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Susan A. Cook

Observed names: S. A. Cook, S. Cook, S.A. Cook, Susan A Cook, Susan Cook
OpenAlex ID: A5111772272
Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration
2006 · Jeong Woong Lee, Kirk Beebe, et al. · Nature · 596
A major gene affecting age-related hearing loss in C57BL/6J mice
1997 · Kenneth R. Johnson, Lawrence C. Erway, et al. · Hearing Research · 366
Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration
1996 · H. O. Sweet, R. T. Bronson, et al. · Mammalian Genome · 155
Motor neuron degeneration of mice is a model of neuronal ceroid lipofuscinosis (Batten's disease)
1993 · Roderick T. Bronson, Brian D. Lake, et al. · Annals of Neurology · 154
A frameshift mutation in the mouse α1 glycine receptor gene (Gira1) results in progressive neurological symptoms and juvenile death
1994 · Marion S. Buckwalter, Susan A. Cook, et al. · Human Molecular Genetics · 115
A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry ( hscy ) mice
2005 · Chantal M. Longo-Guess, Leona H. Gagnon, et al. · Proceedings of the National Academy of Sciences · 99
Inner Ear and Kidney Anomalies Caused by IAP Insertion in an Intron of the Eya1 Gene in a Mouse Model of BOR Syndrome
1999 · K. R. Johnson, S. A. Cook, et al. · Human Molecular Genetics · 87
ZFP191 is required by oligodendrocytes for CNS myelination
2010 · Shen Yi B. Howng, Robin L. Avila, et al. · Genes & Development · 83
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Two novel alleles of tottering with distinct Ca(v)2.1 calcium channel neuropathologies
2008 · T. Miki, T.A. Zwingman, et al. · Neuroscience · 56
Identification and Genetic Mapping of a New Polycystic Kidney Disease on Mouse Chromosome 8
1997 · Poornima M. Janaswami, Edward H. Birkenmeier, et al. · Genomics · 53
Loss of Clcc1 Results in ER Stress, Misfolded Protein Accumulation, and Neurodegeneration
2015 · Yichang Jia, Thomas J. Jucius, et al. · Journal of Neuroscience · 52
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A mouse Col4a4 mutation causing Alport glomerulosclerosis with abnormal collagen α3α4α5(IV) trimers
2014 · Ron Korstanje, Christina R. Caputo, et al. · Kidney International · 51
Neuromuscular degeneration (nmd): a mutation on mouse Chromosome 19 that causes motor neuron degeneration
1995 · S. A. Cook, K. R. Johnson, et al. · Mammalian Genome · 50
A Mouse Model for Meckel Syndrome Type 3
2009 · Susan A. Cook, Gayle B. Collin, et al. · Journal of the American Society of Nephrology · 49
Megencephaly: a new mouse mutation on chromosome 6 that causes hypertrophy of the brain
1996 · L. Rae Donahue, S. A. Cook, et al. · Mammalian Genome · 39
Meckelin Is Necessary for Photoreceptor Intraciliary Transport and Outer Segment Morphogenesis
2012 · Gayle B. Collin, Jungyeon Won, et al. · Investigative Ophthalmology & Visual Science · 37
Identification and genetic mapping of 151 dispersed members of 16 ribosomal protein multigene families in the mouse
1994 · K. R. Johnson, S. A. Cook, et al. · Mammalian Genome · 31
Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5
2003 · Kenneth R Johnson, Priscilla W Lane, et al. · Genomics · 29
Forebrain overgrowth (fog): A new mutation in the mouse affecting neural tube development
1997 · Belinda S. Harris, Thomas Franz, et al. · Teratology · 27
Cerebellar deficient folia (cdf): A new mutation on mouse Chromosome 6
1997 · Susan A. Cook, Roderick T. Bronson, et al. · Mammalian Genome · 24
The original shaker-with-syndactylism mutation ( sy ) is a contiguous gene deletion syndrome
1998 · Kenneth R. Johnson, Susan A. Cook, et al. · Mammalian Genome · 23
Balding: A New Mutation on Mouse Chromosome 18 Causing Hair Loss and Immunological Defects
1994 · M. T. Davisson, S. A. Cook, et al. · Journal of Heredity · 22
The Mouse Congenital Polycystic Kidney (cpk) Locus Maps within 1.3 cM of the Chromosome 12 Marker D12Nyu2
1994 · Elisabeth A. Simon, Susan Cook, et al. · Genomics · 18
A new allele of the lurcher gene, lurcher
1997 · Philip L. De Jager, Jian Zuo, et al. · Mammalian Genome · 14
Mouse paracentric inversion In(3)55Rk mutates the urate oxidase gene
2001 · S.A. Cook, E.C. Akeson, et al. · Cytogenetic and Genome Research · 7
Works count: 36
Citation count: 2,256
H-index: 22
I10-index: 24
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