Shivanand R. Patil - Concepedia

Author

Shivanand R. Patil

University of Iowa Hospitals and Clinics

Also Known As

S Patil, S R Patil, S. R. Patil, Shivanand Patil, Shivanand R Patil, Shivanand R. Patil

Publications

3.7K

Citations

H-Index

113

Concepts

All Affiliations

University of Iowa Hospitals and Clinics University of Iowa Howard Hughes Medical Institute University of Colorado Boulder Oregon Health & Science University

About

Shivanand R. Patil is an author at University of Iowa Hospitals and Clinics specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	20	30	2.1K
2	Public Health	4	4	220
3	Health Sciences	2	2	25
4	Natural Sciences	2	2	196
5	Education	1	1	14

Shivanand R. Patil

Publications

3.4K

Citations

H-Index

Page 1

	Year	Citations
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25 Darryl Nishimura, Ruth E. Swiderski, Wallace L.M. Alward, Nature Genetics Systems BiologyMolecular PhysiologySignaling PathwayCell SignalingGenetics	1998	469
Prognostic Significance of the European LeukemiaNet Standardized System for Reporting Cytogenetic and Molecular Alterations in Adults With Acute Myeloid Leukemia Krzysztof Mrózek, Guido Marcucci, Deedra Nicolet, Journal of Clinical Oncology	2012	405
Abnormality of chromosome 11 in patients withfeatures of Beckwith-Wiedemann syndrome Mary H. Waziri, Shivanand R. Patil, James W. Hanson, The Journal of Pediatrics Developmental AnomalyGenetic DisorderGeneticsCongenital DisordersPathology	1983	233
A Spectrum of FOXC1 Mutations Suggests Gene Dosage as a Mechanism for Developmental Defects of the Anterior Chamber of the Eye Darryl Nishimura, Charles Searby, Wallace L.M. Alward, The American Journal of Human Genetics Ocular DiseaseGene DosageDevelopmental BiologyOphthalmologyGenetic Disorder	2001	214
Identification of Each Human Chromosome with a Modified Giemsa Stain Shivanand R. Patil, Suzanne Merrick, Herbert A. Lubs Science Genetic TestingCytogeneticsGeneticsPathologyMolecular Biology	1971	182
Classification of qh regions in human chromosomes 1, 9, and 16 by C-banding Shivanand R. Patil, Herbert A. Lubs Human Genetics ChromatinHuman Chromosomes 1Cell DivisionGeneticsMolecular Biology	1977	125
Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlations Robert Wallerstein, Ming-Tsung Yu, Richard L. Neu, Prenatal Diagnosis CytogeneticsGeneticsGynecologyEpigeneticsEmbryology	2000	124
Deletions of different segments of the long arm of chromosome 4 Joyce A. Mitchell, Seymour Packman, William D. Loughman, American Journal of Medical Genetics	1981	94
Specific extra chromosomes occur in a modal number dependent pattern in pediatric acute lymphoblastic leukemia Nyla A. Heerema, Susana C. Raimondi, James R. Anderson, Genes Chromosomes and Cancer	2007	89
Characterization of a Novel Gene Disrupted by a Balanced Chromosomal Translocation t(2;19)(q11.2;q13.3) in a Family with Cleft Lip and Palate Koh-ichiro Yoshiura, Junichiro Machida, Sandra Daack‐Hirsch, Genomics Novel Gene DisruptedDevelopmental BiologyCytogeneticsGenetic DisorderGenetics	1998	69

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