Jillene Kogan - Concepedia

Author

Jillene Kogan

Cincinnati Children's Hospital Medical Center

Also Known As

J Kogan, Jillene Kogan, Jillene M. Kogan, Joshua Kogan

Publications

565

Citations

H-Index

Concepts

All Affiliations

Cincinnati Children's Hospital Medical Center University of Cincinnati University of Toronto

About

Jillene Kogan is an author at Cincinnati Children's Hospital Medical Center specializing in medicine, pathology, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	136
2	Molecular Genetics	2	2	29
3	Public Health	1	1	12
4	Biology	1	1	12
5	Microbiology	1	1	17

Jillene Kogan

Publications

312

Citations

H-Index

Page 1

	Year	Citations
Cerebellar and posterior fossa malformations in patients with autism‐associated chromosome 22q13 terminal deletion Kimberly A. Aldinger, Jillene Kogan, Virginia Kimonis, American Journal of Medical Genetics Part A	2012	73
Neurodevelopmental deficits in Pierson (microcoria‐congenital nephrosis) syndrome Elke Wühl, Jillene Kogan, Aleksandra Żurowska, American Journal of Medical Genetics Part A	2007	66
Pierson Syndrome: A Novel Cause of Congenital Nephrotic Syndrome René G. VanDeVoorde, David P. Witte, Jillene Kogan, PEDIATRICS Developmental AnomalyPierson SyndromeUrologyMendelian DisorderOphthalmology	2006	55
Skeletal demineralization and fractures caused by fetal magnesium toxicity Kathy E. Wedig, Jillene Kogan, Elizabeth K. Schorry, Journal of Perinatology Skeletal TraumaBone HealthSkeletal DemineralizationMedicineOsteoporosis	2006	40
Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, <scp>genotype–phenotype</scp> correlations and common mechanisms Maninder Kaur, Justin Blair, Batsal Devkota, American Journal of Medical Genetics Part A	2023	37
Interstitial deletion of 13q associated with polymicrogyria Jillene Kogan, John C. Egelhoff, Howard M. Saal American Journal of Medical Genetics Part A Molecular Diagnostic TechniquesDisease MechanismCytogeneticsGenetic DisorderGenetics	2008	17
High resolution SNP based microarray mapping of mosaic supernumerary marker chromosomes 13 and 17: Delineating novel loci for apraxia Jillene Kogan, Erin Miller, Stephanie M. Ware American Journal of Medical Genetics Part A GeneticsPathologyMolecular GeneticsGenomicsGenome Analysis	2009	12
A novel cytogenetic and molecular characterization of renal metanephric adenoma: Identification of partner genes involved in translocation t(9;15)(p24;q24) Aida Catic, Amina Kurtović-Kozarić, Sarah H. Johnson, Cancer Genetics UrologyGenitourinary CancerKidney ResearchRenal PathologyPathology	2017	12

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