Ina Amarillo - Concepedia

Author

Ina Amarillo

Washington University in St. Louis ORCID

Also Known As

I. Amarillo, I.E. Amarillo, Ina Amarillo, Ina E Amarillo, Ina E. Amarillo

Publications

420

Citations

H-Index

Concepts

All Affiliations

Washington University in St. Louis University of California, Los Angeles

About

Ina Amarillo is an author at Washington University in St. Louis specializing in medicine, genetics, and sex differences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	79
2	Social Sciences	1	1	16
3	Linguistics	1	1	17
4	Neurology	1	1	16
5	Neuroscience	1	1	16

Ina Amarillo

Publications

202

Citations

H-Index

Page 1

	Year	Citations
Familial Microdeletion of 17q24.3 Upstream of <scp><i>SOX</i></scp><i>9</i> Is Associated With Isolated Pierre Robin Sequence Due to Position Effect Ina Amarillo, Katrina M. Dipple, Fabiola Quintero‐Rivera American Journal of Medical Genetics Part A	2013	41
Risk association of congenital anomalies in patients with ambiguous genitalia: A 22-year single-center experience Jennifer Heeley, Abby Hollander, Paul F. Austin, Journal of Pediatric Urology Developmental AnomalyInfertilityPediatric GynecologyRisk AssociationCongenital Anomalies	2017	39
Integrated small copy number variations and epigenome maps of disorders of sex development Ina Amarillo, Nievera Isabelle, Andrew S. Hagan, Human Genome Variation Epigenetic ChangeGeneticsLinkage AnalysisSexual DisordersSmall Cnvs	2016	24
Words matter: The language of difference in human genetics Mildred K. Cho, Maria Laura Duque Lasio, Ina Amarillo, Genetics in Medicine Language EvolutionLinguisticsLanguage ScienceWords Matter	2022	17
Intragenic CNTN4 copy number variants associated with a spectrum of neurobehavioral phenotypes Stephanie Q. Zhang, Julie Fleischer, Hussam Al‐Kateb, European Journal of Medical Genetics Molecular NeuroscienceNeurobehavioral PhenotypesGeneticsPsychiatric GeneticsNeuroscience	2019	16
Acute graft-versus-host disease following lung transplantation in a patient with a novel <i>TERT</i> mutation Jonathan R. Brestoff, Alexandre Teixeira Vessoni, Kirsten Ann Brenner, Thorax	2018	15
Distal chromosome 16p11.2 duplications containing <i>SH2B1</i> in patients with scoliosis Brooke Sadler, Gabe Haller, Lilian Antunes, Journal of Medical Genetics	2019	15
Rare and <i>de novo</i> duplications containing <i>SHOX</i> in clubfoot Brooke Sadler, Gabe Haller, Lilian Antunes, Journal of Medical Genetics	2020	14
Pathogenic paternally inherited <scp><i>NLGN4X</i></scp> deletion in a female with autism spectrum disorder: Clinical, cytogenetic, and molecular characterization Nathan Kopp, Ina Amarillo, Julián A. Martínez-Agosto, American Journal of Medical Genetics Part A	2020	11
Creating Affirmative and Inclusive Practices When Providing Genetic and Genomic Diagnostic and Research Services to Gender-Expansive and Transgender Patients John Theisen, Ina Amarillo The Journal of Applied Laboratory Medicine	2020	10

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