Robert F. Stratton - Concepedia

Author

Robert F. Stratton

The University of Texas Health Science Center at San Antonio

Also Known As

Kara Simpson, R. F. Stratton, R. Stratton, R.F. Stratton, Robert F Stratton, Robert F. Stratton, Robert Stratton, Stratton, Robert, Victoria Enciso

Publications

2.2K

Citations

H-Index

Concepts

All Affiliations

The University of Texas Health Science Center at San Antonio Baylor College of Medicine Wilford Hall Ambulatory Surgical Center United States Air Force Joint Base San Antonio

About

Robert F. Stratton is an author at The University of Texas Health Science Center at San Antonio specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	12	1.3K
2	Health Sciences	1	1	11
3	Public Health	1	1	90
4	Biology	1	1	32
5	Biostatistics	1	1	90

Robert F. Stratton

Publications

Citations

H-Index

Page 1

	Year	Citations
Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly Jeffrey E. Ming, Michelle E. Kaupas, Erich Roessler, Human Genetics Knockout MouseDevelopmental BiologyGeneticsMorphogenesisNeurogenetics	2002	243
Syndromes with lissencephaly. I: Millerdieker and Norman‐Roberts syndromes and isolated lissencephaly William B. Dobyns, Robert F. Stratton, Frank Greenberg American Journal of Medical Genetics Lissencephaly SequenceClinical DisordersDevelopmental AnomalyIsolated LissencephalyNeurological Disorder	1984	218
Miller-Dieker syndrome: Lissencephaly andmonosomy 17p William B. Dobyns, Robert F. Stratton, Julie T. Parke, The Journal of Pediatrics Miller-dieker SyndromeHistopathologyPathologyMedicineHuman Pathology	1983	186
Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18q Jannine D. Cody, Patricia D. Ghidoni, Barbara R. DuPont, American Journal of Medical Genetics	1999	132
Interstitial deletion of (17)(p11.2p11.2): Report of six additional patients with a new chromosome deletion syndrome Robert F. Stratton, William B. Dobyns, Frank Greenberg, American Journal of Medical Genetics	1986	130
New chromosomal syndrome: Miller-Dieker syndrome and monosomy 17p13 Robert F. Stratton, William B. Dobyns, Susan Airhart, Human Genetics New Chromosomal SyndromeCytogeneticsGenetic DisorderGeneticsHistopathology	1984	116
Xq–Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq- karyotype Bruce T. Lahn, Nancy Ma, W. Roy Breg, Nature Genetics Developmental BiologyMendelian DisorderRetarded MalesGenetic DisorderGenetics	1994	116
Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome Margot A. Cousin, Blake A. Creighton, Keith A. Breau, Nature Genetics Developmental AnomalyPathogenic Sptbn1 VariantsBrain DevelopmentMedicineGenetics	2021	98
Narrowing critical regions and determining penetrance for selected 18q‐ phenotypes Jannine D. Cody, Patricia Heard, AnaLisa C. Crandall, American Journal of Medical Genetics Part A Kidney Malformations RegionGeneticsImmunodeficienciesGenetic EpidemiologyMolecular Genetics	2009	90
Establishing a reference group for distal 18q-: clinical description and molecular basis Jannine D. Cody, Minire Hasi, Bridgette Soileau, Human Genetics Translational BiologyGenetic DisorderMedicineGeneticsGenetic Epidemiology	2013	65

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