinoic acid target genes downstream of mesenchymal Tbx1 during inner ear development. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 241: 563-73. PMID 22275070 DOI: 10.1002/dvdy.23731  1
2012 Rosenfeld JA, Amrom D, Andermann E, Andermann F, Veilleux M, Curry C, Fisher J, Deputy S, Aylsworth AS, Powell CM, Manickam K, Heese B, Maisenbacher M, Stevens C, Ellison JW, ... ... Morrow B, et al. Genotype-phenotype correlation in interstitial 6q deletions: a report of 12 new cases. Neurogenetics. 13: 31-47. PMID 22218741 DOI: 10.1007/s10048-011-0306-5  0.8
2012 Herman S, Delio M, Morrow B, Samanich J. Agnathia-otocephaly complex: a case report and examination of the OTX2 and PRRX1 genes. Gene. 494: 124-9. PMID 22198066 DOI: 10.1016/j.gene.2011.11.033  0.4
2011 Freyer L, Aggarwal V, Morrow BE. Dual embryonic origin of the mammalian otic vesicle forming the inner ear. Development (Cambridge, England). 138: 5403-14. PMID 22110056 DOI: 10.1242/dev.069849  1
2011 Guo T, McDonald-McGinn D, Blonska A, Shanske A, Bassett AS, Chow E, Bowser M, Sheridan M, Beemer F, Devriendt K, Swillen A, Breckpot J, Digilio MC, Marino B, Dallapiccola B, ... ... Morrow B, et al. Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. Human Mutation. 32: 1278-89. PMID 21796729 DOI: 10.1002/humu.21568  0.8
2011 Friedman MA, Miletta N, Roe C, Wang D, Morrow BE, Kates WR, Higgins AM, Shprintzen RJ. Cleft palate, retrognathia and congenital heart disease in velo-cardio-facial syndrome: a phenotype correlation study. International Journal of Pediatric Otorhinolaryngology. 75: 1167-72. PMID 21763005 DOI: 10.1016/j.ijporl.2011.06.013  0.8
2011 Petti M, Samanich J, Pan Q, Huang CK, Reinmund J, Farooqi S, Morrow B, Babcock M. Molecular characterization of an interstitial deletion of 1p31.3 in a patient with obesity and psychiatric illness and a review of the literature American Journal of Medical Genetics, Part A. 155: 825-832. PMID 21416589 DOI: 10.1002/ajmg.a.33869  0.8
2011 Guo X, Freyer L, Morrow B, Zheng D. Characterization of the past and current duplication activities in the human 22q11.2 region. Bmc Genomics. 12: 71. PMID 21269513 DOI: 10.1186/1471-2164-12-71  1
2011 Rosenfeld JA, Lacassie Y, El-Khechen D, Escobar LF, Reggin J, Heuer C, Chen E, Jenkins LS, Collins AT, Zinner S, Babcock M, Morrow B, Schultz RA, Torchia BS, Ballif BC, et al. New cases and refinement of the critical region in the 1q41q42 microdeletion syndrome European Journal of Medical Genetics. 54: 42-49. PMID 20951845 DOI: 10.1016/j.ejmg.2010.10.002  0.8
2010 Rosenfeld JA, Crolla JA, Tomkins S, Bader P, Morrow B, Gorski J, Troxell R, Forster-Gibson C, Cilliers D, Hislop RG, Lamb A, Torchia B, Ballif BC, Shaffer LG. Refinement of causative genes in monosomy 1p36 through clinical and molecular cytogenetic characterization of small interstitial deletions American Journal of Medical Genetics, Part A. 152: 1951-1959. PMID 20635359 DOI: 10.1002/ajmg.a.33516  0.8
2010 Atzmon G, Hao L, Pe'er I, Velez C, Pearlman A, Palamara PF, Morrow B, Friedman E, Oddoux C, Burns E, Ostrer H. Abraham's children in the genome era: major Jewish diaspora populations comprise distinct genetic clusters with shared Middle Eastern Ancestry. American Journal of Human Genetics. 86: 850-9. PMID 20560205 DOI: 10.1016/j.ajhg.2010.04.015  0.8
2010 Monks DC, Jahangir A, Shanske AL, Samanich J, Morrow BE, Babcock M. Mutational analysis of HOXA2 and SIX2 in a Bronx population with isolated microtia International Journal of Pediatric Otorhinolaryngology. 74: 878-882. PMID 20542577 DOI: 10.1016/j.ijporl.2010.05.004  0.8
2010 Freyer L, Morrow BE. Canonical Wnt signaling modulates Tbx1, Eya1, and Six1 expression, restricting neurogenesis in the otic vesicle. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 239: 1708-22. PMID 20503367 DOI: 10.1002/dvdy.22308  1
2010 Aggarwal VS, Carpenter C, Freyer L, Liao J, Petti M, Morrow BE. Mesodermal Tbx1 is required for patterning the proximal mandible in mice. Developmental Biology. 344: 669-81. PMID 20501333 DOI: 10.1016/j.ydbio.2010.05.496  1
2010 Shan J, Chobot-Rodd J, Castellanos R, Babcock M, Shanske A, Parikh SR, Morrow BE, Samanich J. GJB2 mutation spectrum in 209 hearing impaired individuals of predominantly Caribbean Hispanic and African descent International Journal of Pediatric Otorhinolaryngology. 74: 611-618. PMID 20381175 DOI: 10.1016/j.ijporl.2010.03.004  0.8
2009 Suzuki G, Harper KM, Hiramoto T, Funke B, Lee M, Kang G, Buell M, Geyer MA, Kucherlapati R, Morrow B, Männistö PT, Agatsuma S, Hiroi N. Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in mice. Human Molecular Genetics. 18: 3914-25. PMID 19617637 DOI: 10.1093/hmg/ddp334  0.8
2009 Braunstein EM, Monks DC, Aggarwal VS, Arnold JS, Morrow BE. Tbx1 and Brn4 regulate retinoic acid metabolic genes during cochlear morphogenesis. Bmc Developmental Biology. 9: 31. PMID 19476657 DOI: 10.1186/1471-213X-9-31  0.8
2009 Fischer TC, Samanich J, Morrow BE, Chobot-Rodd J, Shanske A, Parikh SR. Genetic evaluation of American minority pediatric cochlear implant recipients. International Journal of Pediatric Otorhinolaryngology. 73: 195-203. PMID 19081147 DOI: 10.1016/j.ijporl.2008.10.002  0.8
2008 Aggarwal VS, Morrow BE. Genetic modifiers of the physical malformations in velo-cardio-facial syndrome/DiGeorge syndrome. Developmental Disabilities Research Reviews. 14: 19-25. PMID 18636633 DOI: 10.1002/ddrr.4  0.8
2008 Liao J, Aggarwal VS, Nowotschin S, Bondarev A, Lipner S, Morrow BE. Identification of downstream genetic pathways of Tbx1 in the second heart field. Developmental Biology. 316: 524-37. PMID 18328475 DOI: 10.1016/j.ydbio.2008.01.037  0.8
2008 Braunstein EM, Crenshaw EB, Morrow BE, Adams JC. Cooperative function of Tbx1 and Brn4 in the periotic mesenchyme is necessary for cochlea formation. Journal of the Association For Research in Otolaryngology : Jaro. 9: 33-43. PMID 18231833 DOI: 10.1007/s10162-008-0110-6  0.8
2007 Babcock M, Yatsenko S, Hopkins J, Brenton M, Cao Q, de Jong P, Stankiewicz P, Lupski JR, Sikela JM, Morrow BE. Hominoid lineage specific amplification of low-copy repeats on 22q11.2 (LCR22s) associated with velo-cardio-facial/digeorge syndrome. Human Molecular Genetics. 16: 2560-71. PMID 17675367 DOI: 10.1093/hmg/ddm197  0.8
2007 Funke BH, Brown AC, Ramoni MF, Regan ME, Baglieri C, Finn CT, Babcock M, Shprintzen RJ, Morrow BE, Kucherlapati R. A novel, single nucleotide polymorphism-based assay to detect 22q11 deletions. Genetic Testing. 11: 91-100. PMID 17394398 DOI: 10.1089/gte.2006.0507  0.8
2007 Samanich J, Lowes C, Burk R, Shanske S, Lu J, Shanske A, Morrow BE. Mutations in GJB2, GJB6, and mitochondrial DNA are rare in African American and Caribbean Hispanic individuals with hearing impairment. American Journal of Medical Genetics. Part A. 143: 830-8. PMID 17357124 DOI: 10.1002/ajmg.a.31668  0.4
2007 Babcock M, Yatsenko S, Stankiewicz P, Lupski JR, Morrow BE. AT-rich repeats associated with chromosome 22q11.2 rearrangement disorders shape human genome architecture on Yq12 Genome Research. 17: 451-460. PMID 17284672 DOI: 10.1101/gr.5651507  0.8
2006 Aggarwal VS, Liao J, Bondarev A, Schimmang T, Lewandoski M, Locker J, Shanske A, Campione M, Morrow BE. Dissection of Tbx1 and Fgf interactions in mouse models of 22q11DS suggests functional redundancy. Human Molecular Genetics. 15: 3219-28. PMID 17000704 DOI: 10.1093/hmg/ddl399  0.8
2006 Long JM, LaPorte P, Merscher S, Funke B, Saint-Jore B, Puech A, Kucherlapati R, Morrow BE, Skoultchi AI, Wynshaw-Boris A. Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndrome. Neurogenetics. 7: 247-57. PMID 16900388 DOI: 10.1007/s10048-006-0054-0  0.8
2006 King M, Arnold JS, Shanske A, Morrow BE. T-genes and limb bud development. American Journal of Medical Genetics. Part A. 140: 1407-13. PMID 16688725 DOI: 10.1002/ajmg.a.31250  0.8
2006 Arnold JS, Braunstein EM, Ohyama T, Groves AK, Adams JC, Brown MC, Morrow BE. Tissue-specific roles of Tbx1 in the development of the outer, middle and inner ear, defective in 22q11DS patients. Human Molecular Genetics. 15: 1629-39. PMID 16600992 DOI: 10.1093/hmg/ddl084  0.8
2006 Nowotschin S, Liao J, Gage PJ, Epstein JA, Campione M, Morrow BE. Tbx1 affects asymmetric cardiac morphogenesis by regulating Pitx2 in the secondary heart field. Development (Cambridge, England). 133: 1565-73. PMID 16556915 DOI: 10.1242/dev.02309  0.44
2006 Arnold JS, Werling U, Braunstein EM, Liao J, Nowotschin S, Edelmann W, Hebert JM, Morrow BE. Inactivation of Tbx1 in the pharyngeal endoderm results in 22q11DS malformations. Development (Cambridge, England). 133: 977-87. PMID 16452092 DOI: 10.1242/dev.02264  0.8
2005 Hiroi N, Zhu H, Lee M, Funke B, Arai M, Itokawa M, Kucherlapati R, Morrow B, Sawamura T, Agatsuma S. A 200-kb region of human chromosome 22q11.2 confers antipsychotic-responsive behavioral abnormalities in mice. Proceedings of the National Academy of Sciences of the United States of America. 102: 19132-7. PMID 16365290 DOI: 10.1073/pnas.0509635102  0.8
2005 Yobb TM, Somerville MJ, Willatt L, Firth HV, Harrison K, MacKenzie J, Gallo N, Morrow BE, Shaffer LG, Babcock M, Chernos J, Bernier F, Sprysak K, Christiansen J, Haase S, et al. Microduplication and triplication of 22q11.2: A highly variable syndrome American Journal of Human Genetics. 76: 865-876. PMID 15800846 DOI: 10.1086/429841  0.8
2004 Liao J, Kochilas L, Nowotschin S, Arnold JS, Aggarwal VS, Epstein JA, Brown MC, Adams J, Morrow BE. Full spectrum of malformations in velo-cardio-facial syndrome/DiGeorge syndrome mouse models by altering Tbx1 dosage. Human Molecular Genetics. 13: 1577-85. PMID 15190012 DOI: 10.1093/hmg/ddh176  0.8
2004 Raft S, Nowotschin S, Liao J, Morrow BE. Suppression of neural fate and control of inner ear morphogenesis by Tbx1. Development (Cambridge, England). 131: 1801-12. PMID 15084464 DOI: 10.1242/dev.01067  0.44
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  0.8
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  0.8
2003 Stalmans I, Lambrechts D, De Smet F, Jansen S, Wang J, Maity S, Kneer P, von der Ohe M, Swillen A, Maes C, Gewillig M, Molin DG, Hellings P, Boetel T, Haardt M, ... ... Morrow B, et al. VEGF: a modifier of the del22q11 (DiGeorge) syndrome? Nature Medicine. 9: 173-82. PMID 12539040 DOI: 10.1038/nm819  0.8
2002 Kochilas L, Merscher-Gomez S, Lu MM, Potluri V, Liao J, Kucherlapati R, Morrow B, Epstein JA. The role of neural crest during cardiac development in a mouse model of DiGeorge syndrome. Developmental Biology. 251: 157-66. PMID 12413905 DOI: 10.1006/dbio.2002.0819  0.8
2002 McDermid HE, Morrow BE. Genomic disorders on 22q11. American Journal of Human Genetics. 70: 1077-88. PMID 11925570 DOI: 10.1086/340363  0.8
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