Publications by authors named "Erika Carter"

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Somewhere to go: a position paper on addressing gaps in transition care for adults with childhood-onset rare diseases.
Laura L Tosi, Tracy S Hart, Gabriela Beug, Erika Carter, Eleanor M Perfetto

Orphanet J Rare Dis· October 2025

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Using syringe filtration after lab-scale adsorption processes potentially overestimates PFAS adsorption removal efficiency from non-conventional irrigation water.
Yu-Hua Zheng, Erika Carter, Shiqiang Zou, Clinton F Williams, Alex T Chow

J Environ Qual· January 2025

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"Osteogenesis Imperfecta Patients Wish Orthopedic Surgeons Had Better Strategies to Help with…"-Results of a Patient and Parent-Oriented Survey.
Jill Flanagan, Laura Tosi, Erika Carter, Tracy Hart, Jeanne Franzone

Children (Basel)· August 2023

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Extensor Mechanism Ruptures and Reruptures: Perioperative Opioid Management.
Lafi S Khalil, Toufic R Jildeh, Najib Ussef, Tahsin Rahman, Erika Carter

J Knee Surg· January 2022

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Naturalistic Topography Assessment in a Randomized Clinical Trial of Smoking Unfiltered Cigarettes: Challenges, Opportunities, and Recommendations.
Devan R Romero, Kim Pulvers, Erika Carter, Casey Barber, Nora Satybaldiyeva

Int J Environ Res Public Health· November 2021

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Effects of Unfiltered Cigarettes on Smoking Behavior and Toxicant Exposure: Protocol for a Randomized Crossover Clinical Trial.
Eyal Oren, Kim Pulvers, Devan R Romero, Casey Barber, Erika Carter

JMIR Res Protoc· December 2020

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Consequences of chromsome18q deletions.
Jannine D Cody, Courtney Sebold, Patricia Heard, Erika Carter, Bridgette Soileau

Am J Med Genet C Semin Med Genet· September 2015

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A review of 18p deletions.
Minire Hasi-Zogaj, Courtney Sebold, Patricia Heard, Erika Carter, Bridgette Soileau

Am J Med Genet C Semin Med Genet· September 2015

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Whole arm deletions of 18p: medical and developmental effects.
Courtney Sebold, Bridgette Soileau, Patricia Heard, Erika Carter, Louise O'Donnell

Am J Med Genet A· February 2015

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Ring 18 molecular assessment and clinical consequences.
Erika Carter, Patricia Heard, Minire Hasi, Bridgette Soileau, Courtney Sebold

Am J Med Genet A· January 2015

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Sensorineural hearing loss in people with deletions of 18q: hearing in 18q-.
Brian P Perry, Courtney Sebold, Minire Hasi, Patricia Heard, Erika Carter

Otol Neurotol· June 2014

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Establishing a reference group for distal 18q-: clinical description and molecular basis.
Jannine D Cody, Minire Hasi, Bridgette Soileau, Patricia Heard, Erika Carter

Hum Genet· February 2014

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Mood disorders in individuals with distal 18q deletions.
William B Daviss, Louise O'Donnell, Bridgette T Soileau, Patricia Heard, Erika Carter

Am J Med Genet B Neuropsychiatr Genet· December 2013

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Tetrasomy 18p: report of the molecular and clinical findings of 43 individuals.
Courtney Sebold, Elizabeth Roeder, Marsha Zimmerman, Bridgette Soileau, Patricia Heard, Erika Carter

Am J Med Genet A· September 2010

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Genetic determinants of autism in individuals with deletions of 18q.
Louise O'Donnell, Bridgette Soileau, Patricia Heard, Erika Carter, Courtney Sebold

Hum Genet· August 2010

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Psychiatric syndromes in individuals with chromosome 18 abnormalities.
Juan Zavala, Mercedes Ramirez, Rolando Medina, Patricia Heard, Erika Carter

Am J Med Genet B Neuropsychiatr Genet· April 2010

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A gene dosage map of Chromosome 18: a map with clinical utility.
Jannine D Cody, Erika M Carter, Courtney Sebold, Patricia L Heard, Daniel E Hale

Genet Med· November 2009

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Narrowing critical regions and determining penetrance for selected 18q- phenotypes.
Jannine D Cody, Patricia L Heard, Analisa C Crandall, Erika M Carter, John Li

Am J Med Genet A· July 2009

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High resolution genomic analysis of 18q- using oligo-microarray comparative genomic hybridization (aCGH).
Patricia L Heard, Erika M Carter, Analisa C Crandall, Courtney Sebold, Daniel E Hale

Am J Med Genet A· July 2009

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Molecular and clinical characterization of a recurrent cryptic unbalanced t(4q;18q) resulting in an 18q deletion and 4q duplication.
Craig Horbinski, Erika M Carter, Patricia L Heard, Malini Sathanoori, Jie Hu

Am J Med Genet A· November 2008

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Recurrent interstitial deletions of proximal 18q: a new syndrome involving expressive speech delay.
Jannine D Cody, Courtney Sebold, Amtul Malik, Patricia Heard, Erika Carter

Am J Med Genet A· June 2007

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