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Cathy M. Tuck‐Müller

Observed names: C M Tuck-Muller, C Tuck-Muller, C Tuck‐Muller, C. M. Tuck-Muller, C. M. Tuck‐Muller, C.M. Tuck-Muller, CATHY M. TUCK-MULLER, CATHY TUCK-MULLER, Cathy M Tuck-Muller, Cathy M. Tuck-Miller, Cathy M. Tuck-Muller, Cathy M. Tuck‐Muller, Cathy Tuck-Muller, Tuck-Muller, C.M.
Observed institutions: Tulane University, University of Maryland, Baltimore, University of Maryland Medical System, Johns Hopkins University, University of Alabama, Johns Hopkins Medicine, University of South Alabama Medical Center, Kennedy Institute of Rheumatology, University of South Alabama
OpenAlex ID: A5111597142
DNA hypomethylation and unusual chromosome instability in cell lines fromICF syndrome patients
2000 · C.M. Tuck-Muller, A. Narayan, et al. · Cytogenetic and Genome Research · 209
Isodicentric Y chromosome: cytogenetic, molecular and clinical studies and review of the literature
1995 · Cathy M. Tuck-Muller, Harold Chen, et al. · Human Genetics · 159
Fertility and the cri du chat syndrome
1993 · José E. Martínez, Cathy M. Tuck‐Muller, et al. · Clinical Genetics · 84
Adrenal insufficiency in Smith-Lemli-Opitz syndrome
1999 · Hans C. Andersson, Johnette Frentz, et al. · American Journal of Medical Genetics · 66
Studies of mitotic and centromeric abnormalities in Roberts syndrome: Implications for a defect in the mitotic mechanism
1991 · Ethylin Wang Jabs, Cathy M. Tuck-Muller, et al. · Chromosoma · 58
Sexual discordance in monozygotic twins
1990 · Elizabeth J. Perlman, Gail Stetten, et al. · American Journal of Medical Genetics · 55
Interphase chromosomal abnormalities and mitotic missegregation of hypomethylated sequences in ICF syndrome cells
2005 · David Gisselsson, Chunbo Shao, et al. · Chromosoma · 52
Association of a new chromosomal deletion [del(1)(q32q42)] with diaphragmatic hernia: assignment of a human ferritin gene
1988 · Hagop Youssoufian, Philip Chance, et al. · Human Genetics · 51
Correction of sphingomyelinase deficiency in Niemann‐Pick type C fibroblasts by removal of lipoprotein fraction from culture media
1988 · G. H. Thomas, C. M. Tuck‐Muller, et al. · Journal of Inherited Metabolic Disease · 45
Molecular characterization of a ring chromosome 16 from a patient with bilateral cataracts
2001 · Weigong He, Cathy M. Tuck‐Muller, et al. · American Journal of Medical Genetics · 41
Analysis of marker or complex chromosomal rearrangements present in pre‐ and post‐natal karyotypes utilizing a combination of G‐banding, spectral karyotyping and fluorescence in situ hybridization
2003 · HHQ Heng, CJ Ye, et al. · Clinical Genetics · 39
Partial Monosomy 21, Diminished Activity of Superoxide Dismutase, and Pulmonary Oxygen Toxicity
1988 · Alice D. Ackerman, James C. Fackler, et al. · New England Journal of Medicine · 27
Autosomal Dominant Congenital Cataract Associated With Chromosomal Translocation [t(3;4)(p26.2;p15) ]
1987 · P. D. Reese, C. M. Tuck-Muller, et al. · Archives of Ophthalmology · 26
Prenatal detection of de novo duplication of the short arm of chromosome 18 confirmed by fluorescence in situ hybridization (FISH)
1998 · Shibo Li, Cathy M. Tuck-Muller, et al. · American Journal of Medical Genetics · 24
Confirmation of proximal 1q duplication using fluorescence in situ hybridization
1994 · Harold Chen, Christine J. Kusyk, et al. · American Journal of Medical Genetics · 24
Hypersensitivity to radiation-induced non-apoptotic and apoptotic death in cell lines from patients with the ICF chromosome instability syndrome
2000 · Ajita Narayan, Cathy Tuck-Muller, et al. · Mutation research. Fundamental and molecular mechanisms of mutagenesis · 23
Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization
1995 · Harold Chen, Cathy M. Tuck‐Muller, et al. · American Journal of Medical Genetics · 21
Cytogenetic survey in systemic sclerosis: correlation of aneuploidy with the presence of anticentromere antibodies
2008 · E.W. Jabs, C.M. Tuck-Muller, et al. · Cytogenetics and Cell Genetics · 20
Hyperlipidemia, insulin-dependent diabetes mellitus, and rapidly progressive diabetic retinopathy and nephropathy in Prader-Willi syndrome with del(15)(q11.2q13)
1997 · Reda Bassali, William H. Hoffman, et al. · American Journal of Medical Genetics · 20
A novel RSK2 (RPS6KA3) gene mutation associated with abnormal brain MRI findings in a family with Coffin–Lowry syndrome
2006 · Yueying Wang, Jose E. Martinez, et al. · American Journal of Medical Genetics Part A · 19
A rapid method for PCR amplification of DNA directly from cells fixed in Carnoy's fixative
1995 · Shibo Li, Cathy M. Tuck‐Muller, et al. · American Journal of Medical Genetics · 18
De novo dup (5p) in a patient with congenital hypoplasia of the adrenal gland
1995 · Harold Chen, William H. Hoffman, et al. · American Journal of Medical Genetics · 17
FGFR3 Gene Mutation (Gly380Arg) With Achondroplasia and i(21q) Down Syndrome
2000 · HAROLD CHEN, XINJIE MU, et al. · Southern Medical Journal · 16
Lysosomal chitobiase (CTB) and the G-protein γ 5 subunit (GNG5) genes co-localize to human chromosome 1p22
2008 · W. Ahmad, S. Li, et al. · Cytogenetics and Cell Genetics · 15
Chromosome studies in 10 patients with the rett syndrome
1986 · Jay W. Moore, Cathy M. Tuck-Muller, et al. · American Journal of Medical Genetics · 15
Works count: 46
Citation count: 1,269
H-index: 19
I10-index: 33
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