Publications by authors named "Ina E Amarillo"

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Confirmation of Xp22.11 Duplication as a Germline Susceptibility Alteration in a Wilms Tumor Arising in Horseshoe Kidney.
Hui-Fang Zhou, Ina E Amarillo, Stacy Snyder, Jorge L Granadillo, Christopher J O'Conor

Fetal Pediatr Pathol· August 2022

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Identification of Small Regions of Overlap from Copy Number Variable Regions in Patients with Hypospadias.
Carter H Scott, Ina E Amarillo

Int J Mol Sci· April 2022

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Delineation of the 1q24.3 microdeletion syndrome provides further evidence for the potential role of non-coding RNAs in regulating the skeletal phenotype.
James L Shepherdson, Hongjun Zheng, Ina E Amarillo, Audrey McAlinden, Marwan Shinawi

Bone· January 2021

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Creating Affirmative and Inclusive Practices When Providing Genetic and Genomic Diagnostic and Research Services to Gender-Expansive and Transgender Patients.
J Graham Theisen, Ina E Amarillo

J Appl Lab Med· January 2021

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Mixed Donor Chimerism Following Simultaneous Pancreas-Kidney Transplant.
Armin Rashidi, Daniel C Brennan, Ina E Amarillo, Jason R Wellen, Amanda Cashen

Exp Clin Transplant· June 2018

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Risk association of congenital anomalies in patients with ambiguous genitalia: A 22-year single-center experience.
Jennifer M Heeley, Abby S Hollander, Paul F Austin, Diane F Merritt, Victoria G Wesevich, Ina E Amarillo

J Pediatr Urol· April 2018

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Small copy-number variations involving genes of the FGF pathway in differences in sex development.
Andrew Hagan, Ina E Amarillo

Hum Genome Var· April 2017

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Integrated small copy number variations and epigenome maps of disorders of sex development.
Ina E Amarillo, Isabelle Nievera, Andrew Hagan, Vishwa Huchthagowder, Jennifer Heeley

Hum Genome Var· June 2016

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De novo 9q gain in an infant with tetralogy of Fallot with absent pulmonary valve: Patient report and review of congenital heart disease in 9q duplication syndrome.
Ina E Amarillo, Shawn O'Connor, Caroline K Lee, Marcia Willing, Jennifer A Wambach

Am J Med Genet A· December 2015

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De novo single exon deletion of AUTS2 in a patient with speech and language disorder: a review of disrupted AUTS2 and further evidence for its role in neurodevelopmental disorders.
Ina E Amarillo, Wenhui Laura Li, Xinmin Li, Eric Vilain, Sibel Kantarci

Am J Med Genet A· April 2014

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Familial microdeletion of 17q24.3 upstream of SOX9 is associated with isolated Pierre Robin sequence due to position effect.
Ina E Amarillo, Katrina M Dipple, Fabiola Quintero-Rivera

Am J Med Genet A· May 2013

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