Publications by authors named "Yonit A Addissie"

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EGFR amplification and PI3K pathway mutations identify a subset of breast cancers that synergistically respond to EGFR and PI3K inhibition.
David J Wisniewski, Donna Voeller, Yonit A Addissie, Sachin Kumar Deshmukh, Sharon Wu

Oncogene· January 2026

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EGFR amplification and PI3K pathway mutations identify a subset of breast cancers that synergistically respond to EGFR and PI3K inhibition.
David J Wisniewski, Donna Voeller, Yonit A Addissie, Sachin Kumar Deshmukh, Sharon Wu

bioRxiv· September 2025

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Exome Sequencing and Congenital Heart Disease in Sub-Saharan Africa.
Ekanem N Ekure, Adebowale Adeyemo, Hanhan Liu, Ogochukwu Sokunbi, Nnenna Kalu, Yonit A Addissie

Circ Genom Precis Med· February 2021

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Identifying environmental risk factors and gene-environment interactions in holoprosencephaly.
Yonit A Addissie, Angela Troia, Zoe C Wong, Joshua L Everson, Beth A Kozel

Birth Defects Res· January 2021

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Rubinstein-Taybi syndrome in diverse populations.
Cedrik Tekendo-Ngongang, Babajide Owosela, Nicole Fleischer, Yonit A Addissie, Bryan Malonga

Am J Med Genet A· December 2020

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Prenatal exposure to pesticides and risk for holoprosencephaly: a case-control study.
Yonit A Addissie, Paul Kruszka, Angela Troia, Zoë C Wong, Joshua L Everson

Environ Health· June 2020

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Turner syndrome in diverse populations.
Paul Kruszka, Yonit A Addissie, Cedrik Tekendo-Ngongang, Kelly L Jones, Sarah K Savage

Am J Med Genet A· February 2020

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Circle of Willis anomalies in Turner syndrome: Absent A1 segment of the anterior cerebral artery.
Paul Kruszka, Ashley Buscetta, Maria T Acosta, Nicole Banks, Yonit A Addissie

Birth Defects Res· November 2019

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Tuberous sclerosis in a patient from Nigeria.
Ekanem N Ekure, Yonit A Addissie, Ogochukwu Jidechukwu Sokunbi, Paul Kruszka, Maximilian Muenke

Am J Med Genet A· August 2019

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Williams-Beuren syndrome in diverse populations.
Paul Kruszka, Antonio R Porras, Deise Helena de Souza, Angélica Moresco, Victoria Huckstadt, Yonit A Addissie

Am J Med Genet A· May 2018

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In-depth investigations of adolescents and adults with holoprosencephaly identify unique characteristics.
Karin Weiss, Paul Kruszka, Maria J Guillen Sacoto, Yonit A Addissie, Donald W Hadley

Genet Med· January 2018

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Loss of function in is associated with tetralogy of Fallot and septal defects.
Paul Kruszka, Pranoot Tanpaiboon, Katherine Neas, Kathleen Crosby, Seth I Berger, Yonit A Addissie

J Med Genet· December 2017

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Noonan syndrome in diverse populations.
Paul Kruszka, Antonio R Porras, Yonit A Addissie, Angélica Moresco, Sofia Medrano

Am J Med Genet A· September 2017

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22q11.2 deletion syndrome in diverse populations.
Paul Kruszka, Yonit A Addissie, Daniel E McGinn, Antonio R Porras, Elijah Biggs

Am J Med Genet A· April 2017

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Down syndrome in diverse populations.
Paul Kruszka, Antonio R Porras, Andrew K Sobering, Felicia A Ikolo, Samantha La Qua, Yonit A Addissie

Am J Med Genet A· January 2017

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Muenke syndrome: An international multicenter natural history study.
Paul Kruszka, Yonit A Addissie, Colin M P Yarnell, Donald W Hadley, Maria J Guillen Sacoto

Am J Med Genet A· April 2016

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Craniosynostosis and Noonan syndrome with KRAS mutations: Expanding the phenotype with a case report and review of the literature.
Yonit A Addissie, Udhaya Kotecha, Rachel A Hart, Ariel F Martinez, Paul Kruszka

Am J Med Genet A· November 2015

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Executive Function and Adaptive Behavior in Muenke Syndrome.
Colin M P Yarnell, Yonit A Addissie, Donald W Hadley, Maria J Guillen Sacoto, Nneamaka B Agochukwu

J Pediatr· August 2015

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