Jannine D. Cody - Concepedia

Author

Jannine D. Cody

The University of Texas Health Science Center at San Antonio ORCID

Also Known As

Cody, J.D., Cody, Jannine D., J D Cody, J. Cody, J.D. Cody, Jannine Cody, Jannine D Cody, Jannine D. Cody, Jannine DeMars Cody, Wilson

Publications

2.6K

Citations

H-Index

Concepts

All Affiliations

The University of Texas Health Science Center at San Antonio Chromosome 18 Registry & Research Society Imaging Center Ear Medical Group University of Utah

About

Jannine D. Cody is an author at The University of Texas Health Science Center at San Antonio specializing in genetics, medicine, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	15	815
2	Public Health	2	2	110
3	Social Sciences	2	2	33
4	Natural Sciences	1	1	82
5	Behavioral Sciences	1	1	20

Jannine D. Cody

Publications

2.2K

Citations

H-Index

Page 1

	Year	Citations
Genetic Linkage of Paget Disease of the Bone to Chromosome 18q Jannine D. Cody, Frederick R. Singer, G. David Roodman, The American Journal of Human Genetics Bone DiseaseMendelian DisorderGenetic DisorderGeneticsGenetic Epidemiology	1997	154
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
Three Novel Mutations in SQSTM1 Identified in Familial Paget's Disease of Bone Teresa L. Johnson‐Pais, Julie H Wisdom, Korri Weldon, Journal of Bone and Mineral Research	2003	109
Molecular characterization of a patient with central nervous system dysmyelination and cryptic unbalanced translocation between chromosomes 4q and 18q Shelly Gunn, Xavier T. Reveles, David Viskochil, American Journal of Medical Genetics Part A	2003	109
Magnetic resonance imaging demonstrates incomplete myelination in 18q- syndrome Charles T. Gay, L. Jean Hardies, Ronald A. Rauch, American Journal of Medical Genetics	1997	93
High resolution genomic analysis of 18q− using oligo‐microarray comparative genomic hybridization (aCGH) Patricia Heard, Erika M. Carter, AnaLisa C. Crandall, American Journal of Medical Genetics Part A	2009	90
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
Tetrasomy 18p: Report of the molecular and clinical findings of 43 individuals Courtney Sebold, Elizabeth Roeder, Marsha Zimmerman, American Journal of Medical Genetics Part A	2010	86
Preferential loss of the paternal alleles in the 18q- syndrome Jannine D. Cody, Jessica F. Pierce, Zoran Brkanac, American Journal of Medical Genetics Genetic TestingGeneticsReproductive HealthGynecologyMolecular Genetics	1997	84
Large Inverted Duplications in the Human Genome Form via a Fold-Back Mechanism Karen Hermetz, Scott Newman, Karen N. Conneely, PLoS Genetics Inverted DuplicationGeneticsGenomic MechanismMolecular BiologyDisease Gene Identification	2014	82

Page 1