Avirachan T. Tharapel

Author

University of Tennessee Health Science Center

Also Known As

A T Tharapel, A Tharapel, A. T. THARAPEL, A. T. Tharapel, A. Tharapel, A.T. Tharapel, AVIRACHAN T. THARAPEL, Avirachan T Tharapel, Avirachan T. Tharapel, Avirachan Tharapel

Publications

2.6K

Citations

H-Index

Concepts

All Affiliations

University of Tennessee Health Science Center University of Tennessee at Knoxville Greenwood Genetic Center George Washington University Mission Health

About

Avirachan T. Tharapel is an author at University of Tennessee Health Science Center specializing in medicine, genetics, and cytogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	18	1K
2	Health Sciences	3	3	388
3	Natural Sciences	3	3	78
4	Biology	3	3	119
5	Biochemistry	1	1	15

Avirachan T. Tharapel

Publications

1.8K

Citations

H-Index

Page 1

	Year	Citations
Cytogenetic results from the U.S. collaborative study on CVS David H. Ledbetter, J. M. Zachary, Joe Leigh Simpson, Prenatal Diagnosis	1992	397
Prenatal diagnosis with fetal cells isolated from maternal blood by multiparameter flow cytometry James O. Price, Sherman Elias, Stephen S. Wachtel, American Journal of Obstetrics and Gynecology Fetal CellsHematologyGynecologyMaternal HealthCytometry	1991	237
Resorbed co‐twin as an explanation for discrepant chorionic villus results: Non‐mosaic 47,XX, +16 in villi (direct and culture) with normal (46,XX) amniotic fluid and neonatal blood Avirachan T. Tharapel, Sherman Elias, L.P. Shulman, Prenatal Diagnosis Amniotic FluidCytogeneticsGeneticsNon-mosaic Trisomy 16Fetal Medicine	1989	155
Phenotype-karyotype correlation in patients trisomic for various segments of chromosome 13. Sugandhi A. Tharapel, Raymond Lewandowski, Avirachan T. Tharapel, Journal of Medical Genetics CytogeneticsGeneticsGenetic EpidemiologyPathologyVarious Segments	1986	134
Deletion (X)(q26.1-->q28) in a proband and her mother: molecular characterization and phenotypic-karyotypic deductions. Avirachan T. Tharapel, Kathleen P. Anderson, Joe Leigh Simpson, PubMed	1993	116
A jumping Robertsonian translocation: a molecular and cytogenetic study Susan J. Gross, Avirachan T. Tharapel, Owen P. Phillips, Human Genetics CytogeneticsMedicineGeneticsGenetic MechanismMolecular Genetics	1996	101
Chromosome duplications and deletions and their mechanisms of origin Avirachan T. Tharapel, Ron C. Michaelis, Gopalrao V.N. Velagaleti, Cytogenetic and Genome Research	1999	82
Most Jacobsen syndrome deletion breakpoints occur distal to FRA11B Ron C. Michaelis, Gopalrao V.N. Velagaleti, Christopher T. Jones, American Journal of Medical Genetics CytogeneticsGeneticsPathologyMolecular GeneticsPaternal Origin	1998	79
A simple reproducible method for prometaphase chromosome analysis Joseph Rybak, Avirachan T. Tharapel, Sheldon Robinett, Human Genetics BiologyCytogeneticsGeneticsSimple Reproducible MethodChromosome Biology	1982	56
Apparently balanced <i>de novo</i> translocations in patients with abnormal phenotypes: Report of 6 cases Avirachan T. Tharapel, Robert L. Summitt, Robert S. Wkroy, Clinical Genetics	1977	56

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