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T. Glaser · SciRah

Researcher profile · Semantic Scholar

T. Glaser

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T. Glaser — researcher profile on SciRah

h-index: 30
Works: 55
Citations: 5,481

Most-cited papers

PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects
T. Glaser, L. Jepeal, J. Edwards, S. Young +2 more
1994Nature Genetics722 citations
Semantic Scholar
Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene
T. Glaser, D. Walton, R. Maas
1992Nature Genetics663 citations
Semantic Scholar
An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor.
D. A. Haber, A. Buckler, T. Glaser, K. Call +4 more
1990Cell588 citations
Semantic Scholar
WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour
J. Pelletier, W. Bruening, Frederick P. Li, D. Haber +2 more
1991Nature469 citations
Semantic Scholar
Math5 encodes a murine basic helix-loop-helix transcription factor expressed during early stages of retinal neurogenesis.
N. Brown, Shami Kanekar, M. Vetter, P. Tucker +2 more
1998Development341 citations
Semantic Scholar
Targeting of GFP to newborn rods by Nrl promoter and temporal expression profiling of flow-sorted photoreceptors.
M. Akimoto, Hong Cheng, D. Zhu, Joseph A. Brzezinski +11 more
2006Proceedings of the National Academy of Sciences of the United States of America337 citations Open access
Semantic Scholar
Ribosomal protein L24 defect in Belly spot and tail (Bst), a mouse Minute
E. Oliver, T. Saunders, S. Tarlé, T. Glaser
2004Development303 citations Open access
Semantic Scholar
Deletion of a remote enhancer near ATOH7 disrupts retinal neurogenesis, causing NCRNA disease
N. Ghiasvand, D. Rudolph, M. Mashayekhi, Joseph A. Brzezinski +2 more
2011Nature Neuroscience139 citations Open access
Semantic Scholar
Math5 defines the ganglion cell competence state in a subpopulation of retinal progenitor cells exiting the cell cycle
Joseph A. Brzezinski, L. Prasov, T. Glaser
2012Developmental Biology134 citations Open access
Semantic Scholar
Erratum: PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects (Nature Genetics 7 (463-471))
T. Glaser, L. Jepeal, J. Edwards, S. Young +2 more
1994124 citations
Semantic Scholar
A fine-structure deletion map of human chromosome 11p: Analysis of J1 series hybrids
T. Glaser, D. Housman, W. Lewis, D. Gerhard +1 more
1989Somatic Cell Genetics118 citations
Semantic Scholar
Genomic, transcriptional and mutational analysis of the mouse microphthalmia locus.
Jón Hallsteinn Hallsson, J. Favor, C. Hodgkinson, T. Glaser +7 more
2000Genetics109 citations
Semantic Scholar
The β-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus
T. Glaser, W. H. Lewis, G. Bruns, P. Watkins +7 more
1986Nature103 citations
Semantic Scholar
The eyeless mouse mutation (ey1) removes an alternative start codon from the Rx/rax homeobox gene
P. Tucker, L. Laemle, Amanda Munson, Shami Kanekar +5 more
2001Genesis98 citations Open access
Semantic Scholar
Astrocytes Follow Ganglion Cell Axons to Establish an Angiogenic Template During Retinal Development
Matthew L. O'Sullivan, V. M. Punal, Patrick C. Kerstein, Joseph A. Brzezinski +3 more
2017Glia95 citations Open access
Semantic Scholar
Genes encoding alpha and beta subunits of Na,K-ATPase are located on three different chromosomes in the mouse.
R. Kent, D. Fallows, E. Geissler, T. Glaser +4 more
1987Proceedings of the National Academy of Sciences of the United States of America87 citations Open access
Semantic Scholar
ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous.
L. Prasov, T. Masud, S. Khaliq, S. Mehdi +10 more
2012Human Molecular Genetics76 citations Open access
Semantic Scholar
Math5 expression and function in the central auditory system.
Sara M Saul, Joseph A. Brzezinski, R. Altschuler, S. Shore +7 more
2008Molecular and cellular neurosciences74 citations Open access
Semantic Scholar
Biochemical basis for dominant inheritance, variable penetrance and maternal effects in RBP4 congenital eye disease
Christopher M. Chou, C. Nelson, S. Tarlé, Jonathan T. Pribila +4 more
2015Cell70 citations Open access
Semantic Scholar
Further support of the role of CYP1B1 in patients with Peters anomaly.
A. Vincent, G. Billingsley, M. Priston, T. Glaser +5 more
2006Molecular Vision64 citations
Semantic Scholar
Loss of circadian photoentrainment and abnormal retinal electrophysiology in Math5 mutant mice.
Joseph A. Brzezinski, N. Brown, A. Tanikawa, R. Bush +4 more
2005Investigative Ophthalmology and Visual Science64 citations
Semantic Scholar
Atoh7-independent specification of retinal ganglion cell identity
Justin Brodie-Kommit, Brian S. Clark, Qing Shi, Fion Shiau +14 more
2020Science Advances60 citations Open access
Semantic Scholar
Deficient outgrowth of the ureteric bud underlies the renal agenesis phenotype in mice manifesting the limb deformity (ld) mutation
R. Maas, S. Elfering, T. Glaser, L. Jepeal
1994Developmental Dynamics59 citations
Semantic Scholar
The Atoh7 remote enhancer provides transcriptional robustness during retinal ganglion cell development
Joel B. Miesfeld, N. Ghiasvand, Brennan P. Marsh-Armstrong, N. Marsh-Armstrong +6 more
2020Proceedings of the National Academy of Sciences of the United States of America47 citations Open access
Semantic Scholar
Pushing the envelope of retinal ganglion cell genesis: context dependent function of Math5 (Atoh7)
L. Prasov, T. Glaser
2012Developmental Biology47 citations Open access
Semantic Scholar
Mouse eye gene microarrays for investigating ocular development and disease.
R. Farjo, Jindan Yu, M. Othman, S. Yoshida +4 more
2002Vision Research47 citations Open access
Semantic Scholar
Molecular characterization and mapping of ATOH7, a human atonal homolog with a predicted role in retinal ganglion cell development
N. Brown, S. Dagenais, Chuanfang Chen, T. Glaser
2002Mammalian Genome45 citations Open access
Semantic Scholar
A panel of irradiation-reduced hybrids selectively retaining human chromosome 11p13: their structure and use to purify the WAGR gene complex.
T. Glaser, E. Rose, H. Morse, D. Housman +1 more
1990Genomics45 citations
Semantic Scholar
Direct pulsed field gel electrophoresis of Wilms' tumors shows that dna deletions in 11 p 13 are rare
B. Royer-Pokora, S. Ragg, Brigitte Heckl-Östreicher, M. Held +8 more
1991Genes, Chromosomes and Cancer44 citations
Semantic Scholar
Dynamic expression of ganglion cell markers in retinal progenitors during the terminal cell cycle
L. Prasov, T. Glaser
2012Molecular and cellular neurosciences36 citations Open access
Semantic Scholar
The dynamics of native Atoh7 protein expression during mouse retinal histogenesis, revealed with a new antibody
Joel B. Miesfeld, T. Glaser, N. Brown
2017Gene Expression Patterns29 citations
Semantic Scholar
Math5 (Atoh7) gene dosage limits retinal ganglion cell genesis
L. Prasov, Melinda S. Nagy, D. Rudolph, T. Glaser
2012NeuroReport29 citations Open access
Semantic Scholar
Comprehensive phenotypic and functional analysis of dominant and recessive FOXE3 alleles in ocular developmental disorders
Linda M. Reis, E. Sorokina, L. Dudakova, J. Moravíková +13 more
2021Human Molecular Genetics23 citations Open access
Semantic Scholar
Heterochronic misexpression of Ascl1 in the Atoh7 retinal cell lineage blocks cell cycle exit
R. Hufnagel, Amy N. Riesenberg, M. Quinn, Joseph A. Brzezinski +2 more
2013Molecular and cellular neurosciences23 citations Open access
Semantic Scholar
The recombination activating genes, RAG 1 and RAG 2, are on chromosome 11p in humans and chromosome 2p in mice
M. Oettinger, B. Stanger, D. Schatz, T. Glaser +3 more
2004Immunogenetics22 citations
Semantic Scholar
Conserved and divergent functions of Drosophila atonal, amphibian, and mammalian Ath5 genes
Yan Sun, Shami Kanekar, M. Vetter, S. Gorski +3 more
2003Evolution & Development22 citations Open access
Semantic Scholar
Localization of a human Na+,K+-ATPase alpha subunit gene to chromosome 19q12----q13.2 and linkage to the myotonic dystrophy locus.
H. Harley, J. Brook, C. L. Jackson, T. Glaser +6 more
1988Genomics22 citations
Semantic Scholar
A Critical Analysis of Atoh7 (Math5) mRNA Splicing in the Developing Mouse Retina
L. Prasov, N. Brown, T. Glaser
2010PLoS ONE19 citations Open access
Semantic Scholar
Analysis of FOXD3 sequence variation in human ocular disease
Bethany A. Volkmann Kloss, Linda M. Reis, D. Bremond-Gignac, T. Glaser +1 more
2012Molecular Vision17 citations
Semantic Scholar
Maternal Inheritance of a Recessive RBP4 Defect in Canine Congenital Eye Disease
Maria Kaukonen, S. Woods, S. Ahonen, Seppo Lemberg +5 more
2018Cell Reports16 citations Open access
Semantic Scholar
Erratum: Sequences homologous to glutamic acid decarboxylase cDNA are present on mouse chromosomes 2 and 10 (Genomics, (1990) 6 (115-122))
M. Brilliant, G. Szabó, Zoya Katarova, C. Kozak +3 more
199013 citations
Semantic Scholar
A highly polymorphic locus cloned from the breakpoint of a chromosome 11p13 deletion associated with the WAGR syndrome.
T. Glaser, D. J. Driscoll, S. Antonarakis, David Valle +1 more
1989Genomics13 citations
Semantic Scholar
Isolation and mapping of polymorphic cosmid clones used for sublocalization of the multiple endocrine neoplasia type 1 (MEN1) locus
C. Larsson, G. Weber, E. Kvanta, K. Lewis +5 more
1992Human Genetics9 citations
Semantic Scholar
The rax homeobox gene is mutated in the eyeless axolotl, Ambystoma mexicanum
Erik S. Davis, Gareth J. Voss, Joel B. Miesfeld, Juan Zarate-Sanchez +2 more
2020Developmental Dynamics5 citations Open access
Semantic Scholar
Summary Ribosomal protein L 24 defect in Belly spot and tail ( Bst ) , a mouse Minute
E. Oliver, T. Saunders, S. Tarlé, T. Glaser
20044 citations
Semantic Scholar
Mapping and characterization of 129 cosmids on human chromosome 11p
K. Call, C. Ito, C. Lindberg, Asli Memisoglu +4 more
1992Somatic Cell Genetics4 citations
Semantic Scholar
Isolation and Mapping of 62 New RFLP Markers on Human Chromosome I I
T. Tokino, E. Takahashi, M. Mori, A. Tanigami +5 more
20063 citations
Semantic Scholar
Novel CRB1 pathogenic variant in Chuuk families with Leber congenital amaurosis
Amani S. Albakri, Phattrawan Pisuchpen, Jenina E. Capasso, A. Schneider +6 more
2023American Journal of Medical Genetics. Part A2 citations Open access
Semantic Scholar
[4]Identification and functional analysis of mutations in the human PAX6 gene
R. Maas, J. Epstein, T. Glaser
19962 citations
Semantic Scholar
Phage 8-10 identifies an RFLP on 11q23-qter [HGM9 no. D11S286].
J. Luty, J. Kellogg, C. Maslen, C. Jones +2 more
1988Nucleic Acids Research2 citations Open access
Semantic Scholar

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