Publications by authors named "Ferrin Wheeler"

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A multicenter analysis of individuals with a 47,XXY/46,XX karyotype.
Tiffany Guess, Ferrin C Wheeler, Ashwini Yenamandra, Samantha L P Schilit, Hannah S Anderson

Genet Med· October 2024

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Collaborative efforts to improve genetic testing in the neonatal intensive care unit.
Bryce A Schuler, Mackenzie Mosera, L Dupree Hatch, Angela Grochowsky, Ferrin Wheeler

J Perinatol· December 2023

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Distinct Patterns of Clonal Evolution Drive Myelodysplastic Syndrome Progression to Secondary Acute Myeloid Leukemia.
Tiffany Guess, Chad R Potts, Pawan Bhat, Justin A Cartailler, Austin Brooks, Ferrin C Wheeler

Blood Cancer Discov· July 2022

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Acquisition of aneuploidy drives mutant p53-associated gain-of-function phenotypes.
Lindsay N Redman-Rivera, Timothy M Shaver, Hailing Jin, Clayton B Marshall, Johanna M Schafer, Ferrin C Wheeler

Nat Commun· August 2021

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Clinical diagnosis of neurofibromatosis type I in multiple family members due to cosegregation of a unique balanced translocation with disruption of the NF1 locus: Testing considerations for accurate diagnosis.
Rebecca B Smith, Emily P Solem, Emma C Metz, Ferrin C Wheeler, John A Phillips

Am J Med Genet A· April 2021

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Institutional Training Opportunities for PhD Students in Laboratory Medicine: An Unmet Career Development Need?
Jennifer M Colby, Ferrin C Wheeler, Kimberly A Petrie, Kathleen L Gould, Jonathan E Schmitz

J Appl Lab Med· March 2020

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Preserved expressive language as a phenotypic determinant of Mosaic Angelman Syndrome.
Robert P Carson, Lynne Bird, Anna K Childers, Ferrin Wheeler, Jessica Duis

Mol Genet Genomic Med· September 2019

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A unique evolution of the kidney phenotype in a patient with autosomal recessive Alport syndrome.
Gisella Vischini, Meghan E Kapp, Ferrin C Wheeler, Laszlo Hopp, Agnes B Fogo

Hum Pathol· November 2018

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Limited Utility of Fluorescence In Situ Hybridization for Recurrent Abnormalities in Acute Myeloid Leukemia at Diagnosis and Follow-up.
Ferrin C Wheeler, Annette S Kim, Claudio A Mosse, Aaron C Shaver, Ashwini Yenamandra

Am J Clin Pathol· March 2018

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Bone Marrow-derived Cells Contribute to the Pathogenesis of Pulmonary Arterial Hypertension.
Ling Yan, Xinping Chen, Megha Talati, Bethany Womack Nunley, Santhi Gladson, Ferrin Wheeler

Am J Respir Crit Care Med· April 2016

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The duplication 17p13.3 phenotype: analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes.
Cynthia J Curry, Jill A Rosenfeld, Erica Grant, Karen W Gripp, Carol Anderson, Ferrin C Wheeler

Am J Med Genet A· August 2013

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Tnni3k modifies disease progression in murine models of cardiomyopathy.
Ferrin C Wheeler, Hao Tang, Odessa A Marks, Tracy N Hadnott, Pei-Lun Chu

PLoS Genet· September 2009

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A quantitative trait locus (LSq-1) on mouse chromosome 7 is linked to the absence of tissue loss after surgical hindlimb ischemia.
Ayotunde O Dokun, Sehoon Keum, Surovi Hazarika, Yongjun Li, Gregory M Lamonte, Ferrin Wheeler

Circulation· March 2008

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QTL mapping in a mouse model of cardiomyopathy reveals an ancestral modifier allele affecting heart function and survival.
Ferrin C Wheeler, Liliana Fernandez, Kerri M Carlson, Matthew J Wolf, Howard A Rockman

Mamm Genome· June 2005

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