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Cancer Genetics|February 27, 2019
Multidisciplinary analysis of pediatric T-ALL: 9q34 gene fusionsPeter Papenhausen, Carla A Kelly, Zhenxi Zhang, et al.
Molecular Cytogenetics|July 21, 2021
Clinical significance and mechanisms associated with segmental UPDPeter R Papenhausen, Carla A Kelly, Samuel Harris, et al.
Personalized Medicine|May 26, 2018
Analysis of insurance preauthorization requests for BRCA1 and BRCA2 genetic testing: experience of the Humana Genetic Guidance ProgramAmisha Shah, Heather Harris, Trisha Brown, et al.
American Journal of Medical Genetics. Part A|April 30, 2025
Mosaicism for Genome Wide Homozygosity Identified as an Incidental Finding in Two Apparently Healthy Pregnant WomenGloria T Haskell, S Hussain Askree, Laura Kline, et al.
International Journal of Clinical and Experimental Pathology|January 19, 2013
Double-hit mantle cell lymphoma with MYC gene rearrangement or amplification: a report of four cases and review of the literatureReza Setoodeh, Stuart Schwartz, Peter Papenhausen, et al.
American Journal of Medical Genetics. Part A|December 8, 2005
Breakpoint mapping in a case of mosaicism with partial monosomy 9p23 --> pter and partial trisomy 1q41 --> qter suggests neo-telomere formation in stabilizing the deleted chromosomeLeslie D Kulikowski, Laurie A Christ, Sintia I Nogueira, et al.
Molecular Cytogenetics|June 10, 2023
Laboratory performance of genome-wide cfDNA for copy number variants as compared to prenatal microarrayErica Soster, John Tynan, Clare Gibbons, et al.
Prenatal Diagnosis|March 30, 2026
Cytogenetic and Microarray Analysis Follow-Up of PGT-A Mosaic and Sex Discrepant Embryos During Pregnancy: Absence of Confirmation and Follow-Up RecommendationsLaura A Kline, Vanessa A Nitibhon, Erica L Soster, et al.
American Journal of Medical Genetics. Part A|August 17, 2020
Deletion rescue resulting in segmental homozygosity: A mechanism underlying discordant NIPT resultsSamantha Caldwell, Katelynn Sagaser, Zoe Nelson, et al.
Nature Genetics|December 4, 2001
Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski-/- miceClemencia Colmenares, Heidi A Heilstedt, Lisa G Shaffer, et al.
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