| Year |
Citation |
Score |
| 2022 |
Shao A, Lopez AJ, Chen J, Tham A, Javier S, Quiroz A, Frick S, Levine EM, Lloyd KCK, Leonard BC, Murphy CJ, Glaser TM, Moshiri A. Arap1 loss causes retinal pigment epithelium phagocytic dysfunction and subsequent photoreceptor death. Disease Models & Mechanisms. PMID 35758026 DOI: 10.1242/dmm.049343 |
0.409 |
|
| 2020 |
Davis ES, Voss G, Miesfeld JB, Zarate‐Sanchez J, Voss SR, Glaser T. The rax homeobox gene is mutated in the eyeless axolotl, Ambystoma mexicanum Developmental Dynamics. PMID 32864847 DOI: 10.1002/Dvdy.246 |
0.48 |
|
| 2020 |
Miesfeld JB, Ghiasvand NM, Marsh-Armstrong B, Marsh-Armstrong N, Miller EB, Zhang P, Manna SK, Zawadzki RJ, Brown NL, Glaser T. The remote enhancer provides transcriptional robustness during retinal ganglion cell development. Proceedings of the National Academy of Sciences of the United States of America. PMID 32817515 DOI: 10.1073/Pnas.2006888117 |
0.513 |
|
| 2019 |
Kwon YS, Tham A, Lopez AJ, Edwards S, Woods S, Chen J, Fortunato J, Quiroz A, Javier S, Au I, Clarke M, Humpal D, Lloyd KCK, Thomasy S, Murphy C, ... Glaser TM, et al. Cytoglobin deficiency potentiates Crb1-mediated retinal degeneration in rd8 mice. Developmental Biology. PMID 31634437 DOI: 10.1016/J.Ydbio.2019.10.013 |
0.399 |
|
| 2019 |
Lam PT, Padula SL, Hoang TV, Poth JE, Liu L, Liang C, LeFever AS, Wallace LM, Ashery-Padan R, Riggs PK, Shields JE, Shaham O, Rowan S, Brown NL, Glaser T, et al. Considerations for the use of Cre recombinase for conditional gene deletion in the mouse lens. Human Genomics. 13: 10. PMID 30770771 DOI: 10.1186/S40246-019-0192-8 |
0.382 |
|
| 2018 |
Kaukonen M, Woods S, Ahonen S, Lemberg S, Hellman M, Hytönen MK, Permi P, Glaser T, Lohi H. Maternal Inheritance of a Recessive RBP4 Defect in Canine Congenital Eye Disease. Cell Reports. 23: 2643-2652. PMID 29847795 DOI: 10.1016/J.Celrep.2018.04.118 |
0.366 |
|
| 2017 |
Miesfeld JB, Glaser T, Brown NL. The dynamics of native Atoh7 protein expression during mouse retinal histogenesis, revealed with a new antibody. Gene Expression Patterns : Gep. 27: 114-121. PMID 29225067 DOI: 10.1016/J.Gep.2017.11.006 |
0.475 |
|
| 2017 |
O'Sullivan ML, Puñal VM, Kerstein PC, Brzezinski JA, Glaser T, Wright KM, Kay JN. Astrocytes follow ganglion cell axons to establish an angiogenic template during retinal development. Glia. PMID 28722174 DOI: 10.1002/Glia.23189 |
0.745 |
|
| 2017 |
Moshiri A, Humpal D, Leonard BC, Imai DM, Tham A, Bower L, Clary D, Glaser TM, Lloyd KC, Murphy CJ. Arap1 Deficiency Causes Photoreceptor Degeneration in Mice. Investigative Ophthalmology & Visual Science. 58: 1709-1718. PMID 28324111 DOI: 10.1167/Iovs.16-20062 |
0.347 |
|
| 2015 |
Chou CM, Nelson C, Tarlé SA, Pribila JT, Bardakjian T, Woods S, Schneider A, Glaser T. Biochemical Basis for Dominant Inheritance, Variable Penetrance, and Maternal Effects in RBP4 Congenital Eye Disease. Cell. 161: 634-46. PMID 25910211 DOI: 10.1016/J.Cell.2015.03.006 |
0.377 |
|
| 2013 |
Hufnagel RB, Riesenberg AN, Quinn M, Brzezinski JA, Glaser T, Brown NL. Heterochronic misexpression of Ascl1 in the Atoh7 retinal cell lineage blocks cell cycle exit Molecular and Cellular Neuroscience. 54: 108-120. PMID 23481413 DOI: 10.1016/J.Mcn.2013.02.004 |
0.77 |
|
| 2013 |
Slavotinek AM, Mehrotra P, Nazarenko I, Tang PL, Lao R, Cameron D, Li B, Chu C, Chou C, Marqueling AL, Yahyavi M, Cordoro K, Frieden I, Glaser T, Prescott T, et al. Focal facial dermal dysplasia, type IV, is caused by mutations in CYP26C1. Human Molecular Genetics. 22: 696-703. PMID 23161670 DOI: 10.1093/Hmg/Dds477 |
0.367 |
|
| 2012 |
Prasov L, Nagy M, Rudolph DD, Glaser T. Math5 (Atoh7) gene dosage limits retinal ganglion cell genesis Neuroreport. 23: 631-634. PMID 22660169 DOI: 10.1097/Wnr.0B013E328355F260 |
0.478 |
|
| 2012 |
Prasov L, Masud T, Khaliq S, Mehdi SQ, Abid A, Oliver ER, Silva ED, Lewanda A, Brodsky MC, Borchert M, Kelberman D, Sowden JC, Dattani MT, Glaser T. ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous. Human Molecular Genetics. 21: 3681-94. PMID 22645276 DOI: 10.1093/Hmg/Dds197 |
0.734 |
|
| 2012 |
Prasov L, Glaser T. Pushing the envelope of retinal ganglion cell genesis: context dependent function of Math5 (Atoh7). Developmental Biology. 368: 214-30. PMID 22609278 DOI: 10.1016/J.Ydbio.2012.05.005 |
0.541 |
|
| 2012 |
Prasov L, Glaser T. Dynamic expression of ganglion cell markers in retinal progenitors during the terminal cell cycle Molecular and Cellular Neuroscience. 50: 160-168. PMID 22579728 DOI: 10.1016/J.Mcn.2012.05.002 |
0.492 |
|
| 2012 |
Brzezinski JA, Prasov L, Glaser T. Math5 defines the ganglion cell competence state in a subpopulation of retinal progenitor cells exiting the cell cycle Developmental Biology. 365: 395-413. PMID 22445509 DOI: 10.1016/J.Ydbio.2012.03.006 |
0.777 |
|
| 2011 |
Ghiasvand NM, Rudolph DD, Mashayekhi M, Brzezinski JA, Goldman D, Glaser T. Deletion of a remote enhancer near ATOH7 disrupts retinal neurogenesis, causing NCRNA disease. Nature Neuroscience. 14: 578-86. PMID 21441919 DOI: 10.1038/Nn.2798 |
0.774 |
|
| 2010 |
Prasov L, Brown NL, Glaser T. A critical analysis of Atoh7 (Math5) mRNA splicing in the developing mouse retina. Plos One. 5: e12315. PMID 20808762 DOI: 10.1371/Journal.Pone.0012315 |
0.414 |
|
| 2008 |
Akyol A, Hinoi T, Feng Y, Bommer GT, Glaser TM, Fearon ER. Generating somatic mosaicism with a Cre recombinase-microsatellite sequence transgene. Nature Methods. 5: 231-3. PMID 18264107 DOI: 10.1038/Nmeth.1182 |
0.361 |
|
| 2008 |
Saul SM, Brzezinski JA, Altschuler RA, Shore SE, Rudolph DD, Kabara LL, Halsey KE, Hufnagel RB, Zhou J, Dolan DF, Glaser T. Math5 expression and function in the central auditory system. Molecular and Cellular Neurosciences. 37: 153-69. PMID 17977745 DOI: 10.1016/J.Ydbio.2006.04.184 |
0.681 |
|
| 2006 |
Akimoto M, Cheng H, Zhu D, Brzezinski JA, Khanna R, Filippova E, Oh EC, Jing Y, Linares JL, Brooks M, Zareparsi S, Mears AJ, Hero A, Glaser T, Swaroop A. Targeting of GFP to newborn rods by Nrl promoter and temporal expression profiling of flow-sorted photoreceptors. Proceedings of the National Academy of Sciences of the United States of America. 103: 3890-5. PMID 16505381 DOI: 10.1073/Pnas.0508214103 |
0.767 |
|
| 2005 |
Brzezinski JA, Brown NL, Tanikawa A, Bush RA, Sieving PA, Vitaterna MH, Takahashi JS, Glaser T. Loss of circadian photoentrainment and abnormal retinal electrophysiology in Math5 mutant mice. Investigative Ophthalmology & Visual Science. 46: 2540-51. PMID 15980246 DOI: 10.1167/Iovs.04-1123 |
0.753 |
|
| 2004 |
Oliver ER, Saunders TL, Tarlé SA, Glaser T. Ribosomal protein L24 defect in belly spot and tail (Bst), a mouse Minute. Development (Cambridge, England). 131: 3907-20. PMID 15289434 DOI: 10.1242/Dev.01268 |
0.697 |
|
| 2003 |
Sun Y, Kanekar SL, Vetter ML, Gorski S, Jan YN, Glaser T, Brown NL. Conserved and divergent functions of Drosophila atonal, amphibian, and mammalian Ath5 genes. Evolution & Development. 5: 532-41. PMID 12950631 DOI: 10.1046/J.1525-142X.2003.03058.X |
0.479 |
|
| 2002 |
Brown NL, Dagenais SL, Chen CM, Glaser T. Molecular characterization and mapping of ATOH7, a human atonal homolog with a predicted role in retinal ganglion cell development. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 13: 95-101. PMID 11889557 DOI: 10.1007/S00335-001-2101-3 |
0.45 |
|
| 2002 |
Farjo R, Yu J, Othman MI, Yoshida S, Sheth S, Glaser T, Baehr W, Swaroop A. Mouse eye gene microarrays for investigating ocular development and disease. Vision Research. 42: 463-70. PMID 11853762 DOI: 10.1016/S0042-6989(01)00219-X |
0.413 |
|
| 2001 |
Tucker P, Laemle L, Munson A, Kanekar S, Oliver ER, Brown N, Schlecht H, Vetter M, Glaser T. The eyeless mouse mutation (ey1) removes an alternative start codon from the Rx/rax homeobox gene. Genesis (New York, N.Y. : 2000). 31: 43-53. PMID 11668677 DOI: 10.1002/Gene.10003 |
0.699 |
|
| 2001 |
Vincent A, Billingsley G, Priston M, Williams-Lyn D, Sutherland J, Glaser T, Oliver E, Walter MA, Heathcote G, Levin A, Héon E. Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly. Journal of Medical Genetics. 38: 324-6. PMID 11403040 DOI: 10.1136/Jmg.38.5.324 |
0.687 |
|
| 2000 |
Lauderdale JD, Wilensky JS, Oliver ER, Walton DS, Glaser T. 3' deletions cause aniridia by preventing PAX6 gene expression Proceedings of the National Academy of Sciences of the United States of America. 97: 13755-13759. PMID 11087823 DOI: 10.1073/Pnas.240398797 |
0.699 |
|
| 1998 |
Hodgkinson CA, Nakayama A, Li H, Swenson LB, Opdecamp K, Asher JH, Arnheiter H, Glaser T. Mutation at the anophthalmic white locus in Syrian hamsters: haploinsufficiency in the Mitf gene mimics human Waardenburg syndrome type 2. Human Molecular Genetics. 7: 703-8. PMID 9499424 DOI: 10.1093/Hmg/7.4.703 |
0.408 |
|
| 1994 |
Glaser T, Ton CC, Mueller R, Petzl-Erler ML, Oliver C, Nevin NC, Housman DE, Maas RL. Absence of PAX6 gene mutations in Gillespie syndrome (partial aniridia, cerebellar ataxia, and mental retardation). Genomics. 19: 145-8. PMID 8188215 DOI: 10.1006/Geno.1994.1024 |
0.373 |
|
| 1994 |
Glaser T, Jepeal L, Edwards JG, Young SR, Favor J, Maas RL. PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects. Nature Genetics. 7: 463-71. PMID 7951315 DOI: 10.1038/Ng0894-463 |
0.46 |
|
| 1994 |
Maas R, Elfering S, Glaser T, Jepeal L. Deficient outgrowth of the ureteric bud underlies the renal agenesis phenotype in mice manifesting the limb deformity (ld) mutation. Developmental Dynamics. 199: 214-228. PMID 7517224 DOI: 10.1002/Aja.1001990306 |
0.368 |
|
| 1992 |
Oettinger MA, Stanger B, Schatz DG, Glaser T, Call K, Housman D, Baltimore D. The recombination activating genes, RAG 1 and RAG 2, are on chromosome 11p in humans and chromosome 2p in mice. Immunogenetics. 35: 97-101. PMID 1735560 DOI: 10.1007/Bf00189518 |
0.361 |
|
| 1992 |
Call KM, Ito CY, Lindberg C, Memisoglu A, Petrou C, Glaser T, Jones C, Housman DE. Mapping and characterization of 129 cosmids on human chromosome 11p. Somatic Cell and Molecular Genetics. 18: 463-75. PMID 1475712 DOI: 10.1007/Bf01233086 |
0.332 |
|
| 1992 |
Larsson C, Weber G, Kvanta E, Lewis K, Janson M, Jones C, Glaser TM, Evans G, Nordenskjöld M. Isolation and mapping of polymorphic cosmid clones used for sublocalization of the multiple endocrine neoplasia type 1 (MEN1) locus. Human Genetics. 89: 187-193. PMID 1350263 DOI: 10.1007/Bf00217121 |
0.319 |
|
| 1992 |
Glaser T, Walton DS, Maas RL. Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene Nature Genetics. 2: 232-239. PMID 1345175 DOI: 10.1038/Ng1192-232 |
0.436 |
|
| 1991 |
Buckler AJ, Pelletier J, Haber DA, Glaser T, Housman DE. Isolation, characterization, and expression of the murine Wilms' tumor gene (WT1) during kidney development. Molecular and Cellular Biology. 11: 1707-12. PMID 1671709 DOI: 10.1128/Mcb.11.3.1707 |
0.406 |
|
| 1991 |
Pelletier J, Bruening W, Li FP, Haber DA, Glaser T, Housman DE. WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour. Nature. 353: 431-4. PMID 1654525 DOI: 10.1038/353431A0 |
0.423 |
|
| 1991 |
Royer-Pokora B, Ragg S, Heckl-Ostreicher B, Held M, Loos U, Call K, Glaser T, Housman D, Saunders G, Zabel B. Direct pulsed field gel electrophoresis of Wilms' tumors shows that DNA deletions in 11p13 are rare. Genes, Chromosomes & Cancer. 3: 89-100. PMID 1648959 DOI: 10.1002/Gcc.2870030203 |
0.328 |
|
| 1990 |
Glaser T, Lane J, Housman D. A mouse model of the aniridia-Wilms tumor deletion syndrome. Science (New York, N.Y.). 250: 823-7. PMID 2173141 DOI: 10.1126/Science.2173141 |
0.409 |
|
| 1990 |
Haber DA, Buckler AJ, Glaser T, Call KM, Pelletier J, Sohn RL, Douglass EC, Housman DE. An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor. Cell. 61: 1257-69. PMID 2163761 DOI: 10.1016/0092-8674(90)90690-G |
0.383 |
|
| 1990 |
Glaser T, Rose E, Morse H, Housman D, Jones C. A panel of irradiation-reduced hybrids selectively retaining human chromosome 11p13: their structure and use to purify the WAGR gene complex. Genomics. 6: 48-64. PMID 2154397 DOI: 10.1016/0888-7543(90)90447-3 |
0.36 |
|
| 1990 |
Call KM, Glaser T, Ito CY, Buckler AJ, Pelletier J, Haber DA, Rose EA, Kral A, Yeger H, Lewis WH. Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus. Cell. 60: 509-20. PMID 2154335 DOI: 10.1016/0092-8674(90)90601-A |
0.39 |
|
| 1990 |
Rose EA, Glaser T, Jones C, Smith CL, Lewis WH, Call KM, Minden M, Champagne E, Bonetta L, Yeger H. Complete physical map of the WAGR region of 11p13 localizes a candidate Wilms' tumor gene. Cell. 60: 495-508. PMID 2154334 DOI: 10.1016/0092-8674(90)90600-J |
0.319 |
|
| 1990 |
Brilliant MH, Szabo G, Katarova Z, Kozak CA, Glaser TM, Greenspan RJ, Housman DE. Sequences homologous to glutamic acid decarboxylase cDNA are present on mouse chromosomes 2 and 10. Genomics. 6: 115-22. PMID 1968040 DOI: 10.1016/0888-7543(90)90455-4 |
0.324 |
|
| 1989 |
Glaser T, Housman D, Lewis WH, Gerhard D, Jones C. A fine-structure deletion map of human chromosome 11p: analysis of J1 series hybrids. Somatic Cell and Molecular Genetics. 15: 477-501. PMID 2595451 DOI: 10.1007/Bf01534910 |
0.366 |
|
| 1989 |
Glaser T, Matthews KE, Hudson JW, Seth P, Housman DE, Crerar MM. Localization of the muscle, liver, and brain glycogen phosphorylase genes on linkage maps of mouse chromosomes 19, 12, and 2, respectively. Genomics. 5: 510-21. PMID 2575583 DOI: 10.1016/0888-7543(89)90017-7 |
0.376 |
|
| 1989 |
Glaser T, Driscoll DJ, Antonarakis S, Valle D, Housman D. A highly polymorphic locus cloned from the breakpoint of a chromosome 11p13 deletion associated with the WAGR syndrome. Genomics. 5: 880-93. PMID 2574149 DOI: 10.1016/0888-7543(89)90130-4 |
0.361 |
|
| 1989 |
Bale SJ, Bale AE, Stewart K, Dachowski L, McBride OW, Glaser T, Green JE, Mulvihill JJ, Brandi ML, Sakaguchi K, Aurbach GD, Marx SJ. Linkage analysis of multiple endocrine neoplasia type 1 with INT2 and other markers on chromosome 11 Genomics. 4: 320-322. PMID 2565877 DOI: 10.1016/0888-7543(89)90336-4 |
0.318 |
|
| 1988 |
Harley HG, Brook JD, Jackson CL, Glaser T, Walsh KV, Sarfarazi M, Kent R, Lager M, Koch M, Harper PS. Localization of a human Na+,K+-ATPase alpha subunit gene to chromosome 19q12----q13.2 and linkage to the myotonic dystrophy locus. Genomics. 3: 380-4. PMID 2907504 DOI: 10.1016/0888-7543(88)90131-0 |
0.333 |
|
| 1988 |
Maslen CL, Jones C, Glaser T, Magenis RE, Sheehy R, Kellogg J, Litt M. Seven polymorphic loci mapping to human chromosomal region 11q22-qter. Genomics. 2: 66-75. PMID 2898428 DOI: 10.1016/0888-7543(88)90110-3 |
0.321 |
|
| 1987 |
Arriza JL, Weinberger C, Cerelli G, Glaser TM, Handelin BL, Housman DE, Evans RM. Cloning of human mineralocorticoid receptor complementary DNA: structural and functional kinship with the glucocorticoid receptor. Science (New York, N.Y.). 237: 268-75. PMID 3037703 DOI: 10.1126/Science.3037703 |
0.302 |
|
| 1987 |
Kent RB, Fallows DA, Geissler E, Glaser T, Emanuel JR, Lalley PA, Levenson R, Housman DE. Genes encoding alpha and beta subunits of Na,K-ATPase are located on three different chromosomes in the mouse. Proceedings of the National Academy of Sciences of the United States of America. 84: 5369-73. PMID 2885848 DOI: 10.1073/Pnas.84.15.5369 |
0.302 |
|
| 1986 |
Glaser T, Lewis WH, Bruns GAP, Watkins PC, Rogler CE, Shows TB, Powers VE, Willard HF, Goguen JM, Simola KOJ, Housman DE. The β-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus Nature. 321: 882-887. PMID 3014343 DOI: 10.1038/321882A0 |
0.367 |
|
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