Frederick V. Schaefer

Author

Also Known As

F Schaefer, F V Schaefer, F. Schaefer, F. V. Schaefer, F.V. Schaefer, FREDERICK V. SCHAEFER, Frederick Schaefer, Frederick V Schaefer, Frederick V. Schaefer

Publications

652

Citations

H-Index

Concepts

All Affiliations

Saint Francis University Children's Medical Center National Institute of Standards and Technology University of Tennessee at Knoxville Emory University

About

Frederick V. Schaefer is an author at Saint Francis University specializing in medicine, genetics, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	13	410
2	Cell Biology	5	5	133
3	Health Sciences	3	3	115
4	Public Health	3	3	98
5	Biochemistry	1	1	36

Frederick V. Schaefer

Publications

586

Citations

H-Index

Page 1

	Year	Citations
Novel mutation in the FGFR2 gene at the same codon as the Crouzon syndrome mutations in a severe Pfeiffer syndrome type 2 case Frederick V. Schaefer, Christine B. Anderson, Billur Can, American Journal of Medical Genetics	1998	83
Polymerase chain reaction microanalysis of tumors from stained histological slides. L Whetsell, G Maw, Nancy L. Nadon, PubMed Stained Histological SlidesTumoral PathologyMedicineSurgical PathologyHistopathology	1992	73
Genetic Factors for the Development of Alzheimer Disease in the Cherokee Indian Roger N. Rosenberg, Ralph Richter, R. Risser, Archives of Neurology Geriatric PsychiatryAgingGeneticsGenetic EpidemiologyGenetic Factors	1996	60
Pseudohypoparathyroidism Type 1a with Congenital Hypothyroidism Jordan E. Pinsker, William J. Rogers, Scott McLean, Journal of Pediatric Endocrinology and Metabolism Pseudohypoparathyroidism Type 1AGrowth HormoneGnas GeneGeneticsThyroid Disease	2006	40
The effect of iron on the synthesis and amount of ferritin in red blood cells during ontogeny. Frederick V. Schaefer, E C Theil Journal of Biological Chemistry Iron MetabolismIron StorageIron DeficiencyRedox BiologyOxidative Stress	1981	36
Rearrangement and junctional-site sequence analyses of T-cell receptor gamma genes in intestinal intraepithelial lymphocytes from murine athymic chimeras. Michael Whetsell, R. Lee Mosley, L Whetsell, Molecular and Cellular Biology Lymphocyte DevelopmentImmunologyGamma Gene RearrangementsImmunotherapyIntestinal Intraepithelial Lymphocytes	1991	34
Analyses of Polymorphism for UGT1*1 Exon 1 Promoter in Neonates with Pathologic and Prolonged Jaundice Ayfer Ülgenalp, Nuray Duman, Frederick V. Schaefer, Neonatology Tata Box PolymorphismGenetic TestingGeneticsHuman PolymorphismPathology	2003	32
Mutation analysis of the <i>SLC26A4</i> , <i>FOXI1</i> and <i>KCNJ10</i> genes in individuals with congenital hearing loss Lynn Pique, Marie‐Luise Brennan, C. Davidson, PeerJ	2014	31
Induction of abnormal development and differentiation in cultured mammary glands by cyclic adenine nucleotide and prostaglandins Frederick V. Schaefer, R. Philip Custer, Sam Sorof Nature Developmental BiologyMedicineMammary GlandMammary PhysiologyMorphogenesis	1980	26
Squamous metaplasia in human breast culture: induction by cyclic adenine nucleotide and prostaglandins, and influence of menstrual cycle. Frederick V. Schaefer, R. Philip Custer, Sam Sorof PubMed GynecologyCell ProliferationFemale Reproductive FunctionMenstrual CycleCyclic Adenine Nucleotide	1983	26

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