Cathy M. Tuck‐Müller

Author

Also Known As

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-Muller

Publications

1.3K

Citations

H-Index

Concepts

All Affiliations

University of South Alabama Johns Hopkins University Johns Hopkins Medicine Tulane Medical Center Kennedy Krieger Institute

About

Cathy M. Tuck‐Müller is an author at University of South Alabama specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	15	456
2	Natural Sciences	3	3	33
3	Health Sciences	2	2	87
4	Public Health	2	2	93
5	Allergy	1	1	27

Cathy M. Tuck‐Müller

Publications

Citations

H-Index

Page 1

	Year	Citations
DNA hypomethylation and unusual chromosome instability in cell lines fromICF syndrome patients Cathy M. Tuck‐Müller, Alison R. H. Narayan, Fern Tsien, Cytogenetic and Genome Research	2000	209
Fertility and the cri du chat syndrome José E. Martínez, Cathy M. Tuck‐Müller, Duane Superneau, Clinical Genetics Family MedicineReproductive SciencesFertilityReproductive HealthGynecology	1993	83
Cancer susceptibility in ataxia-telangiectasia. Raymond D. A. Peterson, Jane D. Funkhouser, Cathy M. Tuck‐Müller, PubMed	1992	76
Adrenal insufficiency in Smith-Lemli-Opitz syndrome Hans C. Andersson, Johnette Frentz, Jos� E. Mart�nez, American Journal of Medical Genetics Clinical DisordersHypertonicityHypertensionSmith-lemli-opitz SyndromeUnrelated Patients	1999	66
Studies of mitotic and centromeric abnormalities in Roberts syndrome: Implications for a defect in the mitotic mechanism Ethylin Wang Jabs, Cathy M. Tuck‐Müller, Ronald Cusano, Chromosoma Developmental AnomalyCell DivisionGeneticsMitotic MechanismPathology	1991	59
Interphase chromosomal abnormalities and mitotic missegregation of hypomethylated sequences in ICF syndrome cells David Gisselsson, Chunbo Shao, Cathy M. Tuck‐Müller, Chromosoma ChromatinCell DivisionGenetic DisorderGeneticsMeiosis	2005	54
Association of a new chromosomal deletion [del(1)(q32q42)] with diaphragmatic hernia: assignment of a human ferritin gene Hagop Youssoufian, Philip Chance, Cathy M. Tuck‐Müller, Human Genetics Diaphragmatic HerniaHuman Ferritin GeneGeneticsPathologyMolecular Genetics	1988	51
Correction of sphingomyelinase deficiency in Niemann‐Pick type C fibroblasts by removal of lipoprotein fraction from culture media G. H. Thomas, Cathy M. Tuck‐Müller, Carol S. Miller, Journal of Inherited Metabolic Disease	1988	45
Molecular characterization of a ring chromosome 16 from a patient with bilateral cataracts Weigong He, Cathy M. Tuck‐Müller, José E. Martínez, American Journal of Medical Genetics	2001	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 C.J. Ye, Fengtang Yang, Salah Ebrahim, Clinical Genetics	2003	39

Page 1