| Year |
Citation |
Score |
| 2024 |
Vong KI, Lee S, Au KS, Crowley TB, Capra V, Martino J, Haller M, Araújo C, Machado HR, George R, Gerding B, James KN, Stanley V, Jiang N, Alu K, ... ... Morrow B, et al. Risk of meningomyelocele mediated by the common 22q11.2 deletion. Science (New York, N.Y.). 384: 584-590. PMID 38696583 DOI: 10.1126/science.adl1624 |
0.352 |
|
| 2023 |
Shi L, Song H, Zhou B, Morrow BE. regulates early angiogenesis in mouse embryos by accelerating endothelial cell maturation. Biorxiv : the Preprint Server For Biology. PMID 37503032 DOI: 10.1101/2023.07.12.548782 |
0.339 |
|
| 2023 |
Zhao Y, Wang Y, Shi L, McDonald-McGinn DM, Crowley TB, McGinn DE, Tran OT, Miller D, Lin JR, Zackai E, Johnston HR, Chow EWC, Vorstman JAS, Vingerhoets C, van Amelsvoort T, ... ... Morrow BE, et al. Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS. Npj Genomic Medicine. 8: 17. PMID 37463940 DOI: 10.1038/s41525-023-00363-y |
0.368 |
|
| 2022 |
Campbell IM, Crowley TB, Jobaliya C, Bailey A, McGinn DE, Gaiser K, Bassett A, Gur RE, Morrow B, Emanuel BS, Franco AT, French D, Zackai EH, McDonald-McGinn DM, Lambert MP. Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expression. Clinical Genetics. PMID 36075864 DOI: 10.1111/cge.14227 |
0.33 |
|
| 2021 |
Nomaru H, Liu Y, De Bono C, Righelli D, Cirino A, Wang W, Song H, Racedo SE, Dantas AG, Zhang L, Cai CL, Angelini C, Christiaen L, Kelly RG, Baldini A, ... ... Morrow BE, et al. Single cell multi-omic analysis identifies a Tbx1-dependent multilineage primed population in murine cardiopharyngeal mesoderm. Nature Communications. 12: 6645. PMID 34789765 DOI: 10.1038/s41467-021-26966-6 |
0.648 |
|
| 2021 |
Oluwafemi OO, Musfee FI, Mitchell LE, Goldmuntz E, Xie HM, Hakonarson H, Morrow BE, Guo T, Taylor DM, McDonald-McGinn DM, Emanuel BS, Agopian AJ. Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States. Genes. 12. PMID 34356046 DOI: 10.3390/genes12071030 |
0.361 |
|
| 2020 |
Pastor S, Tran O, Jin A, Carrado D, Silva BA, Uppuluri L, Abid HZ, Young E, Crowley TB, Bailey AG, McGinn DE, McDonald-McGinn DM, Zackai EH, Xie M, Taylor D, ... Morrow BE, et al. Optical mapping of the 22q11.2DS region reveals complex repeat structures and preferred locations for non-allelic homologous recombination (NAHR). Scientific Reports. 10: 12235. PMID 32699385 DOI: 10.1038/S41598-020-69134-4 |
0.339 |
|
| 2019 |
Vervoort L, Demaerel W, Rengifo LY, Odrzywolski A, Vergaelen E, Hestand MS, Breckpot J, Devriendt K, Swillen A, McDonald-McGinn DM, Fiksinski AM, Zinkstok JR, Morrow BE, Heung T, Vorstman JAS, et al. Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins. Human Molecular Genetics. 28: 3724-3733. PMID 31884517 DOI: 10.1093/Hmg/Ddz166 |
0.355 |
|
| 2019 |
Zhao Y, Diacou A, Johnston HR, Musfee FI, McDonald-McGinn DM, McGinn D, Crowley TB, Repetto GM, Swillen A, Breckpot J, Vermeesch JR, Kates WR, Digilio MC, Unolt M, Marino B, ... ... Morrow BE, et al. Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects. American Journal of Human Genetics. PMID 31870554 DOI: 10.1016/J.Ajhg.2019.11.010 |
0.328 |
|
| 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, 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 |
0.429 |
|
| 2019 |
Hasten E, Morrow BE. Tbx1 and Foxi3 genetically interact in the pharyngeal pouch endoderm in a mouse model for 22q11.2 deletion syndrome. Plos Genetics. 15: e1008301. PMID 31412026 DOI: 10.1371/journal.pgen.1008301 |
0.358 |
|
| 2019 |
Xie HM, Taylor DM, Zhang Z, McDonald-McGinn DM, Zackai EH, Stambolian D, Hakonarson H, Morrow BE, Emanuel BS, Goldmuntz E. Copy number variations in individuals with conotruncal heart defects reveal some shared developmental pathways irrespective of 22q11.2 deletion status. Birth Defects Research. PMID 31222980 DOI: 10.1002/Bdr2.1534 |
0.393 |
|
| 2018 |
Morrow BE, McDonald-McGinn DM, Emanuel BS, Vermeesch JR, Scambler PJ. Molecular genetics of 22q11.2 deletion syndrome. American Journal of Medical Genetics. Part A. 176: 2070-2081. PMID 30380194 DOI: 10.1002/ajmg.a.40504 |
0.38 |
|
| 2018 |
Hasten E, McDonald-McGinn DM, Crowley TB, Zackai E, Emanuel BS, Morrow BE, Racedo SE. Dysregulation of TBX1 dosage in the anterior heart field results in congenital heart disease resembling the 22q11.2 duplication syndrome. Human Molecular Genetics. PMID 29509905 DOI: 10.1093/hmg/ddy078 |
0.359 |
|
| 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 |
0.328 |
|
| 2017 |
Guo T, Repetto GM, McDonald McGinn DM, Chung JH, Nomaru H, Campbell CL, Blonska A, Bassett AS, Chow EWC, Mlynarski EE, Swillen A, Vermeesch J, Devriendt K, Gothelf D, Carmel M, ... ... Morrow BE, et al. Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3. Circulation. Cardiovascular Genetics. 10. PMID 29025761 DOI: 10.1161/Circgenetics.116.001690 |
0.31 |
|
| 2017 |
Demaerel W, Hestand MS, Vergaelen E, Swillen A, López-Sánchez M, Pérez-Jurado LA, McDonald-McGinn DM, Zackai E, Emanuel BS, Morrow BE, Breckpot J, Devriendt K, Vermeesch JR. Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements. American Journal of Human Genetics. PMID 28965848 DOI: 10.1016/J.Ajhg.2017.09.002 |
0.43 |
|
| 2017 |
Racedo SE, Hasten E, Lin M, Devakanmalai GS, Guo T, Ozbudak EM, Cai CL, Zheng D, Morrow BE. Reduced dosage of β-catenin provides significant rescue of cardiac outflow tract anomalies in a Tbx1 conditional null mouse model of 22q11.2 deletion syndrome. Plos Genetics. 13: e1006687. PMID 28346476 DOI: 10.1371/Journal.Pgen.1006687 |
0.368 |
|
| 2017 |
Lopez-Rivera E, Liu YP, Verbitsky M, Anderson BR, Capone VP, Otto EA, Yan Z, Mitrotti A, Martino J, Steers NJ, Fasel DA, Vukojevic K, Deng R, Racedo SE, Liu Q, ... ... Morrow BE, et al. Genetic Drivers of Kidney Defects in the DiGeorge Syndrome. The New England Journal of Medicine. PMID 28121514 DOI: 10.1056/Nejmoa1609009 |
0.359 |
|
| 2016 |
Acosta D, Bagchi S, Broin PÓ, Hollern D, Racedo SE, Morrow B, Sellers RS, Greally JM, Golden A, Andrechek E, Wood T, Montagna C. LPA receptor activity is basal specific and coincident with early pregnancy and involution during mammary gland postnatal development. Scientific Reports. 6: 35810. PMID 27808166 DOI: 10.1038/Srep35810 |
0.322 |
|
| 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 |
0.344 |
|
| 2016 |
Mlynarski EE, Xie M, Taylor D, Sheridan MB, Guo T, Racedo SE, McDonald-McGinn DM, Chow EW, Vorstman J, Swillen A, Devriendt K, Breckpot J, Digilio MC, Marino B, Dallapiccola B, ... ... Morrow BE, et al. Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome. Human Genetics. PMID 26742502 DOI: 10.1007/S00439-015-1623-9 |
0.343 |
|
| 2015 |
McDonald-McGinn DM, Sullivan KE, Marino B, Philip N, Swillen A, Vorstman JA, Zackai EH, Emanuel BS, Vermeesch JR, Morrow BE, Scambler PJ, Bassett AS. 22q11.2 deletion syndrome. Nature Reviews. Disease Primers. 1: 15071. PMID 27189754 DOI: 10.1038/nrdp.2015.71 |
0.335 |
|
| 2015 |
Chung JH, Cai J, Suskin BG, Zhang Z, Coleman K, Morrow BE. Whole-Genome Sequencing and Integrative Genomic Analysis Approach on Two 22q11.2 Deletion Syndrome Family Trios for Genotype to Phenotype Correlations. Human Mutation. 36: 797-807. PMID 25981510 DOI: 10.1002/Humu.22814 |
0.334 |
|
| 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 |
0.383 |
|
| 2014 |
Jackson A, Kasah S, Mansour SL, Morrow B, Basson MA. Endoderm-specific deletion of Tbx1 reveals an FGF-independent role for Tbx1 in pharyngeal apparatus morphogenesis. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 243: 1143-51. PMID 24812002 DOI: 10.1002/Dvdy.24147 |
0.374 |
|
| 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 |
0.322 |
|
| 2014 |
Zaveri HP, Beck TF, Hernández-GarcÃa 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 |
0.324 |
|
| 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 |
0.803 |
|
| 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 |
0.337 |
|
| 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 |
0.771 |
|
| 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 |
0.371 |
|
| 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 |
0.789 |
|
| 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 |
0.353 |
|
| 2012 |
Simrick S, Szumska D, Gardiner JR, Jones K, Sagar K, Morrow B, Bhattacharya S, Basson MA. Biallelic expression of Tbx1 protects the embryo from developmental defects caused by increased receptor tyrosine kinase signaling. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 241: 1310-24. PMID 22674535 DOI: 10.1002/Dvdy.23812 |
0.467 |
|
| 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 |
0.777 |
|
| 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 |
0.802 |
|
| 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 |
0.429 |
|
| 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 |
0.739 |
|
| 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 |
0.454 |
|
| 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 |
0.342 |
|
| 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 |
0.768 |
|
| 2011 |
Guo C, Sun Y, Zhou B, Adam RM, Li X, Pu WT, Morrow BE, Moon A, Li X. A Tbx1-Six1/Eya1-Fgf8 genetic pathway controls mammalian cardiovascular and craniofacial morphogenesis. The Journal of Clinical Investigation. 121: 1585-95. PMID 21364285 DOI: 10.1172/JCI58358 |
0.378 |
|
| 2011 |
Alkalay AA, Guo T, Montagna C, Digilio MC, Dallapiccola B, Marino B, Morrow B. Genetic dosage compensation in a family with velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome. American Journal of Medical Genetics. Part A. 155: 548-54. PMID 21337693 DOI: 10.1002/Ajmg.A.33861 |
0.48 |
|
| 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 |
0.777 |
|
| 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 |
0.783 |
|
| 2011 |
Simrick S, Szumska D, Gardiner J, Karun S, Morrow B, Bhattacharya S, Basson MA. Sprouty loss of function mutations in the mouse results in defects characteristic of 22q11 deletion syndrome, which are exacerbated by Tbx1 haploinsufficiency Developmental Biology. 356: 223-224. DOI: 10.1016/J.Ydbio.2011.05.366 |
0.453 |
|
| 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 |
0.454 |
|
| 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 |
0.755 |
|
| 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 |
0.755 |
|
| 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 |
0.782 |
|
| 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 |
0.742 |
|
| 2010 |
Yaguchi Y, Gardiner J, Yu T, Shim K, Morrow B, Basson MA. The control of inner ear morphogenesis by Sprouty and Tbx1 genes in mouse models of 22q11.2 deletion syndrome Developmental Biology. 344: 444. DOI: 10.1016/J.Ydbio.2010.05.131 |
0.489 |
|
| 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 |
0.374 |
|
| 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 |
0.773 |
|
| 2009 |
Monks DC, Braunstein EM, Morrow BE. Tbx1 regulates mesenchymal–epithelial signaling necessary for inner ear development Developmental Biology. 331: 477-478. DOI: 10.1016/J.Ydbio.2009.05.342 |
0.737 |
|
| 2009 |
King M, Ray N, Morrow B. 713: T-box genes and inner ear development American Journal of Obstetrics and Gynecology. 201: S258. DOI: 10.1016/J.Ajog.2009.10.730 |
0.345 |
|
| 2009 |
Alkalay A, Babcock M, Bergsmedh A, Monks D, King ME, Shaffer L, Morrow B. 709: Gene expression profiling of lymphoblastic cell lines from monosomy 1p36 patients reveals differential regulation (expression) of cardiac and neurologic relevant genes American Journal of Obstetrics and Gynecology. 201: S257. DOI: 10.1016/J.Ajog.2009.10.726 |
0.754 |
|
| 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 |
0.361 |
|
| 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 |
0.343 |
|
| 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 |
0.732 |
|
| 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 |
0.78 |
|
| 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 |
0.77 |
|
| 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 |
0.764 |
|
| 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 |
0.319 |
|
| 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 |
0.683 |
|
| 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 |
0.794 |
|
| 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 |
0.335 |
|
| 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 |
0.794 |
|
| 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 |
0.424 |
|
| 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 |
0.774 |
|
| 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 |
0.718 |
|
| 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 |
0.803 |
|
| 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 |
0.791 |
|
| 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 |
0.371 |
|
| 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 |
0.459 |
|
| 2002 |
Gross SJ, Ferreira JC, Morrow B, Dar P, Funke B, Khabele D, Merkatz I. Gene expression profile of trisomy 21 placentas: a potential approach for designing noninvasive techniques of prenatal diagnosis. American Journal of Obstetrics and Gynecology. 187: 457-62. PMID 12193943 DOI: 10.1067/Mob.2002.123542 |
0.343 |
|
| 2002 |
McDermid HE, Morrow BE. Genomic disorders on 22q11. American Journal of Human Genetics. 70: 1077-88. PMID 11925570 DOI: 10.1086/340363 |
0.404 |
|
| 2001 |
Funke B, Epstein JA, Kochilas LK, Lu MM, Pandita RK, Liao J, Bauerndistel R, Schüler T, Schorle H, Brown MC, Adams J, Morrow BE. Mice overexpressing genes from the 22q11 region deleted in velo-cardio-facial syndrome/DiGeorge syndrome have middle and inner ear defects Human Molecular Genetics. 10: 2549-2556. PMID 11709542 DOI: 10.1093/Hmg/10.22.2549 |
0.37 |
|
| 2001 |
Funke B, Pandita RK, Morrow BE. Isolation and characterization of a novel gene containing WD40 repeats from the region deleted in velo-cardio-facial/DiGeorge syndrome on chromosome 22q11 Genomics. 73: 264-271. PMID 11350118 DOI: 10.1006/geno.2000.6506 |
0.437 |
|
| 2001 |
Merscher S, Funke B, Epstein JA, Heyer J, Puech A, Lu MM, Xavier RJ, Demay MB, Russell RG, Factor S, Tokooya K, Jore BS, Lopez M, Pandita RK, Lia M, ... ... Morrow BE, et al. TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome. Cell. 104: 619-29. PMID 11239417 DOI: 10.1016/S0092-8674(01)00247-1 |
0.398 |
|
| 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 |
0.758 |
|
| 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 |
0.752 |
|
| 2000 |
Maldonado-Saldivia J, Funke B, Pandita RK, Schüler T, Morrow BE, Schorle H. Expression of Cdcrel-1 (Pnutl1), a gene frequently deleted in velo-cardio-facial syndrome/DiGeorge syndrome. Mechanisms of Development. 96: 121-4. PMID 10940632 DOI: 10.1016/S0925-4773(00)00370-1 |
0.352 |
|
| 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 |
0.744 |
|
| 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 |
0.762 |
|
| 1999 |
Edelmann L, Pandita RK, Morrow BE. Low-copy repeats mediate the common 3-Mb deletion in patients with velo- cardio-facial syndrome American Journal of Human Genetics. 64: 1076-1086. PMID 10090893 DOI: 10.1086/302343 |
0.401 |
|
| 1999 |
Funke B, Edelmann L, McCain N, Pandita RK, Ferreira J, Merscher S, Zohouri M, Cannizzaro L, Shanske A, Morrow BE. Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a 1.5-Mb region of overlap on chromosome 22q11 American Journal of Human Genetics. 64: 747-758. PMID 10053009 DOI: 10.1086/302284 |
0.41 |
|
| 1998 |
Funke B, Puech A, Saint-Jore B, Pandita R, Skoultchi A, Morrow B. Isolation and characterization of a human gene containing a nuclear localization signal from the critical region for velo-cardio-facial syndrome on 22q11 Genomics. 53: 146-154. PMID 9790763 DOI: 10.1006/Geno.1998.5488 |
0.536 |
|
| 1998 |
Roberts JL, Morrow B, Vega-Rich C, Salafia CM, Nitowsky HM. Incontinentia pigmenti in a newborn male infant with DNA confirmation. American Journal of Medical Genetics. 75: 159-63. PMID 9450877 DOI: 10.1002/(Sici)1096-8628(19980113)75:2<159::Aid-Ajmg7>3.0.Co;2-O |
0.321 |
|
| 1997 |
Funke B, Saint-Jore B, Puech A, Sirotkin H, Edelmann L, Carlson C, Raft S, Pandita RK, Kucherlapati R, Skoultchi A, Morrow BE. Characterization and mutation analysis of goosecoid-like (GSCL), a homeodomain-containing gene that maps to the critical region for VCFS/DGS on 22q11. Genomics. 46: 364-72. PMID 9441739 DOI: 10.1006/Geno.1997.5046 |
0.466 |
|
| 1997 |
Puech A, Saint-Jore B, Funke B, Gilbert DJ, Sirotkin H, Copeland NG, Jenkins NA, Kucherlapati R, Morrow B, Skoultchi AI. Comparative mapping of the human 22q11 chromosomal region and the orthologous region in mice reveals complex changes in gene organization. Proceedings of the National Academy of Sciences of the United States of America. 94: 14608-13. PMID 9405660 DOI: 10.1073/Pnas.94.26.14608 |
0.476 |
|
| 1997 |
Carlson C, Sirotkin H, Pandita R, Goldberg R, McKie J, Wadey R, Patanjali SR, Weissman SM, Anyane-Yeboa K, Warburton D, Scambler P, Shprintzen R, Kucherlapati R, Morrow BE. Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients. American Journal of Human Genetics. 61: 620-9. PMID 9326327 DOI: 10.1086/515508 |
0.421 |
|
| 1997 |
O'Donnell H, McKeown C, Gould C, Morrow B, Scambler P. Detection of an atypical 22q11 deletion that has no overlap with the DiGeorge syndrome critical region [5] American Journal of Human Genetics. 60: 1544-1548. PMID 9199579 DOI: 10.1016/S0002-9297(07)64250-5 |
0.445 |
|
| 1996 |
Papolos DF, Faedda GL, Veit S, Goldberg R, Morrow B, Kucherlapati R, Shprintzen RJ. Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder? The American Journal of Psychiatry. 153: 1541-7. PMID 8942449 DOI: 10.1176/Ajp.153.12.1541 |
0.358 |
|
| 1996 |
Lachman HM, Morrow B, Shprintzen R, Veit S, Parsia SS, Faedda G, Goldberg R, Kucherlapati R, Papolos DF. Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome. American Journal of Medical Genetics. 67: 468-72. PMID 8886163 DOI: 10.1002/(Sici)1096-8628(19960920)67:5<468::Aid-Ajmg5>3.0.Co;2-G |
0.434 |
|
| 1996 |
Sirotkin H, Morrow B, DasGupta R, Goldberg R, Patanjali SR, Shi G, Cannizzaro L, Shprintzen R, Weissman SM, Kucherlapati R. Isolation of a new clathrin heavy chain gene with muscle-specific expression from the region commonly deleted in velo-cardio-facial syndrome. Human Molecular Genetics. 5: 617-24. PMID 8733128 DOI: 10.1093/Hmg/5.5.617 |
0.471 |
|
| 1996 |
Edelmann W, Cohen PE, Kane M, Lau K, Morrow B, Bennett S, Umar A, Kunkel T, Cattoretti G, Chaganti R, Pollard JW, Kolodner RD, Kucherlapati R. Meiotic pachytene arrest in MLH1-deficient mice. Cell. 85: 1125-34. PMID 8674118 DOI: 10.1016/S0092-8674(00)81312-4 |
0.361 |
|
| 1996 |
Papolos DF, Goldberg R, Faedda G, Veit S, Shprintzen R, Kucherlapati R, Morrow B. Psychiatric illness in children and adults with Velo-cardio-facial syndrome with/without 22q11 deletions Psychiatric Genetics. 6: 172. DOI: 10.1097/00041444-199623000-00102 |
0.371 |
|
| 1995 |
Lindsay EA, Goldberg R, Jurecic V, Morrow B, Carlson C, Kucherlapati RS, Shprintzen RJ, Baldini A. Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions. American Journal of Medical Genetics. 57: 514-22. PMID 7677167 DOI: 10.1002/Ajmg.1320570339 |
0.479 |
|
| 1995 |
Karayiorgou M, Morris MA, Morrow B, Shprintzen RJ, Goldberg R, Borrow J, Gos A, Nestadt G, Wolyniec PS, Lasseter VK. Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11. Proceedings of the National Academy of Sciences of the United States of America. 92: 7612-6. PMID 7644464 DOI: 10.1073/Pnas.92.17.7612 |
0.414 |
|
| 1993 |
Das Gupta R, Morrow B, Marondel I, Parimoo S, Goei VL, Gruen J, Weissman S, Skoultchi A, Kucherlapati R. An integrated approach for identifying and mapping human genes. Proceedings of the National Academy of Sciences of the United States of America. 90: 4364-8. PMID 8506274 DOI: 10.1073/Pnas.90.10.4364 |
0.415 |
|
| 1993 |
Morrow B, Kucherlapati R. Gene targeting in mammalian cells by homologous recombination. Current Opinion in Biotechnology. 4: 577-82. PMID 7764209 DOI: 10.1016/0958-1669(93)90080-G |
0.353 |
|
| Show low-probability matches. |