Author

Jack Favor

Observed names: Favor, Jack, J FAVOR, J Favor, J. FAVOR, J. Favor, JACK FAVOR

Observed institutions: Roswell Park Comprehensive Cancer Center, Georgia Institute of Technology, Emory University, Institut Pasteur, Western General Hospital, Churchill Hospital, Helmholtz Munich, University of Oxford, Mary Lyon Centre at MRC Harwell, Amt für Umwelt, Emory Eye Center, Jackson Laboratory, Oxford Centre for Diabetes, Endocrinology and Metabolism, MRC Human Genetics Unit, Institut für Humangenetik, Technical University of Munich, University of Pennsylvania, University of California, Davis, Medical Research Council

OpenAlex ID: A5089969722

Erratum: Mouse Small eye results from mutation in a paired-like homebox-containing gene

1992 · Robert E. Hill, Jack Favor, et al. · Nature · 1,270

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Mouse Small eye results from mutations in a paired-like homeobox-containing gene

1991 · Robert E. Hill, Jack Favor, et al. · Nature · 1,158

PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects

1994 · Tom Glaser, Lisa Jepeal, et al. · Nature Genetics · 713

A Humanized Version of Foxp2 Affects Cortico-Basal Ganglia Circuits in Mice

2009 · Wolfgang Enard, Sabine Gehre, et al. · Cell · 605

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The mouse Pax2 1Neu mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney

1996 · Jack Favor, Rodica Sandulache, et al. · Proceedings of the National Academy of Sciences · 391

COL4A2 Mutations Impair COL4A1 and COL4A2 Secretion and Cause Hemorrhagic Stroke

2011 · Marion Jeanne, Cassandre Labelle-Dumais, et al. · The American Journal of Human Genetics · 219

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Molecular Interaction between Projection Neuron Precursors and Invading Interneurons via Stromal-Derived Factor 1 (CXCL12)/CXCR4 Signaling in the Cortical Subventricular Zone/Intermediate Zone

2006 · Marie-Catherine Tiveron, Mireille Rossel, et al. · Journal of Neuroscience · 207

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Defects of neuronal migration and the pathogenesis of cortical malformations are associated with Small eye (Sey) in the mouse, a point mutation at the Pax-6-locus

1993 · Wolfgang Schmahl, Monika Knoedlseder, et al. · Acta Neuropathologica · 206

Ptf1a is essential for the differentiation of GABAergic and glycinergic amacrine cells and horizontal cells in the mouse retina

2007 · Hassan Nakhai, Saadettin Sel, et al. · Development · 202

Molecular dissection of Pax6 function: the specific roles of the paired domain and homeodomain in brain development

2004 · Nicole Haubst, Joachim Berger, et al. · Development · 191

Introducing the German Mouse Clinic: open access platform for standardized phenotyping

2005 · Valérie Gailus-Durner, Helmut Fuchs, et al. · Nature Methods · 190

pax2.1is required for the development of thyroid follicles in zebrafish

2002 · Thomas Wendl, Klaus Lun, et al. · Development · 177

Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics

2015 · Martin Hrabě de Angelis, George Nicholson, et al. · Nature Genetics · 145

Activating calcium-sensing receptor mutation in the mouse is associated with cataracts and ectopic calcification

2004 · Tertius A. Hough, Debora Bogani, et al. · Proceedings of the National Academy of Sciences · 141

Effects of ENU dosage on mouse strains

2000 · Monica J. Justice, Don A. Carpenter, et al. · Mammalian Genome · 138

Type IV Procollagen Missense Mutations Associated With Defects of the Eye, Vascular Stability, the Brain, Kidney Function and Embryonic or Postnatal Viability in the Mouse, Mus musculus: An Extension of the Col4a1 Allelic Series and the Identification of the First Two Col4a2 Mutant Alleles

2006 · Jack Favor, Christian Johannes Gloeckner, et al. · Genetics · 129

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Erratum: PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects (Nature Genetics 7 (463-471))

1994 · Thomas Gläser, Lisa I. Jepeal, et al. · Nature Genetics · 125

Dominant cataract mutations and specific-locus mutations in mice induced by radiation or ethylnitrosourea

1982 · U.H. Ehling, J. Favor, et al. · Mutation research. Fundamental and molecular mechanisms of mutagenesis · 112

Genomic, Transcriptional and Mutational Analysis of the Mouse microphthalmia Locus

2000 · Jón H Hallsson, Jack Favor, et al. · Genetics · 107

The Transcription Factor Pax6 Regulates Survival of Dopaminergic Olfactory Bulb Neurons via Crystallin αA

2010 · Jovica Ninkovic, Luisa Pinto, et al. · Neuron · 105

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A mutation in the connexin 50 (Cx50) gene is a candidate for the No2 mouse cataract

1998 · Ernest C. Steele Jr., Mary F. Lyon, et al. · Current Eye Research · 99

Induction of gene mutations in mice: The multiple endpoint approach

1985 · U.H. Ehling, D.J. Charles, et al. · Mutation research. Fundamental and molecular mechanisms of mutagenesis · 98

PAX2 Suppresses Apoptosis in Renal Collecting Duct Cells

2000 · Elena Torban, Michael Roger Eccles, et al. · American Journal Of Pathology · 97

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A comparison of the dominant cataract and recessive specific-locus mutation rates induced by treatment of male mice with ethylnitrosourea

1983 · Jack Favor · Mutation research. Fundamental and molecular mechanisms of mutagenesis · 94

Systemic First-Line Phenotyping

2009 · Valérie Gailus-Durner*, Helmut Fuchs*, et al. · Methods in molecular biology · 80

Works count: 173

Citation count: 9,777

H-index: 45

I10-index: 112