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Author/Creator Lebo, Matthew

1. Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centers. (August 2018)

Authors:
Sanghvi, Rashesh; Buhay, Christian; Powell, Bradford; Tsai, Ellen; Dorschner, Michael; Hong, Celine; Lebo, Matthew; Sasson, Ariella; Hanna, David; McGee, Sean; Bowling, Kevin; Cooper, Gregory; Gray, David; Lonigro, Robert; Dunford, Andrew; Brennan, Christine; Cibulskis, Carrie; Walker, Kimberly; ...
Journal:
Genetics in medicine
Issue:
Volume 20:Number 8(2018)
Page Start:
855
Record Type:
Journal Article
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4. Harmonizing variant classification for return of results in the All of Us Research Program. Issue 8 (28th December 2021)

Authors:
Harrison, Steven M.; Austin‐Tse, Christina A.; Kim, Serra; Lebo, Matthew; Leon, Annette; Murdock, David; Radhakrishnan, Aparna; Shirts, Brian H.; Steeves, Marcie; Venner, Eric; Gibbs, Richard A.; Jarvik, Gail P.; Rehm, Heidi L.
Other Names:
Laner Andreas guestEditor.; Maver Ales guestEditor.; den Dunnen Johan T. guestEditor.
Journal:
Human mutation
Issue:
Volume 43:Issue 8(2022)
Page Start:
1114
Record Type:
Journal Article
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5. A Comparison of Whole Genome Sequencing to Multigene Panel Testing in Hypertrophic Cardiomyopathy Patients. (October 2017)

Authors:
Cirino, Allison L.; Lakdawala, Neal K.; McDonough, Barbara; Conner, Lauren; Adler, Dale; Weinfeld, Mark; O'Gara, Patrick; Rehm, Heidi L.; Machini, Kalotina; Lebo, Matthew; Blout, Carrie; Green, Robert C.; MacRae, Calum A.; Seidman, Christine E.; Ho, Carolyn Y.
Journal:
Circulation
Issue:
Volume 10:Number 5(2017)
Page Start:
Record Type:
Journal Article
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6. Elective genomic testing: Practice resource of the National Society of Genetic Counselors. Issue 2 (4th January 2023)

Authors:
Blout Zawatsky, Carrie L.; Bick, David; Bier, Louise; Funke, Birgit; Lebo, Matthew; Lewis, Katie L.; Orlova, Ekaterina; Qian, Emily; Ryan, Lauren; Schwartz, Marci L. B.; Soper, Emily R.
Journal:
Journal of genetic counseling
Issue:
Volume 32:Issue 2(2023)
Page Start:
281
Record Type:
Journal Article
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7. Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease. Issue 5 (10th May 2015)

Authors:
Chopra, Sameer S.; Leshchiner, Ignaty; Duzkale, Hatice; McLaughlin, Heather; Giovanni, Monica; Zhang, Chengsheng; Stitziel, Nathan; Fingeroth, Joyce; Joyce, Robin M.; Lebo, Matthew; Rehm, Heidi; Vuzman, Dana; Maas, Richard; Sunyaev, Shamil R.; Murray, Michael; Cassa, Christopher A.
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 3:Issue 5(2015:Sep.)
Page Start:
413
Record Type:
Journal Article
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